<h2>Job Title: Quality Engineer</h2><h2>Job Description</h2>Join our dynamic Quality team at the Vicksburg Plant as a Quality Engineer. You will be responsible for managing medical device, automotive, and consumer/industrial medical programs. This role involves hands-on engagement with projects from inception to completion, including addressing customer complaints in the field. Your expertise is essential to manage the workload efficiently.<h2>Responsibilities</h2><ul><li>Interpret and review complex engineering drawings and specifications, applying expert-level understanding of GD&amp;T to assess product and process compliance.</li><li>Support and perform medical product validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Process Characterization (PC).</li><li>Ensure compliance with industry-specific standards including IATF and ISO 9001, as well as medical device quality and regulatory requirements.</li><li>Actively participate in new product launches, ensuring quality requirements are integrated into design, process, and production planning.</li><li>Develop, document, and maintain standard work instructions for inspection, testing, and manufacturing processes.</li><li>Conduct first article inspections (FAI) and evaluate results against design specifications.</li><li>Perform and document risk assessments, process capability studies, and tolerance stack-ups.</li><li>Drive Corrective and Preventive Actions (CAPA) using structured problem-solving tools (e.g., 8D, 5 Why, Fishbone).</li><li>Participate in internal and supplier audits, and support regulatory and customer audits.</li><li>Work cross-functionally with Engineering, Manufacturing, and Supply Chain to resolve quality issues and improve processes.</li><li>Lead or assist with the development of control plans, PFMEAs, and process flow diagrams.</li><li>Analyze nonconformities, trends, and quality data to support continuous improvement initiatives.</li></ul><h2>Essential Skills</h2><ul><li>2+ years of experience in a Quality Engineering role within a manufacturing environment.</li><li>Proficient in engineering drawing review and GD&amp;T.</li><li>Experience working with IATF or ISO 9001 standards.</li><li>Experience working directly with customers as the main point of contact.</li><li>Familiarity with quality tools and methodologies such as control plans, process flow, FMEA, and blueprint review.</li><li>Strong willingness to learn, as verified through references.</li><li>Experience with plastic injection molding, IQ/OQ/PQ, statistical analysis, PPAP, APQP, supplier quality, CQE, and Six Sigma (Green Belt or Black Belt).</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with statistical analysis software.</li><li>Experience with precision measurement tools and CMMs.</li><li>Certifications such as CQE (Certified Quality Engineer), Six Sigma Green/Black Belt, or GD&amp;T Professional Certification.</li></ul><h2>Work Environment</h2>This position is based at the Vicksburg Plant, a well-organized, temperature-controlled facility with a cubicle office space. You will be part of a team of four Quality Engineers, reporting to the Quality Manager. The work is production-focused, requiring 60-70% floor time and 30-40% desk work. Work hours are from 7am-4pm or 8am-5pm.Job Type &amp; LocationThis is a Contract to Hire position based out of Vicksburg, MI.Pay and BenefitsThe pay range for this position is $28.85 - $38.46/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Vicksburg,MI.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

public

Quality Engineer

Quality EngineerDescription•Develop, implement, and maintain quality procedures, work instructions, and inspection plans for CNC-machined thermal products (including on-site fundry, machining and electrical assembly)•Review engineering drawings, specifications, and customer requirements to ensure accurate quality planning•Lead root cause analysis and corrective/preventive actions (CAPA) for internal and customer quality issues•Support first article inspections (FAI), in-process inspections, and final inspections•Work closely with CNC machinists, programmers, and supervisors to resolve quality concerns and improve processes•Analyze quality data and trends (scrap, rework, nonconformances) and recommend process improvements•Manage nonconforming material reports (NCMRs) and coordinate disposition activities, both internal rejects and external customer returns (RMA)•Assist with customer, internal, and third-party audits (e.g., ISO 9001)•Ensure proper calibration and maintenance of inspection and measurement equipment•Support supplier quality activities, including supplier evaluations and corrective actions•Support customer-specific quality initiatives and work closely with customer supplier engineers (calls, meetings, emails, projects)•Implement and maintain statistical methodologies for process improvement (SPC, etc.)•Train production and inspection personnel on quality standards and best practices•Daily collaboration with other internal departments, including sales, customer service, engineering, purchasing, and production•Lead / direct the shop-floor quality team (Quality Techs and Inspectors), including training, setting priorities, addressing technical challenges, etc.•Perform other tasks and special projects as needed.Additional Skills &amp; Qualifications•Engineering degree preferred (ME or EE), or equivalent technical experience•5 plus years of Quality Engineering experience.•Ability to read and interpret engineering drawings and GD&amp;T.•Experience using calipers, micrometers, height gauges, CMMs, and other inspection equipment.•Working knowledge of quality tools such as PPAP, FMEA, SPC, root cause analysis, and 8D.•Familiarity with ISO 9001 or other applicable quality management systems.•Proficiency with statistical software, such as MiniTab or JMP•ASQ quality-related certifications preferred (CQE, CQA, or equivalent)•Lean / Six Sigma certifications preferred (Green Belt, Black Belt)•Proficiency with Microsoft Office and quality documentation systems.•Ability to pass pre-employment drug test and background check.Experience LevelExpert LevelJob Type &amp; LocationThis is a Permanent position based out of Batavia, IL.Pay and BenefitsThe pay range for this position is $75000.00 - $100000.00/yr.offers a competitive salary, full benefit package, including medical, dental, vision, life, EAP and 401k with employer match, annual bonus if company hits target numbersWorkplace TypeThis is a fully onsite position in Batavia,IL.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Description:The role of Supplier Quality Engineer is to drive exceptional product quality for customer value beyond expectations while ensuring regulatory assurance and optimized cost quality. Through effective and accurate supplier quality processes, this position ensures product quality, cost-effectiveness, and safe and efficient equipment operation.Responsibilities:<ul><li>Develop and manage supplier quality plans through appropriate risk analysis.</li><li>Support ISO 9000 Quality Process Requirements.</li><li>Support implementation of initiatives related to supplier processes and improvements.</li><li>Ensure Corrective and Preventive Action plans are developed and executed at assigned suppliers.</li><li>Evaluate the need for quality data/reports and provide required quality information beneficial to the specified processes.</li><li>Perform supplier quality audits as required by the verification plan or by the Quality Manager.</li><li>Identify non-conforming materials and workmanship, perform root cause analysis, and implement effective short and long-term corrective actions.</li><li>Participate and lead continuous improvement initiatives.</li><li>Write and submit reports as required for audits, inspections, rejects, root causes, etc.</li></ul>Work Environment:This position requires 30%-40% travel.Job Type &amp; LocationThis is a Contract to Hire position based out of Hamel, MN.Pay and BenefitsThe pay range for this position is $40.00 - $53.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Hamel,MN.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality EngineerJob DescriptionThe ideal candidate will hold a BS degree in Aeronautics Engineering, Mechanical Engineering, or a related discipline focusing on thermodynamics and mechanical systems. Equivalent applicable work experience may be considered. A Part 65 FAA Powerplant mechanics license is preferred. The role requires a minimum of five years of experience in Repair Station or Production, with at least two years in an engineering or test-related role.Responsibilities<ul><li>Perform inspection and release of engines and parts in a timely manner, including visual inspection, borescope inspection, and basic hand measurements.</li><li>Ensure all paperwork associated with product shipment is in compliance, including creation of shipment documentation required by the customer.</li><li>Ensure compliance of engine and component test plans to approved design data, including review and incorporation of engine manual changes and Service Bulletin changes for Repair Station.</li><li>Support review and incorporation of Change in Design and engine drawings/specifications for Production. Support engine and component work plan updates.</li><li>Ensure engine and component test and shop floor activities are executed per internally approved procedures and provide feedback for improvement.</li><li>Review and propose test methods and devices used in support of engine and component testing and miscellaneous part manufacturing and inspection applications.</li><li>Oversee test system and instrument calibrations, review results for acceptability, and coordinate appropriate adjustments.</li><li>Collaborate with a working team to troubleshoot engine test failures for resolution through disposition or rework.</li><li>Facilitate removal, replacement, and investigation of suspect parts issued to engines, including control of physical parts and documentation of condition in appropriate systems.</li><li>Support root cause analysis and countermeasure implementation related to product escape, defect prevention, and systems/databases used to facilitate work.</li><li>Participate in other projects as specified by Quality Management.</li></ul>Essential Skills<ul><li>Knowledge of 14CFR Part 43, Part 145, and Part 21 regulations.</li><li>Ability in written communication, including technical writing and presentations.</li><li>Ability to understand design data (drawings, specifications, manuals).</li><li>Strong attention to detail and adherence to established processes.</li><li>Strong organizational skills.</li><li>Strong analytical, critical thinking, and problem-solving skills.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Burlington, NC.Pay and BenefitsThe pay range for this position is $80000.00 - $95000.00/yr.Competitive Base Wages (pay will be based on several variables that include, but not limited to geographic location, work experience, etc.)
•	Paid Overtime
•	Regional Bonus (when applicable)
•	Industry-leading Benefit Plans (Medical, Dental, Vision, Rx) 
•	Paid time off, including vacation, holidays, shutdown
•	Company Paid Short-Term and Long-Term Disability 
•	401K Plan with company match + additional contribution
Career Growth:
•	Advancement Opportunities
•	Career Mobility
•	Education Reimbursement for Continued Learning
•	Training and Development Programs 
Additional Offerings:
•	Lifestyle Account
•	Childcare Reimbursement Account
•	Tuition Assistance &amp; Student Loan Repayment
•	Elder Care Support
•	Wellbeing Program
•	Community Service and Engagement Programs
•	Product ProgramsWorkplace TypeThis is a fully onsite position in Burlington,NC.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality EngineerJob DescriptionWe are seeking a Quality Engineer with hands-on process quality experience, including manufacturing support, process validation (IQ/OQ/PQ execution), risk-based decision making, and exposure to product or process transfer. Candidates with a cross-functional engineering experience, such as Process, Product, or Manufacturing Engineering, are ideal for this role.Responsibilities<ul><li>Execute process validation (IQ/OQ/PQ).</li><li>Support product and process transfers.</li><li>Provide manufacturing process support, including laser welding, injection molding, extrusion, assembly, and packaging.</li><li>Conduct PFMEA, risk assessment, and develop control plans.</li><li>Utilize SPC, Cp/Cpk, root cause analysis, and DOE for process improvements.</li><li>Troubleshoot production line issues and implement change controls.</li><li>Perform PPAP and supplier process qualifications.</li><li>Develop incoming inspection strategies and offer cross-functional engineering support.</li></ul>Essential Skills<ul><li>4+ years of experience in process improvement.</li><li>4+ years in a manufacturing environment, preferably medical.</li><li>4+ years in a mix of manufacturing, process, and quality engineering roles.</li><li>Proficiency in process validation (IQ/OQ/PQ), product transfer, and root cause analysis.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with continuous improvement methodologies.</li><li>Skilled in cross function engineering roles, quality, manufacturing, and process improvement.</li></ul>Work EnvironmentThe role is based in a manufacturing environment, featuring clean rooms, production floors, and office spaces. The new building fosters a collaborative and family-oriented culture, offering a balance between professional and personal life. Join a team akin to an established start-up, contributing to the development of life-changing medical products.Job Type &amp; LocationThis is a Permanent position based out of Tempe, AZ.Pay and BenefitsThe pay range for this position is $95000.00 - $110000.00/yr.Erbe USA offers comprehensive employee medical benefits, featuring Cigna health insurance with a fully-funded medical deductible via a Health Savings Account (HSA), alongside dental (PPO) and vision insurance. They also provide short-term/long-term disability, basic life insurance, and a fitness center. These benefits aim to support employees with 15 days PTO, sick time, and 401k matchingWorkplace TypeThis is a hybrid position in Tempe,AZ.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>Quality Engineer</h2>Location: Tonawanda, NYSchedule: Rotating shifts (1st, 2nd, and 3rd)Work Environment: Manufacturing floor and office<h3>About the Role</h3>We are seeking a Quality Engineer to serve as a key technical partner across Production, Engineering, Suppliers, and Supplier Quality. In this role, you will play a critical part in ensuring product quality by driving problem‑solving initiatives, supporting manufacturing operations, and leading containment and corrective actions for quality issues. This position offers hands‑on exposure to manufacturing operations while also providing opportunities to influence quality systems, standards, and continuous improvement initiatives.<h2 style="text-align:center;"></h2><h3>What You’ll Do</h3>As a Quality Engineer, you will:<ul><li>Follow and actively enforce all site safety guidelines and policies.</li><li>Partner with Production and Engineering teams to address quality issues, implement containment actions, and drive resolutions.</li><li>Collaborate with Team Leaders and Group Leaders to identify root causes and implement corrective actions.</li><li>Audit elements of Quality Manual and GMS Built‑In Quality Statements.</li><li>Review and approve Standardized Work for assigned departments to ensure compliance with Tonawanda Quality Standards.</li><li>Lead problem‑solving efforts for supplier, internal, and customer quality concerns.</li><li>Ensure effective containment and resolution of non‑conforming product.</li><li>Communicate emerging quality risks and issues in a timely and effective manner.</li><li>Support the PTR (Problem Tracking and Resolution) process by running PTRs and evaluating their impact on product performance and functionality.</li><li>Review and approve Plant Floor Change Management Requests for assigned departments.</li><li>Support departmental scrap reduction and continuous improvement initiatives.</li></ul><h3>Required Qualifications</h3>To be successful in this role, you will bring:<ul><li>Internship experience in Manufacturing or an Engineering discipline.</li><li>Strong critical thinking and analytical problem‑solving skills.</li><li>Ability to work and rotate across all three shifts (1st, 2nd, and 3rd).</li><li>Flexibility to work overtime, weekends, and holidays as business needs require.</li><li>Excellent written and verbal communication skills.</li><li>High integrity, with the ability to work independently, manage ambiguity, and take ownership of responsibilities.</li></ul><h3>Preferred Qualifications</h3>Candidates with the following will have a competitive advantage:<ul><li>Bachelor’s degree in Engineering or equivalent practical experience.</li><li>2+ years of experience in a Quality and/or Manufacturing environment.</li><li>Strong interpersonal and relationship‑building skills, with the ability to collaborate effectively at all levels of the organization.</li><li>Proven ability to solve complex problems by identifying root causes and implementing sustainable corrective actions.</li><li>Proactive mindset with a willingness to ask questions, take initiative, and seek out solutions.</li><li>Knowledge of GMS (Global Manufacturing System) principles and practices.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Buffalo, NY.Pay and BenefitsThe pay range for this position is $25.00 - $30.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Buffalo,NY.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Description
					•	Lead quality investigations related to in-the-market defects to identify root cause and implement corrective actions and preventative actions.
•	Collaborate with cross-functional teams to investigate failure modes and execute impact assessments to ensure appropriate countermeasures are developed and launched.
•	Interface with customers and suppliers to address non-conformances identified during manufacturing.
•	Lead process improvement initiatives utilizing Statistical Process Control (SPC) and Six Sigma methodology such as 5S, Value Stream Mapping, Control Plans, PFEMA, and Process Mapping.
•	Lead Manufacturing Quality Assurance aspects of process control, initiating projects to ensure that targeted process flows are effective and achieves operational requirements, and provide guidance to SME’s on root cause and corrective action (RCCA) activities.
•	Recommend process improvements to management and execute to ensure consistent implementation of internal requirements and external regulations and standards.
•	Provide status reporting regarding manufacturing processes deliverable, dependencies, risks and issues, communicating across teams and management.
•	Advise manufacturing and quality teams on the implementation of international standards (ISO 9001, regulatory standards, etc.) as they relate to manufacturing of product and Good Documentation Practices (GDP).
•	Participate in the investigations and dispositions of product, non-conformances and changes, CARs and MRB.
•	Generate and maintain procedures, work instructions and forms, as necessary to ensure standardization of practices across SaniSure.
•	Implement required changes to existing training programs and assist in training staff members.
•	Perform other tasks as assigned.
										Skills
					Quality engineering, Quality assurance, iso 13485, technical documentation, asq certified, asq certification, asq, capa, complaints, change control, root cause analysis, medical device, pharmaceutical, biotechnology, biotech, 21 CFR
										Top Skills Details
					Quality engineering,Quality assurance,iso 13485,technical documentation,asq certified,asq certification,asq,capa,complaints,change control,root cause analysis,medical device,pharmaceutical,biotechnology,biotech,21 CFR
										Additional Skills &amp; Qualifications
					•	Bachelor’s degree in Business, Sciences or Engineering
•	5+ years of experience in quality operations within a biotechnology or pharmaceutical manufacturing facility.
•	5+ years of experience with technical documentation for complex activities in the areas of the Quality System that includes corrective actions, change control, quality audits and validation of manufacturing processes, or product development in a pharmaceutical or medical device environment.
•	Strong understanding of global pharmaceutical and biotechnology product regulations with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820.
•	Able to drive continuous improvement through collaboration and consensus building.
•	Proficient problem-solving skills using continuous improvement tools; certification desired in ASQ, Green Belt, Lean, or equivalent.
•	Demonstrated proficiency in multiple quality systems including exception management, change control, document control, product release, etc. with strong decision-making skills utilizing risk management.
•	Quality System Knowledge (e.g. ISO 9001, ISO 13485).
•	Advanced skills with MS Office software are preferred.
•	Able to lead change environment across multiple sites and customers globally.
•	Able to communicate effectively, verbally and in writing, and demonstrate good interpersonal skills interdepartmentally and with external vendors, contractors, and customers.
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Permanent position based out of Camarillo, CA.Pay and BenefitsThe pay range for this position is $90000.00 - $110000.00/yr.Medical, dental, 401k, sick pay, pto,Workplace TypeThis is a fully onsite position in Camarillo,CA.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Responsibilities:<ul><li>Develop new processes and products and revise existing ones.</li><li>Create and update project-specific quality plans, ensuring adherence to customer requirements.</li><li>Work as part of a cross-functional team to develop methods to measure products to ensure they meet quality standards.</li><li>Troubleshoot measurement methods and equipment to ensure accuracy and reliability.</li><li>Lead validation of new products and technology (IQ, OQ, PQ) and act as QA lead for equipment validation.</li><li>Collaborate with customers and suppliers on new product processes and lead customer complaints and supplier SCAR management.</li><li>Compile and analyze statistical data to assess process capabilities and conduct PFMEA, GR&amp;R, and SPC studies.</li><li>Create and maintain quality system documentation, including quality plans, inspection and control plans, and work instructions.</li><li>Manage NCR, CAPA, and customer complaints from creation to closure, using problem-solving tools and working as part of a cross-functional team.</li><li>Lead changes in production, ensuring compliance with customer agreements, ISO standards, and internal requirements.</li><li>Prepare, submit, and follow change requests (SCR) with customers.</li><li>Assist production in achieving APU objectives and generate quality KPIs for PSM2.</li><li>Perform internal and external audits.</li><li>Serve as backup for other QEs on customer or internal tasks as requested by the Director of Quality.</li><li>Identify and support continuous improvement opportunities and participate in LEAP workshops.</li></ul>Essential Skills:<ul><li>Bachelor's degree in Manufacturing Engineering or related field.</li><li>Minimum two years of relevant experience or five years for a position.</li><li>Proficient in blueprint reading with GD&amp;T level expected.</li><li>Experience developing manufacturing quality plans.</li><li>Experience conducting process capability, GR&amp;R, PFMEA, and SPC studies.</li><li>Experience working on NCR / CAPA.</li><li>Experience working in an ISO environment, preferably ISO.</li><li>Proficient PC skills in a Windows environment.</li><li>Effective written and verbal communication skills.</li><li>Strong interpersonal and teamwork skills.</li></ul>Additional Skills &amp; Qualifications:<ul><li>Experience in a precision machine shop environment.</li><li>Experience optimizing processes to achieve ongoing cost reductions.</li><li>LEAN / Six Sigma training and demonstrated application.</li><li>Demonstrated use of structured problem-solving methods (i.e., 8D).</li><li>Experience in internal and supplier audits.</li><li>Experience using an ERP system.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Big Lake, MN.Pay and BenefitsThe pay range for this position is $80000.00 - $95000.00/yr.Competitive Benefits Include:
- Medical, dental, vision, life insurance, paid time off and 401K.
- Tuition reimbursement to support your development; floating holidays that you take for days that are important to you.Workplace TypeThis is a fully onsite position in Big Lake,MN.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h1>Job Title: Quality Engineer</h1>Job DescriptionWe are seeking a Quality Engineer who will identify root causes through corrective and preventive actions, implement and validate these plans, and oversee the quality management system. The role involves improving production methods, product quality, and equipment performance. You will be responsible for data collection, entry, and reporting for product conformance and process capability, and for developing and implementing methods and standards for products, materials, equipment, returns, testing, calibration, and processes. Support for AS9100 and ISO 9001 quality management standards, utilizing statistical process control, and supporting mechanical and electrical testing are also key aspects of this role. Our products support multiple industries such as Aerospace/Defense and Medical device. Responsibilities<ul><li>Identify root causes through corrective and preventive actions</li><li>Implement and validate corrective and preventive action plans</li><li>Oversee the quality management system</li><li>Improve production methods, product quality, and equipment performance</li><li>Collect, enter, and report data for product conformance and process capability</li><li>Develop and implement methods and standards for products, materials, equipment, returns, testing, calibration, and processes</li><li>Support AS9100 and ISO 9001 quality management standards</li><li>Utilize statistical process control to support process capability</li><li>Support mechanical and electrical testing</li><li>Execute gap analysis</li></ul>Essential Skills<ul><li>Bachelor's Degree in a related discipline preferred</li><li>2+ years of experience within a quality function</li><li>Working knowledge and experience with problem-solving methodologies</li><li>Experience with quality management systems</li><li>Skills in quality function management</li><li>Continuous improvement and lean/six sigma methodologies</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with root cause analysis and corrective action plans</li></ul>Work EnvironmentYou will report to the Quality Manager and work within a group of engineers and technicians. Our company is a leader in connectors and cables for fiber optics, supporting regulated environments such as government, aerospace, defense, medical, and industrial sectors. This role requires U.S. citizenship, as we cannot provide visa sponsorship. Our work culture promotes growth within the quality and other departments, and we offer a tuition reimbursement program once you are direct with the organization.Job Type &amp; LocationThis is a Permanent position based out of Waseca, MN.Pay and BenefitsThe pay range for this position is $60000.00 - $75000.00/yr.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental &amp; vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Waseca,MN.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2 style="text-align:center;">Quality Engineer</h2>We are seeking a hands‑on Quality Engineer to support product assurance across engineering, manufacturing, supply chain, and program teams. This individual will serve as the primary quality liaison for assigned programs, driving compliance to AS9100/ISO 9001 standards, supporting troubleshooting on the production floor, and leading corrective action efforts. Most work is performed directly on the manufacturing floor, with additional planning and reporting tasks completed at the desk. This position is ideal for someone who enjoys solving problems at the source, collaborating cross‑functionally, and contributing to long‑term product reliability in a regulated environment.Location: Farmingdale, NY 11735Employment Type: PermanentSalary Range: $80,000–$95,000Schedule: 9/80 (Every other Friday off)Key Responsibilities<ul><li>Serve as the program’s single point of contact for all Product Assurance and Quality requirements</li><li>Lead cross‑functional quality efforts and make independent decisions to ensure adherence to quality and reliability standards</li><li>Develop, implement, and maintain program‑specific quality procedures and plans</li><li>Track program budgets, define work scope, and manage assignments for team members</li><li>Support proposals for new programs, including defining quality requirements and estimating scope</li><li>Collect and analyze program quality metrics to identify trends and risks</li><li>Prepare and present status reports to internal leadership and customers</li><li>Generate, track, and close internal and supplier Corrective Action Requests (CARs)</li><li>Perform root cause analysis and drive CAPA effectiveness</li><li>Conduct detailed contract reviews to determine quality and regulatory requirements</li><li>Maintain monitoring systems and PC‑based tools for planning, tracking, and performance evaluation</li><li>Work closely with operations to support troubleshooting, repair, retesting, and floor‑based quality activities</li><li>Occasional overnight travel required</li></ul>Required Qualifications<ul><li>Bachelor’s degree in Engineering (Industrial or Mechanical preferred)</li><li>2+ years of Quality Engineering or related experience</li><li>Strong knowledge of:<ul><li>CAPA</li><li>Internal/external audits</li><li>Root cause analysis</li><li>Quality control methods</li><li>AS9100 &amp; ISO 9001</li></ul></li><li>Hands‑on experience with testing and inspecting electronic components</li><li>Ability to use test equipment such as oscilloscopes, multimeters, and related tools</li><li>Experience developing corrective action plans and working within a Quality Management System</li><li>Excellent interpersonal, written, and verbal communication skills</li></ul>Preferred Qualifications<ul><li>Experience in aerospace, defense, or similarly regulated manufacturing environments</li><li>Exposure to export‑controlled work environments</li><li>Ability to work both independently and within cross‑functional teams</li></ul>Work Environment<ul><li>Primarily located on the manufacturing floor, working at designated benches and workstations</li><li>Involvement in troubleshooting, identifying issues, replacing/repairing components, and retesting</li><li>May work in test or environmental chambers depending on program needs</li><li>Training provided; close support from leads and supervisors</li><li>9/80 schedule (nine‑hour days with every other Friday off)</li><li>Bi‑weekly pay</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Farmingdale, NY.Pay and BenefitsThe pay range for this position is $80000.00 - $95000.00/yr.Medical &amp; Prescription Coverage
Employees have access to a high-deductible comprehensive medical plan through BlueCross
BlueShield, which includes:
- Preventive care at no cost (e.g., routine exams, immunizations, cancer screenings)
- Office visits, lab work, and diagnostic imaging with copays
- Emergency and urgent care services
- Inpatient and outpatient hospitalization
- Maternity care and newborn services
- Mental health and substance abuse treatment
Prescription drug coverage includes a mandatory generic substitution policy, with tiered copays
applied after the deductible.Workplace TypeThis is a fully onsite position in Farmingdale,NY.Application DeadlineThis position is anticipated to close on Feb 21, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h1>Job Title: Quality Engineer</h1>Job DescriptionWe are seeking a Quality Engineer who will identify root causes through corrective and preventive actions, implement and validate these plans, and oversee the quality management system. The role involves improving production methods, product quality, and equipment performance. You will be responsible for data collection, entry, and reporting for product conformance and process capability, and for developing and implementing methods and standards for products, materials, equipment, returns, testing, calibration, and processes. Support for AS9100 and ISO 9001 quality management standards, utilizing statistical process control, and supporting mechanical and electrical testing are also key aspects of this role. Our products support multiple industries such as Aerospace/Defense and Medical device. Responsibilities<ul><li>Identify root causes through corrective and preventive actions</li><li>Implement and validate corrective and preventive action plans</li><li>Oversee the quality management system</li><li>Improve production methods, product quality, and equipment performance</li><li>Collect, enter, and report data for product conformance and process capability</li><li>Develop and implement methods and standards for products, materials, equipment, returns, testing, calibration, and processes</li><li>Support AS9100 and ISO 9001 quality management standards</li><li>Utilize statistical process control to support process capability</li><li>Support mechanical and electrical testing</li><li>Execute gap analysis</li></ul>Essential Skills<ul><li>Bachelor's Degree in a related discipline preferred</li><li>2+ years of experience within a quality function</li><li>Working knowledge and experience with problem-solving methodologies</li><li>Experience with quality management systems</li><li>Skills in quality function management</li><li>Continuous improvement and lean/six sigma methodologies</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with root cause analysis and corrective action plans</li></ul>Work EnvironmentYou will report to the Quality Manager and work within a group of engineers and technicians. Our company is a leader in connectors and cables for fiber optics, supporting regulated environments such as government, aerospace, defense, medical, and industrial sectors. This role requires U.S. citizenship, as we cannot provide visa sponsorship. Our work culture promotes growth within the quality and other departments, and we offer a tuition reimbursement program once you are direct with the organization.Job Type &amp; LocationThis is a Permanent position based out of Owatonna, MN.Pay and BenefitsThe pay range for this position is $60000.00 - $75000.00/yr.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental &amp; vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Owatonna,MN.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Description:The role of Supplier Quality Engineer is to drive exceptional product quality for customer value beyond expectations while ensuring regulatory assurance and optimized cost quality. Through effective and accurate supplier quality processes, this position ensures product quality, cost-effectiveness, and safe and efficient equipment operation.Responsibilities:<ul><li>Develop and manage supplier quality plans through appropriate risk analysis.</li><li>Support ISO 9000 Quality Process Requirements.</li><li>Support implementation of initiatives related to supplier processes and improvements.</li><li>Ensure Corrective and Preventive Action plans are developed and executed at assigned suppliers.</li><li>Evaluate the need for quality data/reports and provide required quality information beneficial to the specified processes.</li><li>Perform supplier quality audits as required by the verification plan or by the Quality Manager.</li><li>Identify non-conforming materials and workmanship, perform root cause analysis, and implement effective short and long-term corrective actions.</li><li>Participate and lead continuous improvement initiatives.</li><li>Write and submit reports as required for audits, inspections, rejects, root causes, etc.</li></ul>Work Environment:This position requires 30%-40% travel.Job Type &amp; LocationThis is a Contract to Hire position based out of Hamel, MN.Pay and BenefitsThe pay range for this position is $40.00 - $53.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Hamel,MN.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>Job Title: Quality Engineer</h2><h2>Job Description</h2>Join our dynamic Quality team at the Vicksburg Plant as a Quality Engineer. You will be responsible for managing medical device, automotive, and consumer/industrial medical programs. This role involves hands-on engagement with projects from inception to completion, including addressing customer complaints in the field. Your expertise is essential to manage the workload efficiently.<h2>Responsibilities</h2><ul><li>Interpret and review complex engineering drawings and specifications, applying expert-level understanding of GD&amp;T to assess product and process compliance.</li><li>Support and perform medical product validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Process Characterization (PC).</li><li>Ensure compliance with industry-specific standards including IATF and ISO 9001, as well as medical device quality and regulatory requirements.</li><li>Actively participate in new product launches, ensuring quality requirements are integrated into design, process, and production planning.</li><li>Develop, document, and maintain standard work instructions for inspection, testing, and manufacturing processes.</li><li>Conduct first article inspections (FAI) and evaluate results against design specifications.</li><li>Perform and document risk assessments, process capability studies, and tolerance stack-ups.</li><li>Drive Corrective and Preventive Actions (CAPA) using structured problem-solving tools (e.g., 8D, 5 Why, Fishbone).</li><li>Participate in internal and supplier audits, and support regulatory and customer audits.</li><li>Work cross-functionally with Engineering, Manufacturing, and Supply Chain to resolve quality issues and improve processes.</li><li>Lead or assist with the development of control plans, PFMEAs, and process flow diagrams.</li><li>Analyze nonconformities, trends, and quality data to support continuous improvement initiatives.</li></ul><h2>Essential Skills</h2><ul><li>2+ years of experience in a Quality Engineering role within a manufacturing environment.</li><li>Proficient in engineering drawing review and GD&amp;T.</li><li>Experience working with IATF or ISO 9001 standards.</li><li>Experience working directly with customers as the main point of contact.</li><li>Familiarity with quality tools and methodologies such as control plans, process flow, FMEA, and blueprint review.</li><li>Strong willingness to learn, as verified through references.</li><li>Experience with plastic injection molding, IQ/OQ/PQ, statistical analysis, PPAP, APQP, supplier quality, CQE, and Six Sigma (Green Belt or Black Belt).</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with statistical analysis software.</li><li>Experience with precision measurement tools and CMMs.</li><li>Certifications such as CQE (Certified Quality Engineer), Six Sigma Green/Black Belt, or GD&amp;T Professional Certification.</li></ul><h2>Work Environment</h2>This position is based at the Vicksburg Plant, a well-organized, temperature-controlled facility with a cubicle office space. You will be part of a team of four Quality Engineers, reporting to the Quality Manager. The work is production-focused, requiring 60-70% floor time and 30-40% desk work. Work hours are from 7am-4pm or 8am-5pm.Job Type &amp; LocationThis is a Contract to Hire position based out of Vicksburg, MI.Pay and BenefitsThe pay range for this position is $28.85 - $38.46/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Vicksburg,MI.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer plays a pivotal role in supporting the commitment to superior craftsmanship and continuous improvement. This position is responsible for driving daily quality initiatives, planning and executing targeted improvement projects, and acting as a key liaison between operations, engineering, and customers. The Quality Engineer analyzes nonconformances, conducts root-cause investigations, implements corrective and preventive actions, enhances inspection methods and procedures, leads AS9102 First Article submissions, conducts internal audits, and supports successful new product introductions. Additionally, this role mentors inspection personnel, maintains compliance with ISO-9001/AS-9100 standards, installs and monitors statistical process controls, and champions 6S activities to ensure a safe, efficient, and high-performing aerospace manufacturing environment.Responsibilities<ul><li>Drive daily quality initiatives and plan targeted improvement projects.</li><li>Serve as a key liaison between operations, engineering, and customers.</li><li>Analyze nonconformances and perform root-cause investigations.</li><li>Implement corrective and preventive actions.</li><li>Enhance inspection methods and procedures.</li><li>Lead AS9102 First Article submissions.</li><li>Conduct internal audits.</li><li>Support successful new product introductions.</li><li>Mentor inspection personnel.</li><li>Maintain compliance with ISO-9001/AS-9100 standards.</li><li>Install and monitor statistical process controls.</li><li>Champion 6S activities in the aerospace manufacturing environment.</li></ul>Essential Skills<ul><li>First article inspection, root cause analysis, and QMS exposure.</li><li>Proficiency in GD&amp;T and blueprint reading.</li><li>Strong leadership potential with excellent communication and soft skills.</li><li>Ability to manage projects and complete them in a timely manner.</li><li>Experience with ISO-9001 or AS-9100 Quality Management Systems.</li><li>Proficient computer skills including Microsoft Office.</li><li>Basic understanding of 6S and blueprint reading.</li></ul>Additional Skills &amp; Qualifications<ul><li>Quality Engineering experience in a manufacturing environment.</li><li>Experience with common machine shop gauging and techniques.</li><li>Ability to identify areas for improvement and think strategically.</li><li>Ability to identify root cause and determine corrective actions.</li><li>Bachelor’s Degree or 5+ years of experience in a Quality Engineering environment.</li><li>ASQ Certified Quality Engineer (CQE) preferred.</li><li>Thorough understanding of inspection methods, techniques, and equipment.</li><li>Experience in the aerospace industry.</li><li>Strong understanding of AS9102 First Article submittal process.</li><li>Ability to perform internal audits independently.</li><li>Must pass an annual eye exam by a licensed optometrist.</li></ul>Work EnvironmentThis position is based onsite in Westfield, MA, with occasional travel to Southwick, MA. The workweek consists of 45 hours, typically from 7:30 AM to 4:30 PM. The work environment is a normal production setting, subject to high noise levels from operating machines, physical hazards from moving equipment and sharp machine parts, exposure to fumes, dust, mist, oil, and cutting fluid, as well as sharp metal edges and forklifts. The company offers a large organization feel with the personal touch of a family-owned business, where employees are known by name. Annual bonuses are provided.Job Type &amp; LocationThis is a Permanent position based out of Westfield, MA.Pay and BenefitsThe pay range for this position is $86000.00 - $107000.00/yr.Health insurance
Dental insurance
Vision insurance
Life insurance
Paid time off (PTO)
401(k)
401(k) matching (noted in some job postings)
Flexible Spending Account (FSA)
Tuition reimbursement
Employee Assistance Program (EAP)Workplace TypeThis is a fully onsite position in Westfield,MA.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer is responsible for providing quality assurance support to the product development team. The role involves resolving bugs, defects, and other potential issues to ensure products meet customer specifications.Responsibilities<ul><li>Implement effective corrective actions through robust root cause analysis and facilitation with process owners.</li><li>Support manufacturing in developing effective procedures and work instructions that meet ISO9001 and other quality management standards.</li><li>Actively engage in root cause identification, corrective actions, and preventative actions for customer concerns, complaints, and queries.</li><li>Approve suppliers and establish appropriate levels of control based on product nature and supplier capability, continuously improving the quality of externally supplied parts.</li><li>Utilize problem-solving techniques for internal and supplier issues, establish robust RCCM through facilitation with process owners, and drive improvements to products and processes using performance data.</li><li>Create visual awareness of quality metrics and communicate them to the business.</li><li>Assist in the development and execution of a process audit plan.</li><li>Review the business to ensure department methodologies, processes, and procedures are adhered to.</li><li>Implement methodologies for establishing the 'cost of quality'.</li></ul>Essential Skills<ul><li>Experience in quality engineering, quality assurance, and manufacturing engineering.</li><li>Strong understanding of supplier quality and root cause analysis.</li><li>Proficiency in audit processes and ISO 9001 standards.</li><li>CAPA and corrective action plans expertise.</li><li>Knowledge of engineering and quality management systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>Degree in Quality, Engineering, Manufacturing or equivalent relevant qualification.</li><li>3-5 years minimum of relevant experience in a mixed volume, assembly environment.</li><li>Excellent problem-solving techniques such as CAPA, 8D, and 5 Whys are desirable.</li><li>In-depth understanding of the manufacturing process within a component and assembly environment.</li><li>Experience in supplier management and driving improvements within the supply chain.</li><li>Internal Auditor Qualification (ISO9001 preferred).</li><li>Ability to motivate and influence people at all levels, building relationships with customers and suppliers.</li><li>Capability to manage several projects and work under pressure without reducing attention to detail.</li></ul>Work EnvironmentThe current team consists of approximately five employees, with opportunities to learn and engage under the guidance of the Quality Manager. The role involves prolonged periods of sitting at a desk and working on a computer, with occasional lifting of up to 15 pounds.Job Type &amp; LocationThis is a Contract to Hire position based out of Rochester, NY.Pay and BenefitsThe pay range for this position is $40.85 - $45.70/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Rochester,NY.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality EngineerJob DescriptionThe Quality Engineer will perform detailed analysis of customer returned parts, using findings to drive Corrective and Preventative Action (CAPA) improvements. The role involves preventing internal recurring failures and reducing risks by performing root cause analysis to identify and address existing issues. The engineer will validate customer RMAs and issue further actions to improve manufacturing processes. Additionally, the engineer will supervise a team of six in the final inspection department, providing guidance, coaching, and training as necessary. The position also involves representing QA in the material review board (MRB) for internal rejections.Responsibilities<ul><li>Perform detailed analysis of customer returned parts and use findings to drive CAPA improvements.</li><li>Prevent internal recurring failures and reduce risks by performing root cause analysis.</li><li>Validate customer RMAs and issue further actions to improve manufacturing processes.</li><li>Supervise a team of six in the final inspection department, providing guidance, coaching, and training.</li><li>Represent QA in the material review board (MRB) for internal rejections.</li></ul>Essential Skills<ul><li>Experience as a Quality Engineer.</li><li>Proficiency with AS9102 standards.</li><li>Ability to perform root cause analysis and implement corrective actions.</li><li>Experience with first article inspections and audits.</li><li>Familiarity with MRB processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in the aerospace industry.</li><li>Familiarity with connector lines.</li></ul>Work EnvironmentThe work environment involves collaborating with a team in the final inspection department. The role requires attention to detail and adherence to aerospace quality standards. The position is integral to maintaining and improving manufacturing processes, ensuring quality and compliance.Job Type &amp; LocationThis is a Contract to Hire position based out of Glendale, CA.Pay and BenefitsThe pay range for this position is $30.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Glendale,CA.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Engineer IIIJob DescriptionWe are seeking a highly experienced Quality Engineer to lead post-acquisition quality remediation efforts at our Irvine, CA site. This onsite role will focus on the remediation, standardization, and sustainment of Process Failure Mode and Effects Analyses (PFMEAs) and Test Method Validation (TMV) documentation to ensure compliance with internal quality standards and applicable regulatory requirements. This role is ideal for a seasoned medical device quality professional with strong expertise in risk management, test method validation, and measurement system analysis, capable of independently assessing legacy documentation, developing remediation strategies, and collaborating cross-functionally to integrate acquired products and processes into an established Quality Management System (QMS).Responsibilities<ul><li>Lead and execute PFMEA remediation activities, including gap assessments, risk re-evaluations, updates, and alignment to current manufacturing and process states.</li><li>Own the remediation, development, and documentation of Test Method Validations (TMVs) for inspection, test, and measurement methods used in manufacturing and product verification.</li><li>Evaluate legacy test methods for adequacy, robustness, and regulatory compliance; identify gaps and define remediation plans.</li><li>Plan, execute, and review Gage Repeatability &amp; Reproducibility (Gage R&amp;R) studies as part of TMV and measurement system validation activities.</li><li>Apply statistical techniques (e.g., GR&amp;R, bias, linearity, stability) to assess measurement system capability and suitability.</li><li>Ensure PFMEAs and TMVs comply with ISO standards, FDA Quality System Regulation (21 CFR 820), and internal quality procedures.</li><li>Collaborate cross-functionally with R&amp;D, Manufacturing Engineering, Quality Control, and Operations to define test requirements, acceptance criteria, and validation strategies.</li><li>Support integration of acquired products, processes, and test methods into the parent company’s QMS.</li><li>Review and approve TMV protocols, reports, and supporting statistical analyses.</li><li>Facilitate risk management and PFMEA reviews to ensure test methods adequately detect and control product and process risks.</li><li>Ensure TMV and PFMEA changes are properly documented and implemented through formal change control processes.</li><li>Support internal and external audits, inspections, and diligence activities related to test method validation and measurement systems.</li><li>Identify opportunities to improve test method robustness and long-term sustainment of validation practices.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Engineering (Biomedical, Mechanical, Manufacturing, Industrial, or related field).</li><li>5+ years of relevant Quality Engineering experience in the medical device industry.</li><li>Proven experience leading PFMEA development and remediation.</li><li>Strong hands-on experience with Test Method Validation (TMV).</li><li>Familiarity and working knowledge of Gage R&amp;R and measurement system analysis.</li><li>Ability to interpret and apply statistical data to validate inspection and test methods.</li><li>Solid working knowledge of ISO standards and FDA QSR (21 CFR 820).</li><li>Experience supporting remediation efforts in a post-acquisition or compliance-driven environment.</li><li>Ability to work onsite in Irvine, CA.</li><li>Excellent technical writing, analytical, and documentation skills.</li><li>Ability to work independently and effectively lead cross-functional teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience validating mechanical, dimensional, functional, or analytical test methods.</li><li>Proficiency with statistical software or analysis tools (e.g., Minitab, JMP, Excel).</li><li>Experience supporting FDA inspections and/or notified body audits.</li><li>Understanding of verification and validation (V&amp;V) activities and their linkage to risk management.</li><li>Experience with electronic QMS systems (e.g., Agile, Windchill, Arena, MasterControl).</li><li>Medical device manufacturing, inspection, or metrology.</li></ul>Work EnvironmentThis role requires working onsite in Irvine, CA, within a dynamic and collaborative environment. Employees enjoy benefits such as 3 weeks of PTO and 10 paid holidays. The position involves a high level of interaction with cross-functional teams and the use of statistical software and electronic QMS systems.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $55.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Irvine,CA.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

HIRING ASAP! If interested in more information/direct feedback, please reach out to me directly at ghilson@actalentservices. com and attach your resume and contact information.﻿Below are some details about the position:<ul><li>BENEFITS: YES</li><li>PAY: $55-65 an hour depending on experience</li><li>SCHEDULE: On-site, M-F (1st shift).</li></ul><h3>Role Overview</h3>Electronics Manufacturing and Quality Engineer – This person is responsible for maximizing the throughput of a new product by working onsite at the supplier to understand issues, debug in real time, optimize product flow through test/repair/debug areas, and resolve incoming quality issues.<h2>Task Breakdown/Workflow</h2>The overall goal of this role is to maximize throughput / ship the most servers. Best estimates for time allocation:<ul><li>20% — Meetings</li><li>30% — Independent analysis</li><li>50% — Collaborative work with internal and external engineers/technicians</li></ul>This role will be on-site at a supplier (non-client owned building). They will need to sync with other engineers that work for the client on overall program status and the tactical daily plan / top issues.From there, their work may include gathering more information through:<ul><li>Physical inspection on the factory floor</li><li>Reviewing logs, Excel data, etc. from their laptop</li></ul>MUST HAVES:<ul><li>BSME, BSIE, BSEE, or related engineering degree (There is no particular degree or certification needed.)</li><li>5 years of experience in an engineering and/or quality role. 3 years is acceptable if that time has been spent in a factory working directly on electronics. If they mostly spend time in an office and only visit factories, more experience is required. There is no particular degree or certification needed. Candidates may have 3 years of experience plus a BS in an engineering discipline, or 20 years of experience with no degree if they worked their way up in a factory.</li><li>Electronics manufacturing experience - In addition to general manufacturing knowledge, they need to have some understanding of electronics.</li><li>Data analysis - Excel proficiency at a minimum</li><li>Manufacturing and Process Engineering bckgrnd - understand how factory flows work and how to optimize them, identify waste, track material, etc.</li><li>Great communication skills (there will be a lot of interaction with the engineering team as well as supply chain, quality, and vendors)</li></ul>NICE TO HAVES:<ul><li>SQL</li></ul>Job Type &amp; LocationThis is a Contract position based out of Nashville, TN.Pay and BenefitsThe pay range for this position is $55.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Nashville,TN.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineer (2 Positions)

Job Title: Quality Engineer - Systems ManagerJob DescriptionThe Quality Systems Manager is a dynamic quality professional with 3-5 years of experience in a regulated industry. This role involves working closely with the Director of Quality and Regulatory Affairs to maintain and enhance the Quality Management System (QMS) through daily quality system activities in a medical device manufacturing environment. The position demands direct engagement in quality processes to ensure compliance with FDA, MDSAP, EU MDR, and other relevant regulatory requirements.Responsibilities<ul><li>Actively maintain and improve the Quality Management System in a medical device manufacturing environment.</li><li>Ensure compliance with regulatory standards including FDA, MDSAP, and EU MDR.</li><li>Conduct root cause analysis and manage corrective and preventive actions (CAPA).</li><li>Review and manage non-conformance reports (NCR) and material review boards (MRB).</li><li>Collaborate with engineers to complete technical documentation.</li><li>Work across multiple departments to ensure proper and efficient documentation.</li><li>Conduct internal and external audits to uphold quality standards.</li></ul>Essential Skills<ul><li>3-5 years of experience working under ISO13485 standards in a manufacturing environment.</li><li>Proficiency in managing Quality Management Systems.</li><li>Experience with RCA, CAPA, NCR, and MRB processes.</li><li>Ability to work cross-functionally across departments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree highly preferred.</li><li>Engineering exposure is beneficial.</li></ul>Work EnvironmentThe role is based in an office setting with working hours from 8 AM to 5 PM. The work environment is collaborative and supportive, offering daily provided lunches and robust benefits. This is an opportunity to contribute to a growing and dynamic organization.Job Type &amp; LocationThis is a Permanent position based out of Middlebury, CT.Pay and BenefitsThe pay range for this position is $90000.00 - $100000.00/yr.Key benefits reported by employees include health and dental insurance, 403(b) retirement matching, tuition reimbursement, and paid holidays. 
Insurance: Medical and dental insurance options are available.
Retirement: The company offers 403(b) matching.
Time Off: Benefits include paid holidays and approximately 6 days of PTO per year.
Work Culture: Employees often cite a supportive environment with flexibility in time and location.
Career Growth: Opportunities for professional development, such as tuition reimbursement, are offered.Workplace TypeThis is a fully onsite position in Middlebury,CT.Application DeadlineThis position is anticipated to close on Mar 3, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineer -  Systems Manager

For immediate consideration, please apply directly to this job posting AND email me at biacosta @actalentservices.com with the following:1) word copy of resume2) 2-3 professional references3) 4-5 brief bullet points highlighting technical qualifications﻿Job Title: Quality Engineer - NPIJob DescriptionAs a Quality Engineer specializing in New Product Introduction (NPI), you will advocate and lead design for manufacture and assembly through technical leadership in quality assurance and control. Your role will be pivotal in supporting the development and introduction of new products, processes, and technologies, with a focus on quality systems development, regulatory compliance, and process risk management, including pFMEA. You will develop and characterize processes that are capable, scalable, and produce high yield, while also supporting the design of robust inspection strategies including CQA’s, CTQ’s, and MSA’s.Responsibilities<ul><li>Foster collaborative relationships across Design Divisions, Advanced Operations, and Quality functions for successful design transfer activities.</li><li>Communicate effectively with internal customers, stakeholders, and project teams to achieve NPI project goals.</li><li>Mentor other groups on design and process transfer expertise.</li><li>Develop and implement methods for process control, improvement, testing, and inspection to ensure product quality.</li><li>Analyze reports and defective products to identify trends and recommend corrective actions.</li><li>Collaborate with supplier representatives on quality problems and contribute to supplier quality improvement programs.</li><li>Apply risk management practices and tools, ensuring compliance with ISO14971.</li><li>Develop and implement lean inspection strategies and plans using state-of-the-art methods and technologies.</li><li>Lead continuous improvements of inspection methods and sampling plans.</li><li>Support the development and execution of validation strategies to achieve highly capable processes.</li><li>Provide expertise in statistical techniques to develop robust quality systems.</li><li>Lead the supplier qualification strategy and approve supplier validations and PPAP.</li><li>Represent quality assurance during the Design Transfer Agreement Plan process to ensure successful product launches.</li></ul>Essential Skills<ul><li>Bachelor of Science in Engineering or related subject.</li><li>3-5 years of experience in a quality or technical discipline.</li><li>Proficiency in mechanical engineering, quality systems, manufacturing processes, and quality engineering.</li><li>Experience in risk management, design control, and validation, particularly within the medical device sector.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of NPI processes and methodologies.</li><li>Familiarity with medical device regulations and standards.</li></ul>Work EnvironmentThis position requires 100% onsite work in Irvine. The work environment is professional, and the role involves collaborating with various teams to ensure successful project outcomes.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $145600.00 - $156000.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Irvine,CA.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineer - NPI

Job Title: Quality Engineer IIJob DescriptionAs a Quality Engineer II, you will play a crucial role in representing the quality function of technical support in collaboration with other internal support groups to address manufacturing issues. You will be responsible for developing and maintaining QA plans and process routings that align with intended and actual activities, and you will provide support for all quoting activities by participating in the initial phases of process design, development, and implementation.Responsibilities<ul><li>Adhere to all safety and health rules and regulations associated with this position.</li><li>Evaluate and support inspection processes through inspection aids and instruction guidelines.</li><li>Develop and implement specialized training sessions for all applicable functions as part of training programs.</li><li>Conduct periodic review and maintenance of all documentation files and develop appropriate systems for document storage and access.</li><li>Review all supplier or customer discrepancies and coordinate the corrective/preventative action effort.</li><li>Provide trend analysis of defects occurring at the customer, supplier, and internally.</li><li>Participate in vendor survey activities as applicable.</li><li>Drive proactive participation with suppliers and aid in their process improvement efforts.</li><li>Interface with all departments concerning Policies and Procedures, with special emphasis on EN4600 and GMP documentation.</li><li>Monitor departmental activities and provide technical and logistical guidance/support for the quality engineering staff as applicable.</li><li>Provide technical support on quality issues with the customer as needed.</li><li>Support and focus corrective action efforts using SPC data and corrective action tracking packages.</li><li>Serve as a liaison between the company and suppliers or customers on quality-related issues.</li><li>Improve technical support for the quality organization.</li><li>Comply with all procedures within the company security policy.</li></ul>Essential Skills<ul><li>Proficiency in quality engineering, process design, and implementation documentation.</li><li>Experience with PFMEA, AS9102, and conducting FAIRs.</li><li>Strong customer interface skills.</li><li>Ability to conduct internal and third-party audits.</li><li>Good time management skills.</li><li>Ability to organize and support on-site visits.</li><li>Bachelor's degree and two years of related experience, or an equivalent combination of education and experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Demonstrated ability in PFMEA/CP readiness.</li><li>Audit experience both internally and with third parties.</li></ul>Work EnvironmentThe position requires working Monday to Friday in an office setting from 8 AM to 5 PM.Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Petersburg, FL.Pay and BenefitsThe pay range for this position is $100.00 - $100.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Petersburg,FL.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineer III

If interested apply to posting and/or email your resume directly to rdegraw @astoncarter.com (no space between the "w" and the "@")Job Title: Quality EngineerJob DescriptionWe are seeking a dedicated and detail-oriented Entry Level Quality Engineer to join our team. The role involves performing detailed analysis of customer returned parts to drive Corrective and Preventative Action (CAPA) improvements, preventing internal recurring failures, and reducing risks by conducting root cause analysis to identify and address existing issues. This is an entry level position- if you have relevant internship experience within Aerospace, this is the right role for you!Must Have:-Aerospace Engineering Degree-Aerospace Manufacturing Internship Responsibilities<ul><li>Perform detailed analysis of customer returned parts and utilize findings to drive CAPA improvements.</li><li>Prevent internal recurring failures and reduce risks by conducting root cause analysis.</li><li>Validate customer RMAs and implement further actions to enhance manufacturing processes.</li><li>Represent the Quality Assurance team in the material review board (MRB) for internal rejections.</li></ul>Essential Skills<ul><li>Experience with AS9102 and aerospace industry standards-- internship experience is okay.</li><li>Proficiency in root cause analysis and implementing corrective actions.</li><li>Ability to conduct first article inspections and manage audits.</li><li>Experience with material review board (MRB) processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>The position involves overseeing different connector lines.</li></ul>Work Environment A professional and detail-oriented approach is essential in this fast-paced, aerospace-focused setting.Job Type &amp; LocationThis is a Contract to Hire position based out of Glendale, CA.Pay and BenefitsThe pay range for this position is $30.00 - $40.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Glendale,CA.Application DeadlineThis position is anticipated to close on Feb 23, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineer | Entry Level

Job DescriptionWe are seeking a Quality Supervisor with experience in manufacturing and quality assurance to lead hourly production teams and ensure operational excellence. This role is responsible for driving productivity, maintaining compliance with safety and company policies, and ensuring products meet strict quality standards.Responsibilities Include<ul><li>Supervise and coordinate the work activities of hourly production employees to ensure quality and production goals are consistently met.</li><li>Establish and adjust manpower to meet production schedules and quality requirements.</li><li>Maintain accurate time and production records.</li><li>Administer disciplinary action as needed, in alignment with company policies and the collective bargaining agreement.</li><li>Coach, develop, and motivate hourly personnel to achieve performance and quality objectives.</li><li>Inspect products to verify conformance to specifications; assist in problem resolution and general maintenance of machinery as needed.</li><li>Provide daily defect feedback to production employees and management, ensuring transparency and timely corrective action.</li><li>Communicate shop floor problems and defects to appropriate personnel responsible for root cause analysis and corrective action.</li><li>Support the achievement of quality and management objectives by ensuring compliance with quality policies, procedures, and processes.</li><li>Initiate actions to prevent nonconformance related to product, processes, and quality systems.</li><li>Identify and document any issues related to the product, process, or quality system.</li><li>Control further processing, delivery, or installation of nonconforming product until deficiencies are corrected.</li><li>Develop and execute inspection and testing schedules for new launches.</li><li>Set up and oversee containment activities when required.</li><li>Recommend improvements to enhance efficiency, production methods, equipment performance, and product quality.</li><li>Interpret, communicate, and enforce company policies and safety regulations.</li><li>Ensure adherence to the collective bargaining agreement.</li></ul>Skills &amp; Qualifications<ul><li>3+ years relevant experience working in quality</li><li>Root cause analysis experience</li><li>ISO 9001 experience</li><li>IATF experience</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Carey, OH.Pay and BenefitsThe pay range for this position is $30.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Carey,OH.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineering Supervisor

Job Title: Quality Engineering TechnicianJob DescriptionQuality Engineering Technician on our battery assembly line, you will play a critical role in ensuring that our battery modules meet the highest standards of quality and reliability. You will be responsible for inspecting, testing, and verifying that our products comply with industry standards and specifications. This position requires a detail-oriented individual with a strong commitment to quality and continuous improvement.Responsibilities<ul><li>Inspect and test battery modules to ensure compliance with industry standards and specifications.</li><li>Verify product quality through detailed inspections and testing procedures.</li><li>Utilize test equipment such as calipers, micrometers, and multimeters.</li><li>Analyze data to identify trends and areas for improvement.</li><li>Conduct root cause analysis to determine sources of defects and implement effective solutions.</li></ul>Essential Skills<ul><li>Experience in quality control or quality assurance in a manufacturing environment, preferably in the automotive or battery industry.</li><li>Proficiency in using inspection and testing equipment like calipers, micrometers, and multimeters.</li><li>Strong analytical and problem-solving skills with the ability to identify root causes and implement solutions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with quality test and inspection procedures.</li><li>Experience with data analysis related to quality control.</li><li>Knowledge of electronics and quality assurance practices.</li></ul>Work EnvironmentThe role involves working with various testing and inspection tools in a manufacturing environment. A commitment to safety standards and continuous quality improvement is essentialJob Type &amp; LocationThis is a Contract position based out of Garden Grove, CA.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Garden Grove,CA.Application DeadlineThis position is anticipated to close on Feb 22, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineering Technician

Job Title: Quality Engineering TechnicianJob DescriptionQuality Engineering Technician on our battery assembly line, you will play a critical role in ensuring that our battery modules meet the highest standards of quality and reliability. You will be responsible for inspecting, testing, and verifying that our products comply with industry standards and specifications. This position requires a detail-oriented individual with a strong commitment to quality and continuous improvement.Responsibilities<ul><li>Inspect and test battery modules to ensure compliance with industry standards and specifications.</li><li>Verify product quality through detailed inspections and testing procedures.</li><li>Utilize test equipment such as calipers, micrometers, and multimeters.</li><li>Analyze data to identify trends and areas for improvement.</li><li>Conduct root cause analysis to determine sources of defects and implement effective solutions.</li></ul>Essential Skills<ul><li>Experience in quality control or quality assurance in a manufacturing environment, preferably in the automotive or battery industry.</li><li>Proficiency in using inspection and testing equipment like calipers, micrometers, and multimeters.</li><li>Strong analytical and problem-solving skills with the ability to identify root causes and implement solutions.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with quality test and inspection procedures.</li><li>Experience with data analysis related to quality control.</li><li>Knowledge of electronics and quality assurance practices.</li></ul>Work EnvironmentThe role involves working with various testing and inspection tools in a manufacturing environment. A commitment to safety standards and continuous quality improvement is essentialJob Type &amp; LocationThis is a Contract position based out of Garden Grove, CA.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Garden Grove,CA.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Engineering TechnicianJob DescriptionWe are seeking a highly skilled Quality Engineering Technician to join our aerospace manufacturing division. This role is ideal for someone with a strong mechanical aptitude, a deep understanding of engineering documentation, and a passion for driving continuous improvement. You will work closely with Quality, Manufacturing, and Engineering teams to ensure components meet stringent aerospace standards and are optimized for manufacturability.Responsibilities<ul><li>Interpret and apply Geometric Dimensioning &amp; Tolerancing (GD&amp;T) to evaluate part conformity.</li><li>Review engineering drawings, specifications, and customer requirements to ensure compliance.</li><li>Support root cause analysis and corrective action activities using methods such as 5-Why, Fishbone, and DMAIC.</li><li>Collaborate with engineers to assess the manufacturability of components and identify potential risks early in the design or production process.</li><li>Provide feedback on engineering drawings and documentation to improve clarity and reduce ambiguity.</li><li>Assist in developing and updating work instructions, inspection plans, and quality documentation.</li><li>Participate in continuous improvement initiatives focused on reducing defects, improving process capability, and increasing efficiency.</li><li>Support the implementation of lean manufacturing tools such as 5S, standard work, and process mapping.</li><li>Collect and analyze quality data to identify trends and recommend improvements.</li></ul>Essential Skills<ul><li>Strong mechanical aptitude.</li><li>Ability to read high-level GD&amp;T blueprints.</li><li>Experience in root cause analysis.</li><li>Familiarity with quality systems such as AS9100 or ISO 9001.</li><li>Minimum of 2-3 years of experience in a manufacturing environment, preferably aerospace or automotive.</li></ul>Additional Skills &amp; Qualifications<ul><li>Engineering tech or recent engineering graduate with a high level of mechanical aptitude.</li><li>Experience in quality assurance and PPAP (Production Part Approval Process).</li></ul>Work EnvironmentThe work environment involves close collaboration with Quality, Manufacturing, and Engineering teams. The role demands the use of lean manufacturing tools and continuous improvement initiatives. Employees are expected to work in a fast-paced aerospace manufacturing setting, contributing to the high standards of quality and efficiency.Job Type &amp; LocationThis is a Permanent position based out of Murfreesboro, TN.Pay and BenefitsThe pay range for this position is $65000.00 - $80000.00/yr.🏥 Health &amp; Wellness
Generous healthcare plan that rewards positive lifestyle choices
Air-conditioned, clean manufacturing spaces for comfort on the job
Supportive environment focused on employee health and safety
💼 Financial &amp; Retirement
Competitive pay structure
Retirement benefits (details not fully disclosed, but commonly include 401(k) plans)
🌴 Time Off &amp; Work-Life Balance
Paid vacation and time off policies
Flexible attendance system (described as lenient by some employees)
Work-life balance rated moderately well by employees

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

🤝 Company Culture
Family-run business with a culture of trust, fairness, and respect
Emphasis on doing right by associates—“we’re in this together” mentality
Positive reviews from employees who value the team atmosphere and leadership supportWorkplace TypeThis is a fully onsite position in Murfreesboro,TN.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Engineering TechnicianJob DescriptionThe Quality Inspector is responsible for conducting inspections of Uninterruptible Power Supply (UPS), Lithium-Ion Battery Cabinets, and other AC Power products through the manufacturing process. This role ensures all AC power-related components meet design specifications, electrical codes, and internal quality standards prior to the Testing phase in the manufacturing process. The inspector plays a key role in identifying defects, verifying safety compliance, and supporting root-cause analysis for continuous improvement.Responsibilities<ul><li>Inspect assembled UPS units and subcomponents (e.g., inverters, rectifiers, transformers, bypass switches) for electrical and mechanical conformity.</li><li>Review blueprints, schematics, and technical diagrams against physical builds.</li><li>Conduct inspections of AC power products including wiring, grounding, and busing against workmanship standards.</li><li>Evaluate proper torquing, cable routing, labeling, and hardware stack ups in accordance with layout diagrams.</li><li>Document all findings, discrepancies in quality records, and inspection checklist.</li><li>Tag nonconforming units and coordinate with production and engineering to resolve issues.</li><li>Participate in root cause analysis and corrective action implementation for recurring defects or process deviations.</li><li>Collaborate with production line leads and assemblers to promote build quality and safety practices.</li><li>Consult Oracle/PD Cloud or the current operating system for part revision numbers, location and availability of parts, quantity of parts, engineering changes, etc.</li></ul>Essential Skills<ul><li>3-5 years of Quality Technician experience.</li><li>Knowledge of ISO 9001 standards.</li><li>Electrical knowledge.</li><li>Strong understanding of AC power systems and UPS design principles.</li><li>Ability to interpret electrical schematics, wiring diagrams, and mechanical drawings.</li><li>Excellent attention to detail and documentation skills.</li><li>Basic computer proficiency (MS Office), Oracle EBS, Outlook, PowerPoint, CAD.</li><li>Strong communication skills and ability to work cross-functionally with production, quality, and engineering teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of ISO 9001 standards, specifically with Product Planning and Verification Clauses.</li><li>Experienced in lean manufacturing concepts, continuous improvement, and/or Six Sigma methods.</li><li>Familiar with torque wrenches, multi-meters, and calibers.</li></ul>Work EnvironmentThis position operates within a manufacturing work environment. The work schedule is 1st shift from 6:00 AM to 2:30 PM, with overtime required, potentially on Saturdays. The role offers a long-term contract to hire position, with a 9-month period before hiring.Job Type &amp; LocationThis is a Contract position based out of Delaware, OH.Pay and BenefitsThe pay range for this position is $30.00 - $30.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Delaware,OH.Application DeadlineThis position is anticipated to close on Mar 3, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Engineering TechnicianJob DescriptionThe Quality Engineering Technician will be responsible for operating test benches in the R&amp;D engineering lab, conducting various tests, troubleshooting test apparatus, and documenting results. The role involves maintaining mechanical test equipment, calibrating tests, and participating in the development of new technology and product modifications.Responsibilities<ul><li>Operate and maintain test benches and lab equipment to ensure accuracy and efficiency.</li><li>Conduct structural, integrity, end-of-life, and efficiency tests.</li><li>Consult with test requestor and/or lab manager to determine appropriate testing methods.</li><li>Set up and conduct performance tests using standardized formats and procedures.</li><li>Identify and communicate test equipment issues to lead technicians or supervisors.</li><li>Assist with equipment calibration and perform basic test bench maintenance.</li><li>Conduct specialized testing without written procedures.</li><li>Fabricate components and assemblies for hydraulic, diesel engine, and alternative power products.</li><li>Build prototypes and retrofit vehicles with products and data acquisition systems.</li><li>Troubleshoot test bench circuits, field equipment systems, and components.</li><li>Maintain a clean and safe work environment.</li><li>Effectively communicate technical information.</li></ul>Essential Skills<ul><li>Mechanical aptitude and testing experience.</li><li>Proficiency in Microsoft Excel and software literacy.</li><li>Experience with Labview and troubleshooting.</li><li>Engineering and automotive manufacturing knowledge.</li><li>Understanding of hydraulics, hydraulic assembly, and valves.</li><li>Ability to read and interpret engineering drawings.</li><li>Fabrication experience in multiple disciplines.</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma or GED with 10+ years of relevant experience.</li><li>Associate's degree preferred.</li><li>Advanced knowledge of test equipment and standards.</li><li>Technical experience in fluid handling, filtration, or diesel engines.</li><li>Advanced computer literacy skills.</li><li>Understanding data logging equipment, dosing systems, and injector characterization stations.</li><li>Strong attention to detail and organizational skills.</li><li>Self-starter with creative and inquisitive nature.</li><li>Excellent interpersonal and communication skills.</li></ul>Work EnvironmentThe work environment is focused on the durability and efficiency of filters for liquid applications, such as diesel fuel. The role requires mechanical testing and upkeep of test benches. The shift is Monday – Thursday from 2:00 p.m. to 11:30 p.m. and Friday from 2:00 p.m. to 6:00 p.m. The dress code is engineering casual with a collared shirt, and personal protective equipment such as safety shoes and safety glasses are required in labs.Job Type &amp; LocationThis is a Permanent position based out of MINNEAPOLIS, MN.Pay and BenefitsThe pay range for this position is $22.00 - $26.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in MINNEAPOLIS,MN.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Environmental Monitoring SpecialistJob DescriptionWe are seeking a Quality Environmental Monitoring Specialist to join our team on the first shift. This role is pivotal in ensuring the cleanliness and safety of our cleanrooms and controlled areas through rigorous environmental monitoring and adherence to quality standards.Responsibilities<ul><li>Perform environmental monitoring of cleanrooms and controlled areas, including viable air, non-viable particles, critical surface monitoring, and personnel monitoring.</li><li>Collect routine environmental samples, including surfaces, air, and water.</li><li>Maintain accurate and complete documentation of sampling information and results in compliance with Good Documentation Practices (GDP).</li><li>Label environmental samples appropriately and submit them to the laboratory via LIMS.</li><li>Submit finished good products for additional testing.</li><li>Review and perform trending on environmental monitoring results.</li><li>Adhere to internal quality procedures related to proper gowning, hygiene, and microbial control to maintain cleanliness within cleanrooms.</li><li>Assist in the development and implementation of processes, reports, data analysis, and procedures within the defined area.</li></ul>Essential Skills<ul><li>High school graduate or GED required.</li><li>Associate or bachelor’s degree in biology, microbiology, or a science-related field preferred.</li><li>0 to 2 years of work experience within a manufacturing environment, with GMP experience preferred.</li><li>Attention to detail in relation to sampling techniques, with previous experience with environmental monitoring and aseptic technique preferred.</li><li>Strong time management skills, communication skills, and critical thinking skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with LIMS or submission of samples to a laboratory.</li><li>Experience working with aseptic technique within an FDA-regulated environment.</li><li>Past participation in regulatory audits (FDA, ISO, etc.).</li></ul>Work EnvironmentThis position operates on the 1st shift from 8:00am-4:30pm. The role is part of a Quality Assurance team consisting of 7 people, including 6 QA Engineers. You will also collaborate with 9-10 Quality Control team members conducting in-process testing and visual inspections. Job Type &amp; LocationThis is a Contract to Hire position based out of Gurnee, IL.Pay and BenefitsThe pay range for this position is $24.00 - $30.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Gurnee,IL.Application DeadlineThis position is anticipated to close on Mar 1, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Environmental Monitoring Specialist

Job Title: Quality Improvement EngineerJob DescriptionWe are seeking a dedicated Quality Improvement Engineer to maintain and enhance the Quality Management System (QMS) at our Brooksville, FL facility. The role involves ensuring compliance with current standards and driving continuous improvement strategies focused on process improvements and the QMS.Responsibilities<ul><li>Maintain and continuously improve the QMS to comply with newly released standards, including ISO 9001.</li><li>Assist with internal audits at various facilities in compliance with ISO standards or NADCAP standards.</li><li>Drive continuous improvement strategies with a focus on process improvements and QMS.</li><li>Facilitate Advanced Product Quality Planning techniques to achieve organizational product quality levels using company metrics and visual aids.</li><li>Collaborate with Program Managers, Engineering, and Operations to ensure new product transfers to Production align with approved data.</li><li>Mentor and support First Article Inspectors and Quality Inspectors to ensure compliance with QMS and customer product specifications.</li><li>Interface with customers regarding all quality requirements, including PPAPs, Validations (IQ, OQ, PQ), complaints, SCARs, CARs, on-site audits, and product quality requirements.</li><li>Manage product inspection activities, including FAI’s, PPAP’s, Validation’s, In-Process, and final inspections.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering or a Technical discipline, or equivalent combination of education and experience.</li><li>Minimum of 4 years' experience as a Quality Assurance Engineer in a Manufacturing Environment.</li><li>American Society for Quality (ASQ) Certified Quality Engineer (CQE) is recommended.</li><li>Self-starter with the ability to motivate others.</li><li>Leadership skills with the ability to make decisions and delegate appropriately.</li><li>Strong written and oral communication skills.</li><li>Experience in good manufacturing practices and quality initiatives.</li><li>In-depth experience with QMS systems, including ISO standards.</li><li>Ability to develop and maintain a team-oriented work environment.</li><li>Strong working knowledge of injection molding processes.</li><li>Experience in implementing continuous improvement, lean, or other process improvement techniques.</li><li>Strategic thinker with experience in statistical analysis and trend identification.</li></ul>Apply to learn more!Job Type &amp; LocationThis is a Permanent position based out of Port Richey, FL.Pay and BenefitsThe pay range for this position is $80000.00 - $110000.00/yr.medical
dental
vision
401k matchWorkplace TypeThis is a fully onsite position in Port Richey,FL.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Improvement Engineer

Job Title: Quality Improvement EngineerJob DescriptionWe are seeking a dedicated Quality Improvement Engineer to maintain and enhance the Quality Management System (QMS) at our Brooksville, FL facility. The role involves ensuring compliance with current standards and driving continuous improvement strategies focused on process improvements and the QMS.Responsibilities<ul><li>Maintain and continuously improve the QMS to comply with newly released standards, including ISO 9001.</li><li>Assist with internal audits at various facilities in compliance with ISO standards or NADCAP standards.</li><li>Drive continuous improvement strategies with a focus on process improvements and QMS.</li><li>Facilitate Advanced Product Quality Planning techniques to achieve organizational product quality levels using company metrics and visual aids.</li><li>Collaborate with Program Managers, Engineering, and Operations to ensure new product transfers to Production align with approved data.</li><li>Mentor and support First Article Inspectors and Quality Inspectors to ensure compliance with QMS and customer product specifications.</li><li>Interface with customers regarding all quality requirements, including PPAPs, Validations (IQ, OQ, PQ), complaints, SCARs, CARs, on-site audits, and product quality requirements.</li><li>Manage product inspection activities, including FAI’s, PPAP’s, Validation’s, In-Process, and final inspections.</li><li>Review and approve employee evaluations.</li><li>Encourage and manage employee development, including counseling and motivation.</li><li>Represent and promote the organization's goodwill and interests throughout the community.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering or a Technical discipline, or equivalent combination of education and experience.</li><li>Minimum of 4 years' experience as a Quality Assurance Engineer in a Manufacturing Environment.</li><li>American Society for Quality (ASQ) Certified Quality Engineer (CQE) is recommended.</li><li>Self-starter with the ability to motivate others.</li><li>Leadership skills with the ability to make decisions and delegate appropriately.</li><li>Strong written and oral communication skills.</li><li>Experience in good manufacturing practices and quality initiatives.</li><li>In-depth experience with QMS systems, including ISO standards.</li><li>Ability to develop and maintain a team-oriented work environment.</li><li>Strong working knowledge of injection molding processes.</li><li>Experience in implementing continuous improvement, lean, or other process improvement techniques.</li><li>Strategic thinker with experience in statistical analysis and trend identification.</li></ul>Additional Skills &amp; Qualifications<ul><li>Travel to other worksites or customer locations: 20% (Must have a personal vehicle with a valid driver's license).</li><li>Limited physical effort required, must be able to carry at least 30lbs.</li><li>Duties are typically performed seated, must be able to sit and type for long periods; involves bending, reaching, pushing, and pulling.</li></ul>Work EnvironmentThis position requires working onsite from Monday to Friday. The role involves working with various technologies and requires adherence to specific standards and practices.Job Type &amp; LocationThis is a Permanent position based out of Port Richey, FL.Pay and BenefitsThe pay range for this position is $80000.00 - $110000.00/yr.medical
dental
vision
401k matchWorkplace TypeThis is a fully onsite position in Port Richey,FL.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Improvement EngineerJob DescriptionWe are seeking a dedicated Quality Improvement Engineer to maintain and enhance the Quality Management System (QMS) at our Brooksville, FL facility. The role involves ensuring compliance with current standards and driving continuous improvement strategies focused on process improvements and the QMS.Responsibilities<ul><li>Maintain and continuously improve the QMS to comply with newly released standards, including ISO 9001.</li><li>Assist with internal audits at various facilities in compliance with ISO standards or NADCAP standards.</li><li>Drive continuous improvement strategies with a focus on process improvements and QMS.</li><li>Facilitate Advanced Product Quality Planning techniques to achieve organizational product quality levels using company metrics and visual aids.</li><li>Collaborate with Program Managers, Engineering, and Operations to ensure new product transfers to Production align with approved data.</li><li>Mentor and support First Article Inspectors and Quality Inspectors to ensure compliance with QMS and customer product specifications.</li><li>Interface with customers regarding all quality requirements, including PPAPs, Validations (IQ, OQ, PQ), complaints, SCARs, CARs, on-site audits, and product quality requirements.</li><li>Manage product inspection activities, including FAI’s, PPAP’s, Validation’s, In-Process, and final inspections.</li><li>Review and approve employee evaluations.</li><li>Encourage and manage employee development, including counseling and motivation.</li><li>Represent and promote the organization's goodwill and interests throughout the community.</li></ul>Essential Skills<ul><li>Bachelor's degree in Engineering or a Technical discipline, or equivalent combination of education and experience.</li><li>Minimum of 4 years' experience as a Quality Assurance Engineer in a Manufacturing Environment.</li><li>American Society for Quality (ASQ) Certified Quality Engineer (CQE) is recommended.</li><li>Self-starter with the ability to motivate others.</li><li>Leadership skills with the ability to make decisions and delegate appropriately.</li><li>Strong written and oral communication skills.</li><li>Experience in good manufacturing practices and quality initiatives.</li><li>In-depth experience with QMS systems, including ISO standards.</li><li>Ability to develop and maintain a team-oriented work environment.</li><li>Strong working knowledge of injection molding processes.</li><li>Experience in implementing continuous improvement, lean, or other process improvement techniques.</li><li>Strategic thinker with experience in statistical analysis and trend identification.</li></ul>Additional Skills &amp; Qualifications<ul><li>Travel to other worksites or customer locations: 20% (Must have a personal vehicle with a valid driver's license).</li><li>Limited physical effort required, must be able to carry at least 30lbs.</li><li>Duties are typically performed seated, must be able to sit and type for long periods; involves bending, reaching, pushing, and pulling.</li></ul>Work EnvironmentThis position requires working onsite from Monday to Friday. The role involves working with various technologies and requires adherence to specific standards and practices.Job Type &amp; LocationThis is a Permanent position based out of Port Richey, FL.Pay and BenefitsThe pay range for this position is $80000.00 - $110000.00/yr.medical
dental
vision
401k matchWorkplace TypeThis is a fully onsite position in Port Richey,FL.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality InspectorPosition SummaryWe are seeking adetail-oriented Quality Inspector to support welding, fabrication, and assemblyoperations by ensuring products meet company, customer, and industry qualitystandards. This role focuses heavily on weld inspection, dimensionalverification, and workmanship evaluation throughout incoming, in-process, andfinal manufacturing stages. The Quality Inspector works closely with Productionand Quality teams to identify nonconformances, maintain compliance, and supportconsistent product quality.Responsibilities·      Perform visual weld inspections in accordance with engineering drawings,weld symbols, and applicable acceptance criteria.·      Verify weld size, profile, continuity, and workmanship against specifiedrequirements.·     Identify weld discontinuities such as cracks, porosity, lack of fusion,undercut, overlap, or distortion.·      Confirm adherence to welding procedures and fabrication standards.·      Support weld traceability and documentation requirements.·      Communicate weld-related quality concerns directly with welders,supervisors, and quality leadership.Incoming, In-Process &amp; Final Inspection·      Perform incoming inspections of castings, machined parts, fabricatedcomponents, and purchased materials.·      Conduct in-process inspections during fabrication and assembly to ensurecompliance with specifications.·      Complete final inspections verifying dimensional accuracy, fit-up, torquerequirements, alignment, and overall product quality.·      Use inspection tools including calipers, micrometers, gauges, andmeasurement devices.	Nonconformance &amp; Documentation·      Document inspection results and maintain accurate quality records.·      Initiate and support nonconformance reports (NCRs) and containmentactivities.·      Assist with Material Review Board (MRB) processes by providing inspectionfindings and supporting documentation.	Quality &amp; Production Support·      Monitor production processes for adherence to work instructions andquality standards.·       Verify calibration status ofinspection tools and measuring equipment.·       Support internal audits and continuousimprovement initiatives.·       Maintain organized inspection areasand promote safe work practices.Qualifications<ul><li>High school diploma or equivalent; technical or vocational training preferred.</li><li>Experience in manufacturing inspection, welding, or fabrication environments.</li><li>Ability to read and interpret engineering drawings, weld symbols, and fabrication specifications.</li><li>Knowledge of visual weld inspection practices; familiarity with AWS standards preferred.</li><li>Experience using mechanical measurement tools.</li><li>Strong attention to detail and problem-solving skills.</li></ul>Preferred <ul><li>AWS Certified Welding Inspector (CWI) or relevant welding inspection training.</li><li>Experience with ISO 9001 quality systems.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Westfield, MA.Pay and BenefitsThe pay range for this position is $86000.00 - $107000.00/yr.Health insurance
Dental insurance
Vision insurance
Life insurance
Paid time off (PTO)
401(k)
401(k) matching (noted in some job postings)
Flexible Spending Account (FSA)
Tuition reimbursement
Employee Assistance Program (EAP)Workplace TypeThis is a fully onsite position in Westfield,MA.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Inspector

Job Title: Quality InspectorJob DescriptionAs a Quality Inspector, you will oversee the inspection of incoming components, conduct in-line and in-process checks, issue labels, and manage special projects. You will also be involved in AQL inspections in case of customer complaints and manage rework processes. The role involves handling over 1200 samples for each production lot and performing quality checks throughout the manufacturing and packaging processes.Responsibilities<ul><li>Perform quality checks of medical products throughout the manufacturing and packaging process.</li><li>Inspect products for defects on bottles, totes, caps, and other packaging.</li><li>Pull labels on batch records for production personnel to use on external packaging.</li><li>Document all quality checks, inspections, and batch record information.</li><li>Ensure production personnel follow GMP's, SOP's, FDA regulations, and quality processes.</li></ul>Essential Skills<ul><li>Quality control experience.</li><li>High School Diploma.</li><li>Computer literacy in document writing such as NCRs, NCMRs, and Batch Records.</li><li>Understanding federal regulations is a plus.</li><li>Experience with GMP, although this can be trained.</li><li>Legible writing and ability to work cross-functionally with production.</li><li>Strong verbal communication skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Quality Auditing.</li><li>Line Auditing.</li><li>Batch Record Review.</li><li>Labeling.</li><li>Experience with NCRs and Deviations.</li><li>GMP and FDA knowledge.</li></ul>Work EnvironmentThis position is for the 1st shift, from 7am to 3:30pm Monday through Thursday, and 5am to 1:30pm on Fridays, with some flexibility. Extended hours may be required occasionally, but there is flexibility for early start or late finish. You will work with drugs, cosmetics, and medical device manufacturers, primarily producing lubricating jellies, shampoos, and saline syringes. 50% of the role involves floor inspections and auditing, while the other 50% involves office work, preparing documentation and project-based tasks. Holidays are paid, with 2 weeks of prorated vacation, and the company encourages career growth from within.Job Type &amp; LocationThis is a Contract to Hire position based out of Hartland, WI.Pay and BenefitsThe pay range for this position is $20.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Hartland,WI.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Description
					Performs inspection of manufacturing goods during the manufacturing process. Conducts dimensional and electrical inspection of sub-assemblies or final systems assemblies. Interprets prints, manufacturing drawings, diagrams, wire cards and lists in approving or rejecting in-process or final assemblies. This position requires knowledge that is acquired through experience, specialized education or training. The role has clearly defined procedures and tasks as well as defined guidelines to aid in decision making
										Skills
					Inspection, Quality control, gd&amp;t, Quality inspection, Micrometer, Quality assurance, Calipers, Blueprint, Quality check, first article, medical device, clean room, gmp
										Top Skills Details
					Inspection,Quality control,gd&amp;t,Quality inspection,Micrometer
										Additional Skills &amp; Qualifications
					he job requires a basic understanding of work routines and procedures in own discipline. The technical procedures for this level are well defined. The job is expected to follow detailed and defined rules / instructions and to make simple judgement in straightforward situations. Typically requires selecting between solutions already established.
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract position based out of Ventura, CA.Pay and BenefitsThe pay range for this position is $23.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Ventura,CA.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Please consider applying if you currently hold GE or Collins DQR certification or can recertify quickly if your certification is inactive.<ul><li>5+ years of aerospace inspection experience</li><li>Familiarity with GE Aviation or Raytheon supplier portal requirements</li></ul>For immediate consideration, please email your resume and interview availability to (sanmalik@actalentservices.com) today or tomorrow. I will be conducting interviews this week and next.<h2 style="text-align:center;">Now Hiring: DQR Quality Inspector – Aerospace Excellence Awaits</h2>📍 Hartford County, CT | Onsite RoleAre you a seasoned DQR Quality Inspector with a passion for aerospace precision? Join a company with 80 years of innovation, a people-first culture, and a reputation for quality that takes flight every day. We’re looking for an experienced inspector who thrives in a fast‑paced aerospace environment and takes pride in ensuring every part meets the highest standards.This is a 100% onsite role at our Hartford County facility, where your expertise will play a critical role in delivering precision components to some of the biggest names in aerospace.<hr><h2>Why You’ll Love This Role</h2>✈️ Work on critical aerospace components📐 Be the authority on dimensional quality and conformance🤝 Collaborate with experts across engineering, manufacturing, and quality🏆 Join a company recognized as a 2025 Mental Health America Bell Seal – Platinum Recipient<hr><h2>What You’ll Do</h2><ul><li>Perform precision dimensional inspections to verify compliance with blueprints, customer specs, and certification requirements.</li><li>Balance your time 50/50 between in‑process and final inspections, ensuring quality at every stage.</li><li>Prepare and review First Article Inspection Reports (FAI), PPAP documentation, and ECAV submissions.</li><li>Partner with internal teams to troubleshoot technical challenges and resolve customer issues.</li><li>Audit inspection processes and produce clear, detailed inspection reports that stand up to scrutiny.</li></ul><hr><h2>What You Bring</h2><h3>Required Expertise</h3><ul><li>5+ years of aerospace inspection experience with deep dimensional inspection knowledge.</li><li>Active GE or Collins DQR certification, or previously held with the ability to recertify quickly.</li><li>Strong experience with FAI, PPAP, and customer-driven quality requirements.</li><li>Direct exposure to GE Aviation, Raytheon Technologies, and other major aerospace OEMs.</li><li>Confidence using inspection equipment, software, and quality systems.</li></ul><h3>Nice to Have</h3><ul><li>A.S. degree in engineering, manufacturing, or a related technical field (or equivalent experience).</li><li>Hands-on experience with GE and Raytheon supplier portals.</li><li>Knowledge of ESA, VSE, and SPS processes.</li><li>Familiarity with DFAR and ITAR export compliance requirements.</li></ul><hr><h2>The Team &amp; Culture</h2><h2>You’ll join a collaborative group of seven inspectors and one inspection supervisor, all reporting to a supportive Quality Manager. Our team values technical excellence, accountability, and continuous improvement—within a company culture recognized nationally for its commitment to employee well-being.</h2>Job Type &amp; LocationThis is a Permanent position based out of East Hartford, CT.Pay and BenefitsThe pay range for this position is $68640.00 - $79040.00/yr.Competitive PTO Package
Paid Company Holidays
401K Match Program
Medical, Dental, Vision Benefits
Tuition Reimbursement/Assistance ProgramWorkplace TypeThis is a fully onsite position in East Hartford,CT.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Inspector Engineer

Job DescriptionWe are seeking a dedicated Quality Lab Technician to join our team in a lab setting. The role involves conducting various tests and measurements to ensure product quality and compliance with standards.Responsibilities• Manage product check‑in procedures and verify specifications of finished goods.• Conduct mechanical testing, including strength and tensile assessments.• Perform precise width measurements with accuracy. • Prepare samples for GC analysis, run tests, and accurately log all results.• Review products to ensure compliance with established color standards.• Test and validate seal strength performance.• Document and maintain detailed records of all laboratory test results. Essential Skills<ul><li>Quality control and assurance experience.</li><li>Laboratory skills.</li><li>Associates degree or high school diploma with quality or laboratory experience.</li><li>Experience with GC and chemistry.</li><li>Ability to work in a fast-paced environment such as production, manufacturing, or food service.</li></ul>Work environment<ul><li>2nd shift hours: 3pm - 11pm</li><li>Training will be on 1st shift for first 4-6 weeks from 7am - 3:00pm</li><li>With shift differential pay it comes out to $22.05/hr</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Addison, IL.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Addison,IL.Application DeadlineThis position is anticipated to close on Feb 25, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Lab Technician

Job Title: Quality Lab TechnicianJoin our dynamic team as a Quality Lab Technician, where you will play a crucial role in ensuring the quality of production batches. You will perform a variety of quality tests and work closely with the Quality Department to maintain high standards in product specifications.Responsibilities<ul><li>Conduct all prescribed testing of production batches according to established methods.</li><li>Ensure all batches meet required color limits and specifications before filling.</li><li>Verify that the product remains within specifications at the time of filling.</li><li>Approve final fill check panels for production.</li><li>Perform quality testing including color, gloss, viscosity, and physical properties.</li><li>Determine adjustments needed to meet quality specifications.</li><li>Keep accurate records of batch adjustments and fill checks on batch tickets.</li><li>Follow all ISO procedures.</li><li>Prepare fill check panels and provide approvals for filling.</li><li>Consult with the Quality Manager on quality issues.</li><li>Work on short-term projects to improve the efficiency of the Quality Department.</li><li>Transfer hazardous wastes to the satellite hazardous waste area as needed.</li><li>Ensure proper labeling of hazardous waste containers.</li><li>Maintain clean and organized workstations and retain storage areas.</li></ul>Essential Skills<ul><li>1-2 years of experience in Quality Control (QC) lab.</li><li>Knowledge of wet chemistry and quality assurance practices.</li><li>Familiarity with testing color, gloss, viscosity, and physical properties.</li><li>Basic math knowledge including percentages and fractions.</li><li>Ability to multi-task and handle various responsibilities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Industry-related QC lab experience preferred but not required.</li><li>Willingness to ask questions.</li><li>Experience in production and familiarity with pulling samples.</li></ul>Work EnvironmentThe position involves working 90% in the lab and 10% on the floor, handling hazardous materials. Lab attire includes wearing lab glasses, button-up shirts, and pants. Job Type &amp; LocationThis is a Contract to Hire position based out of Elk Grove Village, IL.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Elk Grove Village,IL.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Lab TechnicianJoin our dynamic team as a Quality Lab Technician, where you will play a crucial role in ensuring the quality of production batches. You will perform a variety of quality tests and work closely with the Quality Department to maintain high standards in product specifications.Responsibilities<ul><li>Conduct all prescribed testing of production batches according to established methods.</li><li>Ensure all batches meet required color limits and specifications before filling.</li><li>Verify that the product remains within specifications at the time of filling.</li><li>Approve final fill check panels for production.</li><li>Perform quality testing including color, gloss, viscosity, and physical properties.</li><li>Determine adjustments needed to meet quality specifications.</li><li>Keep accurate records of batch adjustments and fill checks on batch tickets.</li><li>Follow all ISO procedures.</li><li>Prepare fill check panels and provide approvals for filling.</li><li>Consult with the Quality Manager on quality issues.</li><li>Work on short-term projects to improve the efficiency of the Quality Department.</li><li>Transfer hazardous wastes to the satellite hazardous waste area as needed.</li><li>Ensure proper labeling of hazardous waste containers.</li><li>Maintain clean and organized workstations and retain storage areas.</li></ul>Essential Skills<ul><li>1-2 years of experience in Quality Control (QC) lab.</li><li>Knowledge of wet chemistry and quality assurance practices.</li><li>Familiarity with testing color, gloss, viscosity, and physical properties.</li><li>Basic math knowledge including percentages and fractions.</li><li>Ability to multi-task and handle various responsibilities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Industry-related QC lab experience preferred but not required.</li><li>Willingness to ask questions.</li><li>Experience in production and familiarity with pulling samples.</li></ul>Work EnvironmentThe position involves working 90% in the lab and 10% on the floor, handling hazardous materials. Lab attire includes wearing lab glasses, button-up shirts, and pants. Job Type &amp; LocationThis is a Contract to Hire position based out of Elk Grove Village, IL.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Elk Grove Village,IL.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Assurance TechnicianJob DescriptionWe are seeking a detail-oriented and proactive Quality Assurance Technician to join our team in a fast-paced food manufacturing environment. The QA Technician plays a critical role in ensuring that all products meet company and regulatory standards for safety, quality, and consistency. This position involves monitoring production processes, conducting inspections, and maintaining accurate documentation to support food safety and quality systems.Responsibilities<ul><li>Perform routine quality checks on raw materials, in-process products, and finished goods.</li><li>Monitor and enforce Good Manufacturing Practices (GMPs), sanitation procedures, and food safety protocols.</li><li>Conduct environmental and product sampling for microbiological and chemical testing.</li><li>Verify compliance with HACCP, FDA, USDA, and other regulatory requirements.</li><li>Maintain and calibrate QA equipment such as scales, thermometers, and pH meters.</li><li>Document and report non-conformances, assist in root cause analysis, and support corrective actions.</li><li>Collaborate with production and sanitation teams to ensure quality standards are upheld.</li><li>Assist in internal audits and support external inspections.</li><li>Maintain accurate records of inspections, test results, and quality metrics.</li><li>Participate in continuous improvement initiatives and training programs.</li></ul>Essential Skills<ul><li>1–2 years of experience in food manufacturing or quality assurance.</li><li>Knowledge of HACCP, GMPs, and food safety regulations.</li><li>Strong attention to detail and organizational skills.</li><li>Ability to work independently and as part of a team.</li><li>Proficient in Microsoft Office and basic data entry.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate or bachelor’s degree in food science, biology, or related field preferred.</li><li>Knowledge of cGMP, quality control, and food safety.</li><li>Eagerness and motivation to learn the Quality Process.</li></ul>Work EnvironmentThis position follows a 12-hour block schedule, working 2 days on and 2 days off, from 6:30 PM to 6:45 AM. Flexibility to cover other shifts when needed is required. The work environment involves spending half of the shift in the lab testing products and the other half retrieving samples and conducting line checks. Conditions may be cold, wet, or noisy, and require standing for extended periods.Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $22.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Lab TechnicianJob DescriptionWe are seeking a detail-oriented and proactive Quality Assurance Technician to join our team in a fast-paced food manufacturing environment. The QA Technician plays a critical role in ensuring that all products meet company and regulatory standards for safety, quality, and consistency. This position involves monitoring production processes, conducting inspections, and maintaining accurate documentation to support food safety and quality systems.Responsibilities<ul><li>Perform routine quality checks on raw materials, in-process products, and finished goods.</li><li>Monitor and enforce Good Manufacturing Practices (GMPs), sanitation procedures, and food safety protocols.</li><li>Conduct environmental and product sampling for microbiological and chemical testing.</li><li>Verify compliance with HACCP, FDA, USDA, and other regulatory requirements.</li><li>Maintain and calibrate QA equipment such as scales, thermometers, and pH meters.</li><li>Document and report non-conformances, assist in root cause analysis, and support corrective actions.</li><li>Collaborate with production and sanitation teams to ensure quality standards are upheld.</li><li>Assist in internal audits and support external inspections.</li><li>Maintain accurate records of inspections, test results, and quality metrics.</li><li>Participate in continuous improvement initiatives and training programs.</li></ul>Essential Skills<ul><li>1–2 years of experience in food manufacturing or quality assurance.</li><li>Knowledge of HACCP, GMPs, and food safety regulations.</li><li>Strong attention to detail and organizational skills.</li><li>Ability to work independently and as part of a team.</li><li>Proficiency in Microsoft Office and basic data entry.</li></ul>Additional Skills &amp; Qualifications<ul><li>An associate or bachelor’s degree in food science, biology, or related field is preferred.</li><li>Comfortable working in cold, wet, or noisy environments and standing for extended periods.</li></ul>Work EnvironmentThe work environment involves half of the shift in the lab testing products and the other half retrieving samples and doing line checks. The position follows a day shift schedule with 12-hour block schedules, working 2 days on and 2 days off from 6:30 am to 6:45 pm. Flexibility to pick up other shifts when others are on PTO is required. The company produces Italy's finest chocolate and other ingredients for well-known products and is willing to train eager and motivated individuals in the Quality Process.Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $21.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality Lab TechnicianJob DescriptionWe are seeking a detail-oriented and proactive Quality Assurance Technician to join our team in a fast-paced food manufacturing environment. The QA Technician plays a critical role in ensuring that all products meet company and regulatory standards for safety, quality, and consistency. This position involves monitoring production processes, conducting inspections, and maintaining accurate documentation to support food safety and quality systems.Responsibilities<ul><li>Perform routine quality checks on raw materials, in-process products, and finished goods.</li><li>Monitor and enforce Good Manufacturing Practices (GMPs), sanitation procedures, and food safety protocols.</li><li>Conduct environmental and product sampling for microbiological and chemical testing.</li><li>Verify compliance with HACCP, FDA, USDA, and other regulatory requirements.</li><li>Maintain and calibrate QA equipment such as scales, thermometers, and pH meters.</li><li>Document and report non-conformances, assist in root cause analysis, and support corrective actions.</li><li>Collaborate with production and sanitation teams to ensure quality standards are upheld.</li><li>Assist in internal audits and support external inspections.</li><li>Maintain accurate records of inspections, test results, and quality metrics.</li><li>Participate in continuous improvement initiatives and training programs.</li></ul>Essential Skills<ul><li>1–2 years of experience in food manufacturing or quality assurance.</li><li>Knowledge of HACCP, GMPs, and food safety regulations.</li><li>Strong attention to detail and organizational skills.</li><li>Ability to work independently and as part of a team.</li><li>Proficiency in Microsoft Office and basic data entry.</li></ul>Additional Skills &amp; Qualifications<ul><li>An associate or bachelor’s degree in food science, biology, or related field is preferred.</li><li>Comfortable working in cold, wet, or noisy environments and standing for extended periods.</li></ul>Work EnvironmentThe work environment involves half of the shift in the lab testing products and the other half retrieving samples and doing line checks. The position follows a day shift schedule with 12-hour block schedules, working 2 days on and 2 days off from 6:30 am to 6:45 pm. Flexibility to pick up other shifts when others are on PTO is required. The company produces Italy's finest chocolate and other ingredients for well-known products and is willing to train eager and motivated individuals in the Quality Process.Job Type &amp; LocationThis is a Contract to Hire position based out of Saint Louis, MO.Pay and BenefitsThe pay range for this position is $21.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job DescriptionWe are seeking a dedicated Quality Lab Technician to join our team in a lab setting. The role involves conducting various tests and measurements to ensure product quality and compliance with standards.Responsibilities• Manage product check‑in procedures and verify specifications of finished goods.• Conduct mechanical testing, including strength and tensile assessments.• Perform precise width measurements with accuracy. • Prepare samples for GC analysis, run tests, and accurately log all results.• Review products to ensure compliance with established color standards.• Test and validate seal strength performance.• Document and maintain detailed records of all laboratory test results. Essential Skills<ul><li>Quality control and assurance experience.</li><li>Laboratory skills.</li><li>Associates degree or high school diploma with quality or laboratory experience.</li><li>Experience with GC and chemistry.</li><li>Ability to work in a fast-paced environment such as production, manufacturing, or food service.</li></ul>About ActalentActalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.Diversity, Equity &amp; InclusionAt Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&amp;I Are Embedded Into Our Culture Through:<ul><li>Hiring diverse talent</li><li>Maintaining an inclusive environment through persistent self-reflection</li><li>Building a culture of care, engagement, and recognition with clear outcomes</li><li>Ensuring growth opportunities for our people</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Addison, IL.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Addison,IL.Application DeadlineThis position is anticipated to close on Feb 25, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Lead (2nd Shift)Job DescriptionPromote the company's overall goals and collaborate with all necessary functions to ensure the shop floor has the resources needed to meet objectives in safety, quality, delivery, and cost. Ensure all inspection team members understand and follow safety policies to maintain a safe workplace.Responsibilities<ul><li>Oversee efficient product flow through quality processes (including first piece, first article, received/purchased product, and in-process), performing inspections as required.</li><li>Ensure nonconforming material is processed according to established procedures and dispositioned promptly.</li><li>Coordinate training activities for Quality and other relevant personnel as needed.</li><li>Prioritize and oversee daily tasks of Quality Inspectors and NDT personnel.</li><li>Maintain IM&amp;T equipment, ensuring timely calibration and proper control of lost, damaged, or out-of-service equipment per procedure.</li><li>Ensure inspection, measuring, and testing equipment is used, handled, stored, and maintained according to QMS and/or manufacturer instructions.</li><li>Maintain work areas in compliance with the 5S system.</li><li>Collaborate with all departments to develop effective fabrication methods that maintain productivity and quality.</li><li>Work with Engineering to determine required fixtures and tooling for production.</li><li>Assist in evaluating and reviewing departmental employees.</li><li>Verify first article packages for completeness and accuracy before submission to the Quality Engineer.</li><li>Help create, develop, and implement programs for Coordinate Measuring Machine (CMM) using Calypso software and inspection arm.</li><li>Set up and operate CMM and inspection arm using existing inspection programs.</li><li>Verify and validate CMM and inspection arm programs per Shapes quality procedures, including correlation using secondary inspection methods.</li><li>Complete DSQR certification training as required by customers and perform DSQR inspections.</li><li>Assist with Source Inspection alongside internal and external DQRs.</li><li>Perform other related duties as assigned.</li></ul>Essential Skills<ul><li>10 years of Quality/Manufacturing experience.</li><li>Demonstrate people management skills.</li><li>Experience with Value Stream Mapping (VSM) of production hardware.</li><li>5S experience.</li><li>Effective in dealing with multiple priorities and simultaneous projects.</li><li>Knowledge of basic math and analytical skills.</li><li>Ability to read drawings and knowledge of GD&amp;T.</li><li>Understanding of customer specifications and AS9100 specifications.</li><li>Good written and verbal communication skills.</li><li>Experience in a demanding fast-paced environment.</li><li>Proficiency with computers and software, including MS Office applications.</li><li>Working knowledge with ERP systems, IFS is a plus.</li></ul>Additional Skills &amp; Qualifications<ul><li>2 years of quality supervisory experience preferred.</li><li>Calypso CMM experience REQUIRED.</li><li>Experience in aerospace/defense industry.</li><li>Knowledge of Machining, Painting, Sheet Metal, and Welding practices beneficial.</li></ul>Work EnvironmentWork in a manufacturing, fabrication, welding tooling shop. The engineering team has cubicles off of the large, clean, indoor machine shop. Clients are in aviation and aerospace, focusing on tooling and fabrication of parts.Job Type &amp; LocationThis is a Permanent position based out of Palm Bay, FL.Pay and BenefitsThe pay range for this position is $50000.00 - $64000.00/yr.health/dental/vision insurance, 401(k) with company match, life/disability insurance, paid time off (PTO), tuition reimbursement, and wellness programs like counseling/dietitian accessWorkplace TypeThis is a fully onsite position in Palm Bay,FL.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Lead

Job Title: Quality LeadJob DescriptionAs a Quality Lead, you will be responsible for ensuring all activities align with our Quality Management System. You will lead a team in creating, revising, and optimizing both offline and online CMM programs and reports, ensuring adherence to customer print specifications. You will also delegate programming and production support priorities within the CMM Programming/Operating team.Responsibilities<ul><li>Create CMM setup and operational instructions specific to parts and machines.</li><li>Analyze and interpret CMM reports to verify compliance with customer specifications.</li><li>Train inspectors in the use of CMM and guide CMM programmers on complex parts and processes.</li><li>Oversee daily and weekly maintenance of CMM machines and ensure that the CMM Software (Calypso) is up-to-date and maintained.</li><li>Ensure correct storage and backup of all programs and data generated by CMM machines.</li><li>Support the QC team with First Article Inspection (FAI), In-Process, or Final Inspection activities as needed.</li><li>Prepare detailed inspection reports, including written descriptions of inspection results and statistical analysis reports.</li><li>Provide technical assistance and training to production, manufacturing engineering, and quality personnel.</li><li>Act as a technical expert on GD&amp;T and interpretation of ASME Y14.5M, staying current with standards, terminology, and inspection methodologies.</li><li>Follow internal inspection procedures and maintain inspection records.</li><li>Maintain the ERP system according to company policies.</li><li>Stay current with industry inspection techniques, practices, and required standards.</li><li>Perform First Piece, Lot, and Final Inspections against customer requirements.</li><li>Perform additional duties as assigned, such as Calibration, Audits, CAPA, Customer Complaints, and RMAs.</li></ul>Essential Skills<ul><li>Eligibility to obtain Secret level security clearance.</li><li>Strong verbal and written communication skills.</li><li>Experience with First Article Inspection and data reporting.</li><li>Proven ability to troubleshoot CMM faults.</li><li>Experience in CMM work is required.</li><li>2+ years of experience with Calypso Zeiss CMM software preferred, but PC-DMIS experience is acceptable.</li><li>Calypso programming language experience.</li><li>Thorough knowledge of Geometric Dimensioning and Tolerancing (GD&amp;T).</li><li>Willingness to work overtime.</li><li>Ability to meet deadlines.</li></ul>Additional Skills &amp; Qualifications<ul><li>Aerospace experience desired.</li></ul>Work EnvironmentThis role is within a mid-size manufacturing company specializing in the Aerospace and Defense industry. The workplace is a CNC shop environment, noted for being very clean compared to non-A&amp;D shops. The company is in the process of streamlining engineering and quality processes for operational efficiency. The environment is stable, offers the potential to gain a Secret Clearance, and combines the resources of a larger company with the close-knit atmosphere of a small company.Job Type &amp; LocationThis is a Contract to Hire position based out of Reisterstown, MD.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Reisterstown,MD.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job TitleQuality ManagerJob DescriptionWe are seeking a dedicated Quality Manager to lead our Quality Management System. This role requires a proactive individual who can lead by example, promote continuous improvement, and implement risk-based thinking. You will be responsible for interpreting and implementing ISO 9001 standards, as well as coordinating and supporting audits.Responsibilities<ul><li>Interpret and implement ISO 9001 standards.</li><li>Coordinate and support surveillance and recertification audits conducted by external providers.</li><li>Evaluate audit findings and implement corrective actions.</li><li>Facilitate Management Review meetings.</li><li>Maintain quality metrics dashboard and QMS board postings monthly.</li><li>Manage internal audit processes and analyze data for improvement.</li><li>Develop, recommend, and monitor corrective and preventive actions.</li><li>Facilitate CAPA and OFI review meetings.</li><li>Ensure quality records retention and control.</li><li>Maintain and schedule annual calibration for measuring equipment.</li><li>Monitor risk management activities according to ISO 9001:2015.</li><li>Promote a quality culture within the organization.</li></ul>Skills and Qualifications Required<ul><li>Proven experience in quality engineering, assurance, and supplier quality.</li><li>Bachelor's degree in Quality Engineering, Manufacturing Engineering, Operations, Business Administration, or a related field. An Associate degree with experience in metal fabrication may be substituted.</li><li>Five plus years of experience in managing or supervising quality assurance and quality control in a manufacturing setting.</li><li>Familiarity with welding, fabrication, and machining specifications.</li><li>Strong analytical and problem-solving skills.</li></ul>Work EnvironmentThe role involves selecting quality equipment, inspection tools, and software to support the inspection team. The Quality Manager will work closely with purchasing and suppliers to ensure quality requirements are met and will be required to conduct supplier quality audits. The position also involves investigating customer complaints and developing corrective actions.Job Type &amp; LocationThis is a Permanent position based out of Green Bay, WI.Pay and BenefitsThe pay range for this position is $100000.00 - $120000.00/yr.Health, vision, dental and competitive PTOWorkplace TypeThis is a fully onsite position in Green Bay,WI.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Manager

Job Title: Quality ManagerJob DescriptionWe are seeking a dedicated Quality Manager to work on-site at a supplier facility, focused on maximizing the throughput of a new product. The role involves collaborating closely with the supplier to understand and resolve issues in real time, optimizing the flow of products through test, repair, and debug areas, and addressing any incoming quality issues.Responsibilities<ul><li>Collaborate with suppliers to understand and resolve production issues in real-time.</li><li>Optimize product flow through test, repair, and debug areas.</li><li>Address and resolve incoming quality issues efficiently.</li><li>Conduct root cause analysis to improve manufacturing processes.</li><li>Track material flow and identify areas of waste for optimization.</li><li>Utilize data analysis tools to assess production timelines and performance.</li></ul>Essential Skills<ul><li>Bachelor's degree in Mechanical, Industrial, Electrical Engineering or a related field.</li><li>5 years of experience in engineering and/or quality roles.</li><li>Proficiency in quality engineering and root cause analysis.</li><li>Understanding of manufacturing and process engineering.</li><li>Basic data analysis skills with Excel proficiency.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in electronics manufacturing.</li><li>Proficiency in SQL is a plus.</li><li>Experience with consumer electronics or similar products.</li><li>3-5 years of experience working in a factory setting, especially with electronics.</li></ul>Work EnvironmentThis role is based on-site at a supplier facility, working closely with the team to ensure quality and production efficiency. The position requires hands-on involvement in the manufacturing process and troubleshooting in real-time.Job Type &amp; LocationThis is a Contract position based out of Nashville, TN.Pay and BenefitsThe pay range for this position is $55.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Nashville,TN.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Position OverviewResponsible for strengthening and advancing the organization’s Quality Management System (QMS) through targeted improvements, while promoting a culture centered on ongoing operational enhancement using Lean, Six Sigma, and related process‑improvement tools.<hr><h3>Essential Duties</h3>Quality Management System (QMS):<ul><li>Review, update, and refine the current QMS to support organizational expansion and align with evolving industry standards.</li><li>Maintain adherence to ISO requirements and all other relevant regulatory expectations.</li></ul>Audits &amp; Compliance:<ul><li>Organize, execute, and oversee both internal and external audit activities.</li><li>Create and manage corrective and preventive action strategies in response to identified gaps.</li></ul>Continuous Improvement:<ul><li>Guide Lean and Six Sigma efforts to streamline processes and minimize inefficiencies.</li><li>Lead improvement initiatives across manufacturing, operations, and supporting departments.</li></ul>Root Cause Analysis &amp; Corrective Measures:<ul><li>Analyze product or process issues using structured problem‑solving techniques.</li><li>Implement robust corrective and preventive actions to prevent repeat issues.</li></ul>Leadership &amp; Culture:<ul><li>Champion a workplace culture that emphasizes ownership, quality, and operational excellence.</li><li>Train and coach employees on quality expectations, methods, and best‑practice standards.</li></ul>Metrics &amp; Reporting:<ul><li>Establish and track key performance metrics related to quality outcomes.</li><li>Communicate quality trends, risk areas, and progress on improvements to leaders.</li></ul><h3>Knowledge, Skills, and Experience Requirements</h3><ul><li>Bachelor’s degree in quality-related studies or a comparable mix of education and hands-on experience that supports strong job performance.</li><li>Degree in Engineering, Quality Management, or a similar discipline (Master’s degree is a plus).</li><li>At least 5 years of experience working in quality oversight or management within a manufacturing setting.</li><li>Solid understanding of ISO 9001 requirements and certification practices.</li><li>Experience working with Lean principles, Six Sigma tools, and continuous improvement systems (Green Belt or Black Belt certification is advantageous).</li><li>Demonstrated ability to perform root cause investigations and drive corrective measures.</li><li>Experience in coordinating audits and maintaining regulatory compliance.</li><li>Strong leadership abilities with excellent communication and analytical thinking skills.</li><li>Skilled in using Microsoft Office programs and database or record‑keeping systems.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Mankato, MN.Pay and BenefitsThe pay range for this position is $90000.00 - $130000.00/yr.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental &amp; vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Mankato,MN.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Quality ManagerJob DescriptionWe are seeking a dedicated Quality Manager to develop, implement, and enforce food safety standards and quality assurance programs. This role involves ensuring compliance with food safety regulations, managing HACCP and regulatory audits, and conducting food safety training programs. Responsibilities<ul><li>Develop, interpret, and implement Quality Assurance and Quality Control procedures and standards, including SOPs, KPIs, and GMPs.</li><li>Evaluate the adequacy of current Quality Assurance and Quality Control standards.</li><li>Ensure compliance with all statutory and system requirements.</li><li>Devise sampling procedures and instructions for recording and reporting quality data.</li><li>Review and enhance the efficiency of quality and inspection systems.</li><li>Plan, conduct, and monitor testing and inspection of materials and products to ensure finished product quality.</li><li>Document internal audits and other quality assurance activities.</li><li>Investigate customer complaints and non-conformance issues, and develop corrective and preventative actions.</li><li>Analyze data to identify areas for improvement in the quality system and prepare reports to communicate outcomes of quality activities.</li><li>Identify training needs and organize training interventions to meet quality standards.</li><li>Coordinate and support on-site audits conducted by external providers and evaluate audit findings to develop and implement corrective actions.</li><li>Ensure quality of processes from supplier materials for production.</li><li>Seek ways to reduce waste and increase efficiency within the organization.</li><li>Manage document systems related to quality management.</li><li>Implement best practices in quality management and related areas.</li><li>Promote product quality and customer service excellence to achieve business goals and culture.</li></ul>Essential Skills<ul><li>3-5 years of experience in food safety/quality in food or food packaging manufacturing.</li><li>Experience implementing SQF quality systems.</li><li>Experience with HACCP and leading SQF Audits.</li><li>Experience developing new SOPs.</li><li>Strong creative problem-solving skills.</li><li>Proficiency in Microsoft Word, Excel, and PowerPoint.</li></ul>Additional Skills &amp; Qualifications<ul><li>Food safety/Audit certifications.</li><li>GFSI certification.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Buffalo Grove, IL.Pay and BenefitsThe pay range for this position is $60000.00 - $100000.00/yr.standard company benefits - will get more infoWorkplace TypeThis is a fully onsite position in Buffalo Grove,IL.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Learn more about free job search tools, learning opportunities, and exclusive member events.

Discover CareerCircle

Access resources to advance your job search and career growth.

Tools & Training

Explore a wide range of job opportunities that match your skills and career goals.

Search Jobs

Create a professional resume that captures the attention of top employers with our easy-to-use tool.

Resume Builder

Prepare for your next interview with our expert tips and strategies.

Interview Prep

Discover in-depth profiles of leading employers to find your ideal workplace.

Search Companies

Develop in-demand skills with curated courses for today’s job market.

Courses

Access career resources and job postings anytime, anywhere with our app.

Mobile App

Source skilled talent and build your team.

Talent Acquisition

Access skilled talent ready to excel via our AI-driven platform, virtual events, and recruitment services.

CareerCircle TalentConnect

Transform your workforce and hiring practices with essential training and continuing education.

InclusiveU

Broaden your talent pool with dedicated support for individuals with disabilities.

Getting Hired Powered by CareerCircle

Mission aligned solutions supporting Non-Profit Organizations, Educational Institutions, Local Workforce Development Boards, and Learning Providers.

Upskilling & Job Advocacy

Upskilling solutions designed to empower members with in-demand skills training and ongoing support for successful certificate completion.

CareerReady

Job advocacy solutions to connect job seekers to inclusive employers through dedicated recruiting support.

CareerAdvocacy

Learn how we connect all communities with careers and build skilled talent pipelines.

About CareerCircle

Discover answers to common questions and gain insights into our goals and services.

Reach out to us for inquiries, support, or to learn more about our mission and services.

Contact

Explore our blog for latest news and trends for job seekers and employers.

Blog

Access our virtual career fairs, job seeker workshops, and employer focused webinars.

Events

Discover valuable resources to enhance your hiring strategy and drive organizational success.

Employer Resources

Get the latest news and updates on our mission, partnerships, and community impact.

Actalent Jobs

Browse Actalent Jobs

JOB SEEKERS

EMPLOYERS

COMMUNITY PARTNERS

ABOUT

RESOURCES