Job Title: Quality ControllerJob DescriptionThis is a corporate Quality Systems / Compliance role responsible for maintaining quality and environmental management systems across multiple locations. The role involves coordinating IATF, ISO 9001, and ISO compliance, supporting audits, managing customer-specific requirements, maintaining document control, and ensuring corrective actions are tracked through closure.Responsibilities<ul><li>Coordinate IATF and ISO management systems across various locations.</li><li>Support certification, surveillance, and recertification audit readiness.</li><li>Coordinate internal, process, external, and customer audits.</li><li>Track audit findings, corrective actions, deadlines, and verification of closure.</li><li>Maintain corporate document control, policies, procedures, revisions, approvals, retention, and obsolete-document controls.</li><li>Coordinate Management Reviews and maintain compliance metrics, dashboards, and risk registers.</li><li>Maintain corporate compliance obligations register.</li><li>Manage Customer-Specific Requirements (CSRs) and determine applicability by customer, plant, program, and process.</li><li>Monitor customer portals/communications for revised requirements and coordinate implementation.</li><li>Partner with Quality, Operations, Engineering, HR, EHS, Purchasing, IT, and Sales to close compliance gaps.</li><li>Identify recurring or cross-site compliance issues and drive corrective actions and continuous improvement.</li><li>Support compliance training and standardization across locations.</li></ul>Essential Skills<ul><li>5+ years of experience within automotive quality systems, QMS, compliance, or a closely related manufacturing quality function.</li><li>Strong working knowledge of IATF.</li><li>Knowledge of ISO 9001 and ISO.</li><li>Experience coordinating or supporting internal/external audits and corrective actions.</li><li>Experience with customer-specific requirements (CSRs) in an automotive environment.</li><li>Understanding of automotive Core Tools.</li><li>Experience with document control, revision/change control, and management-system documentation.</li><li>Ability to maintain compliance matrices, audit records, dashboards, change logs, and traceable documentation.</li><li>Strong cross-functional communication skills and ability to influence people without direct authority.</li><li>Bachelor's degree in Quality, Engineering, Business, Environmental Management, or related discipline OR equivalent relevant experience.</li><li>Comfortable working 100% onsite in Saline.</li></ul>Additional Skills &amp; Qualifications<ul><li>Lead Auditor training/certification for IATF, ISO 9001, or ISO.</li><li>Customer portal experience.</li><li>Multi-site experience.</li><li>Spanish language skills.</li></ul>Work EnvironmentThe position requires working 100% onsite in Saline within a dynamic environment that collaborates across various departments including Quality, Operations, Engineering, HR, EHS, Purchasing, IT, and Sales. The role involves engaging with diverse teams to ensure compliance and drive continuous improvement.Job Type &amp; LocationThis is a Permanent position based out of Saline, MI.Pay and BenefitsThe pay range for this position is $80000.00 - $95000.00/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.Benefits include medical, dental and vision coverage, 401(k) with company match, PTO, up to 10 paid holidays, company-paid short- and long-term disability, tuition reimbursement, wellness benefits, and employee bonus programs.Job Type &amp; LocationThis is a Permanent position based out of Saline, MI.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Saline,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.

Quality Controller

DescriptionWork directly with PTME and Global Quality teams to improve manufacturing system performance, update standard documents, enhance FMA process robustness, and lead continuous improvement training initiatives. Key responsibilities include:	FMA &amp; Quality Deliverables: Assist in the development, review, and maintenance of Process FMA deliverablesincluding PFMEAs and Control Plansto ensure alignment with corporate standards.	Problem Solving &amp; Root Cause Analysis: Support root cause analysis and permanent corrective action (PCA/PRA) processes using structured problem-solving tools such as 3-Legged 5-Why (3L5Y), 8D, and A3.	Launch &amp; Warranty Support: Conduct launch quality and warranty deep-dive reviews to help identify recurring failure modes, risk areas, lessons learned, potential systemic improvements, and ultimately support warranty reduction workstreams.	Lessons Learned &amp; Best Practices: Collaborate with cross-functional partners (Product Development, Plant Quality, and Global Engineering) to support the development and implementation of best practices, drive continuous improvement and issue resolution, and document and cascade Quality Operating System (QOS) lessons learned into forward-model programs.	Continuous Improvement Across Operations: Support the update and enhancement of production quality tools/systems, training materials, and data analysis methods/reporting across manufacturing engineering, including DRIM maintenance.	Plant Support &amp; Travel: Travel to Powertrain Manufacturing Plants as required, including occasional overnight stays, to support launch teams, deep dives, and plant quality initiatives.Additional Skills &amp; QualificationsPreferred Qualifications:Quality Systems Expertise: Demonstrated technical knowledge of Quality Processes, such as Quality Operating System (QOS), Process FMA (SCCAF/SCCP, FMEA, Control Plans), Bill of Process (BOP), Quality Launch Readiness Assessments, 3-Legged 5-Why Problem Solving, DMAIC, and Global 8D methodologies.Six Sigma Certification: Six Sigma Green Belt or Black Belt certification.Core Systems Knowledge: Familiarity with Core Engineering Systems such as MIDAS, FEDE, Global Manufacturing Requirements / Knowledge Packets, engineering standards, and GPDS powertrain deliverables.Technical &amp; CAD Tools: Familiarity with Computer Aided Drafting (CAD) tools (e.g., AutoCAD) and GD&amp;T (Geometric Dimensioning and Tolerancing) knowledge.Job Type &amp; LocationThis is a Contract to Hire position based out of Dearborn, MI.Pay and BenefitsThe pay range for this position is $42.30 - $46.53/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 Dearborn, MI.Application DeadlineThis position is anticipated to close on Nov 11, 2026.Workplace TypeThis is a fully onsite position in Dearborn,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.

Quality Engineer

<h3>Quality Engineer</h3>OverviewThe Quality Engineer ensures customer quality requirements are understood, documented, and met. This role supports new customer onboarding, manages audits, improves quality processes, and helps maintain compliance with aerospace and defense standards such as AS9100 and ISO 9001. The position works closely with quality, manufacturing, and automation teams in a highly technical production environment.<h3></h3><h3>Key Responsibilities</h3><ul><li>Review customer quality requirements and ensure compliance with company processes.</li><li>Identify gaps and develop solutions to meet customer and regulatory requirements.</li><li>Lead quality planning and onboarding activities for new customers.</li><li>Support and manage customer and third-party audits from preparation through closure.</li><li>Drive continuous improvement initiatives using quality data and metrics.</li><li>Develop and maintain the Quality Management System (QMS).</li><li>Create and maintain quality documentation, including control plans, process maps, and SOPs.</li><li>Partner with automation and manufacturing teams to integrate quality requirements into production systems.</li><li>Support inspection activities and AS9102 First Article Inspection requirements.</li><li>Ensure compliance with customer flowdowns and industry quality standards.</li></ul><h3>Required Qualifications</h3><ul><li>5+ years of Quality Engineering experience, preferably in aerospace or defense manufacturing.</li><li>Experience with quality assurance, quality control, and audit support.</li><li>Knowledge of AS9100 and ISO 9001 standards.</li><li>Familiarity with AS9102 First Article Inspection requirements.</li><li>Experience creating quality plans, procedures, and process documentation.</li><li>Strong project management and cross-functional collaboration skills.</li><li>Experience supporting continuous improvement and Lean initiatives.</li><li>Ability to interpret customer specifications and quality requirements.</li></ul><h3>Preferred Qualifications</h3><ul><li>Aerospace or defense manufacturing experience.</li><li>Background in regulated manufacturing environments.</li><li>Experience working with automation systems and quality software tools.</li><li>Strong communication and problem-solving skills.</li></ul><h3>Work Environment</h3>Manufacturing and engineering environment supporting aerospace and defense programs. This role regularly collaborates with quality, manufacturing, and automation teams and participates in audits, process improvement projects, and customer quality initiatives.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 16, 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 EngineerJob DescriptionThe Quality Engineer leads the implementation, maintenance, and continuous improvement of a comprehensive Quality Management System for Class II medical devices. This role provides strategic direction for product quality and reliability, ensures compliance with ISO 9001:2015 and FDA requirements, and drives a culture of continuous improvement across the organization. The Quality Engineer collaborates closely with cross-functional teams to support new product development, supplier quality, and operational excellence.Responsibilities<ul><li>Implement and maintain a robust quality program aligned with ISO 13485 and FDA requirements for medical devices.</li><li>Maintain, review, and continuously improve the Quality Management System based on ISO/IEC 9001:2015 and upcoming standards.</li><li>Develop, review, and maintain the quality manual, policies, objectives, procedures, work instructions, and forms required to comply with ISO 9001:2015 and FDA requirements for Class II medical devices.</li><li>Prepare for external audits and manage all communication with third-party certifying agencies and the FDA during audits, inspections, and investigations.</li><li>Maintain complete and accurate Quality Management System records to ensure readiness for external audits.</li><li>Develop and maintain internal audit programs to proactively identify compliance issues and drive relevant changes to the Quality Management System.</li><li>Review internal quality control processes and coordinate with internal departments to ensure adherence to ISO and FDA requirements.</li><li>Interface with Product Development, Engineering, Purchasing, and Logistics teams to provide expert quality guidance throughout the product lifecycle.</li><li>Collaborate with the sourcing team to drive supplier quality performance and ensure suppliers meet established quality standards.</li><li>Support operations facilities during customer and third-party audits, including developing and implementing effective corrective actions as needed.</li><li>Provide strategic direction for product quality and reliability objectives and oversee the implementation and management of the Quality System.</li><li>Implement and promote a culture of continuous improvement to support the achievement of product quality and reliability goals.</li><li>Coordinate and lead cross-functional projects and special initiatives related to quality, compliance, and process improvement.</li><li>Support cross-functional teams in the implementation of new product development projects, ensuring quality and regulatory requirements are met.</li><li>Create and foster a positive working environment that encourages creative thinking, collaboration, and engagement across teams.</li></ul>Essential Skills<ul><li>Bachelors degree in engineering.</li><li>5+ years of quality engineering experience in the medical device industry.</li><li>Proven experience with ISO-based Quality Management Systems, including ISO 9001:2015.</li><li>Hands-on experience implementing and maintaining quality programs for medical devices.</li><li>Demonstrated experience working with FDA requirements for Class II medical devices.</li><li>Strong knowledge of FDA regulations and audit expectations for medical device manufacturers.</li><li>Experience preparing for and supporting external audits, including third-party and regulatory audits.</li><li>Ability to develop, maintain, and improve quality manuals, policies, procedures, work instructions, and forms.</li><li>Experience developing and executing internal audit programs for Quality Management Systems.</li><li>Strong collaboration skills with Product Development, Engineering, Purchasing, Logistics, and Operations teams.</li><li>Proven ability to drive supplier quality performance in partnership with sourcing or supply chain teams.</li><li>Experience supporting operations during customer and third-party audits and developing corrective actions.</li><li>Demonstrated ability to lead quality initiatives that support product reliability and continuous improvement.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with ISO 13485 or similar medical device quality standards.</li><li>Familiarity with ISO/IEC 9001:2015 and upcoming revisions or related standards.</li><li>Background in implementing and sustaining a culture of continuous improvement.</li><li>Experience coordinating cross-functional teams and managing special projects related to quality or new product development.</li><li>Strong communication skills for interacting with internal teams, external auditors, and regulatory bodies.</li><li>Ability to influence and guide teams in adopting quality best practices and process improvements.</li><li>Experience in a strategic quality role with responsibility for product quality and reliability objectives.</li></ul>Work EnvironmentThe role is based at a fast-paced operations site in Edison, NJ. The Quality Engineer works closely with on-site operations, engineering, and cross-functional teams in a dynamic environment focused on medical device production and compliance. The position involves regular interaction with internal departments, suppliers, and external auditors, as well as active participation in audits, investigations, and project meetings.Job Type &amp; LocationThis is a Permanent position based out of Edison, NJ.Pay and BenefitsThe pay range for this position is $100000.00 - $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.	Medical/Dental insurance (some employee contribution is required)
	Company paid vision and life insurance.
	Transit check and 125 medical plans.
	401k with a company match.
	Paid vacation and sick time.
	Discretionary bonuses and profit sharing.Job Type &amp; LocationThis is a Permanent position based out of Edison, NJ.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Edison,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 Engineer IIJob DescriptionThis Quality Engineer II position offers the opportunity to contribute to a dynamic aerospace and defense electronics supplier in the Kansas City area. You will support a broad range of quality engineering activities, from first article inspections and documentation to internal audits and root cause analysis, helping ensure products meet stringent industry and customer requirements. This role is ideal for a self-starter who wants to be hands-on with new products and grow their expertise in aerospace quality standards and practices.Responsibilities<ul><li>Assist in completing First Article Inspection Reports (FAIRs) and related documentation to verify that new or modified products meet specified requirements.</li><li>Support customer source inspections by preparing comprehensive documentation packages and coordinating required quality information.</li><li>Review sales orders to confirm quality requirements and generate clear, accurate Quality Control Instructions (QCIs) for production and inspection teams.</li><li>Participate in internal investigations and support structured root cause and corrective action activities to address product and process nonconformances.</li><li>Update and maintain quality procedures, forms, and inspection criteria to reflect current standards, customer requirements, and best practices.</li><li>Support training on workmanship standards and quality requirements to ensure consistent understanding and application across teams.</li><li>Assist in preparing basic quality metrics, key performance indicators (KPIs), and trend charts to monitor quality performance and identify improvement opportunities.</li><li>Support internal audits and nonconformance reviews to verify compliance with AS9100/ISO 9001 and internal quality procedures.</li><li>Collaborate with cross-functional teams under guidance and supervision to resolve quality issues and improve processes.</li><li>Perform other quality-related duties as required and assigned to support overall quality system effectiveness.</li></ul>Essential Skills<ul><li>Foundational understanding of AS9100 and ISO 9001 quality management system requirements.</li><li>Ability to read and interpret basic engineering drawings and specifications.</li><li>Strong analytical and problem-solving skills with the ability to participate in structured root cause analysis activities.</li><li>Effective written and verbal communication skills for interaction across departments.</li><li>High attention to detail and strong accuracy in documentation and recordkeeping.</li><li>Ability to learn and apply quality tools, FAIR requirements, and inspection methods.</li><li>Proficiency with Microsoft Office applications for documentation, data analysis, and reporting.</li><li>Exposure to ERP or MES systems, with the ability to navigate and use these tools to support quality activities.</li><li>Ability to work collaboratively with cross-functional teams under guidance and supervision.</li><li>Commitment to learning quality standards, customer requirements, and compliance expectations.</li><li>Ability to perform the essential functions of the job with or without reasonable accommodations in alignment with ADA guidelines.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in Electrical, Mechanical, Industrial, Aerospace, or a related engineering field.</li><li>12 years of engineering or manufacturing experience, including internships or co-op experience.</li><li>Knowledge of AS9100 or ISO 9001 standards beyond a foundational level is preferred.</li><li>Experience or interest in quality engineering, quality control, and continuous improvement.</li><li>Familiarity with root cause analysis and corrective action methodologies.</li><li>Understanding of IPC standards and electronics manufacturing practices.</li><li>Exposure to aerospace and defense industry requirements and practices.</li><li>Experience or coursework related to Six Sigma or similar process improvement methodologies.</li><li>Self-starter mindset with a desire to be hands-on with new products and evolving technologies.</li></ul>Work EnvironmentThis role is based onsite 100% of the time in a manufacturing and engineering environment focused on electronic aerospace products. The typical work schedule is approximately 8:00 a.m. to 5:00 p.m., providing regular daytime hours. You will work closely with engineering, production, and quality teams, using tools such as Microsoft Office and ERP/MES systems, and applying AS9100, ISO 9001, IPC, and other aerospace and defense standards. The environment emphasizes collaboration, continuous learning, and hands-on involvement with new products in a rapidly growing organization.Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.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.Health, Vision, Dental, PTO, Holiday, 401(K)Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Olathe,KS.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 supporting global quality teams by strengthening quality systems, driving continuous improvement, and ensuring strict compliance with FDA and ISO regulatory standards within a medical device manufacturing environment. This role focuses on developing, installing, and revising validation procedures and protocols so that products meet regulatory agency requirements, internal company standards, and current industry practices. The Quality Engineer contributes across the full product lifecycle, from design and development through routine production, and serves as a subject matter expert for validation and risk management programs while reporting to the Quality Manager.Responsibilities<ul><li>Lead the implementation of methods and procedures for inspecting, testing, and evaluating new and transferred products, including executing line trials, conducting process risk analyses, and participating in design and process validations to define appropriate sampling plans for validations and routine production.</li><li>Collaborate with Quality Control, Quality Assurance, Operations, Engineering, Customer Service, Maintenance, and R&amp;D teams to design and plan validation activities, write protocols, execute tests, document results, prepare reports, and secure required approvals for all validation activities, including product processing, product packaging, and utilities.</li><li>Maintain the cleaning validation matrix and evaluate new products against the matrix to determine the appropriate level of cleaning validation required.</li><li>Work closely with Operations, Engineering, and R&amp;D to manage all qualification activities for newly purchased equipment, including Installation Qualification (IQ) and Operational Qualification (OQ), and develop and maintain the validation master plan, qualification schedule, and validation schedule.</li><li>Ensure validation and qualification projects are structured in accordance with FDA regulatory guidelines and communicate validation project status and timelines regularly to Quality Management.</li><li>Resolve complex technical issues during product and process development by applying statistical techniques and analysis to improve the quality system and overall product performance.</li><li>Perform risk management activities, including the development and execution of Failure Modes and Effects Analyses (FMEA).</li><li>Recommend and initiate specification and process changes based on statistical analysis of product performance to ensure product safety, efficacy, and quality.</li><li>Review, develop, revise, and approve quality-related documents, procedures, and records as needed to maintain an effective quality management system.</li><li>Manage the laboratory function, including supervising two direct reports and overseeing day-to-day lab activities.</li><li>Manage and track accelerated and real-time stability studies, summarize results in clear reports, and share findings with customers as appropriate.</li><li>Monitor stability data, identify out-of-specification results, and promptly alert R&amp;D and relevant stakeholders to initiate appropriate actions.</li><li>Support internal and external compliance audits with regulatory agencies and serve as the subject matter expert for validation and risk management programs.</li><li>Act as an internal auditor by planning and conducting internal audits to verify compliance with quality management system and regulatory requirements.</li><li>Assist in investigations of product complaints, including root cause analysis, and support the development and implementation of corrective and preventive actions (CAPA).</li><li>Support quality teams in implementing actions, reviewing procedures, and embedding continuous improvement initiatives within the quality system.</li><li>Conduct training for personnel on quality systems, validation, risk management, and related procedures to ensure understanding and compliance.</li><li>Maintain the integrity of the quality system, product design, and customer product requirements while fostering a strong culture of customer focus.</li><li>Enforce a culture of compliance and performance in alignment with the quality management system, medical device regulations, and applicable standards.</li><li>Perform other work-related duties as assigned by the Quality Manager to support departmental and organizational objectives.</li></ul>Essential Skills<ul><li>Proven ability to maintain the integrity of the quality system, product design, and customer requirements while promoting a strong customer-focused culture.</li><li>Demonstrated capability to enforce compliance with quality management systems and regulatory requirements, particularly within medical device manufacturing.</li><li>Strong problem-solving skills and advanced statistical analysis capabilities using quality engineering tools such as fishbone diagrams, Pareto charts, cause-and-effect matrices, hypothesis testing, control charts, ANOVA, Design of Experiments (DOE), sampling methods, and process capability analysis.</li><li>Experience in project specification, justification, and change management, with the ability to implement and execute continuous improvement initiatives using Lean Six Sigma principles.</li><li>In-depth knowledge of medical device regulations, including FDA 21 CFR Part 820, ISO 13485, ISO 9001, and Good Manufacturing Practice (GMP) requirements.</li><li>Practical experience in project management, including managing multiple projects simultaneously, with strong report writing and presentation skills.</li><li>Demonstrated performance and application of Design Control principles for medical devices, including documentation and validation of design inputs, outputs, and changes.</li><li>Ability to read, analyze, and interpret scientific and technical information, standards, and regulatory guidance.</li><li>Ability to respond professionally to inquiries or complaints from customers, regulatory agencies, and internal stakeholders at healthcare-related sites.</li><li>Strong communication skills with the ability to effectively present information and provide training to team members at various levels.</li><li>Ability to comprehend and apply statistical principles, including statistical process control (SPC), capability indices (Cpk/Ppk), Production Part Approval Process (PPAP), Acceptance Quality Limits (AQL), and operating characteristic (OC) curves.</li><li>Proven ability to define problems, collect relevant data, establish facts, perform root cause analysis, and draw valid conclusions.</li><li>Previous quality engineering experience in the medical device manufacturing industry, with demonstrated compliance to 21 CFR Part 820, ISO 9001, Medical Device Directive (MDD), and related standards.</li><li>Experience working in medical device manufacturing environments, including clean room suites and sterilization processes, is a distinct advantage.</li><li>Bachelors degree in Engineering, Chemistry, Physics, Biology, or another Natural Science discipline.</li><li>Proficiency with personal computers and standard office software, combined with strong verbal and written communication skills.</li><li>Experience using Minitab or similar statistical analysis software for data analysis and reporting.</li><li>Ability to work independently using initiative while also demonstrating strong teamwork and collaboration skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certified Quality Engineer (CQE) or equivalent professional certification is highly desirable.</li><li>Experience with risk management in accordance with ISO 13485 and ISO 9001, including formal risk assessment methodologies.</li><li>Familiarity with pressure sensitive adhesive tape standards and procedures in a quality control environment, including laboratory testing methods.</li><li>Hands-on experience with supplier quality, quality assurance, and quality control in manufacturing settings.</li><li>Knowledge of clean room environments and clean room suite operations within medical device or healthcare-related manufacturing.</li><li>Experience with sterilization and sterilization validation processes, including technologies such as electron beam (e-beam).</li><li>Working history in root cause analysis and structured problem-solving methodologies, including the use of PPAP and other automotive or medical device approval processes.</li><li>Experience supporting or leading validation activities, including equipment, process, and cleaning validations.</li><li>Understanding of sustainable packaging, filtration, and healthcare-related applications is beneficial due to the companys diversified end markets.</li><li>Ability to contribute to innovation and performance enhancement by leveraging materials science, polymers, fibers, and resins across multiple stages of the value chain.</li></ul>Work EnvironmentThis role operates in both office and manufacturing environments within a global specialty materials organization. The work setting is typically quiet to moderate in noise, with periods spent on the manufacturing floor where appropriate protective head coverings may be required. The position involves frequent sitting and communication, as well as occasional standing, walking, and manual handling of objects, tools, or controls. The role may require lifting up to 20 pounds. Close, distance, and color vision are necessary to inspect products, review data, and perform laboratory and validation activities. Work may be performed in clean room environments and laboratories where precision, cleanliness, and adherence to safety and quality procedures are critical. The companys culture emphasizes innovation, continuous improvement, and customer focus, offering exposure to advanced materials technologies, global manufacturing practices, and cross-functional collaboration. Team members benefit from paid holidays and paid time off, and work with modern equipment and statistical tools such as Minitab to support validation, risk management, and quality engineering tasks.Job Type &amp; LocationThis is a Contract position based out of Knoxville, TN.Pay and BenefitsThe pay range for this position is $50.00 - $70.00/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 Knoxville, TN.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Knoxville,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.

Description
					1) On-site availability at Lexington, KY (LEX1)
2) Hands-on experience with hardware device handling, failure analysis triage
3) Ability to diagnose, reproduce, and resolve hardware and system-level failures using appropriate diagnostic tools and methodologies
4) Strong ability to manage multiple failure investigations, escalations, and yield improvement initiatives simultaneously and drive root cause analysis
5) Establish and maintain strong communication channels with cross-functional teams to aid in issue resolution and corrective actions
6) Proficiency with ticketing and documentation systems (e.g., JIRA or equivalent)
7) Ability to coordinate device shipments to external labs and contract manufacturers
8)Excellent written and oral communication skills in English, with the ability to clearly present failure analysis results to cross-functional engineering teams and management
9)Strong time management and organizational skills for coordinating complex failure analysis and cross-functional investigations
10)Expert analytical and problem-solving abilities
 
Preferred:
1. Prior experience supporting quality engineering programs in consumer electronics or comparable hardware environment
2. Familiarity with failure analysis workflows, device tear-down, and defect classification
3. Experience reproducing failures and validating fixes to improve overall platform reliability
4. Experience working within a warehouse, fulfillment center, or reverse logistics facility environment
5. Familiarity with large-format display handling and TV screening
										
					
										
					
										
					
										Experience Level
					Intermediate Level
					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 16, 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 is responsible for developing and continuously improving systems and processes to support receiving inspection, production processes, and customer requirements.Responsibilities<ul><li>Support receiving inspection, production, and shipping processes to maintain product flow and minimize costs.</li><li>Review production work orders to ensure customer requirements are being met.</li><li>Create detailed inspection sheets, work instructions, quality alerts, and dock audits.</li><li>Conduct first article and PPAP submissions.</li><li>Investigate reported MRB rejects and recommend disposition.</li><li>Participate in and lead root cause and corrective action analysis.</li><li>Assist in metrology, gage control, and calibrations.</li><li>May assist Quality Manager in coordinating or performing functions such as internal audits, continuous improvement, internal/external non-conformance reports, and Return Material Authorization (RMA's).</li><li>May perform other duties as assigned.</li></ul>Essential Skills<ul><li>Minimum of an Associate's Degree in Engineering/Quality or related field.</li><li>3+ years of quality experience in an ISO manufacturing environment.</li><li>Ability to read and interpret engineering drawings, GD&amp;T requirements, and customer specifications.</li><li>Proficiency in Microsoft Word, Excel, and PowerPoint.</li><li>Highly organized and able to work independently with various departments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working with CMM, Keyence, and Oasis is desirable.</li><li>Layout background is preferred.</li></ul>Work EnvironmentThe work environment includes both a quality lab and a manufacturing floor. Employees are entitled to 2 weeks of PTO and 9 paid holidays.Job Type &amp; LocationThis is a Contract to Hire position based out of Mansfield, OH.Pay and BenefitsThe pay range for this position is $56.50 - $59.30/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 Mansfield, OH.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Mansfield,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 plays a key role in supporting new program launches and ensuring robust quality processes across both pre-production and post-production activities. In this position, you create and submit PPAPs and APQPs, lead 8D and corrective action meetings, and develop control plans and PFMEAs while collaborating closely with internal teams, customers, and suppliers. You consistently make rational, data-driven decisions and apply strong analytical skills to maintain high standards of quality in an automotive manufacturing environment.Essential Skills<ul><li>Experience working as a Quality Engineer within Automotive Manufacturing (IATF 16949)</li><li>Experience completing and implementing 8D corrective actions and preventative actions</li><li>PPAP, APQP and PFMEA experience </li><li>Strong troubleshooting and root cause analysis experience</li><li>Proficient in blueprint reading and GD&amp;T</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with machined metal products and precision machining processes.</li><li>Experience working with cast iron castings in a production environment.</li><li>Exposure to CNC machining operations and related process development.</li><li>Experience using MeasureLink or similar measurement data collection and analysis software.</li><li>Quality Engineering certifications or additional professional credentials in quality or manufacturing.</li><li>Familiarity with lean manufacturing principles and continuous improvement methodologies.</li><li>Ability to collaborate effectively with cross-functional teams including process engineering, program management, automation, and operations.</li></ul>Work EnvironmentThe typical shift starts at 7:00 a.m., with an expected workweek of approximately 4550 hours. The company culture emphasizes exceptional customer service, problem-solving, and continuous improvement, offering significant exposure to developing machining processes and advanced manufacturing technologies. Team members receive 10 days of paid time off, 6 paid holidays, and access to Udemy learning resources after six months, supporting ongoing professional growth in a dynamic, fast-paced production environment.Job Type &amp; LocationThis is a Contract to Hire position based out of New Troy, MI.Pay and BenefitsThe pay range for this position is $38.46 - $43.27/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 New Troy, MI.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in New Troy,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 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 Engineer IIJob DescriptionThis Quality Engineer II position offers the opportunity to contribute to a dynamic aerospace and defense electronics supplier in the Kansas City area. You will support a broad range of quality engineering activities, from first article inspections and documentation to internal audits and root cause analysis, helping ensure products meet stringent industry and customer requirements. This role is ideal for a self-starter who wants to be hands-on with new products and grow their expertise in aerospace quality standards and practices.Responsibilities<ul><li>Assist in completing First Article Inspection Reports (FAIRs) and related documentation to verify that new or modified products meet specified requirements.</li><li>Support customer source inspections by preparing comprehensive documentation packages and coordinating required quality information.</li><li>Review sales orders to confirm quality requirements and generate clear, accurate Quality Control Instructions (QCIs) for production and inspection teams.</li><li>Participate in internal investigations and support structured root cause and corrective action activities to address product and process nonconformances.</li><li>Update and maintain quality procedures, forms, and inspection criteria to reflect current standards, customer requirements, and best practices.</li><li>Support training on workmanship standards and quality requirements to ensure consistent understanding and application across teams.</li><li>Assist in preparing basic quality metrics, key performance indicators (KPIs), and trend charts to monitor quality performance and identify improvement opportunities.</li><li>Support internal audits and nonconformance reviews to verify compliance with AS9100/ISO 9001 and internal quality procedures.</li><li>Collaborate with cross-functional teams under guidance and supervision to resolve quality issues and improve processes.</li><li>Perform other quality-related duties as required and assigned to support overall quality system effectiveness.</li></ul>Essential Skills<ul><li>Foundational understanding of AS9100 and ISO 9001 quality management system requirements.</li><li>Ability to read and interpret basic engineering drawings and specifications.</li><li>Strong analytical and problem-solving skills with the ability to participate in structured root cause analysis activities.</li><li>Effective written and verbal communication skills for interaction across departments.</li><li>High attention to detail and strong accuracy in documentation and recordkeeping.</li><li>Ability to learn and apply quality tools, FAIR requirements, and inspection methods.</li><li>Proficiency with Microsoft Office applications for documentation, data analysis, and reporting.</li><li>Exposure to ERP or MES systems, with the ability to navigate and use these tools to support quality activities.</li><li>Ability to work collaboratively with cross-functional teams under guidance and supervision.</li><li>Commitment to learning quality standards, customer requirements, and compliance expectations.</li><li>Ability to perform the essential functions of the job with or without reasonable accommodations in alignment with ADA guidelines.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in Electrical, Mechanical, Industrial, Aerospace, or a related engineering field.</li><li>12 years of engineering or manufacturing experience, including internships or co-op experience.</li><li>Knowledge of AS9100 or ISO 9001 standards beyond a foundational level is preferred.</li><li>Experience or interest in quality engineering, quality control, and continuous improvement.</li><li>Familiarity with root cause analysis and corrective action methodologies.</li><li>Understanding of IPC standards and electronics manufacturing practices.</li><li>Exposure to aerospace and defense industry requirements and practices.</li><li>Experience or coursework related to Six Sigma or similar process improvement methodologies.</li><li>Self-starter mindset with a desire to be hands-on with new products and evolving technologies.</li></ul>Work EnvironmentThis role is based onsite 100% of the time in a manufacturing and engineering environment focused on electronic aerospace products. The typical work schedule is approximately 8:00 a.m. to 5:00 p.m., providing regular daytime hours. You will work closely with engineering, production, and quality teams, using tools such as Microsoft Office and ERP/MES systems, and applying AS9100, ISO 9001, IPC, and other aerospace and defense standards. The environment emphasizes collaboration, continuous learning, and hands-on involvement with new products in a rapidly growing organization.Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.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.Health, Vision, Dental, PTO, Holiday, 401(K)Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Olathe,KS.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 new product introductions for automotive programs by developing and maintaining all required quality documentation, driving effective launch processes, and ensuring compliance with industry and customer standards. This role works closely with engineering, production, suppliers, and customers to implement robust quality controls, lead problem-solving activities, and continuously improve processes, costs, and product performance in a Tier One automotive environment.Responsibilities<ul><li>Develop and maintain all documentation required to support new product launches, ensuring completeness, accuracy, and alignment with customer and industry requirements.</li><li>Serve as the gatekeeper for new product introduction activities, confirming that all steps are completed and documented in the correct sequence before launch.</li><li>Support Design Failure Mode and Effects Analysis (DFMEA) and Process Failure Mode and Effects Analysis (PFMEA), and verify that corrective actions are effective and properly implemented.</li><li>Participate in the selection and management of special characteristics for new products, ensuring appropriate control and monitoring.</li><li>Set quality objectives for new product introduction and coordinate associated training related to customer expectations and requirements.</li><li>Investigate opportunities for improvement and cost reduction through troubleshooting, root cause analysis, and implementation of corrective and preventive actions.</li><li>Participate in product design and development activities to embed quality requirements and manufacturability considerations early in the process.</li><li>Conduct and document training for site personnel to support new product introductions and ensure team members are competent in their roles.</li><li>Interface closely with Engineering to ensure flawless product launches, reviewing new product introduction processes for completeness and adequacy against AIAG and internal standards.</li><li>Apply classic quality tools and methodologies, including Statistical Process Control (SPC), Gage Repeatability and Reproducibility (GR&amp;R), and capability studies.</li><li>Evaluate techniques and instructions in site documentation and implement changes as needed to improve clarity, effectiveness, and compliance.</li><li>Perform internal audits and supplier audits during the development phase, and follow up on findings and corrective actions.</li><li>Work to improve inspection, measurement, and test equipment (IMTE) hardware and software, as well as fixtures used at the site to support new product introductions.</li><li>Maintain a strong presence on the production floor, overseeing specific lines such as GM and Ford production lines, and ensuring that daily activities support quality objectives.</li><li>Lead and maintain quality walks on the production floor, documenting findings and driving timely actions to address identified issues.</li><li>Manage supplier portals to validate that no quality issues are present and that required documentation and approvals are in place.</li><li>Lead scrap activity reviews, organize and participate in kaizen events, and drive 5S projects to reduce waste and improve process discipline.</li><li>Participate in scrap meetings and review meetings, providing data-driven insights and action plans to reduce defects and scrap.</li><li>Meet key performance indicator (KPI) targets for new product introduction, including quality, delivery, and cost metrics.</li><li>Take responsibility for customer, internal, and third-party audit findings, ensuring timely resolution and sustainable improvements.</li><li>Support activities related to customer PPAP submissions, including documentation, validation, and communication with customer representatives.</li><li>Assist with testing as needed to validate product and process performance against specifications and customer requirements.</li><li>Ensure all team members involved in new product introduction are properly trained and competent in their respective roles.</li><li>Ensure compliance with applicable plant procedures, human resources policies, safety requirements, and quality systems.</li><li>Follow the requirements of the quality management system and promote adherence across the team and production floor.</li><li>Inform plant operations leadership of any issues affecting product quality or processes, as well as potential issues that may create safety or environmental hazards.</li><li>Participate in audits and drive follow-up on corrective actions to closure.</li><li>Adhere strictly to safety and other company policies and actively work to achieve quality, safety, and environmental objectives while reducing environmental impacts related to site activities.</li><li>Exercise authority to make decisions within the scope of quality engineering responsibilities and stop work processes or quarantine items when quality or safety problems are identified.</li></ul>Essential Skills<ul><li>Proven experience in quality engineering within an automotive or manufacturing environment.</li><li>Strong knowledge of APQP and PPAP processes, including documentation and customer submission requirements.</li><li>Hands-on experience with root cause analysis and structured problem-solving methodologies.</li><li>Demonstrated ability to support and apply DFMEA and PFMEA, including development, review, and follow-up on corrective actions.</li><li>Proficiency with classic quality tools such as Statistical Process Control (SPC), Gage Repeatability and Reproducibility (GR&amp;R), and capability studies.</li><li>Experience conducting internal and supplier audits, and managing findings and corrective actions.</li><li>Familiarity with IATF-related quality system requirements and automotive industry standards.</li><li>Strong documentation skills, with the ability to create, review, and improve work instructions, procedures, and quality plans.</li><li>Ability to interface effectively with engineering, production, suppliers, and customers to support flawless product launches.</li><li>Strong analytical and problem-solving skills with a focus on data-driven decision-making.</li><li>Ability to train and coach site personnel on quality requirements, processes, and tools.</li><li>Capacity to work both on the production floor and in an office environment, balancing strategic and hands-on responsibilities.</li><li>Ability to travel as needed, up to approximately 10%, for supplier visits, audits, and launch support.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in a Tier One automotive environment, particularly with OEMs such as GM, Ford, and Stellantis.</li><li>Background in customer interaction related to quality topics, including PPAP submissions and audit responses.</li><li>Experience leading kaizen events, scrap reduction initiatives, and 5S projects.</li><li>Comfort working in a flexible environment with roughly equal time split between office tasks and production floor activities, with the ability to adjust based on initiatives.</li><li>Strong Spanish and French language skills are highly valued for supporting multilingual teams and suppliers.</li><li>Familiarity with inspection, measurement, and test equipment (IMTE) hardware and software, and production fixtures used in automotive manufacturing.</li><li>Understanding of environmental and safety considerations in manufacturing and commitment to continuous improvement in these areas.</li></ul>Work EnvironmentThis role is based in a Tier One automotive manufacturing facility that designs and produces advanced automotive sensors, actuators, and mechatronic modules. The organization focuses on products that improve powertrain and transmission efficiency, support e-mobility, and enhance overall vehicle performance. The Quality Engineer works in a dynamic environment with approximately a 50/50 split between office-based tasks and time spent on the production floor, although this balance may shift depending on active initiatives. The work involves close collaboration with production lines supplying major automotive manufacturers, including GM, Ford, and Stellantis. The facility operates with established quality, safety, and environmental management systems and uses a range of technologies and equipment, including inspection and measurement tools, test systems, and specialized fixtures to support new product introductions. The culture emphasizes continuous improvement, structured problem solving, and cross-functional teamwork, with regular scrap reviews, kaizen events, and 5S activities. Occasional travel, around 10%, may be required for supplier audits, launch support, and cross-site collaboration.Job Type &amp; LocationThis is a Contract to Hire position based out of Elkmont, AL.Pay and BenefitsThe pay range for this position is $38.46 - $45.67/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 Elkmont, AL.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Elkmont,AL.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 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>Background 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.

Job Title: Quality Engineer IIJob DescriptionThis Quality Engineer II position offers the opportunity to contribute to a dynamic aerospace and defense electronics supplier in the Kansas City area. You will support a broad range of quality engineering activities, from first article inspections and documentation to internal audits and root cause analysis, helping ensure products meet stringent industry and customer requirements. This role is ideal for a self-starter who wants to be hands-on with new products and grow their expertise in aerospace quality standards and practices.Responsibilities<ul><li>Assist in completing First Article Inspection Reports (FAIRs) and related documentation to verify that new or modified products meet specified requirements.</li><li>Support customer source inspections by preparing comprehensive documentation packages and coordinating required quality information.</li><li>Review sales orders to confirm quality requirements and generate clear, accurate Quality Control Instructions (QCIs) for production and inspection teams.</li><li>Participate in internal investigations and support structured root cause and corrective action activities to address product and process nonconformances.</li><li>Update and maintain quality procedures, forms, and inspection criteria to reflect current standards, customer requirements, and best practices.</li><li>Support training on workmanship standards and quality requirements to ensure consistent understanding and application across teams.</li><li>Assist in preparing basic quality metrics, key performance indicators (KPIs), and trend charts to monitor quality performance and identify improvement opportunities.</li><li>Support internal audits and nonconformance reviews to verify compliance with AS9100/ISO 9001 and internal quality procedures.</li><li>Collaborate with cross-functional teams under guidance and supervision to resolve quality issues and improve processes.</li><li>Perform other quality-related duties as required and assigned to support overall quality system effectiveness.</li></ul>Essential Skills<ul><li>Foundational understanding of AS9100 and ISO 9001 quality management system requirements.</li><li>Ability to read and interpret basic engineering drawings and specifications.</li><li>Strong analytical and problem-solving skills with the ability to participate in structured root cause analysis activities.</li><li>Effective written and verbal communication skills for interaction across departments.</li><li>High attention to detail and strong accuracy in documentation and recordkeeping.</li><li>Ability to learn and apply quality tools, FAIR requirements, and inspection methods.</li><li>Proficiency with Microsoft Office applications for documentation, data analysis, and reporting.</li><li>Exposure to ERP or MES systems, with the ability to navigate and use these tools to support quality activities.</li><li>Ability to work collaboratively with cross-functional teams under guidance and supervision.</li><li>Commitment to learning quality standards, customer requirements, and compliance expectations.</li><li>Ability to perform the essential functions of the job with or without reasonable accommodations in alignment with ADA guidelines.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in Electrical, Mechanical, Industrial, Aerospace, or a related engineering field.</li><li>12 years of engineering or manufacturing experience, including internships or co-op experience.</li><li>Knowledge of AS9100 or ISO 9001 standards beyond a foundational level is preferred.</li><li>Experience or interest in quality engineering, quality control, and continuous improvement.</li><li>Familiarity with root cause analysis and corrective action methodologies.</li><li>Understanding of IPC standards and electronics manufacturing practices.</li><li>Exposure to aerospace and defense industry requirements and practices.</li><li>Experience or coursework related to Six Sigma or similar process improvement methodologies.</li><li>Self-starter mindset with a desire to be hands-on with new products and evolving technologies.</li></ul>Work EnvironmentThis role is based onsite 100% of the time in a manufacturing and engineering environment focused on electronic aerospace products. The typical work schedule is approximately 8:00 a.m. to 5:00 p.m., providing regular daytime hours. You will work closely with engineering, production, and quality teams, using tools such as Microsoft Office and ERP/MES systems, and applying AS9100, ISO 9001, IPC, and other aerospace and defense standards. The environment emphasizes collaboration, continuous learning, and hands-on involvement with new products in a rapidly growing organization.Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.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.Health, Vision, Dental, PTO, Holiday, 401(K)Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Olathe,KS.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 ERP Implementation (Contract)Job DescriptionThis contract Quality Engineer role supports a major ERP implementation project over a 9+ month period, with potential extension into 2028. You will begin with a strong focus on core quality engineering activities and progressively transition into a more ERP-focused position as the implementation advances. The role offers the opportunity to help design, configure, and stabilize a new ERP environment in-house, improving on past vendor-led implementations while strengthening quality processes across the organization.Responsibilities<ul><li>Support the ERP implementation by contributing to the configuration and integration of Quality Management System (QMS) processes within SAP ERP and SAP S/4HANA.</li><li>Begin with approximately 75% focus on quality engineering and 25% on ERP implementation, transitioning over time to a more ERP-focused role as the project progresses.</li><li>Communicate proactively with suppliers to address quality issues, clarify requirements, and support continuous improvement in supplier quality.</li><li>Work through the inspection backlog by reviewing, prioritizing, and completing inspections to ensure timely disposition of materials and products.</li><li>Investigate and understand nonconformities, perform root cause analysis, and support corrective and preventive actions in alignment with QMS requirements.</li><li>Update and maintain Quality Management System procedures to align with AS9100 and ISO 9001 standards and with the new ERP processes.</li><li>Review and refine Engineering Change Order (ECO) procedures to ensure accurate, controlled, and traceable changes within the QMS and ERP systems.</li><li>Create, revise, and maintain quality standard operating procedures (SOPs) and documentation to support consistent inspection and quality control practices.</li><li>Perform or support inspections using Coordinate Measuring Machines (CMMs), including Keyence systems, to verify dimensional conformity of components.</li><li>Support quality control and process verification activities in printed circuit board assembly (PCBA) fabrication and related manufacturing operations.</li><li>Collaborate with cross-functional teams, including engineering, manufacturing, and supply chain, to ensure quality requirements are embedded in ERP workflows.</li><li>Ensure quality records, inspection data, and supplier quality documentation are accurately captured and maintained within the ERP and QMS.</li><li>Contribute to continuous improvement initiatives by identifying opportunities to streamline quality processes and enhance system usability within the new ERP environment.</li></ul>Essential Skills<ul><li>Proven background in Quality Engineering with hands-on experience in manufacturing or related environments.</li><li>Experience with Quality Management Systems, including implementation, maintenance, and continuous improvement.</li><li>Practical experience with Engineering Change Orders and associated processes within a controlled environment.</li><li>Experience working with SAP ERP, preferably including SAP S/4HANA, with specific exposure to Quality Management System (QMS) modules or functionality.</li><li>Strong supplier communication skills, including the ability to address supplier quality issues and collaborate on corrective actions.</li><li>Hands-on experience with quality inspections, including use of Coordinate Measuring Machines (CMMs), such as Keyence systems.</li><li>Familiarity with PCBA fabrication and inspection processes for printed circuit board assemblies.</li><li>Working knowledge of AS9100 and ISO 9001 quality standards and their application in a manufacturing environment.</li><li>Mechanical aptitude and the ability to understand technical drawings, specifications, and engineering documentation.</li><li>Ability to create, review, and maintain quality SOPs and documentation with high attention to detail.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience participating in ERP implementation projects, especially those involving SAP ERP or SAP S/4HANA.</li><li>Exposure to integrating quality processes and QMS requirements into ERP systems.</li><li>Experience working in environments certified to AS9100 and ISO 9001 standards.</li><li>Familiarity with inspection backlogs and strategies to reduce them efficiently while maintaining compliance.</li><li>Comfort working with engineering change management processes and ECO workflows.</li><li>Strong documentation skills and the ability to clearly communicate quality requirements and process changes to cross-functional teams.</li></ul>Work EnvironmentYou will work in a combination of office space and a clean printed circuit board assembly (PCBA) manufacturing facility. The environment includes exposure to modern inspection and measurement equipment, such as Keyence CMM machines, and an ERP landscape centered on SAP ERP and SAP S/4HANA. The role supports a large-scale ERP implementation project, providing opportunities to collaborate closely with engineering, manufacturing, and quality teams in a structured, process-driven setting. Dress expectations align with a professional office and clean manufacturing environment, with appropriate attire and any required safety or cleanroom-related considerations provided by the facility.#LI-MH3Job Type &amp; LocationThis is a Contract position based out of Tigard, OR.Pay and BenefitsThe pay range for this position is $58.00 - $72.00/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 Tigard, OR.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Tigard,OR.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 IIJob DescriptionThis Quality Engineer II position offers the opportunity to contribute to a dynamic aerospace and defense electronics supplier in the Kansas City area. You will support a broad range of quality engineering activities, from first article inspections and documentation to internal audits and root cause analysis, helping ensure products meet stringent industry and customer requirements. This role is ideal for a self-starter who wants to be hands-on with new products and grow their expertise in aerospace quality standards and practices.Responsibilities<ul><li>Assist in completing First Article Inspection Reports (FAIRs) and related documentation to verify that new or modified products meet specified requirements.</li><li>Support customer source inspections by preparing comprehensive documentation packages and coordinating required quality information.</li><li>Review sales orders to confirm quality requirements and generate clear, accurate Quality Control Instructions (QCIs) for production and inspection teams.</li><li>Participate in internal investigations and support structured root cause and corrective action activities to address product and process nonconformances.</li><li>Update and maintain quality procedures, forms, and inspection criteria to reflect current standards, customer requirements, and best practices.</li><li>Support training on workmanship standards and quality requirements to ensure consistent understanding and application across teams.</li><li>Assist in preparing basic quality metrics, key performance indicators (KPIs), and trend charts to monitor quality performance and identify improvement opportunities.</li><li>Support internal audits and nonconformance reviews to verify compliance with AS9100/ISO 9001 and internal quality procedures.</li><li>Collaborate with cross-functional teams under guidance and supervision to resolve quality issues and improve processes.</li><li>Perform other quality-related duties as required and assigned to support overall quality system effectiveness.</li></ul>Essential Skills<ul><li>Foundational understanding of AS9100 and ISO 9001 quality management system requirements.</li><li>Ability to read and interpret basic engineering drawings and specifications.</li><li>Strong analytical and problem-solving skills with the ability to participate in structured root cause analysis activities.</li><li>Effective written and verbal communication skills for interaction across departments.</li><li>High attention to detail and strong accuracy in documentation and recordkeeping.</li><li>Ability to learn and apply quality tools, FAIR requirements, and inspection methods.</li><li>Proficiency with Microsoft Office applications for documentation, data analysis, and reporting.</li><li>Exposure to ERP or MES systems, with the ability to navigate and use these tools to support quality activities.</li><li>Ability to work collaboratively with cross-functional teams under guidance and supervision.</li><li>Commitment to learning quality standards, customer requirements, and compliance expectations.</li><li>Ability to perform the essential functions of the job with or without reasonable accommodations in alignment with ADA guidelines.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in Electrical, Mechanical, Industrial, Aerospace, or a related engineering field.</li><li>12 years of engineering or manufacturing experience, including internships or co-op experience.</li><li>Knowledge of AS9100 or ISO 9001 standards beyond a foundational level is preferred.</li><li>Experience or interest in quality engineering, quality control, and continuous improvement.</li><li>Familiarity with root cause analysis and corrective action methodologies.</li><li>Understanding of IPC standards and electronics manufacturing practices.</li><li>Exposure to aerospace and defense industry requirements and practices.</li><li>Experience or coursework related to Six Sigma or similar process improvement methodologies.</li><li>Self-starter mindset with a desire to be hands-on with new products and evolving technologies.</li></ul>Work EnvironmentThis role is based onsite 100% of the time in a manufacturing and engineering environment focused on electronic aerospace products. The typical work schedule is approximately 8:00 a.m. to 5:00 p.m., providing regular daytime hours. You will work closely with engineering, production, and quality teams, using tools such as Microsoft Office and ERP/MES systems, and applying AS9100, ISO 9001, IPC, and other aerospace and defense standards. The environment emphasizes collaboration, continuous learning, and hands-on involvement with new products in a rapidly growing organization.Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.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.Health, Vision, Dental, PTO, Holiday, 401(K)Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Olathe,KS.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 and drives product and supplier quality in a fast-paced manufacturing environment. This role leads root cause investigations, manages corrective and preventive actions, conducts internal and supplier audits, and ensures compliance with quality standards such as IATF and AS9100. The Quality Engineer works closely with suppliers, customers, manufacturing, and quality teams to improve product quality, support new product introductions, and maintain robust quality system documentation.Responsibilities<ul><li>Lead root cause investigations for internal, supplier, and customer quality issues using structured problem-solving methodologies such as 8D.</li><li>Develop, implement, and manage corrective and preventive actions (CAR/SCAR) to address nonconformances and prevent recurrence.</li><li>Conduct internal, supplier, and quality system audits to ensure compliance with IATF, AS9100, and company quality standards.</li><li>Support supplier quality management by monitoring supplier performance, managing supplier scorecards, and driving improvements with key suppliers.</li><li>Collaborate with suppliers and customers to resolve quality concerns, ensuring timely communication and effective issue resolution.</li><li>Support Advanced Product Quality Planning (APQP) activities and new product introductions, including development of Control Plans and quality documentation.</li><li>Manage and participate in Production Part Approval Process (PPAP) activities, including documentation review, submission, and approval for new and modified products.</li><li>Perform and oversee First Article Inspections (FAI) and ensure accurate, complete quality documentation for new and existing products.</li><li>Analyze quality data using SPC and other statistical tools to identify trends, risks, and opportunities for continuous improvement.</li><li>Maintain and improve the quality management system, including procedures, work instructions, records, and compliance documentation.</li><li>Interpret engineering drawings, prints, and specifications to define and validate product requirements and inspection criteria.</li><li>Use metrology tools such as calipers, gauges, Keyence, Nikon, or similar measurement systems to perform dimensional inspections and verify product conformance.</li><li>Develop and update work instructions, inspection plans, and quality reports to support manufacturing and quality operations.</li><li>Partner with cross-functional manufacturing teams to address process issues, improve product quality, and optimize production efficiency.</li><li>Drive continuous improvement initiatives using Lean manufacturing principles to reduce defects, improve processes, and enhance overall quality performance.</li><li>Support new product launches in automotive, aerospace, or similar manufacturing environments, ensuring quality requirements are met throughout the product lifecycle.</li><li>Communicate effectively with other Quality Engineers, supervisors, and cross-functional stakeholders to align on priorities and share quality performance updates.</li></ul>Essential Skills<ul><li>5+ years of Quality Engineering experience in a manufacturing environment.</li><li>Strong experience in automotive quality engineering or similar high-volume manufacturing environments.</li><li>Hands-on experience with IATF and AS9100 quality standards.</li><li>Proficiency in Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP).</li><li>Experience with Failure Mode and Effects Analysis (FMEA) and development of Control Plans.</li><li>Working knowledge of Measurement System Analysis (MSA) and Statistical Process Control (SPC).</li><li>Demonstrated experience conducting internal, supplier, and quality system audits.</li><li>Proven ability to lead 8D root cause analysis and corrective action initiatives.</li><li>Ability to read and interpret engineering drawings, prints, and specifications.</li><li>Experience performing First Article Inspections (FAI) and managing related quality documentation.</li><li>Hands-on metrology experience using calipers, gauges, Keyence, Nikon, or similar measurement systems.</li><li>Experience managing supplier quality issues, including SCARs, CARs, and supplier scorecards.</li><li>Strong written and verbal communication skills, including the ability to create clear work instructions and quality reports.</li><li>Proficiency with Microsoft Office and quality data analysis tools.</li><li>Demonstrated ability to work directly with customers and suppliers to resolve quality concerns.</li><li>Continuous improvement mindset with experience leading process improvement and corrective action projects.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate's degree required; Bachelor's degree preferred in Engineering, Quality, Manufacturing, Industrial, or a related field.</li><li>Experience in automotive manufacturing is strongly preferred, particularly in high-volume production environments.</li><li>Experience in aerospace manufacturing, cable/wire manufacturing, construction-related manufacturing, agricultural equipment manufacturing, or other fast-paced production environments is beneficial.</li><li>Experience working in a PPAP-driven environment with rigorous documentation and approval requirements.</li><li>Practical understanding of Lean manufacturing principles and their application to quality and process improvement.</li><li>Comfort working with suppliers, customers, and cross-functional manufacturing teams in a collaborative setting.</li><li>Ability to thrive in a high-volume, fast-paced production environment with strong attention to detail.</li><li>Strong collaboration skills and ability to work closely with other Quality Engineers and quality leadership.</li></ul>Work EnvironmentThis role operates in a fast-paced, high-volume manufacturing environment with strong quality expectations. The Quality Engineer works standard 8-hour shifts, with flexibility for either 1st or 2nd shift depending on candidate preference and business needs; shift preference is discussed during the interview process. The work involves frequent interaction with production areas, suppliers, customers, and cross-functional teams, as well as use of metrology equipment such as calipers, gauges, Keyence, Nikon, and similar measurement systems. The culture emphasizes collaboration, clear communication, and continuous improvement, and candidates from automotive or similar fast-paced production industries typically adapt well to the environment.Job Type &amp; LocationThis is a Permanent position based out of Akron, PA.Pay and BenefitsThe pay range for this position is $80000.00 - $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.Benefits:
401(k)
401(k) matching
Dental insurance
Employee assistance program
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave
Professional development assistance
Referral program
Tuition reimbursement
Vision insuranceJob Type &amp; LocationThis is a Permanent position based out of Akron, PA.Application DeadlineThis position is anticipated to close on Nov 6, 2026.Workplace TypeThis is a fully onsite position in Akron,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 style="text-align:center;">Job Title: Quality Engineer</h2>Opportunity to join a growing team developing new cutting edge Space technologiesJob DescriptionThe Quality Engineer is responsible for developing, implementing, and maintaining quality assurance programs across mid-sized engineering and manufacturing projects. This role partners closely with engineering and production teams to ensure products meet internal standards and regulatory requirements, while driving continuous improvement in quality and cost.Responsibilities<ul><li>Evaluate product design reliability and overall quality; recommend process and design improvements.</li><li>Identify opportunities to enhance manufacturability, reduce cost, and improve product performance.</li><li>Develop and implement inspection, testing, and evaluation methods to ensure product accuracy and compliance.</li><li>Support functional testing and inspection activities for systems and equipment.</li><li>Conduct internal audits and identify gaps in quality systems; help drive corrective actions.</li><li>Collaborate with suppliers to resolve quality issues and ensure compliance.</li><li>Create in-process inspection plans to ensure products meet customer requirements (Objective Quality Evidence).</li><li>Review and approve manufacturing documentation, including build records and inspection reports.</li><li>Generate and analyze quality data, including statistical reports and technical documentation.</li><li>Support nonconformance reporting, root cause analysis, and corrective action processes.</li><li>Assist with incoming inspection and final acceptance testing as needed.</li><li>Maintain accurate records of quality and as-built documentation for each product.</li><li>Provide guidance and support to junior team members when needed.</li></ul>Essential Skills<ul><li>Proficiency in quality engineering and quality assurance.</li><li>Expertise in root cause analysis, corrective action, and quality management systems.</li><li>Strong knowledge of inspection methods, quality systems, and manufacturing processes.</li><li>Ability to analyze data and develop solutions to both routine and complex quality issues.</li><li>Detail-oriented with strong documentation and reporting skills.</li><li>Experience reviewing electrical and/or mechanical designs against quality standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors or Masters degree in Engineering or related field (or equivalent experience).</li><li>35+ years of experience in quality engineering or a related role.</li><li>Background in aerospace, defense, or highly regulated industries is preferred.</li><li>Familiarity with standards such as AS9100, AS9102, IPC-A-610/620, or similar.</li><li>Experience with advanced inspection techniques like optical inspections, coatings, or precision components.</li><li>Knowledge of nonconformance and Material Review Board (MRB) processes.</li><li>Experience reviewing test procedures and validating system requirements.</li><li>Familiarity with ERP systems such as SAP.</li><li>Experience working in controlled environments like clean rooms.</li></ul>Work EnvironmentThe position may require extended hours to support project demands. Compliance with all applicable regulatory and safety requirements is essential. Eligibility to obtain a U.S. security clearance is required.Job Type &amp; LocationThis is a Contract to Hire position based out of Acton, MA.Pay and BenefitsThe pay range for this position is $35.00 - $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 Acton, MA.Application DeadlineThis position is anticipated to close on Nov 11, 2026.Workplace TypeThis is a fully onsite position in Acton,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.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer plays a key role in supporting new program launches and ensuring robust quality processes across both pre-production and post-production activities. In this position, you create and submit PPAPs and APQPs, lead 8D and corrective action meetings, and develop control plans and PFMEAs while collaborating closely with internal teams, customers, and suppliers. You consistently make rational, data-driven decisions and apply strong analytical skills to maintain high standards of quality in an automotive manufacturing environment.Essential Skills<ul><li>Experience working as a Quality Engineer within Automotive Manufacturing (IATF 16949)</li><li>Experience completing and implementing 8D corrective actions and preventative actions</li><li>PPAP, APQP and PFMEA experience </li><li>Strong troubleshooting and root cause analysis experience</li><li>Proficient in blueprint reading and GD&amp;T</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with machined metal products and precision machining processes.</li><li>Experience working with cast iron castings in a production environment.</li><li>Exposure to CNC machining operations and related process development.</li><li>Experience using MeasureLink or similar measurement data collection and analysis software.</li><li>Quality Engineering certifications or additional professional credentials in quality or manufacturing.</li><li>Familiarity with lean manufacturing principles and continuous improvement methodologies.</li><li>Ability to collaborate effectively with cross-functional teams including process engineering, program management, automation, and operations.</li></ul>Work EnvironmentThe typical shift starts at 7:00 a.m., with an expected workweek of approximately 4550 hours. The company culture emphasizes exceptional customer service, problem-solving, and continuous improvement, offering significant exposure to developing machining processes and advanced manufacturing technologies. Team members receive 10 days of paid time off, 6 paid holidays, and access to Udemy learning resources after six months, supporting ongoing professional growth in a dynamic, fast-paced production environment.Job Type &amp; LocationThis is a Contract to Hire position based out of New Troy, MI.Pay and BenefitsThe pay range for this position is $38.46 - $43.27/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 New Troy, MI.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in New Troy,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.

<h3>Quality Engineer</h3>OverviewThe Quality Engineer ensures customer quality requirements are understood, documented, and met. This role supports new customer onboarding, manages audits, improves quality processes, and helps maintain compliance with aerospace and defense standards such as AS9100 and ISO 9001. The position works closely with quality, manufacturing, and automation teams in a highly technical production environment.<h3></h3><h3>Key Responsibilities</h3><ul><li>Review customer quality requirements and ensure compliance with company processes.</li><li>Identify gaps and develop solutions to meet customer and regulatory requirements.</li><li>Lead quality planning and onboarding activities for new customers.</li><li>Support and manage customer and third-party audits from preparation through closure.</li><li>Drive continuous improvement initiatives using quality data and metrics.</li><li>Develop and maintain the Quality Management System (QMS).</li><li>Create and maintain quality documentation, including control plans, process maps, and SOPs.</li><li>Partner with automation and manufacturing teams to integrate quality requirements into production systems.</li><li>Support inspection activities and AS9102 First Article Inspection requirements.</li><li>Ensure compliance with customer flowdowns and industry quality standards.</li></ul><h3>Required Qualifications</h3><ul><li>5+ years of Quality Engineering experience, preferably in aerospace or defense manufacturing.</li><li>Experience with quality assurance, quality control, and audit support.</li><li>Knowledge of AS9100 and ISO 9001 standards.</li><li>Familiarity with AS9102 First Article Inspection requirements.</li><li>Experience creating quality plans, procedures, and process documentation.</li><li>Strong project management and cross-functional collaboration skills.</li><li>Experience supporting continuous improvement and Lean initiatives.</li><li>Ability to interpret customer specifications and quality requirements.</li></ul><h3>Preferred Qualifications</h3><ul><li>Aerospace or defense manufacturing experience.</li><li>Experience in regulated manufacturing environments.</li><li>Experience working with automation systems and quality software tools.</li><li>Strong communication and problem-solving skills.</li></ul><h3>Work Environment</h3>Manufacturing and engineering environment supporting aerospace and defense programs. This role regularly collaborates with quality, manufacturing, and automation teams and participates in audits, process improvement projects, and customer quality initiatives.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 18, 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 EngineerThis 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.

Job Title: Lead Quality EngineerJob DescriptionThe Lead Quality Engineer will oversee day-to-day quality systems for a Class II medical device within a small, collaborative team in the Twin Cities. This role manages the Quality Management System (QMS), including CAPAs, change reports, continuous improvement initiatives, and test method validations for on-market products. The position focuses on post-market quality and quality assurance, while offering the opportunity to grow into design assurance responsibilities and gain hands-on leadership experience in a smaller medical device organization.Responsibilities<ul><li>Oversee and manage the Quality Management System (QMS) for Class II medical devices, ensuring compliance with applicable standards and regulations.</li><li>Lead and maintain Corrective and Preventive Action (CAPA) processes, including investigation, root cause analysis, implementation of corrective actions, and effectiveness verification.</li><li>Review and manage change reports and quality documentation to ensure accurate, compliant, and timely updates to quality records.</li><li>Drive continuous improvement activities focused on enhancing safety, improving quality cycle times, and reducing lead times to minimize waste.</li><li>Lead the implementation and effectiveness evaluation of continuous improvement systems and methodologies across the quality function.</li><li>Develop, conduct, and control production processes in collaboration with manufacturing teams and quality inspectors to ensure products meet specifications and quality standards.</li><li>Improve measurement and process capability through activities such as gage R&amp;R, test method validation (TMV), statistical process control (SPC), and design of experiments (DOE).</li><li>Initiate and manage nonconforming product or material review board activities, including disposition decisions and follow-up actions.</li><li>Support post-market quality activities for on-market products, including monitoring product performance and implementing quality improvements.</li><li>Collaborate closely with manufacturing and other cross-functional development teams to support product and process improvements.</li><li>Provide day-to-day guidance and oversight to a quality associate, helping to manage workload, priorities, and professional development.</li><li>Work alongside another quality engineer and report to the director of quality, contributing to a cohesive and high-performing quality team.</li><li>Participate in audits and quality control activities to maintain robust quality assurance practices.</li><li>Support and potentially expand into design assurance responsibilities, contributing to risk management and design-related quality activities as experience grows.</li></ul>Essential Skills<ul><li>35 years of experience as a Quality Engineer in a regulated environment.</li><li>At least 3 years of hands-on experience managing and executing CAPA processes.</li><li>Minimum of 3 years of experience working within a formal Quality Management System (QMS).</li><li>At least 5 years of experience in the medical device industry, preferably with Class II devices.</li><li>Strong knowledge of quality engineering principles, including quality control and quality assurance in a manufacturing environment.</li><li>Experience with test method validation (TMV), gage R&amp;R, statistical process control (SPC), and design of experiments (DOE).</li><li>Demonstrated ability to lead continuous improvement initiatives focused on safety, quality, and waste reduction.</li><li>Experience with audits and compliance activities related to medical devices.</li><li>Proven ability to collaborate with manufacturing and cross-functional teams to improve processes and product quality.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to or experience in design assurance is a plus, with the potential to grow into a dedicated design assurance role.</li><li>Experience supporting post-market quality activities for on-market products.</li><li>Ability and interest in gaining management experience by overseeing and mentoring a quality associate.</li><li>Strong analytical and problem-solving skills with a focus on root cause analysis and data-driven decision-making.</li><li>Effective communication skills for working with quality, manufacturing, and other internal teams.</li><li>Motivation to work in a smaller medical device company environment with opportunities for broader responsibility and career growth.</li></ul>Work EnvironmentThe role is based onsite in an office located in Eden Prairie, working Monday through Friday. The quality team is small and collaborative, currently consisting of a director of quality and a quality associate, with this position joining as the third team member. The Lead Quality Engineer will work closely with another quality engineer, the associate, and cross-functional teams such as manufacturing and development. After initial training, there may be some flexibility in work arrangements. The environment offers exposure to a broad range of quality activities, opportunities to gain leadership experience, and close collaboration across departments within a growing medical device organization.Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $43.00 - $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 to Hire position based out of Eden Prairie, MN.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Eden Prairie,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 EngineerJob DescriptionThis is a contract role spanning over nine months, with the potential to extend into 2028, for an ERP implementation project. The position initially involves a focus of 75% on quality engineering and 25% on ERP implementation, gradually transitioning to a more ERP-centric role. The quality engineering tasks include supplier communication, addressing inspection backlogs, understanding nonconformities, updating Quality Management System (QMS) procedures, and reviewing Engineering Change Order (ECO) procedures.Responsibilities<ul><li>Communicate effectively with suppliers to ensure quality standards.</li><li>Work through the inspection backlog to maintain quality assurance.</li><li>Identify and understand nonconformities within the system.</li><li>Update and maintain Quality Management System (QMS) procedures.</li><li>Review Engineering Change Order (ECO) procedures for accuracy and compliance.</li><li>Participate in the ERP implementation process, contributing to its success.</li></ul>Essential Skills<ul><li>Proficient in Quality Engineering practices.</li><li>Experience with ERP implementation, particularly SAP ERP.</li><li>Strong understanding of Quality Management Systems (QMS).</li><li>Familiarity with ISO 9001 and AS9100 standards.</li><li>Experience with SAP S/4HANA and related systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>Mechanical aptitude relevant to quality engineering.</li><li>Experience with Engineering Change Orders.</li><li>Proficiency in using CMM machines, particularly 'Keyence'.</li><li>Knowledge of PCBA fabrication processes.</li></ul>Work EnvironmentThe position is based in an office and a clean Printed Circuit Board Assembly (PCBA) manufacturing facility, providing a professional and structured environment conducive to quality engineering and ERP activities.Job Type &amp; LocationThis is a Contract position based out of Tigard, OR.Pay and BenefitsThe pay range for this position is $58.00 - $72.00/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 Tigard, OR.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Tigard,OR.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: Lead Quality EngineerJob DescriptionThe Lead Quality Engineer will oversee day-to-day quality systems for a Class II medical device within a small, collaborative team in the Twin Cities. This role manages the Quality Management System (QMS), including CAPAs, change reports, continuous improvement initiatives, and test method validations for on-market products. The position focuses on post-market quality and quality assurance, while offering the opportunity to grow into design assurance responsibilities and gain hands-on leadership experience in a smaller medical device organization.Responsibilities<ul><li>Oversee and manage the Quality Management System (QMS) for Class II medical devices, ensuring compliance with applicable standards and regulations.</li><li>Lead and maintain Corrective and Preventive Action (CAPA) processes, including investigation, root cause analysis, implementation of corrective actions, and effectiveness verification.</li><li>Review and manage change reports and quality documentation to ensure accurate, compliant, and timely updates to quality records.</li><li>Drive continuous improvement activities focused on enhancing safety, improving quality cycle times, and reducing lead times to minimize waste.</li><li>Lead the implementation and effectiveness evaluation of continuous improvement systems and methodologies across the quality function.</li><li>Develop, conduct, and control production processes in collaboration with manufacturing teams and quality inspectors to ensure products meet specifications and quality standards.</li><li>Improve measurement and process capability through activities such as gage R&amp;R, test method validation (TMV), statistical process control (SPC), and design of experiments (DOE).</li><li>Initiate and manage nonconforming product or material review board activities, including disposition decisions and follow-up actions.</li><li>Support post-market quality activities for on-market products, including monitoring product performance and implementing quality improvements.</li><li>Collaborate closely with manufacturing and other cross-functional development teams to support product and process improvements.</li><li>Provide day-to-day guidance and oversight to a quality associate, helping to manage workload, priorities, and professional development.</li><li>Work alongside another quality engineer and report to the director of quality, contributing to a cohesive and high-performing quality team.</li><li>Participate in audits and quality control activities to maintain robust quality assurance practices.</li><li>Support and potentially expand into design assurance responsibilities, contributing to risk management and design-related quality activities as experience grows.</li></ul>Essential Skills<ul><li>35 years of experience as a Quality Engineer in a regulated environment.</li><li>At least 3 years of hands-on experience managing and executing CAPA processes.</li><li>Minimum of 3 years of experience working within a formal Quality Management System (QMS).</li><li>At least 5 years of experience in the medical device industry, preferably with Class II devices.</li><li>Strong knowledge of quality engineering principles, including quality control and quality assurance in a manufacturing environment.</li><li>Experience with test method validation (TMV), gage R&amp;R, statistical process control (SPC), and design of experiments (DOE).</li><li>Demonstrated ability to lead continuous improvement initiatives focused on safety, quality, and waste reduction.</li><li>Experience with audits and compliance activities related to medical devices.</li><li>Proven ability to collaborate with manufacturing and cross-functional teams to improve processes and product quality.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to or experience in design assurance is a plus, with the potential to grow into a dedicated design assurance role.</li><li>Experience supporting post-market quality activities for on-market products.</li><li>Ability and interest in gaining management experience by overseeing and mentoring a quality associate.</li><li>Strong analytical and problem-solving skills with a focus on root cause analysis and data-driven decision-making.</li><li>Effective communication skills for working with quality, manufacturing, and other internal teams.</li><li>Motivation to work in a smaller medical device company environment with opportunities for broader responsibility and career growth.</li></ul>Work EnvironmentThe role is based onsite in an office located in Eden Prairie, working Monday through Friday. The quality team is small and collaborative, currently consisting of a director of quality and a quality associate, with this position joining as the third team member. The Lead Quality Engineer will work closely with another quality engineer, the associate, and cross-functional teams such as manufacturing and development. After initial training, there may be some flexibility in work arrangements. The environment offers exposure to a broad range of quality activities, opportunities to gain leadership experience, and close collaboration across departments within a growing medical device organization.Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $43.00 - $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 to Hire position based out of Eden Prairie, MN.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Eden Prairie,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 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 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: Lead Quality EngineerJob DescriptionThe Lead Quality Engineer will oversee day-to-day quality systems for a Class II medical device within a small, collaborative team in the Twin Cities. This role manages the Quality Management System (QMS), including CAPAs, change reports, continuous improvement initiatives, and test method validations for on-market products. The position focuses on post-market quality and quality assurance, while offering the opportunity to grow into design assurance responsibilities and gain hands-on leadership experience in a smaller medical device organization.Responsibilities<ul><li>Oversee and manage the Quality Management System (QMS) for Class II medical devices, ensuring compliance with applicable standards and regulations.</li><li>Lead and maintain Corrective and Preventive Action (CAPA) processes, including investigation, root cause analysis, implementation of corrective actions, and effectiveness verification.</li><li>Review and manage change reports and quality documentation to ensure accurate, compliant, and timely updates to quality records.</li><li>Drive continuous improvement activities focused on enhancing safety, improving quality cycle times, and reducing lead times to minimize waste.</li><li>Lead the implementation and effectiveness evaluation of continuous improvement systems and methodologies across the quality function.</li><li>Develop, conduct, and control production processes in collaboration with manufacturing teams and quality inspectors to ensure products meet specifications and quality standards.</li><li>Improve measurement and process capability through activities such as gage R&amp;R, test method validation (TMV), statistical process control (SPC), and design of experiments (DOE).</li><li>Initiate and manage nonconforming product or material review board activities, including disposition decisions and follow-up actions.</li><li>Support post-market quality activities for on-market products, including monitoring product performance and implementing quality improvements.</li><li>Collaborate closely with manufacturing and other cross-functional development teams to support product and process improvements.</li><li>Provide day-to-day guidance and oversight to a quality associate, helping to manage workload, priorities, and professional development.</li><li>Work alongside another quality engineer and report to the director of quality, contributing to a cohesive and high-performing quality team.</li><li>Participate in audits and quality control activities to maintain robust quality assurance practices.</li><li>Support and potentially expand into design assurance responsibilities, contributing to risk management and design-related quality activities as experience grows.</li></ul>Essential Skills<ul><li>35 years of experience as a Quality Engineer in a regulated environment.</li><li>At least 3 years of hands-on experience managing and executing CAPA processes.</li><li>Minimum of 3 years of experience working within a formal Quality Management System (QMS).</li><li>At least 5 years of experience in the medical device industry, preferably with Class II devices.</li><li>Strong knowledge of quality engineering principles, including quality control and quality assurance in a manufacturing environment.</li><li>Experience with test method validation (TMV), gage R&amp;R, statistical process control (SPC), and design of experiments (DOE).</li><li>Demonstrated ability to lead continuous improvement initiatives focused on safety, quality, and waste reduction.</li><li>Experience with audits and compliance activities related to medical devices.</li><li>Proven ability to collaborate with manufacturing and cross-functional teams to improve processes and product quality.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to or experience in design assurance is a plus, with the potential to grow into a dedicated design assurance role.</li><li>Experience supporting post-market quality activities for on-market products.</li><li>Ability and interest in gaining management experience by overseeing and mentoring a quality associate.</li><li>Strong analytical and problem-solving skills with a focus on root cause analysis and data-driven decision-making.</li><li>Effective communication skills for working with quality, manufacturing, and other internal teams.</li><li>Motivation to work in a smaller medical device company environment with opportunities for broader responsibility and career growth.</li></ul>Work EnvironmentThe role is based onsite in an office located in Eden Prairie, working Monday through Friday. The quality team is small and collaborative, currently consisting of a director of quality and a quality associate, with this position joining as the third team member. The Lead Quality Engineer will work closely with another quality engineer, the associate, and cross-functional teams such as manufacturing and development. After initial training, there may be some flexibility in work arrangements. The environment offers exposure to a broad range of quality activities, opportunities to gain leadership experience, and close collaboration across departments within a growing medical device organization.Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $43.00 - $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 to Hire position based out of Eden Prairie, MN.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Eden Prairie,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 Murfreesboro, 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 Murfreesboro, TN.Application DeadlineThis position is anticipated to close on Nov 14, 2026.Workplace TypeThis is a fully onsite position in Murfreesboro,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 DescriptionThe Quality Engineer supports and improves quality systems, product conformity, and customer satisfaction in a precision aerospace machining environment. This role works cross-functionally with Manufacturing, Engineering, Purchasing, and Supply Chain to ensure compliance with customer, regulatory, and internal quality requirements, with a strong focus on quality metrics, material specifications, and continuous improvement.Responsibilities<ul><li>Support, maintain, and continuously improve quality systems within a precision aerospace machining environment.</li><li>Ensure product conformity to customer, regulatory, and internal quality requirements throughout the manufacturing process.</li><li>Collaborate closely with Manufacturing, Engineering, Purchasing, and Supply Chain teams to address quality issues and drive corrective actions.</li><li>Monitor, analyze, and report on quality metrics and performance data to identify trends and opportunities for improvement.</li><li>Apply geometric dimensioning and tolerancing (GD&amp;T) principles to verify that parts and components meet design and engineering specifications.</li><li>Conduct root cause analysis for nonconformances and implement robust corrective action plans to prevent recurrence.</li><li>Interpret and apply aerospace material specifications and certifications to ensure proper material selection and compliance.</li><li>Utilize and support AS9100 quality management system requirements and customer-specific aerospace standards.</li><li>Participate in the development, documentation, and improvement of quality procedures and work instructions.</li><li>Support first article inspections (FAIs) in accordance with AS9102 when needed, including documentation and validation of special processes.</li><li>Assist with preparation for and participation in customer and regulatory audits, providing evidence of compliance and effective quality controls.</li><li>Work within ERP/MRP and quality management systems to manage quality records, track nonconformances, and maintain accurate documentation.</li><li>Collaborate with cross-functional teams to drive continuous improvement initiatives that enhance product quality and customer satisfaction.</li></ul>Essential Skills<ul><li>Minimum of 3+ years of quality engineering experience in an aerospace or precision machining environment.</li><li>Bachelors degree in Engineering, Quality, Manufacturing, or a related field, or equivalent experience.</li><li>Strong experience working with quality metrics and performance data to monitor and improve quality outcomes.</li><li>Solid understanding of aerospace material specifications and certifications and their application in manufacturing.</li><li>Working knowledge of AS9100 quality management system requirements and customer-specific aerospace standards.</li><li>Proficiency in geometric dimensioning and tolerancing (GD&amp;T) for interpreting drawings and verifying product conformity.</li><li>Experience performing root cause analysis and managing corrective action systems to resolve quality issues.</li><li>Experience in quality engineering and quality control within an aerospace or precision machining setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with first article inspections (FAIs) in accordance with AS9102.</li><li>Exposure to special processes in aerospace or precision machining environments.</li><li>Familiarity with ERP/MRP systems and electronic quality management systems.</li><li>Experience supporting customer and regulatory audits, including preparation of documentation and audit responses.</li><li>Strong quality management mindset with a focus on continuous improvement and customer satisfaction.</li></ul>Work EnvironmentThis position is based onsite five days per week in a precision aerospace machining facility in Decatur, AL. The work environment centers on advanced manufacturing operations, quality systems, and collaboration with cross-functional teams such as Manufacturing, Engineering, Purchasing, and Supply Chain. The role involves frequent interaction with production areas, review of technical documentation and quality records, and use of ERP/MRP and quality management systems to support daily activities.Job Type &amp; LocationThis is a Contract to Hire position based out of Decatur, AL.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 Decatur, AL.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Decatur,AL.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 Quality Engineer to maintain and develop quality systems in a TS16949/IATF certified environment. The role involves following AIAG quality documentation standards such as PPAPs and APQP. You will serve as the main point of contact for suppliers and customers, responsible for corrective actions, problem-solving, and issue resolution. Reporting directly to the Quality Manager, you will collaborate with a team of quality engineers, inspectors, and the process engineering group.Responsibilities<ul><li>Maintain and develop quality systems in compliance with TS16949/IATF standards.</li><li>Follow AIAG quality documentation standards, including PPAPs and APQP.</li><li>Act as the main liaison for suppliers and customers.</li><li>Manage corrective actions and resolve quality issues with customers.</li><li>Collaborate with the quality engineering and process engineering teams.</li></ul>Essential Skills<ul><li>Quality assurance, quality engineering, and quality control expertise.</li><li>Proficiency in APQP and PPAP processes.</li><li>Strong skills in root cause analysis and quality assurance standards.</li><li>Experience in TS16949 or IATF16949 certified facilities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree and 2+ years of quality engineering experience, or 7+ years of experience without a degree.</li><li>Experience in developing corrective actions and control plans.</li><li>Assembly experience is a plus.</li><li>Preferred experience in automotive quality.</li></ul>Work EnvironmentThis position is based in an assembly environment focused on windshield wiper systems. The facility offers a clean floor and a pleasant work atmosphere. Employees benefit from the support of a large company while enjoying the environment of a smaller location. The role involves spending time on the floor investigating quality issues, requiring comfort with being on your feet and working closely with engineers and production associates.Job Type &amp; LocationThis is a Contract position based out of Michigan City, IN.Pay and BenefitsThe pay range for this position is $40.00 - $45.75/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 Michigan City, IN.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Michigan City,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 leads design control quality activities for medical devices, partnering closely with research and development and regulatory affairs to ensure design inputs, outputs, verification, validation, and design risk management comply with FDA and ISO regulations. This role supports the quality management system by maintaining and continuously improving document lifecycle management, CAPA administration, and audit management. The Quality Engineer also provides quality engineering support for manufacturing, including in-process validation, nonconformance management, product release, and equipment qualifications.Responsibilities<ul><li>Own and lead design control quality activities for medical device engineering projects.</li><li>Partner with research and development and regulatory affairs to ensure design inputs and outputs comply with FDA and ISO regulations.</li><li>Plan, execute, and document design verification and validation activities in accordance with regulatory and quality system requirements.</li><li>Lead and maintain design risk management activities, ensuring risks are identified, analyzed, mitigated, and documented appropriately.</li><li>Support and enhance the quality management system, focusing on document lifecycle management and continuous improvement.</li><li>Administer and manage corrective and preventive action (CAPA) processes, including investigation, root cause analysis, implementation of corrective actions, and effectiveness checks.</li><li>Manage and support internal and external audit activities, including preparation, execution, response, and follow-up actions.</li><li>Provide quality engineering support for manufacturing processes, including in-process validation and process improvements.</li><li>Lead and manage nonconformance investigations, including documentation, root cause analysis, and disposition.</li><li>Support product release activities by reviewing quality records and ensuring compliance with applicable standards and procedures.</li><li>Oversee and support equipment qualification activities to ensure equipment used in manufacturing and testing is properly validated and maintained.</li><li>Collaborate with supplier quality and other cross-functional teams to maintain robust quality systems and consistent product quality.</li><li>Apply root cause analysis methodologies to resolve quality issues and prevent recurrence.</li><li>Maintain and update design history files and other quality records to ensure completeness, accuracy, and regulatory compliance.</li></ul>Essential Skills<ul><li>5+ years of experience working with medical devices.</li><li>5+ years of experience with CAPA processes, including investigation, root cause analysis, and corrective action implementation.</li><li>5+ years of experience with nonconformance management.</li><li>5+ years of experience with design verification activities for medical devices.</li><li>Proven experience in quality engineering and quality assurance within a regulated environment.</li><li>Hands-on experience with design control elements, including design inputs, design outputs, design verification, design validation, and design risk management.</li><li>Strong knowledge of medical device regulations, including FDA 21 CFR 820.</li><li>Working knowledge of ISO standards relevant to medical devices and quality management systems.</li><li>Experience with quality systems management and quality system documentation.</li><li>Proficiency in root cause analysis methodologies and tools.</li><li>Experience with CAPA administration and corrective action planning.</li><li>Familiarity with design history files and associated documentation requirements.</li><li>Bachelors degree in Mechanical Engineering or Manufacturing Engineering.</li><li>ASQ certification or equivalent professional quality certification.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working with supplier quality processes in a medical device environment.</li><li>Experience in engineering disciplines relevant to medical device design and manufacturing.</li><li>Experience with document lifecycle management within a quality management system.</li><li>Exposure to audit management, including internal and external audits.</li><li>Ability to collaborate effectively with cross-functional teams, including R&amp;D, regulatory affairs, and manufacturing.</li><li>Strong written and verbal communication skills for documenting quality activities and presenting findings.</li><li>Detail-oriented approach with a focus on regulatory compliance and continuous improvement</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Madison, WI.Pay and BenefitsThe pay range for this position is $38.46 - $76.92/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 Madison, WI.Application DeadlineThis position is anticipated to close on Nov 5, 2026.Workplace TypeThis is a fully onsite position in Madison,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 EngineerJob DescriptionWe are seeking a dedicated and detail-oriented Quality Engineer to ensure the highest standards of product quality and customer satisfaction. The ideal candidate will utilize advanced quality problem-solving methods and lead initiatives to improve processes and products.Responsibilities<ul><li>Establish and ensure conformance to engineering standards and product specifications, maintaining high customer expectations.</li><li>Contain defective products through problem definition, Root Cause Analysis, and tracking resolution effectiveness.</li><li>Detect non-conformances and process variations using Change Control management and auditing.</li><li>Lead cross-functional problem-solving teams to enhance processes and products.</li><li>Guide product development stages focusing on form, fit, function, manufacturability, and durability.</li><li>Prevent customer satisfaction and durability issues through FMEA, design specifications, and past problem history reviews.</li><li>Develop and release control plans, inspection standards, and various manufacturing validations.</li><li>Implement quality compliance, assurance, control, and improvement initiatives across the organization.</li><li>Collaborate with Manufacturing, Engineering, Customer Experience, and Quality teams to resolve quality issues.</li><li>Support the development and management of Material Review Board (MRB) processes.</li><li>Work with Supply Chain and Quality teams to improve supplier quality and enforce compliance.</li><li>Support contract reviews for new awards, customer, and supplier agreements.</li><li>Manage production and quality record retention and management processes.</li></ul>Essential Skills<ul><li>Proficiency in quality engineering methods including Six Sigma.</li><li>Familiarity with ISO 9001 standards.</li><li>Experience in developing and implementing corrective and preventive actions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in supporting and managing Material Review Board (MRB) processes.</li><li>Strong analytical skills for process improvement and problem-solving.</li><li>Ability to collaborate effectively with cross-functional teams.</li></ul>Work EnvironmentThe role involves working closely with multiple departments including Manufacturing, Engineering, and Quality teams. The work environment is dynamic, focusing on continuous improvement and maintaining high-quality standards across all operations.Job Type &amp; LocationThis is a Contract position based out of Torrance, CA.Pay and BenefitsThe pay range for this position is $45.00 - $65.00/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 Torrance, CA.Application DeadlineThis position is anticipated to close on Nov 16, 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 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 to Hire 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 to Hire position based out of Shannon, MS.Application DeadlineThis position is anticipated to close on Nov 17, 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 Title: Corporate Quality Engineer AutomotiveJob DescriptionThe Corporate Quality Engineer Automotive is responsible for partnering with OEMs and Tier 1 suppliers to resolve quality issues during product development and throughout the full program lifecycle. This role focuses on automotive electronic components, including integrated center stack displays, instrument cluster displays, and HVAC switches, ensuring products meet stringent quality standards and customer expectations.Responsibilities<ul><li>Collaborate with OEMs and Tier 1 suppliers to identify, investigate, and resolve quality issues during product development and over the entire program lifetime.</li><li>Support quality activities for integrated center stack displays, instrument cluster displays, HVAC switches, and other automotive electronic cockpit and infotainment components.</li><li>Establish and manage containment activities at customer locations to minimize the impact of defects and quality concerns.</li><li>Perform product testing in the field to assess performance, reliability, and durability, and conduct analysis to minimize defects and failure rates.</li><li>Conduct defect analysis using basic lab diagnostics equipment, collect data logs (QNX experience is a plus), and compile clear reports on root cause analysis.</li><li>Actively participate in issue analysis, root cause identification, technical solution implementation, and lessons learned reporting, including 5 WHYs analysis and 8D problem-solving.</li><li>Carry out hands-on technical work such as software debugging, soldering, ECU flashing, firmware updates in vehicles, and components removal and installation.</li><li>Leverage experience with GM manufacturing methods and processes, including production flow, layout, assembly, and equipment, to improve product quality and production efficiency.</li><li>Use GMs supplier portal to support quality-related activities and maintain accurate documentation and communication with customer teams.</li><li>Support and lead global meetings virtually to coordinate quality actions, share status updates, and align stakeholders on corrective and preventive measures.</li><li>Prepare and maintain detailed quality documentation, reports, and metrics to track issues, corrective actions, and continuous improvement initiatives.</li><li>Travel within the USA and Mexico (approximately 1520%) on short notice when needed to support quality issues related to GM business and other customer programs.</li></ul>Essential Skills<ul><li>Engineering degree in Electrical Engineering (preferred) or Mechanical Engineering.</li><li>5+ years of related experience in quality within the automotive industry, including experience with APQP (Advanced Product Quality Planning).</li><li>Experience or strong foundational knowledge of center stack displays, HVAC switches, and instrument cluster displays as commodities.</li><li>Background working with automotive electronic components as a minimum requirement.</li><li>Basic knowledge of how to establish and manage containment activities at customer locations.</li><li>Thorough knowledge of manufacturing methods and processes, including production flow, layout, assembly operations, and production equipment, gained from experience as a GM supplier or working directly with GM.</li><li>Experience working with GMs supplier portal to manage quality and manufacturing-related activities.</li><li>Proficiency in Microsoft products (such as Word, Excel, PowerPoint) for documentation, reporting, and analysis.</li><li>Familiarity with basic lab diagnostics equipment used for defect analysis and product testing.</li><li>Ability to collect and interpret data logs; experience with QNX operating systems is a plus.</li><li>Ability to compile clear and concise reports on root cause analysis and corrective actions.</li><li>Hands-on capability in software debugging, soldering, ECU flashing, in-vehicle firmware updates, and removal/installation of electronic components.</li><li>Demonstrated experience supporting issue analysis, root cause identification, technical solution implementation, and lessons learned activities using methods such as 5 WHYs and 8D.</li><li>Ability and willingness to travel within the USA and Mexico approximately 1520%, including on short notice, to support customer quality issues.</li><li>Ability to effectively support and participate in global meetings virtually.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with BarTender barcode software for creating, automating, and managing labels, packing slips, barcodes, RFID tags, and related items.</li><li>Experience in automotive infotainment, HMI (Human-Machine Interface), and cockpit display systems.</li><li>Strong analytical and problem-solving skills with a structured approach to quality improvement.</li><li>Effective communication skills for interacting with OEMs, Tier 1 suppliers, manufacturing teams, and global stakeholders.</li><li>Ability to work independently while actively supporting cross-functional teams in a fast-paced environment.</li></ul>Work EnvironmentThis position is based in an office environment with approximately 1520% travel to manufacturing plants to support quality issues and on-site customer activities. The role offers the opportunity to work on new cutting-edge automotive display and electronic technologies within a rapidly growing organization that is winning significant new business. The work culture is relaxed and collaborative, with regular free lunch on Tuesdays, holiday gifts, and a bonus structure that can reach 2040% of annual salary. Employees receive comprehensive benefits, a 401(k) plan with a match, generous paid time off including 17 vacation days and 5 sick days, and company-paid cell phone and necessary technology to perform the job effectively.Job Type &amp; LocationThis is a Contract to Hire position based out of Troy, MI.Pay and BenefitsThe pay range for this position is $40.00 - $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 to Hire position based out of Troy, MI.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Troy,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 Engineer ERP Implementation (Contract)Job DescriptionThis contract Quality Engineer role supports a major ERP implementation project over a 9+ month period, with potential extension into 2028. You will begin with a strong focus on core quality engineering activities and progressively transition into a more ERP-focused position as the implementation advances. The role offers the opportunity to help design, configure, and stabilize a new ERP environment in-house, improving on past vendor-led implementations while strengthening quality processes across the organization.Responsibilities<ul><li>Support the ERP implementation by contributing to the configuration and integration of Quality Management System (QMS) processes within SAP ERP and SAP S/4HANA.</li><li>Begin with approximately 75% focus on quality engineering and 25% on ERP implementation, transitioning over time to a more ERP-focused role as the project progresses.</li><li>Communicate proactively with suppliers to address quality issues, clarify requirements, and support continuous improvement in supplier quality.</li><li>Work through the inspection backlog by reviewing, prioritizing, and completing inspections to ensure timely disposition of materials and products.</li><li>Investigate and understand nonconformities, perform root cause analysis, and support corrective and preventive actions in alignment with QMS requirements.</li><li>Update and maintain Quality Management System procedures to align with AS9100 and ISO 9001 standards and with the new ERP processes.</li><li>Review and refine Engineering Change Order (ECO) procedures to ensure accurate, controlled, and traceable changes within the QMS and ERP systems.</li><li>Create, revise, and maintain quality standard operating procedures (SOPs) and documentation to support consistent inspection and quality control practices.</li><li>Perform or support inspections using Coordinate Measuring Machines (CMMs), including Keyence systems, to verify dimensional conformity of components.</li><li>Support quality control and process verification activities in printed circuit board assembly (PCBA) fabrication and related manufacturing operations.</li><li>Collaborate with cross-functional teams, including engineering, manufacturing, and supply chain, to ensure quality requirements are embedded in ERP workflows.</li><li>Ensure quality records, inspection data, and supplier quality documentation are accurately captured and maintained within the ERP and QMS.</li><li>Contribute to continuous improvement initiatives by identifying opportunities to streamline quality processes and enhance system usability within the new ERP environment.</li></ul>Essential Skills<ul><li>Proven background in Quality Engineering with hands-on experience in manufacturing or related environments.</li><li>Experience with Quality Management Systems, including implementation, maintenance, and continuous improvement.</li><li>Practical experience with Engineering Change Orders and associated processes within a controlled environment.</li><li>Experience working with SAP ERP, preferably including SAP S/4HANA, with specific exposure to Quality Management System (QMS) modules or functionality.</li><li>Strong supplier communication skills, including the ability to address supplier quality issues and collaborate on corrective actions.</li><li>Hands-on experience with quality inspections, including use of Coordinate Measuring Machines (CMMs), such as Keyence systems.</li><li>Familiarity with PCBA fabrication and inspection processes for printed circuit board assemblies.</li><li>Working knowledge of AS9100 and ISO 9001 quality standards and their application in a manufacturing environment.</li><li>Mechanical aptitude and the ability to understand technical drawings, specifications, and engineering documentation.</li><li>Ability to create, review, and maintain quality SOPs and documentation with high attention to detail.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience participating in ERP implementation projects, especially those involving SAP ERP or SAP S/4HANA.</li><li>Exposure to integrating quality processes and QMS requirements into ERP systems.</li><li>Experience working in environments certified to AS9100 and ISO 9001 standards.</li><li>Familiarity with inspection backlogs and strategies to reduce them efficiently while maintaining compliance.</li><li>Comfort working with engineering change management processes and ECO workflows.</li><li>Strong documentation skills and the ability to clearly communicate quality requirements and process changes to cross-functional teams.</li></ul>Work EnvironmentYou will work in a combination of office space and a clean printed circuit board assembly (PCBA) manufacturing facility. The environment includes exposure to modern inspection and measurement equipment, such as Keyence CMM machines, and an ERP landscape centered on SAP ERP and SAP S/4HANA. The role supports a large-scale ERP implementation project, providing opportunities to collaborate closely with engineering, manufacturing, and quality teams in a structured, process-driven setting. Dress expectations align with a professional office and clean manufacturing environment, with appropriate attire and any required safety or cleanroom-related considerations provided by the facility.#LI-MH3Job Type &amp; LocationThis is a Contract position based out of Tualatin, OR.Pay and BenefitsThe pay range for this position is $58.00 - $72.00/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 Tualatin, OR.Application DeadlineThis position is anticipated to close on Nov 21, 2026.Workplace TypeThis is a fully onsite position in Tualatin,OR.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 coordinates and leads day-to-day product and document inspection activities while serving as a key liaison between internal quality teams, external manufacturing partners, engineers, and commercial stakeholders. This role focuses on developing reliability for existing product lines, resolving quality and in-service performance issues, and recommending or implementing process improvements to ensure the highest level of quality assurance and customer satisfaction in an aerospace manufacturing environment.Responsibilities<ul><li>Coordinate and oversee daily product and document inspection activities to ensure compliance with quality standards and customer requirements.</li><li>Analyze and troubleshoot technical specifications and product non-conformance issues across designated phases of process validation.</li><li>Identify current and potential non-conformance problems and proactively drive corrective actions.</li><li>Conduct thorough root cause analysis to determine effective corrective actions and validation procedures for quality issues.</li><li>Collaborate with QA Inspection teams, quality representatives, sales management, and customers to resolve product in-service issues and complaints, following guidance from engineering leadership.</li><li>Monitor and analyze processes, quality metrics, and non-conformance data to identify trends and opportunities for improvement.</li><li>Prepare and maintain a range of documentation, including technical reports, charts, and recommendations for process or quality improvements.</li><li>Develop and maintain detailed knowledge of product characteristics and requirements, performing dimensional evaluations and initiating technical evaluation tests as needed.</li><li>Recommend and support changes to processes and quality engineering practices to enhance product reliability and customer satisfaction.</li><li>Approve and apply analytical and creative problem-solving methods while working collaboratively within a team of experienced quality engineers and commercial stakeholders.</li><li>Interpret complex technical data and translate findings into clear technical reports and actionable recommendations.</li><li>Lead or spearhead quality engineering process improvement and validation projects or cross-functional teams when requested.</li><li>Respond to and attend customer, manufacturer, or supplier quality meetings to represent quality engineering interests and address quality concerns.</li><li>Participate in regularly scheduled or impromptu department and company-sponsored meetings and training sessions.</li><li>Travel domestically and globally as required to support quality engineering activities, customer interactions, and supplier engagements.</li></ul>Essential Skills<ul><li>Bachelors degree in mechanical engineering or a related technical field, or a technical degree with adequate experience in a quality engineering role to offset the degree requirement.</li><li>35 years of related experience in manufacturing and/or quality control, with at least 3 years specifically in a Quality Engineering role.</li><li>Aerospace manufacturing background with strong knowledge of aerospace manufacturing processes.</li><li>In-depth understanding of AS9100 Quality Management Systems and their application in an aerospace environment.</li><li>Hands-on experience with quality documentation, including First Article Inspection Reports (FAIR), Production Part Approval Process (PPAP), and Non-Conformance Corrective Action Plans.</li><li>Experience in supplier quality, including customer-facing interactions and collaboration with external manufacturers and suppliers.</li><li>Proficiency in Advanced Product Quality Planning (APQP) and quality assurance methodologies.</li><li>Strong skills in root cause analysis, particularly related to aerospace products and processes.</li><li>Ability to read and interpret blueprints and technical drawings accurately.</li><li>Knowledge of Geometric Dimensioning and Tolerancing (GD&amp;T) principles and their application in dimensional inspection.</li><li>Familiarity with Gauge Reproducibility and Repeatability (GR&amp;R) studies and external auditing techniques.</li><li>Experience with 3D Model Based Definition tools, such as CATIA and Enovia DMU.</li><li>Ability to interpret technical data, produce clear technical reports, and communicate complex information in a concise and actionable manner.</li><li>Demonstrated analytical and creative problem-solving skills with the ability to work effectively in a team environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working with major aerospace customers, including prior exposure to Rolls-Royce, is highly desirable.</li><li>background in deviation management and handling non-conformance documentation.</li><li>Strong interpersonal and communication skills for effective customer-facing and supplier-facing interactions.</li><li>Ability to collaborate with sales and marketing teams to support product reliability and customer satisfaction initiatives.</li><li>Comfort with leading or participating in cross-functional process improvement and validation projects.</li><li>Willingness and ability to travel globally as needed to support quality engineering and customer requirements.</li><li>Continuous improvement mindset with a focus on enhancing processes, quality performance, and in-service reliability.</li></ul>Work EnvironmentThis role operates primarily onsite in a warehouse-style manufacturing and inspection setting, working closely with internal quality teams and production operations. The Quality Engineer frequently interfaces with customers and suppliers and may visit nearby customer facilities on a regular basis. The environment involves hands-on interaction with aerospace components, inspection tools, and technical documentation, requiring attention to detail and adherence to established quality procedures. Work hours typically follow standard business schedules, with flexibility to attend meetings, training sessions, and customer visits as needed. The culture emphasizes collaboration between engineering, quality, and commercial teams, a strong commitment to aerospace quality standards, and continuous improvement in product reliability and customer satisfaction.Job Type &amp; LocationThis is a Permanent position based out of Indianapolis, IN.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.will provide at a later date please let me know if requestedJob Type &amp; LocationThis is a Permanent position based out of Indianapolis, IN.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Indianapolis,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 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 9, 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 DescriptionWe are seeking a Quality Engineer to maintain and develop quality systems in a TS16949/IATF certified environment. The role involves following AIAG quality documentation standards such as PPAPs and APQP. You will serve as the main point of contact for suppliers and customers, responsible for corrective actions, problem-solving, and issue resolution. Reporting directly to the Quality Manager, you will collaborate with a team of quality engineers, inspectors, and the process engineering group.Responsibilities<ul><li>Maintain and develop quality systems in compliance with TS16949/IATF standards.</li><li>Follow AIAG quality documentation standards, including PPAPs and APQP.</li><li>Act as the main liaison for suppliers and customers.</li><li>Manage corrective actions and resolve quality issues with customers.</li><li>Collaborate with the quality engineering and process engineering teams.</li></ul>Essential Skills<ul><li>Quality assurance, quality engineering, and quality control expertise.</li><li>Proficiency in APQP and PPAP processes.</li><li>Strong skills in root cause analysis and quality assurance standards.</li><li>Experience in TS16949 or IATF16949 certified facilities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree and 2+ years of quality engineering experience, or 7+ years of experience without a degree.</li><li>Experience in developing corrective actions and control plans.</li><li>Assembly experience is a plus.</li><li>Preferred experience in automotive quality.</li></ul>Work EnvironmentThis position is based in an assembly environment focused on windshield wiper systems. The facility offers a clean floor and a pleasant work atmosphere. Employees benefit from the support of a large company while enjoying the environment of a smaller location. The role involves spending time on the floor investigating quality issues, requiring comfort with being on your feet and working closely with engineers and production associates.Job Type &amp; LocationThis is a Contract position based out of Michigan City, IN.Pay and BenefitsThe pay range for this position is $40.00 - $45.75/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 Michigan City, IN.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Michigan City,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 DescriptionWe are seeking a Quality Engineer to monitor production assembly processes, focusing on improving efficiency and participating in production team meetings to drive continuous improvement. You will be responsible for establishing and monitoring inspection plans based on customer acceptance criteria and ensuring compliance with both customer requirements and our Quality Management System. This role requires strong communication and organizational skills, working alongside a diverse range of personnel including Engineers, Manufacturing personnel, management resources, and representatives from the U.S. Government. Additionally, you will provide engineering assistance for lot acceptance test requirements, write and incorporate detailed work instructions, and plan and conduct quality audits while conveying findings through formal reporting.Responsibilities<ul><li>Monitor production assembly processes to improve efficiency.</li><li>Participate in production team meetings to drive continuous improvement.</li><li>Establish and monitor inspection plans based on customer acceptance criteria.</li><li>Ensure compliance with customer requirements and Quality Management System.</li><li>Collaborate with Engineers, Manufacturing personnel, management, and U.S.G. representatives.</li><li>Provide engineering assistance for lot acceptance test requirements.</li><li>Write and incorporate detailed work instructions.</li><li>Plan and conduct quality audits and report findings formally.</li></ul>Essential Skills<ul><li>Quality engineering expertise.</li><li>Familiarity with ISO 9001 standards.</li><li>Experience with corrective actions and audit control plans.</li><li>Proficiency in GD&amp;T and defense industry standards.</li><li>Knowledge of supplier quality and military/government compliance.</li><li>1-3+ years of experience in quality engineering.</li><li>Experience dealing with US government and DoD/Military entities.</li><li>Comfort with inspection experience in shop floor/assembly environments.</li><li>Ability to manage internal audits and support quality inspectors.</li><li>Proficiency in tools like PPAP, corrective action plans, and quality assurance.</li><li>Experience with first article inspection and root cause analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>5+ years of relevant experience.</li><li>A four-year degree is not necessary; relevant experience is key.</li><li>Experience in munitions and firearms is advantageous.</li><li>Understanding of military standards and specifications.</li><li>Ability to think quickly and adapt in a fast-paced environment.</li><li>Ambitious and hands-on approach.</li></ul>Work Environment<ul><li>The work environment offers a clean and growth-oriented setting with a focus on cutting-edge technology and exciting new product initiatives. You will be part of a team that regularly interacts with Inspectors, Manufacturing, and the SQE team. Our business and contracts are secure for the next five years, ensuring stability and growth. The schedule includes a typical workday from 7am-5pm with an hour lunch, consisting of four nine-hour days and an eight-hour Friday. You will have every other Friday off, with potential for flexible hours as long as consistency is maintained. Travel is rare but may occur for supplier issues or offsite product testing, typically lasting a week every 2-4 months. Benefits include tuition reimbursement and opportunities for professional growth</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Janesville, WI.Pay and BenefitsThe pay range for this position is $85000.00 - $95000.00/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.full benefits are available when hired at Amtec.Job Type &amp; LocationThis is a Permanent position based out of Janesville, WI.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Janesville,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 EngineerJob DescriptionWe are seeking a Quality Engineer for an exciting opportunity in Memphis, TN. The role involves supporting new product launches, driving continuous improvement within a manufacturing environment, and ensuring high-quality production and customer satisfaction through the implementation of quality standards and management of corrective actions.Responsibilities<ul><li>Lead quality planning for new product introductions using APQP methodologies.</li><li>Support quoting and process design from a quality perspective.</li><li>Develop inspection processes, control plans, and documentation.</li><li>Investigate customer and supplier discrepancies and drive corrective actions (8D, RCA).</li><li>Partner with suppliers on quality improvements and audits.</li><li>Implement and maintain ISO and quality system requirements.</li><li>Analyze data using SPC and other quality tools to improve processes.</li><li>Support training initiatives related to quality standards and practices.</li><li>Work cross-functionally with engineering, production, and customers.</li><li>Supervise quality technicians and inspectors.</li></ul>Essential Skills<ul><li>Bachelors degree in Engineering (Manufacturing, Industrial, or similar).</li><li>5+ years of quality engineering experience in manufacturing (electronics preferred).</li><li>Experience with core quality tools (PFMEA, Control Plans, 8D, SPC, Lean/Six Sigma, etc.).</li><li>Strong root cause analysis and problem-solving skills.</li><li>Experience with ISO standards and audits.</li></ul>Additional Skills &amp; Qualifications<ul><li>Leadership or supervisory experience is a plus.</li><li>Experience with new product introductions and quality planning.</li><li>Experience in process optimization to enhance customer satisfaction.</li><li>Experience working with suppliers and customers.</li><li>Experience in fast-paced environments.</li><li>Familiarity with quality tools including PFMEA, PFD, Control Plans, 8D, A3, DMAIC, Lean Six Sigma, PDCA, PPAP, AQP, Audit, SPC, Root Cause Analysis, TPM, Value Stream Mapping, 5S, Process Capacity, 3Way 5Whys, Risk Assessment, and Failure Tree Analysis</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Memphis, TN.Pay and BenefitsThe pay range for this position is $43.27 - $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 Permanent position based out of Memphis, TN.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Memphis,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 DescriptionThe Quality Engineer plays a key role in supporting global quality teams by strengthening quality systems, driving continuous improvement, and ensuring strict compliance with FDA and ISO regulatory standards within a medical device manufacturing environment. This role focuses on developing, installing, and revising validation procedures and protocols so that products meet regulatory agency requirements, internal company standards, and current industry practices. The Quality Engineer contributes across the full product lifecycle, from design and development through routine production, and serves as a subject matter expert for validation and risk management programs while reporting to the Quality Manager.Responsibilities<ul><li>Lead the implementation of methods and procedures for inspecting, testing, and evaluating new and transferred products, including executing line trials, conducting process risk analyses, and participating in design and process validations to define appropriate sampling plans for validations and routine production.</li><li>Collaborate with Quality Control, Quality Assurance, Operations, Engineering, Customer Service, Maintenance, and R&amp;D teams to design and plan validation activities, write protocols, execute tests, document results, prepare reports, and secure required approvals for all validation activities, including product processing, product packaging, and utilities.</li><li>Maintain the cleaning validation matrix and evaluate new products against the matrix to determine the appropriate level of cleaning validation required.</li><li>Work closely with Operations, Engineering, and R&amp;D to manage all qualification activities for newly purchased equipment, including Installation Qualification (IQ) and Operational Qualification (OQ), and develop and maintain the validation master plan, qualification schedule, and validation schedule.</li><li>Ensure validation and qualification projects are structured in accordance with FDA regulatory guidelines and communicate validation project status and timelines regularly to Quality Management.</li><li>Resolve complex technical issues during product and process development by applying statistical techniques and analysis to improve the quality system and overall product performance.</li><li>Perform risk management activities, including the development and execution of Failure Modes and Effects Analyses (FMEA).</li><li>Recommend and initiate specification and process changes based on statistical analysis of product performance to ensure product safety, efficacy, and quality.</li><li>Review, develop, revise, and approve quality-related documents, procedures, and records as needed to maintain an effective quality management system.</li><li>Manage the laboratory function, including supervising two direct reports and overseeing day-to-day lab activities.</li><li>Manage and track accelerated and real-time stability studies, summarize results in clear reports, and share findings with customers as appropriate.</li><li>Monitor stability data, identify out-of-specification results, and promptly alert R&amp;D and relevant stakeholders to initiate appropriate actions.</li><li>Support internal and external compliance audits with regulatory agencies and serve as the subject matter expert for validation and risk management programs.</li><li>Act as an internal auditor by planning and conducting internal audits to verify compliance with quality management system and regulatory requirements.</li><li>Assist in investigations of product complaints, including root cause analysis, and support the development and implementation of corrective and preventive actions (CAPA).</li><li>Support quality teams in implementing actions, reviewing procedures, and embedding continuous improvement initiatives within the quality system.</li><li>Conduct training for personnel on quality systems, validation, risk management, and related procedures to ensure understanding and compliance.</li><li>Maintain the integrity of the quality system, product design, and customer product requirements while fostering a strong culture of customer focus.</li><li>Enforce a culture of compliance and performance in alignment with the quality management system, medical device regulations, and applicable standards.</li><li>Perform other work-related duties as assigned by the Quality Manager to support departmental and organizational objectives.</li></ul>Essential Skills<ul><li>Proven ability to maintain the integrity of the quality system, product design, and customer requirements while promoting a strong customer-focused culture.</li><li>Demonstrated capability to enforce compliance with quality management systems and regulatory requirements, particularly within medical device manufacturing.</li><li>Strong problem-solving skills and advanced statistical analysis capabilities using quality engineering tools such as fishbone diagrams, Pareto charts, cause-and-effect matrices, hypothesis testing, control charts, ANOVA, Design of Experiments (DOE), sampling methods, and process capability analysis.</li><li>Experience in project specification, justification, and change management, with the ability to implement and execute continuous improvement initiatives using Lean Six Sigma principles.</li><li>In-depth knowledge of medical device regulations, including FDA 21 CFR Part 820, ISO 13485, ISO 9001, and Good Manufacturing Practice (GMP) requirements.</li><li>Practical experience in project management, including managing multiple projects simultaneously, with strong report writing and presentation skills.</li><li>Demonstrated performance and application of Design Control principles for medical devices, including documentation and validation of design inputs, outputs, and changes.</li><li>Ability to read, analyze, and interpret scientific and technical information, standards, and regulatory guidance.</li><li>Ability to respond professionally to inquiries or complaints from customers, regulatory agencies, and internal stakeholders at healthcare-related sites.</li><li>Strong communication skills with the ability to effectively present information and provide training to team members at various levels.</li><li>Ability to comprehend and apply statistical principles, including statistical process control (SPC), capability indices (Cpk/Ppk), Production Part Approval Process (PPAP), Acceptance Quality Limits (AQL), and operating characteristic (OC) curves.</li><li>Proven ability to define problems, collect relevant data, establish facts, perform root cause analysis, and draw valid conclusions.</li><li>Previous quality engineering experience in the medical device manufacturing industry, with demonstrated compliance to 21 CFR Part 820, ISO 9001, Medical Device Directive (MDD), and related standards.</li><li>Experience working in medical device manufacturing environments, including clean room suites and sterilization processes, is a distinct advantage.</li><li>Bachelors degree in Engineering, Chemistry, Physics, Biology, or another Natural Science discipline.</li><li>Proficiency with personal computers and standard office software, combined with strong verbal and written communication skills.</li><li>Experience using Minitab or similar statistical analysis software for data analysis and reporting.</li><li>Ability to work independently using initiative while also demonstrating strong teamwork and collaboration skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certified Quality Engineer (CQE) or equivalent professional certification is highly desirable.</li><li>Experience with risk management in accordance with ISO 13485 and ISO 9001, including formal risk assessment methodologies.</li><li>Familiarity with pressure sensitive adhesive tape standards and procedures in a quality control environment, including laboratory testing methods.</li><li>Hands-on experience with supplier quality, quality assurance, and quality control in manufacturing settings.</li><li>Knowledge of clean room environments and clean room suite operations within medical device or healthcare-related manufacturing.</li><li>Experience with sterilization and sterilization validation processes, including technologies such as electron beam (e-beam).</li><li>Working history in root cause analysis and structured problem-solving methodologies, including the use of PPAP and other automotive or medical device approval processes.</li><li>Experience supporting or leading validation activities, including equipment, process, and cleaning validations.</li><li>Understanding of sustainable packaging, filtration, and healthcare-related applications is beneficial due to the companys diversified end markets.</li><li>Ability to contribute to innovation and performance enhancement by leveraging materials science, polymers, fibers, and resins across multiple stages of the value chain.</li></ul>Work EnvironmentThis role operates in both office and manufacturing environments within a global specialty materials organization. The work setting is typically quiet to moderate in noise, with periods spent on the manufacturing floor where appropriate protective head coverings may be required. The position involves frequent sitting and communication, as well as occasional standing, walking, and manual handling of objects, tools, or controls. The role may require lifting up to 20 pounds. Close, distance, and color vision are necessary to inspect products, review data, and perform laboratory and validation activities. Work may be performed in clean room environments and laboratories where precision, cleanliness, and adherence to safety and quality procedures are critical. The companys culture emphasizes innovation, continuous improvement, and customer focus, offering exposure to advanced materials technologies, global manufacturing practices, and cross-functional collaboration. Team members benefit from paid holidays and paid time off, and work with modern equipment and statistical tools such as Minitab to support validation, risk management, and quality engineering tasks.Job Type &amp; LocationThis is a Contract position based out of Knoxville, TN.Pay and BenefitsThe pay range for this position is $50.00 - $70.00/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 Knoxville, TN.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Knoxville,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 DescriptionThis role requires an entry-level Quality Engineer who will initially spend 75% of their time on the floor, learning and prioritizing tasks to effectively support the quality team. As a champion for quality, you will ensure that the team has the necessary materials, remove any obstacles hindering project completion, and expedite essential parts. You will handle both internal and external customer issues and participate in AS9100 audits. Over time, the role will transition to a balanced 50/50 split between floor and desk work. Responsibilities also include creating and interpreting SPC charts, conducting PFMEAs, developing control plans, and managing gage R&amp;R and PPAPs. You will work closely with the Quality Manager and eventually transition into an Assistant Quality Manager role, overseeing 9-10 quality technicians.Essential Skills<ul><li>1 year of experience as a Quality Engineer OR an engineering degree.</li><li>Experience with AS9100 standards.</li><li>Audit participation experience.</li><li>Proficiency in SPC charts, PFMEAs, control plans, gage R&amp;R, and PPAPs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with quality system standards.</li><li>Prior audit experience.</li></ul>Work EnvironmentThe position offers a 40-hour workweek with a schedule of Monday-Thursday from 7am-4:30pm and Friday from 7am-11am. Employees enjoy 2 weeks of vacation, a family-like environment with 60 employees, and a growing company culture. Benefits include employee stock ownership, a 401k, and a retirement plan. Access to Udemy courses is available after 6 months of employment.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 9, 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 ensures that high quality standards are consistently maintained across products and manufacturing processes while driving continuous improvement initiatives. This role works closely with engineering, production, and leadership teams to resolve quality issues, support audits, develop and maintain quality systems, and enhance overall manufacturing performance. The position combines hands-on work on the production floor with analytical and documentation responsibilities at the desk.Responsibilities<ul><li>Lead corrective actions and structured problem-solving activities to address product and process quality issues.</li><li>Conduct capability studies, Measurement System Analysis (MSA), Gauge R&amp;R, and process audits to evaluate and improve process performance.</li><li>Support First Article Inspection (FAI) requirements by preparing documentation, coordinating inspections, and ensuring compliance with customer and internal specifications.</li><li>Develop, implement, and maintain Quality Management System (QMS) documentation, including procedures, work instructions, and forms.</li><li>Participate in design reviews and support new product launches to ensure quality requirements are defined, understood, and integrated into manufacturing processes.</li><li>Drive continuous improvement projects focused on improving product quality, process capability, and manufacturing efficiency.</li><li>Support customer quality issues by investigating concerns, identifying root causes, and implementing effective corrective and preventive actions.</li><li>Assist with internal and external audit activities, including preparation, participation, and follow-up on audit findings.</li><li>Utilize precision measurement equipment and metrology tools to perform inspections, verify product conformity, and validate process capability.</li><li>Develop control plans, process controls, and inspection methods to ensure consistent product quality and robust manufacturing processes.</li><li>Support team-based quality processes and collaborate with cross-functional teams to promote a culture of quality and continuous improvement.</li><li>Spend approximately 60% of time on the production floor conducting capability studies, problem solving, and supporting manufacturing teams, and 40% of time performing desk-based analysis, documentation, and planning activities.</li></ul>Essential Skills<ul><li>Associate degree, preferably in engineering or welding.</li><li>35 years of experience in a welding manufacturing or metal manufacturing environment.</li><li>Experience with Production Part Approval Process (PPAP).</li><li>Working knowledge of ISO 9001 quality management systems.</li><li>Quality engineering experience in a manufacturing setting.</li><li>Formal training in problem-solving methodologies such as 8D or 5 Why (5Y).</li><li>Ability to conduct capability studies and perform MSA/Gauge R&amp;R.</li><li>Experience supporting First Article Inspection (FAI) activities.</li><li>Proficiency in using precision measurement equipment and metrology tools.</li><li>Ability to develop and maintain QMS documentation, control plans, and inspection methods.</li><li>Strong analytical and root cause analysis skills.</li><li>Effective communication and collaboration skills for working with engineering, production, and leadership teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Automotive industry experience preferred.</li><li>Certified Welding Inspector (CWI) certification.</li><li>Familiarity with ISO, IATF, AIAG, or ASQ standards and guidelines.</li><li>Lean Six Sigma certification (Green Belt or Black Belt).</li><li>ASQ certification in a relevant discipline.</li><li>Experience participating in design reviews and new product introduction.</li><li>in structured continuous improvement and team-based quality initiatives.</li><li>Interest in career development and progression into leadership roles.</li></ul>Work EnvironmentThis is an onsite role with a typical schedule of 7:00 a.m. to 4:00 p.m. The position involves approximately 60% time on the production floor and 40% time at a desk performing analysis, documentation, and planning. The manufacturing environment is focused on welding and metal fabrication, with frequent use of precision measurement equipment and metrology tools. The workplace offers a flexible schedule, casual dress, and a laid-back atmosphere that emphasizes collaboration and continuous improvement. The organization provides extensive training and certification opportunities, supports career development, and encourages internal promotion, particularly from engineering into leadership roles. While on a contract-to-hire basis, employees receive six paid holidays, three weeks of accrued vacation, and a competitive benefits package with eligibility for medical, dental, and vision coverage on the first day of employment. Once converted to direct employment, additional benefits include a 401(k) with employer match, an Employee Assistance Program, an Educational Assistance Program, career development programs, company bonus potential of up to 10% per year (paid up to 5% every six months), ten paid holidays, three weeks of accrued vacation, and continued access to a comprehensive medical, dental, and vision benefits package.Job Type &amp; LocationThis is a Contract to Hire position based out of Middlebury, IN.Pay and BenefitsThe pay range for this position is $28.85 - $43.27/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 Middlebury, IN.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Middlebury,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 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>Background 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.

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 13, 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 DescriptionWe are seeking a Quality Engineer for an exciting opportunity in Memphis, TN. The role involves supporting new product launches, driving continuous improvement within a manufacturing environment, and ensuring high-quality production and customer satisfaction through the implementation of quality standards and management of corrective actions.Responsibilities<ul><li>Lead quality planning for new product introductions using APQP methodologies.</li><li>Support quoting and process design from a quality perspective.</li><li>Develop inspection processes, control plans, and documentation.</li><li>Investigate customer and supplier discrepancies and drive corrective actions (8D, RCA).</li><li>Partner with suppliers on quality improvements and audits.</li><li>Implement and maintain ISO and quality system requirements.</li><li>Analyze data using SPC and other quality tools to improve processes.</li><li>Support training initiatives related to quality standards and practices.</li><li>Work cross-functionally with engineering, production, and customers.</li><li>Supervise quality technicians and inspectors.</li></ul>Essential Skills<ul><li>Bachelors degree in Engineering (Manufacturing, Industrial, or similar).</li><li>5+ years of quality engineering experience in manufacturing (electronics preferred).</li><li>Experience with core quality tools (PFMEA, Control Plans, 8D, SPC, Lean/Six Sigma, etc.).</li><li>Strong root cause analysis and problem-solving skills.</li><li>Experience with ISO standards and audits.</li></ul>Additional Skills &amp; Qualifications<ul><li>Leadership or supervisory experience is a plus.</li><li>Experience with new product introductions and quality planning.</li><li>Experience in process optimization to enhance customer satisfaction.</li><li>Experience working with suppliers and customers.</li><li>Experience in fast-paced environments.</li><li>Familiarity with quality tools including PFMEA, PFD, Control Plans, 8D, A3, DMAIC, Lean Six Sigma, PDCA, PPAP, AQP, Audit, SPC, Root Cause Analysis, TPM, Value Stream Mapping, 5S, Process Capacity, 3Way 5Whys, Risk Assessment, and Failure Tree Analysis</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Memphis, TN.Pay and BenefitsThe pay range for this position is $43.27 - $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 Memphis, TN.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Memphis,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 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 10, 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 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 1, 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 Title: Quality EngineerKey Role:Serve as a Quality Assurance (QA) engineer and conduct planning, development, engineering, and management of production activities applied in the design and development of a program to reduce the risk of non-conformance to requirements. Develop and maintain QA strategies and plans, provisions, specifications, and associated contract language. Review and analyze policies and regulations for their impact on QA programs and provide feedback on draft publications, specifications, or regulations. Manage the development and execution of final inspection, manufacturing processes, and procedures. Perform audits and surveillance at multiple facilities and lead problem-solving activities. Document lessons learned and continue to drive continuous improvement initiatives and opportunities within QA. Must Have:<ul><li>Experience in collaborating with multifunctional teams of engineers, logistics specialists, quality specialists, fielding managers, system acquisition managers, procurement analysts, budget managers, defense contractors, test and evaluation directors, or contracting officers to certify and quality advance manufacturing technology</li><li>Experience with providing independent oversight and review of project deliverables, including specs, SOWS, qualification plans, test plans and reports, and on-site monitoring of subsystem and component testing</li><li>Experience with the implementation of quality assurance strategy to ensure advanced manufacturing processes yield conforming product</li><li>Ability to review, evaluate, and approve qualification test plans as well as Failure Analysis and Corrective Action Reports (FACAR) associated with testing</li><li>Ability to develop and apply a process control plan that leverages Quality tools DFMEA, PFMEA, or SPC in the certification and qualification of an advanced manufacturing process</li><li>Ability to participate in the change management process to assure products or services continue to meet customer requirements and provide the quality review or concurrence function for engineering changes</li><li>Ability to travel 25% of the time</li><li>Ability to obtain a security clearance</li><li>HS diploma or GED</li></ul> Nice to Have:<ul><li>Knowledge of DoD contractor manufacturing and quality assurance processes</li><li>Bachelors degree</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Warren, MI.Pay and BenefitsThe pay range for this position is $50.00 - $65.00/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 Warren, MI.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Warren,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: Engineer, Quality AssuranceJob DescriptionThe Engineer, Quality Assurance will play a proactive role in supporting quality assurance, quality control, and preventive activities to ensure compliance with regulations and standards. This role involves collaborating with cross-functional teams, assisting in resolving quality issues, and contributing to continuous improvement initiatives within manufacturing and quality processes.Responsibilities<ul><li>Work closely with Operations and Business Functions to ensure quality performance of products and processes.</li><li>Collaborate cross-functionally with internal and external teams to resolve quality issues.</li><li>Own and manage internal and supplier-driven Non-Conformances (NCs), ensuring timely investigation and closure.</li><li>Support or own Corrective and Preventive Actions (CAPAs) through root cause analysis to closure.</li><li>Disposition of non-conforming product through MRB, issuing NCs as appropriate.</li><li>Communicate with suppliers regarding NCs and escalate Supplier Corrective Action Requests (SCARs) as needed.</li><li>Participate in the development and continuous improvement of internal manufacturing processes for existing products.</li><li>Review and support Change Management activities (both supplier and internal).</li><li>Create and/or review new or revised procedures.</li><li>Maintain and analyze KPIs to monitor product and process quality; identify trends and implement corrective actions.</li><li>Support the execution and analysis of manufacturing complaints and product field actions.</li><li>Apply statistical methods for process analysis and control.</li><li>Provide QA support during internal and external audits.</li><li>Support process/equipment validation, qualification, and Measurement System Analysis (MSA).</li><li>Execute internal quality deliverables for engineering changes, manufacturing transfers, and supplier changes.</li><li>Assist in manufacturing/product transfers between plants/facilities, performing appropriate quality activities.</li><li>Execute and analyze Quality Acceptance Tests (QATs).</li><li>Support with product holds and executing containment plans.</li><li>Support in risk management practices and tools, identifying opportunities and weaknesses.</li><li>Support and implement Lean principles through standardization and waste elimination.</li><li>Understand Human Error Prevention and apply those principles to the manufacturing environment.</li><li>Manage supplier relationships, coordinating communications, monitoring performance, managing nonconformities, and ensuring timely delivery of quality materials and services.</li></ul>Essential Skills<ul><li>Proficient in quality engineering, root cause analysis, and Quality/manufacturing engineering.</li><li>Familiar with ISO, medical device standards, and regulatory affairs.</li><li>02 years experience in a Quality or Regulatory Affairs role.</li><li>Solid understanding of engineering and quality principles, including Risk Management, CAPA, Audits, and Statistics.</li><li>Proficient in Microsoft Word, Excel, and PowerPoint.</li><li>Strong problem-solving, analytical, and communication skills with high attention to detail.</li><li>Excellent written and spoken English.</li><li>Confident representing Quality in cross-functional settings.</li><li>Self-starter able to manage multiple tasks in a fast-paced environment.</li><li>Willing to work as part of a multi-site team; some travel required.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiar with GDP and GMP concepts.</li><li>Team player with a customer/stakeholder-focused approach.</li><li>Diplomatic, tactful, and effective at leveraging interpersonal skills.</li><li>Embraces change with a continuous improvement mindset.</li><li>Knowledge of risk-based thinking and statistical concepts is a plus.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Portage, MI.Pay and BenefitsThe pay range for this position is $52.00 - $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 Portage, MI.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Portage,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 Permanent position based out of Tupelo, MS.Pay and BenefitsThe pay range for this position is $80000.00 - $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.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 Tupelo, MS.Application DeadlineThis position is anticipated to close on Nov 13, 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.

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