Job Title: Quality Engineer Job DescriptionThe Quality Engineer is responsible for addressing and resolving quality concerns from clients, such as OEMs like Honda, Subaru, and Chrysler, as well as suppliers. This role requires daily reporting and root cause analysis within client portals and involves leading quality control activities to address issues swiftly.Responsibilities<ul><li>Lead and facilitate Quick Response Quality Control activities to address quality issues at the point of occurrence.</li><li>Utilize robust root cause analysis tools, such as 5-Why, Fishbone, Ishikawa, 8D, and A3, to identify systemic issues and implement corrective and preventive actions.</li><li>Manage internal and external non-conformance, issuing and responding to 8D reports, customer complaints, and internal defect reports.</li><li>Support APQP activities for new product launches and changes.</li><li>Ensure compliance with IATF, customer-specific requirements, and internal procedures.</li><li>Analyze quality data from production and customer feedback to drive improvements in product quality and process reliability.</li><li>Collaborate with manufacturing, engineering, and suppliers to resolve quality issues and implement process improvements.</li><li>Conduct internal and layered process audits and follow up on non-conformities.</li><li>Support PPAP submissions and documentation in accordance with customer requirements.</li><li>Promote a culture of quality, accountability, and continuous improvement on the production floor.</li><li>Participate in FMEA and Control Plan development.</li><li>Provide training and coaching on quality tools, methodology, and problem-solving techniques.</li><li>Drive quality initiatives by engaging on the production floor, setting examples in structured problem-solving, and championing a culture of accountability and operational excellence.</li><li>Lead without formal authority by influencing cross-functional teams and fostering collaboration.</li></ul>Essential Skills<ul><li>Quality engineering experience.</li><li>Tier 1 auto experience.</li><li>Proficient in root cause analysis tools such as 8D, 5-Why, Fishbone, and A3.</li><li>Experience with PPAP, APQP, FMEA, and control plans.</li><li>Strong understanding of IATF standards.</li><li>Experience with customer-specific quality systems.</li><li>Excellent written and verbal communication skills.</li><li>Proficient in Microsoft Office Suite.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Engineering or a related technical discipline, or 5+ years in an automotive quality engineer role.</li><li>3+ years of experience in a quality role within a Tier 1 automotive manufacturing environment.</li><li>Experience with quality management software is a plus.</li><li>Preferred experience with Honda, Subaru, or Chrysler.</li></ul>Work EnvironmentThis role is situated in a manufacturing environment that includes roll forming processes and plastic molding. The position requires being on the floor, working closely with operators to solve issues and problems, rather than working from an office. The company is established with long-standing OEM relationships and offers opportunities to establish updated quality processes and standards.Job Type &amp; LocationThis is a Contract to Hire position based out of Shelbyville, KY.Pay and BenefitsThe pay range for this position is $36.00 - $40.00/hr.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)Workplace TypeThis is a fully onsite position in Shelbyville,KY.Application DeadlineThis position is anticipated to close on Jul 28, 2026.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.

public

Quality Engineer

Job Title: Quality EngineerJob DescriptionThis Quality Engineer role focuses on leading customer-facing quality activities for an automotive manufacturing operation that produces interior components such as carpet and felt. You will serve as the primary contact for customer quality issues, drive corrective actions, and manage quality requirements from prototype through full production launch. The position offers significant exposure to advanced automation, cross-functional collaboration, and clear potential to grow into a Quality Manager position.Responsibilities<ul><li>Serve as the main point of contact for customers on all quality-related issues, ensuring timely and professional communication.</li><li>Lead corrective action requests (CARs) and ensure that quality problems are contained, analyzed, and resolved quickly and effectively.</li><li>Manage customer complaints, product returns, and non-conforming products, including investigation, documentation, and follow-up actions.</li><li>Lead Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP) activities for new product launches.</li><li>Ensure all PPAP documentation is accurately completed, maintained, and submitted on time to meet customer and regulatory requirements.</li><li>Coordinate Run@Rate activities and launch readiness reviews to verify process capability and production readiness.</li><li>Maintain compliance with IATF requirements and support ongoing improvement of the quality management system.</li><li>Oversee Statistical Process Control (SPC), process capability studies, Measurement System Analysis (MSA), calibration systems, and inspection standards.</li><li>Own and maintain key quality documents such as Process FMEAs (PFMEAs), Control Plans, Process Flows, Standard Work, and Work Instructions.</li><li>Lead structured root cause investigations using tools such as 5 Why, Fishbone (Ishikawa) diagrams, Six Sigma methodologies, and Value Stream Mapping.</li><li>Implement corrective and preventive actions to improve product and process quality, reduce defects, and enhance customer satisfaction.</li><li>Manage and coordinate quality requirements for new product launches from prototype through production, ensuring alignment with customer expectations.</li><li>Coordinate dimensional validation, pre-launch inspections, PPAP samples, and other launch-related quality activities.</li><li>Train production teams on new processes, quality requirements, and standards to ensure consistent execution on the shop floor.</li><li>Lead and support the Quality team, promoting a culture of safety, 5S, professionalism, and continuous improvement.</li><li>Work closely with Engineering, Manufacturing, Maintenance, Suppliers, and other internal stakeholders to resolve quality issues and improve processes.</li><li>Provide regular updates to management on launch risks, quality concerns, data-driven findings, and improvement actions.</li><li>Collaborate with suppliers to address supplier quality issues and support development of robust incoming quality controls.</li><li>Apply strong problem-solving and data analysis skills to identify trends, prioritize issues, and drive sustainable improvements.</li><li>Support lean manufacturing initiatives by integrating quality tools and methods into continuous improvement projects.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering or a closely related technical discipline.</li><li>Minimum of three years of experience working with quality systems, procedures, and practices for an automotive supplier in a manufacturing environment.</li><li>Proven problem-solving ability using structured methodologies and tools such as 5 Why, Fishbone, Six Sigma, and Value Stream Mapping.</li><li>Thorough understanding of IATF requirements and APQP procedures and requirements.</li><li>Hands-on experience with APQP and PPAP for new product launches in the automotive industry.</li><li>Experience managing customer interfaces on quality issues, including complaints, returns, and non-conforming products.</li><li>Demonstrated launch experience, including Run@Rate and launch readiness reviews.</li><li>Strong manufacturing process knowledge, particularly in automotive component production.</li><li>Proficiency in quality system documentation and quality systems management.</li><li>Experience with Statistical Process Control (SPC), process capability studies, Measurement System Analysis (MSA), calibration systems, and inspection standards.</li><li>Ability to create, maintain, and own PFMEAs, Control Plans, Process Flows, Standard Work, and Work Instructions.</li><li>Lean Manufacturing experience and familiarity with lean tools and principles.</li><li>Effective leadership without formal authority, with the ability to influence cross-functional teams.</li><li>Strong data analysis skills and the ability to translate data into actionable insights.</li><li>Excellent communication skills, both written and verbal, for interaction with customers, suppliers, and internal teams.</li><li>Knowledge of automotive standards and expectations within the automotive industry.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in automotive interior manufacturing, particularly with products such as headliners, door liners, sound proofing materials, carpet, or felt, is highly desirable.</li><li>Black Belt certification or equivalent Six Sigma training is a strong advantage.</li><li>ISO standards and experience working within ISO-based quality management systems.</li><li>Experience with SAP or similar ERP systems for quality-related data and documentation.</li><li>Supplier quality experience, including working directly with suppliers to resolve quality issues and improve incoming quality.</li><li>Experience in interior automotive manufacturing environments and familiarity with related processes and customer requirements.</li><li>Demonstrated ability to act as a self-starter, taking initiative and working independently with minimal supervision.</li><li>Strong organizational skills and attention to detail in managing multiple projects and priorities.</li><li>Experience working in highly automated manufacturing environments is beneficial.</li><li>Desire and potential to grow into a Quality Manager role over time.</li></ul>Work EnvironmentThe role is based in an automotive supplier manufacturing environment that produces interior components such as headliners, door liners, sound proofing materials, carpet, and felt for vehicles. The facility features a high level of automation and offers significant exposure to modern manufacturing technologies and processes. You will collaborate closely with a cross-functional team that includes Engineering, Manufacturing, Maintenance, and Suppliers, and you will work alongside another Quality Engineer as part of a focused quality team. The environment emphasizes safety, 5S, professionalism, and continuous improvement, with clear opportunities for growth and development, including progression toward a Quality Manager position.Job Type &amp; LocationThis is a Contract to Hire position based out of Jeffersonville, IN.Pay and BenefitsThe pay range for this position is $43.27 - $45.67/hr.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)Workplace TypeThis is a fully onsite position in Jeffersonville,IN.Application DeadlineThis position is anticipated to close on Jul 29, 2026.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.

<h1>Quality Engineer</h1><h2>Join a Growing Aerospace Manufacturing Team</h2>We are seeking a detail-oriented Quality Engineer to support quality operations within a precision aerospace manufacturing environment. This role will partner closely with Engineering, Production, Inspection, Suppliers, and Customers to ensure products and processes meet AS9100 standards and customer requirements. If you have experience with corrective actions, quality systems, FAIR documentation, audits, and supplier quality, we'd love to hear from you.<h2>Key Responsibilities</h2><ul><li>Investigate and resolve quality issues involving production, inspection, engineering, suppliers, and customers.</li><li>Review and disposition nonconforming materials while maintaining accurate quality records and documentation.</li><li>Manage corrective actions, concessions, waivers, and customer quality requests through various customer portals.</li><li>Support First Article Inspection Reports (FAIRs) and coordinate submissions through customer systems and NET-INSPECT.</li><li>Review engineering drawings, specifications, purchase orders, and quality requirements to ensure compliance.</li><li>Verify shipping documentation, certifications, inspection reports, and required quality records prior to shipment.</li><li>Support supplier quality activities, including SCAR management, RMAs, and supplier corrective actions.</li><li>Conduct internal AS9100 audits and assist with continuous improvement initiatives.</li><li>Collaborate with cross-functional teams to ensure customer and regulatory requirements are met.</li><li>Support SPC activities, source inspections, and documentation packages for customer approvals.</li></ul><h2>Required Qualifications</h2><ul><li>Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical field preferred.</li><li>2+ years of Quality Engineering, Quality Assurance, or Supplier Quality experience within a manufacturing environment.</li><li>Experience with corrective actions, nonconforming material processes, root cause analysis, and quality documentation.</li><li>Ability to read and interpret engineering drawings, specifications, and customer quality requirements.</li><li>Working knowledge of AS9100, ISO quality systems, audits, and continuous improvement methodologies.</li><li>Strong organizational skills with exceptional attention to detail.</li><li>Excellent communication skills and ability to work with customers, suppliers, and internal teams.</li></ul><h2>Preferred Experience</h2><ul><li>Aerospace, defense, or highly regulated manufacturing experience.</li><li>Experience with AS9102 FAIR documentation and customer portals such as NET-INSPECT or similar systems.</li><li>Familiarity with DQR, DPRV, DSQR, SCAR, RMA, SPC, and source inspection processes.</li><li>Experience using quality and manufacturing software such as MeasureLink, DISCUS, E2, PRO DOC, or similar platforms.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Clearwater, FL.Pay and BenefitsThe pay range for this position is $36.00 - $36.00/hr.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)Workplace TypeThis is a fully onsite position in Clearwater,FL.Application DeadlineThis position is anticipated to close on Aug 3, 2026.About Actalent 

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



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



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



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



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



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

Job Description: Quality EngineerWe are seeking a skilled Quality Engineer to develop, implement, and maintain quality procedures, work instructions, and inspection plans for CNC-machined thermal products. This role involves reviewing engineering drawings, specifications, and customer requirements to ensure accurate quality planning and leading root cause analysis and corrective/preventive actions for internal and customer quality issues.Responsibilities<ul><li>Develop, implement, and maintain quality procedures, work instructions, and inspection plans for CNC-machined thermal products.</li><li>Review engineering drawings, specifications, and customer requirements to ensure accurate quality planning.</li><li>Lead root cause analysis and corrective/preventive actions for internal and customer quality issues.</li><li>Support first article inspections, in-process inspections, and final inspections.</li><li>Collaborate closely with CNC machinists, programmers, and supervisors to resolve quality concerns and improve processes.</li><li>Analyze quality data and trends, and recommend process improvements.</li><li>Manage nonconforming material reports and coordinate disposition activities.</li><li>Assist with customer, internal, and third-party audits, including ISO 9001.</li><li>Ensure proper calibration and maintenance of inspection and measurement equipment.</li><li>Support supplier quality activities, including supplier evaluations and corrective actions.</li><li>Implement and maintain statistical methodologies for process improvement.</li><li>Train production and inspection personnel on quality standards and best practices.</li><li>Collaborate daily with internal departments, including sales, customer service, engineering, purchasing, and production.</li><li>Lead and direct the shop-floor quality team, including training and addressing technical challenges.</li><li>Perform other tasks and special projects as needed.</li></ul>Essential Skills<ul><li>Mechanical or Electrical Engineering degree is required.</li><li>Minimum of 5 years of Quality Engineering experience.</li><li>Proficiency in reading and interpreting engineering drawings and GD&amp;T.</li><li>Experience with quality tools such as PPAP, FMEA, SPC, root cause analysis, and 8D.</li><li>Familiarity with ISO 9001 or other applicable quality management systems.</li><li>Proficiency with statistical software such as MiniTab or JMP.</li><li>Experience using inspection equipment like calipers, micrometers, height gauges, and CMMs.</li></ul>Additional Skills &amp; Qualifications<ul><li>ASQ quality-related certifications such as CQE or CQA are preferred.</li><li>Lean / Six Sigma certifications such as Green Belt or Black Belt are preferred.</li><li>Proficiency with Microsoft Office and quality documentation systems.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Geneva, IL.Pay and BenefitsThe pay range for this position is $75000.00 - $100000.00/yr.offers a competitive salary, full benefit package, including medical, dental, vision, life, EAP and 401k with employer match, annual bonus if company hits target numbersWorkplace TypeThis is a fully onsite position in Geneva,IL.Application DeadlineThis position is anticipated to close on Aug 4, 2026.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.

Our client in Hayden, ID area is currently hiring for a Quality Engineer. This position is a fully onsite opportunity supporting manufacturing quality initiatives, process improvement efforts, and quality system compliance. The ideal candidate will have experience in Quality Engineering, Root Cause Analysis, SPC, CAPA, and manufacturing environments where quality, consistency, and continuous improvement are critical to success.Pay - $70,000 - $90,000 annuallyLocation - Hayden, IDSchedule - Standard Monday - Friday (40 hours per week)Responsibilities• Support daily Quality Department operations and provide leadership support when needed.• Develop and maintain quality objectives that align with organizational goals and customer requirements.• Create, implement, and improve inspection, testing, and evaluation processes.• Lead quality planning activities related to manufacturing processes, new products, and production support.• Review engineering drawings, specifications, supplier documentation, and quality records for compliance.• Utilize Statistical Process Control (SPC) and other quality tools to monitor performance and drive improvements.• Conduct Root Cause Analysis investigations and implement Corrective and Preventive Actions (CAPA).• Analyze quality data, inspection results, and audit findings to ensure compliance with procedures and standards.• Collaborate with suppliers and internal teams to resolve quality concerns and improve product performance.• Investigate customer quality issues and coordinate corrective actions.• Prepare and present quality metrics, reports, and continuous improvement initiatives to leadership.• Ensure compliance with customer, industry, and regulatory quality standards.• Participate in continuous improvement initiatives including Lean Manufacturing, 5S, and process optimization.• Develop and deliver quality-related training to employees and cross-functional teams.• Support internal, customer, and external quality audits.Qualification Requirements• 3+ years of experience in Quality Engineering, Quality Assurance, or Manufacturing Quality.• Experience supporting production and manufacturing environments.• Strong understanding of Statistical Process Control (SPC).• Experience performing Root Cause Analysis and implementing CAPA initiatives.• Experience collecting, analyzing, and presenting quality data.• Proficiency with Microsoft Office, including Microsoft Excel.• Familiarity with Lean Manufacturing principles and tools.• Experience with 5S, process improvement, and continuous improvement initiatives.• Strong analytical, problem-solving, and communication skills.• Ability to review engineering drawings, specifications, and quality documentation.• Experience supporting audits and quality management systems.Disqualifiers• No experience in manufacturing or production environments.• No Quality Engineering or Quality Assurance experience.• No experience with SPC, Root Cause Analysis, or CAPA methodologies.• Limited experience analyzing quality data and driving corrective actions.• No experience supporting continuous improvement initiatives.• Less than 3 years of relevant quality experience.Employee Value Proposition• Opportunity to play a key role in improving product quality and manufacturing processes.• High visibility position with interaction across quality, engineering, production, and leadership teams.• Opportunity to lead quality improvement initiatives and influence operational performance.• Exposure to complex manufacturing environments and advanced quality methodologies.• Supportive team environment focused on continuous improvement and professional development.• Competitive compensation package with long-term career growth opportunities.• Experience working with quality systems, audits, supplier quality, and process optimization initiatives.Job Type &amp; LocationThis is a Permanent position based out of Hayden, ID.Pay and BenefitsThe pay range for this position is $70000.00 - $90000.00/yr.Health Insurance
Dental Insurance
401(k)
Vacation Time/PTOWorkplace TypeThis is a fully onsite position in Hayden,ID.Application DeadlineThis position is anticipated to close on Aug 6, 2026.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 provides essential quality support and leadership for all new and existing products and processes within the plant. This role involves working closely with internal teams to uphold high quality standards by designing inspection procedures, developing control plans, completing root cause analysis, and managing the PPAP process. The Quality Engineer also maintains relationships with customers and suppliers, ensuring their inquiries and requirements are addressed promptly.Responsibilities<ul><li>Develop and manage essential QMS documents, Process Control Plans, Work Instructions, Inspection Plan, Gauge Instructions, GR&amp;R plan, etc.</li><li>Participate in the development and implementation of new and existing programs through the APQP process.</li><li>Support product launches, engineering changes, and/or improvement changes, ensuring Quality systems are updated to compliance.</li><li>Prepare and submit Production Part Approval Process (PPAP) packages per customer requirements for new/existing products and process changes in a timely manner.</li><li>Complete dimensional reports, capability studies, and measurement systems analysis.</li><li>Lead problem-solving activities for internal/external issues and address and resolve customer concerns in their preferred format.</li><li>Perform internal audits to ensure conformance with IATF and customer-specific requirements.</li><li>Monitor Customer Specific Requirements and customer portals and update documentation as required to ensure compliance.</li><li>Conduct Product Process audits to ensure products are produced to customer specification and inspection activities are conducted in accordance with control plan requirements.</li><li>Train employees in all aspects of Quality inspections, including the use of gauges, fixtures, and in-depth instructions for final inspections, boundary samples, and procedures.</li><li>Organize and lead meetings to identify root causes and implement corrective actions for quality issues.</li><li>Understand customer issues, development, communication, and ensure adherence to Quality alerts.</li><li>Initiate claims to suppliers for defective materials.</li><li>Maintain a clean and safe work environment.</li></ul>Essential Skills<ul><li>Knowledge of PPAP, 8D methodology, supplier quality, quality tools, and customer web-based systems.</li><li>Prior hands-on experience with testing equipment including but not limited to: depth gage, calipers, micrometer, tape measure, product gauges, and CMM preferred.</li><li>At least five years of experience in a Quality role performing similar responsibilities.</li><li>Experience in automotive, IATF, product launch, supplier quality, root cause analysis, and machining.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in a technical area such as Operations Management, Manufacturing Management, Materials/Supply Chain, Engineering, etc., or eight years of directly relevant Quality/Manufacturing experience in lieu of a Bachelor's Degree.</li><li>High School Diploma or equivalency (HSED or GED).</li></ul>Work EnvironmentThe role requires a 40-hour work week, Monday to Friday, primarily in an office environment with some time spent in the production area as required. Schedules and changes to working hours must be approved by the department manager and are subject to change. The work involves standing and walking, occasionally for long periods, within manufacturing facilities and may include heavy lifting up to 50 pounds. The typical manufacturing environment includes elevated noise levels, elevated temperatures near ovens and in summer, and proximity to moving equipment.Job Type &amp; LocationThis is a Contract to Hire position based out of Pleasant Prairie, WI.Pay and BenefitsThe pay range for this position is $43.26 - $48.07/hr.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)Workplace TypeThis is a fully onsite position in Pleasant Prairie,WI.Application DeadlineThis position is anticipated to close on Aug 7, 2026.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 Supplier Quality Engineer provides ongoing support to the business by driving supplier development and improvement activities aligned with corporate quality metrics. This role works closely with Materials/Purchasing, Sourcing, Branch Operations, and Quality Assurance teams to ensure suppliers meet stringent quality standards across multiple industries. The position focuses on auditing and developing suppliers, resolving customer concerns, and supporting new product introductions while maintaining robust quality systems and processes.Responsibilities<ul><li>Conduct comprehensive audits and evaluations for new and existing suppliers to ensure compliance with quality requirements.</li><li>Review and assess self-assessments submitted by potential suppliers and determine their suitability.</li><li>Visit supplier facilities to evaluate their quality systems, processes, and capabilities.</li><li>Complete formal supplier audits, document findings, and communicate results to relevant stakeholders.</li><li>Issue supplier corrective actions based on audit findings and performance issues, and follow up to ensure timely and effective closure.</li><li>Participate in customer audits of suppliers, representing the organization’s quality interests and ensuring supplier readiness.</li><li>Issue monthly supplier performance scorecards and communicate results to suppliers and internal teams.</li><li>Monitor supplier performance, identify trends, and determine areas for improvement in supply quality and delivery performance.</li><li>Perform on-site audits for poor-performing or critical suppliers and develop targeted improvement plans.</li><li>Develop and implement action plans to improve the quality performance of identified suppliers.</li><li>Review and approve Production Part Approval Process (PPAP) submissions when suppliers initiate changes.</li><li>Provide aging reports for quality rejections by branch, supplier, reason code, and associated costs.</li><li>Assist the Quality Assurance team in processing and resolving customer concerns in a timely and effective manner.</li><li>Provide technical support to the organization in new product introduction, ensuring quality requirements are defined and met.</li><li>Support operational excellence initiatives and contribute to continuous improvement in quality processes.</li><li>Apply appropriate quality assurance and improvement methodologies, including structured problem-solving tools.</li><li>Continuously upgrade personal skills and knowledge to improve effectiveness and stay current with industry practices.</li><li>Provide training and guidance to less experienced or less skilled personnel on quality tools, processes, and standards.</li><li>Work closely with key customers to understand issues at the plant level and develop effective solutions.</li><li>Engage directly with major customers in automotive and heavy truck sectors to address quality concerns and drive corrective actions.</li><li>Lead or support corrective action activities that may function as mini Six Sigma projects to address recurring issues.</li><li>Spend significant time on the shop floor and in the laboratory, investigating and resolving quality problems and issues.</li><li>Perform hands-on work in the lab using gauges, inspection tools, and testing equipment to validate product quality.</li><li>Visit domestic suppliers regularly, with travel typically ranging from approximately 10% to 20% depending on project needs.</li><li>Apply Advanced Product Quality Planning (APQP) frameworks and related tools such as PPAP, PFMEA, control plans, and GD&amp;T in supplier and product development activities.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in quality engineering, supplier quality, or a closely related quality-focused role.</li><li>Bachelor’s degree in an engineering discipline.</li><li>Strong knowledge of ISO 9001:2015 quality standards and familiarity with IATF requirements.</li><li>Certification in auditing and demonstrated experience conducting quality system and process audits.</li><li>Proficiency in APQP and PPAP, including the ability to review, approve, and provide training on these processes to suppliers.</li><li>Hands-on experience with corrective action and continuous improvement processes, including 8D, 5 Why, and fishbone (Ishikawa) analysis.</li><li>Familiarity with various manufacturing processes and their impact on product quality.</li><li>Knowledge of material testing and evaluation procedures to assess product conformance.</li><li>Experience with gauging and inspection methods, including the use of precision measurement tools.</li><li>Ability to interpret and apply PFMEA, control plans, and GD&amp;T within supplier and product quality contexts.</li><li>Strong analytical and problem-solving skills with a structured approach to root cause analysis.</li><li>Effective communication skills to interact with suppliers, internal teams, and customers at multiple levels.</li><li>Ability to work hands-on in laboratory and shop-floor environments to investigate and resolve issues.</li><li>Willingness and ability to travel domestically approximately 10% to 20% of the time, depending on project demands.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to the automotive and/or heavy truck industry, including familiarity with sector-specific quality expectations.</li><li>Experience working with customers in industries such as aerospace, automotive, heavy equipment, electronics, and defense.</li><li>Experience with gage calibration and quality-related software tools.</li><li>Hands-on experience using Optical Comparators, Hardness Testers, and plug gages in a lab environment.</li><li>Exposure to lean methodologies and Six Sigma principles, including participation in improvement projects.</li><li>Experience with quality management systems and supplier process or product audits.</li><li>Ability to train suppliers and internal staff on APQP, PPAP, and other quality tools.</li><li>Strong customer-facing skills and experience working directly with key accounts to resolve plant-level issues.</li><li>Demonstrated ability to manage multiple projects and priorities while maintaining attention to detail.</li><li>Motivation to grow supplier quality expertise and work across a variety of industries and product types.</li></ul>Work EnvironmentThe role operates within a small office environment attached to a very clean and well-equipped quality laboratory. The lab includes instruments such as micrometers, calibrated gages, optical comparators, hardness testers, plug gages, and computer-based measurement and reporting systems. The broader facility includes a large warehouse focused on distribution rather than manufacturing, with products such as electrical components and stamped and molded parts. Local sites support operations in nearby locations, and the position involves regular interaction with branch operations and quality teams. Most of the workday is spent on the floor and in the lab, resolving issues and supporting supplier and customer needs, with additional time allocated to supplier visits and audits. Domestic travel typically ranges from about 10% to 20% depending on active projects. The environment supports hands-on problem solving, collaboration with cross-functional teams, and exposure to a wide range of industries and customer applications.OJob Type &amp; LocationThis is a Contract to Hire position based out of Solon, OH.Pay and BenefitsThe pay range for this position is $43.00 - $45.00/hr.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)Workplace TypeThis is a fully onsite position in Solon,OH.Application DeadlineThis position is anticipated to close on Aug 7, 2026.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 Manager/Supplier Quality Engineer to lead the development and implementation of an ISO 9001-compliant Quality Management System while owning key Supplier Quality initiatives. This role involves building quality processes from the ground up, driving certification efforts, improving supplier performance, and ensuring compliance across manufacturing operations. This is an excellent opportunity for a quality professional experienced in creating or enhancing a QMS, leading audits, and partnering with cross-functional teams to drive continuous improvement.Responsibilities<ul><li>Lead the development, implementation, and maintenance of an ISO 9001-compliant Quality Management System (QMS).</li><li>Conduct QMS gap assessments and create implementation roadmaps for certification readiness.</li><li>Establish and manage document control processes, including procedures, work instructions, and revision control.</li><li>Develop and execute internal audit programs, corrective actions, and continuous improvement initiatives.</li><li>Facilitate Management Review meetings and track quality KPIs, risks, and improvement opportunities.</li><li>Prepare for and support external audits and ISO certification activities.</li><li>Own Supplier Quality processes including supplier qualification, onboarding, audits, scorecards, and performance metrics.</li><li>Lead supplier and internal corrective actions utilizing 8D, A3, 5 Why, and Root Cause Analysis methodologies.</li><li>Develop incoming inspection plans, sampling plans, and acceptance criteria.</li><li>Drive quality improvements through SPC, MSA, capability studies, trend analysis, and data-driven decision making.</li><li>Support new product introductions and engineering changes while ensuring supplier readiness and quality controls are established.</li></ul>Essential Skills<ul><li>5+ years of Quality Engineering experience within a manufacturing environment.</li><li>Hands-on experience with Supplier Quality programs and supplier development.</li><li>Experience building, implementing, or improving an ISO 9001 Quality Management System.</li><li>Strong knowledge of ISO 9001 requirements, internal audits, corrective actions, and continuous improvement.</li><li>Internal Auditor certification or training.</li><li>Bachelor's degree in Engineering, Quality, or a related field (or equivalent experience).</li><li>Experience with document control, process mapping, and procedure development.</li><li>Strong problem-solving skills utilizing 8D, A3, 5 Why, Fishbone, or similar methodologies.</li><li>Ability to read and interpret engineering drawings, schematics, GD&amp;T, and inspection requirements.</li></ul>Additional Skills &amp; Qualifications<ul><li>ISO 9001 Lead Auditor Certification.</li><li>Welding inspection experience.</li><li>AWS/CWI Certification.</li><li>Experience with SPC, MSA, capability studies, and statistical quality tools.</li></ul>Work EnvironmentThis position is based on-site.Job Type &amp; LocationThis is a Permanent position based out of Delaware, OH.Pay and BenefitsThe pay range for this position is $85000.00 - $90000.00/yr.• Medical, dental, and vision insurance
 • 401(k) with company match and immediate vesting
 • Paid time off (PTO)
 • Life insurance
 • Disability insurance
 • Employee Assistance Program (EAP)
 • Health Savings Account (HSA) options
 • Flexible work arrangements for eligible positionWorkplace TypeThis is a fully onsite position in Delaware,OH.Application DeadlineThis position is anticipated to close on Aug 3, 2026.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.

Join a fast-paced medical device manufacturing environment where quality drives innovation. As a Quality Engineer, you will play a key role in bringing new products from concept to commercial production, ensuring compliance, reliability, and manufacturing excellence every step of the way.<h4>What You'll Do</h4><ul><li>Lead quality activities for new product development (NPD), design transfer, and manufacturing transfer projects.</li><li>Partner with Engineering, Operations, Supply Chain, and customers to ensure products meet regulatory and quality requirements.</li><li>Drive process qualification and validation activities (IQ/OQ/PQ) to support successful product launches.</li><li>Conduct risk assessments using dFMEA, pFMEA, control plans, and other quality tools to identify and mitigate potential issues.</li><li>Support supplier qualification, process capability studies, and manufacturing readiness initiatives.</li><li>Utilize statistical methods and data analysis tools to improve processes, reduce defects, and drive continuous improvement.</li><li>Lead root cause investigations and CAPA activities to resolve quality issues and strengthen product performance.</li><li>Serve as a trusted quality partner throughout the product lifecycle, communicating project progress, risks, and outcomes to stakeholders.</li></ul><h4>What We're Looking For</h4><ul><li>Bachelor's degree in Engineering or a related technical discipline.</li><li>5+ years of Quality Engineering experience in medical devices or other regulated manufacturing environments.</li><li>Strong experience with NPD, design transfer, process validation, and manufacturing transfer.</li><li>Working knowledge of FDA 21 CFR Part 820, quality systems, and risk management principles.</li><li>Hands-on expertise with FMEA, DOE, SPC, Gauge R&amp;R, process capability analysis, CAPA, and root cause investigations.</li><li>Proficiency with statistical software such as Minitab or JMP.</li><li>Strong project management, communication, and problem-solving skills.</li></ul><h4>Preferred Qualifications</h4><ul><li>Experience in medical device, plating, surface finishing, coatings, or CDMO environments.</li><li>CQE, Lean Six Sigma, or other quality certifications.</li><li>Knowledge of cleanroom manufacturing, sterilization processes, software validation, and eQMS systems.</li><li>Familiarity with Keyence systems, profilometers, and PLC platforms (Allen-Bradley or Siemens).</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Anoka, MN.Pay and BenefitsThe pay range for this position is $45.00 - $58.00/hr.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)Workplace TypeThis is a fully onsite position in Anoka,MN.Application DeadlineThis position is anticipated to close on Jul 29, 2026.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: Supplier Quality EngineerJob DescriptionThe Supplier Quality Engineer serves as the primary point of contact for all supplier-related quality issues. This role verifies non-conforming materials at receiving inspection, coordinates corrective actions with suppliers and internal teams, and ensures that supplier quality management systems and manufacturing processes meet organizational standards. The Supplier Quality Engineer also supports the qualification of new suppliers and contributes to the continuous improvement of overall supplier quality performance.Responsibilities<ul><li>Serve as the primary point of contact for supplier quality issues and act as the liaison between internal product teams and suppliers.</li><li>Work closely with receiving inspection personnel to verify non-conformances at the time of material receipt and ensure accurate documentation of issues.</li><li>Issue and track Supplier Corrective Action Requests (SCARs), ensuring timely responses and effective resolution of supplier-related problems.</li><li>Develop, manage, and monitor timelines to resolve supplier issues, and verify the effectiveness of corrective and preventive actions.</li><li>Conduct supplier visits to perform audits, address ongoing quality issues, and support product validation activities.</li><li>Perform audits of supplier Quality Management Systems (QMS) and manufacturing processes to ensure compliance with organizational and regulatory requirements.</li><li>Collaborate with quality engineering staff and suppliers when Automated Inspection Equipment (AIE) and/or Measurement Systems Evaluation (MSE) are required, ensuring appropriate use and validation of measurement systems.</li><li>Work with suppliers to perform first article inspections at both supplier facilities and internal locations, confirming that initial production meets all specifications and standards.</li><li>Support purchasing personnel in the process of qualifying new suppliers, including participation in evaluations, audits, and ongoing performance reviews.</li><li>Assist with the daily scheduling of priorities in receiving inspection to ensure timely and efficient processing of incoming materials.</li></ul>Essential Skills<ul><li>Proven experience in quality engineering, quality assurance, or supplier quality roles within a manufacturing environment.</li><li>Strong knowledge of quality control and quality management principles, including practical application of Quality Management Systems (QMS).</li><li>Hands-on experience conducting audits of supplier Quality Management Systems and manufacturing processes.</li><li>Ability to work directly with suppliers to perform inspections, including first article inspections, and to address quality issues collaboratively.</li><li>Experience issuing, tracking, and closing Supplier Corrective Actions (SCARs), with a focus on verifying effectiveness of corrective actions.</li><li>Familiarity with Automated Inspection Equipment (AIE) and Measurement Systems Evaluation (MSE), and the ability to support their use with suppliers.</li><li>Strong communication skills to serve as an effective point of contact between internal teams and suppliers.</li><li>Ability to organize and prioritize work, including assisting with daily scheduling of receiving inspection activities.</li><li>Attention to detail and analytical skills to verify non-conformances and evaluate supplier performance.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience performing product validation activities at supplier sites.</li><li>Experience in auditing and improving manufacturing processes in collaboration with suppliers.</li><li>Exposure to supplier qualification processes in partnership with purchasing or procurement teams.</li><li>Ability to travel to supplier locations for audits, inspections, and issue resolution as needed.</li></ul>Work EnvironmentThis role operates in an in-person work environment. The Supplier Quality Engineer works closely with receiving inspection personnel, quality engineering staff, and purchasing teams within a manufacturing or production setting. The position involves regular interaction with suppliers, including on-site visits to supplier facilities for audits, inspections, and product validation activities. Work may include time on the shop floor, in inspection areas, and in office settings for documentation, analysis, and coordination.Job Type &amp; LocationThis is a Permanent position based out of Clear Lake, SD.Pay and BenefitsThe pay range for this position is $60000.00 - $90000.00/yr.Full time benefits offered.Workplace TypeThis is a fully onsite position in Clear Lake,SD.Application DeadlineThis position is anticipated to close on Aug 4, 2026.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 EngineerThe Quality Engineer is responsible for maintaining and improving quality systems, driving continuous improvement initiatives, and ensuring compliance within a regulated manufacturing environment. This role partners with internal teams, customers, and suppliers to resolve quality issues, support new product introductions, and enhance manufacturing processes.Key Responsibilities<ul><li>Maintain and improve Quality Management System (QMS) procedures and regulatory compliance.</li><li>Develop and manage Quality Assurance (QA) plans for new product introductions using APQP and process optimization methodologies.</li><li>Lead root cause investigations and drive CAPA activities for nonconformances.</li><li>Analyze quality and production data to identify trends and improvement opportunities.</li><li>Support process validation, test method validation, and MSA activities.</li><li>Provide quality input during process design, development, and implementation phases.</li><li>Improve inspection methods, quality documentation, and training programs.</li><li>Manage supplier, customer, and internal quality issues, ensuring effective corrective actions.</li><li>Support supplier quality initiatives and continuous improvement efforts.</li><li>Partner with cross-functional teams to standardize manufacturing processes and promote quality excellence.</li><li>Maintain document control systems and provide technical support to customers and internal stakeholders.</li><li>Mentor and support the development of quality assurance team members.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Park City, IL.Pay and BenefitsThe pay range for this position is $42.00 - $46.00/hr.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)Workplace TypeThis is a fully onsite position in Park City,IL.Application DeadlineThis position is anticipated to close on Aug 4, 2026.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 (Contract)Job DescriptionThis short-term Quality Engineer contract role (approximately six months) focuses on providing critical Quality Assurance support by clearing a backlog of investigations and contributing to key QA activities in a regulated environment. You will lead and support investigations related to nonconformances, CAPAs, and complaints, while also assisting with document control, batch release, and document reviews to ensure a full and varied workload throughout the contract. The position requires strong experience in medical devices or similarly regulated industries, excellent root cause analysis capabilities, and clear, precise technical writing skills.Responsibilities<ul><li>Lead and support investigations for nonconformances (NC), CAPAs, and complaints to address a backlog of quality issues in a timely and compliant manner.</li><li>Perform thorough root cause analysis using structured problem-solving methods to identify underlying causes of quality issues and recommend effective corrective and preventive actions.</li><li>Document investigations clearly and accurately, producing high-quality technical reports that meet regulatory and internal quality standards.</li><li>Support additional Quality Assurance activities such as document control, ensuring controlled documents are current, accurate, and properly maintained within the QMS.</li><li>Participate in batch release activities by reviewing relevant documentation for completeness, accuracy, and compliance with applicable standards and procedures.</li><li>Conduct detailed document reviews of procedures, technical documentation, and records to verify compliance with internal quality requirements and regulatory expectations.</li><li>Collaborate closely with the Quality Assurance team and cross-functional partners, including R&amp;D, service, and operations, to gather information and ensure alignment on investigation findings and actions.</li><li>Review and interpret quality system procedures, technical documents, and regulatory requirements to support robust and compliant investigation practices.</li><li>Utilize the QMS system (Qdocs) to manage investigations, documentation, and quality records in an organized and traceable manner.</li><li>Contribute to continuous improvement initiatives within the quality system by identifying trends, recommending process improvements, and supporting implementation of enhanced QA practices.</li></ul>Essential Skills<ul><li>At least 5 years of experience working as a Quality Engineer or QA professional, with a strong focus on investigations.</li><li>Proven experience conducting investigations involving nonconformances (NC), CAPAs, and complaints in a regulated environment.</li><li>Strong understanding of general root cause analysis methodologies and their application to quality issues.</li><li>Excellent technical writing skills, with the ability to produce clear, concise, and well-structured investigation reports and quality documentation.</li><li>Experience working within a Quality Management System (QMS), including use of electronic systems such as Qdocs or similar platforms.</li><li>Background in medical devices is preferred, or substantial experience in a regulated industry such as pharmaceuticals, biotechnology, or other FDA-regulated sectors.</li><li>Knowledge of FDA regulations and expectations related to quality systems, investigations, and CAPA processes.</li><li>Familiarity with ISO standards relevant to quality and medical devices (such as ISO-based QMS frameworks).</li><li>Experience with quality control practices and principles in a regulated environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a medical device environment, including understanding of device lifecycle, risk management, and post-market quality activities.</li><li>Exposure to ISO-based quality standards and their application in daily QA activities.</li><li>Comfort working with cross-functional teams including R&amp;D, service, and operations to gather data and implement corrective and preventive actions.</li><li>Ability to quickly learn and adapt to site-specific QMS tools, including Qdocs, and local procedures.</li><li>Strong attention to detail and organizational skills to manage multiple investigations and documentation tasks simultaneously.</li><li>Effective communication skills, both written and verbal, to present findings and collaborate with stakeholders at different levels.</li><li>Demonstrated ability to work independently while also contributing as a proactive member of a small quality team.</li></ul>Work EnvironmentYou will work as part of a small, collaborative quality team of approximately three other professionals in a hybrid work setting. During the initial phase of the contract, you will spend the majority of your time onsite to receive hands-on training, become familiar with the quality system, and integrate with cross-functional partners. After this training period, a hybrid arrangement with approximately two days in the office each week may be suitable, depending on project needs and performance. The environment is structured and regulated, with a strong emphasis on compliance, documentation accuracy, and adherence to FDA and ISO-based quality standards. You will use a Quality Management System (Qdocs) and other standard office and quality tools to manage investigations, documentation, and batch release activities, working closely with R&amp;D, service, operations, and other stakeholders to support a robust and efficient quality system.Job Type &amp; LocationThis is a Contract position based out of Golden, CO.Pay and BenefitsThe pay range for this position is $40.00 - $65.00/hr.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)Workplace TypeThis is a hybrid position in Golden,CO.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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>Position Overview</h3>We are seeking a Mass Production Parts Quality Analyst to support supplier quality activities and drive continuous improvement initiatives within automotive manufacturing operations. This role is responsible for investigating quality concerns, leading root cause analyses, collaborating with suppliers on corrective actions, and ensuring production parts meet Honda's quality standards.<h3>Key Responsibilities</h3><ul><li>Lead detailed investigations of quality issues, including part measurements and data analysis, to minimize impact on manufacturing operations and downstream customers.</li><li>Prepare and submit technical documentation through the Honda Trouble Report (HTR) system to communicate supplier quality concerns and drive corrective actions.</li><li>Define and manage supplier part change requirements using the Change Point Control System (CPCS), ensuring quality documentation is thoroughly evaluated prior to management review.</li><li>Conduct complex root cause investigations and implement effective corrective and preventive actions.</li><li>Lead Supplier Quality Assurance Visits (QAVs) to review quality concerns, verify countermeasure implementation, and ensure long-term issue resolution.</li><li>Evaluate and disposition non-conforming parts and determine appropriate containment actions.</li><li>Assess incoming supplier parts to ensure compliance with quality standards and specifications.</li><li>Apply PDCA (Plan-Do-Check-Act) methodology and other quality tools to effectively resolve quality issues.</li><li>Review and approve supplier corrective actions, countermeasures, and change points before production implementation.</li><li>Provide guidance and mentorship to newer team members on quality processes, procedures, and best practices.</li></ul><h3>Required Qualifications</h3><ul><li>Bachelor's Degree in Engineering or a related technical field.</li><li>Minimum of 2 years of quality engineering experience within a manufacturing environment.</li><li>Experience leading root cause investigations and implementing corrective actions.</li><li>Strong understanding of quality systems, supplier quality, and continuous improvement methodologies.</li><li>Knowledge of automotive manufacturing processes and industry quality standards.</li></ul><h3>Preferred Qualifications</h3><ul><li>Experience with welding processes or plastic injection molding.</li><li>CMM (Coordinate Measuring Machine) experience.</li><li>Familiarity with supplier quality management and production part approval processes.</li></ul><h3>Required Quality Tools &amp; Methodologies</h3><ul><li>Root Cause Corrective Action (RCCA)</li><li>8D Problem Solving</li><li>5 Why Analysis</li><li>Fishbone (Ishikawa) Analysis</li><li>PDCA (Plan-Do-Check-Act)</li><li>PFMEA (Process Failure Mode and Effects Analysis)</li></ul><h3>Key Skills</h3><ul><li>Quality Engineering</li><li>Root Cause Analysis</li><li>Quality Assurance</li><li>Automotive Manufacturing</li><li>Supplier Quality</li><li>TS/IATF 16949 Standards</li><li>PFMEA</li><li>Corrective and Preventive Actions</li></ul><h3>Experience Level</h3>Entry to Mid-Level (2+ years of relevant quality engineering experience)Job Type &amp; LocationThis is a Contract to Hire position based out of Timmonsville, SC.Pay and BenefitsThe pay range for this position is $33.65 - $36.06/hr.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)Workplace TypeThis is a fully onsite position in Timmonsville,SC.Application DeadlineThis position is anticipated to close on Aug 3, 2026.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
					- Lead improvement initiatives in manufacturing, including automation and digital systems.
- Validate processes through capability studies and gauge R&amp;R analysis.
- Resolve quality issues using root cause analysis and corrective actions.
- Support manufacturing operations with audits and quality analysis.
- Manage supplier corrective actions and collaborate with procurement.
- Assist with New Product Introduction and integration of new technologies.
- Maintain accurate documentation and quality records.
										Skills
					Quality engineering, Ppap, Root cause analysis, Quality management, Apqp, Corrective action plans, new product implementation, blueprint reading, continuous improvement, troubleshooting, Supplier quality
										Top Skills Details
					Quality engineering,Ppap,Root cause analysis,Quality management,Apqp,Corrective action plans
										Additional Skills &amp; Qualifications
					- Bachelors’ Degree within Engineering field preferred 
- Blueprint reading and GDT experience
- APQP experience
- Assembly and manufacturing process knowledge
- Strong Leadership Ability
- Team Player
- Strong Communicator
										Experience Level
					Expert Level
					Job Type &amp; LocationThis is a Contract to Hire position based out of Berea, KY.Pay and BenefitsThe pay range for this position is $28.85 - $38.46/hr.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)Workplace TypeThis is a fully onsite position in Berea,KY.Application DeadlineThis position is anticipated to close on Jul 26, 2026.About Actalent 

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



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



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



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



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



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

Job Title: Quality EngineerJob DescriptionThe Quality Engineer will execute quality control activities within a fabrication shop supporting microelectronics capital projects. This engineering role focuses on ensuring products meet stringent quality standards the first time, with minimal rework or delays. The position requires an experienced, forward-thinking quality professional who contributes actively as a member of the Quality Team and helps secure the expected quality of all fabricated products.Responsibilities<ul><li>Execute quality control activities in a fabrication shop environment for microelectronics capital projects.</li><li>Ensure products meet defined quality requirements on the first pass, minimizing rework, defects, and schedule delays.</li><li>Perform welding inspections to verify compliance with applicable standards and specifications.</li><li>Review and interpret blueprints, mechanical drawings, and structural documentation to validate quality criteria.</li><li>Apply ISO 9001 principles and procedures to maintain and improve the quality management system.</li><li>Conduct supplier audits to assess and monitor supplier quality performance and adherence to standards.</li><li>Support and perform quality assurance activities throughout the production process.</li><li>Identify, investigate, and document nonconformities and quality issues.</li><li>Lead or participate in root cause analysis to determine underlying causes of defects or process deviations.</li><li>Recommend and help implement corrective and preventive actions to improve product and process quality.</li><li>Collaborate with engineering, production, and other cross-functional teams to resolve quality-related concerns.</li><li>Contribute to continuous improvement initiatives, leveraging Six Sigma tools and methodologies where applicable.</li><li>Maintain accurate quality records, inspection reports, and audit documentation.</li><li>Support a culture of quality and accountability within the fabrication shop and broader project teams.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in quality engineering.</li><li>Hands-on experience with quality engineering in a fabrication or manufacturing environment.</li><li>Strong knowledge of ISO 9001 and its application within a quality management system.</li><li>Experience performing welding inspections and evaluating weld quality.</li><li>Ability to read and interpret blueprints, mechanical drawings, and structural documents.</li><li>Proficiency in quality assurance practices and quality control methodologies.</li><li>Experience conducting supplier audits and assessing supplier quality performance.</li><li>Proven ability to perform root cause analysis and develop effective corrective actions.</li><li>Familiarity with Six Sigma principles; Six Sigma Green Belt certification preferred.</li><li>Attention to detail and strong analytical and problem-solving skills.</li><li>Effective communication skills to collaborate with cross-functional teams and document findings clearly.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certified Welding Inspector (CWI) or AWS certification is a strong plus.</li><li>Experience in microelectronics or capital project environments is beneficial.</li><li>Experience in mechanical or structural fabrication quality is advantageous.</li><li>Demonstrated ability to support continuous improvement initiatives using Six Sigma tools.</li><li>Strong organizational skills and ability to manage multiple quality activities simultaneously.</li><li>Forward-thinking mindset with a focus on improving processes and preventing defects.</li><li>Interest in professional growth and taking on increasing responsibility over time.</li></ul>Work EnvironmentThis role is primarily based in a cubicle office setting, with regular collaboration across engineering and production teams. The Quality Engineer will spend occasional time on the fabrication shop floor to conduct inspections, audits, and investigations, and may travel domestically on a minimal basis for supplier visits or project needs. The environment supports complex and technically interesting projects in the microelectronics capital space, offering opportunities for growth and involvement in impactful, high-visibility work.Job Type &amp; LocationThis is a Permanent position based out of Brooklyn Park, MN.Pay and BenefitsThe pay range for this position is $90000.00 - $105000.00/yr.Strong Internal Company Benefits. If you have any questions or wish to see a copy of the benefits, please feel free to reach out.Workplace TypeThis is a fully onsite position in Brooklyn Park,MN.Application DeadlineThis position is anticipated to close on Aug 3, 2026.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 (Contract)Job DescriptionThis short-term Quality Engineer contract role (approximately six months) focuses on providing critical Quality Assurance support by clearing a backlog of investigations and contributing to key QA activities in a regulated environment. You will lead and support investigations related to nonconformances, CAPAs, and complaints, while also assisting with document control, batch release, and document reviews to ensure a full and varied workload throughout the contract. The position requires strong experience in medical devices or similarly regulated industries, excellent root cause analysis capabilities, and clear, precise technical writing skills.Responsibilities<ul><li>Lead and support investigations for nonconformances (NC), CAPAs, and complaints to address a backlog of quality issues in a timely and compliant manner.</li><li>Perform thorough root cause analysis using structured problem-solving methods to identify underlying causes of quality issues and recommend effective corrective and preventive actions.</li><li>Document investigations clearly and accurately, producing high-quality technical reports that meet regulatory and internal quality standards.</li><li>Support additional Quality Assurance activities such as document control, ensuring controlled documents are current, accurate, and properly maintained within the QMS.</li><li>Participate in batch release activities by reviewing relevant documentation for completeness, accuracy, and compliance with applicable standards and procedures.</li><li>Conduct detailed document reviews of procedures, technical documentation, and records to verify compliance with internal quality requirements and regulatory expectations.</li><li>Collaborate closely with the Quality Assurance team and cross-functional partners, including R&amp;D, service, and operations, to gather information and ensure alignment on investigation findings and actions.</li><li>Review and interpret quality system procedures, technical documents, and regulatory requirements to support robust and compliant investigation practices.</li><li>Utilize the QMS system (Qdocs) to manage investigations, documentation, and quality records in an organized and traceable manner.</li><li>Contribute to continuous improvement initiatives within the quality system by identifying trends, recommending process improvements, and supporting implementation of enhanced QA practices.</li></ul>Essential Skills<ul><li>At least 5 years of experience working as a Quality Engineer or QA professional, with a strong focus on investigations.</li><li>Proven experience conducting investigations involving nonconformances (NC), CAPAs, and complaints in a regulated environment.</li><li>Strong understanding of general root cause analysis methodologies and their application to quality issues.</li><li>Excellent technical writing skills, with the ability to produce clear, concise, and well-structured investigation reports and quality documentation.</li><li>Experience working within a Quality Management System (QMS), including use of electronic systems such as Qdocs or similar platforms.</li><li>Background in medical devices is preferred, or substantial experience in a regulated industry such as pharmaceuticals, biotechnology, or other FDA-regulated sectors.</li><li>Knowledge of FDA regulations and expectations related to quality systems, investigations, and CAPA processes.</li><li>Familiarity with ISO standards relevant to quality and medical devices (such as ISO-based QMS frameworks).</li><li>Experience with quality control practices and principles in a regulated environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a medical device environment, including understanding of device lifecycle, risk management, and post-market quality activities.</li><li>Exposure to ISO-based quality standards and their application in daily QA activities.</li><li>Comfort working with cross-functional teams including R&amp;D, service, and operations to gather data and implement corrective and preventive actions.</li><li>Ability to quickly learn and adapt to site-specific QMS tools, including Qdocs, and local procedures.</li><li>Strong attention to detail and organizational skills to manage multiple investigations and documentation tasks simultaneously.</li><li>Effective communication skills, both written and verbal, to present findings and collaborate with stakeholders at different levels.</li><li>Demonstrated ability to work independently while also contributing as a proactive member of a small quality team.</li></ul>Work EnvironmentYou will work as part of a small, collaborative quality team of approximately three other professionals in a hybrid work setting. During the initial phase of the contract, you will spend the majority of your time onsite to receive hands-on training, become familiar with the quality system, and integrate with cross-functional partners. After this training period, a hybrid arrangement with approximately two days in the office each week may be suitable, depending on project needs and performance. The environment is structured and regulated, with a strong emphasis on compliance, documentation accuracy, and adherence to FDA and ISO-based quality standards. You will use a Quality Management System (Qdocs) and other standard office and quality tools to manage investigations, documentation, and batch release activities, working closely with R&amp;D, service, operations, and other stakeholders to support a robust and efficient quality system.Job Type &amp; LocationThis is a Contract position based out of Golden, CO.Pay and BenefitsThe pay range for this position is $40.00 - $65.00/hr.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)Workplace TypeThis is a hybrid position in Golden,CO.Application DeadlineThis position is anticipated to close on Jul 29, 2026.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.

Join a fast-paced medical device manufacturing environment where quality drives innovation. As a Quality Engineer, you will play a key role in bringing new products from concept to commercial production, ensuring compliance, reliability, and manufacturing excellence every step of the way.<h4>What You'll Do</h4><ul><li>Lead quality activities for new product development (NPD), design transfer, and manufacturing transfer projects.</li><li>Partner with Engineering, Operations, Supply Chain, and customers to ensure products meet regulatory and quality requirements.</li><li>Drive process qualification and validation activities (IQ/OQ/PQ) to support successful product launches.</li><li>Conduct risk assessments using dFMEA, pFMEA, control plans, and other quality tools to identify and mitigate potential issues.</li><li>Support supplier qualification, process capability studies, and manufacturing readiness initiatives.</li><li>Utilize statistical methods and data analysis tools to improve processes, reduce defects, and drive continuous improvement.</li><li>Lead root cause investigations and CAPA activities to resolve quality issues and strengthen product performance.</li><li>Serve as a trusted quality partner throughout the product lifecycle, communicating project progress, risks, and outcomes to stakeholders.</li></ul><h4>What We're Looking For</h4><ul><li>Bachelor's degree in Engineering or a related technical discipline.</li><li>5+ years of Quality Engineering experience in medical devices or other regulated manufacturing environments.</li><li>Strong experience with NPD, design transfer, process validation, and manufacturing transfer.</li><li>Working knowledge of FDA 21 CFR Part 820, quality systems, and risk management principles.</li><li>Hands-on expertise with FMEA, DOE, SPC, Gauge R&amp;R, process capability analysis, CAPA, and root cause investigations.</li><li>Proficiency with statistical software such as Minitab or JMP.</li><li>Strong project management, communication, and problem-solving skills.</li></ul><h4>Preferred Qualifications</h4><ul><li>Experience in medical device, plating, surface finishing, coatings, or CDMO environments.</li><li>CQE, Lean Six Sigma, or other quality certifications.</li><li>Knowledge of cleanroom manufacturing, sterilization processes, software validation, and eQMS systems.</li><li>Familiarity with Keyence systems, profilometers, and PLC platforms (Allen-Bradley or Siemens).</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Anoka, MN.Pay and BenefitsThe pay range for this position is $45.00 - $58.00/hr.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)Workplace TypeThis is a fully onsite position in Anoka,MN.Application DeadlineThis position is anticipated to close on Aug 7, 2026.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 product and process quality across the entire product lifecycle, from new product development and validation through manufacturing, production support, and sustaining engineering. This role investigates product and manufacturing quality issues, drives root cause analysis and corrective actions, and partners closely with cross-functional teams to improve quality, reliability, and performance. The Quality Engineer develops and maintains quality documentation, supports validation and testing activities, and ensures that products and processes comply with quality standards and customer requirements.Responsibilities<ul><li>Support product and process quality activities throughout the entire product lifecycle, including new product development, manufacturing, validation, production support, and sustaining engineering.</li><li>Investigate product and manufacturing quality issues, perform detailed root cause analysis, and lead corrective and preventive action efforts to improve quality, reliability, and performance.</li><li>Partner with Engineering, Manufacturing, Test, Quality, and Operations teams to resolve technical issues and drive continuous improvement initiatives.</li><li>Support product validation, reliability testing, environmental testing, and qualification activities to ensure products meet performance, reliability, and quality requirements.</li><li>Develop, update, and maintain quality documentation, including inspection criteria, work instructions, test plans, quality procedures, and quality records.</li><li>Review and support product changes, deviations, and engineering updates to ensure compliance with quality requirements, standards, and regulatory expectations.</li><li>Analyze quality trends, customer issues, field returns, and manufacturing data to identify systemic issues, opportunities for improvement, and defect-reduction strategies.</li><li>Monitor and track quality metrics, prepare reports, and communicate findings, risks, and data-driven recommendations to stakeholders and leadership.</li><li>Support internal audits and Quality Management System activities, contributing to the implementation, maintenance, and improvement of quality processes and best practices.</li><li>Serve as a technical quality resource within cross-functional teams, providing guidance on problem-solving methodologies, quality standards, testing requirements, and product reliability.</li><li>Contribute to new product introduction activities by supporting product validation, verification, and reliability testing plans and execution.</li><li>Apply structured problem-solving tools such as 8D, Fishbone, CAPA, and other methodologies to address complex quality and manufacturing issues.</li><li>Collaborate with Supplier Quality and Manufacturing Engineering to ensure robust manufacturing quality systems, inspection methodologies, and sampling plans.</li><li>Prepare and deliver presentations on quality performance, trends, and improvement initiatives to cross-functional teams.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering or a related technical field.</li><li>5+ years of experience in Quality Engineering, Manufacturing Engineering, or a related field within a manufacturing environment.</li><li>Experience in electronics or electromechanical manufacturing environments, including PCBA, SMT, and board-level products.</li><li>Quality Engineering experience supporting manufacturing and product quality throughout the product lifecycle.</li><li>Strong experience in problem-solving and root cause analysis using tools such as 8D, Fishbone, CAPA, and corrective action methodologies.</li><li>Hands-on experience with product quality in electronics manufacturing, including PCBA quality and electronics manufacturing processes.</li><li>Experience supporting product validation, verification, reliability testing, and environmental testing.</li><li>Working knowledge of ISO 9001 and quality management systems, including internal audits and regulatory or compliance requirements.</li><li>Ability to develop quality metrics, analyze trends, and present data-driven recommendations to stakeholders.</li><li>Understanding of GD&amp;T, inspection methodologies, sampling plans, and manufacturing quality systems.</li><li>Exposure to destructive and non-destructive test methods.</li><li>Proficiency with Microsoft Office applications, including Excel, Word, Visio, Access, and Power BI.</li><li>Ability to work independently with minimal supervision while managing multiple priorities and projects.</li><li>Strong verbal and written communication skills with the ability to collaborate effectively across cross-functional teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a strong technical environment with complex electromechanical and electronics-based products.</li><li>Familiarity with reliability test methods and product qualification processes.</li><li>Lean Six Sigma Green Belt or Black Belt certification is a plus.</li><li>ASQ certifications such as Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or Certified Quality Manager (CQM) are highly desirable.</li><li>IPC-A-610 certification is highly desirable.</li><li>ISO 9001 Lead Auditor certification is highly desirable.</li><li>Experience working with continuous improvement initiatives and lean methodologies.</li><li>Comfortably presenting quality data and improvement plans to cross-functional stakeholders and leadership.</li><li>Interest in supporting products from development through production and sustainment with a focus on long-term reliability and customer satisfaction.</li><li>Motivation to influence product quality and process improvements in a high-visibility role with broad cross-functional interaction.</li></ul>Work EnvironmentThis is an on-site role with a typical schedule of 8:00 AM to 5:00 PM. You will work in a highly collaborative, cross-functional environment alongside Product Quality, Manufacturing Engineering, Test Engineering, Supplier Quality, and Operations teams. The setting involves exposure to complex electromechanical and electronics-based products and offers significant involvement in product development, validation, manufacturing, and continuous improvement initiatives. The organization provides a strong technical environment, comprehensive benefits, tuition reimbursement, and meaningful opportunities for career growth and advancement.Job Type &amp; LocationThis is a Permanent position based out of Carlsbad, CA.Pay and BenefitsThe pay range for this position is $94800.00 - $126400.00/yr.3 weeks PTO + holidays
Medical, dental, vision
401K + life insurance
Tuition reimbursement
Pet insuranceWorkplace TypeThis is a fully onsite position in Carlsbad,CA.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

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



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



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



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



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



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

Quality EngineerJob DescriptionThe Quality Engineer develops and improves manufacturing processes and products, validates new equipment and technologies, supports production with continuous improvement on the shop floor, and manages customer complaints along with NCR and CAPA activities. This role leads change requests with customers, ensures compliance with ISO, FDA, and other applicable standards, and collaborates closely with QA Technicians and Quality Inspectors to maintain and enhance overall product quality.Responsibilities<ul><li>Develop new manufacturing processes and products and revise existing ones to improve quality, efficiency, and reliability.</li><li>Create and update project-specific quality plans that fully meet customer requirements and internal standards.</li><li>Work as an integral member of cross-functional teams to support product and process development activities.</li><li>Develop robust measurement methods to verify that products meet defined quality standards and specifications.</li><li>Troubleshoot measurement methods and equipment to ensure accuracy, repeatability, and reliability of inspection results.</li><li>Lead validation activities for new products and technologies, including IQ, OQ, and PQ phases.</li><li>Serve as the QA lead for equipment validation to ensure new equipment meets regulatory and internal quality requirements.</li><li>Collaborate with customers and suppliers to define and refine new product processes and quality expectations.</li><li>Lead the management of customer complaints and supplier SCARs, ensuring timely investigation and resolution.</li><li>Compile and analyze statistical data to evaluate process capabilities and identify improvement opportunities.</li><li>Conduct PFMEA, GR&amp;R, and SPC studies to assess and control process risks and variation.</li><li>Create and maintain quality system documentation, including quality plans, inspection plans, control plans, and work instructions.</li><li>Manage NCRs, CAPAs, and customer complaints from creation through root cause analysis, corrective action, verification, and closure.</li><li>Apply structured problem-solving tools and work within cross-functional teams to resolve quality issues effectively.</li><li>Lead production changes while ensuring compliance with customer agreements, ISO standards, and internal requirements.</li><li>Prepare, submit, and track change requests (SCR) with customers, ensuring clear communication and approval.</li><li>Support production in achieving APU objectives by providing quality engineering expertise and guidance.</li><li>Generate and report quality KPIs for PSM2 and other performance tracking needs.</li><li>Perform internal and external audits to verify compliance with quality system requirements and drive improvements.</li><li>Provide backup support for other Quality Engineers on customer or internal tasks as needed.</li><li>Identify, lead, and support continuous improvement initiatives across processes and products.</li><li>Participate in LEAN and LEAP workshops to drive waste reduction, process optimization, and cost savings.</li><li>Contribute to risk management activities and ensure that nonconforming material is appropriately controlled and dispositioned.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Manufacturing Engineering or a related technical field.</li><li>Minimum two years of relevant quality engineering experience.</li><li>Strong blueprint reading skills with a solid understanding of GD&amp;T.</li><li>Hands-on experience developing manufacturing quality plans for production environments.</li><li>Demonstrated experience conducting process capability studies, GR&amp;R, PFMEA, and SPC.</li><li>Proven experience working with NCR and CAPA processes from initiation through closure.</li><li>Experience working in an ISO-regulated environment, preferably within a medical or similar regulated industry.</li><li>Proficiency with quality management systems and quality management principles.</li><li>Working knowledge of corrective action planning and root cause analysis methods.</li><li>Proficient PC skills in a Windows environment, including common office and data analysis tools.</li><li>Effective written and verbal communication skills for interaction with cross-functional teams, customers, and suppliers.</li><li>Strong interpersonal and teamwork skills with the ability to collaborate across departments.</li><li>Experience with validation activities, including equipment and process validation.</li><li>Understanding of quality control, quality assurance, and quality management practices in a manufacturing setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a precision machine shop environment, preferably in medical device or similar high-precision manufacturing.</li><li>Experience with PPAP and other advanced product quality planning tools.</li><li>Expereince in supplier quality management and SCAR handling.</li><li>Familiarity with nonconforming material control and documentation requirements.</li><li>Experience optimizing manufacturing processes to achieve ongoing cost reductions and efficiency gains.</li><li>LEAN and/or Six Sigma training with demonstrated application of continuous improvement tools.</li><li>Demonstrated use of structured problem-solving methodologies such as 8D.</li><li>Experience performing internal and supplier audits to ISO and related standards.</li><li>Exposure to risk management practices within a regulated manufacturing environment.</li><li>Experience working within an ERP system to support quality and production activities.</li><li>Knowledge of medical device quality expectations and FDA-related quality practices is a plus.</li><li>Ability to thrive in a growing organization that is investing in new capabilities and technologies.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Big Lake, MN.Pay and BenefitsThe pay range for this position is $80000.00 - $120000.00/yr.Health &amp; Insurance Benefits:
- Medical plans = company contributes a generous portion of the premium cost.
- Dental plan = employer‑supported.
- Voluntary vision plan = low‑cost, employee‑elected.
- Basic Life Insurance = 100% employer‑paid.
- Accidental Death &amp; Dismemberment (AD&amp;D) = 100% employer‑paid.
- Short‑term disability = 100% employer‑paid.
- Long‑term disability = 100% employer‑paid.
- Employee Assistance Program (EAP) = 100% employer‑paid.

Retirement &amp; Savings:
- Retirement contributions (details referenced in the summary, plan documents hold the specifics).

Spending Accounts:
- Flexible Spending Accounts (FSA)
- Dependent Care FSAWorkplace TypeThis is a fully onsite position in Big Lake,MN.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

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



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



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



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



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



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

Job Title: Quality EngineerJob DescriptionWe are seeking a dedicated and skilled Quality Engineer to join our team. The ideal candidate will play a crucial role in supporting our Quality Department, ensuring that all processes and products meet our high standards and align with organizational goals and customer requirements.Responsibilities<ul><li>Support daily Quality Department operations and assume leadership responsibilities when needed.</li><li>Develop and maintain quality objectives that align with organizational goals and customer requirements.</li><li>Create, implement, and improve inspection, testing, and evaluation processes.</li><li>Lead quality planning activities related to manufacturing processes, product development, and production support.</li><li>Review engineering drawings, specifications, supplier documentation, and quality records to ensure compliance.</li><li>Utilize Statistical Process Control (SPC) and other quality tools to monitor performance and identify opportunities for improvement.</li><li>Conduct root cause investigations and implement corrective and preventive actions (CAPA).</li><li>Review quality data, audit findings, and inspection results to ensure consistency with established procedures and standards.</li><li>Collaborate with suppliers and internal teams to resolve quality concerns and improve overall product performance.</li><li>Investigate customer complaints and coordinate quality-related corrective actions.</li><li>Prepare and present quality metrics, reports, and improvement initiatives to leadership.</li><li>Ensure compliance with applicable industry, customer, and regulatory quality standards.</li><li>Participate in continuous improvement efforts, including Lean Manufacturing, 5S, and process optimization initiatives.</li><li>Develop and deliver quality-related training to employees and cross-functional teams.</li><li>Support internal, customer, and external audits as required.</li></ul>Essential Skills<ul><li>3+ years of experience in Quality Engineering, Quality Assurance, or Manufacturing Quality.</li><li>Experience supporting production environments and driving process improvements.</li><li>Strong understanding of SPC, Root Cause Analysis, CAPA, and quality system methodologies.</li><li>Experience collecting, analyzing, and presenting quality data.</li><li>Proficiency with Microsoft Office, particularly Excel.</li><li>Familiarity with Lean Manufacturing tools such as 5S and Value Stream Mapping.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in aerospace, defense, government contracting, or highly regulated manufacturing environments is a plus.</li></ul>Work EnvironmentThe work environment is a normal office setting with quiet noise levels.Job Type &amp; LocationThis is a Permanent position based out of Hayden, ID.Pay and BenefitsThe pay range for this position is $70000.00 - $90000.00/yr.Health Insurance
Dental Insurance
401(k)
Vacation Time/PTOWorkplace TypeThis is a fully onsite position in Hayden,ID.Application DeadlineThis position is anticipated to close on Aug 5, 2026.About Actalent 

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



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



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



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



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



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

Job Title: Quality EngineerJob DescriptionThe Quality Engineer will execute quality control activities within a fabrication shop supporting microelectronics capital projects. This engineering role focuses on ensuring products meet stringent quality standards the first time, with minimal rework or delays. The position requires an experienced, forward-thinking quality professional who contributes actively as a member of the Quality Team and helps secure the expected quality of all fabricated products.Responsibilities<ul><li>Execute quality control activities in a fabrication shop environment for microelectronics capital projects.</li><li>Ensure products meet defined quality requirements on the first pass, minimizing rework, defects, and schedule delays.</li><li>Perform welding inspections to verify compliance with applicable standards and specifications.</li><li>Review and interpret blueprints, mechanical drawings, and structural documentation to validate quality criteria.</li><li>Apply ISO 9001 principles and procedures to maintain and improve the quality management system.</li><li>Conduct supplier audits to assess and monitor supplier quality performance and adherence to standards.</li><li>Support and perform quality assurance activities throughout the production process.</li><li>Identify, investigate, and document nonconformities and quality issues.</li><li>Lead or participate in root cause analysis to determine underlying causes of defects or process deviations.</li><li>Recommend and help implement corrective and preventive actions to improve product and process quality.</li><li>Collaborate with engineering, production, and other cross-functional teams to resolve quality-related concerns.</li><li>Contribute to continuous improvement initiatives, leveraging Six Sigma tools and methodologies where applicable.</li><li>Maintain accurate quality records, inspection reports, and audit documentation.</li><li>Support a culture of quality and accountability within the fabrication shop and broader project teams.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in quality engineering.</li><li>Hands-on experience with quality engineering in a fabrication or manufacturing environment.</li><li>Strong knowledge of ISO 9001 and its application within a quality management system.</li><li>Experience performing welding inspections and evaluating weld quality.</li><li>Ability to read and interpret blueprints, mechanical drawings, and structural documents.</li><li>Proficiency in quality assurance practices and quality control methodologies.</li><li>Experience conducting supplier audits and assessing supplier quality performance.</li><li>Proven ability to perform root cause analysis and develop effective corrective actions.</li><li>Familiarity with Six Sigma principles; Six Sigma Green Belt certification preferred.</li><li>Attention to detail and strong analytical and problem-solving skills.</li><li>Effective communication skills to collaborate with cross-functional teams and document findings clearly.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certified Welding Inspector (CWI) or AWS certification is a strong plus.</li><li>Experience in microelectronics or capital project environments is beneficial.</li><li>Experience in mechanical or structural fabrication quality is advantageous.</li><li>Demonstrated ability to support continuous improvement initiatives using Six Sigma tools.</li><li>Strong organizational skills and ability to manage multiple quality activities simultaneously.</li><li>Forward-thinking mindset with a focus on improving processes and preventing defects.</li><li>Interest in professional growth and taking on increasing responsibility over time.</li></ul>Work EnvironmentThis role is primarily based in a cubicle office setting, with regular collaboration across engineering and production teams. The Quality Engineer will spend occasional time on the fabrication shop floor to conduct inspections, audits, and investigations, and may travel domestically on a minimal basis for supplier visits or project needs. The environment supports complex and technically interesting projects in the microelectronics capital space, offering opportunities for growth and involvement in impactful, high-visibility work.Job Type &amp; LocationThis is a Permanent position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $90000.00 - $105000.00/yr.Strong Internal Company Benefits. If you have any questions or wish to see a copy of the benefits, please feel free to reach out.Workplace TypeThis is a fully onsite position in Minneapolis,MN.Application DeadlineThis position is anticipated to close on Aug 6, 2026.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 DescriptionIn this role, you will serve as a senior technical contributor responsible for preventive quality engineering, systemic problem-solving, and customer quality execution throughout the product lifecycle. You will lead complex quality investigations, drive effective corrective actions, and collaborate across engineering, manufacturing, supply chain, and customer-facing teams to ensure products and processes meet quality, regulatory, and customer requirements. The ideal candidate will have experience working within highly regulated manufacturing environments and a strong understanding of industry quality standards and certifications. Success in this position requires a proactive approach to root cause analysis, data-driven decision making, process improvement, and customer satisfaction.Responsibilities<ul><li>Lead investigations into quality issues and drive sustainable corrective actions.</li><li>Support compliance with applicable aerospace and quality management system requirements.</li><li>Partner with cross-functional teams to improve process capability and product quality.</li><li>Analyze quality data to identify trends, risks, and opportunities for improvement.</li><li>Serve as a technical quality leader for manufacturing and engineering initiatives.</li><li>Drive continuous improvement efforts focused on defect prevention and customer satisfaction.</li></ul>Essential Skills<ul><li>Experience in quality assurance and root cause analysis.</li><li>Familiarity with ISO 9001 and AS9100 standards.</li><li>BS Degree in engineering with 5-10 years of experience or 10+ years without a degree.</li><li>Experience with quality audits including 2nd and 3rd party audits.</li><li>Proficiency in root cause analysis and FEA.</li><li>Mentorship and leadership abilities.</li><li>Six Sigma certification.</li><li>Certified Quality Engineer (CQE).</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong communication skills for exposing ideas and pushing back on other engineers.</li><li>Ability to teach others and present data effectively.</li><li>Experience conducting calls and meetings.</li><li>Excellent collaboration skills.</li></ul>Work EnvironmentThis is an onsite position located in Huntsville, working from 8:00 AM to 3:30 PM CST. You will be part of a team of four other entry to mid-level quality engineers.Job Type &amp; LocationThis is a Contract to Hire position based out of Huntsville, AL.Pay and BenefitsThe pay range for this position is $40.00 - $60.00/hr.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)Workplace TypeThis is a fully onsite position in Huntsville,AL.Application DeadlineThis position is anticipated to close on Aug 6, 2026.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 position involves no supervisory responsibilities but requires the ability to effectively communicate in both oral and written forms with various stakeholders including managers, suppliers, customers, and the public. The role focuses on developing and maintaining a supplier quality system that ensures the supply base is producing, measuring, and maintaining quality standards.Responsibilities<ul><li>Ensure compliance with procedures outlined in the Quality Manual, such as ISO9001 and IATF16949.</li><li>Lead supplier development activities and implement necessary changes.</li><li>Participate in supplier reviews and provide input to the Purchasing Department regarding supplier quality.</li><li>Perform supplier quality audits according to ISO9001, IATF16949, and VDA6 standards.</li><li>Ensure reliability and accuracy of products from the supply base and timely disposition of nonconforming material.</li><li>Coordinate with suppliers on initiatives related to supplier quality performance, track performance trends, and facilitate corrective actions.</li><li>Utilize lean manufacturing, error proofing, and continuous improvement initiatives to support the supplier base and help develop robust processes aligned with zero defect initiatives.</li><li>Provide support to customers regarding supply-based issues.</li></ul>Essential Skills<ul><li>Thorough knowledge of state-of-the-art quality tools and APQP methods such as FMEA, Control Plan, and PPAP.</li><li>Ability to read technical specifications and drawings.</li><li>Problem-solving skills and capability to implement continuous improvement techniques.</li><li>Proficiency in standard business applications software and specialized data analysis tools.</li><li>Six Sigma Green/Black Belt Certification.</li><li>ISO/IATF auditor certification with 2-5 years of related audit experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Spanish language skills.</li><li>Experience in Plastic Molding and Assembly processes.</li><li>Bachelor's Degree is required.</li><li>Experience in quality engineering, documentation review, blueprint reading, and manufacturing processes.</li><li>Proficiency in Microsoft Excel and Microsoft Word.</li><li>Knowledge in PPAP, root cause analysis, 8D, and 5 Why methodologies.</li></ul>Work EnvironmentThe work environment involves collaborating with cross-functional teams and requires the ability to manage communication effectively across various departments. The role may involve using various quality and manufacturing software tools and requires a professional dress code.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.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)Workplace TypeThis is a fully onsite position in Holly Springs,MS.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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 DescriptionJoin a team dedicated to advancing state-of-the-art tactical radios for military applications, contributing to the safety of service men and women in both military and law enforcement capacities. As a Quality Engineer, you will lead quality engineering activities throughout the product lifecycle, ensuring high standards are maintained from design through to production.Responsibilities<ul><li>Lead Quality Engineering activities throughout the product lifecycle, including contract review, requirements management, design reviews, verification/validation, and release to production.</li><li>Initiate and drive internal Corrective Actions Requests (CARs) as required.</li><li>Assist in Supply Chain Quality Assurance activities, including approving/auditing suppliers and conducting Source Inspections of Hardware/Software.</li><li>Support Supplier Corrective Action Requests (SCARs).</li><li>Provide an interface between Purchasing, Engineering, Program Management, and Manufacturing departments during the transition of new products from design to production.</li><li>Support Program Quality Assurance activities for production programs, including First Article Inspections (FAI), Material Review Board (MRB), Change Control Board (CCB), Failure Review Board (FRB), and Work Product review and approval.</li><li>Manage high-priority tasks across multiple projects simultaneously in development.</li><li>Develop Inspection Plans and processes for Receiving and Final Inspection activities.</li><li>Determine Process Capability (Cpk) and defect trends based on statistical analysis.</li><li>Support Continuous Improvement initiatives.</li></ul>Essential Skills<ul><li>BS in Mechanical/Electrical Engineering or equivalent/related technical degree or experience.</li><li>5+ years of Quality Engineering experience.</li><li>Proficiency in ASME/ANSI Y14.5 with the ability to read mechanical drawings.</li><li>Knowledge of electro-mechanical assemblies, IPC standards, schematics, and RF Test equipment.</li><li>Familiarity with Software Quality Assurance, automated MRP systems, and Cause/Corrective Action systems.</li><li>Excellent English communication skills, both written and oral.</li><li>Proficiency in Enterprise Resource Planning (ERP) systems.</li><li>Proficiency in Requirements and Configuration Management tools.</li><li>Proficiency in Microsoft Office Products and Minitab.</li></ul>Additional Skills &amp; Qualifications<ul><li>Efficiency in SAP and/or CostPoint preferred.</li><li>AS9100/CMMI experience is a plus.</li><li>Ability to travel up to 10% of the time domestically.</li></ul>Work EnvironmentThis role is based in a heavy engineering design and manufacturing environment. For the first six months, the position requires onsite work five days a week, transitioning to a hybrid model thereafter. The schedule follows a 9/80 format, with mandatory onsite presence on Monday and Tuesday.Job Type &amp; LocationThis is a Contract to Hire position based out of Germantown, MD.Pay and BenefitsThe pay range for this position is $45.00 - $74.00/hr.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)Workplace TypeThis is a fully onsite position in Germantown,MD.Application DeadlineThis position is anticipated to close on Jul 28, 2026.About Actalent 

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



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



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



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



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



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

Job Title: Quality EngineerJob DescriptionWe are seeking a dedicated and skilled Quality Engineer to join our team. The successful candidate will facilitate and maintain validation project documentation, provide statistical analysis support, and develop SOPs related to validation and risk management. You will monitor and prepare Key Performance Indicators (KPIs) for major customers and conduct quality and engineering studies to support manufacturing operations.Responsibilities<ul><li>Facilitate and maintain validation project documentation.</li><li>Provide statistical analysis support for manufacturing, new product development, trials, and validation activities.</li><li>Develop SOPs relating to validation and risk management.</li><li>Monitor and prepare Key Performance Indicators (KPIs) for major customers.</li><li>Conduct quality and engineering studies to support manufacturing operations.</li><li>Facilitate Corrective Action/Preventative Action (CAPA) activities to identify and resolve root cause issues.</li><li>Train associates on quality topics such as SPC and CAPA.</li><li>Collaborate with customers on equipment and process validations.</li><li>Serve as the database administrator for Infinity QS (Statistical Process Control) software.</li><li>Drive continuous improvement initiatives with internal teams and external partners.</li></ul>Essential Skills<ul><li>Experience in validation protocols, including IQ, OQ, and PQ.</li><li>Proficiency in quality engineering and process validation.</li><li>Strong skills in root cause analysis and problem-solving techniques.</li><li>Ability to develop and execute validation protocols for equipment, sanitation, facilities, software, and processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with Statistical Process Control (SPC) software, particularly Infinity QS.</li><li>Ability to collaborate effectively with customers on equipment and process validations.</li><li>Experience in developing and monitoring Key Performance Indicators (KPIs).</li></ul>Work EnvironmentThe work environment involves supporting manufacturing operations with a focus on quality and validation activities. You will be using various statistical and quality engineering tools and will engage in continuous improvement initiatives. The role requires effective collaboration with both internal teams and external partners.Job Type &amp; LocationThis is a Contract to Hire position based out of Morristown, TN.Pay and BenefitsThe pay range for this position is $85000.00 - $120000.00/hr.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)Workplace TypeThis is a fully onsite position in Morristown,TN.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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 Supplier Quality Engineer provides ongoing support to the business by driving supplier development and improvement activities aligned with corporate quality metrics. This role works closely with Materials/Purchasing, Sourcing, Branch Operations, and Quality Assurance teams to ensure suppliers meet stringent quality standards across multiple industries. The position focuses on auditing and developing suppliers, resolving customer concerns, and supporting new product introductions while maintaining robust quality systems and processes.Responsibilities<ul><li>Conduct comprehensive audits and evaluations for new and existing suppliers to ensure compliance with quality requirements.</li><li>Review and assess self-assessments submitted by potential suppliers and determine their suitability.</li><li>Visit supplier facilities to evaluate their quality systems, processes, and capabilities.</li><li>Complete formal supplier audits, document findings, and communicate results to relevant stakeholders.</li><li>Issue supplier corrective actions based on audit findings and performance issues, and follow up to ensure timely and effective closure.</li><li>Participate in customer audits of suppliers, representing the organization’s quality interests and ensuring supplier readiness.</li><li>Issue monthly supplier performance scorecards and communicate results to suppliers and internal teams.</li><li>Monitor supplier performance, identify trends, and determine areas for improvement in supply quality and delivery performance.</li><li>Perform on-site audits for poor-performing or critical suppliers and develop targeted improvement plans.</li><li>Develop and implement action plans to improve the quality performance of identified suppliers.</li><li>Review and approve Production Part Approval Process (PPAP) submissions when suppliers initiate changes.</li><li>Provide aging reports for quality rejections by branch, supplier, reason code, and associated costs.</li><li>Assist the Quality Assurance team in processing and resolving customer concerns in a timely and effective manner.</li><li>Provide technical support to the organization in new product introduction, ensuring quality requirements are defined and met.</li><li>Support operational excellence initiatives and contribute to continuous improvement in quality processes.</li><li>Apply appropriate quality assurance and improvement methodologies, including structured problem-solving tools.</li><li>Continuously upgrade personal skills and knowledge to improve effectiveness and stay current with industry practices.</li><li>Provide training and guidance to less experienced or less skilled personnel on quality tools, processes, and standards.</li><li>Work closely with key customers to understand issues at the plant level and develop effective solutions.</li><li>Engage directly with major customers in automotive and heavy truck sectors to address quality concerns and drive corrective actions.</li><li>Lead or support corrective action activities that may function as mini Six Sigma projects to address recurring issues.</li><li>Spend significant time on the shop floor and in the laboratory, investigating and resolving quality problems and issues.</li><li>Perform hands-on work in the lab using gauges, inspection tools, and testing equipment to validate product quality.</li><li>Visit domestic suppliers regularly, with travel typically ranging from approximately 10% to 20% depending on project needs.</li><li>Apply Advanced Product Quality Planning (APQP) frameworks and related tools such as PPAP, PFMEA, control plans, and GD&amp;T in supplier and product development activities.</li></ul>Essential Skills<ul><li>Minimum of 3 years of experience in quality engineering, supplier quality, or a closely related quality-focused role.</li><li>Bachelor’s degree in an engineering discipline.</li><li>Strong knowledge of ISO 9001:2015 quality standards and familiarity with IATF requirements.</li><li>Certification in auditing and demonstrated experience conducting quality system and process audits.</li><li>Proficiency in APQP and PPAP, including the ability to review, approve, and provide training on these processes to suppliers.</li><li>Hands-on experience with corrective action and continuous improvement processes, including 8D, 5 Why, and fishbone (Ishikawa) analysis.</li><li>Familiarity with various manufacturing processes and their impact on product quality.</li><li>Knowledge of material testing and evaluation procedures to assess product conformance.</li><li>Experience with gauging and inspection methods, including the use of precision measurement tools.</li><li>Ability to interpret and apply PFMEA, control plans, and GD&amp;T within supplier and product quality contexts.</li><li>Strong analytical and problem-solving skills with a structured approach to root cause analysis.</li><li>Effective communication skills to interact with suppliers, internal teams, and customers at multiple levels.</li><li>Ability to work hands-on in laboratory and shop-floor environments to investigate and resolve issues.</li><li>Willingness and ability to travel domestically approximately 10% to 20% of the time, depending on project demands.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to the automotive and/or heavy truck industry, including familiarity with sector-specific quality expectations.</li><li>Experience working with customers in industries such as aerospace, automotive, heavy equipment, electronics, and defense.</li><li>Experience with gage calibration and quality-related software tools.</li><li>Hands-on experience using Optical Comparators, Hardness Testers, and plug gages in a lab environment.</li><li>Exposure to lean methodologies and Six Sigma principles, including participation in improvement projects.</li><li>Experience with quality management systems and supplier process or product audits.</li><li>Ability to train suppliers and internal staff on APQP, PPAP, and other quality tools.</li><li>Strong customer-facing skills and experience working directly with key accounts to resolve plant-level issues.</li><li>Demonstrated ability to manage multiple projects and priorities while maintaining attention to detail.</li><li>Motivation to grow supplier quality expertise and work across a variety of industries and product types.</li></ul>Work EnvironmentThe role operates within a small office environment attached to a very clean and well-equipped quality laboratory. The lab includes instruments such as micrometers, calibrated gages, optical comparators, hardness testers, plug gages, and computer-based measurement and reporting systems. The broader facility includes a large warehouse focused on distribution rather than manufacturing, with products such as electrical components and stamped and molded parts. Local sites support operations in nearby locations, and the position involves regular interaction with branch operations and quality teams. Most of the workday is spent on the floor and in the lab, resolving issues and supporting supplier and customer needs, with additional time allocated to supplier visits and audits. Domestic travel typically ranges from about 10% to 20% depending on active projects. The environment supports hands-on problem solving, collaboration with cross-functional teams, and exposure to a wide range of industries and customer applications.OJob Type &amp; LocationThis is a Contract to Hire position based out of Solon, OH.Pay and BenefitsThe pay range for this position is $43.00 - $45.00/hr.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)Workplace TypeThis is a fully onsite position in Solon,OH.Application DeadlineThis position is anticipated to close on Aug 3, 2026.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 Engineer ensures that products and processes meet established quality standards and regulatory requirements within a highly technical manufacturing environment. This role focuses on developing and maintaining robust quality systems, analyzing and resolving quality issues, collaborating with suppliers, and leading continuous improvement initiatives that directly impact product performance and end-user safety.Responsibilities Include<ul><li>Develop, implement, and maintain quality control systems and procedures.</li><li>Ensure compliance with industry standards, regulations, and company policies.</li><li>Conduct internal audits and support external audits as required.</li><li>Oversee and perform inspections of materials, products, and processes to ensure compliance with specifications.</li><li>Develop and implement testing protocols and quality standards.</li><li>Investigate and resolve product quality issues by identifying root causes and implementing corrective actions.</li><li>Monitor and report on non-conformance issues and drive continuous improvement efforts.</li><li>Collaborate with suppliers to ensure material and component quality meets specifications.</li><li>Conduct supplier audits and assist in supplier development initiatives.</li><li>Lead quality improvement projects using Lean, Six Sigma, or other methodologies.</li><li>Identify opportunities for process optimization to enhance efficiency and reduce defects.</li><li>Maintain accurate records of quality control processes, audits, and test results.</li><li>Prepare quality reports and present findings to management and stakeholders.</li></ul>Skills &amp; Qualifications<ul><li>2+ years experience working as a Quality Engineer</li><li>Bachelor's degree in Engineering preferred</li><li>Strong understanding of quality systems, 5S methodologies, and tools such as Six Sigma and Lean Manufacturing</li><li>ASQ CQE certification or equivalent experience</li><li>Experience with root cause analysis and corrective action processes such as 8D, Fishbone, and 5-Why</li><li>Experience with Measurement System Analysis (MSA) including Gage R&amp;R</li><li>Experience with Process Failure Mode and Effects Analysis (PFMEA)</li><li>Experience with statistical software such as SQC Pack or Minitab®</li><li>Good understanding of control plans</li><li>Continuous Improvement exposure</li></ul>Preferred Skills<ul><li>ASQ or CQE certification or equivalent experience</li><li>Proficient in measurement, inspection and testing methods, calibration </li><li>DOD- familiarity with government contracts</li><li>Familiarity with regulatory compliance in relevant industries (e.g., FDA, AS9100, IATF 16949)</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Cleveland, OH.Pay and BenefitsThe pay range for this position is $41.00 - $45.00/hr.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)Workplace TypeThis is a fully onsite position in Cleveland,OH.Application DeadlineThis position is anticipated to close on Aug 3, 2026.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 serves as the primary quality representative for a newly established U.S. manufacturing facility, leading the development and implementation of plant-wide quality standards and procedures. The position focuses on driving robust quality systems, resolving customer issues, and partnering closely with production and engineering teams to improve product quality, reduce scrap, and enhance process capability. This role offers a clear pathway for career growth, with the opportunity to advance into a quality management or director-level position within a few years based on performance and contribution.Responsibilities<ul><li>Serve as the primary quality representative for the manufacturing facility and champion plant-wide quality standards and procedures.</li><li>Act as the main point of contact for customer quality concerns, ensuring timely investigation, communication, and resolution of issues.</li><li>Lead root cause analysis and corrective action activities related to customer complaints, internal nonconformances, and supplier quality issues.</li><li>Establish, monitor, and report key quality metrics, and drive continuous improvement initiatives based on data and trends.</li><li>Develop, maintain, and improve quality documentation, including control plans, inspection procedures, work instructions, and standard operating procedures.</li><li>Partner with production and engineering teams to improve product quality, reduce scrap, and increase process capability.</li><li>Support PFMEA, Process Flow Diagram, Control Plan development, and new process development activities.</li><li>Conduct process and quality system audits to ensure compliance with customer requirements and applicable quality standards.</li><li>Manage calibration programs, gauge control activities, and measurement system analysis (MSA) to ensure accuracy and reliability of measurement systems.</li><li>Collaborate with suppliers and global quality teams to ensure consistent quality standards and practices across operations.</li><li>Use tools such as Root Cause Analysis, 5 Why, Fishbone (Ishikawa), SPC, and MSA to solve problems and strengthen processes.</li><li>Prepare and support quality planning documentation, including PPAP submissions and related customer-required documentation.</li><li>Interpret engineering drawings and apply GD&amp;T principles to ensure product and process conformance.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering, Manufacturing Engineering, Industrial Engineering, Mechanical Engineering, or a related technical field.</li><li>1–3 years of experience in a manufacturing quality engineering role.</li><li>Basic understanding of quality management systems such as ISO 9001 and/or IATF.</li><li>Familiarity with Root Cause Analysis, 5 Why, Fishbone (Ishikawa), Control Plans, PFMEA, SPC, and MSA.</li><li>Experience supporting quality documentation and quality planning activities, including Control Plans and PPAP documentation.</li><li>Ability to interpret engineering drawings, with exposure to GD&amp;T concepts.</li><li>Proficiency with Microsoft Office, particularly Excel, for data analysis and reporting.</li><li>Strong analytical skills with the ability to interpret quality data and drive fact-based decisions.</li><li>Strong organizational skills with the ability to manage multiple tasks and priorities.</li><li>Effective written and verbal communication skills for interacting with customers, suppliers, and cross-functional teams.</li><li>Ability to work both independently and collaboratively in a team environment.</li><li>Experience in automotive, industrial, or high-volume manufacturing environments.</li><li>Experience with Lean Manufacturing and continuous improvement initiatives.</li><li>Experience using Statistical Process Control (SPC) to monitor and improve manufacturing processes.</li><li>Demonstrated experience conducting root cause analysis and implementing corrective actions.</li><li>Experience using quality data analysis software such as Minitab.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior experience supporting PPAP documentation and customer-facing quality planning activities is preferred.</li><li>Hands-on experience interpreting complex engineering drawings and applying GD&amp;T is preferred.</li><li>Exposure to high-volume or automotive-related manufacturing processes is highly beneficial.</li><li>Demonstrated ability to drive continuous improvement projects using Lean tools and methods.</li><li>Interest in growing into a leadership role, with potential advancement into quality manager or director responsibilities within 3–4 years based on performance.</li><li>Comfort working in a fast-paced, evolving manufacturing environment where quality systems are being built and refined.</li></ul>Work EnvironmentThis role is fully onsite in a manufacturing facility, with standard hours of approximately 7:00 a.m. to 4:30 p.m. and an expected workweek of around 45 hours. You will work closely with production, engineering, and global quality teams in a hands-on environment focused on high-volume manufacturing and continuous improvement. The facility operates with structured quality systems and uses tools such as SPC, MSA, PFMEA, and quality data analysis software like Minitab, alongside common productivity tools such as Microsoft Excel. The environment emphasizes collaboration, problem-solving, and data-driven decision-making, offering clear opportunities for professional growth and advancement in quality leadership.Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Wayne, IN.Pay and BenefitsThe pay range for this position is $28.85 - $33.65/hr.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)Workplace TypeThis is a fully onsite position in Fort Wayne,IN.Application DeadlineThis position is anticipated to close on Aug 5, 2026.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 Engineer plays a key role in supporting manufacturing operations and quality systems while ensuring products meet customer specifications and technical standards. This position sits within the Technical Services group and works closely with customers, operations, quality control, and quality assurance teams to drive data-based decisions, improve processes, and maintain compliance. The role offers significant long-term growth opportunities, including paths into metallurgy, quality leadership, operations support, and specialized technical services, making it ideal for someone who wants to develop into a future leader or technical expert.Responsibilities<ul><li>Collaborate with manufacturing operations, quality control, and quality assurance teams to ensure products meet customer specifications and internal quality standards.</li><li>Engage directly with customers and internal stakeholders to understand technical requirements and translate them into practical, actionable instructions for production and quality teams.</li><li>Work within established quality systems to monitor performance, identify issues, and support continuous improvement initiatives.</li><li>Use data-driven decision-making to analyze quality performance, identify trends, and recommend corrective and preventive actions.</li><li>Lead or participate in problem-solving activities and root cause analysis to resolve quality issues and prevent recurrence.</li><li>Interpret and apply customer specifications, technical standards, and material requirements to manufacturing processes and quality controls.</li><li>Support compliance with relevant quality requirements, including documentation, audits, and adherence to technical standards.</li><li>Assist in optimizing processes to improve product quality, consistency, and manufacturability.</li><li>Collaborate with cross-functional teams in Technical Services, operations, and quality functions to support key business initiatives and product improvement projects.</li><li>Contribute to supplier quality activities by helping evaluate material performance and addressing supplier-related quality concerns when needed.</li><li>Develop growing expertise in materials engineering, metallurgy, and quality engineering practices to support long-term technical and leadership development.</li><li>Act as a proactive, self-directed contributor who learns the business and manufacturing processes to provide informed, practical quality guidance.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Materials Science or Metallurgical Engineering strongly preferred.</li><li>Strong communication skills with the ability to translate technical requirements and specifications into clear, practical instructions.</li><li>Ability to read, interpret, and work with customer specifications and technical standards.</li><li>Demonstrated problem-solving capability, including structured root cause analysis.</li><li>Self-starter mentality with a strong willingness to learn the business, products, and manufacturing processes.</li><li>Foundational knowledge of materials engineering, metallurgy, or materials science.</li><li>Experience or training in quality engineering or quality assurance concepts.</li><li>Ability to work effectively with cross-functional teams including operations, quality control, and quality assurance.</li></ul>Additional Skills &amp; Qualifications<ul><li>Steel manufacturing experience is a plus but not required.</li><li>Metallurgy background or practical exposure to metallurgical processes.</li><li>Supplier quality experience, including working with external material or component suppliers.</li><li>Exposure to manufacturing environments where technical specifications drive production processes.</li><li>Experience with audits or participation in quality system assessments.</li><li>Familiarity with data-driven decision-making and use of quality data to support improvements.</li><li>background as a Material Science Engineer, Metallurgical Engineer, or Quality Engineer within steel manufacturing is highly relevant.</li><li>Candidates with supplier quality backgrounds are encouraged to apply.</li><li>Strong mechanical engineers with exceptional technical problem-solving aptitude may be considered if they demonstrate the ability to learn materials and quality disciplines.</li><li>Interest in long-term growth into roles such as Technical Services leadership, Metallurgist, Quality Management, Operations or Manufacturing leadership, or customer-facing technical expert positions.</li></ul>Work EnvironmentThe role is based in a heavy manufacturing environment located at the port in Panama City Beach, Florida. The setting involves working in and around industrial production operations, where technical specifications and customer requirements strongly influence how products are manufactured and controlled. The Quality Engineer works on-site within the Technical Services group and regularly interfaces with operations, quality control, and quality assurance teams, as well as customer-facing functions. The environment is fast-paced and highly technical, with a strong emphasis on safety, process discipline, and adherence to standards. Candidates should be comfortable working in a heavy industrial facility and engaging directly with production processes and equipment.Job Type &amp; LocationThis is a Permanent position based out of Panama City, FL.Pay and BenefitsThe pay range for this position is $80000.00 - $85000.00/yr.HEALTH – BLUE CROSS BLUE SHIELD OF ALABAMA 
Option 1 – BlueCross BlueShield Managed Choice (PPO)
In-Network Deductible $1,500 Individual / $3,000 Family, Medical &amp; Pharmacy Copays
Non-Tobacco User $58.10 Individual / $292.42 Family (Monthly)
Tobacco User $134.36 Individual / $490.46 Family (Monthly)
Option 2 – BlueCross BlueShield Managed Choice (High Deductible Health Plan)
In-Network Deductible $2,000 Individual / $4,000 Family, No Medical Copays, Rx Copays after Deductible
Non-Tobacco User No Cost to Employee
Tobacco User $66.47 Individual/ $160.03 Family (Monthly)
Health Savings Account (if enrolled in High Deductible Plan) – All contributions are yours to keep
Employer CONTRIBUTION to account $104.16 Individual / $208.33 Family (Monthly)
Doctor on Demand – 24/7/365 access to board certified doctors for a copay
Rightway Healthcare – Helps employees navigate the health care system and maximize health care benefits. 
DENTAL – LINCOLN FINANCIAL GROUP 
$2,500 Annual Max, Deductible $25 Ind./$50 Family No Cost to Employee
VISION – HUMANA 
Copays: $10 Exam, $15 Lenses, $150 Frame allowance $2.41 Individual / $6.92 Family (Monthly)
FLEXIBLE SPENDING ACCOUNT (maximum annual employee contribution to account) - WEXHEALTH 
Health Care FSA $3,300
Limited Purpose FSA $3,300
Dependent Care FSA $2,500 Individual / $5,000 Joint Filing
SHORT TERM DISABILITY – LINCOLN FINANCIAL GROUP 
Pays 70% of base pay up to $3,500 per week No Cost to Employee 
LONG TERM DISABILITY – LINCOLN FINANCIAL GROUP 
Pays 70% of pre-disability pay up to $15,000 per month No Cost to Employee
BASIC LIFE INSURANCE &amp; AD&amp;D – LINCOLN FINANCIAL GROUP 
1X Salary for Employee / $1,000 each dependent No Cost to Employee
SUPPLEMENTAL LIFE INSURANCE – LINCOLN FINANCIAL GROUP 
Up to $200,000 Including AD&amp;D for Employee Cost Varies
Up to $200,000 on spouse Cost Varies
$10,000 on every child $2.00 Monthly
401(K) DEFINED CONTRIBUTION PLAN – EMPOWER RETIREMENT 
Auto enrolled at a 3% contribution rate
Company matches 100% of your pretax contributions up to 5%
PET INSURANCE – NATIONWIDE 
50% and 70% Reimbursement Cost Varies
IDENTITY PROTECTION – ALLSTATE 
Identity Monitoring &amp; Protection $9.95 Individual / $17.95 Family (Monthly)
VOLUNTARY BENEFITS – TRUSTMARK 
Trustmark Critical Illness Cost Varies
Trustmark Accident Cost Varies
Trustmark Hospital Pay Cost Varies
 
PAID LEAVE 
FIRST CALENDAR YEAR OF SERVICE (Eligible after 90 days) 
Hired Between Vacation Leave Sick Leave
Jan 1 – Mar 31 7 days (56 hours) 5 days (40 hours)
Apr 1 – Jun 30 5 days (40 hours) 4 days (32 hours)
Jul 1 – Sep 30 3 days (24 hours) 3 days (24 hours)
Oct 1 – Dec 31 0 0
 
SUBSEQUENT YEARS OF CONTINUOUS SERVICE 
Vacation Leave Annually Sick Leave Annually
After Year 1 3 Weeks (120 hours) 10 days (80 hours)
After 10 Years 4 Weeks (160 hours)
After 20 Years 5 Weeks (200 hours)
 
HOLIDAYS 
Eleven (11) Paid Holidays Per Year
ADDITIONAL BENEFITS/VARIABLE COMPENSATION 
Annual Performance Bonus – Eligibility based on job grade and performance measured through the assessment 
of individual goals and accomplishments annually with maximum bonus potential starting at 20%. 
Profit Share – Paid per quarter and based on the company’s annual profit.
Tuition Reimbursement – Enables employees to complete an approved higher education program through 
reimbursements for tuition and books. Provides up to 100% reimbursement.
Career Development – Ability to earn and maintain industry certifications.
Wellness Program – Program to help employees find ways to improve their overall health, get answers to health 
care questions and score discounts, earn reimbursements for gym memberships and gift cards.Workplace TypeThis is a fully onsite position in Panama City,FL.Application DeadlineThis position is anticipated to close on Jul 29, 2026.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 skilled Quality Engineer to ensure compliance with Government contracts, customer purchase orders, and flow-down requirements. This role involves serving as a primary quality interface with DCMA, Government Source Inspectors, and customer quality representatives, as well as supporting Government source selection activities. The position requires interpreting Technical Data Packages (TDPs), engineering drawings, specifications, and work instructions to define quality requirements, inspection plans, and acceptance criteria.Responsibilities<ul><li>Review and interpret Government contracts and customer purchase orders to ensure full quality, inspection, and documentation compliance.</li><li>Serve as a primary quality interface with DCMA, Government Source Inspectors, and customer quality representatives.</li><li>Support and participate in Government source selection activities, including supplier evaluations, quality reviews, and compliance assessments.</li><li>Develop, review, and approve quality plans, inspection plans, and quality documentation aligned with contractual and engineering requirements.</li><li>Collaborate with manufacturing and engineering teams to ensure work instructions, routings, and inspection steps accurately reflect contractual, engineering, and quality requirements.</li><li>Lead the identification, documentation, root cause analysis, and corrective action of non-conformances tied to drawings, specifications, suppliers, or contract requirements.</li><li>Support internal, customer, and Government audits, ensuring readiness, documentation accuracy, and effective closeout of findings.</li><li>Ensure compliance with AS9100, customer-specific requirements, and internal quality management system procedures.</li><li>Support supplier quality activities, including source inspection readiness, quality reviews, and issue resolution.</li><li>Maintain accurate quality records and documentation in accordance with aerospace, customer, and Government requirements.</li></ul>Essential Skills<ul><li>Proficiency with inspection tools such as micrometers, calipers, height gauges, pin gauges, and roughometers.</li><li>Ability to read and interpret engineering drawings, schematics, and GD&amp;T.</li><li>Experience with inspection documentation and reporting for receiving, in-process, and final inspections.</li><li>Familiarity with AS9100 quality systems and aerospace quality standards.</li><li>Strong ability to read and interpret engineering drawings, specifications, and technical data packages.</li><li>Experience working with Government contracts and associated quality, inspection, and compliance requirements.</li><li>Direct experience interfacing with DCMA and Government Source Inspection (GSI) representatives.</li></ul>Additional Skills &amp; Qualifications<ul><li>Aerospace or defense manufacturing experience.</li><li>Prior Quality Engineer experience supporting DoD or Government programs.</li><li>Experience working with customer quality portals (Net-Inspect or similar).</li><li>Knowledge of GD&amp;T and inspection methodologies.</li><li>Bachelor’s degree in Engineering, Quality, Manufacturing, or a related technical discipline (or equivalent experience).</li><li>Proficiency with Microsoft Office for technical documentation, reporting, and audit support.</li></ul>Work EnvironmentThe Quality Engineer will work within the Quality department, which consists of a Quality Manager, Quality Supervisor, and one inspector. The role involves working on the manufacturing floor and spending time in an office setting. This position offers a stable workload supporting aerospace and high-precision manufacturing, with hands-on inspection responsibilities and exposure to the full inspection lifecycle. There is potential for conversion to full-time through a contract-to-hire model.Job Type &amp; LocationThis is a Contract to Hire position based out of Los Angeles, CA.Pay and BenefitsThe pay range for this position is $30.00 - $38.00/hr.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)Workplace TypeThis is a fully onsite position in Los Angeles,CA.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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 style="text-align:center;">New Product Introduction Quality Engineer </h3>About the Role:We’re hiring a Quality Engineer to support process validation and manufacturing operations for innovative medical devices. This is a great opportunity for an early-career engineer to gain hands-on experience in IQ/OQ/PQ, process development, and scale-up while working in a highly collaborative, regulated environment. You’ll partner closely with Manufacturing, Quality, and R&amp;D teams and build deep expertise in medical device validation and continuous improvement.<h3>What You’ll Do:</h3><ul><li>Support process validation activities (IQ/OQ/PQ) from planning through execution</li><li>Assist in developing validation protocols, collecting data, and preparing reports</li><li>Contribute to test method validation (TMV) to ensure accuracy and reliability</li><li>Partner with cross-functional teams to improve manufacturing processes</li><li>Support process improvements using Lean principles to increase efficiency and reduce waste</li><li>Assist with manufacturing scale-up, including capacity and throughput analysis</li><li>Help ensure documentation meets regulatory and quality standards</li></ul><h3>Required Qualifications:</h3><ul><li>Bachelor’s degree in Engineering (Mechanical, Manufacturing, Biomedical, or similar)</li><li>~2+ years of experience in manufacturing engineering in a regulated industry</li><li>Exposure to process validation (IQ/OQ/PQ)</li><li>Strong data analysis and technical documentation skills</li><li>Ability to work cross-functionally in a team environment</li></ul><h3>Preferred Qualifications:</h3><ul><li>Experience in medical device manufacturing</li><li>Exposure to test method validation (TMV)</li><li>Familiarity with FDA, ISO, or other regulated environments</li><li>Knowledge of Lean manufacturing or continuous improvement methods</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of White Bear Lake, MN.Pay and BenefitsThe pay range for this position is $40.00 - $52.00/hr.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)Workplace TypeThis is a fully onsite position in White Bear Lake,MN.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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 position supports quality assurance for both the launch of new products and the ongoing production of roll-formed components. The role involves direct communication with customers and suppliers to address corrective actions, the creation of Production Part Approval Process (PPAP) documents, and conducting root cause analysis. Additionally, the role includes programming Coordinate Measuring Machines (CMM).qulaity Responsibilities<ul><li>Communicate directly with customers and suppliers to address corrective actions.</li><li>Create and manage quality documentation, including PPAPs.</li><li>Conduct root cause analysis to identify issues and implement solutions.</li><li>Program CMMs using PC-DMIS or Polyworks software.</li><li>Ensure quality standards are met for new product launches and existing production.</li></ul>Essential Skills<ul><li>2-5 years of experience in automotive quality engineering.</li><li>Proficiency in CMM programming using PC-DMIS or Polyworks.</li><li>Experience with root cause analysis and inspection processes.</li><li>Knowledge of PPAP and automotive quality standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in Engineering is preferred.</li><li>Experience with Wenzel RA1621 CMM.</li><li>Experience in automotive product launches.</li><li>Consideration for candidates with CMM programming experience who have not held an Engineer title.</li></ul>Work EnvironmentThe role involves an 80/20 split between working in the quality lab/office and the production floor. The facility includes roll form and weld lines, as well as secondary forming equipment. Personal Protective Equipment (PPE) is mandatory. The work schedule is Monday through Friday, from 7:00 AM to 3:30 PM, with occasional overtime required.Job Type &amp; LocationThis is a Contract to Hire position based out of Jeffersonville, IN.Pay and BenefitsThe pay range for this position is $38.00 - $43.00/hr.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)Workplace TypeThis is a fully onsite position in Jeffersonville,IN.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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 Job DescriptionThe Quality Systems Engineer position offers an opportunity to provide technical support to the quality and engineering groups, ensuring compliance with AS9100 processes and procedures. The role involves reviewing both external and internal nonconformances, coordinating investigations, and performing RCCA analysis. As a focal point for Internal MRB activities and Customer corrective actions, you will contribute to the continuous improvement of the Quality Management System (QMS) by engaging in functions such as first articles, calibration tracking, customer source inspections, planning verifications, and buyoffs.Responsibilities<ul><li>Manage the QMS system by developing or creating new procedures and processes.</li><li>Track, monitor, analyze, and report performance KPIs and department WIG goals.</li><li>Handle customer corrective action requests and change of charge submittals.</li><li>Create inspection plans and key characteristic/SPC captures.</li><li>Serve as a team member on the AS9100 internal audit team and assist with customer and third-party audits.</li><li>Participate in problem-solving teams to support RCCA activities and MRB-related functions.</li><li>Support planning verifications, job instruction reviews, and MBD drawing approvals.</li><li>Contribute to efforts around APQP, building control plans, PPAP, and FMEA implementation.</li><li>Engage in new work meetings to ensure product quality and compliance requirements are understood.</li></ul>Essential Skills<ul><li>Proficiency in quality engineering and root cause analysis.</li><li>Ability to read and understand blueprints with a working knowledge of GD&amp;T.</li><li>Experience with aerospace requirements and quality concepts.</li><li>Knowledge of AS9102 and experience creating FAI reports in Net-Inspect.</li><li>Strong communication skills (written and verbal) for interaction with customers and auditors.</li><li>Excellent time management and organizational skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Audit support and data analysis capabilities.</li><li>Experience with calibration and inspection processes.</li><li>Familiarity with AS9100 systems, APQP, PPAP, FMEA, and auditing processes.</li><li>A positive attitude, willingness to learn, and ability to collaborate effectively.</li></ul>Work EnvironmentThe role offers a mix of office and manufacturing settings, involving documentation, reporting, and audits in an office environment, and inspections, MRB activities, and quality checks on the production floor. The position is fast-paced and detail-oriented, requiring strong organizational and time management skills. You will work in a collaborative, cross-functional environment with frequent interaction with engineering, production, and quality teams, as well as direct communication with customers and auditors. The work is compliance-driven, revolving around strict aerospace standards (AS9100, AS9102) and continuous improvement initiatives, with a strong focus on problem-solving through involvement in RCCA, MRB, and quality improvement projects.Job Type &amp; LocationThis is a Permanent position based out of Wichita, KS.Pay and BenefitsThe pay range for this position is $65000.00 - $75000.00/yr.Health, Wellness &amp; Insurance
Comprehensive Health, Dental &amp; Vision insurance, with generous employer premium contributions
Short-term and long-term disability coverage 
Life insurance included 

 Financial Benefits &amp; Retirement
Competitive wages
401(k) retirement plan with employer match 
Monthly performance bonuses
Employee referral bonuses at 3-month, 6-month, and 1-year milestones 
Christmas Club savings account 

Paid Time Off &amp; Leave
Paid time off and paid holidays 

Perks &amp; Work Environment
Clean, climate-controlled facility with a modern breakroom featuring food and beverage options 
Gym membership discount 
Employee Assistance Program (EAP)Workplace TypeThis is a fully onsite position in Wichita,KS.Application DeadlineThis position is anticipated to close on Jul 28, 2026.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 Job DescriptionIn this role, you will serve as a senior technical contributor responsible for preventive quality engineering, systemic problem-solving, and customer quality execution throughout the product lifecycle. You will lead complex quality investigations, drive effective corrective actions, and collaborate across engineering, manufacturing, supply chain, and customer-facing teams to ensure products and processes meet quality, regulatory, and customer requirements. The ideal candidate will have experience working within highly regulated manufacturing environments and a strong understanding of industry quality standards and certifications. Success in this position requires a proactive approach to root cause analysis, data-driven decision making, process improvement, and customer satisfaction.Responsibilities<ul><li>Lead investigations into quality issues and drive sustainable corrective actions.</li><li>Support compliance with applicable aerospace and quality management system requirements.</li><li>Partner with cross-functional teams to improve process capability and product quality.</li><li>Analyze quality data to identify trends, risks, and opportunities for improvement.</li><li>Serve as a technical quality leader for manufacturing and engineering initiatives.</li><li>Drive continuous improvement efforts focused on defect prevention and customer satisfaction.</li></ul>Essential Skills<ul><li>Experience in quality assurance and root cause analysis.</li><li>Familiarity with ISO 9001 and AS9100 standards.</li><li>BS Degree in engineering with 5-10 years of experience or 10+ years without a degree.</li><li>Experience with quality audits including 2nd and 3rd party audits.</li><li>Proficiency in root cause analysis and FEA.</li><li>Mentorship and leadership abilities.</li><li>Six Sigma certification.</li><li>Certified Quality Engineer (CQE).</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong communication skills for exposing ideas and pushing back on other engineers.</li><li>Ability to teach others and present data effectively.</li><li>Experience conducting calls and meetings.</li><li>Excellent collaboration skills.</li></ul>Work EnvironmentThis is an onsite position located in Huntsville, working from 8:00 AM to 3:30 PM CST. You will be part of a team of four other entry to mid-level quality engineers.Job Type &amp; LocationThis is a Contract to Hire position based out of Huntsville, AL.Pay and BenefitsThe pay range for this position is $40.00 - $60.00/hr.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)Workplace TypeThis is a fully onsite position in Huntsville,AL.Application DeadlineThis position is anticipated to close on Jul 28, 2026.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.

The Quality Engineer I will be responsible for supporting and improving Quality Management System (QMS) processes to ensure compliance with FDA, ISO, customer, and company requirements within a Contract Development and Manufacturing Organization (CDMO) environment. This position partners with Manufacturing, Operations, Validation, Regulatory Affairs, Supply Chain, R&amp;D, and customers to drive quality initiatives, investigate nonconformances, execute CAPAs, support audits, and improve manufacturing processes for medical device, pharmaceutical, biologic, or combination products.Duties are as follow:<ul><li>Maintain compliance with FDA Quality System Regulation, cGMP requirements, ISO 13485, ISO 9001, and applicable customer requirements.</li><li>Support and execute Quality Management System activities including CAPA, nonconformance management, change control, risk management, deviation investigations, and complaint trending.</li><li>Review and approve quality records to ensure accuracy, completeness, and regulatory compliance.</li><li>Participate in internal, supplier, customer, and regulatory audits and support audit responses and corrective actions.</li><li>Assist in the development, review, and implementation of SOPs, work instructions, forms, and quality procedures.</li><li>Lead investigations involving nonconforming materials, manufacturing deviations, customer complaints, and quality system issues.</li><li>Utilize root cause analysis methodologies including 5 Why, Fishbone, Is/Is Not, Fault Tree Analysis, and Failure Mode and Effects Analysis (FMEA).</li><li>Develop, implement, and verify CAPAs to prevent recurrence of quality issues.</li><li>Analyze quality trends and recommend process improvements based on data-driven findings.</li><li>Partner with Manufacturing and Engineering teams to improve product quality, process capability, and operational efficiency.</li><li>Support process validations, equipment qualifications, and manufacturing transfers.</li><li>Participate in change control reviews and assess quality and regulatory impacts.</li><li>Monitor manufacturing quality metrics and facilitate continuous improvement initiatives.</li><li>Perform risk assessments and facilitate risk management activities throughout product lifecycle stages.</li><li>Establish and monitor quality KPIs and quality metrics.</li><li>Support Lean Manufacturing and Six Sigma initiatives.</li><li>Identify opportunities to streamline processes while maintaining compliance and product quality.</li><li>Serve as a quality representative during customer meetings and project activities.</li><li>Assist with supplier qualification, audits, and supplier corrective actions.</li><li>Support customer quality agreements and quality-related communications.</li><li>Provide technical guidance regarding quality requirements and expectations.</li></ul>Education:<ul><li>Bachelor’s degree in Engineering, Quality, Biomedical Engineering, Mechanical Engineering, Chemical Engineering, Manufacturing Engineering, Industrial Engineering, or a related scientific discipline.</li></ul>Experience:<ul><li>3–5+ years of quality engineering experience in a regulated manufacturing environment.</li><li>Experience in a Medical Device, Pharmaceutical, Biotech, Combination Product, or CDMO environment strongly preferred.</li><li>Experience supporting FDA inspections, ISO audits, and customer audits preferred.</li><li>Knowledge of FDA 21 CFR Part 820, FDA 21 CFR Parts 210/211, ISO 13485, ISO 14971, cGMP requirements, Statistical process control and quality tools</li><li>Experience with: CAPA systems, Nonconformance management, Root cause investigations, Change management systems, Risk assessments, Data analysis and trend reporting, Proficient in Microsoft Excel, Word, PowerPoint, and quality management software.</li></ul>Preferred certification:<ul><li>ASQ Certified Quality Engineer (CQE)</li><li>ASQ Certified Quality Auditor (CQA)</li><li>Six Sigma Green Belt or higher</li><li>Lead Auditor Certification (ISO 13485 or ISO 9001)</li></ul>Job Type &amp; LocationThis is a Contract position based out of Dallas, TX.Pay and BenefitsThe pay range for this position is $30.00 - $38.00/hr.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)Workplace TypeThis is a fully onsite position in Dallas,TX.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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 daily quality assurance activities, analyzes production data to drive continuous improvement, and refines methods to enhance overall performance. This position develops effective testing, sampling, and training procedures to ensure compliance with customer and industry standards. The Quality Engineer also conducts audits, prepares reports, and drives corrective and preventative actions to resolve quality issues and prevent recurrence.Responsibilities<ul><li>Comply with all BOS, ISO/TS, and customer-specific requirements.</li><li>Understand plant/customer KPIs and work with the team to meet and exceed them.</li><li>Participate as a Layered Process Auditor if instructed by the manager.</li><li>Ensure continuous improvement in all production quality deliverables.</li><li>Provide support on PPAP package preparation for product submissions and approval by appropriate customer personnel.</li><li>Develop and update Control Plan as required.</li><li>Support the manufacturing engineer in updating the PFMEA as required.</li><li>Develop appropriate inspection plans and containment plans.</li><li>Utilize all customer-specific systems.</li><li>Conduct capability studies and ensure they are performed and documented for special characteristics, meeting customer and internal requirements.</li><li>Support the continuous improvement of the Operation Description Sheets (ODS).</li><li>Identify and utilize appropriate statistical tools, mentoring team members on proper statistical application and techniques.</li><li>Interface with assigned external customers as the single point of contact for issue resolution.</li><li>Complete any customer-specific advanced quality planning requirements.</li><li>Write and submit 8-Ds to the customer in a timely manner.</li><li>Visit the customer as needed.</li><li>Communicate between the customer and the plant.</li><li>Initiate Quality Alerts when concerns arise and follow the alert until it is closed.</li><li>Confirm all customer return material analysis root cause and corrective actions.</li></ul>Essential Skills<ul><li>2+ years of quality engineering experience within the automotive industry.</li><li>Experience with PPAP and APQP requirements.</li><li>Internal auditing experience.</li><li>Customer interaction experience.</li><li>Experience managing suppliers.</li><li>Experience in training others.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with root cause analysis.</li><li>Knowledge of automotive industry standards.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Greenfield, OH.Pay and BenefitsThe pay range for this position is $33.65 - $39.00/hr.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)Workplace TypeThis is a fully onsite position in Greenfield,OH.Application DeadlineThis position is anticipated to close on Jul 31, 2026.About Actalent 

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



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



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



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



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



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

Job Title: Quality EngineerJob DescriptionWe are seeking a dedicated Quality Engineer with a passion for excellence in electronic assemblies. The ideal candidate will hold a Bachelor's Degree in Engineering and possess 3-5 years of quality control experience related to electronic assemblies, or a Master's degree with a minimum of 1 year in the same field. This role involves developing and operating quality control systems, using metrology and statistical methods to improve practices, and planning long-term improvements to enhance quality structures.Responsibilities<ul><li>Develop and execute short- and long-term quality strategies to ensure high standards across electronic assembly products.</li><li>Implement quality systems, manage corrective actions, and lead audits.</li><li>Drive continuous improvement initiatives across internal operations and the supplier base.</li><li>Create and establish short-term quality plans and support the execution of long-term quality plans.</li><li>Introduce new product release systems to ensure quality aligns with company philosophy.</li><li>Establish and monitor quality metrics and collection systems, providing monthly reports.</li><li>Coordinate with the parent company on new product development and technical/quality issues.</li><li>Manage internal and external corrective actions.</li><li>Create, implement, and upgrade quality processes and procedures.</li><li>Schedule and lead ISO and customer audits, training internal auditors, and resolving open issues with auditing agencies and customers.</li><li>Support supplier audit teams, evaluate and authorize new suppliers, and conduct regular supplier quality meetings.</li><li>Support customer audits and prepare necessary information.</li><li>Identify and implement opportunities for continual improvement, including cost reduction and process improvements.</li></ul>Essential Skills<ul><li>Bachelor's Degree in Engineering or a Master's Degree with relevant experience.</li><li>3-5 years of quality control experience in electronic assemblies or related field.</li><li>Ability to develop and operate quality control systems and training programs.</li><li>Proficiency in using metrology and statistical methods.</li><li>Familiarity with quality cost concepts and auditing quality systems.</li><li>Excellent problem-solving, training, and follow-up skills.</li><li>Strong communication and interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with CAPA Process, PPAP, Internal Audit, External Audit, and ISO 9001.</li><li>Knowledge of supplier quality management and root cause analysis.</li></ul>Work EnvironmentThe position is based in an electro-mechanical assembly environment, working closely with one other Quality Engineer and 3-5 Manufacturing/Industrial Engineers. The role requires hands-on involvement on the manufacturing floor, troubleshooting quality issues approximately 25-30% of the time.Job Type &amp; LocationThis is a Contract to Hire position based out of Deerfield, IL.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/hr.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)Workplace TypeThis is a fully onsite position in Deerfield,IL.Application DeadlineThis position is anticipated to close on Aug 7, 2026.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 EngineerThe Quality Engineer is responsible for maintaining and improving quality systems, driving continuous improvement initiatives, and ensuring compliance within a regulated manufacturing environment. This role partners with internal teams, customers, and suppliers to resolve quality issues, support new product introductions, and enhance manufacturing processes.Key Responsibilities<ul><li>Maintain and improve Quality Management System (QMS) procedures and regulatory compliance.</li><li>Develop and manage Quality Assurance (QA) plans for new product introductions using APQP and process optimization methodologies.</li><li>Lead root cause investigations and drive CAPA activities for nonconformances.</li><li>Analyze quality and production data to identify trends and improvement opportunities.</li><li>Support process validation, test method validation, and MSA activities.</li><li>Provide quality input during process design, development, and implementation phases.</li><li>Improve inspection methods, quality documentation, and training programs.</li><li>Manage supplier, customer, and internal quality issues, ensuring effective corrective actions.</li><li>Support supplier quality initiatives and continuous improvement efforts.</li><li>Partner with cross-functional teams to standardize manufacturing processes and promote quality excellence.</li><li>Maintain document control systems and provide technical support to customers and internal stakeholders.</li><li>Mentor and support the development of quality assurance team members.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Waukegan, IL.Pay and BenefitsThe pay range for this position is $42.00 - $46.00/hr.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)Workplace TypeThis is a fully onsite position in Waukegan,IL.Application DeadlineThis position is anticipated to close on Aug 7, 2026.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 (Sterilization) Job DescriptionThe Quality Engineer plays a key role in ensuring that innovative medical devices meet rigorous internal and external quality standards. In this position, you collaborate closely with doctors and engineers to develop creative, high-quality products, define methods and equipment for measuring quality, and support regulatory and quality assurance activities. You also partner with and train quality inspectors and technicians, help lead a junior Quality Engineer, and drive continuous improvement by identifying defects, uncovering their root causes, and implementing effective solutions.Responsibilities<ul><li>Collaborate with doctors and engineers to develop creative, high-quality medical devices that meet regulatory and customer expectations.</li><li>Define and implement appropriate methods, measurement techniques, and equipment to assess and control product quality.</li><li>Participate in and support internal and external quality audits, ensuring compliance with applicable standards and regulations.</li><li>Maintain and oversee document control processes to ensure accurate, current, and compliant quality documentation.</li><li>Support sterilization processes and verification activities to ensure medical devices meet required sterilization standards.</li><li>Contribute to the development, maintenance, and improvement of the Quality Management System (QMS) in alignment with ISO and GMP requirements.</li><li>Identify defects and nonconformities in products and processes, investigate their origin, and implement effective corrective and preventive actions using root cause analysis.</li><li>Assist in regulatory and quality assurance efforts to ensure products conform to US FDA and international regulatory requirements.</li><li>Partner with and train quality inspectors and technicians on quality standards, procedures, and inspection techniques.</li><li>Support supplier quality management activities, including supplier approval, auditing, and oversight of incoming inspection processes.</li><li>Participate in new product development activities for medical devices, ensuring quality requirements are integrated into design and manufacturing.</li><li>Use statistical analysis tools, including Minitab, to analyze data, monitor process performance, and support data-driven decision making.</li><li>Prepare clear, concise technical and quality documentation, including reports, procedures, and work instructions.</li><li>Collaborate with leadership, including the VP of Quality, and help guide and support a junior Quality Engineer.</li><li>Contribute to continuous improvement initiatives to enhance product quality, process robustness, and overall quality system effectiveness.</li></ul>Essential Skills &amp; Qualifications<ul><li>Bachelor’s degree in Engineering or a related scientific discipline.</li><li>At least 1 year of experience as a Quality Engineer, Quality Technician, or Microbiologist in the medical device industry.</li><li>Experience with sterilization processes and related quality controls in a medical device context.</li><li>Strong communication skills, with the ability to collaborate effectively with cross-functional teams including doctors, engineers, and quality staff.</li><li>Strong analytical and technical writing skills for preparing reports, procedures, and quality documentation.</li><li>Hands-on experience with Quality Management Systems (QMS).</li><li>Experience performing internal and external quality audits.</li><li>Experience with document control processes within a regulated environment.</li><li>Experience supporting new product development of medical devices.</li><li>Working knowledge of US FDA and international regulatory requirements for medical devices.</li><li>Experience with supplier quality management, including supplier approval, auditing, and incoming inspection.</li><li>Familiarity with ISO and Good Manufacturing Practice (GMP) requirements.</li><li>Proficiency in root cause analysis methodologies to investigate and resolve quality issues.</li><li>Experience using statistical analysis software, including Minitab.</li><li>ASQ certification is preferred.</li><li>Experience with PPAP (Production Part Approval Process) or similar qualification processes.</li><li>Experience working within a formal quality management system for medical devices.</li><li>Ability to work independently while also contributing effectively to a small, growing team.</li><li>Demonstrated ability to train and mentor quality inspectors, technicians, or junior engineers.</li><li>Strong attention to detail and a continuous improvement mindset.</li></ul>Work EnvironmentThis role is based in an office setting within a brand-new, modern building in the Kendall area. The quality team operates from a high-rise office, while a separate two-story facility houses a surgery center on the first floor and the design team on the second floor, fostering close collaboration between clinical and engineering functions. The company is a growing medical device organization of approximately 40 individuals that has expanded every year, offering a dynamic environment where your work directly supports individuals who are severely injured. The workplace culture emphasizes flexibility, collaboration, and innovation, with a professional yet supportive atmosphere and opportunities to work closely with both technical and clinical professionals.Job Type &amp; LocationThis is a Contract to Hire position based out of MIAMI, FL.Pay and BenefitsThe pay range for this position is $35.00 - $45.00/hr.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)Workplace TypeThis is a fully onsite position in MIAMI,FL.Application DeadlineThis position is anticipated to close on Jul 27, 2026.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 position supports quality assurance for both the launch of new products and the ongoing production of roll-formed components. The role involves direct communication with customers and suppliers to address corrective actions, the creation of Production Part Approval Process (PPAP) documents, and conducting root cause analysis. Additionally, the role includes programming Coordinate Measuring Machines (CMM).qulaity Responsibilities<ul><li>Communicate directly with customers and suppliers to address corrective actions.</li><li>Create and manage quality documentation, including PPAPs.</li><li>Conduct root cause analysis to identify issues and implement solutions.</li><li>Program CMMs using PC-DMIS or Polyworks software.</li><li>Ensure quality standards are met for new product launches and existing production.</li></ul>Essential Skills<ul><li>2-5 years of experience in automotive quality engineering.</li><li>Proficiency in CMM programming using PC-DMIS or Polyworks.</li><li>Experience with root cause analysis and inspection processes.</li><li>Knowledge of PPAP and automotive quality standards.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in Engineering is preferred.</li><li>Experience with Wenzel RA1621 CMM.</li><li>Experience in automotive product launches.</li><li>Consideration for candidates with CMM programming experience who have not held an Engineer title.</li></ul>Work EnvironmentThe role involves an 80/20 split between working in the quality lab/office and the production floor. The facility includes roll form and weld lines, as well as secondary forming equipment. Personal Protective Equipment (PPE) is mandatory. The work schedule is Monday through Friday, from 7:00 AM to 3:30 PM, with occasional overtime required.Job Type &amp; LocationThis is a Contract to Hire position based out of Jeffersonville, IN.Pay and BenefitsThe pay range for this position is $38.00 - $43.00/hr.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)Workplace TypeThis is a fully onsite position in Jeffersonville,IN.Application DeadlineThis position is anticipated to close on Jul 29, 2026.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 Job DescriptionThis Quality Engineer role serves as the primary quality representative for a newly established U.S. manufacturing facility, leading the development and implementation of plant-wide quality standards and procedures. The position focuses on driving robust quality systems, resolving customer issues, and partnering closely with production and engineering teams to improve product quality, reduce scrap, and enhance process capability. This role offers a clear pathway for career growth, with the opportunity to advance into a quality management or director-level position within a few years based on performance and contribution.Responsibilities<ul><li>Serve as the primary quality representative for the manufacturing facility and champion plant-wide quality standards and procedures.</li><li>Act as the main point of contact for customer quality concerns, ensuring timely investigation, communication, and resolution of issues.</li><li>Lead root cause analysis and corrective action activities related to customer complaints, internal nonconformances, and supplier quality issues.</li><li>Establish, monitor, and report key quality metrics, and drive continuous improvement initiatives based on data and trends.</li><li>Develop, maintain, and improve quality documentation, including control plans, inspection procedures, work instructions, and standard operating procedures.</li><li>Partner with production and engineering teams to improve product quality, reduce scrap, and increase process capability.</li><li>Support PFMEA, Process Flow Diagram, Control Plan development, and new process development activities.</li><li>Conduct process and quality system audits to ensure compliance with customer requirements and applicable quality standards.</li><li>Manage calibration programs, gauge control activities, and measurement system analysis (MSA) to ensure accuracy and reliability of measurement systems.</li><li>Collaborate with suppliers and global quality teams to ensure consistent quality standards and practices across operations.</li><li>Use tools such as Root Cause Analysis, 5 Why, Fishbone (Ishikawa), SPC, and MSA to solve problems and strengthen processes.</li><li>Prepare and support quality planning documentation, including PPAP submissions and related customer-required documentation.</li><li>Interpret engineering drawings and apply GD&amp;T principles to ensure product and process conformance.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering, Manufacturing Engineering, Industrial Engineering, Mechanical Engineering, or a related technical field.</li><li>1–3 years of experience in a manufacturing quality engineering role.</li><li>Basic understanding of quality management systems such as ISO 9001 and/or IATF.</li><li>Familiarity with Root Cause Analysis, 5 Why, Fishbone (Ishikawa), Control Plans, PFMEA, SPC, and MSA.</li><li>Experience supporting quality documentation and quality planning activities, including Control Plans and PPAP documentation.</li><li>Ability to interpret engineering drawings, with exposure to GD&amp;T concepts.</li><li>Proficiency with Microsoft Office, particularly Excel, for data analysis and reporting.</li><li>Strong analytical skills with the ability to interpret quality data and drive fact-based decisions.</li><li>Strong organizational skills with the ability to manage multiple tasks and priorities.</li><li>Effective written and verbal communication skills for interacting with customers, suppliers, and cross-functional teams.</li><li>Ability to work both independently and collaboratively in a team environment.</li><li>Experience in automotive, industrial, or high-volume manufacturing environments.</li><li>Experience with Lean Manufacturing and continuous improvement initiatives.</li><li>Experience using Statistical Process Control (SPC) to monitor and improve manufacturing processes.</li><li>Demonstrated experience conducting root cause analysis and implementing corrective actions.</li><li>Experience using quality data analysis software such as Minitab.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior experience supporting PPAP documentation and customer-facing quality planning activities is preferred.</li><li>Hands-on experience interpreting complex engineering drawings and applying GD&amp;T is preferred.</li><li>Exposure to high-volume or automotive-related manufacturing processes is highly beneficial.</li><li>Demonstrated ability to drive continuous improvement projects using Lean tools and methods.</li><li>Interest in growing into a leadership role, with potential advancement into quality manager or director responsibilities within 3–4 years based on performance.</li><li>Comfort working in a fast-paced, evolving manufacturing environment where quality systems are being built and refined.</li></ul>Work EnvironmentThis role is fully onsite in a manufacturing facility, with standard hours of approximately 7:00 a.m. to 4:30 p.m. and an expected workweek of around 45 hours. You will work closely with production, engineering, and global quality teams in a hands-on environment focused on high-volume manufacturing and continuous improvement. The facility operates with structured quality systems and uses tools such as SPC, MSA, PFMEA, and quality data analysis software like Minitab, alongside common productivity tools such as Microsoft Excel. The environment emphasizes collaboration, problem-solving, and data-driven decision-making, offering clear opportunities for professional growth and advancement in quality leadership.Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Wayne, IN.Pay and BenefitsThe pay range for this position is $28.85 - $33.65/hr.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)Workplace TypeThis is a fully onsite position in Fort Wayne,IN.Application DeadlineThis position is anticipated to close on Jul 30, 2026.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.

<h1>Quality Engineer</h1>Clearwater, FL | Up to $75,000 Salary <h2>Join a Growing Aerospace Manufacturing Team</h2>We are seeking a detail-oriented Quality Engineer to support quality operations within a precision aerospace manufacturing environment. This role will partner closely with Engineering, Production, Inspection, Suppliers, and Customers to ensure products and processes meet AS9100 standards and customer requirements. If you have experience with corrective actions, quality systems, FAIR documentation, audits, and supplier quality, we'd love to hear from you.<h2>Key Responsibilities</h2><ul><li>Investigate and resolve quality issues involving production, inspection, engineering, suppliers, and customers.</li><li>Review and disposition nonconforming materials while maintaining accurate quality records and documentation.</li><li>Manage corrective actions, concessions, waivers, and customer quality requests through various customer portals.</li><li>Support First Article Inspection Reports (FAIRs) and coordinate submissions through customer systems and NET-INSPECT.</li><li>Review engineering drawings, specifications, purchase orders, and quality requirements to ensure compliance.</li><li>Verify shipping documentation, certifications, inspection reports, and required quality records prior to shipment.</li><li>Support supplier quality activities, including SCAR management, RMAs, and supplier corrective actions.</li><li>Conduct internal AS9100 audits and assist with continuous improvement initiatives.</li><li>Collaborate with cross-functional teams to ensure customer and regulatory requirements are met.</li><li>Support SPC activities, source inspections, and documentation packages for customer approvals.</li></ul><h2>Required Qualifications</h2><ul><li>Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical field preferred.</li><li>2+ years of Quality Engineering, Quality Assurance, or Supplier Quality experience within a manufacturing environment.</li><li>Experience with corrective actions, nonconforming material processes, root cause analysis, and quality documentation.</li><li>Ability to read and interpret engineering drawings, specifications, and customer quality requirements.</li><li>Working knowledge of AS9100, ISO quality systems, audits, and continuous improvement methodologies.</li><li>Strong organizational skills with exceptional attention to detail.</li><li>Excellent communication skills and ability to work with customers, suppliers, and internal teams.</li></ul><h2>Preferred Experience</h2><ul><li>Aerospace, defense, or highly regulated manufacturing experience.</li><li>Experience with AS9102 FAIR documentation and customer portals such as NET-INSPECT or similar systems.</li><li>Familiarity with DQR, DPRV, DSQR, SCAR, RMA, SPC, and source inspection processes.</li><li>Experience using quality and manufacturing software such as MeasureLink, DISCUS, E2, PRO DOC, or similar platforms.</li></ul>If you're passionate about quality, continuous improvement, and supporting mission-critical aerospace products, apply today to learn more about this Clearwater, FL opportunity.Job Type &amp; LocationThis is a Contract to Hire position based out of Clearwater, FL.Pay and BenefitsThe pay range for this position is $36.00 - $36.00/hr.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)Workplace TypeThis is a fully onsite position in Clearwater,FL.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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 evaluates and investigates product complaints and nonconformances, drives corrective and preventive actions, and supports new product introduction to ensure consistent compliance with quality standards. This role serves as a key liaison between the plant, customers, and internal teams, authoring and maintaining quality system documentation, performing internal audits, and promoting continual improvement in processes and product design within a regulated manufacturing environment.Responsibilities<ul><li>Perform and document evaluations and investigations resulting from customer complaints, product nonconformances, and corrective and preventive actions (CAPA).</li><li>Deploy formal root cause analysis methods and tools to identify underlying issues and implement effective corrective actions.</li><li>Validate and approve Production Part Approval Process (PPAP) submissions for new product introduction (NPI) programs.</li><li>Serve as a representative of the plant to customers, providing professional communication and support on quality-related topics.</li><li>Collaborate with cross-functional internal groups to respond to product inquiries, resolve issues, and support continuous improvement initiatives.</li><li>Disposition returned products in accordance with established procedures and quality system requirements.</li><li>Perform internal audits in accordance with ISO 9001 and other applicable quality standards to ensure ongoing compliance.</li><li>Ensure continual improvement in process and product design by identifying opportunities, recommending changes, and supporting implementation.</li><li>Participate in customer audits and notified body audits, providing documentation, explanations, and follow-up actions as needed.</li><li>Author and maintain quality management system (QMS) documents, specifications, and work instructions that meet and sustain quality standards.</li><li>Track plant performance against quality requirements using established measurement standards and metrics.</li><li>Verify the effectiveness of CAPA actions by reviewing data, monitoring outcomes, and updating records.</li><li>Interact with customers in a professional manner to address quality concerns, provide status updates, and support long-term relationships.</li><li>Support process validation, advanced product quality planning (APQP), and related activities for new product development and ongoing production.</li><li>Contribute to a culture of quality and continuous improvement within a manufacturing environment, particularly for medical and electro-mechanical products.</li></ul>Essential Skills<ul><li>1–3 years of experience in a quality or regulatory affairs role.</li><li>Hands-on ownership of CAPA activities, including investigation, implementation, and verification of effectiveness.</li><li>Strong root cause analysis skills using formal methodologies and tools.</li><li>Experience with internal auditing, preferably to ISO 9001 or similar quality management system standards.</li><li>Experience with complaint and nonconformance management in a manufacturing environment.</li><li>Familiarity with PPAP and APQP processes for new product introduction and ongoing production.</li><li>Exposure to medical device or GMP-related industries, with understanding of regulated quality systems.</li><li>Knowledge of process validation in a manufacturing or product development context.</li><li>Proficiency with Microsoft Office Suite (such as Word, Excel, and PowerPoint) for documentation and reporting.</li><li>Strong organizational skills with the ability to manage multiple tasks and priorities.</li><li>Strong problem-solving skills with a quality- and results-oriented mindset.</li><li>Ability to interact with customers in a professional and collaborative manner.</li><li>Comfort working in or around production environments within a manufacturing facility.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of GMP-related industries is preferred.</li><li>Experience with quality system standards, including ISO 9001, is preferred.</li><li>ASQ Certified Quality Engineer (CQE) or ASQ Certified Quality Auditor (CQA) certification is preferred.</li><li>Experience in a medical device or healthcare-related manufacturing environment is an advantage.</li><li>Familiarity with electro-mechanical products, such as surgical medical carts, is beneficial.</li><li>Exposure to new product development processes and cross-functional collaboration.</li><li>Strong written communication skills for authoring QMS documents, specifications, and work instructions.</li><li>Ability to work effectively in a growing organization undergoing investment and expansion.</li></ul>Work EnvironmentThe role is based in a standard office environment with regular visits to production areas. Production areas may be hot, cool, or dusty and have a moderate noise level, reflecting an active manufacturing setting. The organization is undergoing significant investment and growth, expanding into more electro-mechanical products, including surgical medical carts. Team members work with a mix of office technology and manufacturing equipment, collaborating closely with production, engineering, and quality teams in a dynamic, improvement-focused culture.Job Type &amp; LocationThis is a Permanent position based out of Milwaukee, WI.Pay and BenefitsThe pay range for this position is $90000.00 - $100000.00/yr.401k
Dental, Health, VisionWorkplace TypeThis is a fully onsite position in Milwaukee,WI.Application DeadlineThis position is anticipated to close on Aug 3, 2026.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 optimizes product quality by serving as a key liaison between engineering, manufacturing, assembly, test, packaging, and supply chain functions. This role defines and implements quality standards, inspection plans, and test methods, while supporting internal operations through training, problem resolution, and performance data analysis. The Quality Engineer also partners closely with suppliers to communicate quality plans, address issues, and support both new product introductions and ongoing production, with strong opportunities to develop leadership skills and contribute to new product launches.Responsibilities<ul><li>Act as the primary link between engineering, manufacturing, assembly, test, packaging, and supply chain teams to ensure quality requirements are clearly defined and consistently met.</li><li>Provide input to product documentation, including drawings, specifications, inspection plans, and testing methods, to embed quality requirements throughout the product life cycle.</li><li>Define quality standards, create inspection plans, and develop test methods that ensure products, components, and processes meet specified requirements.</li><li>Implement statistical process control methods and techniques to monitor and control manufacturing processes, and use data to drive improvements.</li><li>Inspect raw materials, components, assemblies, and processes personally or by directing Quality Technicians to verify conformance to requirements.</li><li>Ensure all gauges and measuring equipment are properly calibrated, compliant with applicable standards, and accurately documented.</li><li>Track performance data, analyze quality results, and generate clear reports to identify trends, issues, and opportunities for improvement.</li><li>Investigate non-conformances to determine root causes, recommend corrective actions, and follow through to ensure issues are resolved effectively.</li><li>Lead cross-functional problem-solving teams to address complex quality issues and drive sustainable corrective and preventive actions.</li><li>Implement corrective and preventive actions internally and with suppliers, and verify the effectiveness of these actions over time.</li><li>Identify and recommend opportunities for improvement in manufacturing processes and product quality, using structured methodologies and statistical analysis.</li><li>Collaborate with engineering, manufacturing, and other teams to integrate quality requirements into designs, processes, and product launches.</li><li>Interact with suppliers, including performing supplier visits, to communicate quality expectations, review performance, and support new product introductions.</li><li>Maintain detailed quality documentation, including quality plans, inspection reports, validation protocols, and related records.</li><li>Communicate quality plans, issues, and performance data clearly to internal departments, suppliers, and auditors in both verbal and written formats.</li><li>Maintain current knowledge of industry regulations and standards, and ensure that practices remain compliant with applicable quality management system requirements.</li><li>Identify gaps in the Quality Management System and initiate updates or improvements to address those gaps.</li><li>Train employees in quality processes, procedures, tools, and methodologies to build organizational capability and consistency.</li><li>Participate in interviewing, hiring, and onboarding new employees as appropriate, particularly within the quality function.</li><li>Support activities such as Advanced Product Quality Planning (APQP), Production Part Approval Process (PPAP), and validation activities including IQ/OQ/PQ and PFMEA.</li><li>Assist with leadership responsibilities related to overseeing Quality Technicians and supporting the development of the quality team.</li></ul>Essential Skills<ul><li>Minimum of 3+ years of experience in quality-related roles, with increasing responsibilities over time.</li><li>Experience working within Quality Management Systems such as ISO 9001 or similar standards.</li><li>Demonstrated experience in problem solving, corrective actions, and project management within a manufacturing or production environment.</li><li>Proficiency in Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP).</li><li>Strong knowledge of inspection equipment and techniques, including hands-on use and interpretation of results.</li><li>Ability to read and interpret engineering drawings and standards, including Geometric Dimensioning and Tolerancing (GD&amp;T).</li><li>Practical experience with statistical analysis and statistical process control methods to monitor and improve processes.</li><li>Proven ability to conduct root cause analysis using structured methodologies and logical, data-driven approaches.</li><li>Experience with validation activities such as Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).</li><li>Experience contributing to Process Failure Modes and Effects Analysis (PFMEA).</li><li>Strong verbal and written communication skills for interacting with internal teams, suppliers, and auditors.</li><li>Ability to train others in quality processes, procedures, and tools.</li><li>Engineering degree or equivalent technical education or experience in a relevant field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certification to a recognized body of knowledge, such as ASQ Certified Quality Engineer, is preferred.</li><li>Experience working within formal Quality Management Systems, including ISO-based frameworks.</li><li>Leadership experience or demonstrated potential to take on leadership responsibilities, particularly in overseeing Quality Technicians.</li><li>Experience supporting new product introductions and launches from a quality perspective.</li><li>Experience with statistical analysis tools and methods, with a structured and methodical approach to problem solving.</li><li>Familiarity with industry regulations and standards relevant to manufacturing quality and compliance.</li><li>Ability to travel occasionally to supplier locations and between company facilities.</li><li>Interest in gaining or expanding leadership experience and taking ownership of quality aspects of new product launches.</li></ul>Work EnvironmentThe role splits time between an office environment and modern production and manufacturing facilities equipped with heating and air conditioning. The position requires regular movement throughout the facilities, including sitting, standing, using hands to handle and touch components and equipment, and frequent visual, verbal, and auditory communication. The role involves travel between company facilities and occasional travel to supplier locations. The position requires the ability to lift up to 10 pounds regularly and up to 50 pounds occasionally while working in a clean, professional production and office setting.Job Type &amp; LocationThis is a Permanent position based out of Oconomowoc, WI.Pay and BenefitsThe pay range for this position is $80000.00 - $95000.00/yr.401k
Health, Dental, Vision Insurance
STD/LTDWorkplace TypeThis is a fully onsite position in Oconomowoc,WI.Application DeadlineThis position is anticipated to close on Aug 3, 2026.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 Engineer provides expert leadership in post‑market surveillance for finished medical devices, with a strong focus on root cause analysis, risk assessment, failure mode determination, product reliability, and ongoing product performance monitoring. This role collaborates closely with Development, Operations, Manufacturing, Quality functions, and global field teams to ensure activities comply with established procedures and applicable geographic regulations. The position requires flexibility in managing changing priorities, the ability to work independently with minimal supervision, and a commitment to continuous improvement in product quality and patient outcomes.Responsibilities<ul><li>Lead the product reporting process for complaint handling across all products, including initial evaluation, escalation, risk evaluation, investigation, root cause determination, product disposition, and report closure.</li><li>Manage the returned product analysis process, including coordination of decontamination, external vendor sterilization, detailed root cause analysis, and root cause determination, while supporting other root cause investigations as requested.</li><li>Lead failure mode determination activities, including collaboration with external laboratories when necessary.</li><li>Collect, manage, and analyze data related to returned product results and post‑market therapy outcomes generated from the product reporting process.</li><li>Organize and lead cross‑functional reviews with Development, Operations, and Manufacturing on emerging quality issues and participate in defining and implementing corrective actions.</li><li>Work with Operations to obtain product returns from the field and initiate warranty replacements as appropriate.</li><li>Lead and participate in post‑market reviews covering product performance, therapy performance, safety, and system risk management.</li><li>Lead and participate in post‑market risk management reviews with cross‑functional teams to minimize risks and initiate potential corrective and preventive actions (CAPAs).</li><li>Lead and support cross‑functional teams to resolve quality issues and drive completion of CAPAs.</li><li>Generate and approve design history file documents, device master record documents, engineering change orders (ECOs), and other quality management system (QMS) records.</li><li>Support internal and external QMS audits by preparing documentation, participating in audit activities, and following up on findings.</li><li>Perform design reliability, process quality, and product quality assurance functions as needed.</li><li>Document product and therapy‑related field reports within prescribed timelines and provide all necessary documentation to support investigations, including follow‑up reporting.</li><li>Complete required training and competency confirmations within established timelines and maintain up‑to‑date knowledge of relevant procedures.</li><li>Comply with applicable quality system procedures and policies while actively suggesting and supporting continuous process improvements.</li><li>Effectively prioritize, execute, and report on multiple concurrent projects and tasks in a dynamic environment.</li></ul>Essential Skills<ul><li>Minimum of 2+ years of experience in a quality or design function within the finished medical device industry.</li><li>Hands‑on medical device work history, ideally with electromechanical devices.</li><li>Strong work history in post‑market quality engineering, including complaint handling, product reliability, and product quality assurance.</li><li>Demonstrated experience in root cause analysis and risk management for medical devices.</li><li>Experience using risk management tools such as dFMEA, pFMEA, and fault tree analysis (FTA).</li><li>Experience applying the medical device risk management standard ISO 14971.</li><li>Knowledge of global harmonization task force (GHTF) requirements for process validation and related activities.</li><li>Solid understanding of ISO standards and FDA Quality System Requirements, including FDA 21 CFR Part 820, 821, and 822.</li><li>Experience with quality systems management and quality management systems in a regulated environment.</li><li>Ability to perform design reliability assessments and process and product quality assurance functions.</li><li>Demonstrated team leadership skills with the ability to prioritize, execute, and report on projects.</li><li>Strong project management and time management capabilities, with the ability to handle multiple tasks concurrently and adapt to changing priorities.</li><li>Proven creative and effective problem‑solving skills and original thinking in developing compliance solutions.</li><li>Proficiency with MS Word, Excel, and PowerPoint.</li><li>Ability to work independently without direct supervision while maintaining high standards of accuracy and compliance.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working with Class III active implantable medical devices.</li><li>Experience in design reliability engineering, process validation, and product quality assurance functions.</li><li>ASQ certifications such as CRE, CQM, CQE, or CQA are highly desirable.</li><li>Formal training in ISO standards and quality systems.</li><li>Experience with industry standards such as IEC and EN standards relevant to medical devices.</li><li>Auditing experience, including internal or external quality system audits.</li><li>Certification as an auditor through recognized bodies is an advantage.</li><li>Familiarity with cleanroom environments and process validation in regulated manufacturing settings.</li><li>Experience with product quality monitoring and post‑market surveillance for medical therapies.</li><li>Strong communication skills for effective interaction with cross‑functional teams and global field personnel.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $43.00 - $53.00/hr.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)Workplace TypeThis is a fully onsite position in Minneapolis,MN.Application DeadlineThis position is anticipated to close on Jul 29, 2026.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 Engineer provides expert leadership in post‑market surveillance for finished medical devices, with a strong focus on root cause analysis, risk assessment, failure mode determination, product reliability, and ongoing product performance monitoring. This role collaborates closely with Development, Operations, Manufacturing, Quality functions, and global field teams to ensure activities comply with established procedures and applicable geographic regulations. The position requires flexibility in managing changing priorities, the ability to work independently with minimal supervision, and a commitment to continuous improvement in product quality and patient outcomes.Responsibilities<ul><li>Lead the product reporting process for complaint handling across all products, including initial evaluation, escalation, risk evaluation, investigation, root cause determination, product disposition, and report closure.</li><li>Manage the returned product analysis process, including coordination of decontamination, external vendor sterilization, detailed root cause analysis, and root cause determination, while supporting other root cause investigations as requested.</li><li>Lead failure mode determination activities, including collaboration with external laboratories when necessary.</li><li>Collect, manage, and analyze data related to returned product results and post‑market therapy outcomes generated from the product reporting process.</li><li>Organize and lead cross‑functional reviews with Development, Operations, and Manufacturing on emerging quality issues and participate in defining and implementing corrective actions.</li><li>Work with Operations to obtain product returns from the field and initiate warranty replacements as appropriate.</li><li>Lead and participate in post‑market reviews covering product performance, therapy performance, safety, and system risk management.</li><li>Lead and participate in post‑market risk management reviews with cross‑functional teams to minimize risks and initiate potential corrective and preventive actions (CAPAs).</li><li>Lead and support cross‑functional teams to resolve quality issues and drive completion of CAPAs.</li><li>Generate and approve design history file documents, device master record documents, engineering change orders (ECOs), and other quality management system (QMS) records.</li><li>Support internal and external QMS audits by preparing documentation, participating in audit activities, and following up on findings.</li><li>Perform design reliability, process quality, and product quality assurance functions as needed.</li><li>Document product and therapy‑related field reports within prescribed timelines and provide all necessary documentation to support investigations, including follow‑up reporting.</li><li>Complete required training and competency confirmations within established timelines and maintain up‑to‑date knowledge of relevant procedures.</li><li>Comply with applicable quality system procedures and policies while actively suggesting and supporting continuous process improvements.</li><li>Effectively prioritize, execute, and report on multiple concurrent projects and tasks in a dynamic environment.</li></ul>Essential Skills<ul><li>Minimum of 2+ years of experience in a quality or design function within the finished medical device industry.</li><li>Hands‑on medical device work history, ideally with electromechanical devices.</li><li>Strong work history in post‑market quality engineering, including complaint handling, product reliability, and product quality assurance.</li><li>Demonstrated experience in root cause analysis and risk management for medical devices.</li><li>Experience using risk management tools such as dFMEA, pFMEA, and fault tree analysis (FTA).</li><li>Experience applying the medical device risk management standard ISO 14971.</li><li>Knowledge of global harmonization task force (GHTF) requirements for process validation and related activities.</li><li>Solid understanding of ISO standards and FDA Quality System Requirements, including FDA 21 CFR Part 820, 821, and 822.</li><li>Experience with quality systems management and quality management systems in a regulated environment.</li><li>Ability to perform design reliability assessments and process and product quality assurance functions.</li><li>Demonstrated team leadership skills with the ability to prioritize, execute, and report on projects.</li><li>Strong project management and time management capabilities, with the ability to handle multiple tasks concurrently and adapt to changing priorities.</li><li>Proven creative and effective problem‑solving skills and original thinking in developing compliance solutions.</li><li>Proficiency with MS Word, Excel, and PowerPoint.</li><li>Ability to work independently without direct supervision while maintaining high standards of accuracy and compliance.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working with Class III active implantable medical devices.</li><li>Experience in design reliability engineering, process validation, and product quality assurance functions.</li><li>ASQ certifications such as CRE, CQM, CQE, or CQA are highly desirable.</li><li>Formal training in ISO standards and quality systems.</li><li>Experience with industry standards such as IEC and EN standards relevant to medical devices.</li><li>Auditing experience, including internal or external quality system audits.</li><li>Certification as an auditor through recognized bodies is an advantage.</li><li>Familiarity with cleanroom environments and process validation in regulated manufacturing settings.</li><li>Experience with product quality monitoring and post‑market surveillance for medical therapies.</li><li>Strong communication skills for effective interaction with cross‑functional teams and global field personnel.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $43.00 - $53.00/hr.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)Workplace TypeThis is a fully onsite position in Minneapolis,MN.Application DeadlineThis position is anticipated to close on Aug 5, 2026.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 Job DescriptionThe Quality Engineer investigates product and process quality issues, identifies root causes, and drives effective corrective and preventive actions. This role develops and monitors key performance indicators (KPIs) to uncover opportunities for product and process improvement, and leads cross-functional initiatives to implement sustainable changes that enhance operational effectiveness and customer satisfaction.Responsibilities<ul><li>Investigate product and process quality issues in a manufacturing environment and document findings in a clear and structured manner.</li><li>Identify root causes of quality problems using formal methodologies such as 8D, 5 Why Analysis, Fishbone/Ishikawa Diagrams, and other quality tools.</li><li>Develop, implement, and track corrective and preventive actions (CAPA) to address identified root causes and prevent recurrence.</li><li>Create, monitor, and analyze key performance indicators (KPIs) to identify trends, risks, and opportunities for continuous improvement in product and process quality.</li><li>Lead cross-functional problem-solving activities with technicians, supervisors, engineers, and other stakeholders to resolve quality issues and implement robust solutions.</li><li>Drive process improvements that enhance operational effectiveness, yield, and overall customer satisfaction.</li><li>Apply quality engineering tools such as FMEA and SPC to assess risk, monitor process stability, and ensure consistent product performance.</li><li>Work directly on the production floor to observe processes, collaborate with production teams, and verify the effectiveness of implemented improvements.</li><li>Document and communicate quality findings, recommendations, and improvement results to relevant stakeholders in a clear and timely manner.</li></ul>Essential Skills<ul><li>Bachelor’s degree in mechanical, manufacturing, or a closely related engineering discipline.</li><li>5+ years of quality engineering experience in a manufacturing environment.</li><li>Hands-on experience in industries such as semiconductor, medical device, automotive, or aerospace is preferred.</li><li>Proficiency with quality engineering tools and methods, including 8D, FMEA, 5 Why Analysis, Fishbone/Ishikawa Diagrams, and Statistical Process Control (SPC).</li><li>Demonstrated experience performing root cause analysis and managing corrective and preventive actions (CAPA).</li><li>Ability to work comfortably and effectively on the production floor alongside technicians, supervisors, and engineers.</li><li>Strong analytical skills to interpret data, monitor KPIs, and drive data-based decision-making.</li><li>Effective communication and collaboration skills to lead cross-functional teams and influence stakeholders.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in highly regulated or high-reliability manufacturing sectors such as semiconductor, medical device, automotive, or aerospace.</li><li>Familiarity with continuous improvement and structured problem-solving methodologies, including Six Sigma.</li><li>Demonstrated ability to implement sustainable process improvements that enhance quality and operational performance.</li></ul>Work EnvironmentThis role operates within a manufacturing environment that requires frequent presence on the production floor to observe processes, collaborate with technicians and supervisors, and validate improvements. The Quality Engineer works closely with cross-functional engineering and operations teams, using quality tools such as 8D, FMEA, SPC, 5 Why Analysis, and Fishbone/Ishikawa Diagrams to drive data-driven decisions and continuous improvement. The position involves a balance of hands-on floor engagement and office-based analysis and documentation, in a setting focused on operational excellence and high product quality.Job Type &amp; LocationThis is a Permanent position based out of Horsham, PA.Pay and BenefitsThe pay range for this position is $85000.00 - $107000.00/yr.Medical, Dental, and Vision
Employee Stock Purchase Plan (ESPP)
401(k) with Company Match
Holiday, Vacation, and Sick Time
Flexible Spending Accounts (FSA)
Commuter Benefits
Life and Accident Insurance
Disability Insurance
Tuition Reimbursement
Employee Assistance Program (EAP)
Identity Theft Remediation
Emergency Travel AssistanceWorkplace TypeThis is a fully onsite position in Horsham,PA.Application DeadlineThis position is anticipated to close on Jul 29, 2026.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 Job DescriptionWe are seeking a highly skilled Quality Engineer to play a pivotal role in supporting a critical manufacturing transition and launch initiative. Our high-volume automotive manufacturing facility specializes in advanced metal stamping, welding, and assembly operations. As a Quality Engineer, you will focus on Production Part Approval Process (PPAP) ownership, customer submissions, quality documentation, and launch readiness activities related to tooling transfers, equipment installations, engineering changes, and future production programs.Responsibilities<ul><li>Coordinate and manage PPAP submissions involving initial samples, engineering changes, prototype builds, and pilot programs.</li><li>Prepare and submit complete PPAP packages through applicable customer portals.</li><li>Serve as the primary owner of customer submission activities, ensuring compliance with customer-specific requirements.</li><li>Support manufacturing transfers, tooling moves, equipment launches, and production readiness activities.</li><li>Prepare and maintain required quality documentation, including Control Plans, Process Flow Diagrams, PFMEAs, Inspection Instructions, and more.</li><li>Review supplier PPAP documentation and determine acceptance or rejection based on customer and internal requirements.</li><li>Develop and maintain inspection, testing, and evaluation standards.</li><li>Create forms, procedures, and instructions used to collect and report quality and reliability data.</li><li>Investigate and resolve internal and customer quality concerns.</li><li>Perform Layered Process Audits (LPAs) and follow up on corrective actions.</li><li>Ensure timely completion of customer corrective actions and verification of preventive actions to eliminate repeat issues.</li><li>Provide guidance and training to production associates and quality technicians regarding quality requirements and documentation practices.</li><li>Support continuous improvement initiatives, waste reduction efforts, and operational excellence programs.</li><li>Support compliance with IATF, ISO, TPM, and other company quality initiatives.</li></ul>Essential Skills<ul><li>5+ years of Quality Engineering experience within automotive manufacturing.</li><li>Extensive hands-on experience developing and submitting complete PPAP packages.</li><li>Strong understanding of customer quality requirements and customer portal submissions.</li><li>Strong knowledge of APQP, PPAP, Control Plans, PFMEA, Process Flow Diagrams, MSA, SPC, and Corrective Action Methodologies.</li><li>Willingness to work on a contract basis with potential for direct hire.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in Engineering, Manufacturing, Quality, or related technical discipline preferred.</li><li>Experience in automotive stamping, welding, or assembly.</li><li>Experience supporting structural automotive components or vehicle frame/body systems.</li><li>Familiarity with IATF, ISO, Layered Process Audits (LPA), and TPM initiatives.</li></ul>Work EnvironmentThe position is based in a high-volume automotive manufacturing facility with over 300 associates. The facility houses approximately 30 presses along with extensive robotic welding and assembly equipment. The work involves supporting production launches and ensuring manufacturing readiness during a significant transition phase. The role requires attention to detail and adherence to quality standards in a fast-paced environment.Job Type &amp; LocationThis is a Contract position based out of Belleville, MI.Pay and BenefitsThe pay range for this position is $40.00 - $48.00/hr.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)Workplace TypeThis is a fully onsite position in Belleville,MI.Application DeadlineThis position is anticipated to close on Jul 23, 2026.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 high-volume advanced manufacturing operations involving laser processing, fragile material handling, inspection, cleaning, packaging, and customer quality requirements. This role develops, maintains, and improves data collection systems to understand process performance, identify defect trends, support root-cause analysis, and ensure effective, well-documented production controls. A key focus is creating reliable process data at every production step, from incoming inspection through shipment, while partnering closely with Operations, Engineering, Manufacturing, Materials, and customer-facing teams. This position is critical to scaling production while protecting yield, customer confidence, product traceability, and process control within a cutting-edge, high-growth environment.Responsibilities<ul><li>Develop, maintain, and improve production quality data collection systems to monitor process performance and drive continuous improvement.</li><li>Create and manage reliable process data across all production steps, including incoming inspection, lamination, laser processing, cleaning, final inspection, packaging, and shipment.</li><li>Analyze production data to identify defect trends, process variation, and quality risks, and translate findings into practical corrective and preventive actions.</li><li>Support root-cause analysis and implement disciplined corrective actions to address quality issues and prevent recurrence.</li><li>Ensure production controls are effective, documented, and aligned with quality management system requirements, including ISO 9001.</li><li>Collaborate closely with Operations, Engineering, Manufacturing, Materials, and customer-facing program teams to identify and mitigate quality risks early.</li><li>Support and maintain documentation such as Control Plans, PFMEA, work instructions, inspection plans, and nonconforming material processes.</li><li>Collect data, compile it into graphs and charts, and present it in a clear and meaningful way to internal stakeholders and customers.</li><li>Interface directly with customers to address quality concerns, present data and proposals, and respond to quality-related requests.</li><li>Support customer audits, supplier qualifications, Control Plan reviews, PFMEA reviews, and corrective-action reviews as needed.</li><li>Contribute to process control, defect tracking, and process capability analysis to support stable, scalable production.</li><li>Participate in and support production ramps, new product introductions, and high-growth manufacturing activities to ensure quality is maintained as volume increases.</li><li>Use structured problem-solving methods and statistical tools such as MSA, gage R&amp;R, SPC, capability analysis, and Pareto analysis to improve processes.</li><li>Support optical inspection, metrology, and automated inspection methods where applicable, ensuring measurement systems are suitable and reliable.</li><li>Prepare and deliver proposals and technical presentations to internal teams and external customers, explaining quality strategies, findings, and recommendations.</li></ul>Essential Skills<ul><li>3–5 years of experience as a Quality Engineer in a manufacturing or production environment.</li><li>Experience working within an ISO 9001 quality management system and familiarity with ISO 9001 QMS requirements.</li><li>Ability to interface effectively with customers regarding quality issues, data, and corrective actions.</li><li>Strong ability to collect data, compile it into graphs and charts, and present it in a clear and meaningful way.</li><li>Experience with root-cause analysis, corrective action, process control, and defect tracking.</li><li>Bachelor’s degree in Engineering, Quality, Manufacturing, Materials Science, or a related technical field, or equivalent practical experience such as an associate degree or substantial non-degreed technical experience.</li><li>Strong capability to develop and maintain production quality data systems.</li><li>Familiarity with Control Plans, PFMEA, work instructions, inspection plans, and nonconforming material processes.</li><li>Ability to analyze data, identify trends, and convert findings into practical actions that improve quality and process performance.</li><li>Strong communication skills for working with Operations, Engineering, Quality, Materials, and customer-facing teams.</li><li>Strong attention to detail and a high level of commitment to documentation accuracy.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in aerospace, industrial manufacturing, or medical device manufacturing environments is highly preferred.</li><li>Experience supporting production ramps, new product introductions, or high-growth manufacturing environments.</li><li>Experience with laser processing, semiconductor materials, wafer handling, micro-machining, optics, electronics, medical devices, aerospace, or other precision manufacturing environments.</li><li>Experience working with fragile materials such as wafers, thin films, coated materials, or thermal interface materials.</li><li>Experience with optical inspection, digital microscopy, profilometry, metrology systems, SWIR/IR inspection, or automated inspection methods.</li><li>Experience supporting customer audits, supplier qualification activities, Control Plan reviews, PFMEA reviews, or corrective-action reviews.</li><li>Experience with measurement system analysis (MSA), gage R&amp;R, statistical process control (SPC), capability analysis, Pareto analysis, and structured problem-solving methodologies.</li><li>Interest in working with cutting-edge technology and contributing to a high-growth organization focused on precision manufacturing.</li></ul>Work EnvironmentThis is a fully onsite role in a high-volume advanced manufacturing environment that focuses on precision processes such as laser processing, optical inspection, and metrology. The Quality Engineer works closely with operators, team leads, quality inspectors, manufacturing engineers, and customer quality teams, and regularly presents proposals and findings to internal stakeholders and external customers. The position requires frequent interaction with customer representatives, including fielding calls and responding promptly to quality-related requests. Standard hours are Monday through Friday, either 8:00 a.m. to 5:00 p.m. or 9:00 a.m. to 6:00 p.m. The environment emphasizes collaboration, technical excellence, and the use of advanced inspection and measurement technologies, offering the opportunity to work with cutting-edge technology in a company experiencing significant growth.Job Type &amp; LocationThis is a Permanent position based out of Columbia, MD.Pay and BenefitsThe pay range for this position is $68000.00 - $90000.00/yr.Competitive salary, dependent on experience.
Generous time-off package including paid PTO starting at 12 days (rising to 25
with service), 9 public holidays plus a floating holiday, paid birthday leave, sick
&amp; safe leave, and paid bereavement and public-duty leave (pro-rated for
part-time roles).
Company medical insurance plan, including health, dental, and vision
coverage
Life Insurance and Disability Insurance for added financial protection
Generous 401K scheme
Professional development opportunities, where applicable, including training
and support for qualificationsWorkplace TypeThis is a fully onsite position in Columbia,MD.Application DeadlineThis position is anticipated to close on Jul 30, 2026.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 Quality Engineer. This role involves managing customer quality issues, conducting root cause analysis, and implementing corrective actions. The Quality Engineer will develop and track quality metrics and KPIs, lead inspection activities for fabricated sheet metal components, and ensure supplier compliance with quality standards.Responsibilities<ul><li>Maintain and improve the Quality Management System (QMS), including NCR, CAR, RCA, 8D, ECN, and internal audit processes.</li><li>Manage customer quality issues, complaints, and warranty claims, ensuring timely root cause analysis and corrective actions.</li><li>Develop and track quality metrics and KPIs to monitor product, process, and supplier performance.</li><li>Lead inspection activities across supplier, receiving, in-process, and final inspection for fabricated sheet metal components.</li><li>Qualify, onboard, and develop suppliers to ensure compliance with quality and fabrication standards.</li><li>Support production through NCR management, quality training, and collaboration with manufacturing and engineering teams.</li><li>Drive continuous improvement initiatives focused on reducing scrap, rework, and process inefficiencies in fabrication operations.</li><li>Promote a strong safety and quality culture throughout the manufacturing floor.</li></ul>Essential Skills<ul><li>Quality engineering</li><li>Continuous improvement</li><li>Quality assurance</li><li>Supplier quality</li><li>Root cause analysis</li><li>Sheet metal fabrication</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Engineering or a related discipline.</li><li>Minimum of 5 years of quality assurance experience in a production or manufacturing environment.</li><li>Preferred experience includes metal fabrication, welding, painting processes, SolidWorks, PDM/MRP/ERP systems, and drafting standards (ANSI Y14).</li><li>Experience with ISO 9001 and/or Lean Six Sigma certification is preferred.</li></ul>Work EnvironmentThe work environment involves collaborating with manufacturing and engineering teams on the production floor. You will be working in a dynamic and fast-paced setting that requires adherence to safety and quality standards. The role may involve using SolidWorks, PDM/MRP/ERP systems, and adhering to ANSI Y14 drafting standards.Job Type &amp; LocationThis is a Permanent position based out of Winneconne, WI.Pay and BenefitsThe pay range for this position is $90000.00 - $125000.00/yr.Health Insurace
Dental Insurance
Vision Insurance
PTO &amp; Holiday Pay
401k + BonusWorkplace TypeThis is a fully onsite position in Winneconne,WI.Application DeadlineThis position is anticipated to close on Jul 27, 2026.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 Quality Engineer. This role involves managing customer quality issues, conducting root cause analysis, and implementing corrective actions. The Quality Engineer will develop and track quality metrics and KPIs, lead inspection activities for fabricated sheet metal components, and ensure supplier compliance with quality standards.Responsibilities<ul><li>Maintain and improve the Quality Management System (QMS), including NCR, CAR, RCA, 8D, ECN, and internal audit processes.</li><li>Manage customer quality issues, complaints, and warranty claims, ensuring timely root cause analysis and corrective actions.</li><li>Develop and track quality metrics and KPIs to monitor product, process, and supplier performance.</li><li>Lead inspection activities across supplier, receiving, in-process, and final inspection for fabricated sheet metal components.</li><li>Qualify, onboard, and develop suppliers to ensure compliance with quality and fabrication standards.</li><li>Support production through NCR management, quality training, and collaboration with manufacturing and engineering teams.</li><li>Drive continuous improvement initiatives focused on reducing scrap, rework, and process inefficiencies in fabrication operations.</li><li>Promote a strong safety and quality culture throughout the manufacturing floor.</li></ul>Essential Skills<ul><li>Quality engineering</li><li>Continuous improvement</li><li>Quality assurance</li><li>Supplier quality</li><li>Root cause analysis</li><li>Sheet metal fabrication</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Engineering or a related discipline.</li><li>Minimum of 5 years of quality assurance experience in a production or manufacturing environment.</li><li>Preferred experience includes metal fabrication, welding, painting processes, SolidWorks, PDM/MRP/ERP systems, and drafting standards (ANSI Y14).</li><li>Experience with ISO 9001 and/or Lean Six Sigma certification is preferred.</li></ul>Work EnvironmentThe work environment involves collaborating with manufacturing and engineering teams on the production floor. You will be working in a dynamic and fast-paced setting that requires adherence to safety and quality standards. The role may involve using SolidWorks, PDM/MRP/ERP systems, and adhering to ANSI Y14 drafting standards.Job Type &amp; LocationThis is a Permanent position based out of Winneconne, WI.Pay and BenefitsThe pay range for this position is $90000.00 - $125000.00/yr.Health Insurace
Dental Insurance
Vision Insurance
PTO &amp; Holiday Pay
401k + BonusWorkplace TypeThis is a fully onsite position in Winneconne,WI.Application DeadlineThis position is anticipated to close on Jul 31, 2026.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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