Quality ManagerJob DescriptionThe Quality Manager leads and continuously improves the companys quality management system (QMS) to ensure full compliance with FDA regulations, ISO standards, and other applicable regulatory requirements within the medical device industry. This role oversees quality engineering, quality assurance, and quality control activities, drives effective corrective and preventive actions, and partners closely with cross-functional teams to embed quality into every stage of the product lifecycle. The Quality Manager serves as a key liaison during internal and external audits and provides clear, data-driven quality insights to senior leadership.Responsibilities<ul><li>Lead, maintain, and continually improve the companys quality management system (QMS) in compliance with FDA regulations, ISO standards, and other applicable regulatory requirements.</li><li>Plan, manage, and host internal and external audits, including FDA inspections and ISO certification audits, ensuring audit readiness at all times.</li><li>Oversee corrective and preventive action (CAPA) processes, nonconformance investigations, and complaint handling to ensure timely, effective, and compliant resolutions.</li><li>Collaborate with cross-functional teams, including Research and Development, Manufacturing, and Regulatory, to ensure quality is built into every stage of the product lifecycle.</li><li>Develop, track, and analyze quality metrics and key performance indicators (KPIs), and present findings, trends, and recommendations to senior leadership.</li><li>Lead and coordinate training programs on quality standards, procedures, and best practices to ensure organization-wide understanding and adherence.</li><li>Manage document control and change control processes to maintain accurate, current, and compliant quality documentation and records.</li><li>Oversee risk management processes, ensuring that product and process risks are identified, evaluated, and mitigated in accordance with applicable standards.</li><li>Supervise quality assurance and quality control staff, providing coaching, guidance, and performance feedback to build a high-performing quality team.</li><li>Support and lead root cause analysis activities to identify underlying issues and implement sustainable corrective and preventive actions.</li><li>Participate in and lead special projects and other duties as assigned to support broader organizational goals related to quality and compliance.</li></ul>Essential Skills<ul><li>Bachelors degree in Engineering, Life Sciences, or a related field.</li><li>5+ years of experience in quality management within the medical device industry.</li><li>Strong knowledge of FDA Quality System Regulation (QSR) and relevant ISO-based quality management system requirements.</li><li>Demonstrated experience managing and maintaining a quality management system (QMS) in a regulated environment.</li><li>Hands-on experience with CAPA processes, including initiation, investigation, implementation, and effectiveness verification.</li><li>Proficiency in root cause analysis methodologies and tools to resolve quality issues and prevent recurrence.</li><li>Experience preparing for and managing internal and external audits, including regulatory inspections and ISO certification audits.</li><li>Solid background in quality engineering and quality assurance practices within medical device manufacturing.</li><li>Strong understanding of risk management principles and their application in product and process development.</li><li>Excellent leadership skills with experience supervising or leading quality assurance and quality control staff.</li><li>Effective written and verbal communication skills, with the ability to present quality metrics and findings to senior leadership.</li><li>Strong problem-solving and analytical skills, with the ability to interpret data and drive evidence-based decisions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Masters degree in Engineering, Life Sciences, or a related field is preferred.</li><li>Familiarity with aerospace quality standards such as AS9100 is beneficial, especially for organizations serving multiple regulated markets.</li><li>Experience developing and delivering training programs on quality standards, procedures, and best practices.</li><li>background in medical device quality systems, including complaint handling, nonconformance management, and audit readiness.</li><li>ASQ certifications, such as Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA), are a plus.</li><li>Demonstrated ability to collaborate effectively with cross-functional teams, including R&amp;D, Manufacturing, and Regulatory.</li><li>Proven capability to develop, monitor, and report on quality metrics and key performance indicators (KPIs).</li></ul>Work EnvironmentThe Quality Manager works in a regulated medical device environment that emphasizes compliance, documentation integrity, and continuous improvement. The role involves close collaboration with cross-functional teams such as Research and Development, Manufacturing, Regulatory, and quality assurance and quality control staff. Work typically takes place in an office and manufacturing or laboratory setting where access to quality documentation systems, QMS tools, and audit preparation materials is essential. The position requires regular participation in internal meetings, audit activities, and training sessions, as well as periodic interaction with external auditors and regulatory representatives. The environment is structured, detail-oriented, and process-driven, with a strong focus on maintaining high product quality and meeting regulatory expectations.Job Type &amp; LocationThis is a Permanent position based out of Lawndale, CA.Pay and BenefitsThe pay range for this position is $130000.00 - $150000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.health, dental, vision, pto, sick pay, retirement plan, and moreJob Type &amp; LocationThis is a Permanent position based out of Lawndale, CA.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Lawndale,CA.About Actalent 

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



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



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



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



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



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

Quality Manager

Job Title: Quality ManagerJob DescriptionThe Quality Manager plans, coordinates, and directs all Quality Assurance and Quality Control activities to ensure manufactured products consistently meet customer, company, and industry requirements. This role provides strategic and hands-on leadership to the Quality Department, driving quality objectives, performance metrics, corrective and preventive actions, inspection processes, testing methodologies, compliance, and continuous improvement across a manufacturing environment. The position offers significant influence over the Quality organization, with visibility across manufacturing, engineering, operations, senior leadership, and customers, and plays a key role in supporting advanced manufacturing and modernization programs.Responsibilities<ul><li>Establish and maintain quality objectives that align with corporate goals and overall business strategy.</li><li>Lead, develop, and mentor Quality Department personnel, including Engineers, Inspectors, Technicians, and other quality staff.</li><li>Utilize key performance indicators (KPIs) to monitor quality performance and implement corrective and improvement initiatives.</li><li>Own and manage the Corrective and Preventive Action (CAPA) process, ensuring timely resolution of quality issues.</li><li>Develop standards, procedures, and methodologies for inspection, testing, and evaluation of products and components.</li><li>Oversee product and component inspection, testing, analysis, and all related quality activities within the manufacturing environment.</li><li>Review engineering and design documentation to verify compliance with stated customer, company, and industry requirements.</li><li>Review vendor quality documentation and internal company quality records to ensure adherence to quality standards.</li><li>Represent the organization during customer visits, surveys, meetings, audits, and presentations related to quality.</li><li>Analyze and review quality data to confirm compliance with company policies, procedures, and regulatory requirements.</li><li>Escalate significant quality issues to senior leadership and drive effective corrective actions to closure.</li><li>Prepare and present technical and program-level quality information to senior management and customers.</li><li>Direct inspection and testing personnel to maintain control over materials, components, and finished products.</li><li>Maintain current knowledge of applicable government and industry quality standards and requirements.</li><li>Develop and deliver quality-related training programs to support employee development and compliance.</li><li>Utilize PLEX ERP to manage and support quality activities, including documentation, tracking, and reporting.</li><li>Lead employee development and training efforts within the Quality Department, including performance management and coaching.</li><li>Manage work assignment, prioritization, and resource allocation for quality personnel to meet operational needs.</li><li>Participate in interviewing and hiring of Quality Department employees to build a strong and capable team.</li><li>Collaborate cross-functionally with manufacturing, engineering, program management, operations, supply chain, and customers to resolve quality issues and improve processes.</li><li>Support continuous improvement initiatives, including Lean Manufacturing and other quality enhancement methodologies.</li><li>Contribute to the establishment and tracking of Quality KPIs and support the development of Quality training programs.</li></ul>Essential Skills<ul><li>8+ years of experience in Quality Assurance, Quality Engineering, Quality Management, or a comparable discipline within a manufacturing environment.</li><li>Minimum 2+ years of direct management experience leading employees in a manufacturing-focused Quality organization.</li><li>Proven experience managing Quality Engineers, Inspectors, Technicians, or other quality personnel.</li><li>Strong Quality Assurance and Quality Control background in a manufacturing setting, including inspection, testing, evaluation, and product quality processes.</li><li>Hands-on proficiency with PLEX ERP, including the ability to navigate and utilize the system to support manufacturing and quality activities.</li><li>Experience owning and driving CAPA (Corrective and Preventive Action) processes from issue identification through resolution and verification.</li><li>Demonstrated ability to identify quality issues, determine root causes, implement corrective actions, and monitor effectiveness.</li><li>Working knowledge of government and industry quality standards applicable to manufacturing operations.</li><li>Experience representing Quality during customer meetings, audits, visits, presentations, and surveys.</li><li>Comfort presenting technical and program-level quality information to senior management and customers.</li><li>Strong skills in quality engineering, quality management systems (QMS), and overall quality management.</li><li>Proficiency in root cause analysis and corrective action planning.</li><li>Experience with quality documentation, inspection, testing and validation, and manufacturing quality processes.</li><li>Demonstrated leadership skills, including employee development and training, performance management, work assignment and prioritization, interviewing and hiring, employee coaching and corrective action, cross-functional communication, and executive/customer presentations.</li><li>Bachelors degree in Engineering, Management, Business, or a related discipline.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in aerospace and defense manufacturing environments.</li><li>background in military vehicle or ground vehicle manufacturing.</li><li>Experience in automotive OEM or Tier 1 manufacturing.</li><li>Familiarity with AS9100 quality management standards.</li><li>Experience with IATF quality standards.</li><li>Knowledge of ISO 9001 quality management systems.</li><li>Understanding of government and Department of Defense (DoD) quality requirements.</li><li>Internal or external audit experience, including planning and execution.</li><li>Supplier quality experience, including supplier evaluation and performance monitoring.</li><li>Experience with APQP (Advanced Product Quality Planning) and PPAP (Production Part Approval Process).</li><li>Knowledge of PFMEA (Process Failure Mode and Effects Analysis) and Control Plans.</li><li>Experience with Lean Manufacturing and continuous improvement methodologies.</li><li>Six Sigma certification or equivalent process improvement credentials.</li><li>ASQ certifications such as Certified Quality Engineer (CQE), Certified Quality Manager/Organizational Excellence (CQM/OE), or similar.</li><li>Experience establishing and tracking Quality KPIs to drive performance and improvement.</li><li>Experience developing and delivering Quality training programs for employees.</li><li>Comfort working in a defense-oriented, advanced manufacturing environment supporting modernization programs.</li></ul>Work EnvironmentThis role is based in Plymouth, Michigan in a manufacturing-focused Quality leadership position. The work environment is a combination of office, quality lab and inspection areas, and manufacturing floor activity. The Quality Manager interacts extensively with manufacturing, engineering, program management, operations, supply chain, customers, and senior leadership, and directly manages employees within the Quality Department. The position may occasionally require lifting up to 25 pounds and involves periodic standing, walking, sitting, reaching, and hands-on activities within the manufacturing environment. The setting is professional, collaborative, and focused on advanced manufacturing and continuous improvement, with regular cross-functional engagement and customer-facing responsibilities.Job Type &amp; LocationThis is a Contract position based out of Sterling Heights, MI.Pay and BenefitsThe pay range for this position is $45.00 - $55.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job DescriptionAs the Quality Assurance Manager, you lead and oversee all quality assurance and quality control activities within a manufacturing operation. You manage the quality management system, drive continuous improvement, and ensure that products consistently meet customer and regulatory requirements while fostering a culture of quality across the organization.Responsibilities<ul><li>Manage and maintain the Quality Management System (QMS), ensuring compliance with internal requirements as well as customer and industry standards.</li><li>Develop, implement, and monitor quality standards, procedures, and detailed work instructions to support consistent and reliable manufacturing processes.</li><li>Analyze quality metrics and performance data to identify trends, root causes, and opportunities for improvement in products and processes.</li><li>Lead internal quality audits, supplier audits, and customer audits to verify compliance and drive corrective actions where needed.</li><li>Direct supplier quality initiatives, including supplier qualification, performance scorecards, corrective actions, and PPAP activities.</li><li>Plan and lead corrective and preventive action (CAPA) programs, ensuring actions are properly documented, tracked, and effectively closed.</li><li>Conduct root cause analysis using methodologies such as 8D, 5 Why, Fishbone (Ishikawa), and Fault Tree Analysis to resolve complex quality issues.</li><li>Collaborate closely with Operations, Engineering, Supply Chain, and Customer Service teams to resolve quality concerns and improve cross-functional processes.</li><li>Drive continuous improvement projects focused on defect reduction, waste reduction, process optimization, and increased customer satisfaction.</li><li>Ensure compliance with applicable industry standards, regulatory requirements, and company policies related to quality and manufacturing.</li><li>Manage customer quality issues in a customer-facing capacity, providing timely communication, thorough investigation, and effective corrective actions.</li><li>Recruit, develop, coach, and lead quality team members, setting clear expectations and driving accountability for departmental objectives.</li><li>Champion lean manufacturing and process improvement initiatives to enhance efficiency and overall operational performance.</li><li>Oversee quality reporting tools and systems, ensuring accurate documentation and effective use of data for decision-making.</li><li>Support project management activities related to quality, including planning, execution, and monitoring of quality-focused projects.</li><li>Apply advanced quality tools such as FMEA, APQP, PPAP, MSA, and GD&amp;T in the development and control of manufacturing processes.</li><li>Coordinate and support compliance activities, ensuring that all quality-related processes align with relevant standards and customer requirements.</li><li>Utilize ERP systems to manage and track quality-related information, documentation, and workflows.</li></ul>Essential Skills<ul><li>Bachelor's degree in Quality, Engineering, Manufacturing, Industrial Technology, or a related field.</li><li>5+ years of progressive quality management experience in a manufacturing environment.</li><li>Proven experience leading quality teams and driving continuous improvement initiatives.</li><li>Strong understanding of quality systems, auditing practices, and statistical analysis methods.</li><li>Experience implementing, maintaining, and auditing ISO 9001-compliant quality management systems.</li><li>Hands-on experience with root cause analysis methodologies such as 8D, 5 Why, Fishbone (Ishikawa), and Fault Tree Analysis.</li><li>Demonstrated ability to lead internal audits, supplier audits, and customer audits.</li><li>Experience developing, tracking, and closing corrective and preventive actions (CAPA).</li><li>Quality management leadership experience, including managing teams, coaching employees, and driving accountability.</li><li>Supplier quality management experience, including supplier qualification, scorecards, corrective actions, and PPAP activities.</li><li>Strong continuous improvement mindset with experience in lean manufacturing and process improvement initiatives.</li><li>Excellent communication, leadership, and problem-solving skills.</li><li>Proficiency in Microsoft Office and quality reporting tools.</li><li>Ability to work effectively in a customer-facing role to address and resolve quality issues.</li><li>Familiarity with compliance requirements related to quality and manufacturing.</li><li>Experience using ERP systems to support quality management activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>ASQ certifications such as Certified Quality Manager (CQM), Certified Quality Engineer (CQE), or related credentials.</li><li>Formal experience with ISO 9001 quality management systems, including implementation and continuous maintenance.</li><li>Lean Manufacturing and Six Sigma training or certification.</li><li>Experience with metal fabrication, assembly, machining, or electromechanical manufacturing processes.</li><li>Knowledge of advanced quality tools and methodologies, including FMEA, APQP, PPAP, MSA, and GD&amp;T.</li><li>Experience supporting supplier quality management programs and customer audit requirements.</li><li>Strong background in continuous improvement, waste reduction, and process optimization.</li><li>Experience in project management related to quality initiatives.</li></ul>Work EnvironmentThis role operates within an established manufacturing facility that uses older equipment and an older production environment. You work in a collaborative and supportive setting where quality is central to the culture and where innovation, accountability, teamwork, and continuous improvement are highly valued. The organization offers competitive compensation, a comprehensive benefits package, a 401(k) with company match, paid time off and holidays, and structured career development opportunities. You have the chance to make a meaningful impact on products trusted by customers worldwide and to help shape the future of quality excellence within a respected manufacturing organizationJob Type &amp; LocationThis is a Contract to Hire position based out of Nicholasville, KY.Pay and BenefitsThe pay range for this position is $52.00 - $62.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

<h2 style="text-align:center;">Quality Manager</h2>Are you passionate about building quality into breakthrough medical technologies? We're seeking a Quality Manager to lead quality operations for an innovative structural heart medical device program advancing through pivotal clinical trials and toward global commercialization. In this highly visible leadership role, you will oversee manufacturing quality, inspection, compliance, investigations, and quality systems while leading a team of quality professionals supporting the production of Class III implantable medical devices. This is an opportunity to influence product quality, regulatory readiness, and operational excellence while helping bring life-changing cardiovascular therapies to patients around the world.<h2></h2><h2>What You'll Do</h2><ul><li>Lead quality operations supporting manufacturing, inspection, testing, and release activities.</li><li>Ensure compliance with FDA, ISO 13485, MDSAP, and applicable international regulations.</li><li>Maintain a continuous state of audit and inspection readiness.</li><li>Lead investigations involving nonconformances, deviations, complaints, and quality events.</li><li>Drive CAPA activities from investigation through implementation and effectiveness verification.</li><li>Partner with manufacturing teams to improve process capability, product quality, and operational performance.</li><li>Oversee environmental monitoring, cleanroom controls, and manufacturing quality processes.</li><li>Support supplier quality initiatives, including supplier corrective actions and incoming inspection strategies.</li><li>Develop and coach quality engineers and quality inspectors while fostering a culture of accountability and continuous improvement.</li><li>Monitor quality metrics and identify opportunities to improve efficiency, compliance, and product quality.</li><li>Collaborate across functions to support clinical, regulatory, and commercialization objectives.</li><li>Contribute to long-term quality strategy while remaining actively involved in day-to-day operations.</li></ul><h3>Required Qualifications</h3><ul><li>Bachelor's degree in Engineering, Life Sciences, Quality, or a related technical discipline.</li><li>7+ years of experience in Quality Engineering, Quality Assurance, Manufacturing Quality, or Quality Operations within a regulated industry.</li><li>Experience working in FDA-regulated medical device manufacturing environments.</li><li>Strong knowledge of quality systems, CAPA, nonconformance management, root cause analysis, and regulatory compliance.</li><li>Experience leading investigations and driving corrective and preventive actions.</li><li>Prior people leadership or team management experience.</li><li>Strong understanding of manufacturing quality, inspection methods, process controls, and quality improvement methodologies.</li><li>Excellent communication and cross-functional collaboration skills.</li></ul><h3>Preferred Qualifications</h3><ul><li>Experience supporting Class III or implantable medical devices.</li><li>Cardiovascular, structural heart, electrophysiology, orthopedic, neuromodulation, or other complex medical device experience.</li><li>Experience supporting products through clinical studies and commercialization.</li><li>Familiarity with MDSAP, EU MDR, and Health Canada requirements.</li><li>Experience working in cleanroom manufacturing environments.</li><li>Experience with supplier quality and critical component management.</li><li>Knowledge of risk management, validation, design controls, and design assurance principles.</li><li>Proven success in fast-paced or high-growth medical device organizations.</li></ul>Don't meet every qualification? We encourage you to apply. We value diverse medical device backgrounds and recognize that strong candidates may bring transferable experience from other highly regulated product environments.Job Type &amp; LocationThis is a Permanent position based out of Maple Grove, MN.Pay and BenefitsThe pay range for this position is $120000.00 - $145000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.We recognize that meaningful work is supported by meaningful benefits. Thats why we offer a competitive compensation package along with comprehensive benefits designed to support you and your familys health, well-being, and financial future. Our benefits package includes:
	Medical
	Dental
	Vision
	Flexible Spending Account (FSA)
	Basic Life 
	401(k) Retirement Plan
	Paid Holidays
	PTO
	Maternity/Paternity paid leaveJob Type &amp; LocationThis is a Permanent position based out of Maple Grove, MN.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Maple Grove,MN.About Actalent 

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



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



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



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



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



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

Job Title: Quality ManagerJob DescriptionThe Quality Manager oversees quality engineering activities to ensure products consistently meet established requirements and standards. This role gathers and analyzes factual data to solve complex quality-related problems, identifies and applies solutions based on technical experience and established precedents, and plans and leads quality projects with realistic timelines and clear sequencing of activities. The Quality Manager works collaboratively across all departments to build a strong team environment and drives the implementation of quality goals through audits, inspections, and testing, while closely engaging with suppliers and external experts.Responsibilities<ul><li>Gather and analyze relevant, factual information and data to identify, investigate, and resolve quality-related issues.</li><li>Apply technical experience and established precedents to develop and implement effective solutions to quality problems.</li><li>Plan, organize, and lead quality projects by defining activities, sequencing tasks, and establishing realistic timelines.</li><li>Evaluate process methods and equipment to ensure they meet performance and quality requirements.</li><li>Establish quality plans for equipment and processes that support general and specific product performance needs.</li><li>Monitor process performance against established standards and implement corrective actions when necessary.</li><li>Apply ISO and Quality System Regulation (QSR) requirements to internal processes and procedures, as well as to those of external suppliers.</li><li>Collaborate with suppliers on new product introductions to ensure quality and performance requirements are fully met.</li><li>Assist Manufacturing, Sourcing, and Development teams in interpreting and applying applicable regulations and quality standards.</li><li>Develop and maintain department and project budgets to support quality initiatives and continuous improvement efforts.</li><li>Facilitate team efforts on quality engineering projects and promote a collaborative, results-oriented environment.</li><li>Communicate clearly and effectively in both oral and written form with multiple levels across the organization and with external stakeholders.</li><li>Use optical comparators, coordinate measuring machines (CMMs), and other measurement tools to support inspection and testing activities.</li><li>Conduct and support product testing, design assurance activities, and risk analysis using FMEA and related methodologies.</li><li>Apply statistical methods, process control techniques, and process capability analysis to monitor and improve product and process quality.</li><li>Maintain thorough knowledge of existing products and a basic understanding of competitive products to inform quality decisions.</li><li>Identify inaccurate or incomplete information from supporting departments, discern potential issues, and propose corrective actions.</li></ul>Essential Skills<ul><li>57 years of experience in a Quality Engineering role, with medical device industry experience strongly preferred.</li><li>Bachelors degree in engineering or an alternative bachelors degree combined with certification as a quality engineer (e.g., CQE).</li><li>Strong background in quality engineering within regulated environments, ideally in medical devices.</li><li>Proficiency in applying ISO standards and QSR requirements to processes, procedures, and supplier activities.</li><li>Hands-on experience with FMEA, design assurance, and product testing methods.</li><li>Expert knowledge of blueprint reading and geometric dimensioning and tolerancing (GD&amp;T).</li><li>Proficiency with Microsoft Office Suite for data analysis, documentation, and communication.</li><li>Ability to use optical comparators and coordinate measuring machines (CMMs) for inspection and measurement.</li><li>Solid understanding of statistics, process control, and process capability analysis.</li><li>Ability to work effectively within a team environment and build strong relationships across departments and with external partners such as suppliers and regulatory agencies.</li><li>Demonstrated ability to deliver results, meet deadlines, and maintain a strong results orientation.</li><li>Strong oral and written communication skills, with the ability to communicate at multiple levels of the organization.</li><li>Full working knowledge of supporting departmental needs and capabilities, including the ability to recognize inaccurate information and suggest improvements.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certification as a Quality Engineer (CQE) or Reliability Engineer Certification (CRE) granted through the American Society for Quality (ASQ) is preferred.</li><li>Experience working directly with suppliers on new product introductions and supplier quality management.</li><li>Experience implementing and maintaining quality plans for equipment and processes.</li><li>Familiarity with medical device regulations and standards beyond ISO and QSR.</li><li>Thorough knowledge of existing product lines and a basic understanding of competitive products in the market.</li><li>Strong analytical and problem-solving skills with the ability to interpret complex technical information.</li><li>Ability to facilitate cross-functional team efforts and drive consensus on quality initiatives.</li><li>Budget development and management experience for department and project-level activities.</li></ul>Work EnvironmentThe Quality Manager works in a professional, engineering-focused environment that emphasizes cross-functional collaboration among Manufacturing, Sourcing, Development, and other supporting departments. The role involves regular interaction with suppliers and regulatory agencies, as well as hands-on work with inspection and measurement equipment such as optical comparators and coordinate measuring machines (CMMs). Daily work includes using Microsoft Office Suite for documentation, reporting, and communication, and applying ISO and QSR-based quality systems in a regulated setting, particularly aligned with medical device standards. The environment supports structured project work with defined timelines and budgets, and encourages a team-oriented, results-driven culture focused on continuous improvement and product quality.Job Type &amp; LocationThis is a Contract position based out of Warsaw, IN.Pay and BenefitsThe pay range for this position is $45.00 - $53.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality ManagerJob DescriptionThe Quality Manager leads and continuously improves the companys quality management system (QMS) to ensure full compliance with FDA regulations, ISO standards, and other applicable regulatory requirements within the medical device industry. This role oversees quality engineering, quality assurance, and quality control activities, drives effective corrective and preventive actions, and partners closely with cross-functional teams to embed quality into every stage of the product lifecycle. The Quality Manager serves as a key liaison during internal and external audits and provides clear, data-driven quality insights to senior leadership.Responsibilities<ul><li>Lead, maintain, and continually improve the companys quality management system (QMS) in compliance with FDA regulations, ISO standards, and other applicable regulatory requirements.</li><li>Plan, manage, and host internal and external audits, including FDA inspections and ISO certification audits, ensuring audit readiness at all times.</li><li>Oversee corrective and preventive action (CAPA) processes, nonconformance investigations, and complaint handling to ensure timely, effective, and compliant resolutions.</li><li>Collaborate with cross-functional teams, including Research and Development, Manufacturing, and Regulatory, to ensure quality is built into every stage of the product lifecycle.</li><li>Develop, track, and analyze quality metrics and key performance indicators (KPIs), and present findings, trends, and recommendations to senior leadership.</li><li>Lead and coordinate training programs on quality standards, procedures, and best practices to ensure organization-wide understanding and adherence.</li><li>Manage document control and change control processes to maintain accurate, current, and compliant quality documentation and records.</li><li>Oversee risk management processes, ensuring that product and process risks are identified, evaluated, and mitigated in accordance with applicable standards.</li><li>Supervise quality assurance and quality control staff, providing coaching, guidance, and performance feedback to build a high-performing quality team.</li><li>Support and lead root cause analysis activities to identify underlying issues and implement sustainable corrective and preventive actions.</li><li>Participate in and lead special projects and other duties as assigned to support broader organizational goals related to quality and compliance.</li></ul>Essential Skills<ul><li>Bachelors degree in Engineering, Life Sciences, or a related field.</li><li>5+ years of experience in quality management within the medical device industry.</li><li>Strong knowledge of FDA Quality System Regulation (QSR) and relevant ISO-based quality management system requirements.</li><li>Demonstrated experience managing and maintaining a quality management system (QMS) in a regulated environment.</li><li>Hands-on experience with CAPA processes, including initiation, investigation, implementation, and effectiveness verification.</li><li>Proficiency in root cause analysis methodologies and tools to resolve quality issues and prevent recurrence.</li><li>Experience preparing for and managing internal and external audits, including regulatory inspections and ISO certification audits.</li><li>Solid background in quality engineering and quality assurance practices within medical device manufacturing.</li><li>Strong understanding of risk management principles and their application in product and process development.</li><li>Excellent leadership skills with experience supervising or leading quality assurance and quality control staff.</li><li>Effective written and verbal communication skills, with the ability to present quality metrics and findings to senior leadership.</li><li>Strong problem-solving and analytical skills, with the ability to interpret data and drive evidence-based decisions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Masters degree in Engineering, Life Sciences, or a related field is preferred.</li><li>Familiarity with aerospace quality standards such as AS9100 is beneficial, especially for organizations serving multiple regulated markets.</li><li>Experience developing and delivering training programs on quality standards, procedures, and best practices.</li><li>background in medical device quality systems, including complaint handling, nonconformance management, and audit readiness.</li><li>ASQ certifications, such as Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA), are a plus.</li><li>Demonstrated ability to collaborate effectively with cross-functional teams, including R&amp;D, Manufacturing, and Regulatory.</li><li>Proven capability to develop, monitor, and report on quality metrics and key performance indicators (KPIs).</li></ul>Work EnvironmentThe Quality Manager works in a regulated medical device environment that emphasizes compliance, documentation integrity, and continuous improvement. The role involves close collaboration with cross-functional teams such as Research and Development, Manufacturing, Regulatory, and quality assurance and quality control staff. Work typically takes place in an office and manufacturing or laboratory setting where access to quality documentation systems, QMS tools, and audit preparation materials is essential. The position requires regular participation in internal meetings, audit activities, and training sessions, as well as periodic interaction with external auditors and regulatory representatives. The environment is structured, detail-oriented, and process-driven, with a strong focus on maintaining high product quality and meeting regulatory expectations.Job Type &amp; LocationThis is a Permanent position based out of Lawndale, CA.Pay and BenefitsThe pay range for this position is $130000.00 - $150000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.health, dental, vision, pto, sick pay, retirement plan, and moreJob Type &amp; LocationThis is a Permanent position based out of Lawndale, CA.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Lawndale,CA.About Actalent 

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



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



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



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



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



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

Quality ManagerJob DescriptionThe Quality Manager leads and continuously improves the companys quality management system (QMS) to ensure full compliance with FDA regulations, ISO standards, and other applicable regulatory requirements within the medical device industry. This role oversees quality engineering, quality assurance, and quality control activities, drives effective corrective and preventive actions, and partners closely with cross-functional teams to embed quality into every stage of the product lifecycle. The Quality Manager serves as a key liaison during internal and external audits and provides clear, data-driven quality insights to leadership.Responsibilities<ul><li>Lead, maintain, and continually improve the companys quality management system (QMS) in compliance with FDA regulations, ISO standards, and other applicable regulatory requirements.</li><li>Plan, manage, and host internal and external audits, including FDA inspections and ISO certification audits, ensuring audit readiness at all times.</li><li>Oversee corrective and preventive action (CAPA) processes, nonconformance investigations, and complaint handling to ensure timely, effective, and compliant resolutions.</li><li>Collaborate with cross-functional teams, including Research and Development, Manufacturing, and Regulatory, to ensure quality is built into every stage of the product lifecycle.</li><li>Develop, track, and analyze quality metrics and key performance indicators (KPIs), and present findings, trends, and recommendations to leadership.</li><li>Lead and coordinate training programs on quality standards, procedures, and best practices to ensure organization-wide understanding and adherence.</li><li>Manage document control and change control processes to maintain accurate, current, and compliant quality documentation and records.</li><li>Oversee risk management processes, ensuring that product and process risks are identified, evaluated, and mitigated in accordance with applicable standards.</li><li>Supervise quality assurance and quality control staff, providing coaching, guidance, and performance feedback to build a high-performing quality team.</li><li>Support and lead root cause analysis activities to identify underlying issues and implement sustainable corrective and preventive actions.</li><li>Participate in and lead special projects and other duties as assigned to support broader organizational goals related to quality and compliance.</li></ul>Essential Skills<ul><li>Bachelors degree in Engineering, Life Sciences, or a related field.</li><li>5+ years of experience in quality management within the medical device industry.</li><li>Strong knowledge of FDA Quality System Regulation (QSR) and relevant ISO-based quality management system requirements.</li><li>Demonstrated experience managing and maintaining a quality management system (QMS) in a regulated environment.</li><li>Hands-on experience with CAPA processes, including initiation, investigation, implementation, and effectiveness verification.</li><li>Proficiency in root cause analysis methodologies and tools to resolve quality issues and prevent recurrence.</li><li>Experience preparing for and managing internal and external audits, including regulatory inspections and ISO certification audits.</li><li>Solid experience in quality engineering and quality assurance practices within medical device manufacturing.</li><li>Strong understanding of risk management principles and their application in product and process development.</li><li>Excellent leadership skills with experience supervising or leading quality assurance and quality control staff.</li><li>Effective written and verbal communication skills, with the ability to present quality metrics and findings to leadership.</li><li>Strong problem-solving and analytical skills, with the ability to interpret data and drive evidence-based decisions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Masters degree in Engineering, Life Sciences, or a related field is preferred.</li><li>Familiarity with aerospace quality standards such as AS9100 is beneficial, especially for organizations serving multiple regulated markets.</li><li>Experience developing and delivering training programs on quality standards, procedures, and best practices.</li><li>Experience in medical device quality systems, including complaint handling, nonconformance management, and audit readiness.</li><li>ASQ certifications, such as Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA), are a plus.</li><li>Demonstrated ability to collaborate effectively with cross-functional teams, including R&amp;D, Manufacturing, and Regulatory.</li><li>Proven capability to develop, monitor, and report on quality metrics and key performance indicators (KPIs).</li></ul>Work EnvironmentThe Quality Manager works in a regulated medical device environment that emphasizes compliance, documentation integrity, and continuous improvement. The role involves close collaboration with cross-functional teams such as Research and Development, Manufacturing, Regulatory, and quality assurance and quality control staff. Work typically takes place in an office and manufacturing or laboratory setting where access to quality documentation systems, QMS tools, and audit preparation materials is essential. The position requires regular participation in internal meetings, audit activities, and training sessions, as well as periodic interaction with external auditors and regulatory representatives. The environment is structured, detail-oriented, and process-driven, with a strong focus on maintaining high product quality and meeting regulatory expectations.If interested, simply apply.Or send your resume to Patrick at prager @ actalentservices.comJob Type &amp; LocationThis is a Permanent position based out of Lawndale, CA.Pay and BenefitsThe pay range for this position is $130000.00 - $150000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.health, dental, vision, pto, sick pay, retirement plan, and moreJob Type &amp; LocationThis is a Permanent position based out of Lawndale, CA.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Lawndale,CA.About Actalent 

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



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



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



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



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



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

Food Quality ManagerJob DescriptionThe Quality Manager oversees all aspects of quality assurance and food safety within a food manufacturing environment, ensuring that products, processes, and documentation meet regulatory, customer, and internal standards. This role develops and maintains quality systems, leads audits and inspections, manages quality staff, and drives continuous improvement across the organization.Responsibilities<ul><li>Oversee quality assurance, food safety, HACCP, SSOP, GMP, SQF, and regulatory compliance programs, ensuring all required documentation is accurate, timely, and complete.</li><li>Develop, maintain, and update quality procedures, reports, product specifications, sanitation records, maintenance logs, and other quality system documentation.</li><li>Lead, support, and participate in HACCP, SSOP, Food Defense, Quality Team, and company quality meetings, including delivering training and communicating key quality topics.</li><li>Manage internal and external audits, inspections, certifications, verifications, laboratory testing, mock recalls, lot tracking, and product release communication.</li><li>Monitor supplier, cold storage, shipping, receiving, pest control, sanitation, and raw material programs, following up on issues and implementing corrective actions as needed.</li><li>Support label approval processes, UPC creation, carton and bag blueprint review, nutritional documentation, net weight compliance, and product specification accuracy.</li><li>Respond to customer, supplier, cold storage, and USDA concerns, leading timely investigation, resolution, and documentation of product or compliance issues.</li><li>Provide leadership and oversight for QA staff, including the QA Supervisor, managing department supplies and budgets while supporting training, accountability, and overall quality department performance.</li><li>Collaborate with cross-functional teams to resolve quality and food safety issues and drive continuous improvement initiatives.</li><li>Ensure ongoing compliance with USDA regulations and GFSI audit requirements, maintaining readiness for regulatory and third-party audits.</li></ul>Essential Skills<ul><li>Minimum 5+ years of quality assurance experience in food manufacturing or a closely related industry.</li><li>Strong working knowledge of food safety and quality systems, including HACCP, SSOP, GMP, SQF, and Food Defense programs.</li><li>Demonstrated understanding of USDA regulatory compliance and regulatory and GFSI audit processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in Food Science, Meat Science, Microbiology, Food Technology, Chemistry, Biological Sciences, or a related field preferred.</li><li>Experience in quality control, quality checks, and food safety programs within a manufacturing setting.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of St. Cloud, MN.Pay and BenefitsThe pay range for this position is $80000.00 - $120000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Base salary is one component of a competitive compensation package for employees. Full benefits package, including medical/vision/dental/life insurance, 401(k) with company match, and paid time off. We take into consideration a variety of factors including, but not limited to, skills, abilities, experience, education, credentials, and internal equity when determining the base salary offered. Roles are eligible for additional rewards, including an annual incentive program based on individual and company performance.Job Type &amp; LocationThis is a Permanent position based out of St. Cloud, MN.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in St. Cloud,MN.About Actalent 

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



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



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



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



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



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

Quality Manager - Food Safety And Quality

Job Title: Quality Operator 2nd ShiftJob DescriptionThe Quality Operator on 2nd shift (MondayFriday, 4:00 p.m. to 12:00 a.m.) sets up, operates, adjusts, and changes over packaging line equipment in a regulated pharmaceutical manufacturing environment. This role ensures continuous packaging operations by supplying materials, monitoring product quality attributes, performing in-process checks, and accurately documenting results in accordance with Good Manufacturing Practices (GMP). The Quality Operator also performs minor mechanical adjustments, participates in cleaning and validation activities, and supports cross-functional trials to maintain high standards of product quality and operational efficiency.Responsibilities<ul><li>Set up, adjust, operate, and perform changeovers on packaging machinery to support continuous production runs.</li><li>Start packaging equipment and closely observe operations to detect mechanical or operational malfunctions.</li><li>Stop equipment when issues arise and promptly report malfunctions to the Production Supervisor or appropriate personnel.</li><li>Analyze mechanical or operational problems, determine root causes, and take appropriate corrective actions within defined procedures.</li><li>Test and verify equipment performance after changeovers to ensure quality operation before returning to production.</li><li>Monitor and inspect product during packaging to confirm it meets all specifications and quality standards.</li><li>Measure and track product variables and attributes throughout the production run to ensure designated parameters are maintained.</li><li>Document in-process testing results, batch progress, and equipment activities accurately and on time in the Packaging Batch Record and other GMP documentation.</li><li>Comply with all internal policies and procedures, as well as applicable FDA, DEA, OSHA, and other regulatory requirements.</li><li>Maintain a clean, organized, and safe work area, following all housekeeping and safety guidelines.</li><li>Perform required facility and equipment cleaning in accordance with the master cleaning schedule and cleanroom requirements.</li><li>Assist with equipment and process validation efforts, including setup, execution support, and documentation as needed.</li><li>Support Research and Development, Manufacturing Technology, and engineering teams during trials and studies on the packaging line.</li><li>Collaborate effectively with production, quality, and other team members to meet production, quality, and safety goals.</li><li>Use computer/PLC-controlled systems to input and monitor machine settings, track performance, and support troubleshooting activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associates degree or equivalent from a two-year college or technical school is acceptable.</li><li>Experience in the sciences is preferred, particularly for candidates interested in progressing into quality or laboratory roles over time.</li><li>Experience in a manufacturing, production, or general labor environment is beneficial.</li><li>Previous exposure to GMP, FDA-regulated, or pharmaceutical manufacturing environments is an advantage.</li><li>Strong people skills and the ability to work effectively within a tight-knit, collaborative team.</li><li>Demonstrated ability to prioritize tasks, stay organized, and maintain high accuracy in a fast-paced setting.</li><li>Interest in learning pharmaceutical industry regulations and best practices, with a desire to grow into roles in QA, manufacturing quality assurance, or laboratory/office functions.</li><li>Comfort working with computer-based systems and automated equipment in a production setting.</li><li>Ability to identify recurring equipment issues and communicate insights to management to support continuous improvement.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Portage, IN.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Operator

Job Title: Quality Process EngineerJob DescriptionThe Quality Process Engineer leads critical quality initiatives across manufacturing, suppliers, and customers to ensure robust processes, prevent defects, and support new product launches. This role focuses on root cause analysis, continuous process improvement, and driving standardized quality systems and tools throughout the organization while providing technical leadership to quality teams.Responsibilities<ul><li>Lead root cause investigations and implement effective corrective actions for manufacturing, supplier, and customer quality issues.</li><li>Improve manufacturing processes by applying Statistical Process Control (SPC), process capability analysis, and robust control plans to enhance consistency and reduce variation.</li><li>Drive defect prevention initiatives that reduce scrap, rework, warranty claims, and customer complaints by strengthening processes and controls.</li><li>Support new product launches and manufacturing process validation activities to ensure stable, capable, and compliant production processes.</li><li>Lead Production Part Approval Process (PPAP) activities for new and modified products, processes, tooling, and suppliers, ensuring complete and accurate submissions and on-time approvals.</li><li>Develop, review, and approve PPAP elements, including process flow diagrams, control plans, dimensional results, material and performance test records, capability studies, and Part Submission Warrants (PSWs).</li><li>Plan and execute Measurement System Analysis (MSA), including variable and attribute studies, to verify that measurement systems are accurate, repeatable, reproducible, and suitable for production use.</li><li>Support ISO quality system requirements, internal and external audits, and continuous improvement initiatives to maintain and enhance certification and compliance.</li><li>Train and coach employees on quality tools, standards, and structured problem-solving methodologies to build quality awareness and capability across the organization.</li><li>Provide day-to-day technical leadership, coaching, and work direction to Quality Technicians to ensure effective inspection activities, containment actions, and problem-solving efforts.</li><li>Ensure adherence to established quality standards, procedures, and documentation requirements across production and quality functions.</li></ul>Essential Skills<ul><li>1015 years of experience in quality, with a strong track record of running a team and driving quality improvement initiatives.</li><li>Proven experience in quality engineering and process engineering within a manufacturing environment.</li><li>Demonstrated expertise in leading root cause analysis and implementing corrective and preventive actions.</li><li>Hands-on experience with Production Part Approval Process (PPAP), including preparation, review, and approval of all required elements.</li><li>Strong skills in process improvement using tools such as Statistical Process Control (SPC) and process capability analysis.</li><li>Practical knowledge and application of Lean and Six Sigma methodologies for defect reduction and process optimization.</li><li>Experience planning and conducting Measurement System Analysis (MSA) for both variable and attribute measurement systems.</li><li>Ability to train, coach, and provide technical leadership to quality teams and cross-functional stakeholders.</li><li>Familiarity with ISO-based quality management systems and support of audits and continuous improvement activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience driving structured defect prevention programs that reduce scrap, rework, and warranty exposure.</li><li>Experience in supporting new product introductions and process validation activities in a manufacturing setting.</li><li>Ability to develop and maintain comprehensive control plans and process documentation.</li><li>Strong communication and collaboration skills to work effectively with production, engineering, suppliers, and customers.</li><li>Demonstrated ability to influence and lead continuous improvement initiatives across multiple teams.</li></ul>Work EnvironmentThe role operates in a manufacturing environment where significant investments are being made to modernize and enhance production capabilities. The organization emphasizes bringing manufacturing processes directly to the shop floor and fostering a culture of continuous improvement. Team members benefit from strong support for quality initiatives and access to robust benefits, while working closely with production, engineering, and quality personnel to drive high-performance operations.Job Type &amp; LocationThis is a Contract to Hire position based out of Manitowoc, WI.Pay and BenefitsThe pay range for this position is $110000.00 - $120000.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Process Engineer

Job Title: Quality SpecialistJob DescriptionThe Quality Specialist ensures that all quality documentation is accurate, compliant, and completed on time, while supporting investigations, deviations, and customer complaint management within a pharmaceutical environment.Responsibilities<ul><li>Complete quality documentation accurately and in a timely manner, including investigation reports and deviation records.</li><li>Review batch records to ensure compliance with Good Manufacturing Practice (GMP) standards and internal quality procedures.</li><li>Assist in the investigation of quality issues, including deviations and nonconformances, and document findings and corrective actions.</li><li>Support the management and resolution of customer complaints by gathering data, performing root cause analysis, and documenting outcomes.</li><li>Collaborate with cross-functional teams to ensure consistent application of quality assurance processes and procedures.</li><li>Participate in validation activities by reviewing and supporting documentation to confirm compliance with regulatory and internal requirements.</li><li>Contribute to continuous improvement initiatives by identifying trends in investigations, deviations, and customer complaints and recommending process enhancements.</li><li>Maintain organized, complete, and audit-ready quality records and documentation in accordance with regulatory expectations and company policies.</li></ul>Essential Skills<ul><li>Bachelor's degree in Science or a related discipline.</li><li>45+ years of experience in a pharmaceutical quality role.</li><li>Strong understanding of Good Manufacturing Practice (GMP) principles and their application in a pharmaceutical setting.</li><li>Hands-on experience with investigations related to quality issues.</li><li>Proven experience managing and documenting deviations.</li><li>Experience handling and documenting customer complaints within a regulated environment.</li><li>Proficiency in batch record review and quality documentation review.</li><li>Solid background in quality assurance practices and processes.</li><li>Ability to perform and document root cause analysis in support of investigations and deviations.</li><li>Strong attention to detail and accuracy in completing quality documentation.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience supporting validation activities and reviewing validation documentation.</li><li>Familiarity with regulatory expectations related to pharmaceutical quality systems.</li><li>Ability to work collaboratively with cross-functional teams to resolve quality issues.</li><li>Strong written communication skills for clear, concise, and compliant documentation.</li><li>Organizational skills to manage multiple investigations, deviations, and documentation tasks simultaneously.</li></ul>Work EnvironmentThis role operates within a regulated pharmaceutical environment that adheres to Good Manufacturing Practice (GMP) standards. The position involves extensive work with quality documentation, batch records, and investigation reports, often using electronic and paper-based systems. Work is typically performed during standard business hours in an office or quality operations setting within a manufacturing or laboratory facility. The environment emphasizes compliance, attention to detail, and collaboration with quality assurance, production, and other technical teams.Job Type &amp; LocationThis is a Contract position based out of Cherry Hill, NJ.Pay and BenefitsThe pay range for this position is $32.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Specialist

<h1>Quality Assurance Specialist</h1><h2>Position Details</h2><ul><li>Job Title: Quality Assurance Specialist</li><li>Employment Type: Contract</li><li>Schedule: Monday-Friday, 1st Shift</li><li>Location: 100% Onsite</li><li>Pay Rate: $35.00-$39.00/hour</li></ul><h2>Key Responsibilities</h2><ul><li>Manage and maintain quality documentation and records within the Quality Management System (QMS).</li><li>Support compliance with applicable quality standards and regulatory requirements.</li><li>Assist with internal and external audits to ensure audit readiness and successful outcomes.</li><li>Collaborate with cross-functional teams to develop, review, and update standard operating procedures (SOPs), work instructions, and quality guidelines.</li><li>Support quality processes including:<ul><li>CAPA (Corrective and Preventive Actions)</li><li>Change Control</li><li>Non-Conformance Investigations</li><li>Risk Management</li><li>Root Cause Analysis</li></ul></li><li>Review and approve customer projects for delivery.</li><li>Support the qualification, maintenance, calibration, and control of laboratory instruments and equipment.</li><li>Partner with both internal stakeholders and external customers to ensure quality expectations are met</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor's degree in Biology, Biotechnology, Life Sciences, Chemistry, or a related scientific discipline.</li><li>Experience working in a Quality Assurance, Quality Control, or laboratory environment.</li><li>Familiarity with quality systems supporting:<ul><li>GCP</li><li>ISO 17025</li><li>GMP (preferred)</li></ul></li><li>Experience participating in audits and compliance activities.</li><li>Strong understanding of:<ul><li>Quality Management Systems (QMS)</li><li>CAPA processes</li><li>Root Cause Analysis</li><li>Regulatory Compliance</li></ul></li><li>Proficiency with Microsoft Office applications.</li><li>Strong analytical, organizational, and problem-solving skills.</li><li>Excellent written and verbal communication abilities</li></ul>Job Type &amp; LocationThis is a Contract position based out of Waltham, MA.Pay and BenefitsThe pay range for this position is $35.00 - $39.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Description Internal customers (AS and other departments) and external customers Management and organization of quality documentation Ensure successful completion of external and internal audits. Collaborate cross-functionally to develop, update and review instructions and guidelines. Support continuous improvements, CAPA (corrective and preventive actions), CC (change control), non-conformance, and risk management processes. Review and approve customer projects for delivery. support qualification, maintenance and control of instruments and equipmentAdditional Skills &amp; QualificationsBachelor degree in the Life Science field or similar ( Science, Biology, Biotech) Experience in Quality, contract laboratory, or QC laboratory with a quality system adapted for GCP, ISO17025, or equivalent. Proven computer experience, especially with Microsoft Office. Experience with LIMS and document management systems. Strong communication and interpersonal skills. Excellent analytical and problem-solving skills.Experience LevelEntry LevelJob Type &amp; LocationThis is a Contract position based out of Waltham, MA.Pay and BenefitsThe pay range for this position is $35.00 - $39.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

<h3>Description</h3><ul><li>Author and maintain reference standard Certificates of Analysis (CoAs) and specification documents.</li><li>Plan, design, and oversee testing processes to ensure reference standards are fit for purpose and meet specifications, including characterization and requalification.</li><li>Coordinate cross-functionally to manage incoming new reference materials for upcoming projects.</li><li>Manage reference material logistics with contract laboratories, maintaining communication regarding characterization and testing.</li><li>Perform both on-site and back-office audits of reference standard usage, documentation, and compliance with regulatory requirements, including FDA, ICH, EU, and ISO standards.</li><li>Provide QC review of documentation, data accuracy, and regulatory compliance for reference standard-related processes.</li><li>Assist in training QC personnel on the handling, documentation, and regulatory requirements for reference standards.</li><li>Act as a liaison between Quality Control and other internal departments, including Analytical Development (AD), Project Management (PM), and Manufacturing (MFG), as it relates to sample management, testing requirements, project documentation, and contract laboratory management.</li></ul><h3>Skills</h3><ul><li>Quality Control</li><li>Chemistry</li><li>Reference Materials</li><li>Chemistry Testing</li><li>Characterization</li><li>Certificates of Analysis (CoAs)</li><li>GMP</li><li>FDA</li><li>ICH</li><li>EU</li><li>ISO</li></ul><h3>Top Skills</h3><ul><li>Quality Control</li><li>Chemistry</li><li>Reference Materials</li><li>Chemistry Testing</li><li>Characterization</li><li>Certificates of Analysis (CoAs)</li></ul><h3>Additional Qualifications</h3><ul><li>Bachelors degree in Chemistry or a related field with 5+ years of experience in a GMP laboratory, or a Masters degree with 3+ years of experience.</li><li>Strong communication, collaboration, and attention to detail.</li><li>Solid understanding of reference standard specifications and scheduling.</li><li>Working knowledge of SQL, databases, and ALCOA+ data integrity principles.</li><li>Understanding of Smartsheet and audit readiness.</li></ul><h3>Schedule</h3><ul><li>MondayFriday, 8:00 AM5:00 PM</li></ul><h3>Experience Level</h3><ul><li>Experienced-level QC professional with 35+ years of relevant GMP laboratory experience, depending on degree level.</li></ul><h3></h3><h3></h3>Job Type &amp; LocationThis is a Contract position based out of Milford, MA.Pay and BenefitsThe pay range for this position is $38.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

<h2>Quality Control Specialist</h2>We are seeking a detail-oriented Quality Control Specialist to support reference standard management programs within a GMP-regulated laboratory environment. This individual will play a critical role in ensuring reference materials are properly qualified, maintained, documented, and compliant with applicable regulatory standards.<h3></h3><h3>Key Responsibilities</h3><ul><li>Author, review, and maintain Certificates of Analysis (CoAs), specifications, and supporting documentation for reference standards.</li><li>Plan, coordinate, and oversee characterization, qualification, and requalification activities to ensure reference standards remain fit for purpose.</li><li>Collaborate with cross-functional teams to manage incoming reference materials and support project timelines.</li><li>Coordinate testing and characterization activities with external contract laboratories, serving as the primary point of contact throughout the process.</li><li>Conduct on-site and remote audits related to reference standard usage, documentation, and regulatory compliance.</li><li>Perform Quality Control reviews of data, documentation, and processes to ensure accuracy, completeness, and compliance with GMP requirements.</li><li>Support training initiatives for QC personnel on reference standard handling, documentation practices, and compliance requirements.</li><li>Act as a liaison between Quality Control and internal departments including Analytical Development, Project Management, and Manufacturing to support sample management, testing schedules, and project documentation.</li><li>Maintain audit readiness and ensure adherence to applicable regulatory and quality standards.</li></ul><h3>Required Qualifications</h3><ul><li>Bachelor's degree in Chemistry or a related scientific discipline with 5+ years of GMP laboratory experience, or a Master's degree with 3+ years of relevant experience.</li><li>Strong knowledge of Quality Control processes within a regulated pharmaceutical, biotechnology, or life sciences environment.</li><li>Experience managing reference standards, reference materials, specifications, and Certificates of Analysis (CoAs).</li><li>Experience supporting characterization and testing activities for laboratory materials.</li><li>Familiarity with FDA, ICH, EU, ISO, and GMP requirements.</li><li>Strong attention to detail, organizational skills, and documentation practices.</li><li>Excellent communication and cross-functional collaboration skills.</li></ul><h3>Preferred Qualifications</h3><ul><li>Working knowledge of SQL, databases, and data integrity principles, including ALCOA+.</li><li>Experience utilizing Smartsheet or similar project-tracking tools.</li><li>Understanding of audit readiness and inspection support activities.</li><li>Ability to manage multiple priorities in a fast-paced, regulated environment.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Milford, MA.Pay and BenefitsThe pay range for this position is $38.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality SpecialistLong-Term Opportunity | Day Shift | Offers BenefitsJob DescriptionThe Quality Specialist ensures exceptional product quality by auditing the facility and production lines, evaluating raw materials, bulk, and finished products, and driving continuous improvement initiatives. This role plays a key part in maintaining a world-class manufacturing control program and supporting a culture of quality across the organization.Responsibilities<ul><li>Complete packaging batch record paperwork accurately and in a timely manner where required.</li><li>Perform regular audits of manufacturing lines and the manufacturing plant to maintain a world-class manufacturing control program.</li><li>Ensure quality events, including deviations, non-conformances, and potential issues, are properly documented, escalated, and resolved to support efficient and effective decision making.</li><li>Maintain compliance with current Standard Operating Procedures (SOPs), Work Instructions, and test procedures.</li><li>Proactively update SOPs, Work Instructions, controlled forms, and test methods to support process improvements and regulatory compliance.</li><li>Ensure documentation records are accurate, complete, and compliant with current Good Manufacturing Practice (GMP) requirements.</li><li>Document and investigate deviations and out-of-specification (OOS) situations, determining root causes and proposing corrective and preventive actions.</li><li>Coach personnel to improve compliance with regulatory and quality requirements and reinforce best practices.</li><li>Verify that products meet quality specifications and customer standards prior to release.</li><li>Ensure current reference and product standards are properly maintained and updated as needed.</li><li>Accurately record data and pertinent information in accordance with cGMP requirements.</li><li>Maintain compliance with current regulatory expectations and practices, such as USP and 21 CFR drug manufacturing regulations.</li></ul>Qualifications &amp; Requirements: <ul><li>2+yrs of experience in a GMP manufacturing environment such as pharmaceutical, cosmetics, personal care, food processing, or medical device (preferred).</li><li>HS Diploma required, but Associate's or Bachelor's degree preferred.</li><li>Working knowledge of cGMP and 21 CFR drug manufacturing regulations.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $26.50 - $32.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

<h3>Operations Specialist Quality - 2 openings one on 1st shift one on 2nd shift </h3>Schedule:<ul><li>On-site manufacturing environment.</li><li>1st Shift: 7:30 AM 3:30 PM</li><li>2nd Shift: 3:00 PM 11:30 PM</li></ul>We are seeking an experienced Quality Inspection Specialist to perform precision inspections of manufactured parts and ensure compliance with engineering specifications and tolerances. This is a hands-on role within a manufacturing environment, working closely with production and quality teams.Key Responsibilities:<ul><li>Perform dimensional inspections using micrometers, height gages, plug gages, bore gages, and other precision measurement tools.</li><li>Read and interpret blueprints, technical drawings, and GD&amp;T requirements.</li><li>Verify manufactured parts meet dimensional and tolerance specifications.</li><li>Review inspection results and accurately document findings.</li><li>Interpret CMM reports when applicable.</li><li>Work with manufacturing and quality teams to address nonconformances and improve inspection processes.</li></ul>Qualifications:<ul><li>3+ years of quality inspection experience in a manufacturing environment.</li><li>Strong hands-on experience with precision measurement and inspection equipment.</li><li>Solid understanding of GD&amp;T.</li><li>Ability to read and interpret blueprints and technical drawings.</li><li>Strong attention to detail, problem-solving, and communication skills.</li><li>Experience interpreting CMM reports is a plus.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Loves Park, IL.Pay and BenefitsThe pay range for this position is $27.00 - $37.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Specialist 1st And 2nd Shift

The Quality Specialist II will support product disposition activities while ensuring compliance with established quality systems, cGMP requirements, and regulatory expectations. This role will collaborate with cross-functional teams to review manufacturing and quality documentation, assess product impact, investigate quality issues, and support product release decisions.The ideal candidate will have experience in a regulated biopharmaceutical, pharmaceutical, or biotechnology environment, with a strong skills in batch record review, product disposition, deviation investigations, and quality systems.RequirementsAdvanced degree plus 2 years of experience, or Bachelors degree plus 3 years of experience in Quality Assurance, Quality Control, Manufacturing, or a related function within a regulated biopharmaceutical, pharmaceutical, or biotechnology environment.Preferred fields of study include Life Sciences, Biology, Microbiology, Biochemistry, Chemistry, Engineering, or a related technical discipline.Strong knowledge of cGMP regulations, regulatory expectations, and industry guidance applicable to biologics and pharmaceutical manufacturing.Experience performing batch record review and approval, product disposition, and assessment of manufacturing documentation for commercial and clinical products.Working knowledge of deviation investigations, CAPA management, change control systems, and risk assessment methodologies.Ability to evaluate product impact and make disposition decisions based on manufacturing, testing, validation, and quality system data.Experience reviewing and interpreting analytical testing results, environmental monitoring data, process monitoring data, validation reports, and quality documentation to support product release decisions.Knowledge of manufacturing processes, aseptic operations, upstream and downstream processing, and/or fill-finish operations preferred.Experience with electronic quality and enterprise systems such as TrackWise, Veeva, SAP, LIMS, document management systems, and electronic batch record platforms.Strong technical writing and documentation review skills with the ability to clearly document quality decisions and rationale.Excellent attention to detail with the ability to identify discrepancies, compliance risks, and potential product quality impacts.Strong problem-solving, critical-thinking, and risk-based decision-making skills.Ability to effectively communicate quality requirements and disposition decisions to cross-functional stakeholders, including Manufacturing, MSAT, QC, Supply Chain, Validation, and Regulatory Affairs.Strong organizational skills with the ability to manage multiple disposition activities and competing priorities in a fast-paced manufacturing environment.Ability to work independently while exercising sound judgment within established quality systems and procedures.Working knowledge of statistical concepts, trending tools, and quality metrics preferred.Experience supporting regulatory inspections and customer audits preferred.Demonstrated experience making GMP product disposition decisions, including evaluation of batch record exceptions, deviations, change controls, laboratory results, process monitoring data, product impact assessments, and completion of all required release documentation prior to disposition.Job Type &amp; LocationThis is a Contract position based out of Plainville, MA.Pay and BenefitsThe pay range for this position is $45.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Specialist II

Job DescriptionWe are seeking a Quality Specialist II to support product disposition and ensure compliance with cGMP regulations, quality systems, and regulatory requirements within a biotech/pharmaceutical manufacturing environment.Key Responsibilities<ul><li>Perform batch record review and product disposition for clinical and commercial products</li><li>Review manufacturing, testing, validation, and quality documentation to support product release</li><li>Investigate deviations, support CAPAs, change controls, and risk assessments</li><li>Evaluate product impact using analytical, environmental monitoring, process, and validation data</li><li>Partner with Manufacturing, QC, MSAT, Validation, Supply Chain, and Regulatory teams</li><li>Support audits, inspections, and continuous improvement initiatives</li></ul>Qualifications<ul><li>Advanced degree with 2+ years, or Bachelor's degree with 3+ years of experience in QA, QC, Manufacturing, or a related GMP-regulated biotech/pharmaceutical environment</li><li>Degree in Life Sciences, Biology, Microbiology, Biochemistry, Chemistry, Engineering, or related field</li><li>Strong knowledge of cGMPs, batch record review, product disposition, deviations, CAPAs, change controls, and risk assessments</li><li>Experience reviewing analytical, validation, environmental monitoring, and process data to support release decisions</li><li>Familiarity with aseptic manufacturing, upstream/downstream processing, or fill-finish operations preferred</li><li>Experience with TrackWise, Veeva, SAP, LIMS, electronic batch records, and document management systems preferred</li><li>Strong technical writing, problem-solving, communication, and organizational skills</li></ul>Job Type &amp; LocationThis is a Contract position based out of Plainville, MA.Pay and BenefitsThe pay range for this position is $45.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality SupervisorJob DescriptionThe Quality Supervisor is a hands-on leader responsible for maintaining product safety, upholding high standards, and optimizing team performance. Reporting to the Quality Manager, this role involves supervising and coaching technicians, driving daily performance, and ensuring compliance with food safety and quality standards. The supervisor plays a key role in strengthening Good Manufacturing Practices (GMPs) and fostering a culture of continuous improvement.Responsibilities<ul><li>Ensure accountability for quality and food safety practices during operations.</li><li>Maintain holds and develop corrective actions (CAPA) using root cause analysis and monitor their effectiveness.</li><li>Manage the quality and sanitation team by scheduling, approving timecards, assigning tasks, and providing ongoing training and mentoring.</li><li>Work with production to monitor processes and procedures for effectiveness and continuous improvement.</li><li>Initiate, track, and trend NCRs/CAPAs.</li><li>Participate actively in scheduled food safety and facility GMP audits as part of the internal audit team.</li><li>Coordinate pre-op, post-op, and glass/brittle plastic inspections.</li><li>Act as a communication liaison between management and quality staff to support corporate and plant-driven initiatives.</li><li>Maintain the food safety plan and update SOPs as required as part of the food safety team.</li><li>Ensure associates at all levels are trained on quality programs.</li><li>Interact with other supervisors and managers to share best practices.</li><li>Perform and maintain the environmental monitoring program and product testing program.</li></ul>Essential Skills<ul><li>3-5 years of quality experience with a minimum of 1 year in a quality leadership role.</li><li>B.S. Degree in Food Science, Microbiology, Chemistry, or related field preferred.</li><li>Experience with CAPAs and root cause analysis.</li><li>HACCP certification and GFSI audits experience such as FSSC or SQF is a plus.</li><li>PCQI certification preferred.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with new quality software like Redzone is beneficial.</li><li>Strong focus on innovation and team support.</li></ul>Work EnvironmentThe work schedule is mainly Monday to Friday, from 7 am to 4 pm. Flexibility is required for occasional weekends or off-shift work. The role is based in a 24/7 manufacturing facility with free daily lunch provided.Job Type &amp; LocationThis is a Permanent position based out of Oak Park, IL.Pay and BenefitsThe pay range for this position is $85000.00 - $90000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.full standard benefits with PTOJob Type &amp; LocationThis is a Permanent position based out of Oak Park, IL.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Oak Park,IL.About Actalent 

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



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



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



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



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



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

Quality Supervisor

Job Title: Quality SupervisorJob DescriptionThe Quality Supervisor is a hands-on leader responsible for maintaining product safety, upholding high standards, and optimizing team performance. Reporting to the Quality Manager, this role involves supervising and coaching technicians, driving daily performance, and ensuring compliance with food safety and quality standards. The supervisor plays a key role in strengthening Good Manufacturing Practices (GMPs) and fostering a culture of continuous improvement.Responsibilities<ul><li>Ensure accountability for quality and food safety practices during operations.</li><li>Maintain holds and develop corrective actions (CAPA) using root cause analysis and monitor their effectiveness.</li><li>Manage the quality and sanitation team by scheduling, approving timecards, assigning tasks, and providing ongoing training and mentoring.</li><li>Work with production to monitor processes and procedures for effectiveness and continuous improvement.</li><li>Initiate, track, and trend NCRs/CAPAs.</li><li>Participate actively in scheduled food safety and facility GMP audits as part of the internal audit team.</li><li>Coordinate pre-op, post-op, and glass/brittle plastic inspections.</li><li>Act as a communication liaison between management and quality staff to support corporate and plant-driven initiatives.</li><li>Maintain the food safety plan and update SOPs as required as part of the food safety team.</li><li>Ensure associates at all levels are trained on quality programs.</li><li>Interact with other supervisors and managers to share best practices.</li><li>Perform and maintain the environmental monitoring program and product testing program.</li></ul>Essential Skills<ul><li>3-5 years of quality experience with a minimum of 1 year in a quality leadership role.</li><li>B.S. Degree in Food Science, Microbiology, Chemistry, or related field preferred.</li><li>Experience with CAPAs and root cause analysis.</li><li>HACCP certification and GFSI audits experience such as FSSC or SQF is a plus.</li><li>PCQI certification preferred.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with new quality software like Redzone is beneficial.</li><li>Strong focus on innovation and team support.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Forest Park, IL.Pay and BenefitsThe pay range for this position is $85000.00 - $90000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.full standard benefits with PTOJob Type &amp; LocationThis is a Permanent position based out of Forest Park, IL.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Forest Park,IL.About Actalent 

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



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



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



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



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



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

Job Title: Quality SupervisorJob DescriptionThe Quality Supervisor is a hands-on leader responsible for maintaining product safety, upholding high standards, and optimizing team performance. Reporting to the Quality Manager, this role involves supervising and coaching technicians, driving daily performance, and ensuring compliance with food safety and quality standards. The supervisor plays a key role in strengthening Good Manufacturing Practices (GMPs) and fostering a culture of continuous improvement.Responsibilities<ul><li>Ensure accountability for quality and food safety practices during operations.</li><li>Maintain holds and develop corrective actions (CAPA) using root cause analysis and monitor their effectiveness.</li><li>Manage the quality and sanitation team by scheduling, approving timecards, assigning tasks, and providing ongoing training and mentoring.</li><li>Work with production to monitor processes and procedures for effectiveness and continuous improvement.</li><li>Initiate, track, and trend NCRs/CAPAs.</li><li>Participate actively in scheduled food safety and facility GMP audits as part of the internal audit team.</li><li>Coordinate pre-op, post-op, and glass/brittle plastic inspections.</li><li>Act as a communication liaison between management and quality staff to support corporate and plant-driven initiatives.</li><li>Maintain the food safety plan and update SOPs as required as part of the food safety team.</li><li>Ensure associates at all levels are trained on quality programs.</li><li>Interact with other supervisors and managers to share best practices.</li><li>Perform and maintain the environmental monitoring program and product testing program.</li></ul>Essential Skills<ul><li>3-5 years of quality experience with a minimum of 1 year in a quality leadership role.</li><li>B.S. Degree in Food Science, Microbiology, Chemistry, or related field preferred.</li><li>Experience with CAPAs and root cause analysis.</li><li>HACCP certification and GFSI audits experience such as FSSC or SQF is a plus.</li><li>PCQI certification preferred.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with new quality software like Redzone is beneficial.</li><li>Strong focus on innovation and team support.</li></ul>Work EnvironmentThe work schedule is mainly Monday to Friday, from 7 am to 4 pm. Flexibility is required for occasional weekends or off-shift work. The role is based in a 24/7 manufacturing facility with free daily lunch provided.Job Type &amp; LocationThis is a Permanent position based out of Elmhurst, IL.Pay and BenefitsThe pay range for this position is $85000.00 - $90000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.full standard benefits with PTOJob Type &amp; LocationThis is a Permanent position based out of Elmhurst, IL.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Elmhurst,IL.About Actalent 

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



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



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



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



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



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

Job Title: Quality SupervisorJob DescriptionThe Quality Supervisor leads quality assurance and food safety activities in a candy packaging facility, ensuring all operations meet regulatory, customer, and internal standards. This role oversees quality programs, drives continuous improvement, and provides hands-on leadership to a team of quality technicians while supporting corporate and plant initiatives.Responsibilities<ul><li>Take accountability for quality and food safety practices during all packaging operations.</li><li>Maintain product holds and develop effective corrective and preventive actions (CAPA) using root cause analysis, and monitor CAPA implementation for effectiveness.</li><li>Schedule and approve timecards in the time and attendance system, assign daily tasks, and provide ongoing training and mentoring to quality staff.</li><li>Monitor quality processes and procedures to ensure effectiveness, compliance, and continuous improvement across the facility.</li><li>Initiate and track nonconformance reports (NCRs) and CAPAs for all deviations from quality or food safety standards.</li><li>Serve as an active member of the internal audit team and participate in scheduled food safety and Good Manufacturing Practices (GMP) facility audits.</li><li>Coordinate and oversee pre-operational, post-operational, and glass/brittle plastic inspections to minimize contamination risks.</li><li>Act as a communication liaison between plant management and quality staff to support corporate and plant-driven quality and food safety initiatives.</li><li>Contribute as part of the food safety team by maintaining the food safety plan and updating standard operating procedures (SOPs) as required.</li><li>Ensure associates at all levels receive training on quality and food safety programs and verify training effectiveness.</li><li>Collaborate with other supervisors and managers to share best practices and drive consistency in quality processes.</li><li>Perform and maintain the environmental monitoring program, including sampling and testing of the production environment.</li><li>Manage the product testing program, including testing for allergens, contaminants, and other critical food safety parameters.</li><li>Trend monthly key performance indicator (KPI) data for the Quality Manager and assist in preparing quality and food safety reports for leadership.</li></ul>Essential Skills<ul><li>Minimum 5 years of experience in food quality or an equivalent food industry quality assurance role.</li><li>Experience testing allergens, contaminants, and other critical food safety parameters.</li><li>Strong knowledge of food safety principles and practices, including HACCP and preventive controls.</li><li>6 months to 1 year of proven leadership experience in a quality or operations environment.</li><li>Demonstrated experience conducting and supporting CAPA investigations, including root cause analysis.</li><li>Hands-on experience with GFSI-based audits and standards.</li><li>Ability to manage and monitor quality processes, NCRs, CAPAs, and KPI trends.</li><li>Strong communication skills to effectively liaise between management and quality staff.</li><li>Ability to train and mentor associates at all levels on quality and food safety programs.</li><li>Proficiency in using time and attendance systems for scheduling and approving timecards.</li><li>Detail-oriented approach with strong organizational and documentation skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree, preferably in food science, quality, microbiology, or a related field.</li><li>HACCP certification.</li><li>PCQI (Preventive Controls Qualified Individual) certification.</li><li>Experience participating in internal food safety and GMP audits.</li><li>Experience coordinating pre-op, post-op, and glass/brittle plastic inspections.</li><li>Experience managing environmental monitoring and product testing programs.</li><li>Experience preparing and presenting quality and food safety reports for leadership.</li><li>Demonstrated ability to drive continuous improvement in quality systems and processes.</li></ul>Work EnvironmentThis role is based in a candy packaging facility where finished candy products are packaged rather than manufactured onsite. The position primarily supports 2nd shift, typically from 3:00 p.m. to 12:00 a.m. The Quality Supervisor oversees approximately seven direct reports on 2nd shift and supports a broader team of about twenty quality technicians across all shifts. The environment follows strict food safety, GMP, and quality standards, including routine inspections, environmental monitoring, and product testing. Team members work closely with production and leadership to maintain a clean, safe, and compliant facility, with appropriate attire and hygiene practices required for food packaging operations.Job Type &amp; LocationThis is a Permanent position based out of Dekalb, IL.Pay and BenefitsThe pay range for this position is $88000.00 - $95000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.strong benefits including PTOJob Type &amp; LocationThis is a Permanent position based out of Dekalb, IL.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Dekalb,IL.About Actalent 

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



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



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



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



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



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

Quality Supervisor 1st ShiftSeeking an experienced Quality Supervisor to lead first-shift quality operations in a food manufacturing setting. This role will oversee quality staff, support food safety programs, investigate quality issues, and ensure products and processes meet established standards.What Youll Do<ul><li>Lead and develop quality team members.</li><li>Monitor food safety, GMP, and quality compliance.</li><li>Manage CAPAs, nonconformances, and root cause investigations.</li><li>Support HACCP, preventive controls, audits, and environmental monitoring.</li><li>Analyze quality trends and drive process improvements.</li><li>Partner with production teams to resolve quality concerns.</li></ul>What Were Looking For<ul><li>5+ years of food quality/QA experience.</li><li>Prior team leadership experience.</li><li>HACCP and food safety experience.</li><li>Knowledge of CAPA and root cause analysis.</li><li>GFSI audit experience preferred.</li><li>PCQI certification preferred.</li><li>Bachelors degree in a related scientific discipline preferred.</li></ul>Work EnvironmentMonday - Friday first shift Job Type &amp; LocationThis is a Permanent position based out of Oak Brook, IL.Pay and BenefitsThe pay range for this position is $88000.00 - $95000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.strong benefits including PTOJob Type &amp; LocationThis is a Permanent position based out of Oak Brook, IL.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Oak Brook,IL.About Actalent 

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



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



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



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



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



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

Quality Supervisor 1st ShiftSeeking an experienced Quality Supervisor to lead first-shift quality operations in a food manufacturing setting. This role will oversee quality staff, support food safety programs, investigate quality issues, and ensure products and processes meet established standards.What Youll Do<ul><li>Lead and develop quality team members.</li><li>Monitor food safety, GMP, and quality compliance.</li><li>Manage CAPAs, nonconformances, and root cause investigations.</li><li>Support HACCP, preventive controls, audits, and environmental monitoring.</li><li>Analyze quality trends and drive process improvements.</li><li>Partner with production teams to resolve quality concerns.</li></ul>What Were Looking For<ul><li>5+ years of food quality/QA experience.</li><li>Prior team leadership experience.</li><li>HACCP and food safety experience.</li><li>Knowledge of CAPA and root cause analysis.</li><li>GFSI audit experience preferred.</li><li>PCQI certification preferred.</li><li>Bachelors degree in a related scientific discipline preferred.</li></ul>Work EnvironmentMonday - Friday first shift Job Type &amp; LocationThis is a Permanent position based out of Chicago, IL.Pay and BenefitsThe pay range for this position is $88000.00 - $95000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.strong benefits including PTOJob Type &amp; LocationThis is a Permanent position based out of Chicago, IL.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Chicago,IL.About Actalent 

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



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



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



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



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



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

Quality Supervisor 2nd ShiftSeeking an experienced Quality Supervisor to lead second-shift quality operations in a food manufacturing setting. This role will oversee quality staff, support food safety programs, investigate quality issues, and ensure products and processes meet established standards.What Youll Do<ul><li>Lead and develop quality team members.</li><li>Monitor food safety, GMP, and quality compliance.</li><li>Manage CAPAs, nonconformances, and root cause investigations.</li><li>Support HACCP, preventive controls, audits, and environmental monitoring.</li><li>Analyze quality trends and drive process improvements.</li><li>Partner with production teams to resolve quality concerns.</li></ul>What Were Looking For<ul><li>5+ years of food quality/QA experience.</li><li>Prior team leadership experience.</li><li>HACCP and food safety experience.</li><li>Knowledge of CAPA and root cause analysis.</li><li>GFSI audit experience preferred.</li><li>PCQI certification preferred.</li><li>Bachelors degree in a related scientific discipline preferred.</li></ul>Work EnvironmentMonday - Friday second shift Job Type &amp; LocationThis is a Permanent position based out of Rochelle, IL.Pay and BenefitsThe pay range for this position is $88000.00 - $95000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.strong benefits including PTOJob Type &amp; LocationThis is a Permanent position based out of Rochelle, IL.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Rochelle,IL.About Actalent 

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



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



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



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



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



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

Job Title: Quality SupervisorJob DescriptionThe Quality Supervisor is a hands-on leader responsible for maintaining product safety, upholding high standards, and optimizing team performance. Reporting to the Quality Manager, this role involves supervising and coaching technicians, driving daily performance, and ensuring compliance with food safety and quality standards. The supervisor plays a key role in strengthening Good Manufacturing Practices (GMPs) and fostering a culture of continuous improvement.Responsibilities<ul><li>Ensure accountability for quality and food safety practices during operations.</li><li>Maintain holds and develop corrective actions (CAPA) using root cause analysis and monitor their effectiveness.</li><li>Manage the quality and sanitation team by scheduling, approving timecards, assigning tasks, and providing ongoing training and mentoring.</li><li>Work with production to monitor processes and procedures for effectiveness and continuous improvement.</li><li>Initiate, track, and trend NCRs/CAPAs.</li><li>Participate actively in scheduled food safety and facility GMP audits as part of the internal audit team.</li><li>Coordinate pre-op, post-op, and glass/brittle plastic inspections.</li><li>Act as a communication liaison between management and quality staff to support corporate and plant-driven initiatives.</li><li>Maintain the food safety plan and update SOPs as required as part of the food safety team.</li><li>Ensure associates at all levels are trained on quality programs.</li><li>Interact with other supervisors and managers to share best practices.</li><li>Perform and maintain the environmental monitoring program and product testing program.</li><li>Trend KPI data for the Quality Manager and assist in preparing reports for senior leadership management.</li></ul>Essential Skills<ul><li>3-5 years of quality experience with a minimum of 1 year in a quality leadership role.</li><li>B.S. Degree in Food Science, Microbiology, Chemistry, or related field preferred.</li><li>Experience with CAPAs and root cause analysis.</li><li>HACCP certification and GFSI audits experience such as FSSC or SQF is a plus.</li><li>PCQI certification preferred.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with new quality software like Redzone is beneficial.</li><li>Strong focus on innovation and team support.</li></ul>Work EnvironmentThe work schedule is mainly Monday to Friday, from 7 am to 4 pm, aligning with the technicians' shifts from 4 am to 4 pm. Flexibility is required for occasional weekends or off-shift work. The role is based in a 24/7 manufacturing facility with free daily lunch provided. The building is older, consisting of five floors without an elevator.Job Type &amp; LocationThis is a Permanent position based out of Forest Park, IL.Pay and BenefitsThe pay range for this position is $85000.00 - $90000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.full standard benefits with PTOJob Type &amp; LocationThis is a Permanent position based out of Forest Park, IL.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Forest Park,IL.About Actalent 

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



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



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



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



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



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

Job Title: Quality Systems Specialist Job DescriptionThe Quality Systems Specialist is responsible for supporting and maintaining the company's Quality Management System (QMS) within a regulated pharmaceutical manufacturing environment. This role involves managing document control activities, authoring and revising Standard Operating Procedures (SOPs), administering employee training records, supporting audits, processing quality events such as CAPAs, deviations, and change controls, and facilitating customer quality agreements. The position requires cross-functional collaboration with Operations, Quality, Regulatory, and leadership teams to drive continuous improvement and ensure quality system compliance.Responsibilities<ul><li>Manage document control activities and maintain the Quality Management System.</li><li>Author and revise Standard Operating Procedures (SOPs).</li><li>Administer and maintain employee training records and training matrices.</li><li>Support internal and external audits.</li><li>Process quality events such as CAPAs, deviations, and change controls.</li><li>Facilitate customer quality agreements and respond to supplier qualification requests.</li><li>Ensure compliance with cGMP, ICH, ISO, and customer requirements.</li><li>Collaborate with cross-functional teams to drive continuous improvement.</li></ul>Essential Skills<ul><li>Bachelor's degree in a scientific discipline.</li><li>3-4 years of Quality Assurance experience in a cGMP, GxP, ISO-regulated manufacturing environment.</li><li>Experience developing, maintaining, and improving quality systems in regulated manufacturing environments.</li><li>Understanding of CAPA, deviations, change controls, complaints, audits, and training systems.</li><li>Experience ensuring procedures and quality systems meet cGMP, ISO, and customer requirements.</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong technical writing skills.</li><li>Ability to investigate quality issues and perform root cause analysis.</li><li>Excellent organizational and follow-up skills.</li><li>Experience with audits and regulatory inspections.</li><li>Strong communication skills and cross-functional collaboration.</li><li>Intermediate Microsoft Office skills.</li><li>Experience with electronic quality systems such as MasterControl preferred.</li><li>Pharmaceutical or life sciences manufacturing experience highly preferred.</li></ul>Work EnvironmentThe work environment includes standard business hours from Monday to Friday, with an onsite office and manufacturing support environment. The role involves close collaboration with Quality, Operations, Manufacturing, Regulatory, and Management teams. It predominantly involves office-based work with extensive use of computer systems and documentation platforms in a fast-paced, regulated life sciences environment with shifting priorities and deadlines. This is a 6-month contract assignment.Job Type &amp; LocationThis is a Contract position based out of Carlsbad, CA.Pay and BenefitsThe pay range for this position is $28.50 - $35.61/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Systems Specialist

Description
					The Quality Systems &amp; Scientific Quality Specialist will serve as a technical quality resource responsible for supporting and improving Quality Management Systems, quality investigations, auditing, employee qualification, and continuous improvement within a highly technical manufacturing environment.

This role requires someone who approaches quality from an analytical and scientific perspective. The individual will evaluate quality data, investigate deviations and failures, identify root causes, assess product and process conformance, and translate findings into controlled procedures, corrective actions, and technical training.

The role is currently structured as an individual contributor position. However, the organization is open to expanding the scope for a candidate with previous Quality Manager or supervisory experience. A strong leadership candidate could potentially oversee approximately 45 Quality Technicians.

Quality Systems
Support development, execution, and continuous improvement of the Quality Management System.
Maintain quality procedures, specifications, SOPs, and controlled documentation.
Ensure quality records are accurate, traceable, and audit-ready.
Evaluate quality-system performance and identify opportunities for improvement.
Maintain alignment with ISO 9001 and applicable customer requirements.
Support additional laboratory-oriented standards such as ISO 17025 when applicable.

Quality Investigations &amp; Root Cause Analysis
Investigate product nonconformances, quality deviations, customer complaints, and returned materials.
Evaluate available quality data to determine potential failure mechanisms.
Perform or facilitate structured root cause investigations.
Develop corrective and preventive actions.
Assess corrective-action effectiveness after implementation.
Partner with technical teams when investigation requires additional product testing or analysis.

Product &amp; Process Quality
Evaluate products and components against specifications and established acceptance criteria.
Support investigation of inconsistencies in product performance, workmanship, or specifications.
Review returned products and support RMA investigations through appropriate quality workflows.
Partner with Quality Technicians to ensure inspection and testing activities are consistently performed.
Identify trends that could indicate systemic quality problems.

Quality Data &amp; Continuous Improvement
Collect, review, and trend quality data.
Analyze:
Nonconformances
Audit findings
Customer returns
Corrective actions
Inspection results
Training and qualification data
Identify recurring trends and potential systemic failure mechanisms.
Translate quality findings into measurable continuous improvement initiatives.
Monitor results to determine whether improvements are scientifically and operationally effective.

Auditing &amp; Compliance
Develop and maintain internal audit schedules.
Conduct QMS and process audits.
Train internal auditors.
Prepare technical documentation for customer and external audits.
Document findings and ensure corrective actions are appropriately addressed.
Analyze audit findings for broader trends rather than treating findings as isolated events.

Technical Training &amp; Qualification
This is not HR/L&amp;D training. Training is directly connected to technical competency and quality.
Develop technical training programs for Quality Technicians and other manufacturing personnel.
Establish competency matrices and qualification requirements.
Translate SOPs and quality procedures into effective hands-on training.
Track certifications, qualifications, and recertification requirements.
Evaluate whether training is producing consistent technical performance.
Update training when investigations, audits, or quality trends indicate a knowledge gap.

Potential Scientific Quality Leadership
For candidates brought in at a manager level:
Lead approximately 45 Quality Technicians.
Provide technical guidance for inspection, QC, and quality investigations.
Review quality findings and determine appropriate escalation.
Develop technicians' technical competencies.
Assign quality priorities and ensure appropriate coverage.
Serve as a technical escalation point between Quality leadership and frontline quality personnel.
										Skills
					qms, quality management system, quality assurance, auditing, root cause, capa, technical training, ISO9001, ISO17025, Metrology, technical leadership
										Top Skills Details
					qms,quality management system,quality assurance,auditing,root cause,capa,technical training
										Additional Skills &amp; Qualifications
					Required
35+ years in:
Quality Assurance
Quality Systems
Quality Control
Laboratory Quality
Technical Compliance
Related scientific/technical quality environment
Strong QMS experience.
ISO 9001 experience.
Quality auditing experience.
Root cause investigation experience.
CAPA / corrective action experience.
Strong documentation and data-integrity practices.
Experience using quality data to make technical decisions.
Experience developing or maintaining SOPs and controlled documentation.
Scientific Backgrounds to Target

Recruiters should strongly consider candidates with backgrounds in:

Chemistry
Biology / Biotechnology
Materials Science
Pharmaceutical Sciences
Laboratory Sciences
Quality Sciences
Applied Sciences

Relevant technical experience may be more important than the exact degree.

Preferred Qualifications
Experience within a large, mature quality organization
Biotechnology
Pharmaceutical manufacturing
Aerospace
Medical device
Semiconductor
Automotive
Advanced materials
Laboratory or analytical testing environments
ISO 17025 experience
Quality Manager or QA Manager experience
Internal Auditor Certification
Lean / Six Sigma training
Previous leadership of QC/QA technicians

A Successful Candidate Will...
Think like a quality scientist, not merely a document-control specialist.
Ask why a failure occurred, not just whether the paperwork was completed.
Be comfortable examining quality data and identifying patterns.
Understand the relationship between product specifications, testing, process controls, and final product performance.
Use root cause analysis and evidence to drive decisions.
Bring technical credibility when working with Quality Technicians.
Build scalable quality systems appropriate for a rapidly growing organization.
Develop technical training that improves actual competency rather than simply checking a compliance box.
Bring practices learned within a larger, established quality organization into a rapidly expanding team.
										Experience Level
					Entry Level
					Job Type &amp; LocationThis is a Contract position based out of Portland, OR.Pay and BenefitsThe pay range for this position is $37.00 - $47.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

<h1>Quality Systems &amp; Quality Specialist</h1><h2>Position Overview</h2>We are seeking a detail-oriented Quality Systems &amp; Quality Specialist to support and continuously improve our Quality Management System (QMS). This role will focus on quality investigations, auditing, technical training, documentation control, and continuous improvement initiatives across the organization.The ideal candidate is a strong analytical problem-solver who enjoys using data, structured investigation techniques, and quality tools to identify root causes, strengthen systems, improve compliance, and drive product and process quality.<h2>Key Responsibilities</h2><ul><li>Maintain, support, and continuously improve Quality Management System (QMS) processes.</li><li>Lead and support quality investigations, nonconformance reviews, and root cause analyses.Quality Management System</li><li>Analyze customer complaints, product returns, deviations, and quality trends to identify improvement opportunities.</li><li>Coordinate and support Corrective and Preventive Actions (CAPA).</li><li>Plan and conduct internal quality audits.</li><li>Support external, customer, and regulatory audits.</li><li>Develop, revise, and maintain SOPs, work instructions, forms, and controlled documentation.</li><li>Create and deliver competency-based training programs for technical personnel.</li><li>Monitor and analyze quality metrics, KPIs, and performance trends.</li><li>Support product and process quality improvement initiatives.</li><li>Collaborate with cross-functional teams to resolve recurring quality issues and implement sustainable solutions.</li><li>Support ISO compliance efforts and maintain audit readiness.</li></ul><h2>Required Qualifications</h2><ul><li>3+ years of experience in Quality Assurance, Quality Control, Quality Systems, Laboratory Quality, or a related field.</li><li>Working knowledge of Quality Management Systems (QMS).</li><li>Experience supporting ISO-compliant quality systems.</li><li>Experience conducting investigations, root cause analysis, and problem-solving activities.</li><li>Internal auditing experience.</li><li>Strong technical writing and documentation skills.</li><li>Excellent analytical, organizational, and communication skills.</li><li>Ability to manage multiple priorities in a fast-paced environment.</li></ul><h2>Preferred Qualifications</h2><ul><li>Experience in biotechnology, pharmaceuticals, medical devices, aerospace, semiconductor manufacturing, automotive, laboratory environments, or advanced materials.</li><li>Experience with ISO 9001 and/or ISO 17025 standards.</li><li>CAPA program experience.</li><li>Lean Manufacturing and/or Six Sigma training or certification.</li><li>Previous leadership, supervisory, or Quality Manager experience.</li><li>Experience developing and delivering technical training programs.</li><li>ASQ certifications such as Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or Certified Quality Improvement Associate (CQIA) preferred.</li></ul>This position offers an opportunity to play a key role in strengthening quality systems, driving continuous improvement, and supporting operational excellence within a growing organization.Job Type &amp; LocationThis is a Contract position based out of Portland, OR.Pay and BenefitsThe pay range for this position is $37.00 - $47.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

We are seeking a technical quality professional to support Quality Management Systems, investigations, auditing, technical training, and continuous improvement within a rapidly growing organization.This role is ideal for someone who enjoys applying an analytical approach to quality, using data and structured investigation techniques to understand failures, identify root causes, strengthen quality systems, and improve product consistency.<h3></h3><h3>Responsibilities</h3><ul><li>Maintain and continuously improve QMS processes.</li><li>Lead or support quality investigations and root cause analysis.</li><li>Analyze nonconformances, customer returns, and quality trends.</li><li>Support corrective and preventive actions.</li><li>Conduct internal quality audits.</li><li>Support external and customer audits.</li><li>Develop SOPs, work instructions, and controlled technical documentation.</li><li>Develop competency-based training for technical personnel.</li><li>Analyze quality metrics and identify opportunities for continuous improvement.</li><li>Support product and process quality investigations.</li><li>Partner across technical teams to resolve recurring quality concerns.</li><li>Support ISO compliance and audit readiness.</li></ul><h3>Essential Qualifications</h3><ul><li>35+ years of QA, QC, Quality Systems, Laboratory Quality, or related experience.</li><li>Strong QMS knowledge.</li><li>ISO quality-system experience.</li><li>Experience with quality investigations and root cause analysis.</li><li>Internal auditing experience.</li><li>Strong technical documentation skills.</li><li>Demonstrated analytical and problem-solving ability.</li></ul><h3>Preferred Qualifications</h3><ul><li>Biotechnology, pharmaceutical, medical device, aerospace, semiconductor, automotive, laboratory, or advanced materials experience.</li><li>ISO 9001 and ISO 17025 experience.</li><li>CAPA experience.</li><li>Lean or Six Sigma experience.</li><li>Previous leadership or Quality Manager experience.</li><li>Experience training and developing technical quality personnel.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Portland, OR.Pay and BenefitsThe pay range for this position is $37.00 - $47.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality Systems Specialist III- *Hybrid, onsite in Parsippany, NJ OR Foster City, CA*Job DescriptionThe Quality Systems Specialist III serves as the Quality Site Lead for assigned contract organizations, providing risk-based quality oversight across development, technology transfer, validation, launch, and commercial supply. This role implements external quality plans, monitors compliance with regulatory and internal standards, and ensures robust quality governance for outsourced manufacturing and testing activities. The position works cross-functionally with internal and external partners to maintain product quality, regulatory compliance, and continuity of supply in a dynamic, GMP-regulated environment.Responsibilities<ul><li>Serve as the Quality Site Lead for assigned external manufacturing and testing organizations, with guidance from senior quality leadership.</li><li>Provide routine, risk-based quality oversight across development, technology transfer, validation, launch, and commercial supply activities.</li><li>Implement the external quality plan for assigned sites in alignment with product, network, regulatory, and supply objectives.</li><li>Monitor contract organizations compliance with internal standards, regulatory requirements, and Quality Agreements, and escalate significant gaps in a timely manner.</li><li>Represent Quality on Product Quality Teams and cross-functional CMC, development, commercialization, supply, and governance teams.</li><li>Build and maintain productive working relationships with external Quality counterparts, ensuring clear communication, governance, and accountability.</li><li>Participate in quality governance forums and business reviews, using metrics, trends, audit outcomes, and operational performance data to identify and drive corrective actions.</li><li>Coordinate the development, implementation, and maintenance of Quality Agreements covering manufacturing, testing, disposition, change control, investigations, validation, data governance, communication, and regulatory support.</li><li>Oversee timely management and closure of deviations, investigations, CAPAs, change controls, complaints, validation activities, and other quality events at assigned sites.</li><li>Support batch record review, release, and disposition activities, and facilitate resolution of issues that may affect product quality, patient safety, regulatory compliance, or supply continuity.</li><li>Track the performance of contract organizations using defined metrics and coordinate remediation or capability-building actions when expectations are not met.</li><li>Partner with Manufacturing, Supply Chain, Development, Quality Control, Regulatory CMC, Auditing, and Quality Systems teams to implement quality and regulatory requirements and support the production plan.</li><li>Support quality issue escalations and risk assessments involving potential product impact, batch disposition decisions, regulatory reporting, or continuity of supply.</li><li>Apply Quality Risk Management principles to identify, document, mitigate, and escalate compliance, product, and supply risks associated with external operations.</li><li>Maintain inspection readiness, including PAI/PLI readiness, for assigned sites and support regulatory inspections, responses, commitments, and remediation activities.</li><li>Review audit and inspection findings, monitor CAPA completion and effectiveness, and support the generation and maintenance of compliant GMP documentation.</li><li>Stay current with relevant regulatory expectations and industry standards and help translate changes into site oversight practices and quality system improvements.</li><li>Contribute to continuous improvement of external quality systems, governance structures, metrics, processes, and training related to outsourced operations.</li><li>Provide work direction, coaching, and project leadership to Quality professionals as needed, without direct people-management responsibility.</li><li>Review records and documents, including change controls and deviations, ensuring accuracy, completeness, and compliance with GMP requirements.</li><li>Support multiple clinical contract manufacturing organizations, including those based in China, with a focus on manufacturing-related quality oversight.</li><li>Leverage expertise in biologics, parenterals, aseptic operations, or drug product filling to provide effective oversight of relevant manufacturing processes.</li><li>Demonstrate flexibility in managing changing priorities with a strong sense of urgency, particularly in support of clinical and commercial supply needs.</li></ul>Essential Skills<ul><li>5+ years of relevant experience and a bachelors degree in science or a related field, or 4+ years of relevant experience and an advanced science or business degree.</li><li>Relevant experience in Quality Assurance, Quality Control, manufacturing, validation, or another GMP-regulated function within the biopharmaceutical or pharmaceutical industry.</li><li>Working knowledge of GMP manufacturing processes, including testing, packaging, labeling, validation, product lifecycle management, batch documentation, or outsourced operations.</li><li>Demonstrated ability to provide quality oversight of contract manufacturing or testing organizations, or strong readiness to do so.</li><li>Experience with key quality system elements such as validation, shop-floor quality support, batch record review, deviation management, CAPA management, and inspection readiness.</li><li>Working experience in parenteral, aseptic, and/or biologics operations, particularly in a manufacturing or quality oversight capacity.</li><li>Ability to review and assess change controls and deviations, with the capability to author such documentation when required.</li><li>Strong understanding and practical application of Quality Risk Management principles in a GMP environment.</li><li>Proficiency in interpreting and applying regulatory requirements and internal quality standards to external operations.</li><li>Ability to analyze metrics, trends, and audit outcomes and translate them into meaningful quality and performance improvements.</li><li>Strong communication skills to effectively collaborate with internal stakeholders and external quality counterparts.</li><li>Demonstrated ability to manage multiple priorities and adapt to changing demands with a sense of urgency.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree in a scientific or business discipline is preferred when combined with relevant industry experience.</li><li>Experience supporting contract manufacturing or testing operations is preferred, particularly for clinical or commercial supply.</li><li>Exposure to validation activities, including process validation, cleaning validation, or equipment qualification, within GMP environments.</li><li>Experience in shop-floor quality support, including real-time decision-making and issue resolution in manufacturing areas.</li><li>Background in inspection readiness activities, including preparation for regulatory inspections and support during and after inspections.</li><li>Experience with biologics, parenteral products, aseptic processing, and drug product filling operations.</li><li>Ability to provide coaching, guidance, or project leadership to other Quality professionals without direct line management responsibilities.</li><li>Comfort working with global contract manufacturing organizations, including those located in China, and navigating cross-cultural collaboration.</li><li>Strong organizational skills and attention to detail in reviewing records, documents, and quality system data.</li><li>Capability to work effectively in cross-functional CMC, development, commercialization, and supply teams.</li></ul>Work EnvironmentThis hybrid role is based in either South San Francisco, CA or Parsippany, NJ, combining on-site work with remote flexibility as business needs require. The position operates within a GMP-regulated biopharmaceutical environment focused on manufacturing-related activities and oversight of multiple clinical contract manufacturing organizations, including sites in China. The work involves frequent interaction with cross-functional teams and external partners, extensive review of GMP records and documentation, and participation in quality governance forums and business reviews. The environment emphasizes inspection readiness, data integrity, and adherence to established quality systems and regulatory expectations, while requiring adaptability to changing priorities and timelines.Job Type &amp; LocationThis is a Contract position based out of Parsippany-Troy Hills, NJ.Pay and BenefitsThe pay range for this position is $58.00 - $65.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Systems Specialist III

Job Title: Quality Systems Specialist III- *Hybrid, onsite in Parsippany, NJ OR Foster City, CA*Job DescriptionThe Quality Systems Specialist III serves as the Quality Site Lead for assigned contract organizations, providing risk-based quality oversight across development, technology transfer, validation, launch, and commercial supply. This role implements external quality plans, monitors compliance with regulatory and internal standards, and ensures robust quality governance for outsourced manufacturing and testing activities. The position works cross-functionally with internal and external partners to maintain product quality, regulatory compliance, and continuity of supply in a dynamic, GMP-regulated environment.Responsibilities<ul><li>Serve as the Quality Site Lead for assigned external manufacturing and testing organizations, with guidance from senior quality leadership.</li><li>Provide routine, risk-based quality oversight across development, technology transfer, validation, launch, and commercial supply activities.</li><li>Implement the external quality plan for assigned sites in alignment with product, network, regulatory, and supply objectives.</li><li>Monitor contract organizations compliance with internal standards, regulatory requirements, and Quality Agreements, and escalate significant gaps in a timely manner.</li><li>Represent Quality on Product Quality Teams and cross-functional CMC, development, commercialization, supply, and governance teams.</li><li>Build and maintain productive working relationships with external Quality counterparts, ensuring clear communication, governance, and accountability.</li><li>Participate in quality governance forums and business reviews, using metrics, trends, audit outcomes, and operational performance data to identify and drive corrective actions.</li><li>Coordinate the development, implementation, and maintenance of Quality Agreements covering manufacturing, testing, disposition, change control, investigations, validation, data governance, communication, and regulatory support.</li><li>Oversee timely management and closure of deviations, investigations, CAPAs, change controls, complaints, validation activities, and other quality events at assigned sites.</li><li>Support batch record review, release, and disposition activities, and facilitate resolution of issues that may affect product quality, patient safety, regulatory compliance, or supply continuity.</li><li>Track the performance of contract organizations using defined metrics and coordinate remediation or capability-building actions when expectations are not met.</li><li>Partner with Manufacturing, Supply Chain, Development, Quality Control, Regulatory CMC, Auditing, and Quality Systems teams to implement quality and regulatory requirements and support the production plan.</li><li>Support quality issue escalations and risk assessments involving potential product impact, batch disposition decisions, regulatory reporting, or continuity of supply.</li><li>Apply Quality Risk Management principles to identify, document, mitigate, and escalate compliance, product, and supply risks associated with external operations.</li><li>Maintain inspection readiness, including PAI/PLI readiness, for assigned sites and support regulatory inspections, responses, commitments, and remediation activities.</li><li>Review audit and inspection findings, monitor CAPA completion and effectiveness, and support the generation and maintenance of compliant GMP documentation.</li><li>Stay current with relevant regulatory expectations and industry standards and help translate changes into site oversight practices and quality system improvements.</li><li>Contribute to continuous improvement of external quality systems, governance structures, metrics, processes, and training related to outsourced operations.</li><li>Provide work direction, coaching, and project leadership to Quality professionals as needed, without direct people-management responsibility.</li><li>Review records and documents, including change controls and deviations, ensuring accuracy, completeness, and compliance with GMP requirements.</li><li>Support multiple clinical contract manufacturing organizations, including those based in China, with a focus on manufacturing-related quality oversight.</li><li>Leverage expertise in biologics, parenterals, aseptic operations, or drug product filling to provide effective oversight of relevant manufacturing processes.</li><li>Demonstrate flexibility in managing changing priorities with a strong sense of urgency, particularly in support of clinical and commercial supply needs.</li></ul>Essential Skills<ul><li>5+ years of relevant experience and a bachelors degree in science or a related field, or 4+ years of relevant experience and an advanced science or business degree.</li><li>Relevant experience in Quality Assurance, Quality Control, manufacturing, validation, or another GMP-regulated function within the biopharmaceutical or pharmaceutical industry.</li><li>Working knowledge of GMP manufacturing processes, including testing, packaging, labeling, validation, product lifecycle management, batch documentation, or outsourced operations.</li><li>Demonstrated ability to provide quality oversight of contract manufacturing or testing organizations, or strong readiness to do so.</li><li>Experience with key quality system elements such as validation, shop-floor quality support, batch record review, deviation management, CAPA management, and inspection readiness.</li><li>Working experience in parenteral, aseptic, and/or biologics operations, particularly in a manufacturing or quality oversight capacity.</li><li>Ability to review and assess change controls and deviations, with the capability to author such documentation when required.</li><li>Strong understanding and practical application of Quality Risk Management principles in a GMP environment.</li><li>Proficiency in interpreting and applying regulatory requirements and internal quality standards to external operations.</li><li>Ability to analyze metrics, trends, and audit outcomes and translate them into meaningful quality and performance improvements.</li><li>Strong communication skills to effectively collaborate with internal stakeholders and external quality counterparts.</li><li>Demonstrated ability to manage multiple priorities and adapt to changing demands with a sense of urgency.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree in a scientific or business discipline is preferred when combined with relevant industry experience.</li><li>Experience supporting contract manufacturing or testing operations is preferred, particularly for clinical or commercial supply.</li><li>Exposure to validation activities, including process validation, cleaning validation, or equipment qualification, within GMP environments.</li><li>Experience in shop-floor quality support, including real-time decision-making and issue resolution in manufacturing areas.</li><li>Background in inspection readiness activities, including preparation for regulatory inspections and support during and after inspections.</li><li>Experience with biologics, parenteral products, aseptic processing, and drug product filling operations.</li><li>Ability to provide coaching, guidance, or project leadership to other Quality professionals without direct line management responsibilities.</li><li>Comfort working with global contract manufacturing organizations, including those located in China, and navigating cross-cultural collaboration.</li><li>Strong organizational skills and attention to detail in reviewing records, documents, and quality system data.</li><li>Capability to work effectively in cross-functional CMC, development, commercialization, and supply teams.</li></ul>Work EnvironmentThis hybrid role is based in either South San Francisco, CA or Parsippany, NJ, combining on-site work with remote flexibility as business needs require. The position operates within a GMP-regulated biopharmaceutical environment focused on manufacturing-related activities and oversight of multiple clinical contract manufacturing organizations, including sites in China. The work involves frequent interaction with cross-functional teams and external partners, extensive review of GMP records and documentation, and participation in quality governance forums and business reviews. The environment emphasizes inspection readiness, data integrity, and adherence to established quality systems and regulatory expectations, while requiring adaptability to changing priorities and timelines.Job Type &amp; LocationThis is a Contract position based out of Foster City, CA.Pay and BenefitsThe pay range for this position is $58.00 - $65.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality Systems Specialist III- *Hybrid, onsite in Parsippany, NJ OR Foster City, CA*Job DescriptionThe Quality Systems Specialist III serves as the Quality Site Lead for assigned contract organizations, providing risk-based quality oversight across development, technology transfer, validation, launch, and commercial supply. This role implements external quality plans, monitors compliance with regulatory and internal standards, and ensures robust quality governance for outsourced manufacturing and testing activities. The position works cross-functionally with internal and external partners to maintain product quality, regulatory compliance, and continuity of supply in a dynamic, GMP-regulated environment.Responsibilities<ul><li>Serve as the Quality Site Lead for assigned external manufacturing and testing organizations, with guidance from senior quality leadership.</li><li>Provide routine, risk-based quality oversight across development, technology transfer, validation, launch, and commercial supply activities.</li><li>Implement the external quality plan for assigned sites in alignment with product, network, regulatory, and supply objectives.</li><li>Monitor contract organizations compliance with internal standards, regulatory requirements, and Quality Agreements, and escalate significant gaps in a timely manner.</li><li>Represent Quality on Product Quality Teams and cross-functional CMC, development, commercialization, supply, and governance teams.</li><li>Build and maintain productive working relationships with external Quality counterparts, ensuring clear communication, governance, and accountability.</li><li>Participate in quality governance forums and business reviews, using metrics, trends, audit outcomes, and operational performance data to identify and drive corrective actions.</li><li>Coordinate the development, implementation, and maintenance of Quality Agreements covering manufacturing, testing, disposition, change control, investigations, validation, data governance, communication, and regulatory support.</li><li>Oversee timely management and closure of deviations, investigations, CAPAs, change controls, complaints, validation activities, and other quality events at assigned sites.</li><li>Support batch record review, release, and disposition activities, and facilitate resolution of issues that may affect product quality, patient safety, regulatory compliance, or supply continuity.</li><li>Track the performance of contract organizations using defined metrics and coordinate remediation or capability-building actions when expectations are not met.</li><li>Partner with Manufacturing, Supply Chain, Development, Quality Control, Regulatory CMC, Auditing, and Quality Systems teams to implement quality and regulatory requirements and support the production plan.</li><li>Support quality issue escalations and risk assessments involving potential product impact, batch disposition decisions, regulatory reporting, or continuity of supply.</li><li>Apply Quality Risk Management principles to identify, document, mitigate, and escalate compliance, product, and supply risks associated with external operations.</li><li>Maintain inspection readiness, including PAI/PLI readiness, for assigned sites and support regulatory inspections, responses, commitments, and remediation activities.</li><li>Review audit and inspection findings, monitor CAPA completion and effectiveness, and support the generation and maintenance of compliant GMP documentation.</li><li>Stay current with relevant regulatory expectations and industry standards and help translate changes into site oversight practices and quality system improvements.</li><li>Contribute to continuous improvement of external quality systems, governance structures, metrics, processes, and training related to outsourced operations.</li><li>Provide work direction, coaching, and project leadership to Quality professionals as needed, without direct people-management responsibility.</li><li>Review records and documents, including change controls and deviations, ensuring accuracy, completeness, and compliance with GMP requirements.</li><li>Support multiple clinical contract manufacturing organizations, including those based in China, with a focus on manufacturing-related quality oversight.</li><li>Leverage expertise in biologics, parenterals, aseptic operations, or drug product filling to provide effective oversight of relevant manufacturing processes.</li><li>Demonstrate flexibility in managing changing priorities with a strong sense of urgency, particularly in support of clinical and commercial supply needs.</li></ul>Essential Skills<ul><li>5+ years of relevant experience and a bachelors degree in science or a related field, or 4+ years of relevant experience and an advanced science or business degree.</li><li>Relevant experience in Quality Assurance, Quality Control, manufacturing, validation, or another GMP-regulated function within the biopharmaceutical or pharmaceutical industry.</li><li>Working knowledge of GMP manufacturing processes, including testing, packaging, labeling, validation, product lifecycle management, batch documentation, or outsourced operations.</li><li>Demonstrated ability to provide quality oversight of contract manufacturing or testing organizations, or strong readiness to do so.</li><li>Experience with key quality system elements such as validation, shop-floor quality support, batch record review, deviation management, CAPA management, and inspection readiness.</li><li>Working experience in parenteral, aseptic, and/or biologics operations, particularly in a manufacturing or quality oversight capacity.</li><li>Ability to review and assess change controls and deviations, with the capability to author such documentation when required.</li><li>Strong understanding and practical application of Quality Risk Management principles in a GMP environment.</li><li>Proficiency in interpreting and applying regulatory requirements and internal quality standards to external operations.</li><li>Ability to analyze metrics, trends, and audit outcomes and translate them into meaningful quality and performance improvements.</li><li>Strong communication skills to effectively collaborate with internal stakeholders and external quality counterparts.</li><li>Demonstrated ability to manage multiple priorities and adapt to changing demands with a sense of urgency.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree in a scientific or business discipline is preferred when combined with relevant industry experience.</li><li>Experience supporting contract manufacturing or testing operations is preferred, particularly for clinical or commercial supply.</li><li>Exposure to validation activities, including process validation, cleaning validation, or equipment qualification, within GMP environments.</li><li>Experience in shop-floor quality support, including real-time decision-making and issue resolution in manufacturing areas.</li><li>Background in inspection readiness activities, including preparation for regulatory inspections and support during and after inspections.</li><li>Experience with biologics, parenteral products, aseptic processing, and drug product filling operations.</li><li>Ability to provide coaching, guidance, or project leadership to other Quality professionals without direct line management responsibilities.</li><li>Comfort working with global contract manufacturing organizations, including those located in China, and navigating cross-cultural collaboration.</li><li>Strong organizational skills and attention to detail in reviewing records, documents, and quality system data.</li><li>Capability to work effectively in cross-functional CMC, development, commercialization, and supply teams.</li></ul>Work EnvironmentThis hybrid role is based in either South San Francisco, CA or Parsippany, NJ, combining on-site work with remote flexibility as business needs require. The position operates within a GMP-regulated biopharmaceutical environment focused on manufacturing-related activities and oversight of multiple clinical contract manufacturing organizations, including sites in China. The work involves frequent interaction with cross-functional teams and external partners, extensive review of GMP records and documentation, and participation in quality governance forums and business reviews. The environment emphasizes inspection readiness, data integrity, and adherence to established quality systems and regulatory expectations, while requiring adaptability to changing priorities and timelines.Job Type &amp; LocationThis is a Contract position based out of Foster City, CA.Pay and BenefitsThe pay range for this position is $58.00 - $65.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Tech

Job Title: Quality Technical WriterJob DescriptionThis role focuses on supporting quality and microbiology teams by conducting particulate matter investigations related to microbiology deviations and documenting findings through clear, detailed technical reports. The Quality Technical Writer works closely with QC laboratories and quality assurance teams in a contained facility, ensuring investigations, deviations, and corrective actions are accurately recorded and compliant with GMP and FDA expectations.Responsibilities<ul><li>Conduct particulate matter investigations in collaboration with QC laboratories and microbiology teams, focusing on deviations related to microbiology and materials.</li><li>Perform root cause analysis using methodologies such as 5 Whys, Fishbone diagrams, or other structured problem-solving tools to determine the underlying causes of non-conformances and deviations.</li><li>Write clear, detailed CAPA (Corrective and Preventive Action) deviation reports, ensuring all relevant data, analysis, and conclusions are thoroughly documented.</li><li>Assist with corrective action investigations by gathering information, organizing evidence, and documenting findings in a structured and compliant format.</li><li>Obtain information from cross-functional team members and translate technical input into accurate, user-friendly documentation such as manuals, reports, and process descriptions.</li><li>Draft detailed descriptions of processes and procedures related to deviations involving particulate matter and materials, ensuring alignment with quality and regulatory requirements.</li><li>Document non-conformances, out-of-specification (OOS) investigations, and deviation reports in accordance with GMP and internal quality standards.</li><li>Collaborate closely with microbiology, quality assurance, and technical writing teams to ensure consistency, clarity, and completeness of all investigation-related documentation.</li><li>Work interdependently with other departments to gather data, clarify issues, and ensure timely completion of investigations and CAPA documentation.</li><li>Maintain high standards of written communication, ensuring all reports are precise, logically structured, and suitable for internal review and regulatory scrutiny.</li></ul>Essential Skills<ul><li>Strong technical writing skills with proven experience drafting detailed investigation reports, deviation reports, non-conformance reports, and OOS investigations.</li><li>Experience working in a laboratory or GMP environment, with 35 years of industry experience in a scientific or quality-focused setting.</li><li>Hands-on experience with CAPA processes, including documenting corrective and preventive actions for quality investigations.</li><li>Proficiency in root cause analysis techniques such as 5 Whys and Fishbone (Ishikawa) methodologies.</li><li>Knowledge of GMP (Good Manufacturing Practice) principles and their application in pharmaceutical or medical device environments.</li><li>Experience conducting or supporting investigations related to non-conformances, deviations, and OOS results.</li><li>Familiarity with FDA-regulated environments and expectations for documentation and quality investigations.</li><li>Bachelors degree in a scientific discipline or a closely related field.</li><li>Ability to collaborate effectively with laboratory, microbiology, quality assurance, and cross-functional teams to gather and interpret technical information.</li><li>Strong attention to detail and ability to produce accurate, clear, and compliant documentation under timelines driven by quality and regulatory needs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the pharmaceutical industry is preferred, with openness to candidates from medical device environments.</li><li>Prior involvement in CAPA investigations and non-conformance management is highly beneficial.</li><li>Exposure to FDA audits or inspections and familiarity with documentation expectations in such contexts.</li><li>Ability to translate complex scientific or technical concepts into clear written documentation for diverse internal stakeholders.</li><li>Comfort working on multiple open investigations simultaneously while maintaining organization and prioritization.</li><li>Demonstrated ability to work within structured quality systems and follow established procedures and templates.</li><li>Experience collaborating with technical writing teams or investigation teams in a quality or QA department.</li></ul>Work EnvironmentThis is a 612 month contract role with the potential for extension in six-month increments, supported by a high volume of open investigations. The position is based in a contained facility environment and involves close collaboration with the microbiology team within the quality assurance department. The Quality Technical Writer works primarily at a cubicle workstation alongside the quality department and a technical writing team that includes other investigators. The role requires frequent interaction with multiple departments, fostering a collaborative and interdependent work culture focused on quality, compliance, and continuous improvement.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Technical Writer

Job Title: Quality TechnicianJob DescriptionThe Quality Technician will primarily work in the Quality Control Laboratory, supporting the testing and analysis of cGMP-produced viral vectors and cells. This role involves close collaboration with the QC manager and senior QC staff to develop and implement strategic directions within the GMP area. The technician will perform assays, ensuring they are run efficiently five nights a week, and will maintain proper operation, calibration, validation, cleaning, and maintenance of QC lab equipment.Responsibilities<ul><li>Perform QC methods and develop methods under the guidance of senior staff.</li><li>Analyze microbiological environmental monitoring samples.</li><li>Write and revise Standard Operating Procedures (SOPs).</li><li>Maintain and monitor lab equipment.</li><li>Manage materials for QC and production supplies.</li><li>Participate in periodic cleaning of the clean room facility and assist in manufacturing viral vector products.</li><li>Operate within the Quality Management System for manufacturing phase-appropriate material.</li><li>Ensure product samples are properly labeled and documented.</li><li>Evaluate and improve sample management processes.</li><li>Maintain compliance with regulatory requirements for cellular and gene therapy products.</li><li>Complete, review, file, and archive documentation according to SOPs.</li><li>Work under close supervision and within established policies and procedures.</li><li>Collaborate in a diverse team environment and communicate effectively to ensure high productivity.</li><li>Document all activities performed according to established guidelines.</li></ul>Essential Skills<ul><li>Experience in biology, virology, GMP, cGMP, GLP, QC, and clean room environments.</li><li>Strong communication skills and accountability.</li><li>Ability to handle documentation, conduct quality checks, write reports, and manage samples.</li></ul>Additional Skills &amp; Qualifications<ul><li>Preferred experience with aseptic techniques, mammalian cell culture, PCR, and ELISA procedures.</li><li>Understanding of regulatory and documentation constraints in a GMP environment.</li><li>Experience in GMP manufacturing is highly preferred.</li></ul>Work EnvironmentJoin a rapidly growing company that is expanding with two new sites in Columbus, Ohio. The work environment features state-of-the-art clean rooms and equipment. You will work in cross-functional teams during the 1st shift from 9 AM to 5 PM, with flexibility to start between 7:30 AM and 9 AM, Monday through Friday.Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality Technician

Job Title: Quality TechnicianJob DescriptionThe Quality Technician plays a key role in quality assurance and control by performing advanced inspections, audits, and testing on raw materials, components, and finished products. This role validates compliance with internal specifications and external standards, supports root cause analysis and continuous improvement initiatives, and collaborates closely with engineering, production, and supply chain teams to enhance product quality and manufacturing processes.Responsibilities<ul><li>Perform advanced inspections, product and workstation audits, and testing on raw materials, components, and finished products, including capability studies, validations, and root-cause investigations.</li><li>Validate that products and processes comply with internal specifications and relevant external standards.</li><li>Interpret engineering drawings and specifications with a high degree of accuracy, including both dimensional and visual or aesthetic requirements.</li><li>Support root cause investigations using structured problem-solving tools such as 5 Whys, Fishbone diagrams, and DMAIC methodologies.</li><li>Collaborate with design, quality, and process engineering to baseline and drive continuous improvement of products, manufacturing processes, and metrology systems.</li><li>Execute gage repeatability and reproducibility (GRR) studies to ensure measurement systems are reliable and consistent.</li><li>Identify trends in defects and nonconformances, analyze data, and propose data-driven solutions to improve quality and reduce variation.</li><li>Assist in the implementation of Statistical Process Control (SPC) methods to support stable, in-control production operations.</li><li>Support metrology system improvement efforts by providing input into system and gage designs, procedures, and reproducibility enhancements.</li><li>Maintain precise, accurate, and timely records within quality management systems and related documentation platforms.</li><li>Prepare inspection data, test results, and quality evidence to support internal and external audits.</li><li>Participate in design reviews, process validations, and metrology systems analysis to ensure robust quality controls are in place.</li><li>Work closely with quality, production, engineering, and supply chain teams to support program implementation and rollout related to quality and metrology initiatives.</li></ul>Essential Skills<ul><li>At least 5 years of quality experience in a manufacturing environment.</li><li>At least 5 years of experience in quality engineering or inspection roles.</li><li>At least 5 years of experience working with measurement tools.</li><li>Expert-level proficiency in measurement tools such as calipers, gauges, micrometers, and XYZ tables.</li><li>Hands-on experience with inspection, metrology, and auditing activities.</li><li>Strong Experience in root cause analysis using methods such as 5 Whys, Fishbone, and DMAIC.</li><li>Experience with quality documentation and maintaining records in quality management systems.</li><li>Experience in continuous improvement, quality assurance, and technical documentation.</li><li>Strong understanding of lean manufacturing principles.</li><li>Strong understanding of Six Sigma principles and methodologies.</li><li>Exceptional attention to detail and analytical thinking in evaluating data and inspection results.</li><li>Strong communication skills, including the ability to summarize data and findings and present results clearly to diverse audiences.</li><li>Effective communication skills for collaborating with cross-functional teams in production, engineering, and supply chain.</li><li>Familiarity with Microsoft Office tools, including Excel, Word, PowerPoint, and Copilot.</li><li>Familiarity with quality management systems and their associated processes.</li><li>Familiarity with statistical software such as Minitab for data analysis and process improvement.</li></ul>Additional Skills &amp; Qualifications<ul><li>Quality experience specifically in windows and doors manufacturing is highly desirable.</li><li>Demonstrated ability to interpret complex engineering drawings and specifications accurately.</li><li>Experience conducting capability studies, validations, and gage repeatability and reproducibility (GRR) studies.</li><li>Experience implementing or supporting Statistical Process Control (SPC) in manufacturing environments.</li><li>Proven ability to identify defect trends and recommend data-driven corrective and preventive actions.</li><li>Experience preparing inspection data and quality evidence for internal and external audits.</li><li>Comfort working in a team-centric environment with a focus on growth and continuous improvement.</li></ul>Work EnvironmentThis role operates in a new, modern manufacturing facility with a team-centric environment focused on growth and continuous improvement. The Quality Technician works closely with production, engineering, quality, and supply chain teams, using a variety of measurement tools such as calipers, gauges, micrometers, and XYZ tables, as well as software tools including Microsoft Office, Copilot, quality management systems, and statistical software like Minitab. The setting emphasizes collaboration, precision, and adherence to robust quality processes, providing opportunities to contribute to ongoing improvements in products, processes, and metrology systems.Job Type &amp; LocationThis is a Contract to Hire position based out of Cottage Grove, MN.Pay and BenefitsThe pay range for this position is $30.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality TechnicianJob DescriptionThis contract Quality Technician role supports a growing Quality organization by owning the day-to-day health, accuracy, and closure of quality-related tickets and processes. You will manage non-conformances, RMAs, and MRB dispositions, while helping to establish and support a new function focused on field and fleet hardware issues. The position centers on rigorous ticket hygiene, efficient Material Review Board (MRB) operations, and smooth handoff of field quality issues into the existing RMA process as Field Quality capabilities mature.Responsibilities<ul><li>Own the day-to-day triage, cleanup, and closure of tickets in the Quality Jira project, ensuring timely and accurate handling of all quality issues.</li><li>Ensure all required Jira fields are correctly and completely populated to maintain high-quality data integrity across quality records.</li><li>Maintain and clear the backlog across MRB, QA, and RMA Jira dashboards by closing out stale or completed tickets and flagging aging items for disposition.</li><li>Support the Quality Alert intake process through the Slack channel, Enjo bot, and Jira automation, ensuring that new issues enter the system correctly and efficiently.</li><li>Run daily MRB logistics, including preparing the MRB list, identifying MRB stakeholders and subject-matter experts, and driving prioritization of tickets and products for MRB agendas based on technical impact, safety impact, timelines, product demand, and R&amp;D needs.</li><li>Update Jira records and physical or electronic inventory status to reflect MRB dispositions accurately.</li><li>Execute MRB disposition activities by coordinating with manufacturing for rework work orders, scrap orders, and supplier RMA requests, and directing the physical and electronic movement of non-conforming products within inventory.</li><li>Perform ERP transactions for non-conforming material moved to MRB status to ensure accurate inventory and status tracking.</li><li>Support the Field Quality functions handoff into the Manufacturing Quality RMA process by creating and linking RMA tickets with sufficient triage context, including failure mode, severity, and troubleshooting performed, once root-cause and corrective action cannot be completed in the field.</li><li>Transfer ownership of field-originated issues at the point of MRB disposition to ensure a seamless transition into standard quality processes.</li><li>Help maintain the Field Quality Dashboard to provide clear visibility into field and fleet hardware issues and their status.</li><li>Assist with day-to-day field quality issue processing as ticket volume flows into standard Quality Jira, RMA, and MRB handling, partnering with the Field Quality directly responsible individual and Manufacturing Quality stakeholders on closure-loop tracking back to source tickets.</li><li>Participate in weekly MRB standups and vendor or contract manufacturer meetings tied to field-originated issues to drive timely resolutions and continuous improvement.</li></ul>Essential Skills<ul><li>Working proficiency in Jira, including creating and editing tickets, understanding issue linking, and using filters and dashboards across multiple projects.</li><li>Familiarity with MRB, RMA, and non-conformance or NCMR workflows, or a demonstrated willingness to ramp quickly using documented processes.</li><li>Comfort with ERP transaction processing for inventory and MRB status moves.</li><li>Strong attention to detail and commitment to ticket data hygiene, with a focus on cleanup and closure rather than only new-ticket creation.</li><li>Ability to work effectively in a cross-functional environment with Quality Engineers, Hardware Engineering, Manufacturing, Global Supply Management or Inventory, and Supplier Quality Engineering to keep dispositions and closures moving.</li><li>Prior experience as a Quality Technician in a manufacturing or hardware environment.</li><li>Exposure to root-cause and corrective-action processes such as RCCA, SCAR, and 8D or CAPA.</li><li>Willingness to learn and apply evolving Field Quality frameworks and processes as the function matures.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working with non-conformance management, including MRB and RMA processes in a manufacturing or hardware context.</li><li>Familiarity with field quality frameworks and structured approaches for tracking and resolving field-originated issues, or openness to quickly learning such frameworks.</li><li>Strong organizational skills and the ability to manage multiple dashboards, ticket queues, and priorities simultaneously.</li><li>Effective communication skills to collaborate with technical and operations stakeholders and to represent quality issues clearly in meetings and standups.</li><li>Demonstrated ability to adapt to new tools, automations, and workflows as quality processes evolve.</li></ul>Work EnvironmentThis role operates in a technology-driven manufacturing and hardware environment that relies heavily on digital tools and structured processes. You will work extensively with Jira for ticket and workflow management, Slack and automation tools such as the Enjo bot for alert intake and communication, and an ERP system for inventory and MRB-related transactions. The position involves close collaboration with cross-functional teams, including Quality Engineering, Hardware Engineering, Manufacturing, Inventory or Supply Management, and Supplier Quality, as well as participation in weekly MRB standups and vendor or contract manufacturer meetings. Work is primarily focused on managing digital records, dashboards, and process flows, while coordinating closely with manufacturing and inventory teams who handle physical materials and non-conforming products.Job Type &amp; LocationThis is a Contract to Hire position based out of Pittsburgh, PA.Pay and BenefitsThe pay range for this position is $47.00 - $47.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

<h1>Quality Technician / QA Process Quality Inspector</h1>Shift: 2nd shift: 2:00-10:30pm. Will train on 1st shift for roughly 3 months prior to moving to 2nd shift. We're seeking a Quality Technician to join our clients growing Quality team. In this highly visible role, you'll be at the center of manufacturing operations, partnering closely with production teams to ensure products are manufactured safely, consistently, and in compliance with cGMP standards. This is an excellent opportunity for a quality professional who enjoys being hands-on, solving problems in real time, and coaching others on quality best practices. You'll have the chance to build your expertise in investigations, CAPA activities, documentation review, training, and quality systems while working in a collaborative environment where your contributions are recognized and valued.Key Responsibilities<ul><li>Monitor manufacturing operations to ensure compliance with cGMP requirements and internal procedures.</li><li>Conduct routine floor inspections and walkthroughs to verify quality standards are being followed.</li><li>Review production and quality documentation for accuracy, completeness, and compliance.</li><li>Partner with production teams to correct documentation issues and ensure proper record keeping.</li><li>Support investigations involving deviations, incidents, and nonconformances.</li><li>Assist with CAPA development and implementation activities.</li><li>Verify suite cleanliness, line clearances, equipment readiness, and cleaning activities.</li><li>Conduct in-process quality inspections and provide real-time feedback to production teams.</li><li>Support training efforts related to quality procedures, deviations, and compliance requirements.</li><li>Serve as a quality resource to operators, leads, and supervisors throughout production activities.</li><li>Assist with sampling, raw material labeling, and other QA support activities as needed.</li><li>Identify opportunities for process improvements and help drive quality initiatives across the facility.</li></ul>Minimum Qualifications<ul><li>At least 1 year of Quality Assurance, Quality Control, auditing, or quality-related experience in a regulated manufacturing environment.</li><li>1-3+ years of experience in pharmaceutical, biotechnology, dietary supplement, food manufacturing, or other cGMP-regulated industries.</li><li>Previous experience working directly on a manufacturing or production floor.</li><li>Working knowledge of GMP/cGMP regulations and quality systems.</li><li>Experience reviewing and maintaining controlled documentation and manufacturing records.</li><li>Strong communication skills and the ability to work effectively with cross-functional teams.</li><li>Ability to identify issues, provide coaching, and hold teams accountable to quality standards.</li><li>Strong organizational skills and attention to detail.</li><li>High School Diploma or equivalent.</li></ul>Work Environment &amp; Growth OpportunityYou'll join a collaborative QA team of fewer than ten professionals where every team member plays an important role in maintaining product quality and compliance. The position is primarily based on the production floor, providing direct interaction with manufacturing teams and opportunities to influence quality culture every day.Employees enjoy manageable workloads, strong support from leadership, excellent benefits, and a generous PTO program. Most importantly, this role offers a clear pathway for professional growth within Quality Assurance, including opportunities to expand into investigations, quality systems, compliance, and other advanced QA functions.Job Type &amp; LocationThis is a Contract to Hire position based out of Verona, WI.Pay and BenefitsThe pay range for this position is $21.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality TechnicianShift: 6 PM - 6:30 AMOVERNIGHT ROLETucker, GADescriptionThis Quality Technician role supports a quality control laboratory within a manufacturing environment, ensuring that products meet established standards and customer expectations. The position focuses on performing quality tests, maintaining accurate documentation, and supporting production and distribution with timely quality information. The role offers the opportunity to work with experienced team members, develop technical skills in testing and chemistry, and contribute to a stable, long-term career path.Primary Responsibilities<ul><li>Execute and adhere to all EHS requirements as well as maintain a safe work environment and follow internal safety rules and procedures including wearing proper, PPE as appropriate.</li><li>Participates in the general housekeeping of lab area</li><li>Enters and back-up all QA data test results in SAP</li><li>Maintains critical equipment and laboratory inventory supplies to support continuous uninterrupted QA lab support.</li><li>Maintains and manages obsolete (Expired, damaged &amp; returned goods), Off-spec and rejected material storage area for finished products to minimize waste generation.</li><li>Ensures that all customer complaints are checked within 48 hours and reported to management.</li><li>Complies with company policies and procedures.</li><li>Collects time sensitive samples. Retains inventory for raw materials and finished products.</li><li>Provides timely and accurate QA information to production and distribution such as proper documentation, communication of released material, and labeling of pallets that are rejected.</li><li>Completes, maintains, and process all other pertinent paperwork and records.</li><li>Immediately notify all affected personnel of any rejected batch/ lot number prior to release of material.</li><li>Proactive in meeting functions for Quality, Safety, Housekeeping, and waste minimization.</li><li>Communicates all critical issues and problems concerning QA, test equipment problems, schedule changes, and assignments to the facility technical manager.</li><li>A Team player: volunteers to help where needed to get job done and enhance skills.</li><li>Works with some direction and supervision of Sr. Lab Technicians and the facility technical manager</li></ul>Additional Skills &amp; Qualifications<ul><li>At least 1 year of experience working in a manufacturing environment.</li><li>High school diploma or GED.</li><li>Experience in manufacturing, quality control, testing, quality assurance, and quality inspection.</li><li>Ability to complete documentation accurately and correctly.</li><li>Ability to add, subtract, multiply, and divide in all units of measure using whole numbers, common fractions, and decimals.</li><li>Comfort working in a quality control laboratory within a manufacturing setting.</li><li>Ability to use or learn systems such as SAP for entering and backing up QA test results.</li><li>Strong attention to detail and ability to follow established procedures and safety rules.</li><li>Capability to work independently during assigned shifts while maintaining communication with the team.</li><li>Willingness to work a 12-hour night shift on a 2-2-3 schedule.</li></ul>Work EnvironmentThe role is based in a quality control laboratory within an adhesive manufacturing facility. You will work primarily in a lab environment that supports production operations, using testing equipment such as viscometers and other analytical tools to evaluate chemical and adhesive products. The position follows a 12-hour night shift from approximately 6:00 p.m. to 6:30 a.m. on a 2-2-3 schedule, which includes working every other weekend. During these shifts, you will often work independently in the lab while coordinating closely with production, distribution, and technical staff. The company offers a stable and established environment with long-tenured employees, a pleasant and collaborative culture, and opportunities to learn from experienced team members. Proper PPE is required, and adherence to safety procedures and housekeeping standards is expected at all times.Job Type &amp; LocationThis is a Contract to Hire position based out of TUCKER, GA.Pay and BenefitsThe pay range for this position is $18.00 - $20.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of TUCKER, GA.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in TUCKER,GA.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 TechnicianJob DescriptionThe Quality Technician inspects incoming materials and components, programs and operates coordinate measuring machines (CMM), and supports the development and improvement of inspection methodologies within an ISO 9001 quality management system. This role works closely with Engineering to ensure products meet stringent dimensional, cleanliness, and electro-static discharge (ESD) requirements, while accurately documenting inspection results and contributing to continuous improvement of quality standards.Responsibilities<ul><li>Inspect incoming materials and parts from suppliers using visual and mechanical inspection tools, ensuring they meet all specified requirements.</li><li>Review and verify First Article Inspection (FAI) reports from suppliers, confirming compliance with drawings, specifications, and quality standards.</li><li>Program inspection routines on CMM equipment, including setup and execution of measurement programs.</li><li>Work closely with Engineering to develop, refine, and modify inspection methodologies for new and existing products.</li><li>Use conventional and advanced inspection devices and methods to verify dimensions against engineering drawings and specifications.</li><li>Create and maintain standards for inspection processes and author clear, detailed quality inspection reports.</li><li>Record inspection results, measurement data, and related information accurately in accordance with the Quality Management System (QMS).</li><li>Set up and perform inspections on intricate components with tight tolerances, ensuring consistent and repeatable results.</li><li>Interpret blueprints, schematics, sketches, and other design documents to determine inspection criteria and methods.</li><li>Handle and inspect parts in a Class 1,000 (ISO Class 6) cleanroom environment while following all cleanroom protocols.</li><li>Handle electro-static sensitive (ESD) components properly to prevent damage and ensure product integrity.</li><li>Apply and interpret Geometric Dimensioning and Tolerancing (GD&amp;T) on engineering drawings and inspection plans.</li><li>Use MS Office applications, especially Excel, Word, and PowerPoint, to document inspection data and prepare reports.</li><li>Manage and organize inspection data using appropriate software tools for inspection data management.</li><li>Work independently with minimal supervision, prioritizing tasks in a dynamic, fast-paced environment.</li><li>Collaborate effectively with cross-functional teams by communicating inspection findings and quality issues clearly.</li><li>Maintain compliance with ISO 9001 quality systems and internal QMS procedures during all inspection activities.</li></ul>Essential Skills<ul><li>Proficiency in Geometric Dimensioning and Tolerancing (GD&amp;T), including interpretation and application on engineering drawings.</li><li>Experience with CMM inspection utilizing PC-DMIS software.</li><li>Ability to program and run CMM equipment for complex and intricate components with tight tolerances.</li><li>Ability to interpret blueprints, schematics, sketches, and other design documents for inspection purposes.</li><li>Hands-on experience with visual inspection techniques and mechanical measuring tools such as gages and other conventional inspection devices.</li><li>Knowledge and practical understanding of ISO 9001 quality management systems and QMS procedures.</li><li>Ability to handle parts in a Class 1,000 (ISO Class 6) cleanroom environment while following strict protocols.</li><li>Ability to properly handle electro-static sensitive (ESD) components.</li><li>Strong organizational, communication, and analytical skills.</li><li>Ability to work independently with minimal supervision.</li><li>Proficiency with MS Office Suite, especially Excel, Word, and PowerPoint.</li><li>Ability to multitask and prioritize work in a dynamic, fast-paced environment.</li><li>Strong attention to detail and a high degree of accuracy in all inspection tasks.</li><li>Computer skills and familiarity with software tools used for inspection data management.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience using advanced inspection devices and methods in addition to conventional tools.</li><li>Experience editing engineering drawings and designs for GD&amp;T compliance.</li><li>Familiarity with CMM programming software such as PC-DMIS and Calypso.</li><li>Experience with calibration activities related to inspection equipment and gages.</li><li>Experience in quality inspection, quality assurance, and incoming inspections.</li><li>Experience creating inspection standards and authoring formal quality reports.</li><li>Comfort working within an established Quality Management System and contributing to continuous improvement initiatives.</li><li>Interest in ongoing training and skills development, supported by a company that invests in training the right person.</li></ul>Work EnvironmentThis role is primarily based in a Class 1,000 (ISO Class 6) cleanroom environment, where the Quality Technician spends most of the day following all cleanroom protocols. The position involves regular standing, walking, bending, squatting, and kneeling while performing inspections and handling components. The role requires the ability to grasp, lift, and move items weighing up to 50 pounds. Some portion of the day is spent working at a computer to program CMM equipment, manage inspection data, and prepare reports using MS Office and other software tools. The environment is dynamic and fast paced, with a strong focus on precision, cleanliness, and adherence to quality and ESD handling procedures.Job Type &amp; LocationThis is a Permanent position based out of Bedford, MA.Pay and BenefitsThe pay range for this position is $62400.00 - $72800.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

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

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



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



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



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



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



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

Description
					1st Shift - CTH - $20 - 25/hour
- 1-3+ Years as a Quality Technician/Inspection role
- Willing to take on more Entry Level candidates and train
- Experienced w/ Calipers, Micrometers, Gauges
- Computer Skills: Basic Data Input, Emails
- Able to Stand, Walk, Lift (Products from 5-25lbs) for the majority of day

Plus Haves:
- PPAP Experience
- ISO-9001 Experience

Day-to-Day:
Audits of Production Line
- Measurement of production to ensure within compliance
- Walking around majority of day
- Working with Engineering to confirm product issues and assign case
- Send professional emails across teams, inputting measurement data into Excel
										Skills
					Calipers
										Top Skills Details
					Calipers
										Additional Skills &amp; Qualifications
					Quality Technician
	Documenting anything found that doesn't meet our high quality standards and helping contain and action of these issues in a timely manner.
	Helping create or update documentation. 
	Identifying and leading efforts to improve manufacturing processes
	Collaborating with Engineering to test and inspect products 
	Evaluating and processing Production Part Approval Process (PPAP) documentation

Key Qualifications:
	1-2 years of related Quality or Manufacturing experience
	Ability to read and interpret blueprints
	Ability to use standard measurement equipment and tools ie; Micrometers, Gauges, Calipers
	Basic computer skills (e.g. Excel, Word, Outlook)

Physical Requirements:
	Ability to stand, lift, carry, push, bend, twist, kneel, squat for long durations
	Near vision, color discrimination, depth perception
	Tactile discrimination
	Ability to concentrate for extended periods of time in a disruptive workspace
										Experience Level
					Entry Level
					Job Type &amp; LocationThis is a Contract to Hire position based out of Bartlett, IL.Pay and BenefitsThe pay range for this position is $20.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality TechnicianJob DescriptionThe Quality Technician supports mission-critical defense manufacturing by ensuring that all materials, parts, and documentation conform to purchase orders, contracts, and applicable material and military specifications. This role focuses on documentation, certification review, data package preparation, auditing, and compliance rather than hands-on inspection. The position offers an excellent entry point into defense manufacturing quality, providing exposure to Navy and government quality requirements and opportunities for long-term career growth in quality assurance and regulatory compliance.Responsibilities<ul><li>Review supplier software and documentation to verify that incoming materials conform to purchase orders, contracts, and material specifications.</li><li>Perform quality assurance reviews of part orders, ensuring all contract requirements are met and preparing complete and accurate quality data packages.</li><li>Maintain and update the supplier database, ensuring supplier software and documentation for incoming materials are uploaded into Central Apps in a timely manner.</li><li>Maintain, organize, and update Objective Quality Evidence (OQE) records and project documents as required by Naval customer orders.</li><li>Read and interpret customer drawings, contracts, written work instructions, routes, bills of material (BOMs), work sampling plans, and process and material specifications.</li><li>Work with computer-based Enterprise Resource Planning (ERP) systems to manage and track quality-related data and documentation.</li><li>Prepare pump kits and assembly packages prior to assembly and test, ensuring all required components and documentation are complete and accurate.</li><li>Perform internal quality audits at required intervals to verify compliance with internal procedures, customer requirements, and applicable standards.</li><li>Participate in the implementation and utilization of continuous improvement tools (such as CBS tools) to enhance processes, documentation, and overall quality performance.</li><li>Review material documentation such as Mill Test Reports (MTRs), Certificates of Conformance (CoCs), and other quality-related records for completeness and accuracy.</li><li>Ensure material traceability and compliance with Navy and government quality requirements, including OQE and applicable defense regulations.</li><li>Collaborate with cross-functional teams to resolve quality issues, support problem solving, and ensure timely completion of quality-related tasks.</li><li>Apply knowledge of AS9100, ISO 9001, DFARS, military specifications, and Navy requirements when reviewing documentation and quality data packages.</li></ul>Essential Skills<ul><li>Experience with quality and manufacturing documentation, including reviewing and managing MTRs, CoCs, and quality data packages.</li><li>Ability to read and interpret bills of material (BOMs), work orders, drawings, specifications, certificates of conformance, routers, and other production documents.</li><li>Knowledge of material traceability and Objective Quality Evidence (OQE) requirements in a regulated or defense-related environment.</li><li>Familiarity with defense-related quality and contractual requirements, including DFARS and military specifications.</li><li>Understanding of quality management standards such as AS9100 and ISO 9001.</li><li>Proficiency with ERP systems for managing quality and production data; ERP knowledge is required.</li><li>Proficiency in Microsoft Office applications for documentation, reporting, and communication.</li><li>Strong attention to detail with the ability to identify discrepancies in documentation and ensure accuracy and completeness.</li><li>Effective problem-solving skills with the ability to analyze issues and support corrective actions.</li><li>Ability to multitask, prioritize work, and manage time effectively in a documentation-intensive environment.</li><li>Strong organizational skills and the ability to work independently with minimal supervision.</li><li>Excellent communication skills, both written and verbal, with the ability to convey technical and quality-related information clearly.</li><li>Ability to make sound decisions within the scope of quality and compliance responsibilities.</li><li>Demonstrated ability to work collaboratively as a team player, set clear agendas, and follow through on tasks and plans.</li><li>Education: High school student or graduate, or preferably an Associates degree (A.A.) from a two-year college or technical school.</li><li>Experience: One to three years of related experience in quality, manufacturing, or a similar documentation-focused role.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with military contracts and associated documentation requirements.</li><li>Experience with material document review in a manufacturing or defense environment.</li><li>Familiarity with Navy-specific quality requirements and customer documentation expectations.</li><li>Knowledge of CMM (Coordinate Measuring Machine) and NDT (Non-Destructive Testing) processes is a plus.</li><li>Experience with AS9100 and ISO 9001 quality management systems.</li><li>IFS ERP experience is a plus.</li><li>Exposure to low-volume, high-mix manufacturing environments, with emphasis on specialized products and documentation.</li><li>Interest in building a career in quality assurance and government/defense manufacturing compliance.</li><li>Comfort working with complex documentation, including military specifications and Navy requirements.</li></ul>Work EnvironmentThis role operates in a manufacturing environment that supports pumps, valves, and fluid-control equipment used on naval vessels and submarines. The position is primarily documentation-focused and does not involve physically touching or inspecting product. Work centers around computer-based systems, including ERP platforms and digital documentation tools, in a low-volume, high-mix production setting where products are specialized and documentation requirements are detailed and rigorous. The environment emphasizes adherence to Navy and government quality requirements, including DFARS, military specifications, OQE, and material traceability. Team members collaborate closely with engineering, production, and quality functions while working independently on documentation, audits, and compliance activities. The culture supports continuous improvement and offers opportunities to grow expertise in quality assurance and defense manufacturing compliance.Job Type &amp; LocationThis is a Contract to Hire position based out of Warren, MA.Pay and BenefitsThe pay range for this position is $32.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality TechnicianJob DescriptionThe Quality Technician plays a key role in quality assurance and control by performing advanced inspections, audits, and testing on raw materials, components, and finished products. This role validates compliance with internal specifications and external standards, supports root cause analysis and continuous improvement initiatives, and collaborates closely with engineering, production, and supply chain teams to enhance product quality and manufacturing processes.Responsibilities<ul><li>Perform advanced inspections, product and workstation audits, and testing on raw materials, components, and finished products, including capability studies, validations, and root-cause investigations.</li><li>Validate that products and processes comply with internal specifications and relevant external standards.</li><li>Interpret engineering drawings and specifications with a high degree of accuracy, including both dimensional and visual or aesthetic requirements.</li><li>Support root cause investigations using structured problem-solving tools such as 5 Whys, Fishbone diagrams, and DMAIC methodologies.</li><li>Collaborate with design, quality, and process engineering to baseline and drive continuous improvement of products, manufacturing processes, and metrology systems.</li><li>Execute gage repeatability and reproducibility (GRR) studies to ensure measurement systems are reliable and consistent.</li><li>Identify trends in defects and nonconformances, analyze data, and propose data-driven solutions to improve quality and reduce variation.</li><li>Assist in the implementation of Statistical Process Control (SPC) methods to support stable, in-control production operations.</li><li>Support metrology system improvement efforts by providing input into system and gage designs, procedures, and reproducibility enhancements.</li><li>Maintain precise, accurate, and timely records within quality management systems and related documentation platforms.</li><li>Prepare inspection data, test results, and quality evidence to support internal and external audits.</li><li>Participate in design reviews, process validations, and metrology systems analysis to ensure robust quality controls are in place.</li><li>Work closely with quality, production, engineering, and supply chain teams to support program implementation and rollout related to quality and metrology initiatives.</li></ul>Essential Skills<ul><li>At least 5 years of quality experience in a manufacturing environment.</li><li>At least 5 years of experience in quality engineering or inspection roles.</li><li>At least 5 years of experience working with measurement tools.</li><li>Expert-level proficiency in measurement tools such as calipers, gauges, micrometers, and XYZ tables.</li><li>Hands-on experience with inspection, metrology, and auditing activities.</li><li>Strong Experience in root cause analysis using methods such as 5 Whys, Fishbone, and DMAIC.</li><li>Experience with quality documentation and maintaining records in quality management systems.</li><li>Experience in continuous improvement, quality assurance, and technical documentation.</li><li>Strong understanding of lean manufacturing principles.</li><li>Strong understanding of Six Sigma principles and methodologies.</li><li>Exceptional attention to detail and analytical thinking in evaluating data and inspection results.</li><li>Strong communication skills, including the ability to summarize data and findings and present results clearly to diverse audiences.</li><li>Effective communication skills for collaborating with cross-functional teams in production, engineering, and supply chain.</li><li>Familiarity with Microsoft Office tools, including Excel, Word, PowerPoint, and Copilot.</li><li>Familiarity with quality management systems and their associated processes.</li><li>Familiarity with statistical software such as Minitab for data analysis and process improvement.</li></ul>Additional Skills &amp; Qualifications<ul><li>Quality experience specifically in windows and doors manufacturing is highly desirable.</li><li>Demonstrated ability to interpret complex engineering drawings and specifications accurately.</li><li>Experience conducting capability studies, validations, and gage repeatability and reproducibility (GRR) studies.</li><li>Experience implementing or supporting Statistical Process Control (SPC) in manufacturing environments.</li><li>Proven ability to identify defect trends and recommend data-driven corrective and preventive actions.</li><li>Experience preparing inspection data and quality evidence for internal and external audits.</li><li>Comfort working in a team-centric environment with a focus on growth and continuous improvement.</li></ul>Work EnvironmentThis role operates in a new, modern manufacturing facility with a team-centric environment focused on growth and continuous improvement. The Quality Technician works closely with production, engineering, quality, and supply chain teams, using a variety of measurement tools such as calipers, gauges, micrometers, and XYZ tables, as well as software tools including Microsoft Office, Copilot, quality management systems, and statistical software like Minitab. The setting emphasizes collaboration, precision, and adherence to robust quality processes, providing opportunities to contribute to ongoing improvements in products, processes, and metrology systems.Job Type &amp; LocationThis is a Contract to Hire position based out of Cottage Grove, MN.Pay and BenefitsThe pay range for this position is $30.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Quality TechnicianOffers Benefits | 1st Shift | Monday - FridayJob DescriptionThe Quality Technician is responsible for ensuring products and processes meet established quality standards through testing, inspection, and data collection. This role partners closely with Manufacturing, Engineering, Product Development, and Operations to identify issues, drive compliance, and support continuous improvement efforts.Responsibilities<ul><li>Conduct sampling, testing, and inspections of raw materials, work-in-process, and finished products.</li><li>Perform physical measurements using precision testing and inspection equipment.</li><li>Verify product quality through visual inspections and compliance checks.</li><li>Investigate, document, and communicate quality concerns and non-conforming products.</li><li>Conduct raw material testing and product retesting as needed.</li><li>Troubleshoot quality-related equipment and testing issues.</li><li>Maintain accurate quality records, test results, and calibration documentation.</li><li>Perform equipment calibrations and support gauge management programs.</li></ul>Additional Skills &amp; Qualifications:<ul><li>Experience in inspection, quality check, quality control, and quality assurance.</li><li>High School Diploma required.</li><li>2+ years of manufacturing and/or quality experience in an industrial environment.</li></ul>Work EnvironmentThe work schedule is Monday to Friday, 7 AM to 3:30 PM. The role is within a production, manufacturing environment.Job Type &amp; LocationThis is a Contract to Hire position based out of Rockford, MN.Pay and BenefitsThe pay range for this position is $20.00 - $26.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality TechnicianJob DescriptionThe Quality Technician programs and edits CMM programs, performs precise measurements, and supports the inspection process across new product development and receiving inspection activities. This role helps maintain and improve the certified quality management system by validating processes, documenting results, and participating in in-process audits. The position focuses heavily on measurement of tight tolerance parts, working closely with engineering, purchasing, and suppliers to resolve issues and ensure consistent product quality.Responsibilities<ul><li>Program, edit, and operate coordinate measuring machines (CMMs) to inspect tight tolerance parts using PCDMIS and related software.</li><li>Perform detailed measurements and inspections of products in process and at final stages, ensuring they meet specifications and quality standards.</li><li>Support receiving inspection by measuring new parts from suppliers, identifying issues, and validating that components meet drawing and specification requirements.</li><li>Contribute to the new product development (NPD) process by measuring and validating new parts that have not previously been produced or inspected, helping to establish robust measurement methods.</li><li>Collaborate with engineers, purchasing, and suppliers to resolve part-related issues, including methods of measurement, interpretation of drawings, and understanding of GD&amp;T requirements.</li><li>Support and maintain the certified quality management system (QMS) by validating processes, participating in in-process audits, and providing accurate documentation.</li><li>Use a variety of inspection tools such as calipers, micrometers, gauges, optical comparators, and Keyence systems to perform precise measurements.</li><li>Take ownership of measurement activities at the facility, including CMM operation, drawing interpretation, and selection of appropriate inspection methods.</li><li>Assist with cross-training efforts within the quality team to ensure coverage across inspection, calibration, and other quality functions.</li><li>Manage assigned projects and tasks independently, organizing and prioritizing work to meet required deadlines without constant supervision.</li><li>Maintain accurate records of inspection results, measurements, and quality documentation in accordance with internal procedures.</li><li>Participate in continuous improvement initiatives within a 5S environment, helping to enhance quality processes and overall efficiency.</li><li>Demonstrate reliable attendance and work a full scheduled shift, ensuring consistent support for production and NPD activities.</li></ul>Essential Skills<ul><li>Minimum 3 years of experience operating coordinate measuring machines (CMMs), with CMM programming experience preferred.</li><li>Experience with CMM software such as PCDMIS, CALYPSO, or MCOSMOS, with the ability to learn PCDMIS if not already proficient.</li><li>Minimum 3 years of experience performing measurements with calipers and micrometers.</li><li>Minimum 3 years of experience working with tight tolerance parts in aerospace, automotive, or medical industries.</li><li>Practical knowledge of reading part drawings, including an understanding of GD&amp;T symbols, their meanings, and how they apply to measurement and inspection.</li><li>Hands-on experience using inspection tools such as calipers, micrometers, gauges, and optical comparators.</li><li>Ability to operate or learn to operate Hexagon CMMs using PCDMIS software.</li><li>Capability to take ownership of measurement activities and work as a self-starter with limited direct supervision.</li><li>Strong attention to detail and accuracy in measurement, documentation, and inspection processes.</li><li>Ability to manage time effectively, handle multiple tasks, and complete projects within required timelines.</li><li>Willingness to work a full 8-hour shift with consistent, on-time attendance.</li></ul>Additional Skills &amp; Qualifications<ul><li>CMM programming experience using PCDMIS is highly preferred.</li><li>Experience with other CMM software platforms such as MCOSMOS or CALYPSO, with the ability to transition to PCDMIS.</li><li>Familiarity with Keyence measurement systems, with training available for candidates who do not yet have this experience.</li><li>Experience using optical comparators and a variety of gauges for dimensional inspection.</li><li>Experience in blueprint reading, quality control, and inspection of custom manufactured components.</li><li>Interest in working within new product development environments and supporting the launch of new parts and processes.</li><li>Willingness to participate in cross-training within the quality team, including inspection and calibration activities.</li><li>Comfort working in a dynamic environment with variety in daily tasks and measurement challenges.</li><li>Motivation to grow within the organization and take on additional responsibility over time.</li></ul>Work EnvironmentThe role is based in a climate-controlled facility that operates under 5S principles, providing a clean, organized, and comfortable work area. The quality team consists of a small group of specialists and engineers, and this position adds to that core team, offering significant ownership over measurement and inspection activities. The environment emphasizes custom manufacturing and new product development, creating variety in the types of parts and measurement challenges encountered. The facility uses Hexagon CMMs with PCDMIS software, along with calipers, micrometers, gauges, optical comparators, and Keyence systems for inspection. Standard hours are 7:00 a.m. to 3:30 p.m., Monday through Friday. The culture supports internal promotions, professional growth, and increasing involvement in the aerospace industry, offering opportunities to develop skills, take ownership of work, and contribute meaningfully to quality and process improvement.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 $30.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Description: Quality TechnicianWe are seeking a detail-oriented Quality Technician to support product quality and incoming inspections as the company continues to grow. This role will play a critical part in ensuring products meet specifications, fit properly, and function as designed before reaching customers. The ideal candidate enjoys hands-on inspection work, is comfortable using measurement tools, and has experience interpreting drawings, tolerances, and quality requirements in a manufacturing environment.Responsibilities<ul><li>Perform incoming inspections on components and finished products.</li><li>Use calipers, gauges, go/no-go gauges, and other inspection equipment to verify product conformance.</li><li>Interpret engineering drawings, specifications, and tolerance requirements.</li><li>Verify fit, form, and function of manufactured components and assemblies.</li><li>Inspect CNC machined, injection molded, and manufactured parts for defects and dimensional compliance.</li><li>Document inspection results and communicate quality concerns to engineering and operations teams.</li><li>Support containment, corrective action, and continuous improvement efforts.</li><li>Identify recurring quality issues from suppliers and incoming shipments.</li><li>Assist with product validation and approval processes.</li><li>Maintain inspection records and quality documentation.</li><li>Work closely with Engineering and Operations to ensure consistency across a growing product portfolio.</li></ul>Essential Skills<ul><li>High school diploma or technical degree/certificate.</li><li>5+ years of quality inspection experience in a manufacturing environment.</li><li>Experience using calipers, micrometers, gauges, and other precision measuring tools.</li><li>Ability to read and interpret engineering drawings and basic GD&amp;T.</li><li>Strong attention to detail and documentation skills.</li><li>Comfortable performing hands-on inspections throughout the day.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience inspecting machined components.</li><li>Experience with injection molded plastic parts.</li><li>Understanding of go/no-go gauge applications.</li><li>Familiarity with first article and incoming inspection processes.</li><li>Exposure to supplier quality or overseas manufacturing environments.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Chicago, IL.Pay and BenefitsThe pay range for this position is $34.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality TechnicianJob DescriptionWe are seeking a Lead Mechanical Inspector to provide hands-on inspection expertise and technical leadership throughout the manufacturing process, from incoming materials through final product release. This role serves as a key resource for inspection methods, quality standards, and customer requirements, including complex and serialized production parts. The successful candidate will guide inspection activities, mentor other inspectors, ensure quality and regulatory requirements are met, and collaborate closely with manufacturing and quality teams to improve processes and deliver high-quality products.Responsibilities<ul><li>Perform incoming, in-process, and final inspections.</li><li>Read and interpret engineering drawings, specifications, and GD&amp;T.</li><li>Operate FARO, portable CMMs, and other precision inspection equipment.</li><li>Complete First Article Inspections (FAIRs) per AS9102 standards.</li><li>Review and validate inspection results.</li><li>Create, manage, and close NCRs for nonconforming material.</li><li>Lead and provide technical guidance to inspectors.</li><li>Train inspectors on inspection methods, GD&amp;T, and quality requirements.</li><li>Prioritize inspection work based on production needs.</li><li>Troubleshoot complex inspection and quality issues.</li><li>Maintain compliance with AS9100 and ISO 9001 standards.</li><li>Support audits, root cause analysis, and corrective actions.</li><li>Maintain accurate inspection and quality documentation.</li></ul>Essential Skills<ul><li>Proficiency in inspection techniques and quality assurance.</li><li>Experience with AS9102 FAIR, ISO 9001, and AS9100 standards.</li><li>Capability in GD&amp;T, blueprint reading, and visual inspection.</li><li>Proficiency with CMM and portable metrology equipment.</li><li>Ability to lead and train other inspectors.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in quality control and assurance.</li><li>Strong troubleshooting skills for complex inspection and quality issues.</li><li>Ability to maintain compliance and documentation accurately.</li></ul>Work EnvironmentThe work environment is collaborative, innovative, and fast-paced. Employees are encouraged to take ownership, solve problems, share new ideas, and work across teams to deliver high-quality solutions for customers.Job Type &amp; LocationThis is a Contract to Hire position based out of Tucson, AZ.Pay and BenefitsThe pay range for this position is $25.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

Job Title: Quality TechnicianJob DescriptionThe Quality Technician will play a crucial role in ensuring our products meet design specifications and quality standards. This position involves assisting in various quality assurance processes, including first article, FMEA, PFMEA, and out-of-box audits, as well as qualifying raw materials and component parts. The role also involves creating quality processes, inspecting incoming materials, and maintaining accurate quality records.Responsibilities<ul><li>Assist in first article, FMEA, PFMEA, and out-of-box audits to ensure product meets design specifications and identify areas of weakness.</li><li>Assist in qualifying raw materials and component parts, ensuring they meet quality standards via PPAP and ongoing quality monitoring.</li><li>Support in-process controls and resolve component issues.</li><li>Assist in the creation of quality processes and documentation to ensure products and processes from suppliers meet technical standards.</li><li>Inspect selected incoming materials for compliance with specifications such as drawings, BOMs, routing guides, workmanship standards, and safety.</li><li>Collect data, generate inspection reports, discrepant material reports, and track product movements.</li><li>Perform source inspections and audits to validate product conformance, internal manufacturing/assembly processes, and supplier process controls.</li><li>Maintain accurate quality records of inspection and audit activities.</li><li>Support routine maintenance and calibration of quality equipment.</li></ul>Essential Skills<ul><li>Experience with quality and inspection equipment.</li><li>Proficient in interpreting 3D CAD drawings and Bill of Material structures.</li><li>Experience using Microsoft Office.</li><li>Prior experience with ERP systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with quality, inspection, and control processes.</li><li>Ability to use calipers, micrometres, micrometers, and gages.</li><li>Experience in first article inspection.</li></ul>Work EnvironmentThe position involves working in a dynamic environment where attention to detail and adherence to quality standards are paramount. The role requires the use of advanced quality inspection equipment and software, including Microsoft Office and ERP systems. The technician will collaborate with various departments to ensure quality standards are maintained throughout the production process.Job Type &amp; LocationThis is a Contract position based out of Saint Paul, MN.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

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



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



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



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



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



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

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