Job Title: Quality Systems Engineer / Quality EngineerJob DescriptionThe Quality Systems Engineer / Quality Engineer maintains and continuously improves the automotive Quality Management System to ensure compliance with IATF standards, customer-specific requirements, and applicable regulations. This role leads audits, drives corrective and preventive actions, supports new product launches, and partners closely with manufacturing and engineering teams to enhance process capability, product quality, and overall plant performance. It is an excellent opportunity for a quality professional who wants to own and improve an IATF-based quality system while building a clear path toward future quality leadership roles.Responsibilities<ul><li>Maintain, improve, and ensure compliance of the Quality Management System (QMS) with IATF requirements and customer-specific standards.</li><li>Lead, coordinate, and perform internal, process, product, and layered process audits, and effectively manage audit findings and follow-up actions.</li><li>Support customer, regulatory, and third-party certification audits, including preparation, on-site support, and post-audit activities.</li><li>Develop, implement, and monitor corrective and preventive actions (CAPA) to address nonconformities and prevent recurrence.</li><li>Investigate quality issues using structured problem-solving methodologies such as 8D, 5-Why, DMAIC, and Fishbone analysis.</li><li>Support Advanced Product Quality Planning (APQP) activities for new product launches, collaborating with cross-functional teams to ensure robust quality plans.</li><li>Prepare, review, and submit Production Part Approval Process (PPAP) documentation to obtain customer approval for production parts.</li><li>Facilitate the development, review, and ongoing maintenance of Process Failure Mode and Effects Analyses (PFMEA) to identify risks and implement preventive controls.</li><li>Conduct Measurement Systems Analysis (MSA) studies, including gauge evaluations and related studies, to validate measurement system capability and reliability.</li><li>Monitor and analyze quality metrics, Statistical Process Control (SPC) data, process capability, and key performance indicators (KPIs) to identify trends and drive improvement.</li><li>Ensure ongoing compliance with customer-specific requirements, automotive quality standards, and internal procedures.</li><li>Train employees on quality procedures, standards, tools, and best practices to strengthen the overall quality culture.</li><li>Partner with manufacturing, engineering, operations, suppliers, and customers to drive continuous improvement and resolve quality issues.</li><li>Lead or support continuous improvement and Six Sigma projects that reduce defects, improve efficiency, and deliver measurable quality improvements.</li><li>Support the development and maintenance of control plans to ensure consistent and controlled manufacturing processes.</li><li>Utilize ERP and MES quality system capabilities to support quality planning, data collection, and reporting where applicable.</li></ul>Essential Skills<ul><li>Bachelors degree and 2+ years of relevant quality experience, or Associates degree and 4+ years of related quality experience.</li><li>Hands-on experience supporting or managing an IATF-certified Quality Management System in an automotive or closely related environment.</li><li>Strong knowledge of automotive quality tools and methodologies, including APQP, PPAP, PFMEA, MSA, and SPC.</li><li>Proven experience planning, conducting, and leading internal, process, product, and system audits, and managing audit findings through closure.</li><li>Demonstrated ability to perform root cause analysis and implement effective corrective and preventive actions using methods such as 8D and 5-Why.</li><li>Experience with Measurement Systems Analysis (MSA), including gauge studies and calibration-related controls.</li><li>Practical understanding of automotive manufacturing processes, standards, and customer-specific requirements.</li><li>Ability to analyze quality data, monitor process capability, and interpret quality metrics and KPIs for decision-making.</li><li>Experience driving continuous improvement and applying Six Sigma or similar methodologies to reduce variation and improve quality.</li><li>Proficiency with Microsoft Excel and Word for data analysis, reporting, and documentation.</li><li>Strong verbal and written communication skills to interact effectively with cross-functional teams, suppliers, and customers.</li><li>Effective organizational and leadership abilities to coordinate audits, projects, and quality system initiatives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive manufacturing experience, particularly in high-volume production environments.</li><li>IATF or ISO 9001 Lead Auditor certification.</li><li>Six Sigma Green Belt or Six Sigma Black Belt certification.</li><li>Experience in Supplier Quality management, including supplier development and performance monitoring.</li><li>Experience in Customer Quality, including customer interface, complaint management, and customer-specific requirements.</li><li>Experience with Statistical Process Control (SPC), control plan development, and advanced statistical analysis.</li><li>Knowledge of Lean Manufacturing principles and continuous improvement methodologies.</li><li>Project management experience, including leading cross-functional quality or improvement projects.</li><li>Experience with ERP and MES quality systems for tracking, analyzing, and reporting quality data.</li><li>Ability to work collaboratively in cross-functional teams and influence others without direct authority.</li><li>Strong attention to detail and a systematic, process-oriented mindset.</li></ul>Work EnvironmentThis role offers a balanced mix of technical quality engineering work, hands-on manufacturing support, and strategic ownership of the quality management system. You will split your time between the plant floor and an office environment, engaging directly with production teams, engineering, leadership, suppliers, and customers. The position operates within an automotive manufacturing setting that emphasizes compliance, data-driven decision-making, and continuous improvement. You will regularly use tools such as ERP and MES systems, Microsoft Office applications, and standard quality engineering instruments and software. The work environment supports collaboration, visibility, and meaningful impact on plant performance, with clear opportunities to grow into future quality leadership roles.Job Type &amp; LocationThis is a Contract to Hire position based out of Versailles, KY.Pay and BenefitsThe pay range for this position is $38.00 - $41.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Versailles, KY.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Versailles,KY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Engineer

Job Title: Quality EngineerJob DescriptionWe are seeking a Quality Engineer for a fully onsite role in Newton, North Carolina. In this position, you ensure that products and processes meet established quality standards and customer expectations while directly interfacing with OEM customers. You develop and maintain quality control systems, monitor production performance, identify defects, and lead continuous improvement initiatives in a highly automated manufacturing environment. The role offers the opportunity to work with advanced automation, robotics, machine vision, and smart manufacturing technologies, driving meaningful improvements that directly impact production, quality, and operational performance.Responsibilities<ul><li>Develop, implement, and maintain quality assurance and quality control processes to ensure products meet internal and customer requirements.</li><li>Monitor production operations to verify compliance with quality standards, specifications, and regulatory requirements.</li><li>Perform detailed root cause analysis of defects and nonconformities, and implement corrective and preventive actions (CAPA) to prevent recurrence.</li><li>Conduct internal quality audits and support external audits, including customer, regulatory, and IATF audits.</li><li>Collaborate closely with engineering, manufacturing, supply chain, and operations teams to identify, investigate, and resolve quality issues.</li><li>Analyze quality data and metrics to drive improvement activities that achieve established KPIs such as scrap cost, non-right-first-time (NRFT), and first-time-through (FTT).</li><li>Lead continuous improvement and value-saving initiatives using methodologies such as Lean, Six Sigma, and Kaizen.</li><li>Review engineering designs, drawings, specifications, and design changes to identify potential quality risks and recommend mitigation strategies.</li><li>Ensure compliance with relevant regulatory and industry standards, including IATF 16949, ISO 9001, and other applicable ISO standards.</li><li>Train production and engineering staff on quality standards, procedures, tools, and best practices to strengthen the overall quality culture.</li><li>Lead automation-related quality projects from concept through implementation and optimization, ensuring robust quality controls are integrated into automated systems.</li><li>Drive quality-focused improvements in advanced automation, robotics, machine vision, and smart manufacturing technologies.</li><li>Support the creation and maintenance of quality documentation such as control plans, FMEAs, PPAPs, and inspection plans.</li><li>Interpret and apply GD&amp;T principles to ensure parts and assemblies meet dimensional and geometric requirements.</li><li>Contribute to continuous improvement initiatives that enhance production performance, reduce defects, and improve operational efficiency.</li><li>Perform all other duties related to quality engineering and continuous improvement as assigned.</li></ul>Essential Skills<ul><li>Bachelors degree in Engineering or a related technical field.</li><li>At least 2 years of experience in quality engineering or quality assurance within a production environment, preferably in automotive manufacturing.</li><li>Strong knowledge of quality engineering principles and practices, including quality assurance and quality control methodologies.</li><li>Hands-on experience with IATF 16949 and ISO quality standards, including ISO 9001.</li><li>Proficiency in corrective and preventive action (CAPA) processes and documentation.</li><li>Strong GD&amp;T skills with the ability to read and interpret engineering blueprints and technical drawings.</li><li>Solid understanding and practical use of core quality tools such as FMEA, SPC, control plans, and PPAP.</li><li>Experience applying root cause analysis techniques, including 5 Whys and Fishbone (Ishikawa) diagrams.</li><li>Ability to analyze quality data and production metrics to identify trends, issues, and improvement opportunities.</li><li>Proficiency in data analysis tools such as Excel, Minitab, or similar statistical software.</li><li>Excellent written and verbal communication skills for interacting with OEM customers and cross-functional teams.</li><li>Strong problem-solving and analytical skills, with the ability to tackle complex technical issues in a manufacturing environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in an automotive manufacturing environment or with OEM customers.</li><li>Shainin certification or experience with Shainin problem-solving methodologies.</li><li>Familiarity with advanced automation, robotics, machine vision, and smart manufacturing technologies.</li><li>Experience leading automation projects from concept through implementation and optimization.</li><li>Experience in process optimization, manufacturing engineering, or industrial engineering within a production environment.</li><li>Demonstrated ability to lead continuous improvement and value-saving initiatives using Lean, Six Sigma, or Kaizen.</li><li>Comfort working in cross-functional teams and collaborating with engineering, operations, maintenance, and supply chain.</li><li>Ability to take ownership of automation systems and quality processes that directly impact production performance.</li><li>Motivation to solve complex technical challenges and drive measurable improvements in quality and efficiency.</li><li>Strong organizational skills and attention to detail in managing quality documentation and audit activities.</li></ul>Work EnvironmentThis role is fully onsite in a fast-paced, highly automated manufacturing facility in Newton, North Carolina. You work directly on the production floor and in engineering spaces, balancing hands-on troubleshooting with project execution and continuous improvement initiatives. The environment features advanced automation, robotics, machine vision, and smart manufacturing technologies supporting the future of mobility. You collaborate closely with experienced engineering, operations, maintenance, and supply chain teams in a global manufacturing setting where engineering and quality contributions are recognized and valued. The culture emphasizes teamwork, continuous improvement, data-driven decision-making, and strong career growth opportunities. Typical hours align with standard manufacturing schedules, with flexibility as needed to support production and audit activities. Attire is appropriate for a manufacturing environment, including safety-conscious clothing and any required personal protective equipment.Job Type &amp; LocationThis is a Permanent position based out of Newton, NC.Pay and BenefitsThe pay range for this position is $85000.00 - $105000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Medical, dental, and vision insurance plans.
401(k) retirement savings plan with company-sponsored retirement benefits.
Paid time off and company holidays.
Life and disability insurance offerings.
Employee assistance and wellness programs.
Career development and advancement opportunities within a global manufacturing organization operating in numerous countries and facilities worldwide.Job Type &amp; LocationThis is a Permanent position based out of Newton, NC.Application DeadlineThis position is anticipated to close on Nov 5, 2026.Workplace TypeThis is a fully onsite position in Newton,NC.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer will initially spend 75% of their time on the floor to learn and understand prioritization needs. They will champion the quality team, ensuring they have necessary materials, removing obstacles, and assisting in the advancement of parts. The role involves responding to customer issues both internally and externally and participating in AS9100 audits. Over time, the position will transition to a 50/50 split between floor and desk work. Responsibilities include creating and analyzing SPC charts, conducting PFMEA's, developing control plans, performing gage R&amp;R, and preparing PPAPS. The Quality Engineer will serve as the Quality Manager's right-hand individual, with potential growth into an Assistant Quality Manager role, overseeing 9-10 quality technicians.Responsibilities<ul><li>Champion the quality team by ensuring material availability and removing project obstacles.</li><li>Respond to customer issues internally and externally.</li><li>Participate in AS9100 audits.</li><li>Create and analyze SPC charts, conduct PFMEA's, develop control plans, perform gage R&amp;R, and prepare PPAPS.</li><li>Serve as the right hand to the Quality Manager with potential growth to Assistant Quality Manager overseeing 9-10 quality technicians.</li></ul>Essential Skills<ul><li>1 year of experience as a Quality Engineer or an engineering degree.</li><li>Knowledge of AS9100 and audit processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with quality system standards.</li><li>Prior audit experience.</li></ul>Work EnvironmentThe position operates on a schedule of four 10-hour days, Monday through Thursday, from 6:00 AM to 4:30 PM with a 30-minute lunch break. Due to a heavy workload, availability for work on Fridays is also required, totaling 40-50 hours per week. The company offers a family-like environment with 60 employees, employee stock ownership, and good benefits including a 401k retirement plan. Employees receive two weeks of vacation. The company is growing and offers access to Udemy after six months for aerospace experience.Job Type &amp; LocationThis is a Contract to Hire position based out of Ithaca, MI.Pay and BenefitsThe pay range for this position is $28.85 - $36.05/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Ithaca, MI.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Ithaca,MI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer plays a key role in ensuring that automotive interior components, specifically center consoles made from plastics and metal, meet stringent customer and industry quality standards. This position serves as the primary quality liaison to customers, overseeing qualification of new parts, maintaining compliance with automotive quality standards, and driving continuous improvement through data-driven analysis and robust documentation.Responsibilities<ul><li>Represent the manufacturing facility to designated automotive customers as the primary quality contact, building strong, professional relationships.</li><li>Ensure all delivered parts meet customer specifications and are free from defects through rigorous quality control and validation processes.</li><li>Lead and manage the Production Part Approval Process (PPAP) documentation to qualify new parts for customers, ensuring all required records are complete, accurate, and submitted on time.</li><li>Apply Advanced Product Quality Planning (APQP) methodologies to support the launch of new products and changes to existing products.</li><li>Implement and maintain Statistical Process Control (SPC) methods to monitor production processes, analyze trends, and take action to maintain process stability and capability.</li><li>Conduct root cause analysis and root cause failure analysis for nonconformances, customer complaints, and internal quality issues, and develop effective corrective action plans.</li><li>Drive corrective action activities, ensuring containment, root cause identification, implementation of long-term solutions, and verification of effectiveness.</li><li>Prepare, maintain, and organize quality documentation, including control plans, inspection records, reports, and customer-required quality documents.</li><li>Develop and deliver clear, data-driven reports and presentations to internal teams and customers, explaining quality performance, issues, and improvement plans.</li><li>Collaborate with supplier quality and production teams to resolve supplier-related quality concerns and improve incoming material quality.</li><li>Support ongoing compliance with ISO 9001 and TS 16949 (IATF 16949) automotive quality management system requirements.</li><li>Participate in continuous improvement initiatives to enhance product quality, process efficiency, and customer satisfaction within the automotive plastics and metal fabrication environment.</li></ul>Essential Skills<ul><li>Quality engineering experience within the automotive industry.</li><li>Strong knowledge of Statistical Process Control (SPC) and its application in a manufacturing environment.</li><li>Hands-on experience with Advanced Product Quality Planning (APQP).</li><li>Demonstrated expertise with the Production Part Approval Process (PPAP), including documentation and customer submission.</li><li>Practical experience developing and executing corrective action plans.</li><li>Proficiency in root cause analysis and root cause failure analysis methodologies.</li><li>Familiarity with ISO 9001 quality management systems.</li><li>Familiarity with TS 16949 / IATF 16949 automotive quality standards.</li><li>Ability to create, manage, and maintain detailed quality documentation.</li><li>Strong skills in reporting and analyzing quality data, with the ability to present findings clearly to internal stakeholders and customers.</li><li>Experience working in automotive manufacturing, preferably with plastics and metal fabrication processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree is preferred but not required.</li><li>Experience in supplier quality is beneficial.</li><li>Ability to collaborate effectively with cross-functional teams in manufacturing and engineering.</li><li>Strong communication and presentation skills for customer-facing interactions.</li><li>Detail-oriented mindset with a focus on accuracy and compliance in documentation.</li><li>Comfort working in a fast-paced, growing automotive manufacturing environment.</li></ul>Work EnvironmentThis role is based in an automotive plastics and metal manufacturing facility that produces center consoles for cars. The environment is typical of a modern manufacturing plant, with production equipment, fabrication processes, and quality inspection areas. The company operates as a strong, growing automotive manufacturer in the Tupelo area, offering opportunities to work with advanced manufacturing technologies and established automotive quality systems. Team members collaborate closely across production, engineering, and quality functions in a professional, safety-conscious setting.Job Type &amp; LocationThis is a Contract position based out of Shannon, MS.Pay and BenefitsThe pay range for this position is $38.00 - $50.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Shannon, MS.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Shannon,MS.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionThe Quality Engineering team is seeking a passionate and highly motivated Engineer to join their dynamic team. The primary responsibility of this role is to monitor, maintain, and improve Quality indicators from both our manufacturing shops and supply base. The successful candidate will support the Quality objective to provide the highest quality vehicle to the customers. Responsibilities<ul><li>Develop and manage Quality Standards related to Suppliers, In-House Manufacturing Shops, and Completed Vehicle.</li><li>Assure Change-point Management for Suppliers, In-House Manufacturing Shops, and Design.</li><li>Provide technical support and daily problem-solving for part and shop issues within the Manufacturing Shop.</li><li>Communicate, coordinate, and negotiate to solve complex problems with cross-functional teams.</li><li>Act as Quality Window Person to Design and provide Design Technical Support.</li><li>Develop technical procedures and produce engineering reports.</li><li>Manage field and warranty issues for the responsible area.</li></ul>Qualifications <ul><li>Bachelor of Science in Engineering.</li><li>Ability to work effectively in a team setting with strong communication skills.</li><li>Experience developing and reviewing technical documents such as drawings, reports, manuals, and technical specifications.</li><li>Ability to create presentations for diverse audiences.</li><li>Basic understanding of Problem-Solving Tools such as TBP, 8D, Fishbone, 4M, and 5 Why.</li><li>Basic understanding of Risk Analysis Tools such as PFMEA.</li><li>Basic understanding of automotive systems.</li><li>Manufacturing experience.</li><li>Automotive experience is a significant advantage.</li><li>Experience in Lean manufacturing, Root cause analysis, Process engineering, Mechanical engineering, Manufacturing processes, Continuous improvement, Assembly, and Electrical engineering.</li><li>Familiarity with the automotive industry and PPAP.</li><li>Knowledge of ISO 9001.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Holly Springs, MS.Pay and BenefitsThe pay range for this position is $40.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Holly Springs, MS.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Holly Springs,MS.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThis Quality Engineer role focuses on investigating customer-reported product and quality issues, identifying root causes, and driving effective corrective and preventive actions in a manufacturing environment. You will work closely with production and engineering teams, communicate directly with customers about quality concerns and resolutions, and ensure that products consistently meet dimensional and quality requirements. The position requires strong problem-solving skills, hands-on use of measurement tools, and the ability to manage multiple quality concerns simultaneously.Responsibilities<ul><li>Investigate customer-reported product and quality issues in a timely and thorough manner.</li><li>Review initial customer quality reports and gather all necessary data to support detailed investigations.</li><li>Perform structured root cause analysis and lead 8D problem-solving activities to identify underlying issues.</li><li>Develop, implement, and document corrective and preventive actions to address identified problems and prevent recurrence.</li><li>Partner closely with production, manufacturing, and engineering teams to resolve quality issues and improve processes.</li><li>Communicate directly with customers regarding quality concerns, investigation findings, and implemented resolutions.</li><li>Manage multiple customer quality concerns simultaneously while maintaining clear priorities and timelines.</li><li>Track nonconformances, corrective actions, and quality trends to identify recurring issues and opportunities for improvement.</li><li>Inspect products and evaluate dimensional and quality requirements using appropriate tools and methods.</li><li>Verify that corrective actions are effective, sustainable, and properly integrated into existing processes.</li><li>Read and interpret engineering drawings and blueprints to support investigations and product evaluations.</li><li>Collaborate cross-functionally to promote a culture of quality and continuous improvement within the organization.</li></ul>Essential Skills<ul><li>Minimum of 2 years of Quality Engineering or related manufacturing experience.</li><li>Strong root cause analysis skills with demonstrated experience in structured problem-solving.</li><li>Proficiency in 8D problem-solving methodologies for addressing product and process issues.</li><li>Experience investigating and resolving manufacturing or product quality issues.</li><li>Strong customer-facing communication skills, including the ability to explain technical findings clearly and professionally.</li><li>Ability to work effectively with production, manufacturing, and engineering teams in a cross-functional environment.</li><li>Ability to read and interpret engineering drawings and blueprints.</li><li>Familiarity with basic measurement tools such as calipers and micrometers.</li><li> in quality engineering, quality assurance, or supplier quality within a manufacturing setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive or high-volume manufacturing experience preferred, but not required.</li><li>Experience tracking nonconformances, corrective actions, and quality trends.</li><li>Exposure to supplier quality processes and collaboration with external partners.</li><li>Comfort working with structured problem-solving tools and documentation such as 8D reports.</li><li>Degree is not required; equivalent practical experience in quality or manufacturing is valued.</li></ul>Work EnvironmentThis role operates in a manufacturing environment where you will regularly collaborate with production, manufacturing, and engineering teams on the shop floor and in office settings. You will use basic measurement tools such as calipers and micrometers to inspect products and verify dimensional and quality requirements. The position involves managing multiple customer quality concerns at once, participating in cross-functional meetings, and engaging directly with customers to discuss quality issues and resolutions. The environment emphasizes continuous improvement, structured problem-solving, and clear communication across teams to maintain high product quality and customer satisfaction.Job Type &amp; LocationThis is a Contract to Hire position based out of Upper Sandusky, OH.Pay and BenefitsThe pay range for this position is $33.65 - $36.06/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Upper Sandusky, OH.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Upper Sandusky,OH.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Description
					A Quality Engineer II is responsible for investigating returned products and customer complaints to determine root cause, implement corrective and preventive actions, and ensure alignment with internal and external quality standards. This role combines hands-on failure analysis with broader quality engineering responsibilities, including supporting the Quality Management System (QMS), contributing to continuous improvement initiatives, and driving customer-focused quality outcomes. In addition, a Quality Engineer II may provide quality-related guidance during product development efforts and/or the establishment of quality systems. Success in this role includes but is not limited to identifying quality-related improvement opportunities for products and processes and ensuring adherence to internal and external quality standards. Quality Engineer II is the second level within the Quality Engineer career path.
										Skills
					failure analysis, RMA investigations, root cause analysis, electrical testing, electrical troubleshooting, mechanical product testing, CAPA, ISO 9001, schematics, Electrical engineering, CQE certification, ISO certifications, Salesforce, quality auditing
										Top Skills Details
					failure analysis,RMA investigations,root cause analysis,electrical testing,electrical troubleshooting,mechanical product testing,CAPA,ISO 9001,schematics,Electrical engineering
										Additional Skills &amp; Qualifications
					Bachelor's degree in the field of Engineering, Electrical, Industrial, etc.
3 (+) years of relevant professional level work experience preferred. 
Experience with root cause analysis methodologies (5 Whys, Fishbone, 8D/4D)
Experience with RMA processes or customer complaint investigation
Demonstrated ability successfully using electrical inspection and test equipment.
Knowledge of ISO 9001. 
Knowledge of Error Proofing and related techniques. 
Knowledge of Lean/Six Sigma. 
Demonstrated ability interpreting and effectively using engineering drawings, schematics, and technical documentation.
Computer proficiency, including Microsoft Office applications (Word, Excel, and PowerPoint). 
Demonstrated ability communicating and working effectively with others. 
Demonstrated ability to effectively work with data and apply data analysis techniques to solve quality-related problems.
Demonstrates a willingness to collaborate with others, build relationships, and involve others in decision making. 
Demonstrates the ability to deliver results by solving or supporting others in solving problems, prioritizing tasks and/or resources, and focusing on outcomes. 
Demonstrates self-awareness and the willingness to learn and grow, accept changes, and effectively adapt to changing work demands. 
Demonstrates the ability to drive customer value through knowledge of the business, putting effort into identifying customer needs, and delivering work to maximize the value for customers. 
Demonstrates a willingness to promote the value of improvement and innovation by staying ahead of trends, creating ideas and opportunities, and generating speed. 
Demonstrates a willingness to take ownership by making decisions, taking responsibility, and driving things forward.
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract to Hire position based out of Middletown, PA.Pay and BenefitsThe pay range for this position is $30.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Middletown, PA.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Middletown,PA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionWe are seeking a dedicated Quality Engineer to join our team. The successful candidate will be responsible for conducting supplier audits, supporting incoming inspections, and developing quality system improvements for critical suppliers. This role involves contributing to supply chain risk assessments, reviewing customer requirements, and determining inspection processes.Responsibilities<ul><li>Conduct supplier audits to qualify and evaluate new and existing suppliers.</li><li>Support incoming inspection and communicate with suppliers regarding SCARs.</li><li>Develop critical suppliers on quality system improvements.</li><li>Contribute to supply chain risk assessments and scorecards.</li><li>Review customer requirements and specifications related to vendor-supplied materials.</li><li>Determine inspection processes and device capabilities.</li><li>Work with various gauges, instruments, and inspection devices.</li><li>Collaborate with Process Engineering to develop data collection techniques.</li><li>Conduct First Article Inspections and review documentation with Engineering.</li><li>Assist in training individuals in inspection methods.</li><li>Review root causes and corrective actions in response to supplier issues.</li><li>Travel for vendor visits and audits.</li></ul>Essential Skills<ul><li>5+ years of quality engineering experience in manufacturing.</li><li>Experience working with customers or suppliers on quality issues and corrective actions.</li><li>Proficiency in inspection techniques, including FAI, inspection plans, and measuring tools.</li><li>Familiarity with SCAR, ISO 9001, AS9100, PPAP, SPC, and metal components.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in Mechanical, Industrial, Chemical, Electrical Engineering, or a related field.</li><li>Two years of related experience in a manufacturing environment.</li><li>Excellent communication skills.</li><li>Ability to manage multiple tasks and coordinate deadlines effectively.</li></ul>Work EnvironmentThis position is based at a manufacturing site. The facility is a smaller, approximately 75-person establishment, offering visibility and influence. The role involves direct impact on improving and strengthening a critical supplier base, supporting major aerospace, defense, missile, communications, and space programs. The company is experiencing significant growth, offering opportunities for professional development and advancement.Job Type &amp; LocationThis is a Permanent position based out of Southbridge, MA.Pay and BenefitsThe pay range for this position is $82000.00 - $112000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.401k
Medical
Dental 
Vision
Retention BonusJob Type &amp; LocationThis is a Permanent position based out of Southbridge, MA.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Southbridge,MA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality EngineerJob DescriptionThe Quality Engineer supports quality and compliance activities for new labeling processes and related manufacturing operations in a highly regulated, FDA-governed environment. This role focuses on investigations and root cause analysis, technical documentation aligned with design control requirements, and collaboration with cross-functional teams to ensure products and processes meet regulatory and quality standards throughout the product lifecycle.Responsibilities<ul><li>Support quality and compliance work tied to new labeling processes, including conducting investigations, performing root cause analysis, and working cross-functionally to identify, resolve, and prevent issues.</li><li>Create, update, and maintain technical documentation in alignment with FDA and design control requirements, including design history files (DHF), validation documentation, and quality records.</li><li>Contribute to quality planning activities and partner with manufacturing and engineering teams across the product lifecycle to ensure robust quality controls and continuous improvement.</li><li>Assist with risk management activities using tools such as Failure Modes and Effects Analysis (FMEA) and hazard analysis in accordance with ISO-related standards.</li><li>Support validation efforts for new and existing processes, helping to define requirements, execute validation activities, and document results in compliance with regulatory expectations.</li><li>Maintain and improve quality system procedures and documentation, ensuring they remain current, compliant, and effective in supporting operations.</li><li>Assist with internal and external audits and other compliance activities by preparing documentation, responding to findings, and supporting corrective and preventive actions.</li><li>Help drive change management by supporting documentation updates, coordinating approvals, and assisting with implementation of changes in a regulated manufacturing environment.</li><li>Collaborate with cross-functional stakeholders, including manufacturing, engineering, and quality teams, to promote a process-oriented, quality-focused culture.</li></ul>Essential Skills<ul><li>Bachelors degree in Biomedical Engineering, Mechanical Engineering, or a related technical field.</li><li>02 years of experience, including internships or co-op roles, in manufacturing, product development, or quality engineering within a regulated industry such as medical device or pharmaceutical.</li><li>Hands-on experience with root cause analysis methods and investigation writing, including the ability to structure clear, logical reports.</li><li>Strong technical writing skills for creating and maintaining quality and regulatory documentation.</li><li>Understanding of quality engineering principles and practices in a regulated environment.</li><li>Ability to work effectively in complex, highly regulated manufacturing settings and follow established processes and procedures.</li><li>Attention to detail and accuracy in documentation, analysis, and compliance-related activities.</li><li>Ability to collaborate cross-functionally and communicate clearly with engineering, manufacturing, and quality teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>2+ years of experience performing root cause analysis and technical writing within a bioscience-related industry such as medical devices, biotechnology, or pharmaceuticals.</li><li>Familiarity with FDA regulations and design control requirements, including documentation such as DHF, validation records, and quality system documentation.</li><li>Experience with risk management tools such as FMEA and hazard analysis, ideally aligned with ISO-related standards.</li><li>or coursework in biomedical engineering, mechanical engineering, or closely related disciplines with a focus on regulated product development.</li><li>Demonstrated process-oriented mindset and interest in continuous improvement within manufacturing and quality systems.</li></ul>Work EnvironmentThis role operates in an FDA-regulated manufacturing environment that emphasizes adherence to quality systems, documentation standards, and regulatory compliance. The position follows a Monday through Friday, first-shift schedule, typically from 7:00 a.m. to 3:30 p.m., providing a structured workday within a production and engineering setting. The environment involves close collaboration with manufacturing and engineering teams, use of standard office and production documentation tools, and consistent engagement with established procedures and validation protocols.Job Type &amp; LocationThis is a Contract to Hire position based out of Vandalia, OH.Pay and BenefitsThe pay range for this position is $70000.00 - $80000.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Vandalia, OH.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Vandalia,OH.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer will play a crucial role in overseeing and maintaining the Quality Systems, as well as conducting both internal and external audits including NADCAP, AS9100, and ISO9001. This position involves generating and implementing procedures, interpreting blueprints, and managing root cause corrective actions. The role requires interaction with internal employees, customers, and suppliers to ensure quality is built into the product.Responsibilities<ul><li>Lead and participate in cross-functional teams to initiate quality improvement ideas within key operating departments.</li><li>Develop and improve processes and procedures, providing tactical support for production and inspection.</li><li>Promote continuous improvement activities and lead related projects.</li><li>Conduct root cause and failure analysis for products and related processes, recommending corrective and preventive actions.</li><li>Support product monitoring by establishing procedures, troubleshooting processes and equipment issues, training personnel, and addressing quality concerns.</li><li>Function as the lead internal auditor, establishing audit schedules as required.</li><li>Manage multiple projects concurrently.</li><li>Represent the company with external auditors such as ISO and NADCAP, as necessary.</li><li>Assist in maintaining compliance with ISO and AS 9100 standards.</li><li>Perform inspections as required to support the quality function.</li><li>Maintain the quality manual and related work instructions as needed.</li><li>Assist in implementing and maintaining Statistical Process Control (SPC).</li></ul>Essential Skills<ul><li>3+ years of Quality Engineering experience.</li><li>Experience with Root Cause Corrective Action.</li><li>Experience interacting with customers and suppliers.</li><li>Ability to read blueprints and schematics.</li><li>Experience in Aerospace or Automotive industries.</li></ul>Additional Skills &amp; Qualifications<ul><li>Proactive approach to problem-solving.</li><li>Familiarity with AS9100 and ISO9001 standards.</li><li>Experience with PPAP and APQP processes.</li></ul>Work EnvironmentThe Quality Engineer will report to the Quality Manager and will be involved in customer audits as well as compliance with AS-9100 and other regulatory bodies. The role requires active participation in internal quality program execution and process improvement. Collaboration with various groups to facilitate improvements is essential. The company is experiencing significant growth and offers opportunities for advancement, with strong financial backing and a supportive work environment. Employees can benefit from a 4% bonus based on attendance and goal attainment, along with a 401K match up to 4% after a vesting period.Job Type &amp; LocationThis is a Contract to Hire position based out of PHOENIX, AZ.Pay and BenefitsThe pay range for this position is $43.27 - $55.29/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of PHOENIX, AZ.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in PHOENIX,AZ.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2>Overview</h2>As a Quality Engineer, you will play a critical role in new product introduction, process validation, and manufacturing transfer activities, partnering with engineering, operations, suppliers, and customers to bring products from development into commercial production.<h2>Responsibilities</h2><ul><li>Represent Quality on cross-functional product development teams.</li><li>Support design transfer and product commercialization activities.</li><li>Review and approve specifications, validation protocols, engineering changes, and quality documentation.</li><li>Lead or support IQ/OQ/PQ validation activities and process qualification efforts.</li><li>Facilitate manufacturing transfers between sites, suppliers, and customers.</li><li>Drive risk management activities including FMEAs and Control Plans.</li><li>Partner with manufacturing and engineering teams to improve process capability and manufacturing readiness.</li><li>Support supplier qualification, quality investigations, and continuous improvement initiatives.</li><li>Ensure compliance with FDA regulations, quality systems, and applicable industry standards.</li></ul><h2>Qualifications</h2><ul><li>Bachelor's degree in Engineering or related technical discipline.</li><li>5+ years of Quality Engineering experience within medical device or regulated manufacturing environments.</li><li>Experience with new product introduction, design transfer, process validation, and manufacturing transfers.</li><li>Strong knowledge of FDA regulations, risk management, CAPA, SPC, FMEA, and root cause analysis tools.</li><li>Proficiency with Minitab, JMP, or similar statistical software.</li><li>Excellent communication, analytical, and project management skills.</li></ul><h2>Preferred Qualifications</h2><ul><li>Medical device CDMO or contract manufacturing experience.</li><li>CQE, Lean Six Sigma, or related quality certifications.</li><li>Knowledge of cleanroom operations, sterilization processes, and eQMS platforms.</li><li>Experience with DOE, measurement system analysis, and process capability studies.</li></ul><h2>Work Environment</h2>On-site role within a manufacturing and engineering environment. Occasional travel may be required to customer, supplier, or company locations. Exposure to production and plating areas requires adherence to safety and quality procedures.Job Type &amp; LocationThis is a Permanent position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $95000.00 - $120000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.PTO, 401K match, and 10 Paid HolidaysJob Type &amp; LocationThis is a Permanent position based out of Minneapolis, MN.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Minneapolis,MN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Engineer Medical Device ManufacturingJob DescriptionThis Quality Engineer role offers the opportunity to support a medical device manufacturing environment by driving continuous improvement and ensuring strict compliance with regulatory requirements. You will work closely with cross-functional teams to maintain robust quality systems, support manufacturing operations, and enhance product reliability through data-driven decision-making and proactive quality initiatives.Responsibilities<ul><li>Support and maintain standard quality manufacturing practices in compliance with FDA regulations and applicable quality standards.</li><li>Assist in the development, implementation, and continuous improvement of quality systems, procedures, and documentation.</li><li>Participate in root cause analysis activities and lead or support corrective and preventive action (CAPA) processes to address nonconformances and recurring issues.</li><li>Collaborate with cross-functional teams on quality-related projects, including process validation, risk management, and new or existing product development initiatives.</li><li>Conduct internal quality audits to verify compliance with internal procedures and regulatory requirements, and support external regulatory inspections as needed.</li><li>Analyze quality data and metrics, such as defect trends and process capability, to identify opportunities for improvement and drive continuous improvement projects.</li><li>Review and approve manufacturing and quality documentation, including batch records, change documentation, and other controlled records.</li><li>Apply quality engineering tools such as FMEA, SPC, and structured root cause analysis to improve process capability, reduce variation, and enhance product reliability.</li><li>Support manufacturing process improvements on the shop floor, working closely with production teams to resolve quality issues and optimize processes.</li><li>Manage and support quality-related projects, ensuring deliverables are completed on time and effectively communicated to stakeholders.</li><li>Interface with clients and external stakeholders on quality matters, providing clear, professional communication and technical support when required.</li></ul>Essential Skills<ul><li>35 years of experience in a quality engineering role within a regulated manufacturing environment, preferably in medical device manufacturing.</li><li>Working knowledge of FDA Quality System Regulation (QSR) and risk management principles applicable to medical devices or other regulated products.</li><li>Strong analytical and problem-solving skills, with demonstrated experience using structured root cause analysis methods.</li><li>Proficiency with quality engineering tools such as Failure Modes and Effects Analysis (FMEA) and Statistical Process Control (SPC).</li><li>Experience supporting or conducting internal audits in a manufacturing or quality systems environment.</li><li>Hands-on experience with manufacturing processes and quality control in a production setting.</li><li>Ability to work effectively in cross-functional teams and collaborate with engineering, manufacturing, and quality personnel.</li><li>Strong verbal and written communication skills, including the ability to communicate clearly with client-facing stakeholders.</li><li>Ability to work approximately 4550 hours per week, as required by production and project demands.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in engineering, life sciences, or a related field preferred.</li><li>Candidates with 7+ years of relevant quality engineering experience may be considered in lieu of a degree.</li><li>Experience in medical device manufacturing, including familiarity with relevant standards such as ISO 9001, is strongly preferred.</li><li>Experience with Production Part Approval Process (PPAP) in a manufacturing environment.</li><li>Experience working with CNC-based manufacturing processes is beneficial.</li><li>Strong organizational skills and attention to detail, with the ability to manage multiple tasks and documentation requirements in a regulated environment.</li></ul>Work EnvironmentThe role is based in a manufacturing plant environment with extensive use of CNC machines and other production equipment. You will spend significant time on the shop floor, collaborating with production and engineering teams to monitor processes and address quality issues in real time. The position typically requires working 4550 hours per week to support production schedules, project timelines, and audit or inspection activities. The environment is fast-paced and project-driven, with full benefits offered and a strong focus on continuous improvement, regulatory compliance, and cross-functional teamwork.Job Type &amp; LocationThis is a Permanent position based out of Manchester, TN.Pay and BenefitsThe pay range for this position is $80000.00 - $85000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Health &amp; Wellness
Generous healthcare plan that rewards positive lifestyle choices
Air-conditioned, clean manufacturing spaces for comfort on the job
Supportive environment focused on employee health and safety
 Financial &amp; Retirement
Competitive pay structure
Retirement benefits (details not fully disclosed, but commonly include 401(k) plans)
 Time Off &amp; Work-Life Balance
Paid vacation and time off policies
Flexible attendance system (described as lenient by some employees)
Work-life balance rated moderately well by employees

 Career Development
Opportunities for internal advancement
On-the-job learning and training programs
Roles available across engineering, manufacturing, and quality assurance

 Company Culture
Family-run business with a culture of trust, fairness, and respect
Emphasis on doing right by associateswere in this together mentality
Positive reviews from employees who value the team atmosphere and leadership supportJob Type &amp; LocationThis is a Permanent position based out of Manchester, TN.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Manchester,TN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionAs a Quality Engineer, you will be responsible for reviewing new and revised manufacturing jobs to ensure material selection, heat treatment requirements, processing routes, and compliance with customer specifications. You will investigate metallurgical, quality, and heat-treatment issues, perform root cause analysis, and implement corrective actions for non-conforming materials, processes, and products. Additionally, you will manage third-party laboratory testing, including sample submissions, result tracking, technical report review, and the disposition of failed results. Your role will also involve verifying incoming material chemistry against certifications and specifications, supporting supplier quality initiatives, and driving corrective actions when needed. You will collaborate with Quality, Engineering, Production, heat treatment vendors, and steel suppliers to develop metallurgical programs, support new product launches, improve process capability, and drive continuous improvement using Lean, Six Sigma, and other quality methodologies.Responsibilities<ul><li>Review and validate material selection, heat treatment requirements, and processing routes for manufacturing jobs.</li><li>Investigate and resolve metallurgical, quality, and heat-treatment issues.</li><li>Perform root cause analysis and implement corrective actions for non-conforming materials, processes, and products.</li><li>Manage third-party laboratory testing and track results.</li><li>Verify incoming material chemistry against certifications and specifications.</li><li>Support supplier quality initiatives and drive corrective actions.</li><li>Collaborate with various teams to develop metallurgical programs and improve process capability.</li></ul>Essential Skills<ul><li>Bachelors degree in Materials Engineering, Engineering Physics, Chemistry, or a related field.</li><li>3-5 years of experience in a quality engineering role in a manufacturing setting.</li><li>Proficiency in statistical analysis tools and data analytics (Minitab, JMP, or equivalent).</li><li>Strong attention to detail and ability to identify minute surface defects.</li><li>Strong problem-solving and analytical skills.</li><li>Excellent verbal and written communication abilities.</li><li>Ability to work collaboratively in a team environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Direct heat treatment experience or metal background.</li><li>Experience with ISO 9001, AS9100, or regulated industry is a plus.</li><li>Experience in automotive, aerospace, or other highly regulated industries.</li><li>Familiarity with ERP and PLM systems.</li><li>Attention to detail and a proactive approach to quality improvement.</li><li>High level of initiative and ability to work in a fast-paced environment.</li><li>Familiarity with safety and environmental regulations.</li></ul>Work EnvironmentThe work environment is primarily in a forging setting, which involves spending about 40% of the time on the floor, depending on project needs. The environment can be hot and dirty, requiring adaptability. While the position is office-based, it requires engagement with the manufacturing floor.Job Type &amp; LocationThis is a Contract to Hire position based out of Portland, IN.Pay and BenefitsThe pay range for this position is $38.46 - $52.88/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Portland, IN.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Portland,IN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer reviews customer and program quality requirements and ensures they are fully identified, clearly understood, and effectively met through existing policies, procedures, and systems. When current capabilities do not meet customer expectations, this role leads the development and implementation of new processes and systems to achieve full compliance. The position focuses on onboarding new customers, supporting audits, driving data-driven process improvements, and enhancing the Quality Management System in a highly technical, automation-focused environment, particularly within aerospace or defense manufacturing.Responsibilities<ul><li>Review customer and program quality requirements and ensure alignment with existing policies, procedures, and systems.</li><li>Identify gaps between customer requirements and current capabilities and lead the development of new processes and systems to close those gaps.</li><li>Onboard new customers by mapping their quality requirements and performing detailed gap assessments against current capabilities.</li><li>Collaborate closely with the automation team to integrate new customer quality processes into automation systems.</li><li>Act as a project manager for customer and third-party audits, ensuring all pre-audit tasks are accurately completed and post-audit action items are clearly documented and tracked to closure.</li><li>Drive and implement data-driven process improvements based on quality specifications and customer flowdowns.</li><li>Develop and refine the Quality Management System to meet industry benchmarks and ensure seamless integration with automation tools.</li><li>Create comprehensive quality plans and protocols in collaboration with quality and manufacturing teams.</li><li>Serve as a product owner for quality-related automation tools, ensuring they meet customer-specific requirements, production system needs, and applicable industry standards.</li><li>Develop standards for customer-specific quality documentation, including process maps, control plans, and standard operating procedures.</li><li>Work with complex quality specifications and customer flowdowns to ensure consistent and compliant execution across operations.</li><li>Support inspection-related activities and quality-focused manufacturing processes, including adherence to AS9102 First Article Inspection requirements.</li></ul>Essential Skills<ul><li>Minimum of 5 years of experience in a quality engineering role, preferably in aerospace or defense manufacturing.</li><li>Hands-on experience in quality engineering, including quality assurance and quality control activities.</li><li>Experience conducting and supporting audits, including customer and third-party audits.</li><li>In-depth knowledge of AS9100 standards and experience managing customer audits and quality requirements (preferred).</li><li>Strong understanding of ISO 9001 quality management principles.</li><li>Awareness of lean principles and continuous improvement methodology.</li><li>Experience working with complex quality specifications, including customer flowdowns.</li><li>Strong understanding of manufacturing processes with a focus on quality-related tasks such as inspection processes.</li><li>Familiarity with AS9102 First Article Inspection requirements.</li><li>Ability to develop and maintain quality plans, process maps, control plans, and standard operating procedures.</li><li>Ability to manage projects and coordinate cross-functional activities related to audits and process improvements.</li><li>Capability to act as a product owner for quality-related automation tools and ensure alignment with customer and production needs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in aerospace or defense manufacturing environments.</li><li>Background in quality assurance within regulated industries.</li><li>Exposure to or experience with lean and continuous improvement projects.</li><li>Comfort working with advanced automation tools and systems in a production environment.</li><li>Strong communication and collaboration skills to work effectively with quality, manufacturing, and automation teams.</li><li>Ability to interpret and apply industry standards and customer-specific quality requirements.</li></ul>Work EnvironmentThe role operates in a manufacturing and engineering environment with a strong focus on aerospace and defense quality standards. The Quality Engineer works closely with automation teams, quality professionals, and manufacturing staff to integrate quality processes into advanced automation systems. The environment emphasizes structured quality management systems such as AS9100 and ISO 9001, as well as formal documentation including process maps, control plans, and standard operating procedures. Work typically involves participation in customer and third-party audits, engagement in continuous improvement activities, and regular interaction with complex customer quality specifications and flowdowns. The position requires a professional presence in production and office settings, with appropriate attire suited to both manufacturing floor and technical meeting environments.Job Type &amp; LocationThis is a Permanent position based out of Torrance, CA.Pay and BenefitsThe pay range for this position is $100000.00 - $180000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Medical, dental, vision, and life insurance plans for employees 401k

Relocation support may be provided for certain situations, based on business need.

Flexible vacation policy

EquityJob Type &amp; LocationThis is a Permanent position based out of Torrance, CA.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Torrance,CA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Systems Engineer / Quality EngineerJob DescriptionThe Quality Systems Engineer / Quality Engineer maintains and continuously improves the automotive Quality Management System to ensure compliance with IATF standards, customer-specific requirements, and applicable regulations. This role leads audits, drives corrective and preventive actions, supports new product launches, and partners closely with manufacturing and engineering teams to enhance process capability, product quality, and overall plant performance. It is an excellent opportunity for a quality professional who wants to own and improve an IATF-based quality system while building a clear path toward future quality leadership roles.Responsibilities<ul><li>Maintain, improve, and ensure compliance of the Quality Management System (QMS) with IATF requirements and customer-specific standards.</li><li>Lead, coordinate, and perform internal, process, product, and layered process audits, and effectively manage audit findings and follow-up actions.</li><li>Support customer, regulatory, and third-party certification audits, including preparation, on-site support, and post-audit activities.</li><li>Develop, implement, and monitor corrective and preventive actions (CAPA) to address nonconformities and prevent recurrence.</li><li>Investigate quality issues using structured problem-solving methodologies such as 8D, 5-Why, DMAIC, and Fishbone analysis.</li><li>Support Advanced Product Quality Planning (APQP) activities for new product launches, collaborating with cross-functional teams to ensure robust quality plans.</li><li>Prepare, review, and submit Production Part Approval Process (PPAP) documentation to obtain customer approval for production parts.</li><li>Facilitate the development, review, and ongoing maintenance of Process Failure Mode and Effects Analyses (PFMEA) to identify risks and implement preventive controls.</li><li>Conduct Measurement Systems Analysis (MSA) studies, including gauge evaluations and related studies, to validate measurement system capability and reliability.</li><li>Monitor and analyze quality metrics, Statistical Process Control (SPC) data, process capability, and key performance indicators (KPIs) to identify trends and drive improvement.</li><li>Ensure ongoing compliance with customer-specific requirements, automotive quality standards, and internal procedures.</li><li>Train employees on quality procedures, standards, tools, and best practices to strengthen the overall quality culture.</li><li>Partner with manufacturing, engineering, operations, suppliers, and customers to drive continuous improvement and resolve quality issues.</li><li>Lead or support continuous improvement and Six Sigma projects that reduce defects, improve efficiency, and deliver measurable quality improvements.</li><li>Support the development and maintenance of control plans to ensure consistent and controlled manufacturing processes.</li><li>Utilize ERP and MES quality system capabilities to support quality planning, data collection, and reporting where applicable.</li></ul>Essential Skills<ul><li>Bachelors degree and 2+ years of relevant quality experience, or Associates degree and 4+ years of related quality experience.</li><li>Hands-on experience supporting or managing an IATF-certified Quality Management System in an automotive or closely related environment.</li><li>Strong knowledge of automotive quality tools and methodologies, including APQP, PPAP, PFMEA, MSA, and SPC.</li><li>Proven experience planning, conducting, and leading internal, process, product, and system audits, and managing audit findings through closure.</li><li>Demonstrated ability to perform root cause analysis and implement effective corrective and preventive actions using methods such as 8D and 5-Why.</li><li>Experience with Measurement Systems Analysis (MSA), including gauge studies and calibration-related controls.</li><li>Practical understanding of automotive manufacturing processes, standards, and customer-specific requirements.</li><li>Ability to analyze quality data, monitor process capability, and interpret quality metrics and KPIs for decision-making.</li><li>Experience driving continuous improvement and applying Six Sigma or similar methodologies to reduce variation and improve quality.</li><li>Proficiency with Microsoft Excel and Word for data analysis, reporting, and documentation.</li><li>Strong verbal and written communication skills to interact effectively with cross-functional teams, suppliers, and customers.</li><li>Effective organizational and leadership abilities to coordinate audits, projects, and quality system initiatives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive manufacturing experience, particularly in high-volume production environments.</li><li>IATF or ISO 9001 Lead Auditor certification.</li><li>Six Sigma Green Belt or Six Sigma Black Belt certification.</li><li>Experience in Supplier Quality management, including supplier development and performance monitoring.</li><li>Experience in Customer Quality, including customer interface, complaint management, and customer-specific requirements.</li><li>Experience with Statistical Process Control (SPC), control plan development, and advanced statistical analysis.</li><li>Knowledge of Lean Manufacturing principles and continuous improvement methodologies.</li><li>Project management experience, including leading cross-functional quality or improvement projects.</li><li>Experience with ERP and MES quality systems for tracking, analyzing, and reporting quality data.</li><li>Ability to work collaboratively in cross-functional teams and influence others without direct authority.</li><li>Strong attention to detail and a systematic, process-oriented mindset.</li></ul>Work EnvironmentThis role offers a balanced mix of technical quality engineering work, hands-on manufacturing support, and strategic ownership of the quality management system. You will split your time between the plant floor and an office environment, engaging directly with production teams, engineering, leadership, suppliers, and customers. The position operates within an automotive manufacturing setting that emphasizes compliance, data-driven decision-making, and continuous improvement. You will regularly use tools such as ERP and MES systems, Microsoft Office applications, and standard quality engineering instruments and software. The work environment supports collaboration, visibility, and meaningful impact on plant performance, with clear opportunities to grow into future quality leadership roles.Job Type &amp; LocationThis is a Contract to Hire position based out of Versailles, KY.Pay and BenefitsThe pay range for this position is $38.00 - $41.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Versailles, KY.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Versailles,KY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer plays a key role in ensuring that medical device products and processes comply with FDA 21 CFR 820, ISO standards, and international medical device regulations. This position focuses on managing quality systems activities, including sterilization qualification, CAPA management, validation review, and maintaining documentation needed for audits. The role requires strong organizational skills, attention to detail, and the ability to drive quality improvements across the organization.Responsibilities<ul><li>Ensure compliance with FDA 21 CFR 820, Quality System Regulations (QSR), Good Manufacturing Practices (GMP), ISO standards, and international medical device regulations (including MDR) in assigned areas.</li><li>Understand and support sterilization qualification and ongoing maintenance activities as they relate to medical devices.</li><li>Manage the corrective and preventive action (CAPA) process from initial investigation through implementation and effectiveness checks.</li><li>Maintain Design History Files and Technical Files, ensuring documentation is complete, accurate, and ready for internal and external audits.</li><li>Organize and prioritize assigned tasks to ensure projects meet expectations, milestones, and timelines.</li><li>Create, deliver, and maintain department and company training related to quality systems, procedures, and regulatory requirements.</li><li>Review and approve verification and validation protocols and reports to ensure they meet regulatory and company standards.</li><li>Utilize quality tools such as Failure Modes and Effects Analysis (FMEA), Control Plans, and Process Flow diagrams to support risk management and process improvement.</li><li>Support and maintain the medical device Quality Management System (QMS), including ISO-related activities and documentation.</li><li>Collaborate with cross-functional teams to resolve quality issues and implement sustainable corrective actions.</li><li>Prepare for and participate in internal and external audits by providing required quality and regulatory documentation.</li></ul>Essential Skills<ul><li>Relevant quality engineering work experience in an ISO-regulated medical device environment.</li><li>Demonstrated experience reviewing verification and validation protocols and reports.</li><li>Proven ability to manage CAPA processes from investigation through effectiveness checks.</li><li>Experience supporting and maintaining medical device Quality Management System (QMS) activities.</li><li>Knowledge of FDA 21 CFR 820, QSR, GMP, ISO standards, and international medical device regulations (including MDR).</li><li>Understanding of sterilization qualification and maintenance for medical devices.</li><li>Proficiency with quality tools such as FMEA, Control Plans, and Process Flow diagrams.</li><li>Bachelors degree in Engineering or a related field of study.</li><li>Proficiency in Microsoft Excel, Word, and other common office software.</li><li>Strong verbal and written communication skills in English.</li><li>Ability to stand, sit, and work at a computer for normal periods.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working within a laid-back, collaborative, and team-oriented environment.</li><li>Ability to organize and prioritize multiple tasks to meet project deadlines.</li><li>Comfort collaborating across departments to support training and continuous improvement initiatives.</li><li>Strong attention to detail and commitment to maintaining accurate and audit-ready documentation.</li></ul>Work EnvironmentThis is a fully onsite position, Monday through Friday, typically from 8:00 a.m. to 5:00 p.m., with some flexibility in hours depending on employee needs. The company culture is laid-back and family-like, with a tight-knit group that values collaboration and open communication. Leadership maintains an open-door policy and fosters a welcoming environment. The team regularly engages in fun activities outside of work, promoting strong relationships and a positive atmosphere. Work is primarily performed in an office setting, involving regular standing or sitting and working at a computer for normal periods, with standard business-casual attire appropriate for a professional environment.Job Type &amp; LocationThis is a Contract to Hire position based out of Phillipsburg, NJ.Pay and BenefitsThe pay range for this position is $40.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Phillipsburg, NJ.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Phillipsburg,NJ.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer reviews customer and program quality requirements and ensures they are fully identified, clearly understood, and effectively met through existing policies, procedures, and systems. When current capabilities do not meet customer expectations, this role leads the development and implementation of new processes and systems to achieve full compliance. The position focuses on onboarding new customers, supporting audits, driving data-driven process improvements, and enhancing the Quality Management System in a highly technical, automation-focused environment, particularly within aerospace or defense manufacturing.Responsibilities<ul><li>Review customer and program quality requirements and ensure alignment with existing policies, procedures, and systems.</li><li>Identify gaps between customer requirements and current capabilities and lead the development of new processes and systems to close those gaps.</li><li>Onboard new customers by mapping their quality requirements and performing detailed gap assessments against current capabilities.</li><li>Collaborate closely with the automation team to integrate new customer quality processes into automation systems.</li><li>Act as a project manager for customer and third-party audits, ensuring all pre-audit tasks are accurately completed and post-audit action items are clearly documented and tracked to closure.</li><li>Drive and implement data-driven process improvements based on quality specifications and customer flowdowns.</li><li>Develop and refine the Quality Management System to meet industry benchmarks and ensure seamless integration with automation tools.</li><li>Create comprehensive quality plans and protocols in collaboration with quality and manufacturing teams.</li><li>Serve as a product owner for quality-related automation tools, ensuring they meet customer-specific requirements, production system needs, and applicable industry standards.</li><li>Develop standards for customer-specific quality documentation, including process maps, control plans, and standard operating procedures.</li><li>Work with complex quality specifications and customer flowdowns to ensure consistent and compliant execution across operations.</li><li>Support inspection-related activities and quality-focused manufacturing processes, including adherence to AS9102 First Article Inspection requirements.</li></ul>Essential Skills<ul><li>Minimum of 5 years of experience in a quality engineering role, preferably in aerospace or defense manufacturing.</li><li>Hands-on experience in quality engineering, including quality assurance and quality control activities.</li><li>Experience conducting and supporting audits, including customer and third-party audits.</li><li>In-depth knowledge of AS9100 standards and experience managing customer audits and quality requirements (preferred).</li><li>Strong understanding of ISO 9001 quality management principles.</li><li>Awareness of lean principles and continuous improvement methodology.</li><li>Experience working with complex quality specifications, including customer flowdowns.</li><li>Strong understanding of manufacturing processes with a focus on quality-related tasks such as inspection processes.</li><li>Familiarity with AS9102 First Article Inspection requirements.</li><li>Ability to develop and maintain quality plans, process maps, control plans, and standard operating procedures.</li><li>Ability to manage projects and coordinate cross-functional activities related to audits and process improvements.</li><li>Capability to act as a product owner for quality-related automation tools and ensure alignment with customer and production needs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in aerospace or defense manufacturing environments.</li><li>Background in quality assurance within regulated industries.</li><li>Exposure to or experience with lean and continuous improvement projects.</li><li>Comfort working with advanced automation tools and systems in a production environment.</li><li>Strong communication and collaboration skills to work effectively with quality, manufacturing, and automation teams.</li><li>Ability to interpret and apply industry standards and customer-specific quality requirements.</li></ul>Work EnvironmentThe role operates in a manufacturing and engineering environment with a strong focus on aerospace and defense quality standards. The Quality Engineer works closely with automation teams, quality professionals, and manufacturing staff to integrate quality processes into advanced automation systems. The environment emphasizes structured quality management systems such as AS9100 and ISO 9001, as well as formal documentation including process maps, control plans, and standard operating procedures. Work typically involves participation in customer and third-party audits, engagement in continuous improvement activities, and regular interaction with complex customer quality specifications and flowdowns. The position requires a professional presence in production and office settings, with appropriate attire suited to both manufacturing floor and technical meeting environments.Job Type &amp; LocationThis is a Permanent position based out of Torrance, CA.Pay and BenefitsThe pay range for this position is $100000.00 - $180000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Medical, dental, vision, and life insurance plans for employees 401k

Relocation support may be provided for certain situations, based on business need.

Flexible vacation policy

EquityJob Type &amp; LocationThis is a Permanent position based out of Torrance, CA.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Torrance,CA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Systems Engineer / Quality EngineerJob DescriptionThe Quality Systems Engineer / Quality Engineer maintains and continuously improves the automotive Quality Management System to ensure compliance with IATF standards, customer-specific requirements, and applicable regulations. This role leads audits, drives corrective and preventive actions, supports new product launches, and partners closely with manufacturing and engineering teams to enhance process capability, product quality, and overall plant performance. It is an excellent opportunity for a quality professional who wants to own and improve an IATF-based quality system while building a clear path toward future quality leadership roles.Responsibilities<ul><li>Maintain, improve, and ensure compliance of the Quality Management System (QMS) with IATF requirements and customer-specific standards.</li><li>Lead, coordinate, and perform internal, process, product, and layered process audits, and effectively manage audit findings and follow-up actions.</li><li>Support customer, regulatory, and third-party certification audits, including preparation, on-site support, and post-audit activities.</li><li>Develop, implement, and monitor corrective and preventive actions (CAPA) to address nonconformities and prevent recurrence.</li><li>Investigate quality issues using structured problem-solving methodologies such as 8D, 5-Why, DMAIC, and Fishbone analysis.</li><li>Support Advanced Product Quality Planning (APQP) activities for new product launches, collaborating with cross-functional teams to ensure robust quality plans.</li><li>Prepare, review, and submit Production Part Approval Process (PPAP) documentation to obtain customer approval for production parts.</li><li>Facilitate the development, review, and ongoing maintenance of Process Failure Mode and Effects Analyses (PFMEA) to identify risks and implement preventive controls.</li><li>Conduct Measurement Systems Analysis (MSA) studies, including gauge evaluations and related studies, to validate measurement system capability and reliability.</li><li>Monitor and analyze quality metrics, Statistical Process Control (SPC) data, process capability, and key performance indicators (KPIs) to identify trends and drive improvement.</li><li>Ensure ongoing compliance with customer-specific requirements, automotive quality standards, and internal procedures.</li><li>Train employees on quality procedures, standards, tools, and best practices to strengthen the overall quality culture.</li><li>Partner with manufacturing, engineering, operations, suppliers, and customers to drive continuous improvement and resolve quality issues.</li><li>Lead or support continuous improvement and Six Sigma projects that reduce defects, improve efficiency, and deliver measurable quality improvements.</li><li>Support the development and maintenance of control plans to ensure consistent and controlled manufacturing processes.</li><li>Utilize ERP and MES quality system capabilities to support quality planning, data collection, and reporting where applicable.</li></ul>Essential Skills<ul><li>Bachelors degree and 2+ years of relevant quality experience, or Associates degree and 4+ years of related quality experience.</li><li>Hands-on experience supporting or managing an IATF-certified Quality Management System in an automotive or closely related environment.</li><li>Strong knowledge of automotive quality tools and methodologies, including APQP, PPAP, PFMEA, MSA, and SPC.</li><li>Proven experience planning, conducting, and leading internal, process, product, and system audits, and managing audit findings through closure.</li><li>Demonstrated ability to perform root cause analysis and implement effective corrective and preventive actions using methods such as 8D and 5-Why.</li><li>Experience with Measurement Systems Analysis (MSA), including gauge studies and calibration-related controls.</li><li>Practical understanding of automotive manufacturing processes, standards, and customer-specific requirements.</li><li>Ability to analyze quality data, monitor process capability, and interpret quality metrics and KPIs for decision-making.</li><li>Experience driving continuous improvement and applying Six Sigma or similar methodologies to reduce variation and improve quality.</li><li>Proficiency with Microsoft Excel and Word for data analysis, reporting, and documentation.</li><li>Strong verbal and written communication skills to interact effectively with cross-functional teams, suppliers, and customers.</li><li>Effective organizational and leadership abilities to coordinate audits, projects, and quality system initiatives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive manufacturing experience, particularly in high-volume production environments.</li><li>IATF or ISO 9001 Lead Auditor certification.</li><li>Six Sigma Green Belt or Six Sigma Black Belt certification.</li><li>Experience in Supplier Quality management, including supplier development and performance monitoring.</li><li>Experience in Customer Quality, including customer interface, complaint management, and customer-specific requirements.</li><li>Experience with Statistical Process Control (SPC), control plan development, and advanced statistical analysis.</li><li>Knowledge of Lean Manufacturing principles and continuous improvement methodologies.</li><li>Project management experience, including leading cross-functional quality or improvement projects.</li><li>Experience with ERP and MES quality systems for tracking, analyzing, and reporting quality data.</li><li>Ability to work collaboratively in cross-functional teams and influence others without direct authority.</li><li>Strong attention to detail and a systematic, process-oriented mindset.</li></ul>Work EnvironmentThis role offers a balanced mix of technical quality engineering work, hands-on manufacturing support, and strategic ownership of the quality management system. You will split your time between the plant floor and an office environment, engaging directly with production teams, engineering, leadership, suppliers, and customers. The position operates within an automotive manufacturing setting that emphasizes compliance, data-driven decision-making, and continuous improvement. You will regularly use tools such as ERP and MES systems, Microsoft Office applications, and standard quality engineering instruments and software. The work environment supports collaboration, visibility, and meaningful impact on plant performance, with clear opportunities to grow into future quality leadership roles.Job Type &amp; LocationThis is a Contract to Hire position based out of Versailles, KY.Pay and BenefitsThe pay range for this position is $38.00 - $41.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Versailles, KY.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Versailles,KY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Engineer/ Hardware Failure Analysis EngineerLocation: Lexington, KY-- occasional travel (once per month) to additional sites located in Louisville and Cincinnati<h3>Description</h3><ul><li>Hands-on experience with hardware device handling, troubleshooting, and failure analysis.</li><li>Ability to diagnose, reproduce, and resolve hardware and system-level issues using appropriate diagnostic tools and methodologies.</li><li>Proven ability to manage multiple failure investigations, escalations, and yield improvement initiatives concurrently while driving root cause analysis and corrective actions.</li><li>Strong cross-functional collaboration skills with the ability to establish and maintain effective communication channels to support issue resolution.</li><li>Experience using ticketing and documentation systems such as JIRA or similar platforms.</li><li>Ability to coordinate and manage device shipments to external laboratories, vendors, and contract manufacturers.</li><li>Excellent written and verbal communication skills, with the ability to clearly present technical findings and failure analysis results to engineering teams and leadership.</li><li>Strong organizational and time management skills, capable of coordinating complex investigations across multiple stakeholders.</li><li>Exceptional analytical, troubleshooting, and problem-solving skills.</li></ul><h3>Preferred Qualifications</h3><ul><li>Experience supporting quality engineering programs within consumer electronics, hardware manufacturing, or a related industry.</li><li>Familiarity with failure analysis processes, device teardown procedures, and defect classification methodologies.</li><li>Experience reproducing hardware or system failures and validating corrective actions to improve product reliability.</li><li>Experience working in a warehouse, fulfillment center, reverse logistics, or similar operational environment.</li><li>Familiarity with large-format display handling, testing, and TV screening processes.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Lexington, KY.Pay and BenefitsThe pay range for this position is $45.00 - $90.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Lexington, KY.Application DeadlineThis position is anticipated to close on Nov 14, 2026.Workplace TypeThis is a fully onsite position in Lexington,KY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer will focus on the review, creation, and completion of First Article Inspection (FAI) documentation in accordance with AS9102 requirements. The role centers on documentation review and verification rather than hands-on product inspection. You will evaluate supplier-submitted FAIRs, prepare and review internal FAIRs, verify that all required product characteristics are properly measured and documented, and collaborate with suppliers and internal stakeholders to resolve discrepancies. The initial assignment is expected to last 3 to 6 months to address a backlog of approximately 100 to 150 full and partial FAIRs, with the potential to transition into a full-time Quality Engineer role supporting Quality Management System development and production growth.Responsibilities<ul><li>Review supplier First Article Inspection (FAI) packages for accuracy, completeness, and compliance with AS9102 requirements.</li><li>Create, review, and complete internal full and partial First Article Inspections (FAIs).</li><li>Verify that drawing characteristics, specifications, materials, and all applicable requirements are properly captured within FAI documentation.</li><li>Identify missing, incomplete, or inaccurate information within FAI packages and ensure issues are clearly documented.</li><li>Coordinate with suppliers to resolve documentation issues, measurement discrepancies, and noncompliant submissions.</li><li>Maintain organized, accurate, and traceable FAI records in alignment with Quality Management System expectations.</li><li>Prioritize and manage a high volume of FAIs to support production schedules and rapid product development activities.</li><li>Review and validate new and updated First Article Inspection Reports (FAIRs) in accordance with AS9102 and internal QMS requirements.</li><li>Collaborate with internal stakeholders to clarify technical requirements and ensure consistent application of quality standards.</li><li>Support continuous improvement of FAI documentation processes and practices within the quality function.</li></ul>Essential Skills<ul><li>Three or more years of experience in quality engineering, supplier quality, First Article Inspection, or a related aerospace manufacturing quality role.</li><li>Hands-on experience creating and reviewing First Article Inspection packages.</li><li>Working knowledge of AS9102 First Article Inspection requirements.</li><li>Experience operating within an AS9100 or similar regulated Quality Management System (QMS).</li><li>Ability to read and interpret engineering drawings, specifications, bills of material, and technical requirements.</li><li>Understanding of dimensional inspection principles and mechanical measurement methods.</li><li>Ability to verify inspection results produced using tools such as calipers, micrometers, and go/no-go gauges.</li><li>Strong documentation review and technical writing skills for preparing clear and compliant FAIRs.</li><li>Strong record-keeping skills to maintain accurate, traceable quality documentation.</li><li>Ability to identify discrepancies in inspection data and documentation and to resolve them effectively.</li><li>Effective communication skills to work with suppliers and internal stakeholders on quality and documentation issues.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in quality engineering within aerospace or avionics manufacturing environments.</li><li>Experience with First Article Inspection Reporting (FAIR) tools and processes.</li><li>Familiarity with structured Quality Management Systems and continuous improvement practices.</li><li>Ability to manage priorities and deadlines while handling a high volume of FAI documentation.</li><li>Strong attention to detail and a methodical approach to reviewing technical data.</li><li>Comfort working with rapidly evolving product designs and frequent engineering revisions.</li></ul>Work EnvironmentThe role supports a facility that designs and manufactures low-SWaP certified avionics, including transponders, identification friend or foe systems, and ACAS/DAA modules for military and commercial aircraft. Work takes place within a regulated environment operating under an AS9100-based Quality Management System with AS9102-compliant First Article Inspection processes. The position focuses primarily on office-based tasks involving detailed documentation review, interaction with digital quality records, and regular communication with suppliers and internal engineering and production teams. The assignment is structured around addressing a defined backlog of approximately 100 to 150 full and partial FAIRs generated by rapid product development and engineering changes, and may evolve into a longer-term quality engineering role as production grows.Job Type &amp; LocationThis is a Contract position based out of Bingen, WA.Pay and BenefitsThe pay range for this position is $40.00 - $52.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Bingen, WA.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Bingen,WA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionAs a Quality Engineer, you will be responsible for reviewing new and revised manufacturing jobs to ensure material selection, heat treatment requirements, processing routes, and compliance with customer specifications. You will investigate metallurgical, quality, and heat-treatment issues, perform root cause analysis, and implement corrective actions for non-conforming materials, processes, and products. Additionally, you will manage third-party laboratory testing, including sample submissions, result tracking, technical report review, and the disposition of failed results. Your role will also involve verifying incoming material chemistry against certifications and specifications, supporting supplier quality initiatives, and driving corrective actions when needed. You will collaborate with Quality, Engineering, Production, heat treatment vendors, and steel suppliers to develop metallurgical programs, support new product launches, improve process capability, and drive continuous improvement using Lean, Six Sigma, and other quality methodologies.Responsibilities<ul><li>Review and validate material selection, heat treatment requirements, and processing routes for manufacturing jobs.</li><li>Investigate and resolve metallurgical, quality, and heat-treatment issues.</li><li>Perform root cause analysis and implement corrective actions for non-conforming materials, processes, and products.</li><li>Manage third-party laboratory testing and track results.</li><li>Verify incoming material chemistry against certifications and specifications.</li><li>Support supplier quality initiatives and drive corrective actions.</li><li>Collaborate with various teams to develop metallurgical programs and improve process capability.</li></ul>Essential Skills<ul><li>Bachelors degree in Materials Engineering, Engineering Physics, Chemistry, or a related field.</li><li>3-5 years of experience in a quality engineering role in a manufacturing setting.</li><li>Proficiency in statistical analysis tools and data analytics (Minitab, JMP, or equivalent).</li><li>Strong attention to detail and ability to identify minute surface defects.</li><li>Strong problem-solving and analytical skills.</li><li>Excellent verbal and written communication abilities.</li><li>Ability to work collaboratively in a team environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Direct heat treatment or metal experience.</li><li>Experience with ISO 9001, AS9100, or regulated industry is a plus.</li><li>Experience in automotive, aerospace, or other highly regulated industries.</li><li>Familiarity with ERP and PLM systems.</li><li>Attention to detail and a proactive approach to quality improvement.</li><li>High level of initiative and ability to work in a fast-paced environment.</li><li>Familiarity with safety and environmental regulations.</li></ul>Work EnvironmentThe work environment is primarily in a forging setting, which involves spending about 40% of the time on the floor, depending on project needs. The environment can be hot and dirty, requiring adaptability. While the position is office-based, it requires engagement with the manufacturing floor.Job Type &amp; LocationThis is a Contract to Hire position based out of Portland, IN.Pay and BenefitsThe pay range for this position is $38.46 - $52.88/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Portland, IN.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Portland,IN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer supports quality activities within an on-site manufacturing operation, with primary responsibility for investigating and documenting manufacturing nonconformances across two production business units. The role focuses on identifying root causes of manufacturing and product issues, assessing impacted products and lots, and driving timely, compliant resolutions in a regulated environment.Responsibilities<ul><li>Own and perform nonconformance investigations related to manufacturing and product quality issues across two production business units.</li><li>Conduct thorough root cause analysis to determine the source of manufacturing discrepancies and quality events.</li><li>Write clear, technically sound investigation reports that document findings, root cause, impacted lots and products, and recommended actions.</li><li>Support approximately four nonconformance closures per week, adapting to varying investigation complexity, timelines, and related change controls.</li><li>Partner with upstream and downstream teams to investigate issues across the entire manufacturing process, from raw materials to finished products.</li><li>Analyze manufacturing and quality data using tools such as Excel, Power BI, and PI Vision to identify trends, risks, and improvement opportunities.</li><li>Work cross-functionally with Operations, Quality, Manufacturing Engineering, supervisors, technicians, and production personnel to resolve quality issues.</li><li>Maintain complete, accurate, and compliant investigation documentation in accordance with applicable quality system requirements and good documentation practices (GDP).</li><li>Support and participate in CAPA activities, including risk mitigation and implementation of corrective and preventive actions stemming from investigations.</li><li>Contribute to and support change control processes associated with manufacturing and quality improvements.</li><li>Review drawings, procedures, and related technical documentation to ensure quality requirements are clearly defined and met.</li><li>Apply knowledge of regulatory expectations, including FDA and ISO-related requirements, within a medical device or pharmaceutical manufacturing context.</li><li>Support audits and internal quality assurance activities as needed.</li><li>Collaborate with cross-functional teams to continuously improve nonconformance investigation processes and overall product quality.</li></ul>Essential Skills<ul><li>Bachelor's degree in an engineering discipline or a related technical field.</li><li>Minimum 12+ years of professional industry experience after graduation.</li><li>13 years of experience within medical device or pharmaceutical manufacturing, or another regulated manufacturing environment.</li><li>Hands-on experience conducting nonconformance, NCR, NCMR, or deviation investigations, including ownership of investigations rather than only participation.</li><li>Demonstrated experience performing structured root cause analysis.</li><li>Experience with CAPA, risk mitigation, and change control in a manufacturing or production environment.</li><li>Proven ability to write high-quality technical investigation reports and other quality documentation.</li><li>Strong technical writing skills with attention to clarity, accuracy, and compliance with GDP.</li><li>Strong problem-solving skills with the ability to analyze complex manufacturing and quality issues.</li><li>Effective cross-functional communication skills, including the ability to work closely with Operations, Quality, Manufacturing Engineering, and production teams.</li><li>Experience supporting a manufacturing or production environment, including interaction with technicians, supervisors, and engineering staff.</li><li>Proficiency with Excel for data analysis and reporting.</li><li>Familiarity with FDA-regulated or ISO-based quality systems and quality engineering or quality assurance practices.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience within medical device or pharmaceutical manufacturing environments is strongly preferred.</li><li>Exposure to or experience with Power BI and PI Vision for data visualization and analysis.</li><li>Experience in quality engineering, quality assurance, or related engineering disciplines.</li><li>Experience with audits in regulated manufacturing environments.</li><li>Knowledge of ISO standards relevant to quality systems and medical products.</li><li>Experience managing and documenting nonconformances, including NCMR and NCR processes.</li><li>Experience supporting investigations that lead to CAPA and change control activities.</li><li>Ability to interpret and review engineering drawings, procedures, and related technical documentation.</li><li>Comfort working in a growth-oriented organization with evolving processes and continuous improvement initiatives.</li><li>Interest in long-term assignment opportunities, with potential for a 12month contract and possible extension based on performance and business needs.</li></ul>Work EnvironmentThis position is based on-site in a manufacturing environment that develops, manufactures, and markets innovative medical products and services for the healthcare industry. The facility focuses on products with inherent safety features that help address critical healthcare challenges, including opioid abuse issues, hospital-acquired malnutrition, and hazardous drug exposure. You will work closely with a large, diverse operations and quality team that includes technicians, supervisors, and engineering staff who manage raw materials, in-process work, and finished products. The environment is highly regulated and quality-focused, with established quality systems, FDA and ISO expectations, and strong emphasis on data-driven decision-making using tools such as Excel, Power BI, and PI Vision. The role involves regular interaction on the production floor, review of drawings and procedures, and participation in cross-functional projects. This is a 12month contract assignment with the potential to extend, offering the opportunity to contribute to a market-leading organization in a growth phase while supporting meaningful healthcare-focused productsJob Type &amp; LocationThis is a Contract to Hire position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $40.00 - $55.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Irvine, CA.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Irvine,CA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Engineer  Nonconformance & CAPA

Job Description: Quality Engineer IIThis Quality Engineer II role focuses on driving robust quality processes within a fast-growing manufacturing environment that produces switchgear, busbars, and electrical distribution equipment for data centers. You will lead and improve quality systems, support key customer requirements such as PPAP, and perform root cause analysis to ensure products meet stringent industry standards, including ISO 9001, UL, and milspec specifications. This position is fully on-site and requires close collaboration with manufacturing and engineering teams to support both low- and high-volume, engineer-to-order production.Responsibilities<ul><li>Lead and manage quality engineering activities on the manufacturing floor, ensuring products meet internal and external quality standards.</li><li>Perform and oversee Production Part Approval Process (PPAP) activities for major customers, ensuring all documentation and validation requirements are met.</li><li>Update and maintain quality procedures and documentation within the ISO 9001 quality management system, supporting ongoing certification and compliance.</li><li>Participate in and lead root cause analysis (RCA) investigations using tools such as Fishbone diagrams and 5 Why analysis to resolve quality issues and prevent recurrence.</li><li>Support and improve the Quality Management System (QMS), including processes for incoming, in-process, and final inspection.</li><li>Conduct and oversee quality inspections on electrical distribution equipment, switchgear, and related components to ensure conformance to specifications, UL standards, and milspec requirements.</li><li>Collaborate closely with manufacturing and engineering teams to address quality concerns in low- to high-volume and engineer-to-order production environments.</li><li>Review and manage Material Review Board (MRB) activities, including disposition of nonconforming materials and components.</li><li>Utilize Bills of Materials (BOM) and engineering documentation to verify product configuration and ensure accurate build and inspection criteria.</li><li>Apply knowledge of UL standards, including UL 891 switchboard commercial standards, and milspec requirements to guide design, manufacturing, and inspection practices.</li><li>Monitor and report on quality-related key performance indicators (KPIs) to drive continuous improvement in product and process quality.</li><li>Support efforts to maintain and enhance certifications and standards, particularly ISO 9001, and contribute to quality-related initiatives in a growing organization.</li><li>Engage confidently with internal teams and customers to communicate quality requirements, findings, and improvement plans.</li></ul>Essential Skills<ul><li>At least 5 years of experience in quality engineering within a manufacturing floor environment.</li><li>Hands-on experience with PPAP (Production Part Approval Process) for key customers.</li><li>Demonstrated experience updating and maintaining quality procedures within an ISO 9001 environment.</li><li>Strong proficiency in root cause analysis (RCA) using tools such as Fishbone diagrams and 5 Why techniques.</li><li>Experience with quality inspection processes, including incoming inspection, in-process inspection, and final inspection.</li><li>Knowledge of Quality Management Systems (QMS) and practical experience implementing and improving QMS processes.</li><li>Experience working with electrical, mechanical, and power distribution equipment, including switchgear and variable frequency applications.</li><li>Understanding of UL standards, particularly UL 891 switchboard commercial standards.</li><li>Familiarity with milspec standards and their application to manufacturing and inspection.</li><li>Ability to interpret and work with Bills of Materials (BOM) and engineering documentation.</li><li>Experience supporting Material Review Board (MRB) activities and handling nonconforming material.</li><li>Comfort working in both low- and high-volume production environments and with engineer-to-order products.</li><li>Strong collaboration skills for working closely with manufacturing and engineering teams.</li><li>Confidence in decision-making and communication when addressing quality issues and improvement initiatives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree preferred, ideally in engineering, quality, or a related technical field.</li><li>Experience working in organizations that are establishing or expanding certifications and quality systems, such as ISO 9001, is a strong plus.</li><li>Experience in companies focused on electrical and automation equipment is beneficial.</li><li>Familiarity with electrical distribution equipment, switchgear, and power conversions in data center or similar environments.</li><li>Experience using and tracking quality-related KPIs to support continuous improvement.</li><li>Ability to thrive in a rapidly growing company and adapt to evolving processes and customer requirements.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Cudahy, WI.Pay and BenefitsThe pay range for this position is $45.00 - $60.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Cudahy, WI.Application DeadlineThis position is anticipated to close on Nov 6, 2026.Workplace TypeThis is a fully onsite position in Cudahy,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Engineer II

Job Description: Quality Engineer IIThis Quality Engineer II role focuses on driving robust quality processes within a fast-growing manufacturing environment that produces switchgear, busbars, and electrical distribution equipment for data centers. You will lead and improve quality systems, support key customer requirements such as PPAP, and perform root cause analysis to ensure products meet stringent industry standards, including ISO 9001, UL, and milspec specifications. This position is fully on-site and requires close collaboration with manufacturing and engineering teams to support both low- and high-volume, engineer-to-order production.Responsibilities<ul><li>Lead and manage quality engineering activities on the manufacturing floor, ensuring products meet internal and external quality standards.</li><li>Perform and oversee Production Part Approval Process (PPAP) activities for major customers, ensuring all documentation and validation requirements are met.</li><li>Update and maintain quality procedures and documentation within the ISO 9001 quality management system, supporting ongoing certification and compliance.</li><li>Participate in and lead root cause analysis (RCA) investigations using tools such as Fishbone diagrams and 5 Why analysis to resolve quality issues and prevent recurrence.</li><li>Support and improve the Quality Management System (QMS), including processes for incoming, in-process, and final inspection.</li><li>Conduct and oversee quality inspections on electrical distribution equipment, switchgear, and related components to ensure conformance to specifications, UL standards, and milspec requirements.</li><li>Collaborate closely with manufacturing and engineering teams to address quality concerns in low- to high-volume and engineer-to-order production environments.</li><li>Review and manage Material Review Board (MRB) activities, including disposition of nonconforming materials and components.</li><li>Utilize Bills of Materials (BOM) and engineering documentation to verify product configuration and ensure accurate build and inspection criteria.</li><li>Apply knowledge of UL standards, including UL 891 switchboard commercial standards, and milspec requirements to guide design, manufacturing, and inspection practices.</li><li>Monitor and report on quality-related key performance indicators (KPIs) to drive continuous improvement in product and process quality.</li><li>Support efforts to maintain and enhance certifications and standards, particularly ISO 9001, and contribute to quality-related initiatives in a growing organization.</li><li>Engage confidently with internal teams and customers to communicate quality requirements, findings, and improvement plans.</li></ul>Essential Skills<ul><li>At least 5 years of experience in quality engineering within a manufacturing floor environment.</li><li>Hands-on experience with PPAP (Production Part Approval Process) for key customers.</li><li>Demonstrated experience updating and maintaining quality procedures within an ISO 9001 environment.</li><li>Strong proficiency in root cause analysis (RCA) using tools such as Fishbone diagrams and 5 Why techniques.</li><li>Experience with quality inspection processes, including incoming inspection, in-process inspection, and final inspection.</li><li>Knowledge of Quality Management Systems (QMS) and practical experience implementing and improving QMS processes.</li><li>Experience working with electrical, mechanical, and power distribution equipment, including switchgear and variable frequency applications.</li><li>Understanding of UL standards, particularly UL 891 switchboard commercial standards.</li><li>Familiarity with milspec standards and their application to manufacturing and inspection.</li><li>Ability to interpret and work with Bills of Materials (BOM) and engineering documentation.</li><li>Experience supporting Material Review Board (MRB) activities and handling nonconforming material.</li><li>Comfort working in both low- and high-volume production environments and with engineer-to-order products.</li><li>Strong collaboration skills for working closely with manufacturing and engineering teams.</li><li>Confidence in decision-making and communication when addressing quality issues and improvement initiatives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree preferred, ideally in engineering, quality, or a related technical field.</li><li>Experience working in organizations that are establishing or expanding certifications and quality systems, such as ISO 9001, is a strong plus.</li><li>Experience in companies focused on electrical and automation equipment is beneficial.</li><li>Familiarity with electrical distribution equipment, switchgear, and power conversions in data center or similar environments.</li><li>Experience using and tracking quality-related KPIs to support continuous improvement.</li><li>Ability to thrive in a rapidly growing company and adapt to evolving processes and customer requirements.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Cudahy, WI.Pay and BenefitsThe pay range for this position is $45.00 - $60.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Cudahy, WI.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Cudahy,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Description: Quality Engineer IIThis Quality Engineer II role focuses on driving robust quality processes within a fast-growing manufacturing environment that produces switchgear, busbars, and electrical distribution equipment for data centers. You will lead and improve quality systems, support key customer requirements such as PPAP, and perform root cause analysis to ensure products meet stringent industry standards, including ISO 9001, UL, and milspec specifications. This position is fully on-site and requires close collaboration with manufacturing and engineering teams to support both low- and high-volume, engineer-to-order production.Responsibilities<ul><li>Lead and manage quality engineering activities on the manufacturing floor, ensuring products meet internal and external quality standards.</li><li>Perform and oversee Production Part Approval Process (PPAP) activities for major customers, ensuring all documentation and validation requirements are met.</li><li>Update and maintain quality procedures and documentation within the ISO 9001 quality management system, supporting ongoing certification and compliance.</li><li>Participate in and lead root cause analysis (RCA) investigations using tools such as Fishbone diagrams and 5 Why analysis to resolve quality issues and prevent recurrence.</li><li>Support and improve the Quality Management System (QMS), including processes for incoming, in-process, and final inspection.</li><li>Conduct and oversee quality inspections on electrical distribution equipment, switchgear, and related components to ensure conformance to specifications, UL standards, and milspec requirements.</li><li>Collaborate closely with manufacturing and engineering teams to address quality concerns in low- to high-volume and engineer-to-order production environments.</li><li>Review and manage Material Review Board (MRB) activities, including disposition of nonconforming materials and components.</li><li>Utilize Bills of Materials (BOM) and engineering documentation to verify product configuration and ensure accurate build and inspection criteria.</li><li>Apply knowledge of UL standards, including UL 891 switchboard commercial standards, and milspec requirements to guide design, manufacturing, and inspection practices.</li><li>Monitor and report on quality-related key performance indicators (KPIs) to drive continuous improvement in product and process quality.</li><li>Support efforts to maintain and enhance certifications and standards, particularly ISO 9001, and contribute to quality-related initiatives in a growing organization.</li><li>Engage confidently with internal teams and customers to communicate quality requirements, findings, and improvement plans.</li></ul>Essential Skills<ul><li>At least 5 years of experience in quality engineering within a manufacturing floor environment.</li><li>Hands-on experience with PPAP (Production Part Approval Process) for key customers.</li><li>Demonstrated experience updating and maintaining quality procedures within an ISO 9001 environment.</li><li>Strong proficiency in root cause analysis (RCA) using tools such as Fishbone diagrams and 5 Why techniques.</li><li>Experience with quality inspection processes, including incoming inspection, in-process inspection, and final inspection.</li><li>Knowledge of Quality Management Systems (QMS) and practical experience implementing and improving QMS processes.</li><li>Experience working with electrical, mechanical, and power distribution equipment, including switchgear and variable frequency applications.</li><li>Understanding of UL standards, particularly UL 891 switchboard commercial standards.</li><li>Familiarity with milspec standards and their application to manufacturing and inspection.</li><li>Ability to interpret and work with Bills of Materials (BOM) and engineering documentation.</li><li>Experience supporting Material Review Board (MRB) activities and handling nonconforming material.</li><li>Comfort working in both low- and high-volume production environments and with engineer-to-order products.</li><li>Strong collaboration skills for working closely with manufacturing and engineering teams.</li><li>Confidence in decision-making and communication when addressing quality issues and improvement initiatives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree preferred, ideally in engineering, quality, or a related technical field.</li><li>Experience working in organizations that are establishing or expanding certifications and quality systems, such as ISO 9001, is a strong plus.</li><li>Experience in companies focused on electrical and automation equipment is beneficial.</li><li>Familiarity with electrical distribution equipment, switchgear, and power conversions in data center or similar environments.</li><li>Experience using and tracking quality-related KPIs to support continuous improvement.</li><li>Ability to thrive in a rapidly growing company and adapt to evolving processes and customer requirements.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Cudahy, WI.Pay and BenefitsThe pay range for this position is $45.00 - $60.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Cudahy, WI.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Cudahy,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Engineer IIIJob DescriptionAs a Quality Engineer III (QE III), you will play a critical role in supporting quality activities across the product lifecyclefrom New Product Introduction (NPI) through Process Performance Qualification (PPQ) and into commercial manufacturing. This high-level individual contributor role is responsible for ensuring programs are compliant, inspection-ready, and aligned with commercialization quality strategies. You will collaborate cross-functionally to deliver high-quality outcomes that support successful product launches and sustained commercial operations. The role requires you to be on the floor for operations between 30-40% of the day, conducting risk assessments, managing deviations, reviewing Master Batch Records, and supporting documents.Responsibilities<ul><li>Serve as Quality representative/lead on cross-functional program teams to enable successful commercialization readiness, from late-stage development through launch and post-launch support.</li><li>Provide phase-appropriate QA oversight for technology transfer, process validation/PPQ readiness, control strategy implementation, and manufacturing scale-up activities.</li><li>Partner with Product/Program Leadership to ensure quality deliverables, timelines, and risk mitigations are built into program plans, including risk assessments, readiness reviews, and documentation strategy.</li><li>Ensure alignment to applicable regulations and guidance such as FDA, EMA, ICH, and site quality standards.</li><li>Review and approve GMP documentation, including batch records, SOPs, technical reports, and quality records.</li><li>Support material disposition and product release activities.</li><li>Conduct compliance walkthroughs to ensure adherence to GMP standards.</li><li>Provide QA support during manufacturing 'hypercare' and critical operations.</li><li>Support investigations for deviations, CAPAs, and change controls.</li><li>Apply risk-based decision-making to ensure compliant and effective outcomes.</li><li>Identify, assess, and mitigate quality risks across operations.</li><li>Contribute to continuous improvement initiatives.</li></ul>Essential Skills<ul><li>5+ years experience in a regulated GMP manufacturing environment, including Quality oversight.</li><li>Experience supporting different pharmaceutical clinical phases and/or commercial manufacturing.</li><li>Strong knowledge of quality systems, deviation management, and risk assessment.</li><li>Master Batch Record review experience and regulatory technical review (FDA, GMP).</li><li>Strong working knowledge of cGMP, data integrity expectations, and inspection readiness.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in a scientific discipline or equivalent experience.</li><li>Effective communication skills and attention to detail.</li><li>Ability to influence cross-functionally and manage competing priorities.</li><li>Proven ability to make key and timely decisions.</li><li>Leadership skills and organizational abilities.</li><li>Technical knowledge of biopharmaceutical manufacturing is desirable.</li><li>Ability to aseptically gown and work in environmental clean rooms.</li></ul>Work EnvironmentThe St. Louis site is a fast-paced biologic drug substance manufacturing facility operating around the clock with approximately 1,000 employees. The facility focuses on cell process development to support clinical and commercial manufacturing. You will work Monday to Friday with flexible start times, typically 8am-5pm. The role requires 60% desk work and 30-40% on-floor operations, where you will need to gown up in a bunny suit or blues.Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $36.00 - $48.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Saint Louis,MO.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Engineer III - Process Validation

Job Title: Quality Engineering TechnicianJob DescriptionAs a Quality Engineering Technician, you will conduct in-process and final inspections to verify dimensions, workmanship, process compliance, and technical standards. You will utilize automated and precision inspection equipment, including Keyence and profilometers, to measure components and document results. Additionally, you will identify and document nonconformances, generate Quality Notifications (QNs), and support problem-solving, root cause analysis, and disposition activities. You will also perform job audits, operational certification surveillance, and over-inspects while maintaining knowledge of applicable customer, FAA, JAA, and technical requirements. Following established procedures and standard work, you will obtain and maintain required inspection certifications/stamps and provide technical support or training to other employees when qualified.Responsibilities<ul><li>Conduct in-process and final inspections to verify dimensions, workmanship, and process compliance.</li><li>Utilize automated and precision inspection equipment, including Keyence and profilometers, for measurements.</li><li>Document results and identify nonconformances, generating Quality Notifications (QNs).</li><li>Support problem-solving, root cause analysis, and disposition activities.</li><li>Perform job audits, operational certification surveillance, and over-inspects.</li><li>Maintain knowledge of applicable customer, FAA, JAA, and technical requirements.</li><li>Obtain and maintain required inspection certifications/stamps.</li><li>Provide technical support or training to other employees when qualified.</li></ul>Essential Skills<ul><li>Inspection and quality control in a manufacturing process.</li><li>Ability to read and interpret blueprints, drawings, inspection procedures, and technical specifications.</li><li>Experience with precision measuring tools and equipment such as Keyence and profilometers.</li><li>Knowledge in engineering documentation and manufacturing processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate's degree with 3+ years of relevant experience or 7+ years of relevant experience without a degree.</li><li>Experience with SAP, Solumina, and proficiency with Microsoft Office, including Excel, Word, and PowerPoint.</li><li>Experience with PPAP, APQP, and root cause failure analysis.</li></ul>Work EnvironmentThe role is based in a manufacturing setting where you will work with advanced equipment and resources. The site is growing tremendously with significant investments, providing a career-based opportunity. Employees enjoy strong benefits, including paid holidays, vacation, and PTO, while working for a Fortune 500 company with a backlog and demand for current and evolving products.Job Type &amp; LocationThis is a Contract position based out of Asheville, NC.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Asheville, NC.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Asheville,NC.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Engineering Technician

Job Title: Quality Engineering TechnicianJob DescriptionThe Quality Engineering Technician develops, modifies, and maintains quality inspection programs for Optical Gaging Products (OGP) and Keyence systems to ensure accurate, efficient, and repeatable measurement processes. This role designs and implements robust inspection programs, creates fixtures, and supports inspection activities to meet production and quality requirements. The technician coordinates programming projects from initial concept through final validation, ensuring compliance with quality standards while collaborating closely with production and quality teams.Responsibilities<ul><li>Develop, modify, and maintain quality inspection programs for OGP and Keyence systems to ensure accurate and repeatable measurements.</li><li>Design and implement robust inspection programs that support efficient and reliable measurement processes.</li><li>Create, design, and refine fixtures required to support inspection activities and ensure part stability and repeatability during measurement.</li><li>Coordinate quality programming projects from initial concept through final validation, ensuring timelines and quality standards are met.</li><li>Support inspection activities by troubleshooting and optimizing measurement programs as production needs evolve.</li><li>Ensure all inspection programs comply with established quality standards and customer requirements.</li><li>Collaborate with production and quality teams to align inspection programming with manufacturing processes and product specifications.</li><li>Interpret engineering blueprints and apply Geometric Dimensioning &amp; Tolerancing (GD&amp;T) principles to develop accurate inspection routines.</li><li>Utilize SolidWorks and/or AutoCAD to support fixture design and inspection-related tooling.</li><li>Work with precision equipment such as surface grinders, mills, lathes, and wash tanks as needed to support inspection and fixture preparation.</li><li>Support validation activities, including measurement verification and documentation of inspection program performance.</li><li>Maintain organized documentation for inspection programs, fixtures, and validation results to support audits and continuous improvement.</li></ul>Essential Skills<ul><li>5+ years of experience in quality engineering or precision inspection.</li><li>Strong proficiency in blueprint reading and interpretation of engineering drawings.</li><li>Proficiency in Geometric Dimensioning &amp; Tolerancing (GD&amp;T).</li><li>Familiarity with operating and working around surface grinders, mills, lathes, and wash tanks.</li><li>Proficiency in SolidWorks and/or AutoCAD for designing fixtures and supporting inspection processes.</li><li>Ability to coordinate projects from concept through final validation in a quality or manufacturing environment.</li><li>Strong attention to detail and ability to ensure accurate, efficient, and repeatable measurement processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience using OGP and Keyence systems in a manufacturing or quality environment.</li><li>Knowledge of statistical analysis tools such as Minitab and QcCalc.</li><li>Experience supporting PPAP (Production Part Approval Process), First Article Inspection (FAI), Gauge R&amp;R (Repeatability and Reproducibility), and Capability Studies.</li><li>Ability to work effectively in a collaborative, production-oriented environment.</li><li>Strong communication skills to support coordination with production, engineering, and quality teams.</li></ul>Work EnvironmentThe role is based in a busy, highly social inspection room where multiple activities and conversations may occur simultaneously. The technician must maintain focus, accuracy, and professionalism while managing frequent interpersonal interactions and supporting ongoing production needs. The environment involves working around precision equipment such as surface grinders, mills, lathes, and wash tanks, as well as using OGP and Keyence inspection systems and CAD tools like SolidWorks and AutoCAD. Permanent employees may be eligible for a discretionary bonus program, paid time off, and holidays, and the organization may offer sign-on incentives and opportunities for conversion to a permanent role. The culture emphasizes collaboration, technical excellence, and supporting high-quality manufacturing outcomes.Job Type &amp; LocationThis is a Permanent position based out of York, PA.Pay and BenefitsThe pay range for this position is $29.00 - $39.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of York, PA.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in York,PA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2>Quality Engineering Technician</h2><h3>Job Description</h3>The Quality Engineering Technician is responsible for ensuring architectural precast concrete products meet project specifications, dimensional tolerances, and quality standards throughout the manufacturing process. This role performs inspections, maintains quality documentation, and partners with production and engineering teams to support continuous improvement and product excellence.<h3>Responsibilities</h3><ul><li>Review construction drawings, specifications, and project requirements to establish quality expectations.</li><li>Conduct pre-pour inspections of forms, reinforcement, embeds, and inserts to ensure compliance with design and project specifications.</li><li>Inspect finished precast products for dimensional accuracy, structural integrity, and architectural appearance.</li><li>Verify proper product identification, marking, and traceability throughout production.</li><li>Maintain inspection reports, quality records, and production documentation.</li><li>Utilize measuring tools and mathematical calculations to verify dimensions, quantities, and tolerances.</li><li>Identify quality concerns, document findings, and assist in implementing corrective actions.</li><li>Collaborate with production, engineering, and drafting teams to resolve issues and improve manufacturing processes.</li><li>Support the development and refinement of quality control procedures and best practices.</li><li>Maintain a safe, organized work environment and comply with all company safety standards.</li></ul><h3>Required Qualifications</h3><ul><li>Bachelor's degree in Engineering or a related technical field.</li><li>1-2 years of experience in construction materials, concrete production, field testing, quality control, or a related industry.</li><li>Ability to read and interpret construction drawings, blueprints, and technical specifications.</li><li>Knowledge of quality control principles and inspection practices.</li><li>Proficiency with basic measuring tools, including tape measures and dimensional inspection equipment.</li><li>Strong math, problem-solving, and analytical skills.</li><li>Effective written and verbal communication skills.</li><li>Strong attention to detail and ability to work independently in a fast-paced environment.</li><li>Ability to perform shop-floor inspections, including standing, walking, and climbing as required.</li></ul><h3>Preferred Qualifications</h3><ul><li>Experience with precast concrete manufacturing or related construction materials.</li><li>FE certification or interest in pursuing FE/PE licensure (company support available).</li><li>Interest in leadership development and long-term career growth.</li><li>Commitment to continuous learning and professional development.</li></ul><h3>Work Environment</h3>This position is approximately 70% shop floor and 30% office-based. The manufacturing environment involves exposure to concrete production, dust, noise, and active equipment, while the office setting supports collaboration with engineering and drafting teams. The company offers a family-oriented culture, opportunities for professional growth, profit-sharing eligibility after one year, a 401(k) with company match, and plans for a new, modern office and manufacturing facility.Job Type &amp; LocationThis is a Contract to Hire position based out of Omaha, NE.Pay and BenefitsThe pay range for this position is $24.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Omaha, NE.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Omaha,NE.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Engineering TechnicianJob DescriptionAs a Quality Engineering Technician, you will conduct in-process and final inspections to verify dimensions, workmanship, process compliance, and technical standards. You will utilize automated and precision inspection equipment, including Keyence and profilometers, to measure components and document results. Additionally, you will identify and document nonconformances, generate Quality Notifications (QNs), and support problem-solving, root cause analysis, and disposition activities. You will also perform job audits, operational certification surveillance, and over-inspects while maintaining knowledge of applicable customer, FAA, JAA, and technical requirements. Following established procedures and standard work, you will obtain and maintain required inspection certifications/stamps and provide technical support or training to other employees when qualified.Responsibilities<ul><li>Conduct in-process and final inspections to verify dimensions, workmanship, and process compliance.</li><li>Utilize automated and precision inspection equipment, including Keyence and profilometers, for measurements.</li><li>Document results and identify nonconformances, generating Quality Notifications (QNs).</li><li>Support problem-solving, root cause analysis, and disposition activities.</li><li>Perform job audits, operational certification surveillance, and over-inspects.</li><li>Maintain knowledge of applicable customer, FAA, JAA, and technical requirements.</li><li>Obtain and maintain required inspection certifications/stamps.</li><li>Provide technical support or training to other employees when qualified.</li></ul>Essential Skills<ul><li>Inspection and quality control in a manufacturing process.</li><li>Ability to read and interpret blueprints, drawings, inspection procedures, and technical specifications.</li><li>Experience with precision measuring tools and equipment such as Keyence and profilometers.</li><li>Knowledge in engineering documentation and manufacturing processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate's degree with 3+ years of relevant experience or 7+ years of relevant experience without a degree.</li><li>Experience with SAP, Solumina, and proficiency with Microsoft Office, including Excel, Word, and PowerPoint.</li><li>Experience with PPAP, APQP, and root cause failure analysis</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Asheville, NC.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Asheville, NC.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Asheville,NC.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 

 The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law. 

 If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options. 

 San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records. 

 Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability. 

 Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2>Quality Engineering Technician</h2><h3>Job Description</h3>The Quality Engineering Technician is responsible for ensuring architectural precast concrete products meet project specifications, dimensional tolerances, and quality standards throughout the manufacturing process. This role performs inspections, maintains quality documentation, and partners with production and engineering teams to support continuous improvement and product excellence.<h3>Responsibilities</h3><ul><li>Review construction drawings, specifications, and project requirements to establish quality expectations.</li><li>Conduct pre-pour inspections of forms, reinforcement, embeds, and inserts to ensure compliance with design and project specifications.</li><li>Inspect finished precast products for dimensional accuracy, structural integrity, and architectural appearance.</li><li>Verify proper product identification, marking, and traceability throughout production.</li><li>Maintain inspection reports, quality records, and production documentation.</li><li>Utilize measuring tools and mathematical calculations to verify dimensions, quantities, and tolerances.</li><li>Identify quality concerns, document findings, and assist in implementing corrective actions.</li><li>Collaborate with production, engineering, and drafting teams to resolve issues and improve manufacturing processes.</li><li>Support the development and refinement of quality control procedures and best practices.</li><li>Maintain a safe, organized work environment and comply with all company safety standards.</li></ul><h3>Required Qualifications</h3><ul><li>Bachelor's degree in Engineering or a related technical field.</li><li>1-2 years of experience in construction materials, concrete production, field testing, quality control, or a related industry.</li><li>Ability to read and interpret construction drawings, blueprints, and technical specifications.</li><li>Knowledge of quality control principles and inspection practices.</li><li>Proficiency with basic measuring tools, including tape measures and dimensional inspection equipment.</li><li>Strong math, problem-solving, and analytical skills.</li><li>Effective written and verbal communication skills.</li><li>Strong attention to detail and ability to work independently in a fast-paced environment.</li><li>Ability to perform shop-floor inspections, including standing, walking, and climbing as required.</li></ul><h3>Preferred Qualifications</h3><ul><li>Experience with precast concrete manufacturing or related construction materials.</li><li>FE certification or interest in pursuing FE/PE licensure (company support available).</li><li>Interest in leadership development and long-term career growth.</li><li>Commitment to continuous learning and professional development.</li></ul><h3>Work Environment</h3>This position is approximately 70% shop floor and 30% office-based. The manufacturing environment involves exposure to concrete production, dust, noise, and active equipment, while the office setting supports collaboration with engineering and drafting teams. The company offers a family-oriented culture, opportunities for professional growth, profit-sharing eligibility after one year, a 401(k) with company match, and plans for a new, modern office and manufacturing facility.Job Type &amp; LocationThis is a Contract to Hire position based out of Omaha, NE.Pay and BenefitsThe pay range for this position is $24.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Omaha, NE.Application DeadlineThis position is anticipated to close on Nov 8, 2026.Workplace TypeThis is a fully onsite position in Omaha,NE.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Description: Quality InspectorAs a Quality Inspector, you will conduct assembly line audits to ensure proper equipment set-ups, availability of calibrated tools, and adherence to approved work instructions. You will reinforce Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) among production personnel. Your role involves reviewing production records for completeness, accuracy, and legibility, ensuring all records comply with Quality System requirements. You will execute product releases, perform independent final inspections, and authorize shipment of conforming assemblies. Additionally, you will evaluate nonconforming materials, coordinate disposition activities, and document investigations per Quality System requirements.Responsibilities<ul><li>Conduct assembly line audits to verify equipment set-ups and calibrated tools.</li><li>Reinforce GMP and GDP to production personnel.</li><li>Review production records for completeness, accuracy, and legibility.</li><li>Execute product release, including final inspections and sign-offs.</li><li>Evaluate nonconforming material and document investigations per Quality System requirements.</li><li>Participate in assembly line validations by collecting and documenting objective evidence.</li><li>Maintain operator training records and ensure personnel qualification for assembly tasks.</li><li>Issue quality alerts for complaints and nonconformances to prevent recurrence.</li><li>Document process deviations and in-process changes for necessary approvals.</li><li>Support evaluation and documentation of rework for assemblies per Quality System requirements.</li></ul>Essential Skills<ul><li>1-2 years of experience in a manufacturing environment, preferably in device assembly.</li><li>Blueprint reading.</li><li>Use of measurement tools such as calipers and micrometers.</li><li>Material Review Board (MRB) and Nonconformance management.</li><li>Intermediate-level Geometric Dimensioning &amp; Tolerancing (GD&amp;T).</li><li>Familiarity with Good Documentation Practices and production record review.</li><li>Proficiency with Microsoft Outlook and Microsoft Excel.</li></ul>Additional Skills &amp; Qualifications<ul><li>Broad understanding of materials, manufacturing technologies, and processes preferred.</li><li>Proficiency with electronic ERP systems and inspection management systems preferred.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Pay and BenefitsThe pay range for this position is $24.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Milwaukee,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Inspector

Job Title: Quality Inspector - 2nd Shift, 2:30pm-11pm + $1/hr shift differential. Job DescriptionThe Quality Inspector ensures that production assemblies meet all established quality standards by auditing assembly lines, reviewing documentation, and authorizing product release. This role focuses on reinforcing Good Manufacturing Practices and Good Documentation Practices, evaluating nonconforming materials, and supporting continuous improvement within a clean and organized manufacturing environment.Responsibilities<ul><li>Conduct assembly line audits to verify proper equipment set-ups, availability of calibrated tools, and adherence to approved work instructions.</li><li>Reinforce Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) with production personnel to ensure consistent compliance.</li><li>Review each production record (Device History Record, DHR) for completeness, accuracy, and legibility, ensuring records are retained or archived according to Quality System requirements.</li><li>Execute product release activities, including performing independent final inspections, completing sign-offs, and processing system transactions to authorize shipment of conforming assemblies.</li><li>Evaluate nonconforming material, coordinate disposition activities, and document investigations and dispositions in accordance with Quality System requirements.</li><li>Participate in assembly line validations by collecting objective evidence and documenting results for formal approval.</li><li>Maintain operator training records and verify that personnel are qualified before performing assembly tasks.</li><li>Issue quality alerts to production personnel in response to complaints and nonconformances to prevent recurrence.</li><li>Document process deviations and in-process changes and obtain applicable approvals as required by the Quality System.</li><li>Identify work instruction and process gaps and provide information to support continuous improvement initiatives.</li><li>Support evaluation and documentation of rework for assemblies, including product returns, in alignment with Quality System requirements.</li><li>Perform inspections involving sheet metal components and first article inspections using appropriate measurement tools.</li><li>Use calipers, micrometers, gauges, and other measurement devices to verify product dimensions and conformance.</li><li>Apply intermediate-level Geometric Dimensioning &amp; Tolerancing (GD&amp;T) concepts during inspection and documentation activities.</li><li>Collaborate with Material Review Board (MRB) and support Nonconformance management processes.</li><li>Utilize Microsoft Outlook, Microsoft Excel, and electronic ERP or inspection management systems to manage records, track inspections, and support reporting.</li></ul>Essential Skills<ul><li>12 years of experience in a manufacturing environment, preferably in device assembly.</li><li>Ability to read and interpret blueprints and technical drawings.</li><li>Hands-on experience using measurement tools such as calipers, micrometers, and gauges.</li><li>Knowledge of Material Review Board (MRB) processes and Nonconformance management.</li><li>Intermediate-level understanding of Geometric Dimensioning &amp; Tolerancing (GD&amp;T).</li><li>Familiarity with Good Documentation Practices and production record review.</li><li>Proficiency with Microsoft Outlook and Microsoft Excel.</li><li>Experience conducting first article inspections and working with sheet metal components.</li><li>Ability to follow and enforce ISO and Quality System requirements.</li><li>Strong attention to detail and ability to assess product conformity through inspection and documentation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Broad understanding of materials, manufacturing technologies, and production processes is preferred.</li><li>Proficiency with electronic ERP systems and inspection management systems is preferred.</li><li>Experience with CAPA (Corrective and Preventive Action) activities is beneficial.</li><li>Comfort working in an electro-mechanical environment with evolving technologies.</li><li>Strong communication skills to issue quality alerts and collaborate with production personnel.</li><li>Organizational skills to maintain accurate training records and quality documentation.</li><li>Interest in continuous improvement and identifying process and work instruction gaps.</li></ul>Work EnvironmentThis role is based in a very clean, organized manufacturing facility with a cubicle located on the production floor, providing close proximity to the workstations and assembly lines. The position is on a second shift schedule from 2:30 p.m. to 11:00 p.m., with a shift differential added to the hourly pay. The environment offers strong opportunities for growth, including exposure to increasingly electro-mechanical assemblies and the chance to learn new skills. The facility promotes a professional, collaborative atmosphere focused on quality, continuous improvement, and employee development.Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Pay and BenefitsThe pay range for this position is $24.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Milwaukee,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality InspectorJob DescriptionAs a Quality Inspector, you will conduct assembly line audits to ensure proper equipment set-ups, availability of calibrated tools, and adherence to approved work instructions. You will reinforce Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) among production personnel. Your role involves reviewing production records for completeness, accuracy, and legibility, ensuring all records comply with Quality System requirements. You will execute product releases, perform independent final inspections, and authorize shipment of conforming assemblies. Additionally, you will evaluate nonconforming materials, coordinate disposition activities, and document investigations per Quality System requirements.Responsibilities<ul><li>Conduct assembly line audits to verify equipment set-ups and calibrated tools.</li><li>Reinforce GMP and GDP to production personnel.</li><li>Review production records for completeness, accuracy, and legibility.</li><li>Execute product release, including final inspections and sign-offs.</li><li>Evaluate nonconforming material and document investigations per Quality System requirements.</li><li>Participate in assembly line validations by collecting and documenting objective evidence.</li><li>Maintain operator training records and ensure personnel qualification for assembly tasks.</li><li>Issue quality alerts for complaints and nonconformances to prevent recurrence.</li><li>Document process deviations and in-process changes for necessary approvals.</li><li>Support evaluation and documentation of rework for assemblies per Quality System requirements.</li></ul>Essential Skills<ul><li>1-2 years of experience in a manufacturing environment, preferably in device assembly.</li><li>Blueprint reading.</li><li>Use of measurement tools such as calipers and micrometers.</li><li>Material Review Board (MRB) and Nonconformance management.</li><li>Intermediate-level Geometric Dimensioning &amp; Tolerancing (GD&amp;T).</li><li>Familiarity with Good Documentation Practices and production record review.</li><li>Proficiency with Microsoft Outlook and Microsoft Excel.</li></ul>Additional Skills &amp; Qualifications<ul><li>Broad understanding of materials, manufacturing technologies, and processes preferred.</li><li>Proficiency with electronic ERP systems and inspection management systems preferred.</li></ul>Work EnvironmentThe work environment is very clean and organized, with a cubicle close to the work station, allowing you to be close to the action. The shift is 1st Shift from 6am to 2:30pm, providing a great balance of work-life. This is a great place to work, with ample room for growth and opportunities to learn new electro-mechanical skills.Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Pay and BenefitsThe pay range for this position is $24.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Milwaukee,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Description: Quality InspectorAs a Quality Inspector, you will conduct assembly line audits to ensure proper equipment set-ups, availability of calibrated tools, and adherence to approved work instructions. You will reinforce Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) among production personnel. Your role involves reviewing production records for completeness, accuracy, and legibility, ensuring all records comply with Quality System requirements. You will execute product releases, perform independent final inspections, and authorize shipment of conforming assemblies. Additionally, you will evaluate nonconforming materials, coordinate disposition activities, and document investigations per Quality System requirements.Responsibilities<ul><li>Conduct assembly line audits to verify equipment set-ups and calibrated tools.</li><li>Reinforce GMP and GDP to production personnel.</li><li>Review production records for completeness, accuracy, and legibility.</li><li>Execute product release, including final inspections and sign-offs.</li><li>Evaluate nonconforming material and document investigations per Quality System requirements.</li><li>Participate in assembly line validations by collecting and documenting objective evidence.</li><li>Maintain operator training records and ensure personnel qualification for assembly tasks.</li><li>Issue quality alerts for complaints and nonconformances to prevent recurrence.</li><li>Document process deviations and in-process changes for necessary approvals.</li><li>Support evaluation and documentation of rework for assemblies per Quality System requirements.</li></ul>Essential Skills<ul><li>1-2 years of experience in a manufacturing environment, preferably in device assembly.</li><li>Blueprint reading.</li><li>Use of measurement tools such as calipers and micrometers.</li><li>Material Review Board (MRB) and Nonconformance management.</li><li>Intermediate-level Geometric Dimensioning &amp; Tolerancing (GD&amp;T).</li><li>Familiarity with Good Documentation Practices and production record review.</li><li>Proficiency with Microsoft Outlook and Microsoft Excel.</li></ul>Additional Skills &amp; Qualifications<ul><li>Broad understanding of materials, manufacturing technologies, and processes preferred.</li><li>Proficiency with electronic ERP systems and inspection management systems preferred.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Pay and BenefitsThe pay range for this position is $24.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Milwaukee,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality InspectorJob DescriptionThe Quality Inspector role is responsible for inspecting a wide variety of parts, assemblies, tooling fixtures, and materials to ensure they meet customer requirements, company specifications, and applicable quality standards. Working under limited supervision, this position sets up, operates, inspects, tests, and adjusts new and reworked tools, dies, gauges, jigs, and fixtures for conformance to engineering drawings and specifications. The role also maintains, processes, and compiles confidential electronic and hard copy reports, records, and statistics, and handles non-routine assignments that require sound judgment to resolve moderately complex issues. Occasional inspections at customer or vendor sites may be required.Responsibilities<ul><li>Inspect machined parts, components, assemblies, and materials to ensure compliance with regulatory guidelines and industry standards such as Military Standards, ASTM, AWS, ANSI, and ASME Code.</li><li>Prepare and deliver electronic and hard copy inspection reports and communicate results to appropriate stakeholders, including project engineers.</li><li>Set up and operate measuring and test equipment, applying Geometric Dimensioning and Tolerancing (GD&amp;T) principles to verify part conformance.</li><li>Operate Coordinate Measurement Machines (CMM) or other portable metrology equipment to achieve part acceptance, including equipment setup and execution of final dimensional and in-process manufacturing inspections.</li><li>Observe testing activities and provide quality oversight to verify compliance with applicable requirements and standards.</li><li>Interact with and respond to regulatory agencies and customers during audits and reviews of inspection and calibration activities.</li><li>Monitor and verify quality using statistical process control or other control procedures as required.</li><li>Coordinate the procurement of standard materials, services, and parts needed to perform inspections.</li><li>Maintain, update, and manage computer databases related to inspections, calibration, and quality records.</li><li>Ensure adherence to all applicable laws, regulations, and company obligations whenever conducting business on behalf of the organization.</li><li>Work safely at all times, following established operating procedures and practices.</li><li>Travel to customer or vendor sites as needed to perform inspections or support quality activities.</li><li>Perform other related duties as assigned to support the overall quality assurance function.</li></ul>Essential Skills<ul><li>Associate degree, trade school certificate, military training, or equivalent in quality inspection or a related field, or certification by a professional group such as ASQ or AWS.</li><li>Three or more years of progressive experience in electrical, mechanical, electromechanical, or metrology inspection and calibration.</li><li>Strong ability to read and understand engineering drawings and specifications and perform complex mathematical computations.</li><li>Intermediate to subject matter expert-level knowledge of Geometric Dimensioning and Tolerancing (GD&amp;T).</li><li>Proficiency with hand inspection tools including micrometers, calipers, height gages, plug and ring gages, profilometers, and radius gages.</li><li>Experience performing hand inspections and visual checks in a production or manufacturing environment.</li><li>Experience with CMM or Laser Tracker equipment for part acceptance.</li><li>Working knowledge of metrology software such as PC-DMIS, Spatial Analyzer, or Polyworks.</li><li>Experience with quality systems and standards including ISO 9001 and AS9100/9102.</li><li>Strong communication skills to effectively interface with employees at all levels, including management.</li><li>Ability to interpret complex information and respond to a variety of complex quality and inspection issues.</li><li>Ability to work independently and as part of a team, including the flexibility to work extended hours when required.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certification by professional organizations such as ASQ or AWS in quality or inspection disciplines.</li><li>Experience with optical comparators, including Keyence vision systems, scanners, and Micro-Vu equipment.</li><li>Experience with Coordinate Measuring Machines, portable arms, and Laser Tracker equipment (such as LEICA models or similar) for part acceptance.</li><li>Intermediate-level knowledge of coordinate metrology software, including PC-DMIS, Spatial Analyzer, or Polyworks.</li><li>Strong data entry skills and proficiency with the Microsoft Office suite.</li><li>Experience with Department of Defense (DoD) quality assurance program requirements in a manufacturing environment.</li><li>Ability to obtain and maintain DoD clearance is desired.</li><li>Familiarity with statistical process control and other quality control procedures.</li><li>Experience preparing, updating, and maintaining electronic and hard copy quality records, reports, and statistics.</li></ul>Work EnvironmentThis position is based onsite at a manufacturing facility in Tupelo, Mississippi, working on a 4x10 schedule with four ten-hour days each week and Fridays off. The role is performed in a production and inspection environment that involves regular interaction with precision measurement equipment, inspection tools, optical comparators, CMMs, and metrology software. Work may occasionally require travel to customer or vendor locations to conduct inspections or support audits. The environment emphasizes adherence to established safety procedures, regulatory requirements, and quality standards, with a focus on accurate documentation and collaboration across engineering and quality teams.Job Type &amp; LocationThis is a Contract to Hire position based out of Tupelo, MS.Pay and BenefitsThe pay range for this position is $25.77 - $41.35/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Tupelo, MS.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Tupelo,MS.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Inspector - 2nd Shift, 2:30pm-11pm + $1/hr shift differential. Job DescriptionThe Quality Inspector ensures that production assemblies meet all established quality standards by auditing assembly lines, reviewing documentation, and authorizing product release. This role focuses on reinforcing Good Manufacturing Practices and Good Documentation Practices, evaluating nonconforming materials, and supporting continuous improvement within a clean and organized manufacturing environment.Responsibilities<ul><li>Conduct assembly line audits to verify proper equipment set-ups, availability of calibrated tools, and adherence to approved work instructions.</li><li>Reinforce Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) with production personnel to ensure consistent compliance.</li><li>Review each production record (Device History Record, DHR) for completeness, accuracy, and legibility, ensuring records are retained or archived according to Quality System requirements.</li><li>Execute product release activities, including performing independent final inspections, completing sign-offs, and processing system transactions to authorize shipment of conforming assemblies.</li><li>Evaluate nonconforming material, coordinate disposition activities, and document investigations and dispositions in accordance with Quality System requirements.</li><li>Participate in assembly line validations by collecting objective evidence and documenting results for formal approval.</li><li>Maintain operator training records and verify that personnel are qualified before performing assembly tasks.</li><li>Issue quality alerts to production personnel in response to complaints and nonconformances to prevent recurrence.</li><li>Document process deviations and in-process changes and obtain applicable approvals as required by the Quality System.</li><li>Identify work instruction and process gaps and provide information to support continuous improvement initiatives.</li><li>Support evaluation and documentation of rework for assemblies, including product returns, in alignment with Quality System requirements.</li><li>Perform inspections involving sheet metal components and first article inspections using appropriate measurement tools.</li><li>Use calipers, micrometers, gauges, and other measurement devices to verify product dimensions and conformance.</li><li>Apply intermediate-level Geometric Dimensioning &amp; Tolerancing (GD&amp;T) concepts during inspection and documentation activities.</li><li>Collaborate with Material Review Board (MRB) and support Nonconformance management processes.</li><li>Utilize Microsoft Outlook, Microsoft Excel, and electronic ERP or inspection management systems to manage records, track inspections, and support reporting.</li></ul>Essential Skills<ul><li>12 years of experience in a manufacturing environment, preferably in device assembly.</li><li>Ability to read and interpret blueprints and technical drawings.</li><li>Hands-on experience using measurement tools such as calipers, micrometers, and gauges.</li><li>Knowledge of Material Review Board (MRB) processes and Nonconformance management.</li><li>Intermediate-level understanding of Geometric Dimensioning &amp; Tolerancing (GD&amp;T).</li><li>Familiarity with Good Documentation Practices and production record review.</li><li>Proficiency with Microsoft Outlook and Microsoft Excel.</li><li>Experience conducting first article inspections and working with sheet metal components.</li><li>Ability to follow and enforce ISO and Quality System requirements.</li><li>Strong attention to detail and ability to assess product conformity through inspection and documentation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Broad understanding of materials, manufacturing technologies, and production processes is preferred.</li><li>Proficiency with electronic ERP systems and inspection management systems is preferred.</li><li>Experience with CAPA (Corrective and Preventive Action) activities is beneficial.</li><li>Comfort working in an electro-mechanical environment with evolving technologies.</li><li>Strong communication skills to issue quality alerts and collaborate with production personnel.</li><li>Organizational skills to maintain accurate training records and quality documentation.</li><li>Interest in continuous improvement and identifying process and work instruction gaps.</li></ul>Work EnvironmentThis role is based in a very clean, organized manufacturing facility with a cubicle located on the production floor, providing close proximity to the workstations and assembly lines. The position is on a second shift schedule from 2:30 p.m. to 11:00 p.m., with a shift differential added to the hourly pay. The environment offers strong opportunities for growth, including exposure to increasingly electro-mechanical assemblies and the chance to learn new skills. The facility promotes a professional, collaborative atmosphere focused on quality, continuous improvement, and employee development.Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Pay and BenefitsThe pay range for this position is $24.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Milwaukee,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Lab Associate IJob DescriptionThe Quality Lab Associate I primarily supports QC Microbiology Laboratory operations at a pharmaceutical manufacturing facility in Round Lake, IL. This role focuses on biological testing for biologics and drugs throughout all stages of the manufacturing process, including incoming raw materials, in-process samples, finished products, and facility environmental and critical systems microbiological monitoring. The position is a first-shift role with flexible hours between 8:00 a.m. and 5:00 p.m., requires weekend and holiday work, and involves working in both Drug Delivery and Penicillin facilities.Responsibilities<ul><li>Conduct microbial analyses on raw materials, in-process samples, finished products, and samples collected from environmental monitoring programs within the manufacturing facility.</li><li>Perform routine facility environmental monitoring, including surfaces, air, particulate, and personnel monitoring, as well as critical systems monitoring such as water, clean steam, process compressed air, and nitrogen.</li><li>Prepare media and reagents used within the laboratory to support microbiological testing and routine laboratory operations.</li><li>Operate laboratory instrumentation, including particle counters, pH meters, SAS equipment, autoclaves, and computer systems such as LIMS, to collect, record, and manage data.</li><li>Monitor inventory of supplies, equipment, reagents, and media; order, receive, and stock supplies as necessary to ensure uninterrupted laboratory operations.</li><li>Maintain a clean, safe, and organized laboratory area and perform regular laboratory housekeeping activities in accordance with internal procedures and safety standards.</li><li>Conduct and document laboratory and nonconformance investigations, including data review, root cause analysis, impact assessment, and development of appropriate corrective and preventive actions.</li><li>Maintain data integrity and ensure compliance with standard operating procedures, FDA Quality System Regulations, and current Good Manufacturing Practice (cGMP) regulations.</li><li>Follow, understand, and comply with established procedures and policies related to cGMPs and safety requirements.</li><li>Contribute to other laboratory tasks and projects as assigned, supporting team objectives and continuous improvement initiatives.</li><li>Work in both Drug Delivery and Penicillin facilities as needed to support manufacturing and laboratory operations.</li></ul>Essential Skills<ul><li>Ability to perform all essential laboratory duties satisfactorily, including microbiological testing and documentation.</li><li>Must not be allergic to Penicillin, Cephalosporin, or their related products and minerals due to work in Penicillin facilities.</li><li>Knowledge in basic biology and microbiology principles, including aseptic technique.</li><li>Proficiency in Laboratory Information Management Systems (LIMS) for data entry, tracking, and reporting.</li><li>Ability to handle multiple tasks concurrently and complete them in a timely manner while maintaining accuracy.</li><li>Strong attention to detail, conscientious work habits, and high reading comprehension skills for reviewing data and documentation.</li><li>Ability to lift up to 50 pounds when required to handle laboratory supplies and equipment.</li><li>Capability to work independently and as part of a team in a laboratory and manufacturing environment.</li><li>Flexibility to work weekends and holidays as needed to support production and laboratory schedules.</li><li>Bachelors degree in microbiology or biological science.</li><li>Minimum of 2 years of experience in a laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of Good Laboratory Practice (GLP) principles and pharmaceutical aseptic processing cGMP requirements is preferred.</li><li>Demonstrated technical writing skills for documenting investigations, procedures, and reports.</li><li>Familiarity with structured root cause investigation methodologies, including DMAIC (Define, Measure, Analyze, Improve, Control).</li><li>Self-motivation, adaptability, and a positive attitude in a highly dynamic environment.</li><li>Strong organizational skills to manage inventory, documentation, and multiple ongoing tasks.</li><li>Ability to collaborate effectively with cross-functional teams in manufacturing and quality.</li><li>Comfort working in both Drug Delivery and Penicillin facilities and adapting to different process areas.</li></ul>Work EnvironmentThis is a first-shift position with hours typically between 8:00 a.m. and 5:00 p.m., operating on a Thursday through Monday schedule. Weekend and holiday work is required, and occasional off-shift work may be needed to support manufacturing and testing demands. The role is based in a QC Microbiology Laboratory within a pharmaceutical manufacturing facility in Round Lake, IL, and involves work in both Drug Delivery and Penicillin production areas. The environment includes routine exposure to biologics, drugs, and related materials, as well as critical systems such as purified water, clean steam, compressed air, and nitrogen. Laboratory work involves regular use of instrumentation such as particle counters, pH meters, SAS equipment, autoclaves, and computer systems including LIMS. The facility maintains strict cGMP, GLP, and FDA QSR standards, emphasizing data integrity, safety, and cleanliness. Showers are required when leaving the facility, and employees are expected to follow all safety procedures and dress appropriately for a controlled laboratory and manufacturing environment. The work requires standing for extended periods, handling laboratory materials, and occasionally lifting up to 50 pounds in a clean, highly regulated setting.Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Application DeadlineThis position is anticipated to close on Nov 5, 2026.Workplace TypeThis is a fully onsite position in Round Lake,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Lab Associate I

Job Title: QC Lab Associate Job DescriptionThe QC Lab Associate primarily supports QC Microbiology Laboratory operations at a pharmaceutical manufacturing facility in Round Lake, IL. This role focuses on biological testing for biologics and drugs throughout all stages of the manufacturing process, including incoming raw materials, in-process samples, finished products, and facility environmental and critical systems microbiological monitoring. The position is a first-shift role with flexible hours between 8:00 a.m. and 5:00 p.m., requires weekend and holiday work, and involves working in both Drug Delivery and Penicillin facilities.Responsibilities<ul><li>Conduct microbial analyses on raw materials, in-process samples, finished products, and samples collected from environmental monitoring programs within the manufacturing facility.</li><li>Perform routine facility environmental monitoring, including surfaces, air, particulate, and personnel monitoring, as well as critical systems monitoring such as water, clean steam, process compressed air, and nitrogen.</li><li>Prepare media and reagents used within the laboratory to support microbiological testing and routine laboratory operations.</li><li>Operate laboratory instrumentation, including particle counters, pH meters, SAS equipment, autoclaves, and computer systems such as LIMS, to collect, record, and manage data.</li><li>Monitor inventory of supplies, equipment, reagents, and media; order, receive, and stock supplies as necessary to ensure uninterrupted laboratory operations.</li><li>Maintain a clean, safe, and organized laboratory area and perform regular laboratory housekeeping activities in accordance with internal procedures and safety standards.</li><li>Conduct and document laboratory and nonconformance investigations, including data review, root cause analysis, impact assessment, and development of appropriate corrective and preventive actions.</li><li>Maintain data integrity and ensure compliance with standard operating procedures, FDA Quality System Regulations, and current Good Manufacturing Practice (cGMP) regulations.</li><li>Follow, understand, and comply with established procedures and policies related to cGMPs and safety requirements.</li><li>Contribute to other laboratory tasks and projects as assigned, supporting team objectives and continuous improvement initiatives.</li><li>Work in both Drug Delivery and Penicillin facilities as needed to support manufacturing and laboratory operations.</li></ul>Essential Skills<ul><li>Ability to perform all essential laboratory duties satisfactorily, including microbiological testing and documentation.</li><li>Must not be allergic to Penicillin, Cephalosporin, or their related products and minerals due to work in Penicillin facilities.</li><li>Knowledge in basic biology and microbiology principles, including aseptic technique.</li><li>Proficiency in Laboratory Information Management Systems (LIMS) for data entry, tracking, and reporting.</li><li>Ability to handle multiple tasks concurrently and complete them in a timely manner while maintaining accuracy.</li><li>Strong attention to detail, conscientious work habits, and high reading comprehension skills for reviewing data and documentation.</li><li>Ability to lift up to 50 pounds when required to handle laboratory supplies and equipment.</li><li>Capability to work independently and as part of a team in a laboratory and manufacturing environment.</li><li>Flexibility to work weekends and holidays as needed to support production and laboratory schedules.</li><li>Bachelors degree in microbiology or biological science.</li><li>Minimum of 2 years of experience in a laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of Good Laboratory Practice (GLP) principles and pharmaceutical aseptic processing cGMP requirements is preferred.</li><li>Demonstrated technical writing skills for documenting investigations, procedures, and reports.</li><li>Familiarity with structured root cause investigation methodologies, including DMAIC (Define, Measure, Analyze, Improve, Control).</li><li>Self-motivation, adaptability, and a positive attitude in a highly dynamic environment.</li><li>Strong organizational skills to manage inventory, documentation, and multiple ongoing tasks.</li><li>Ability to collaborate effectively with cross-functional teams in manufacturing and quality.</li><li>Comfort working in both Drug Delivery and Penicillin facilities and adapting to different process areas.</li></ul>Work EnvironmentThis is a first-shift position with hours typically between 8:00 a.m. and 5:00 p.m., operating on a Thursday through Monday schedule. Weekend and holiday work is required, and occasional off-shift work may be needed to support manufacturing and testing demands. The role is based in a QC Microbiology Laboratory within a pharmaceutical manufacturing facility in Round Lake, IL, and involves work in both Drug Delivery and Penicillin production areas. The environment includes routine exposure to biologics, drugs, and related materials, as well as critical systems such as purified water, clean steam, compressed air, and nitrogen. Laboratory work involves regular use of instrumentation such as particle counters, pH meters, SAS equipment, autoclaves, and computer systems including LIMS. The facility maintains strict cGMP, GLP, and FDA QSR standards, emphasizing data integrity, safety, and cleanliness. Showers are required when leaving the facility, and employees are expected to follow all safety procedures and dress appropriately for a controlled laboratory and manufacturing environment. The work requires standing for extended periods, handling laboratory materials, and occasionally lifting up to 50 pounds in a clean, highly regulated setting.Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Application DeadlineThis position is anticipated to close on Nov 6, 2026.Workplace TypeThis is a fully onsite position in Round Lake,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Lab Associate Job DescriptionThe QC Lab Associate primarily supports QC Microbiology Laboratory operations at a pharmaceutical manufacturing facility in Round Lake, IL. This role focuses on biological testing for biologics and drugs throughout all stages of the manufacturing process, including incoming raw materials, in-process samples, finished products, and facility environmental and critical systems microbiological monitoring. The position is a first-shift role with flexible hours between 8:00 a.m. and 5:00 p.m., requires weekend and holiday work, and involves working in both Drug Delivery and Penicillin facilities.Responsibilities<ul><li>Conduct microbial analyses on raw materials, in-process samples, finished products, and samples collected from environmental monitoring programs within the manufacturing facility.</li><li>Perform routine facility environmental monitoring, including surfaces, air, particulate, and personnel monitoring, as well as critical systems monitoring such as water, clean steam, process compressed air, and nitrogen.</li><li>Prepare media and reagents used within the laboratory to support microbiological testing and routine laboratory operations.</li><li>Operate laboratory instrumentation, including particle counters, pH meters, SAS equipment, autoclaves, and computer systems such as LIMS, to collect, record, and manage data.</li><li>Monitor inventory of supplies, equipment, reagents, and media; order, receive, and stock supplies as necessary to ensure uninterrupted laboratory operations.</li><li>Maintain a clean, safe, and organized laboratory area and perform regular laboratory housekeeping activities in accordance with internal procedures and safety standards.</li><li>Conduct and document laboratory and nonconformance investigations, including data review, root cause analysis, impact assessment, and development of appropriate corrective and preventive actions.</li><li>Maintain data integrity and ensure compliance with standard operating procedures, FDA Quality System Regulations, and current Good Manufacturing Practice (cGMP) regulations.</li><li>Follow, understand, and comply with established procedures and policies related to cGMPs and safety requirements.</li><li>Contribute to other laboratory tasks and projects as assigned, supporting team objectives and continuous improvement initiatives.</li><li>Work in both Drug Delivery and Penicillin facilities as needed to support manufacturing and laboratory operations.</li></ul>Essential Skills<ul><li>Ability to perform all essential laboratory duties satisfactorily, including microbiological testing and documentation.</li><li>Must not be allergic to Penicillin, Cephalosporin, or their related products and minerals due to work in Penicillin facilities.</li><li>Knowledge in basic biology and microbiology principles, including aseptic technique.</li><li>Proficiency in Laboratory Information Management Systems (LIMS) for data entry, tracking, and reporting.</li><li>Ability to handle multiple tasks concurrently and complete them in a timely manner while maintaining accuracy.</li><li>Strong attention to detail, conscientious work habits, and high reading comprehension skills for reviewing data and documentation.</li><li>Ability to lift up to 50 pounds when required to handle laboratory supplies and equipment.</li><li>Capability to work independently and as part of a team in a laboratory and manufacturing environment.</li><li>Flexibility to work weekends and holidays as needed to support production and laboratory schedules.</li><li>Bachelors degree in microbiology or biological science.</li><li>Minimum of 2 years of experience in a laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of Good Laboratory Practice (GLP) principles and pharmaceutical aseptic processing cGMP requirements is preferred.</li><li>Demonstrated technical writing skills for documenting investigations, procedures, and reports.</li><li>Familiarity with structured root cause investigation methodologies, including DMAIC (Define, Measure, Analyze, Improve, Control).</li><li>Self-motivation, adaptability, and a positive attitude in a highly dynamic environment.</li><li>Strong organizational skills to manage inventory, documentation, and multiple ongoing tasks.</li><li>Ability to collaborate effectively with cross-functional teams in manufacturing and quality.</li><li>Comfort working in both Drug Delivery and Penicillin facilities and adapting to different process areas.</li></ul>Work EnvironmentThis is a first-shift position with hours typically between 8:00 a.m. and 5:00 p.m., operating on a Thursday through Monday schedule. Weekend and holiday work is required, and occasional off-shift work may be needed to support manufacturing and testing demands. The role is based in a QC Microbiology Laboratory within a pharmaceutical manufacturing facility in Round Lake, IL, and involves work in both Drug Delivery and Penicillin production areas. The environment includes routine exposure to biologics, drugs, and related materials, as well as critical systems such as purified water, clean steam, compressed air, and nitrogen. Laboratory work involves regular use of instrumentation such as particle counters, pH meters, SAS equipment, autoclaves, and computer systems including LIMS. The facility maintains strict cGMP, GLP, and FDA QSR standards, emphasizing data integrity, safety, and cleanliness. Showers are required when leaving the facility, and employees are expected to follow all safety procedures and dress appropriately for a controlled laboratory and manufacturing environment. The work requires standing for extended periods, handling laboratory materials, and occasionally lifting up to 50 pounds in a clean, highly regulated setting.Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Application DeadlineThis position is anticipated to close on Nov 11, 2026.Workplace TypeThis is a fully onsite position in Round Lake,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Lab Associate Job DescriptionThe QC Lab Associate primarily supports QC Microbiology Laboratory operations at a pharmaceutical manufacturing facility in Round Lake, IL. This role focuses on biological testing for biologics and drugs throughout all stages of the manufacturing process, including incoming raw materials, in-process samples, finished products, and facility environmental and critical systems microbiological monitoring. The position is a first-shift role with flexible hours between 8:00 a.m. and 5:00 p.m., requires weekend and holiday work, and involves working in both Drug Delivery and Penicillin facilities.Responsibilities<ul><li>Conduct microbial analyses on raw materials, in-process samples, finished products, and samples collected from environmental monitoring programs within the manufacturing facility.</li><li>Perform routine facility environmental monitoring, including surfaces, air, particulate, and personnel monitoring, as well as critical systems monitoring such as water, clean steam, process compressed air, and nitrogen.</li><li>Prepare media and reagents used within the laboratory to support microbiological testing and routine laboratory operations.</li><li>Operate laboratory instrumentation, including particle counters, pH meters, SAS equipment, autoclaves, and computer systems such as LIMS, to collect, record, and manage data.</li><li>Monitor inventory of supplies, equipment, reagents, and media; order, receive, and stock supplies as necessary to ensure uninterrupted laboratory operations.</li><li>Maintain a clean, safe, and organized laboratory area and perform regular laboratory housekeeping activities in accordance with internal procedures and safety standards.</li><li>Conduct and document laboratory and nonconformance investigations, including data review, root cause analysis, impact assessment, and development of appropriate corrective and preventive actions.</li><li>Maintain data integrity and ensure compliance with standard operating procedures, FDA Quality System Regulations, and current Good Manufacturing Practice (cGMP) regulations.</li><li>Follow, understand, and comply with established procedures and policies related to cGMPs and safety requirements.</li><li>Contribute to other laboratory tasks and projects as assigned, supporting team objectives and continuous improvement initiatives.</li><li>Work in both Drug Delivery and Penicillin facilities as needed to support manufacturing and laboratory operations.</li></ul>Essential Skills<ul><li>Ability to perform all essential laboratory duties satisfactorily, including microbiological testing and documentation.</li><li>Must not be allergic to Penicillin, Cephalosporin, or their related products and minerals due to work in Penicillin facilities.</li><li>Knowledge in basic biology and microbiology principles, including aseptic technique.</li><li>Proficiency in Laboratory Information Management Systems (LIMS) for data entry, tracking, and reporting.</li><li>Ability to handle multiple tasks concurrently and complete them in a timely manner while maintaining accuracy.</li><li>Strong attention to detail, conscientious work habits, and high reading comprehension skills for reviewing data and documentation.</li><li>Ability to lift up to 50 pounds when required to handle laboratory supplies and equipment.</li><li>Capability to work independently and as part of a team in a laboratory and manufacturing environment.</li><li>Flexibility to work weekends and holidays as needed to support production and laboratory schedules.</li><li>Bachelors degree in microbiology or biological science.</li><li>Minimum of 2 years of experience in a laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of Good Laboratory Practice (GLP) principles and pharmaceutical aseptic processing cGMP requirements is preferred.</li><li>Demonstrated technical writing skills for documenting investigations, procedures, and reports.</li><li>Familiarity with structured root cause investigation methodologies, including DMAIC (Define, Measure, Analyze, Improve, Control).</li><li>Self-motivation, adaptability, and a positive attitude in a highly dynamic environment.</li><li>Strong organizational skills to manage inventory, documentation, and multiple ongoing tasks.</li><li>Ability to collaborate effectively with cross-functional teams in manufacturing and quality.</li><li>Comfort working in both Drug Delivery and Penicillin facilities and adapting to different process areas.</li></ul>Work EnvironmentThis is a first-shift position with hours typically between 8:00 a.m. and 5:00 p.m., operating on a Thursday through Monday schedule. Weekend and holiday work is required, and occasional off-shift work may be needed to support manufacturing and testing demands. The role is based in a QC Microbiology Laboratory within a pharmaceutical manufacturing facility in Round Lake, IL, and involves work in both Drug Delivery and Penicillin production areas. The environment includes routine exposure to biologics, drugs, and related materials, as well as critical systems such as purified water, clean steam, compressed air, and nitrogen. Laboratory work involves regular use of instrumentation such as particle counters, pH meters, SAS equipment, autoclaves, and computer systems including LIMS. The facility maintains strict cGMP, GLP, and FDA QSR standards, emphasizing data integrity, safety, and cleanliness. Showers are required when leaving the facility, and employees are expected to follow all safety procedures and dress appropriately for a controlled laboratory and manufacturing environment. The work requires standing for extended periods, handling laboratory materials, and occasionally lifting up to 50 pounds in a clean, highly regulated setting.Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Application DeadlineThis position is anticipated to close on Nov 2, 2026.Workplace TypeThis is a fully onsite position in Round Lake,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality Laboratory ManagerJob DescriptionThis role leads a brand-new quality laboratory within a metal finishing, electroplating, and surface treatment manufacturing environment. The Quality Laboratory Manager oversees all laboratory operations and provides technical leadership for quality, analytical chemistry, and process control. The position works closely with production and quality teams to maintain plating chemistry, resolve process issues, improve product quality, and ensure compliance with internal standards and external regulations.Responsibilities<ul><li>Lead and manage daily laboratory operations, including scheduling, testing priorities, staffing, documentation, and equipment needs.</li><li>Supervise, train, and develop laboratory technicians and assigned quality personnel, fostering a strong culture of safety, quality, and continuous improvement.</li><li>Oversee chemical analysis and process control for plating baths, pretreatment systems, passivates, sealers, rinses, wastewater, and incoming chemicals.</li><li>Review analytical results and determine appropriate chemical additions or process adjustments to maintain stable operating conditions and product quality.</li><li>Monitor plating chemistry and process trends to ensure consistent performance and adherence to specifications.</li><li>Partner closely with production and quality teams to troubleshoot plating defects, chemistry issues, and process deviations.</li><li>Oversee operation, calibration, maintenance, and troubleshooting of analytical equipment, including ICP-OES, ICP-MS, and other laboratory instrumentation.</li><li>Lead root-cause investigations and implement corrective and preventive actions related to quality concerns, customer complaints, and process failures.</li><li>Maintain and update laboratory procedures, testing methods, calibration records, and quality documentation in alignment with quality management systems.</li><li>Support internal audits, customer audits, and quality-system audits by providing accurate laboratory data and documentation.</li><li>Ensure laboratory compliance with chemical safety, environmental, wastewater, and regulatory requirements.</li><li>Monitor laboratory performance, chemical usage, testing accuracy, and key quality metrics to ensure reliable and efficient operations.</li><li>Identify and implement opportunities to improve process control, laboratory efficiency, product quality, and operating costs.</li><li>Contribute to building and establishing workflows, standards, and best practices in a new laboratory within a new facility.</li></ul>Essential Skills<ul><li>Bachelors degree in Chemistry, Chemical Technology, Materials Science, Chemical Engineering, or a related scientific or technical discipline.</li><li>At least 5 years of experience in an industrial laboratory, manufacturing laboratory, chemical processing, or quality environment.</li><li>Previous experience in laboratory leadership, supervision, or management.</li><li>Strong knowledge of analytical chemistry, wet chemistry, titration, and chemical process control.</li><li>Demonstrated ability to interpret laboratory results and make appropriate process or chemical adjustments based on analytical data.</li><li>Hands-on experience with laboratory instrumentation such as ICP-OES and/or ICP-MS.</li><li>Proven troubleshooting, root-cause analysis, and problem-solving skills in a technical environment.</li><li>Experience with quality assurance, quality control, and quality management systems.</li><li>Strong communication skills, with the ability to collaborate effectively with production, quality, and laboratory teams.</li><li>Strong organizational skills and attention to detail in managing documentation, testing schedules, and laboratory records.</li><li>Ability to lead, mentor, and develop laboratory and quality personnel.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in electroplating, metal finishing, coatings, surface treatment, or specialty chemical manufacturing.</li><li>Experience supporting zinc, zinc-nickel, zinc-iron, or similar plating processes.</li><li>Knowledge of plating baths, pretreatment processes, passivation, sealing, coating thickness measurement, and corrosion testing.</li><li>Experience with wastewater treatment operations and environmental compliance requirements.</li><li>Familiarity with quality systems such as IATF and ISO 9001.</li><li>Knowledge of statistical process control (SPC), measurement system analysis (MSA), 8D problem solving, Lean, Six Sigma, or other continuous-improvement methodologies.</li><li>Experience supporting automotive or other high-volume manufacturing environments.</li><li>Interest in a hands-on laboratory leadership role within a new facility and new laboratory setup.</li></ul>Work EnvironmentThe role involves a combination of laboratory and production floor responsibilities in a metal finishing and electroplating manufacturing setting. You will frequently interact with manufacturing personnel and process equipment while working with chemicals, industrial machinery, and active production lines. Personal protective equipment (PPE) is required and provided, reflecting a strong emphasis on safety. The position requires the ability to stand and walk for extended periods, climb stairs, and occasionally lift up to 40 pounds. You will work in a modern, brand-new facility and laboratory, offering a hands-on environment where you can shape laboratory practices, systems, and culture in close collaboration with operations and quality teams.Job Type &amp; LocationThis is a Permanent position based out of Fort Wayne, IN.Pay and BenefitsThe pay range for this position is $80000.00 - $120000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.holiday pay, health, dental, vision, 401k, paid time off.Job Type &amp; LocationThis is a Permanent position based out of Fort Wayne, IN.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Fort Wayne,IN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Lab Manager

Job Title: Quality Laboratory SpecialistJob DescriptionThe Quality Laboratory Specialist supports quality assurance and quality control activities within a manufacturing environment. This role performs physical, chemical, and analytical testing on raw materials, in-process batches, compounded products, and finished goods to ensure they meet established specifications and quality standards. The specialist serves as a key laboratory resource, providing technical support to manufacturing operations, maintaining accurate documentation, and helping ensure product quality throughout the production process. This position offers the opportunity to operate as the sole laboratory professional on site, with strong potential for growth and development.Responsibilities<ul><li>Perform physical, chemical, and analytical testing on raw materials, in-process batches, compounded products, and finished goods using established laboratory methods and procedures.</li><li>Conduct quality inspections and testing, including measurements such as pH, viscosity, specific gravity, appearance, concentration, and other product-specific characteristics.</li><li>Evaluate test results, identify trends or out-of-specification conditions, and support the implementation of corrective actions when quality concerns arise.</li><li>Perform incoming raw material inspections and release testing to verify compliance with specifications before materials are used in production.</li><li>Support manufacturing operations by providing quality guidance, troubleshooting product and process issues, and assisting with quality-related investigations.</li><li>Maintain accurate laboratory records, certificates of analysis, testing reports, and other quality documentation in accordance with internal procedures and regulatory expectations.</li><li>Operate, calibrate, maintain, and troubleshoot laboratory equipment to ensure reliable and consistent test results.</li><li>Manage laboratory chemical inventory and ensure compliance with storage, labeling, and shelf-life requirements.</li><li>Assist with nonconformance investigations, root cause analysis, corrective and preventive action (CAPA) activities, internal audits, and continuous improvement initiatives.</li><li>Coordinate material holds and communicate quality concerns to appropriate stakeholders to prevent the release or shipment of nonconforming products.</li><li>Prepare customer, production, and sales support samples as needed to support business and operational requirements.</li><li>Follow all safety, quality, and regulatory requirements while maintaining a clean, organized, and compliant laboratory environment.</li></ul>Essential Skills<ul><li>3+ years of laboratory, quality control, or quality assurance experience in a manufacturing environment.</li><li>Experience performing analytical testing, quality inspections, and maintaining laboratory documentation.</li><li>Knowledge of quality systems, nonconformance investigations, and continuous improvement methodologies.</li><li>Hands-on experience with laboratory chemistry and biochemistry techniques.</li><li>Experience working with quality control and quality assurance processes in a manufacturing or industrial setting.</li><li>Familiarity with Good Manufacturing Practices (GMP) and their application in a laboratory and production environment.</li><li>Ability to operate, calibrate, and troubleshoot laboratory equipment, including analytical instruments such as HPLC or similar technologies.</li><li>Strong analytical and problem-solving skills with the ability to interpret test data and identify trends or issues.</li><li>Strong organizational skills with the ability to manage multiple priorities and tasks independently.</li><li>Effective written and verbal communication skills for documenting results and collaborating with cross-functional teams.</li><li>Ability to work independently as the primary laboratory resource on site while supporting a broader manufacturing team.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in Chemistry, Chemical Technology, Laboratory Science, or a related technical field preferred; equivalent experience considered.</li><li>Experience with HPLC and other analytical chemistry techniques.</li><li>Experience supporting CAPA activities, internal audits, and continuous improvement projects.</li><li>Familiarity with laboratory chemical inventory management and shelf-life control.</li><li>Comfort working in both laboratory and manufacturing environments.</li><li>Demonstrated ability to prioritize work, meet deadlines, and adapt to changing production needs.</li><li>Interest in professional growth and development within a quality and laboratory-focused career path.</li></ul>Work EnvironmentThe role operates in both laboratory and manufacturing settings with regular exposure to industrial chemicals, laboratory equipment, and production processes. The position requires the ability to stand, walk, and perform routine laboratory activities for extended periods. Appropriate personal protective equipment (PPE) is required and provided, and adherence to safety procedures is essential. The environment emphasizes cleanliness, organization, and compliance with safety and quality standards. Work hours follow a standard schedule, with occasional overtime or weekend work that may be required based on production needs. As the sole laboratory specialist on site, the role offers a high level of ownership and responsibility within a collaborative manufacturing operation.Job Type &amp; LocationThis is a Contract to Hire position based out of Huntington, IN.Pay and BenefitsThe pay range for this position is $25.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Huntington, IN.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Huntington,IN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Lab Specialist

Job Title: Quality Lab TechnicianJob DescriptionThe Quality Laboratory Technician is responsible for performing routine laboratory testing and inspection activities that support the manufacture and packaging of aerospace and medical adhesives. This position ensures raw materials, in-process materials, intermediates, and finished products meet established quality standards and customer specifications.Responsibilities<ul><li>Conduct physical property testing including viscosity, density, color, cure characteristics, and other product-specific quality evaluations.</li><li>Record and report test results accurately and promptly.</li><li>Notify Quality Leadership and Production personnel of out-of-specification results or quality concerns.</li><li>Maintain accurate laboratory records and test documentation in accordance with quality system requirements.</li><li>Enter test results and quality data into SAP and other electronic systems.</li><li>Support preparation of Certificates of Analysis (COAs) and product quality documentation.</li><li>Maintain retained samples and associated records in accordance with established procedures.</li><li>Ensure complete traceability of laboratory data and testing processes.</li><li>Maintain laboratory equipment in a clean and organized condition.</li><li>Perform routine calibration checks, equipment verification, and basic troubleshooting activities.</li><li>Assist with inventory management of laboratory supplies, standards, and consumables.</li><li>Support housekeeping activities and maintain a safe laboratory environment.</li><li>Ensure all laboratory work is performed in compliance with safety and environmental requirements.</li><li>Follow AS9100, NADCAP, ISO 9001, customer specifications, and internal quality procedures.</li><li>Support internal audits, customer audits, and accreditation activities as requested.</li><li>Assist with investigations involving non-conforming products, customer complaints, and process deviations.</li><li>Participate in continuous improvement activities focused on quality, safety, and laboratory efficiency.</li></ul>Essential Skills<ul><li>Proficiency in Chemistry, Quality Control, and GMP.</li><li>Bachelor's Degree in Chemistry, Materials Science, or a Scientific Discipline.</li><li>1-2 years of experience in quality or manufacturing in a regulated industry.</li><li>Ability to follow written procedures, specifications, and test methods.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with SAP preferred.</li></ul>Work EnvironmentThe position involves working in a lab environment and office space, collaborating with a small team. The role requires compliance with safety standards and maintaining a clean and organized work area.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $28.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Irvine,CA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Lab Technician

Job Title: Quality Lab TechnicianJob DescriptionThe Quality Lab Technician will support the manufacturing quality laboratory by performing physical testing in the lab. This role involves operating metrology instruments, collecting data, and comparing it against defined criteria for disposition, including thickness, density, roughness, durometer, SEM, and confocal microscope. The technician will perform routine and non-routine inspections, collect, analyze, and document results in accordance with quality procedures, and compare testing results to established specifications and acceptance criteria. The technician will support product disposition activities by accurately reporting lab findings.Responsibilities<ul><li>Operate and maintain laboratory instrumentation such as Scanning Electron Microscope, Confocal Microscope, Thickness Measurement Systems, Surface Roughness Measurement Equipment, Density Testing Equipment, and Durometer Hardness Testers.</li><li>Complete testing documentation and maintain accurate laboratory records.</li><li>Run tests, input data into the system, analyze and interpret results.</li><li>Collect, analyze, and document results according to quality procedures.</li><li>Compare testing results to established specifications and acceptance criteria.</li></ul>Essential Skills<ul><li>Bachelor's degree in Chemistry, Material Science, Biology, or related science/engineering degree.</li><li>Previous experience working in a manufacturing quality lab.</li><li>Hands-on experience operating laboratory or metrology instrumentation.</li><li>Strong attention to detail and data accuracy.</li><li>Experience documenting results and working within quality systems.</li><li>Ability to interpret specifications and compare results against acceptance criteria.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prefer experience with SEM and/or confocal microscopy.</li><li>Experience in a materials characterization lab, specialty chemical manufacturing, or advanced manufacturing environments.</li><li>Knowledge of metrology.</li><li>Experience working within ISO-regulated manufacturing environments.</li><li>Familiarity with statistical analysis and quality tools.</li></ul>Work EnvironmentThe role is based in a quality lab with working hours from Monday to Friday, 10AM-6PM. There is an opportunity for flexible scheduling if preferred. The company is hiring for several positions across departments due to increased sales growth, offering contractors the chance to apply for full-time roles.Job Type &amp; LocationThis is a Contract position based out of Aurora, IL.Pay and BenefitsThe pay range for this position is $25.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Aurora, IL.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Aurora,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Laboratory Technician - Quality and Food SafetyJob DescriptionWe are seeking a dedicated Laboratory Technician to support quality and food safety operations within a dynamic manufacturing environment. This role involves testing raw materials, in-process samples, and finished products to ensure they meet established quality and safety specifications. The position requires hands-on involvement with routine analytical and sensory testing, documentation of results, equipment maintenance, and effective communication with production and quality teams. Strong attention to detail, organizational skills, and the ability to work independently are essential.Responsibilities<ul><li>Perform routine laboratory testing on in-process and finished product samples.</li><li>Conduct analytical and sensory testing according to established procedures and record, review, and enter test results into laboratory systems.</li><li>Identify results that fall outside expected specifications and promptly communicate concerns to appropriate personnel.</li><li>Collect, receive, label, handle, store, and retain laboratory samples according to established procedures.</li><li>Follow Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), HACCP, and applicable food safety requirements.</li><li>Follow laboratory SOPs and standardized testing methods.</li><li>Perform routine checks and verifications of laboratory equipment, testing methods, instruments, and standards.</li><li>Maintain, calibrate, and troubleshoot laboratory equipment as needed.</li><li>Safely handle and store chemicals, solutions, compressed gases, and other laboratory materials according to applicable safety procedures and Safety Data Sheets.</li><li>Maintain accurate laboratory records and documentation.</li><li>Monitor testing supplies and communicate inventory or reordering needs.</li><li>Compare analytical results against established specifications to verify product quality.</li><li>Participate in proficiency testing and other quality-control activities.</li><li>Maintain a clean, organized, and professional laboratory workspace.</li><li>Communicate effectively with Quality, Production, Operations, and other departments.</li><li>Assist with training other laboratory personnel as needed.</li><li>Follow all environmental, health, food safety, and workplace safety procedures.</li><li>Perform additional laboratory and quality-related responsibilities as assigned.</li></ul>Essential Skills<ul><li>Quality control</li><li>Laboratory operations</li><li>Chemistry</li><li>Biology</li><li>Quality assurance</li><li>Wet chemistry</li><li>Titration</li><li>Good Manufacturing Practices (GMP)</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma or GED required.</li><li>Associates or Bachelors degree in Biology, Chemistry, Food Science, Laboratory Science, or another applied science preferred.</li><li>1+ years of previous laboratory, quality-control, food manufacturing, or analytical testing experience preferred.</li><li>Strong attention to detail and ability to accurately document test results.</li><li>Basic math skills and ability to read, write, and communicate effectively in English.</li><li>Ability to follow written procedures, testing methods, and safety requirements.</li><li>Comfortable working independently while also contributing to a team environment.</li><li>Ability to manage multiple tasks and maintain organization in a fast-paced setting.</li><li>Basic computer proficiency, including Microsoft Office and laboratory or instrument software.</li><li>Willingness to learn new testing procedures, equipment, and quality processes.</li><li>Reliable attendance and ability to work the required schedule.</li></ul>Work EnvironmentThe work environment is a laboratory setting within a manufacturing plant, requiring the ability to stand, walk, and sit for extended periods. The role involves bending, kneeling, climbing stairs, and other physical activities associated with a manufacturing laboratory environment. The position requires lifting and moving up to 50 pounds and safely working with laboratory chemicals and compressed gases. There may be exposure to chemicals, food ingredients, and potential allergens. The role requires flexibility to work weekends and holidays when needed. The typical schedule is Thursday to Monday, 6 am to 2 pm.Job Type &amp; LocationThis is a Contract to Hire position based out of Frankfort, IN.Pay and BenefitsThe pay range for this position is $22.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Frankfort, IN.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Frankfort,IN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h2 style="text-align:center;">Quality Technician </h2>Job DescriptionThe Quality Technician supports a dairy manufacturing facility that produces milk, flavored milks, and cultured dairy products by performing routine testing on in-process and finished products to ensure they meet established food safety and quality standards. This role focuses on laboratory testing, accurate documentation, and close collaboration with production and quality teams to maintain consistent product quality and regulatory compliance.Responsibilities<ul><li>Collect in-process and finished product samples from the production line to verify that quality and safety standards are consistently met.</li><li>Perform basic analytical testing, including pH measurements, wet chemistry techniques, and basic microbiological testing on dairy products.</li><li>Use laboratory equipment and pipetting techniques accurately to conduct analyses and generate reliable test results.</li><li>Document and record all test results clearly and accurately in accordance with company procedures and applicable regulatory standards.</li><li>Support other technicians by assisting with daily lab activities and contributing to efficient lab operations and workflow.</li><li>Participate in organoleptic (taste) testing of dairy products as part of overall quality evaluation and product assessment.</li><li>Maintain a clean, organized, and compliant laboratory environment by following good laboratory practices and housekeeping standards.</li><li>Follow standard operating procedures and quality protocols to ensure consistent testing practices and data integrity.</li><li>Collaborate with production personnel to communicate test results, support troubleshooting, and help resolve quality-related issues.</li><li>Demonstrate a quality-focused mindset and a long-term commitment to building a career in food quality and safety.</li></ul>Essential Skills<ul><li>Bachelors degree in a science-related field such as Biology, Chemistry, Food Science, or a closely related discipline preferred.</li><li>Quality control and quality assurance mindset with strong attention to detail.</li><li>Basic understanding of laboratory practices, including safe handling of samples and equipment, or a strong willingness to learn.</li><li>Comfort working in a fast-paced manufacturing environment while managing multiple tasks and priorities.</li><li>Ability to follow standard operating procedures precisely and maintain accurate records.</li><li>Comfort with consuming dairy products as part of organoleptic (taste) testing for product evaluation.</li><li>Strong communication skills and the ability to work effectively with both laboratory and production teams.</li><li>Interest in building a long-term career in quality, food safety, or food science within a manufacturing setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior laboratory or quality experience in food, beverage, or manufacturing environments is a plus but not required; entry-level candidates are welcome.</li><li>Experience or coursework in food safety, food science, or related disciplines is beneficial.</li><li>Familiarity with wet chemistry techniques, pH testing, and basic microbiological methods is advantageous.</li><li>Comfort using laboratory equipment and pipetting techniques to perform routine analyses.</li><li>Demonstrated ability to be quality minded, reliable, and committed to continuous learning.</li><li>Ability to build positive working relationships and communicate clearly with a relatively new team.</li><li>Openness to working 2nd shift hours and maintaining consistent attendance.</li></ul>Work EnvironmentThis role is primarily based in a laboratory within a dairy manufacturing facility that produces milk, flavored milks, and cultured dairy products. The Quality Technician works closely with a relatively new and collaborative team, where clear communication and an easygoing, professional demeanor are important. While most tasks take place in the lab, the role also requires regularly going out onto the production floor to collect samples and interact with production staff. The environment is fast paced and production-oriented, with exposure to typical food manufacturing conditions such as chilled areas, processing equipment, and active production lines. The position follows 2nd shift hours, and the dress code aligns with standard food manufacturing and laboratory expectations, including appropriate hygiene and safety attireJob Type &amp; LocationThis is a Contract position based out of O Fallon, IL.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of O Fallon, IL.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in O Fallon,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Lab Technician ($17/hr) - Lubbock, TX<h3>Overview</h3>As a Quality Lab Technician, you will perform testing and inspections on seed samples to help ensure product quality, accuracy, and consistency throughout the production process.Estimated Start Date: November 23, 2026<h3>Key Responsibilities</h3><ul><li>Perform visual quality inspections on seed samples</li><li>Conduct lab testing (pH, moisture, protein assays, titrations)</li><li>Complete germination testing (warm &amp; cool)</li><li>Analyze seed purity and perform accurate seed counts</li><li>Collect and organize product samples</li></ul><h3>Requirements</h3><ul><li>High school diploma or GED</li><li>Degree in Agriculture, Plant Science, Natural Science, Chemistry, Biology or Science related field is a plus**</li><li>Experience in quality inspection, lab work, or agriculture preferred</li><li>Experience with seed testing, farm work, or manufacturing QC</li><li>Basic knowledge of biology, chemistry, or QC processes</li><li>Must provide Passport or Birth Certificate for onboarding</li></ul>Job Type &amp; LocationThis is a Contract position based out of Shallowater, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Shallowater, TX.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Shallowater,TX.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Laboratory Technician

Quality Lab Technician ($17/hr) - Lubbock, TX<h3></h3><h3>Overview</h3>As a Quality Lab Technician, you will perform testing and inspections on seed samples to help ensure product quality, accuracy, and consistency throughout the production process.Estimated Start Date: November 23, 2026<h3>Key Responsibilities</h3><ul><li>Perform visual quality inspections on seed samples</li><li>Conduct lab testing (pH, moisture, protein assays, titrations)</li><li>Complete germination testing (warm &amp; cool)</li><li>Analyze seed purity and perform accurate seed counts</li><li>Collect and organize product samples</li></ul><h3>Requirements</h3><ul><li>High school diploma or GED</li><li>Degree in Agriculture, Plant Science, Natural Science, Chemistry, Biology or Science related field is a plus**</li><li>Experience in quality inspection, lab work, or agriculture preferred</li><li>Experience with seed testing, farm work, or manufacturing QC</li><li>Basic knowledge of biology, chemistry, or QC processes</li><li>Must provide Passport or Birth Certificate for onboarding</li></ul>Job Type &amp; LocationThis is a Contract position based out of Lubbock, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Lubbock, TX.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Lubbock,TX.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Lab Technician ($17/hr) - Lubbock, TX<h3>Overview</h3>As a Quality Lab Technician, you will perform testing and inspections on seed samples to help ensure product quality, accuracy, and consistency throughout the production process.Estimated Start Date: November 23, 2026<h3>Key Responsibilities</h3><ul><li>Perform visual quality inspections on seed samples</li><li>Conduct lab testing (pH, moisture, protein assays, titrations)</li><li>Complete germination testing (warm &amp; cool)</li><li>Analyze seed purity and perform accurate seed counts</li><li>Collect and organize product samples</li></ul><h3>Requirements</h3><ul><li>High school diploma or GED</li><li>Degree in Agriculture, Plant Science, Natural Science, Chemistry, Biology or Science related field is a plus**</li><li>Experience in quality inspection, lab work, or agriculture preferred</li><li>Experience with seed testing, farm work, or manufacturing QC</li><li>Basic knowledge of biology, chemistry, or QC processes</li><li>Must provide Passport or Birth Certificate for onboarding</li></ul>Job Type &amp; LocationThis is a Contract position based out of Idalou, TX.Pay and BenefitsThe pay range for this position is $17.00 - $17.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Idalou, TX.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Idalou,TX.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Quality LeadJob DescriptionThe Parts Quality Lead is responsible for driving supplier and part quality throughout the new model development lifecycle, ensuring all outsourced components meet stringent quality, manufacturing, and performance requirements before mass production launch. This role serves as the primary quality liaison among suppliers, engineering, purchasing, manufacturing, research and development, supply chain, and program teams. The Parts Quality Lead leads part maturation, supplier readiness, risk reduction, corrective actions, and final part approval while providing clear, timely status updates to quality leadership.Responsibilities<ul><li>Lead supplier quality activities throughout the new model development process and ensure readiness for mass production launch.</li><li>Build and maintain effective relationships with suppliers to ensure quality expectations, timing, documentation, and deliverables are fully met.</li><li>Evaluate supplier manufacturing processes during the development phase to identify quality risks, determine root causes, and establish clear countermeasure direction.</li><li>Lead supplier Quality Review Meetings and Design Review Meetings in alignment with the overall model development plan.</li><li>Drive thorough root cause analysis and implementation of sustainable corrective actions for supplier and part quality concerns.</li><li>Track, analyze, and report part tooling development throughout the new model cycle for assigned suppliers.</li><li>Provide tooling authorization to suppliers at appropriate new model development milestones based on quality and readiness criteria.</li><li>Request, manage, and review all Quality Assurance Notice documents from suppliers, evaluate technical content, and request countermeasures as needed to achieve part approval.</li><li>Lead detailed part-by-part reviews, trial event inspections, and quality evaluations to confirm product readiness for launch.</li><li>Lead New Model Reviews to confirm full part maturation prior to mass production and provide status updates to the Parts Quality management team.</li><li>Achieve full approval for all assigned parts before mass production launch, ensuring all requirements are met.</li><li>Ensure all design changes are reviewed, approved, documented, and processed within program timing and quality standards.</li><li>Prioritize part concerns based on quality risk, production impact, launch timing, and customer requirements.</li><li>Evaluate the effectiveness of process countermeasures, change point controls, and supplier resource allocation to mitigate quality risks.</li><li>Analyze inspection results, supplier performance, and launch concerns to identify trends and drive continuous improvement.</li><li>Properly perform and guide quality evaluations of parts leading up to final approval, ensuring compliance with specifications and standards.</li><li>Document and communicate concern items, analysis, recommendations, and countermeasures through New Model Evaluation reports and management updates.</li><li>Schedule and lead new model meetings and events with research and development teams according to the model development schedule.</li><li>Partner with engineering, manufacturing, purchasing, supply chain, supplier development, and program teams to support quality and launch objectives.</li><li>Coordinate issue resolution across internal teams and suppliers to protect program timing and production readiness.</li><li>Provide technical guidance and quality leadership during supplier reviews, trial events, and launch preparation activities.</li></ul>Essential Skills<ul><li>Minimum of two years of experience in quality, manufacturing engineering, supplier quality, product quality, project management, supply chain, or a related manufacturing environment.</li><li>Experience working directly with original equipment manufacturers or manufacturing suppliers.</li><li>Strong knowledge of root cause analysis and corrective action methodologies.</li><li>Solid understanding of manufacturing processes and process controls.</li><li>Hands-on experience with part inspection and quality evaluation techniques.</li><li>Proven ability to lead cross-functional activities and manage multiple priorities in a fast-paced manufacturing environment.</li><li>Strong problem-solving skills with the ability to identify issues, analyze data, and implement effective solutions.</li><li>Excellent organization and documentation skills to manage reports, records, and quality documentation.</li><li>Effective presentation and communication skills for engaging suppliers and internal stakeholders.</li><li>Strong supplier communication skills to influence and drive quality improvements.</li><li>Two-year or four-year degree in Quality, Engineering, Manufacturing, Project Management, Supply Chain, or a related technical field, or an equivalent combination of education and relevant experience.</li><li>Experience supporting new product launches or new model development programs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Working knowledge of Advanced Product Quality Planning (APQP).</li><li>Experience with Production Part Approval Process (PPAP).</li><li>Familiarity with Process Failure Mode and Effects Analysis (PFMEA).</li><li>Ability to develop and manage control plans for critical processes and parts.</li><li>Experience with statistical process control (SPC) for monitoring and improving manufacturing performance.</li><li>Understanding of geometric dimensioning and tolerancing (GD&amp;T).</li><li>Knowledge of lean manufacturing principles and their application in a production environment.</li><li>Experience conducting supplier audits to assess process capability and compliance</li></ul>Job Type &amp; LocationThis is a Contract position based out of Haw River, NC.Pay and BenefitsThe pay range for this position is $38.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Haw River, NC.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Haw River,NC.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Lead

CMM ProgrammerCMM Programming | Metrology | Dimensional Inspection | Leadership | Quality Systems | MSA | Manufacturing QualityAbout the RoleWe're seeking a hands-on Quality Lab Lead with a strong experience in CMM programming, metrology, and quality systems who enjoys solving technical challenges, mentoring others, and driving continuous improvement.What You'll Do<ul><li>Lead day-to-day operations of the quality lab, ensuring inspections and measurements are completed on time.</li><li>Manage CMM schedules to support production and customer requirements.</li><li>Supervise, coach, and train laboratory technicians on equipment, procedures, and quality standards.</li><li>Perform and oversee dimensional inspections using CMMs, portable arms, scanners, and other metrology tools.</li><li>Analyze measurement data and support root cause investigations for quality issues.</li><li>Maintain quality records, inspection reports, and laboratory documentation.</li><li>Troubleshoot measurement equipment and coordinate repairs, calibrations, and maintenance.</li><li>Manage lab tooling, supplies, and instrumentation inventory.</li><li>Support software updates, validation activities, and user training for metrology systems.</li><li>Partner with engineering, production, and suppliers to ensure quality requirements are met.</li><li>Identify and implement improvements to lab processes, tooling, and inspection methods.</li></ul>What We're Looking For<ul><li>3+ years of experience working with CMMs, metrology equipment, and dimensional inspection.</li><li>Experience leading or mentoring technicians in a manufacturing or quality environment.</li><li>Strong understanding of Measurement Systems Analysis (MSA) and quality control principles.</li><li>Hands-on experience with portable arm CMMs, scanners, and measurement software.</li><li>Ability to interpret drawings, specifications, and inspection requirements.</li><li>Strong troubleshooting, problem-solving, and organizational skills.</li><li>Excellent communication skills and ability to work cross-functionally.</li></ul>Work EnvironmentThis role works closely with production in a fast-paced manufacturing environment. The quality lab is a central hub supporting inspection, troubleshooting, and process improvement efforts across the facility. You'll collaborate with engineering, operations, and quality teams while helping drive a culture focused on accuracy, teamwork, and continuous improvement.Job Type &amp; LocationThis is a Contract to Hire position based out of Elk River, MN.Pay and BenefitsThe pay range for this position is $30.00 - $38.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Elk River, MN.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Elk River,MN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

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