For immediate consideration, please email resume to jonukwugha@actalentservices.com! I will be conducting the phone screen for this role!Job Title: Quality ManagerJob DescriptionWe are seeking an experienced Quality Manager with a proven track record in leading quality teams within aerospace or similarly regulated manufacturing environments. The ideal candidate will possess strong expertise in AS9100 standards, practical audit execution, and blueprint interpretation, with a focus on GD&amp;T literacy. This role requires hands-on leadership, the ability to manage the MRB process, and to drive corrective actions from identification to closure, while partnering effectively with inspection leadership.Responsibilities<ul><li>Lead the site quality function to ensure aerospace components comply with blueprint and customer certification requirements.</li><li>Stabilize inspection throughput and ensure documentation accuracy following recent staff changes.</li><li>Oversee quality management systems execution, maintain audit readiness, manage MRB cadence, and ensure corrective action closure.</li><li>Collaborate with production, engineering, and leadership teams to prevent product escapes and maintain customer trust.</li></ul>Essential Skills<ul><li>Proven management experience in aerospace quality teams within a production environment.</li><li>Comprehensive understanding of AS9100 standards and audit readiness.</li><li>Strong experience with managing aerospace OEM expectations and customer requirements.</li><li>Expertise in MRB leadership, RCCA, CAPA closure, and nonconformance reduction.</li><li>Capability to stabilize a team and drive throughput without compromising accuracy.</li></ul>Additional Skills &amp; Qualifications<ul><li>Direct experience with GE Aviation, Collins Aerospace, Pratt and Whitney, and Raytheon customer requirements.</li><li>Familiarity with supplier portals, FAI, PPAP, and ECAV workflows.</li><li>Knowledge of DFAR/ITAR export compliance fundamentals.</li><li>Lean or Six Sigma experience for quality throughput and escape reduction.</li><li>DQR awareness and ability to support DQR inspection strategy.</li></ul>Work EnvironmentThis position is based 100% onsite at the East Hartford facility. The work environment involves direct collaboration with inspectors, inspection supervisors, production, and engineering teams. The role demands high urgency, sensitivity to customer needs, and a strong commitment to quality discipline.Job Type &amp; LocationThis is a Permanent position based out of East Hartford, CT.Pay and BenefitsThe pay range for this position is $115000.00 - $145000.00/yr.Competitive base salary with 10 percent annual manager bonus
Comprehensive medical, dental, and vision insurance
401(k) retirement plan with company match
Competitive PTO package
Paid company holidays
Tuition reimbursement and education assistance program
Stable, long‑tenured organization with over 80 years of operation
Strong workplace culture, including recognition as a 2025 Platinum recipient of Mental Health America’s Bell Seal for Workplace Mental Health
Onsite leadership role with direct impact on quality, operations, and customer outcomesWorkplace TypeThis is a fully onsite position in East Hartford,CT.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.

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Quality Manager

Job Title: Quality ManagerJob DescriptionWe are seeking a Quality Manager to lead our Quality Assurance efforts and ensure compliance with ISO 9001 standards. Reporting to the President, this role oversees the company’s Quality Management System, manages audits, and drives quality initiatives across departments. Responsibilities include maintaining quality documentation, developing testing and inspection procedures, and ensuring product quality from raw materials to finished goods. If you are proactive, collaborative, and committed to continuous improvement, we encourage you to apply.Responsibilities<ul><li>Oversee quality checks before products leave the facility and inspect incoming products from customers.</li><li>Coordinate quality activities and participate as part of the staff.</li><li>Conduct and manage ISO 9001:2015 audits.</li><li>Track Key Performance Indicators (KPIs) monthly and address non-conformances.</li><li>Manage scrap numbers and work closely with the molding department to minimize scrap during production startup.</li><li>Supervise a team of 4 direct reports, including 3 quality techs on the first shift and 1 quality tech on the second shift.</li></ul>Essential Skills<ul><li>Experience with ISO audits and ISO 9001 standards.</li><li>Strong understanding of Quality Management Systems in a manufacturing environment.</li><li>Ability to address non-conforming products and implement corrective actions.</li><li>Experience in coordinating quality activities and leading a team.</li><li>Familiarity with plastic injection molding processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in a related industrial, scientific, or business field.</li><li>5–8 years of related experience in manufacturing and production with an emphasis on Quality Management Systems.</li><li>Analytical, critical-thinking, and problem-solving skills to review systems and propose solutions.</li><li>Strong interpersonal, leadership, management, and communication skills.</li><li>Professional certifications and experience with ERP systems are a plus.</li></ul>Work EnvironmentThe role is set within a manufacturing environment, focusing on quality assurance and management. The Quality Manager will work closely with various departments to ensure product quality and compliance with standards. The position involves managing a team across different shifts and requires collaboration with the molding department. The work environment emphasizes continuous improvement, teamwork, and adherence to quality standards.Job Type &amp; LocationThis is a Permanent position based out of Caledonia, WI.Pay and BenefitsThe pay range for this position is $100000.00 - $120000.00/yr.401k
Dental, health, visionWorkplace TypeThis is a fully onsite position in Caledonia,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.

Job Title: Quality Program ManagerJob DescriptionAs a Quality Program Manager, you will manage quality projects and orchestrate results to achieve broad program goals. You will plan and implement schedules and monitor programs from inception through delivery. Your role involves defining and reporting program roadmaps, status updates, development issues, and success metrics. You will identify and monitor areas of risk while continuously seeking opportunities to improve cost, performance, and schedules. You will also build and manage budgets, facilitate communication and coordination among projects, manage stakeholder engagement and satisfaction, and maintain awareness of trends, business conditions, and internal processes impacting component projects or the overall program.Responsibilities<ul><li>Manage quality projects to achieve program goals.</li><li>Plan and implement project schedules from inception through delivery.</li><li>Define and report on program roadmaps, status, development issues, and success metrics.</li><li>Identify and monitor areas of risk.</li><li>Continuously seek opportunities to improve cost, performance, and schedules.</li><li>Build and manage budgets.</li><li>Facilitate communication and coordination among projects.</li><li>Manage stakeholder engagement and satisfaction.</li><li>Maintain awareness of trends, business conditions, and internal processes impacting projects.</li></ul>Essential Skills<ul><li>Expertise in quality engineering and quality assurance.</li><li>Proficiency in root cause analysis and audit processes.</li><li>Experience with medical devices and technical writing.</li><li>Knowledge of ISO standards, non-conformances, investigations, CAPA's, FDA regulations, and risk mitigation.</li><li>Strong writing skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree with 5 - 10 or more years of relevant experience.</li><li>Experience in managing a team of quality engineers.</li></ul>Work EnvironmentThe role is based in an on-site manufacturing setting where innovative medical products and services are developed, manufactured, and marketed to the healthcare industry. These products offer inherent safety features addressing significant healthcare challenges, including opioid abuse, hospital-acquired malnutrition, and hazardous drug exposure. You will lead a team of 10 quality engineers.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $79.00 - $80.00/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 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 Program Manager

Job Title: Quality Program ManagerJob DescriptionAs a Quality Program Manager, you will manage quality projects, maintain CAPA Investigations and orchestrate results to achieve a broad program goal. You will plan and implement schedules, monitor the program from inception through delivery, and define and report program roadmap, status, development issues, and success metrics. Your role involves identifying and monitoring areas of risk, continuously seeking opportunities to improve cost, performance, and schedule. You will build and manage budgets, facilitate communication and coordination among projects, and manage stakeholder engagement and satisfaction. Staying aware of trends, business conditions, and internal processes impacting component projects or the overall program is essential.Responsibilities<ul><li>Manage quality projects and orchestrate results to achieve broad program goals.</li><li>Plan and implement schedules, monitoring the program from inception through delivery.</li><li>Define and report program roadmap, status, development issues, and success metrics.</li><li>Identify and monitor areas of risk.</li><li>Continuously seek opportunities to improve cost, performance, and schedule.</li><li>Build and manage budgets.</li><li>Facilitate communication and coordination among projects.</li><li>Manage stakeholder engagement and satisfaction.</li><li>Maintain awareness of trends, business conditions, and internal processes impacting component projects or the overall program.</li></ul>Essential Skills<ul><li>Quality engineering</li><li>Quality assurance</li><li>Root cause analysis</li><li>Audit</li><li>Medical device expertise</li><li>Technical writing</li><li>Knowledge of ISO standards</li><li>Non-conformances</li><li>Investigations</li><li>Corrective and Preventive Actions (CAPA)</li><li>FDA regulations</li><li>Risk mitigation</li><li>Product discrepancies</li><li>Change control</li><li>Engineering skills</li><li>Strong writing skills</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree</li><li>5 - 10 or more years of experience</li></ul>Work EnvironmentThis role is based on-site at a manufacturing facility. The company develops, manufactures, and markets innovative medical products and services to the healthcare industry. Their products offer inherent safety features addressing significant healthcare challenges, including opioid abuse, hospital-acquired malnutrition, and hazardous drug exposure. You will lead a team of 10 quality engineers.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $79.00 - $80.00/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 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.

Job Title: Quality Program ManagerJob DescriptionAs a Quality Program Manager, you will manage quality projects, maintain CAPA Investigations and orchestrate results to achieve a broad program goal. You will plan and implement schedules, monitor the program from inception through delivery, and define and report program roadmap, status, development issues, and success metrics. Your role involves identifying and monitoring areas of risk, continuously seeking opportunities to improve cost, performance, and schedule. You will build and manage budgets, facilitate communication and coordination among projects, and manage stakeholder engagement and satisfaction. Staying aware of trends, business conditions, and internal processes impacting component projects or the overall program is essential.Responsibilities<ul><li>Manage quality projects and orchestrate results to achieve broad program goals.</li><li>Plan and implement schedules, monitoring the program from inception through delivery.</li><li>Define and report program roadmap, status, development issues, and success metrics.</li><li>Identify and monitor areas of risk.</li><li>Continuously seek opportunities to improve cost, performance, and schedule.</li><li>Build and manage budgets.</li><li>Facilitate communication and coordination among projects.</li><li>Manage stakeholder engagement and satisfaction.</li><li>Maintain awareness of trends, business conditions, and internal processes impacting component projects or the overall program.</li></ul>Essential Skills<ul><li>Quality engineering</li><li>Quality assurance</li><li>Root cause analysis</li><li>Audit</li><li>Medical device expertise</li><li>Technical writing</li><li>Knowledge of ISO standards</li><li>Non-conformances</li><li>Investigations</li><li>Corrective and Preventive Actions (CAPA)</li><li>FDA regulations</li><li>Risk mitigation</li><li>Product discrepancies</li><li>Change control</li><li>Engineering skills</li><li>Strong writing skills</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree</li><li>5 - 10 or more years of experience</li></ul>Work EnvironmentThis role is based on-site at a manufacturing facility. The company develops, manufactures, and markets innovative medical products and services to the healthcare industry. Their products offer inherent safety features addressing significant healthcare challenges, including opioid abuse, hospital-acquired malnutrition, and hazardous drug exposure. You will lead a team of 10 quality engineers.Job Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $79.00 - $80.00/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 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 TechnicianJob DescriptionAs a Quality Technician, you will inspect incoming materials and parts from suppliers using visual and mechanical tools, review and verify First Article Inspection (FAI) from suppliers, and use both conventional and advanced inspection devices to verify dimensions to drawing specifications. You will be responsible for managing or helping manage the calibration program, participating in Material Review Board (MRB) meetings for disposition of non-compliant materials, maintaining records and data as required by the Quality Management System, and recommending improvements to the QMS database to enhance information availability for improvements.Responsibilities<ul><li>Inspect incoming materials and parts using visual and mechanical tools.</li><li>Review and verify First Article Inspection (FAI) from suppliers.</li><li>Use conventional and advanced inspection devices to verify dimensions to drawing specifications.</li><li>Manage or assist in managing the calibration program.</li><li>Participate in MRB meetings for disposition of non-compliant materials.</li><li>Maintain records, data, and related information as required by the Quality Management System.</li><li>Recommend improvements to the QMS database to better provide information for improvements.</li></ul>Essential Skills<ul><li>Proficient with Geometric Dimensioning and Tolerancing (GD&amp;T).</li><li>Experience with CMM inspection and instruments utilizing PC-DMIS.</li><li>Ability to set up inspection for intricate components with tight tolerances.</li><li>Able to interpret blueprints, schematics, and other design documents.</li><li>Proper handling of parts in Class 1,000 (ISO Class 6) cleanroom environment.</li><li>Proper handling of Electro-static sensitive (ESD) components.</li><li>Good organizational, communication, and analytical skills.</li><li>Understanding of ISO 9001 quality systems requirements.</li><li>Proficiency with MS Office Suite, especially Excel, Word, and PowerPoint.</li><li>Ability to work independently with minimal supervision.</li><li>Ability to multitask and prioritize in a dynamic, fast-paced environment.</li><li>Strong attention to detail and accuracy.</li><li>Computer skills and knowledge of software tools for inspection data management.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with calibration, CMM programming, and quality assurance.</li><li>Knowledge of creating standards for inspection and authoring quality reports.</li><li>Familiarity with editing engineering drawings and designs for GD&amp;T.</li></ul>Work EnvironmentYou will be working in a Class 6 cleanroom environment. The position is currently based in Wakefield, with plans to move to a new site in Bedford. Some teams have started the move, and the entire site will be relocated by the end of Q1 at the latest.Job Type &amp; LocationThis is a Contract to Hire position based out of Wakefield, MA.Pay and BenefitsThe pay range for this position is $38.00 - $42.00/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 Wakefield,MA.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 Specialist

<h2 style="text-align:center;">Quality Specialist - Microbiology</h2>Job DescriptionWe are seeking a dedicated Quality Specialist in Microbiology to join our team. This role involves performing daily microbiological testing and ensuring quality control of microbiological supplies. You will be working in a sterile lab environment and collaborating closely with the manufacturing team to perform environmental monitoring. This is an excellent opportunity for professionals looking to enhance their skills in microbiological validation and quality assurance.<h2>PAY - $22/hour</h2>Responsibilities<ul><li>Conduct daily microbiological testing, including work under a sterile hood, spread plate techniques, enrichments, sub-cultures, gram staining, coagulation tests, AI20E, fungal identification, and microscope work.</li><li>Perform quality control of microbiological supplies and growth promotion testing.</li><li>Conduct water testing and complete paperwork in SAP and by hand following SOPs and GMPs.</li><li>Perform environmental monitoring and swabbing in the manufacturing areas at scheduled times.</li><li>Coordinate the shipping of samples for outsourced testing to third-party labs.</li></ul>Essential Skills<ul><li>Proficiency in microbiology and aseptic techniques.</li><li>Strong understanding of cleaning and disinfection procedures.</li><li>Detailed documentation and reporting skills.</li><li>Experience with gram staining, spread plate techniques, and membrane filtration.</li></ul>Additional Skills &amp; Qualifications<ul><li>BS Degree in Biology required, Master’s degree preferred.</li><li style="text-align:center;">Experience in quality control, GMP, laboratory settings, and environmental monitoring is a plus.</li></ul>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 - $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.

Quality Specialist - Microbiology

Quality Specialist - MicrobiologyJob DescriptionWe are seeking a dedicated Quality Specialist in Microbiology to join our team. This role involves performing daily microbiological testing and ensuring quality control of microbiological supplies. You will be working in a sterile lab environment and collaborating closely with the manufacturing team to perform environmental monitoring. This is an excellent opportunity for professionals looking to enhance their skills in microbiological validation and quality assurance.Responsibilities<ul><li>Conduct daily microbiological testing, including work under a sterile hood, spread plate techniques, enrichments, sub-cultures, gram staining, coagulation tests, AI20E, fungal identification, and microscope work.</li><li>Perform quality control of microbiological supplies and growth promotion testing.</li><li>Conduct water testing and complete paperwork in SAP and by hand following SOPs and GMPs.</li><li>Perform environmental monitoring and swabbing in the manufacturing areas at scheduled times.</li><li>Coordinate the shipping of samples for outsourced testing to third-party labs.</li></ul>Essential Skills<ul><li>Proficiency in microbiology and aseptic techniques.</li><li>Strong understanding of cleaning and disinfection procedures.</li><li>Detailed documentation and reporting skills.</li><li>Experience with gram staining, spread plate techniques, and membrane filtration.</li></ul>Additional Skills &amp; Qualifications<ul><li>BS Degree in Biology required, Master’s degree preferred.</li><li>Experience in quality control, GMP, laboratory settings, and environmental monitoring is a plus.</li></ul>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 - $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 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.

Job Title: Quality Systems EngineerJob DescriptionWe are seeking a Quality Systems Engineer responsible for maintaining IATF / ISO 9001 compliance and conducting audit activities. This role involves developing and implementing quality documentation, analyzing SPC data, and resolving out-of-spec issues through root cause analysis.Responsibilities<ul><li>Develop, implement, and control quality documentation, control plans, and specifications.</li><li>Analyze SPC data, monitor capability, and resolve out-of-spec issues.</li><li>Conduct root cause analysis and drive corrective and preventive actions.</li><li>Collaborate with engineering and production on quality standards and process improvements.</li><li>Oversee process audits, inspections, and disposition of nonconforming material.</li><li>Participate in APQP, capability studies, and gauge R&amp;R analysis.</li><li>Manage supplier quality requirements and compliance.</li><li>Prepare and report quality KPIs and performance metrics.</li><li>Support customer quality requirements and satisfaction initiatives.</li><li>Contribute to continuous improvement initiatives and quality training efforts.</li><li>Ensure compliance with regulatory, safety, and legal requirements.</li></ul>Essential Skills<ul><li>Experience in quality engineering, IATF, and ISO 9001.</li><li>Proficiency in root cause analysis and data analysis.</li><li>Capability in IATF / ISO 9001 Lead Auditing.</li><li>Experience with SPC &amp; Statistical Data Analysis.</li><li>Knowledge of APQP, Control Plans, Capability Studies &amp; Gage R&amp;R.</li><li>Experience in Manufacturing Process Quality.</li><li>Supplier &amp; Customer Quality Management expertise.</li><li>Continuous Improvement, Audit, Compliance, Lean Manufacturing, Six Sigma.</li><li>Understanding of Total Quality System and Quality Management System.</li><li>Document control experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Open to working occasionally on weekends.</li><li>Interest in professional growth and taking on future leadership roles.</li><li>Flexibility, teamwork, and interaction with all areas in manufacturing, engineering, and document control.</li><li>Ability to verify part dimensions using engineering drawings/specifications.</li><li>Physical ability to lift 40-50 lbs as needed.</li><li>Willingness to travel domestically and internationally.</li><li>Experience in automotive manufacturing.</li></ul>Work EnvironmentJoin a family-owned company known for its excellence in the processing, manufacturing, and distribution of steel for over 40 years. Enjoy a supportive culture where team events such as spring cookouts and Christmas dinners are common. The company values growth and development, offering opportunities for internal promotion. Uniforms are provided but not mandatory, and monthly giveaways are a perk. Work in a flexible and collaborative environment with options for shifts from 8-5, 7-4, or 9-6. The work setting is an automotive manufacturing environment, with a 5-day work week, primarily from Monday to Friday. The facility is not climate-controlled and involves 70% office work and 30% floor work, with a focus on audits and systems.Job Type &amp; LocationThis is a Permanent position based out of Bowling Green, KY.Pay and BenefitsThe pay range for this position is $75000.00 - $90000.00/yr.Benefits:

401(k)
401(k) matching
Dental insurance
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance
Competitive Pay.
Medical, Dental, and Vision Plans.
Deferred Compensation (401k) Plan with a company match.
No-cost Life Insurance, Short Term Disability, Long Term Disability overages.Workplace TypeThis is a fully onsite position in Bowling Green,KY.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 Systems Engineer

<h2>Job Title: Quality Systems Engineer</h2>Client is unable to provide visa sponsorship now or in the future. Job DescriptionWe are seeking a Quality Systems Engineer responsible for maintaining IATF / ISO 9001 compliance and conducting audit activities. This role involves developing and implementing quality documentation, analyzing SPC data, and resolving out-of-spec issues through root cause analysis.Responsibilities<ul><li>Develop, implement, and control quality documentation, control plans, and specifications.</li><li>Analyze SPC data, monitor capability, and resolve out-of-spec issues.</li><li>Conduct root cause analysis and drive corrective and preventive actions.</li><li>Collaborate with engineering and production on quality standards and process improvements.</li><li>Oversee process audits, inspections, and disposition of nonconforming material.</li><li>Participate in APQP, capability studies, and gauge R&amp;R analysis.</li><li>Manage supplier quality requirements and compliance.</li><li>Prepare and report quality KPIs and performance metrics.</li><li>Support customer quality requirements and satisfaction initiatives.</li><li>Contribute to continuous improvement initiatives and quality training efforts.</li><li>Ensure compliance with regulatory, safety, and legal requirements.</li></ul>Essential Skills<ul><li>Experience in quality engineering, IATF, and ISO 9001.</li><li>Proficiency in root cause analysis and data analysis.</li><li>Capability in IATF / ISO 9001 Lead Auditing.</li><li>Experience with SPC &amp; Statistical Data Analysis.</li><li>Knowledge of APQP, Control Plans, Capability Studies &amp; Gage R&amp;R.</li><li>Experience in Manufacturing Process Quality.</li><li>Supplier &amp; Customer Quality Management expertise.</li><li>Continuous Improvement, Audit, Compliance, Lean Manufacturing, Six Sigma.</li><li>Understanding of Total Quality System and Quality Management System.</li><li>Document control experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Open to working occasionally on weekends.</li><li>Interest in professional growth and taking on future leadership roles.</li><li>Flexibility, teamwork, and interaction with all areas in manufacturing, engineering, and document control.</li><li>Ability to verify part dimensions using engineering drawings/specifications.</li><li>Physical ability to lift 40-50 lbs as needed.</li><li>Willingness to travel domestically and internationally.</li><li>Experience in automotive manufacturing.</li></ul>Work EnvironmentJoin a family-owned company known for its excellence in the processing, manufacturing, and distribution of steel for over 40 years. Enjoy a supportive culture where team events such as spring cookouts and Christmas dinners are common. The company values growth and development, offering opportunities for internal promotion. Uniforms are provided but not mandatory, and monthly giveaways are a perk. Work in a flexible and collaborative environment with options for shifts from 8-5, 7-4, or 9-6. The work setting is an automotive manufacturing environment, with a 5-day work week, primarily from Monday to Friday. The facility is not climate-controlled and involves 70% office work and 30% floor work, with a focus on audits and systems.Job Type &amp; LocationThis is a Permanent position based out of Bowling Green, KY.Pay and BenefitsThe pay range for this position is $75000.00 - $90000.00/yr.Benefits:

401(k)
401(k) matching
Dental insurance
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance
Competitive Pay.
Medical, Dental, and Vision Plans.
Deferred Compensation (401k) Plan with a company match.
No-cost Life Insurance, Short Term Disability, Long Term Disability overages.
PTO: 24 personal hrs, 40 hrs sick, 80 hrs vacation, 10 paid holidays
401k 100% invested up to 5% and 4% match
reviews benefits annuallyWorkplace TypeThis is a fully onsite position in Bowling Green,KY.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.

For immediate consideration, please email resume to jonukwugha@actalentservices.com! I will be conducting the phone screen for this role!Job Title: Quality 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 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 Systems Manager

POSITION SUMMARYThe Quality Systems Manager is a hands-on quality professional with 3–5 years of experience in a regulated industry. This role works closely with the Director of Quality and Regulatory Affairs to actively maintain and improve the Quality Management System (QMS) through daily execution of quality system activities in a medical device manufacturing environment. The position requires direct involvement in quality processes to ensure compliance with FDA, ISO 13485, MDSAP, EU MDR, and other applicable regulatory requirements.PRIMARY RESPONSIBILITIES· Own and execute the Nonconforming Product (NCR) process, including product quarantine, documentation, vendor and supplier communication, product returns and rework, root cause investigations, and issue resolution in collaboration with the QA Engineer.o Serve as the Quality representative on the Material Review Board (MRB) and provide direct support for manufacturing quality issues.o Actively manage quarantine inventory and prepare routine reports on return status and part performance.· Prepare, manage, and document Quality Assurance metrics and performance tracking meetings.o Collect, analyze, and trend quality data such as in-process component performance, final test failures, and other key quality indicators.· Execute employee training activities and maintain training records, ensuring employees are trained to current procedures and quality system requirements.· Actively participate in the Corrective and Preventive Action (CAPA) process, including initiating CAPAs, scheduling meetings, documenting actions, and ensuring timely completion of assigned tasks.· Participate directly in internal and external audits, including preparation, execution, and follow-up activities.o Perform hands-on internal documentation audits to verify compliance with established procedures and regulatory requirements.· Draft, revise, and maintain quality documentation to support regulatory compliance, process changes, and manufacturing updates. Documentation may include Nonconformance Reports, Risk Assessments, ECRs/ECOs, QMS procedures and forms, and other related records.· Perform additional duties and responsibilities as needed to support daily quality operations, regulatory compliance, and evolving business needs.KNOWLEDGE AND SKILL REQUIREMENTS· Strong oral and written communication skills.· Excellent organizational skills with a high level of attention to detail.· Hands-on, investigative mindset with demonstrated root cause analysis skills.· Proficiency in Microsoft Office Suite and basic data analysis tools.· Solid understanding of quality control procedures and applicable regulatory standards.· Working knowledge of ISO 13485, FDA 21 CFR 820, and/or ISO 9001 preferred.· Experience with MDSAP, MDR, MDD, and EU Technical File documentation is a plus.· Technical writing experience is a plus.Job Type &amp; LocationThis is a Permanent position based out of Middlebury, CT.Pay and BenefitsThe pay range for this position is $90000.00 - $125000.00/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 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 Technical Writer - CAPA InvestigationsDescriptionThe candidate will be helping the team by predominantly doing deviation report writing and will work in one of their contained facility labs. They will also be transcribing and editing many documents within their SAP program and helping with investigations.Job Responsibilities - Using 5 why's or Fishbone or other methodology in determining root cause analysis and writing detailed descriptions on the CAPA (corrective actions)- Help heavily with CAPA deviation report writing- Assist with corrective action investigations - Obtain information from team and writing manuals and other sources- Writes descriptions of processes of materials- Help with document redlining - Experience in documenting in SAP System is a plus.Skillstechnical writing, capa, quality assurance, gmp, investigations, non-conformances, writing skills, pharmaceutical, medical deviceTop Skills Detailstechnical writing,capa,quality assurance,gmp,investigations,non-conformancesAdditional Skills &amp; QualificationsBachelors Degree: Scientific degree 3-5 years of experience technical writing Experience writing deviation reports Experience with CAPA is a plusExperience with 5 why's or Fishbone methodologyFDA experienceGDP experiencePharmaceutical experience preferred, open to medical device.Experience LevelIntermediate LevelJob Type &amp; LocationThis is a Contract position based out of Irvine, CA.Pay and BenefitsThe pay range for this position is $40.00 - $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 Irvine,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 Technical Writer

Job Title: Quality TechnicianJob DescriptionThe Quality Technician will work on the engineering team and support engineers with non-routine engineering development activities. This role involves evaluating returned products from customers, providing expertise in inspection methods, and ensuring the correct use of metrology and calibration. The technician will support the inspection of incoming components, materials, in-process inspection of fabricated parts and assemblies, and final inspection before shipments. The Quality Technician will oversee and lead activities within the Quality Lab, ensuring proper use and calibration of measurement instruments.Responsibilities<ul><li>Participate in the development of inspection plans for receiving, in-process, and final inspections.</li><li>Lead and conduct inspections as necessary to support quality lab operations and overall operations requirements.</li><li>Provide training and guidance to inspector staff and operations personnel regarding the correct use and care of metrological instrumentation, storage, and maintenance.</li><li>Inspect metrology for cleanliness, status of calibration, and general good operation.</li><li>Guide and make recommendations regarding the sourcing of new metrology and methods for ongoing improvement of technology.</li><li>Manage rejections of material directly with the supplier, including NC and CA reporting requirements as necessary.</li><li>Oversee calibration processes.</li></ul>Essential Skills<ul><li>Experience with PPAP documentation.</li><li>Proficiency in GD&amp;T and reading/interpreting engineering drawings.</li><li>Experience with measurement instruments such as CMMs (Mitutoyo) and/or calibration devices.</li><li>Familiarity with ISO standards.</li><li>First Article Inspection experience.</li><li>Experience in documentation and records control.</li></ul>Additional Skills &amp; Qualifications<ul><li>An Associate's Degree in Engineering is nice to have.</li><li>Experience with Optical Comparator is beneficial.</li></ul>Work EnvironmentThe position is based at the Kalamazoo facility, which is a satellite operation with 50-60 employees. The Quality Team consists of 2 Quality Engineers, 2 Quality Technicians, and Quality Inspectors. The role involves working in the quality lab, directly supporting the engineering team, with direction from 2 Quality Engineers. Standard work hours range from 40-45 hours per week. The company provides end-to-end contract manufacturing and assembly of medical devices and components, registered with the U.S. FDA and Health Canada. Employees receive 10 days PTO and 6 standard holidays.Job Type &amp; LocationThis is a Contract to Hire position based out of Kalamazoo, MI.Pay and BenefitsThe pay range for this position is $24.00 - $28.00/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 Kalamazoo,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.

Quality Technician

Responsibilities<ul><li>Comply with applicable FDA regulations and ISO requirements.</li><li>Adhere to company Quality Management System (QMS).</li><li>Perform and document incoming, in-progress, and final product acceptance testing.</li><li>Create inspection documents and maintain the incoming inspection room.</li><li>Verify that documents required of suppliers, such as certificates of conformance and first article inspection results, are provided for incoming goods.</li><li>Use standard measuring instruments, gauges, and controlled components to verify functional fit and dimensional checks.</li><li>Test incoming goods, such as electronic devices and PCBs.</li><li>Develop and maintain incoming inspection files and records.</li><li>Document in-house inspection results.</li><li>Update and maintain manufacturing product files upon final inspection and acceptance of products.</li><li>Log defects in the QA defect management reporting system and assist in analysis.</li><li>Create detailed Quality Reports as required, initiate non-conformance reports, and work with Engineering and Manufacturing to resolve problems.</li><li>Review the disposition of parts, sub-assemblies, and products, and release finished goods into inventory.</li><li>Participate in root cause analysis and support corrective and preventive actions.</li><li>Work with Supply Chain in returning nonconforming goods to suppliers.</li><li>Maintain calibration program, including reviews and approvals of calibration reports.</li><li>Analyze problems and recommend changes.</li><li>Support FDA inspections, and external and internal ISO audits.</li></ul>Additional Skills &amp; Qualifications<ul><li>Identification of patterns and trends in unplanned events and non-conformances.</li><li>Meticulous documentation and recordkeeping habits.</li><li>Calibration system maintenance.</li><li>Intermediate Computer skills: Microsoft Office Suite (including PowerPoint, Office, Outlook, Visio, Word, Excel).</li><li>Functional understanding of the ISO International Standard.</li><li>Practical knowledge of the FDA Code of Federal Regulations (CFR), Title 21, Part 820.</li><li>QMS requirements, including nonconformance reporting (NCR), corrective and preventive action (CAPA).</li><li>Incoming, in-process, and outgoing inspection techniques.</li><li>Use of gauges and standard measuring instruments.</li><li>Familiarity with current good manufacturing practices (cGMP).</li><li>Understanding of common manufacturing processes.</li><li>Knowledge of first article inspection (FAI) and certificates of conformance (CofC).</li><li>Support of FDA inspections, and external and internal ISO audits.</li><li>Associate degree preferred.</li><li>1-2 years in a quality assurance role in a regulated industry—medical device manufacturing preferred.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Wheeling, IL.Pay and BenefitsThe pay range for this position is $25.00 - $27.00/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 Wheeling,IL.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.

<h2 style="text-align:center;">Hiring for a Quality Technician in Bloomfield, CT</h2>Job DescriptionThe Quality Technician will provide crucial support for aero-derivative gas turbine programs, extending beyond mere inspection of parts. This role involves reviewing paperwork, inspection plans, working with suppliers to rectify issues, and overseeing first article inspections. Proficiency in Microsoft Office and Excel is essential.Responsibilities<ul><li>Perform inspection of new and overhauled parts received from suppliers.</li><li>Inspect parts stored in the warehouse before they are moved to the parent company/owner.</li><li>Inspect parts at supplier, partner, or customer locations as needed.</li><li>Ensure all supplier documentation is accurate and meets requirements as part of the inspection process.</li><li>Execute supplier source inspections.</li></ul>Essential Skills<ul><li>Quality engineering and materials engineering knowledge.</li><li>Experience with ISO Standards, Auditing, Root Cause Analysis, Quality Standards, and Quality Assurance.</li><li>Mechanical Engineering, including Heat Treating, Brazing, and Welding.</li><li>Proficiency in Process Analysis.</li><li>Bachelor's Degree in a technical field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working effectively with cross-functional groups.</li><li>Ability to develop and sustain change activities.</li><li>Project management skills with proven accomplishments.</li><li>Engineering drawing interpretation and GD&amp;T skills, with the ability to interpret CMM data outputs.</li><li>Hard gaging experience, including the use of calipers and micrometers.</li><li>Ability to engage, interact with, and hold suppliers accountable.</li><li>Experience using root cause analysis tools such as 8D, 5 Whys, and Ishikawa diagrams.</li><li>Strong analytical, problem-solving, and communication skills.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Bloomfield, CT.Pay and BenefitsThe pay range for this position is $80000.00 - $85000.00/yr.Mitsubishi Power Aero offers a comprehensive health package:

Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability coverage
Health &amp; wellness programs

Bonus Program
401KWorkplace TypeThis is a fully onsite position in Bloomfield,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.

Job Title: Quality TechnicianJob DescriptionWe are seeking a diligent Quality Technician to uphold and maintain superior quality standards within our food manufacturing facility. You will be integral in ensuring product compliance and safety while contributing to our commitment to high-quality, organic products.Responsibilities<ul><li>Conduct line clearance to verify that lines are clear before startup.</li><li>Perform equipment swabbing after sanitation procedures.</li><li>Execute quality audits for each production line throughout shifts.</li><li>Document in-line process check results for each production run according to pre-approved specifications.</li><li>Report any Out of Specification (OOS) or non-conformance issues to production and management.</li><li>Ensure immediate corrective actions are implemented before startup for any non-conformance.</li><li>Label and store non-compliant products in designated areas, following the MRB process.</li><li>Perform periodic quality and Good Manufacturing Practice (GMP) audits of production areas, focusing on product handling compliance.</li><li>Audit staged ingredients for manufacturing, ensuring no expired materials are used.</li><li>Conduct temperature audits of ingredients, Work-In-Process (WIP), and finished products during production.</li><li>Prepare shift reports for follow-up by the next shift.</li><li>Perform case count audits on all products.</li><li>Carry out daily pre-operational inspections.</li><li>Assist in metal detector validations and regular in-process metal detector line checks.</li><li>Ensure operators adhere to metal detector Standard Operating Procedures (SOP).</li><li>Report any food safety risks to the supervisor.</li><li>Perform other duties as assigned.</li></ul>Essential Skills<ul><li>Experience in inspection and quality control within a food manufacturing environment.</li><li>Proficiency in GMP practices.</li><li>Ability to work 3rd shift: Monday to Friday, some Saturdays, from 10:00 PM to 6:30 AM.</li><li>Microsoft Office experience.</li><li>Strong communication and organizational skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience in food manufacturing quality assurance.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Bourbonnais, IL.Pay and BenefitsThe pay range for this position is $20.00 - $23.00/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 Bourbonnais,IL.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 Technician Location: Dubuque, Iowa Shift: Offering 1st and 2nd Description<ul><li>Perform product audits on the production floor</li><li>Support specification reviews and communicate quality requirements</li><li>Conduct and document test procedures (air/water/structural testing)</li><li>Build and install test fixtures and prototypes</li><li>Use measurement tools (tape measures, calipers, micrometers) to verify parts</li><li>Partner with Quality Engineers, Operations, and OPD teams to resolve issues</li><li>Participate in root cause investigations and corrective actions</li><li>Maintain quality documentation and standard work instructions</li><li>Assist with calibration and care of quality/test equipment</li><li>Attend daily shift debriefs and contribute to continuous improvement activities</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong computer skills</li><li>Technical degree or related education preferred</li><li>Ability to read and interpret technical drawings/specifications</li><li>Strong communication and interpersonal skills</li><li>Detail-oriented with excellent follow-through</li><li>Comfortable working on the production floor</li><li>Measurement tool familiarity (training provided)</li><li>Interest in long-term growth within Quality</li></ul>Job Type &amp; LocationThis is a Contract position based out of Dubuque, IA.Pay and BenefitsThe pay range for this position is $28.00 - $35.00/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 Dubuque,IA.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.

Quality TechnicianJob DescriptionThis position performs quality inspection and quality acceptance of incoming components, in-progress product assembly, and final product inspection. The role is crucial for ensuring the manufacturing quality of our products. The ideal candidates will have a strong mechanical acumen, with sound logical reasoning and analytical skills.Responsibilities<ul><li>Comply with applicable FDA regulations and ISO requirements.</li><li>Adhere to company Quality Management System (QMS).</li><li>Perform and document incoming, in-progress, and final product acceptance testing.</li><li>Create inspection documents and maintain the incoming inspection room.</li><li>Verify that documents required of suppliers, such as certificates of conformance and first article inspection results, are provided for incoming goods.</li><li>Use standard measuring instruments, gauges, and controlled components to verify functional fit and dimensional checks.</li><li>Test incoming goods, such as electronic devices and PCBs.</li><li>Develop and maintain incoming inspection files and records.</li><li>Document in-house inspection results.</li><li>Update and maintain manufacturing product files upon final inspection and acceptance of products.</li><li>Log defects in the QA defect management reporting system and assist in analysis.</li><li>Create detailed Quality Reports as required, initiate non-conformance reports, and work with Engineering and Manufacturing to resolve problems.</li><li>Review the disposition of parts, sub-assemblies, and products, and release finished goods into inventory.</li><li>Participate in root cause analysis and support corrective and preventive actions.</li><li>Work with Supply Chain in returning nonconforming goods to suppliers.</li><li>Maintain calibration program, including reviews and approvals of calibration reports.</li><li>Analyze problems and recommend changes.</li><li>Support FDA inspections, and external and internal ISO audits.</li></ul>Essential Skills<ul><li>Inspection, Calipers, Blueprint, Micrometer, documentation, ISO, cGMP, Quality measurement, medical device</li><li>Documentation, Quality control, Reporting, Quality assurance, FDA compliance</li></ul>Additional Skills &amp; Qualifications<ul><li>Identification of patterns and trends in unplanned events and non-conformances.</li><li>Meticulous documentation and recordkeeping habits.</li><li>Calibration system maintenance.</li><li>Intermediate Computer skills: Microsoft Office Suite (including PowerPoint, Office, Outlook, Visio, Word, Excel).</li><li>Functional understanding of the ISO International Standard.</li><li>Practical knowledge of the FDA Code of Federal Regulations (CFR), Title 21, Part 820.</li><li>QMS requirements, including nonconformance reporting (NCR), corrective and preventive action (CAPA).</li><li>Incoming, in-process, and outgoing inspection techniques.</li><li>Use of gauges and standard measuring instruments.</li><li>Familiarity with current good manufacturing practices (cGMP).</li><li>Understanding of common manufacturing processes.</li><li>Knowledge of first article inspection (FAI) and certificates of conformance (CofC).</li><li>Support of FDA inspections, and external and internal ISO audits.</li><li>Associate degree preferred.</li><li>1-2 years in a quality assurance role in a regulated industry—medical device manufacturing preferred.</li></ul>Work EnvironmentThis role operates in a mid-sized manufacturing environment, requiring onsite work from Monday to Friday between 7:30 AM and 4:00 PM.Job Type &amp; LocationThis is a Contract to Hire position based out of Lincolnshire, IL.Pay and BenefitsThe pay range for this position is $25.00 - $27.00/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 Lincolnshire,IL.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 TechnicianJob DescriptionWe are seeking a dedicated Quality Technician to join our team. The ideal candidate will be responsible for developing and delivering technical, quality, and on-the-job training to ensure workforce competency and compliance. This role involves creating and managing training materials and providing hands-on instruction in soldering and inspection techniques.Responsibilities<ul><li>Develop and deliver technical, quality, and on-the-job training to ensure workforce competency and compliance.</li><li>Create, maintain, and manage training materials, curricula, certifications, and training records.</li><li>Provide hands-on instruction, including soldering and inspection techniques, for new and existing employees.</li><li>Support quality compliance by communicating inspection results, quality issues, and training needs to cross-functional areas.</li><li>Identify training gaps and recommend improvements to training programs, methods, and materials.</li><li>Perform additional duties as assigned to support operational needs.</li></ul>Essential Skills<ul><li>Strong attention to detail with well-developed observational skills.</li><li>Proficiency in the use of inspection tools and equipment, including calipers, micrometers, gauges, and related measurement devices.</li><li>Working knowledge of quality standards and methodologies such as AS9100, ISO standards, and Lean Manufacturing principles.</li><li>Ability to read, interpret, and train to engineering drawings, blueprints, specifications, and work instructions.</li><li>Strong written and verbal communication skills with the ability to present information clearly to diverse audiences.</li><li>Basic computer proficiency, including Microsoft Office applications and quality management systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma or GED required; technical or vocational training in quality, manufacturing, engineering, or a related field preferred.</li><li>Previous experience in quality, inspection, manufacturing, training, or a related technical role is preferred.</li><li>Demonstrated ability to read, analyze, and interpret technical documents, procedures, and manuals.</li><li>Ability to use and interpret measurement and inspection tools, including calipers, micrometers, feeler gauges, and x-ray (as applicable).</li></ul>Work EnvironmentThe role follows a normal business hours schedule and is an hourly non-exempt position. The work environment is part of an expanding Aerospace and Defense company that is heavily involved with electronics.Job Type &amp; LocationThis is a Permanent position based out of Olathe, KS.Pay and BenefitsThe pay range for this position is $54000.00 - $75000.00/yr.Health, Vision, Dental, 401(K), Holiday, PTOWorkplace TypeThis is a fully onsite position in Olathe,KS.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 TechnicianJob DescriptionThe Quality Technician will be responsible for reviewing products as they progress through the production line, from start to finish. This role is integral to the ramp-up for the snow season, requiring an understanding of basic measurements using micrometers and calipers. Familiarity with CMM is an advantage. The technician will follow the product journey from the fabrication shop through the weld shop to the final product, documenting each stage using programs such as Excel, SharePoint, and Minitab. The role requires basic math skills and involves a balance of 50% documentation and 50% hands-on work.Responsibilities<ul><li>Review and inspect products throughout the production process.</li><li>Utilize micrometers and calipers for measurement.</li><li>Document processes using Excel, SharePoint, and Minitab.</li><li>Understand and apply measurement scales and terminology.</li><li>Perform basic mathematical operations and measurement conversions.</li><li>Select appropriate measuring tools and techniques.</li><li>Measure using surface plate layouts.</li><li>Collaborate with other departments to reduce waste.</li></ul>Essential Skills<ul><li>Proficiency in using calipers and micrometers.</li><li>Strong understanding of quality control and inspection procedures.</li><li>Knowledge of measurement types, scales, and terminology.</li><li>Ability to perform basic math and solve for x.</li><li>Experience with measurement conversions and adding/subtracting degrees, minutes, and seconds.</li><li>Capability to select and use appropriate measuring tools.</li></ul>Additional Skills &amp; Qualifications<ul><li>CMM experience is a plus.</li><li>Familiarity with PPAP and other quality certifications is advantageous.</li><li>Knowledge of quality methodologies such as SPC, 8D, and 5 Whys is beneficial.</li><li>Blueprint reading skills required with detailed understanding.</li><li>Problem-solving and diagnostic skills.</li><li>Good communication skills.</li></ul>Work EnvironmentThe position involves working in a fabrication shop and manufacturing/assembly floor across two different plants. The role includes working across inspection lines, with an emphasis on reducing waste. There is significant room for growth within the quality team, contributing to initiatives aimed at minimizing waste costs.Job Type &amp; LocationThis is a Contract to Hire position based out of Appleton, WI.Pay and BenefitsThe pay range for this position is $23.00 - $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 Appleton,WI.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.

Job Title: Quality TechnicianJob DescriptionIn this role, you will work with tight tolerance parts and be responsible for programming and editing the Coordinate Measuring Machine (CMM) programs. You will support the measurements of the inspection process and be involved in in-process audits. The Quality Technician will complete measurements and inspections of products both in-process and at final stages. Additionally, you will provide support for the certified Quality Management System (QMS) as needed, helping to assure consistent quality of production by validating processes and providing documentation.Responsibilities<ul><li>Program and edit CMM programs.</li><li>Conduct measurements and inspections of products during in-process and final stages.</li><li>Support the Quality Management System and participate in in-process audits.</li><li>Validate production processes to assure consistent quality.</li><li>Provide necessary documentation to support quality assurance.</li></ul>Essential Skills<ul><li>Minimum 3 years of experience with CMMs.</li><li>Proficiency in using calipers and micrometers for measurements.</li><li>Experience with tight tolerance parts in aerospace, automotive, or medical industries.</li><li>Knowledge of inspection techniques, including GD&amp;T, blueprint reading, and quality control.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with PCDMIS or CALYPSO is beneficial.</li><li>Strong attention to detail and analytical skills.</li></ul>Work EnvironmentYou will work in a climate-controlled environment alongside a team consisting of a quality specialist and a quality engineer. The facility operates Monday to Friday, from 7 am to 3:30 pm, with occasional half-days based on production needs. The facility is open from 6 am to 2:30 pm, providing the opportunity for a flexible schedule if required. Our work environment encourages personal ownership and offers opportunities for growth, with a focus on custom manufacturing, variety of work, and a commitment to a 5S environment.Job Type &amp; LocationThis is a Contract to Hire position based out of Pleasant Prairie, WI.Pay and BenefitsThe pay range for this position is $25.00 - $28.00/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 Pleasant Prairie,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.

Job Description: Quality TechnicianResponsibilities <ol><li>Inspecting incoming parts. – Visual inspections, Micrometers and Calipers</li><li>Documentation and quality approval of the work orders. Help with non-confirming reports</li><li>Calibration coordination.</li><li>Documents and training procedures. Managing document changes. Comfortable with computer, getting into Microsoft word.</li></ol>Additional Skills &amp; Qualifications<ul><li>High attention to detail in a regulated environment.</li><li>Associate degree preferred. Highschool or GED required.</li><li>1-2 years of experience in a quality assurance role in a regulated industry—medical device manufacturing preferred.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Long Grove, IL.Pay and BenefitsThe pay range for this position is $25.00 - $27.00/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 Long Grove,IL.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.

Job Title: Quality TechnicianJob DescriptionJoin our team as a Quality Technician, where you will play a crucial role in ensuring the quality and compliance of our products. You will conduct thorough inspections and tests, maintain testing equipment, and collaborate with production teams to address any quality concerns. Your efforts will contribute to continuous improvement initiatives and help us uphold our standards.Responsibilities<ul><li>Perform in-process and final product inspections.</li><li>Conduct tests to ensure compliance with specifications.</li><li>Maintain and calibrate testing equipment.</li><li>Document and report quality issues.</li><li>Work with production teams to resolve quality concerns.</li><li>Assist in audits and continuous improvement initiatives.</li></ul>Essential Skills<ul><li>Proficiency in inspection and quality control.</li><li>Experience with laboratory and quality assurance processes.</li><li>Knowledge of GMP and HACCP</li><li>Ability to conduct quality inspections and checks.</li><li>Understanding of production processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma, Associate's or Bachelor's Degree in Sciences or equivalent.</li><li>2 years of quality experience within manufacturing.</li></ul>Work EnvironmentThis position is 1st shift, Monday through Friday. 6:00am-2:30pm. Job Type &amp; LocationThis is a Contract to Hire position based out of Milwaukee, WI.Pay and BenefitsThe pay range for this position is $23.00 - $28.00/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 Milwaukee,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.

Job Title: Quality TechnicianJob DescriptionThe Quality Technician is responsible for ensuring the highest quality standards in the production of premium sauces. The role involves performing line clearance, equipment swabbing, and quality audits across production lines. The technician will document process check results, report any out-of-specification issues, and ensure corrective actions are completed promptly.Responsibilities<ul><li>Verify that production lines are clear before startup.</li><li>Perform equipment swabbing after sanitation.</li><li>Conduct quality audits on each production line throughout the shift.</li><li>Document in-line process check results according to pre-approved specifications.</li><li>Report any Out of Specification (OOS) or non-conformance issues to production.</li><li>Ensure immediate corrective action is completed before startup for any non-conformance.</li><li>Label and store non-compliant products following the MRB process.</li><li>Perform periodic quality and GMP audits of the production area, particularly at the mix deck.</li><li>Audit staged ingredients to ensure no expired materials are used.</li><li>Conduct temperature audits of ingredients, work-in-progress, and finished products during production.</li><li>Prepare shift reports for follow-up by the next shift.</li><li>Perform case counts audits on all products.</li><li>Execute daily pre-operational inspections.</li><li>Assist in metal detector validations and perform regular in-process metal detector line checks.</li><li>Ensure operators follow metal detector Standard Operating Procedures (SOP).</li><li>Report any food safety risks to the supervisor.</li><li>Collect samples from raw materials, in-process, and finished products for lab testing.</li></ul>Essential Skills<ul><li>Experience in inspection, quality control, and food manufacturing.</li><li>Proficiency in GMP (Good Manufacturing Practices).</li><li>Experience working night shifts: Monday to Friday, and some Saturdays from 10:00 PM to 6:30 AM.</li><li>Microsoft Office proficiency.</li><li>Strong communication and organizational skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in a related field.</li><li>Experience in food manufacturing quality control.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Manteno, IL.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/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 Manteno,IL.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.

Responsibilities<ul><li>Calibrate and verify measuring and test equipment in accordance with ISO quality standards.</li><li>Interpret engineering drawings, technical specifications, and GD&amp;T symbols to validate part conformity.</li><li>Generate detailed inspection reports for incoming, in-process, and final parts, documenting measurements and deviations.</li><li>Collaborate with manufacturing and quality teams to resolve dimensional discrepancies and recommend corrective actions.</li><li>Perform dimensional inspections using precision instruments such as micrometers, bore gauges, dial indicators, calipers, and height gauges.</li><li>Conduct NDT Level 2 MT, UT, and PT testing in the lab, ensuring parts are correct after manufacturing and upon arrival.</li></ul>Essential Skills<ul><li>Proficient in interpreting engineering drawings and GD&amp;T symbols.</li><li>Skilled in using precision instruments like micrometers, calipers, and gauges.</li><li>Experience with documentation review and control.</li><li>Strong understanding of quality assurance, control, and inspection processes.</li><li>Experience with ERP systems.</li><li>Ability to read and understand blueprints and sketches.</li><li>Proficient in heavy documentation tasks.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Chicago, IL.Pay and BenefitsThe pay range for this position is $28.00 - $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 Chicago,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 Title: Quality Engineering TechnicianJob DescriptionWe are seeking an experienced Quality Engineering Technician to join our team. The ideal candidate will be responsible for the qualification and verification of inspection tools, conducting measurement system analyses, and ensuring adherence to compliance and quality system standards. This role demands a detail-oriented individual with experience in engineering technology and precision measurement.Responsibilities<ul><li>Execute inspection tool qualifications in accordance with approved protocols and procedures.</li><li>Measure and verify inspection tools against engineering drawings and specifications.</li><li>Confirm tools meet dimensional, functional, and performance requirements prior to release.</li><li>Support re-qualification activities following tool changes, repairs, or significant use.</li><li>Support and execute measurement system analysis (MSA) studies, including data collection and documentation.</li><li>Assist with bias, linearity, and stability evaluations where applicable.</li><li>Ensure measurement data is collected accurately and consistently.</li><li>Partner with Engineering and Quality to resolve measurement system concerns.</li><li>Generate inspection tool qualification reports, including test methods, results, and acceptance criteria.</li><li>Ensure documentation is complete, accurate, and compliant with ISO and FDA requirements.</li><li>Maintain inspection tool records per document control procedures.</li><li>Assist with out-of-tolerance investigations related to inspection tools and gauges.</li><li>Support root cause activities by collecting measurement data and performing tool checks.</li><li>Document findings and corrective actions in accordance with procedures.</li><li>Support containment actions when inspection tool issues are identified.</li><li>Perform dimensional inspections using hand tools, fixtures, and custom inspection tools.</li><li>Support verification of tools prior to production release or supplier use.</li><li>Follow proper handling and care of inspection tools to maintain accuracy and repeatability.</li><li>Work directly with the Inspection Tool Design Engineer during tool development and qualification.</li><li>Support Quality Engineering during audits, investigations, and validation activities.</li><li>Assist Manufacturing and Incoming Inspection teams with inspection tool usage and questions.</li><li>Perform all activities in compliance with ISO, FDA 21 CFR 820, and internal procedures.</li><li>Follow established procedures for inspection tool qualification, MSA, and change control.</li><li>Support internal and external audits related to inspection and measurement systems.</li></ul>Essential Skills<ul><li>At least 2 years of experience in inspection, metrology, quality, or manufacturing support in a regulated environment.</li><li>Hands-on experience using precision measurement tools such as calipers, micrometers, and gauges.</li><li>Experience supporting or executing measurement system analysis (MSA) activities.</li><li>Ability to read and interpret engineering drawings and GD&amp;T.</li><li>Strong attention to detail and documentation accuracy.</li><li>Fluent in English, both written and verbal communication.</li></ul>Work EnvironmentThis position requires working onsite Monday through Friday from 9 AM to 5 PM. The work environment is collaborative, with opportunities to engage with cross-functional teams in engineering and quality assurance. You will have access to state-of-the-art equipment and tools to support your role.Job Type &amp; LocationThis is a Contract to Hire position based out of Miami, FL.Pay and BenefitsThe pay range for this position is $28.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

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

For immediate consideration, please email resume to jonukwugha@actalentservices.com! I will be conducting the phone screen for this role!<h2 style="text-align:center;">Hiring for a Quality Technician in Bloomfield!</h2>Job DescriptionThe Quality Technician will provide crucial support for aero-derivative gas turbine programs, extending beyond mere inspection of parts. This role involves reviewing paperwork, inspection plans, working with suppliers to rectify issues, and overseeing first article inspections. Proficiency in Microsoft Office and Excel is essential.Responsibilities<ul><li>Perform inspection of new and overhauled parts received from suppliers.</li><li>Inspect parts stored in the warehouse before they are moved to the parent company/owner.</li><li>Inspect parts at supplier, partner, or customer locations as needed.</li><li>Ensure all supplier documentation is accurate and meets requirements as part of the inspection process.</li><li>Execute supplier source inspections.</li></ul>Essential Skills<ul><li>Quality engineering and materials engineering knowledge.</li><li>Experience with ISO Standards, Auditing, Root Cause Analysis, Quality Standards, and Quality Assurance.</li><li>Mechanical Engineering, including Heat Treating, Brazing, and Welding.</li><li>Proficiency in Process Analysis.</li><li>Bachelor's Degree in a technical field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working effectively with cross-functional groups.</li><li>Ability to develop and sustain change activities.</li><li>Project management skills with proven accomplishments.</li><li>Engineering drawing interpretation and GD&amp;T skills, with the ability to interpret CMM data outputs.</li><li>Hard gaging experience, including the use of calipers and micrometers.</li><li>Ability to engage, interact with, and hold suppliers accountable.</li><li>Experience using root cause analysis tools such as 8D, 5 Whys, and Ishikawa diagrams.</li><li>Strong analytical, problem-solving, and communication skills.</li></ul>Work EnvironmentThe work environment is a mid-level high-rise modern office building, primarily employing engineers to work on Aero-Derivative Pratt and Whitney engines for power generation globally. Flexible hours are offered along with banked PTO and multiple employee outings, including contractors and charity events. The facility is sophisticated, supporting the development and manufacturing of energy solutions for power generation with a portfolio of gas turbines ranging from 30 to 140 MW packages.Job Type &amp; LocationThis is a Permanent position based out of Glastonbury, CT.Pay and BenefitsThe pay range for this position is $80000.00 - $85000.00/yr.Mitsubishi Power Aero offers a comprehensive health package:

Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability coverage
Health &amp; wellness programs

Bonus Program
401KWorkplace TypeThis is a fully onsite position in Glastonbury,CT.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 TechnicianJob DescriptionWe are seeking a Quality Technician to support our comprehensive, enterprise-wide Quality Management System. This role is ideal for a candidate who thrives in a fast-paced, cross-functional manufacturing environment.Responsibilities<ul><li>Perform sample inspections and measurements of incoming parts.</li><li>Process non-conforming materials for testing or disposition.</li><li>Conduct First Article Inspections (FAIs) of new parts and/or parts from new suppliers.</li><li>Complete internal audits and associated documentation.</li><li>Interpret engineering prints and schematics.</li><li>Support safety and quality initiatives such as 5S, ESD, FOD, and ISO.</li><li>Assist in the Material Review Board process.</li><li>Maintain information systems.</li><li>Prepare reports by collecting, analyzing, and summarizing data; making recommendations.</li><li>Review, analyze, and report on quality discrepancies.</li></ul>Essential Skills<ul><li>A two-year technical degree is required; a four-year technical degree is preferred</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Pittsburgh, PA.Pay and BenefitsThe pay range for this position is $25.00 - $27.00/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 Pittsburgh,PA.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.

<h2 style="text-align:center;">Hiring for a Quality Technician in Bloomfield!</h2>Job DescriptionThe Quality Technician will provide crucial support for aero-derivative gas turbine programs, extending beyond mere inspection of parts. This role involves reviewing paperwork, inspection plans, working with suppliers to rectify issues, and overseeing first article inspections. Proficiency in Microsoft Office and Excel is essential.Responsibilities<ul><li>Perform inspection of new and overhauled parts received from suppliers.</li><li>Inspect parts stored in the warehouse before they are moved to the parent company/owner.</li><li>Inspect parts at supplier, partner, or customer locations as needed.</li><li>Ensure all supplier documentation is accurate and meets requirements as part of the inspection process.</li><li>Execute supplier source inspections.</li></ul>Essential Skills<ul><li>Quality engineering and materials engineering knowledge.</li><li>Experience with ISO Standards, Auditing, Root Cause Analysis, Quality Standards, and Quality Assurance.</li><li>Mechanical Engineering, including Heat Treating, Brazing, and Welding.</li><li>Proficiency in Process Analysis.</li><li>Bachelor's Degree in a technical field.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working effectively with cross-functional groups.</li><li>Ability to develop and sustain change activities.</li><li>Project management skills with proven accomplishments.</li><li>Engineering drawing interpretation and GD&amp;T skills, with the ability to interpret CMM data outputs.</li><li>Hard gaging experience, including the use of calipers and micrometers.</li><li>Ability to engage, interact with, and hold suppliers accountable.</li><li>Experience using root cause analysis tools such as 8D, 5 Whys, and Ishikawa diagrams.</li><li>Strong analytical, problem-solving, and communication skills.</li></ul>Work EnvironmentThe work environment is a mid-level high-rise modern office building, primarily employing engineers to work on Aero-Derivative Pratt and Whitney engines for power generation globally. Flexible hours are offered along with banked PTO and multiple employee outings, including contractors and charity events. The facility is sophisticated, supporting the development and manufacturing of energy solutions for power generation with a portfolio of gas turbines ranging from 30 to 140 MW packages.Job Type &amp; LocationThis is a Permanent position based out of Glastonbury, CT.Pay and BenefitsThe pay range for this position is $80000.00 - $85000.00/yr.Mitsubishi Power Aero offers a comprehensive health package:

Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability coverage
Health &amp; wellness programs

Bonus Program
401KWorkplace TypeThis is a fully onsite position in Glastonbury,CT.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.

Job Title: Quality TechnicianJob DescriptionThe Quality Technician role is primarily focused on ensuring quality on the production floor through thorough quality checks and maintaining proper documentation. This position involves minimal lab work, limited to preparing samples for third-party testing. The role requires accurate interpretation and adherence to reference documents such as specifications and Standard Operating Procedures (SOPs). The technician must comply with Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs), and effectively communicate quality-related information both verbally and in writing.Responsibilities<ul><li>Perform quality checks on the production floor.</li><li>Ensure adherence to quality processes and maintain documentation.</li><li>Prepare samples for third-party testing.</li><li>Interpret and follow reference documentation, including specifications and SOPs.</li><li>Comply with GMPs and GLPs.</li><li>Communicate quality-related information effectively.</li></ul>Essential Skills<ul><li>At least 1 year of experience in quality control or quality assurance.</li><li>Ability to perform quality inspections and checks.</li><li>Strong attention to detail and basic math skills.</li><li>Excellent communication skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Quality Control Experience.</li><li>Associates degree in the sciences is a plus.</li><li>Interest in manufacturing and quality settings with potential for upward mobility.</li></ul>Work EnvironmentThe position is for the 2nd shift, from 3:30 pm to 12:00 am, Monday through Friday. The work environment is a clean manufacturing facility with several production lines. The candidate will be required to walk around and pull samples from various lines. The company fosters a positive environment with a strong culture.Job Type &amp; LocationThis is a Contract to Hire position based out of Allentown, PA.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 Allentown,PA.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 TechnicianJob DescriptionThe Quality Technician role is primarily focused on ensuring quality on the production floor through thorough quality checks and maintaining proper documentation. This position involves minimal lab work, limited to preparing samples for third-party testing. The role requires accurate interpretation and adherence to reference documents such as specifications and Standard Operating Procedures (SOPs). The technician must comply with Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs), and effectively communicate quality-related information both verbally and in writing.Responsibilities<ul><li>Perform quality checks on the production floor.</li><li>Ensure adherence to quality processes and maintain documentation.</li><li>Prepare samples for third-party testing.</li><li>Interpret and follow reference documentation, including specifications and SOPs.</li><li>Comply with GMPs and GLPs.</li><li>Communicate quality-related information effectively.</li></ul>Essential Skills<ul><li>At least 1 year of experience in quality control or quality assurance.</li><li>Ability to perform quality inspections and checks.</li><li>Strong attention to detail and basic math skills.</li><li>Excellent communication skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Quality Control Experience.</li><li>Associates degree in the sciences is a plus.</li><li>Interest in manufacturing and quality settings with potential for upward mobility.</li></ul>Work EnvironmentThe position is for the 2nd shift, from 3:30 pm to 12:00 am, Monday through Friday. The work environment is a clean manufacturing facility with several production lines. The candidate will be required to walk around and pull samples from various lines. The company fosters a positive environment with a strong culture.Job Type &amp; LocationThis is a Contract to Hire position based out of Allentown, PA.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 Allentown,PA.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 TechnicianJob DescriptionThe Quality Technician is responsible for ensuring the highest quality standards. The role involves performing line clearance, equipment swabbing, and quality audits across production lines. The technician will document process check results, report any out-of-specification issues, and ensure corrective actions are completed promptly.Responsibilities<ul><li>Verify that production lines are clear before startup.</li><li>Perform equipment swabbing after sanitation.</li><li>Conduct quality audits on each production line throughout the shift.</li><li>Document in-line process check results according to pre-approved specifications.</li><li>Report any Out of Specification (OOS) or non-conformance issues to production.</li><li>Ensure immediate corrective action is completed before startup for any non-conformance.</li><li>Label and store non-compliant products following the MRB process.</li><li>Perform periodic quality and GMP audits of the production area, particularly at the mix deck.</li><li>Audit staged ingredients to ensure no expired materials are used.</li><li>Conduct temperature audits of ingredients, work-in-progress, and finished products during production.</li><li>Prepare shift reports for follow-up by the next shift.</li><li>Perform case counts audits on all products.</li><li>Execute daily pre-operational inspections.</li><li>Assist in metal detector validations and perform regular in-process metal detector line checks.</li><li>Ensure operators follow metal detector Standard Operating Procedures (SOP).</li><li>Report any food safety risks to the supervisor.</li><li>Collect samples from raw materials, in-process, and finished products for lab testing.</li></ul>Essential Skills<ul><li>Experience in inspection, quality control, and food manufacturing.</li><li>Proficiency in GMP (Good Manufacturing Practices).</li><li>Experience working night shifts: Monday to Friday, and some Saturdays from 10:00 PM to 6:30 AM.</li><li>Microsoft Office proficiency.</li><li>Strong communication and organizational skills.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Kankakee, IL.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/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 Kankakee,IL.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.

Job Title: Quality TechnicianJob DescriptionThe Quality Technician is responsible for ensuring the highest quality standards in the production of premium sauces. The role involves performing line clearance, equipment swabbing, and quality audits across production lines. The technician will document process check results, report any out-of-specification issues, and ensure corrective actions are completed promptly.Responsibilities<ul><li>Verify that production lines are clear before startup.</li><li>Perform equipment swabbing after sanitation.</li><li>Conduct quality audits on each production line throughout the shift.</li><li>Document in-line process check results according to pre-approved specifications.</li><li>Report any Out of Specification (OOS) or non-conformance issues to production.</li><li>Ensure immediate corrective action is completed before startup for any non-conformance.</li><li>Label and store non-compliant products following the MRB process.</li><li>Perform periodic quality and GMP audits of the production area, particularly at the mix deck.</li><li>Audit staged ingredients to ensure no expired materials are used.</li><li>Conduct temperature audits of ingredients, work-in-progress, and finished products during production.</li><li>Prepare shift reports for follow-up by the next shift.</li><li>Perform case counts audits on all products.</li><li>Execute daily pre-operational inspections.</li><li>Assist in metal detector validations and perform regular in-process metal detector line checks.</li><li>Ensure operators follow metal detector Standard Operating Procedures (SOP).</li><li>Report any food safety risks to the supervisor.</li><li>Collect samples from raw materials, in-process, and finished products for lab testing.</li></ul>Essential Skills<ul><li>Experience in inspection, quality control, and food manufacturing.</li><li>Proficiency in GMP (Good Manufacturing Practices).</li><li>Experience working night shifts: Monday to Friday, and some Saturdays from 10:00 PM to 6:30 AM.</li><li>Microsoft Office proficiency.</li><li>Strong communication and organizational skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in a related field.</li><li>Experience in food manufacturing quality control.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Manteno, IL.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/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 Manteno,IL.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 TechnicianJob DescriptionWe are seeking a Quality Technician to support our comprehensive, enterprise-wide Quality Management System. This role is ideal for a candidate who thrives in a fast-paced, cross-functional manufacturing environment.Responsibilities<ul><li>Perform sample inspections and measurements of incoming parts.</li><li>Process non-conforming materials for testing or disposition.</li><li>Conduct First Article Inspections (FAIs) of new parts and/or parts from new suppliers.</li><li>Complete internal audits and associated documentation.</li><li>Interpret engineering prints and schematics.</li><li>Support safety and quality initiatives such as 5S, ESD, FOD, and ISO.</li><li>Assist in the Material Review Board process.</li><li>Maintain information systems.</li><li>Prepare reports by collecting, analyzing, and summarizing data; making recommendations.</li><li>Review, analyze, and report on quality discrepancies.</li></ul>Essential Skills<ul><li>A two-year technical degree is required; a four-year technical degree is preferred</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Pittsburgh, PA.Pay and BenefitsThe pay range for this position is $25.00 - $27.00/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 Pittsburgh,PA.Application DeadlineThis position is anticipated to close on Mar 2, 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 TechnicianJob DescriptionProvide support for Quality Engineering functions, including manufacturing, sterility assurance, or supplier quality, and lead projects and improvement initiatives. Conduct investigations for product or supplier nonconformance and process noncompliance issues, documenting exceptions in the Corrective Action / Preventative Action (CAPA) System.Responsibilities<ul><li>Lead investigations for product or supplier nonconformance and process noncompliance issues.</li><li>Perform CAPA activities, including root cause analysis, investigations, product and process disposition, and effectiveness checks.</li><li>Participate in the review and disposition of non-conforming product or controlled process inputs, including the Product Quality Review Board, returns, and complaints.</li><li>Support validation activities by reviewing and approving data sheets, drafting validation protocols, and documenting results in a validation report.</li><li>Conduct process and safety audits and document results appropriately.</li><li>Assist in Change Management functions, including maintaining Work Instructions and Standard Operating Procedures.</li><li>Perform product acceptance testing, quality inspections, data entry, and data corrections accurately.</li><li>Support environmental monitoring investigations and document quality inspections on controlled suppliers.</li><li>Identify and support process improvement initiatives and implementation.</li><li>Support projects as a quality resource as assigned.</li><li>Mentor or train other team members.</li></ul>Essential Skills<ul><li>Quality control and quality inspection skills.</li><li>Experience with micrometers, calipers, and quality assurance processes.</li><li>Familiarity with CAPA systems.</li><li>Medical device and lab testing knowledge.</li></ul>Additional Skills &amp; Qualifications<ul><li>High School diploma or equivalent required.</li><li>2+ years of experience in quality assurance or quality control.</li><li>Experience in Microbiology or Biology preferred.</li><li>ASQ certification preferred.</li><li>Strong verbal and written communication skills.</li><li>Proficiency in Microsoft Office Suite, especially basic Excel.</li><li>Technical writing skills.</li><li>Problem-solving methodologies and investigation experience.</li></ul>Work EnvironmentThe work environment is highly organized, featuring clean rooms that are bright and welcoming. Employees work in small teams that collaborate daily. The role requires the ability to move or lift objects up to 25 pounds and frequent stationary positioning, either standing or sitting, while utilizing digital tools. Fine manipulation using hands and fingers is often required for typing, writing, and other tasks.Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $27.50 - $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 Eden Prairie,MN.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.

Responsibilities<ul><li>Develop and update Job Instructions, Control Plans, and Quality Alerts; process Engineering Change Instructions (ECIs).</li><li>Review training records and assist with Production Part Approval Process (PPAP) audits and submissions.</li><li>Present warranty data and charts in quality meetings.</li><li>Collaborate with cross-functional teams to resolve gaging and fixturing issues.</li><li>Perform weekly Layered Process Audits (LPAs) and support inspection, containment, and sorting activities.</li><li>Investigate production issues, determine root causes, and manage nonconforming material.</li><li>Interface with labs and use Quality Assurance Database (QAD) to track suspect material.</li><li>Conduct inspections using precision tools and maintain Visual Factory standards.</li></ul>Essential Skills<ul><li>Proficiency in inspection, quality control, and quality assurance.</li><li>Ability to read and interpret blueprints.</li><li>Experience with nonconforming material management and control plans.</li><li>Strong understanding of IATF and ISO 9001 standards.</li><li>Proficient in GD&amp;T (Geometric Dimensioning and Tolerancing) and PPAP documentation.</li><li>Ability to perform root cause analysis and lead audits.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Westchester, IL.Pay and BenefitsThe pay range for this position is $50000.00 - $65000.00/yr.401K
Health Dental vision
PTO HolidayWorkplace TypeThis is a fully onsite position in Westchester,IL.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.

Job Title: Quality TechnicianShifts: <ul><li>2nd shift 6:00PM-2:30AM paying $22.50/hr</li><li>3rd shift 1:30AM-10:00AM paying $23.50/hr</li></ul>Job DescriptionAs a Quality Technician, you will split your time equally between working on the plant floor and in a lab setting. Your primary role will be to ensure the highest standards of quality and safety in our production processes.Responsibilities<ul><li>Perform inspections, including pre-operative and food safety, and document and communicate results.</li><li>Conduct daily operating inspections to ensure compliance with GMPs and USDA requirements.</li><li>Perform magnet and metal detector record checks and inform the supervisor of any deficiencies.</li><li>Conduct ATP swab tests, including daily and weekly line swabs.</li><li>Calibrate lab equipment such as scales, pH meters, and salt analyzers.</li><li>Conduct organic start-up tests, ensuring documentation of appropriate cleaning processes and pH levels.</li><li>Review previous day's HACCP records daily.</li><li>Change thermometer recorder charts as needed.</li><li>Perform quality audits, including systems, production scales, and salt analyzers, and document findings.</li><li>Conduct in-bound checks and verify COAs to ensure they meet requirements.</li><li>Maintain stock of laboratory and production supplies as directed.</li><li>Serve as a liaison with the USDA.</li><li>Distribute weekly code date sheets promptly.</li><li>Report and follow up on food safety and quality concerns.</li><li>Perform pizza line coverage checks.</li><li>Notify the supervisor of all downtimes.</li><li>Enforce food safety PPE/GMP requirements and report any concerns.</li><li>Perform other duties as assigned by the supervisor.</li></ul>Additional Skills &amp; Qualifications<ul><li>High school diploma with science classes or lab courses and 6 months to 1+ years of manufacturing experience in the food industry, or</li><li>B.S. degree in Life Sciences with no industry experience, or</li><li>Associates degree in Life Sciences with 6 months to 1 year of manufacturing experience in the food industry.</li><li>6 months to 1+ years of GMP experience, open to ISO and GLP environments.</li><li>0 to 2 years of quality experience is ideal but not required.</li></ul>Work EnvironmentThe role involves a 50/50 split between a lab setting and the plant floor.Job Type &amp; LocationThis is a Contract to Hire position based out of Beaver Dam, WI.Pay and BenefitsThe pay range for this position is $21.00 - $22.25/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 Beaver Dam,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.

Job Title: Quality TechnicianJob DescriptionIn this role, you will work with tight tolerance parts and be responsible for programming and editing the Coordinate Measuring Machine (CMM) programs. You will support the measurements of the inspection process and be involved in in-process audits. The Quality Technician will complete measurements and inspections of products both in-process and at final stages. Additionally, you will provide support for the certified Quality Management System (QMS) as needed, helping to assure consistent quality of production by validating processes and providing documentation.Responsibilities<ul><li>Program and edit CMM programs.</li><li>Conduct measurements and inspections of products during in-process and final stages.</li><li>Support the Quality Management System and participate in in-process audits.</li><li>Validate production processes to assure consistent quality.</li><li>Provide necessary documentation to support quality assurance.</li></ul>Essential Skills<ul><li>Minimum 3 years of experience with CMMs.</li><li>Proficiency in using calipers and micrometers for measurements.</li><li>Experience with tight tolerance parts in aerospace, automotive, or medical industries.</li><li>Knowledge of inspection techniques, including GD&amp;T, blueprint reading, and quality control.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with PCDMIS or CALYPSO is beneficial.</li><li>Strong attention to detail and analytical skills.</li></ul>Work EnvironmentYou will work in a climate-controlled environment alongside a team consisting of a quality specialist and a quality engineer. The facility operates Monday to Friday, from 7 am to 3:30 pm, with occasional half-days based on production needs. The facility is open from 6 am to 2:30 pm, providing the opportunity for a flexible schedule if required. Our work environment encourages personal ownership and offers opportunities for growth, with a focus on custom manufacturing, variety of work, and a commitment to a 5S environment.Job Type &amp; LocationThis is a Contract to Hire position based out of Pleasant Prairie, WI.Pay and BenefitsThe pay range for this position is $25.00 - $28.00/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 Pleasant Prairie,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.

Job Title: Quality TechnicianJob DescriptionAs a Quality Technician, you will be responsible for testing finished products for various parameters such as acid, salt, pH, and sulfites. You will also perform metal detection and assess fill weights, drained weights, defects, and abnormal colors or flavors. Additionally, you will ensure that coding is correct on packaging and cases, perform audits, and resolve all issues related to product quality.Responsibilities<ul><li>Test finished products for acid, salt, pH, and sulfites.</li><li>Perform metal detection and assess fill weights, drained weights, defects, and abnormal colors or flavors.</li><li>Ensure coding is correct on packaging and cases.</li><li>Perform audits and resolve issues related to product quality.</li><li>Complete Quality Assurance/Control paperwork.</li><li>Comply with GMPs, safety and quality standards, food safety measures, and OSHA regulations.</li></ul>Essential Skills<ul><li>Degree in the Sciences (Biology, Environmental Science, Agriculture, Food Science, Biochemistry, etc.).</li><li>Strong attention to detail.</li><li>Ability to uphold quality standards and hold manufacturing accountable to those.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous Food Manufacturing or HACCP/Food Safety Experience is a plus.</li><li>1 plus years of experience in Quality.</li><li>1 plus year of GMP and FDA/USDA experience.</li></ul>Work EnvironmentThis position is based in a food manufacturing facility specializing in sauerkraut production, where the smell can be intense at times. The role is lab-based but requires sample collection on the production floor. The position offers a shift opening, with initial training on the Day Shift lasting 2-4 weeks.Job Type &amp; LocationThis is a Permanent position based out of Bear Creek, WI.Pay and BenefitsThe pay range for this position is $41600.00 - $52000.00/yr.401k
two weeks vacation accrued &amp; 2 hours accrued sick time per month
medical, dental, vision
company paid life insurance, short term and long term disabilityWorkplace TypeThis is a fully onsite position in Bear Creek,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.

Job Title: Quality TechnicianJob DescriptionThis full-time, onsite position from Monday to Friday, 7:30 AM to 4:00 PM, involves performing quality inspection and acceptance of incoming components, in-progress product assembly, and final product inspection. The role ensures the manufacturing quality of the products, demanding strong mechanical acumen, logical reasoning, and analytical skills.Responsibilities3 parts of the job. <ol><li>Inspecting incoming parts. – Visual inspections, Micrometers and Calipers</li><li>documentation and quality approval of the work orders. Help with non-confirming reports </li><li>Calibration coordination. </li><li>Documents and training procedures. Managing document changes. Comfortable with computer, getting into Microsoft word. </li></ol>Additional Skills &amp; Qualifications<ul><li>high attention to detail in a regulated environment. </li><li>Associate degree preferred. Highschool or GED required. </li><li>1-2 years of experience in a quality assurance role in a regulated industry—medical device manufacturing preferred.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Lincolnshire, IL.Pay and BenefitsThe pay range for this position is $25.00 - $27.00/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 Lincolnshire,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 Technician 1st Shift

Job Title: Quality Validation EngineerJob DescriptionWe are seeking a skilled and detail-oriented Quality Validation Engineer to play a crucial role in equipment validations for pharmaceutical manufacturing and laboratory settings. The successful candidate will ensure compliance with industry regulations by executing and overseeing equipment qualification processes, including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Factory Acceptance Tests (FATs), Site Acceptance Tests (SATs), Cleaning Commissions, and Cleaning Validations. This role involves creating, reviewing, and executing validation documents and protocols to maintain the highest quality standards in our manufacturing processes and facilities.Responsibilities<ul><li>Develop and design detailed validation documents, including User Requirements Specifications (URS), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and process validation protocols.</li><li>Conduct comprehensive process validations and facility qualifications to ensure adherence to company and regulatory standards.</li><li>Lead cleaning validation efforts to ensure equipment cleaning processes meet standards for preventing cross-contamination and maintaining product integrity.</li><li>Oversee facility qualification activities, ensuring all equipment and infrastructure comply with validation standards.</li><li>Draft and finalize validation reports, summarizing the results of tests, inspections, and data analyses.</li><li>Collaborate closely with production, quality control, and regulatory teams to ensure alignment with regulatory standards and company policies.</li></ul>Essential Skills<ul><li>5 years of experience in validation within a pharmaceutical manufacturing environment.</li><li>Strong understanding of validation protocols and documentation, including URS, IQ, OQ, PQ.</li><li>Excellent written and verbal communication skills, with experience writing clear, concise reports.</li><li>Familiarity with pharmaceutical regulatory requirements and standards (e.g., FDA, ISO).</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Engineering, Chemistry, Biology, Physics, or a related field.</li><li>Experience with compounding and packaging of liquid drug products (highly preferred).</li><li>Experience with validation of computer systems (preferred).</li><li>Experience with serialization (preferred).</li></ul>Work EnvironmentThe candidate will work at the Mount Prospect site, starting in the staging room before moving to the manufacturing floor and quality group. The manufacturing operates 9 lines, all on the first shift from 8 am to 5 pm. The Quality team consists of 6-8 members, and the company follows FDA and GMP guidelines. The company has a strong growth plan for its future in the generic drug and European markets, with ongoing expansion to ensure FDA compliance.Job Type &amp; LocationThis is a Contract to Hire position based out of Mount Prospect, IL.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Mount Prospect,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.

Quality Validation Engineer

Job Title: Quality/Blending TechnicianJob DescriptionThe Quality/Blending Technician plays a critical role in ensuring product integrity and compliance with customer requirements. This position supports both internal operations and customer-facing initiatives through rigorous testing, documentation, and collaboration with technical and sales teams.Responsibilities<ul><li>Batch, mix, and blend products according to specifications for customer orders.</li><li>Measure, weigh, and load raw materials into machines.</li><li>Monitor mixtures for consistency and viscosity.</li><li>Sample, test, and approve incoming raw materials and finished products to meet specifications and customer requirements.</li><li>Provide support for manufacturing areas.</li><li>Perform routine and advanced quality tests, including appearance, specific gravity, pH, and refractive index measurements, coating weight, and adhesion testing.</li><li>Execute various panel tests for corrosion resistance and coating performance.</li><li>Prepare internal lab samples.</li><li>Maintain inventory of retained samples and manage rotation schedules.</li><li>Generate Certificates of Analysis and maintain accurate records of all testing activities.</li><li>Ensure compliance with quality standards and internal SOPs.</li><li>Assist chemists and technical staff with special projects under the direction of leadership.</li><li>Provide technical support for sales initiatives and customer projects.</li></ul>Essential Skills<ul><li>Quality control</li><li>Laboratory skills</li><li>Blending and mixing experience</li><li>Quality assurance</li><li>QC analysis</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma required</li><li>Associates or Bachelor’s degree in a scientific discipline preferred</li><li>1-3 years of experience in GMP quality operations environment</li><li>Experience with blending, mixing, or other related manufacturing preferred</li></ul>Work EnvironmentThis role operates in a manufacturing environment involving metal working fluids, lubricants, and coolants. The standard work schedule is Monday through Friday, from 7 am to 4 pm. The company is currently renovating a new facility for expansion, offering the opportunity to develop SOPs and implement quality functions. The work setting includes a small team where independent work is expected post-training.Job Type &amp; LocationThis is a Contract to Hire position based out of Huntington, IN.Pay and BenefitsThe pay range for this position is $24.00 - $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 Huntington,IN.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/Blending Technician

Job Title: Quality/Blending TechnicianJob DescriptionThe Quality/Blending Technician plays a critical role in ensuring product integrity and compliance with customer requirements. This position supports both internal operations and customer-facing initiatives through rigorous testing, documentation, and collaboration with technical and sales teams.Responsibilities<ul><li>Batch, mix, and blend products according to specifications for customer orders.</li><li>Measure, weigh, and load raw materials into machines.</li><li>Monitor mixtures for consistency and viscosity.</li><li>Sample, test, and approve incoming raw materials and finished products to meet specifications and customer requirements.</li><li>Provide support for manufacturing areas.</li><li>Perform routine and advanced quality tests, including appearance, specific gravity, pH, and refractive index measurements, coating weight, and adhesion testing.</li><li>Execute various panel tests for corrosion resistance and coating performance.</li><li>Prepare internal lab samples.</li><li>Maintain inventory of retained samples and manage rotation schedules.</li><li>Generate Certificates of Analysis and maintain accurate records of all testing activities.</li><li>Ensure compliance with quality standards and internal SOPs.</li><li>Assist chemists and technical staff with special projects under the direction of leadership.</li><li>Provide technical support for sales initiatives and customer projects.</li></ul>Essential Skills<ul><li>Quality control</li><li>Laboratory skills</li><li>Blending and mixing experience</li><li>Quality assurance</li><li>QC analysis</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma required</li><li>Associates or Bachelor’s degree in a scientific discipline preferred</li><li>1-3 years of experience in GMP quality operations environment</li><li>Experience with blending, mixing, or other related manufacturing preferred</li></ul>Work EnvironmentThis role operates in a manufacturing environment involving metal working fluids, lubricants, and coolants. The standard work schedule is Monday through Friday, from 7 am to 4 pm. The company is currently renovating a new facility for expansion, offering the opportunity to develop SOPs and implement quality functions. The work setting includes a small team where independent work is expected post-training.Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Wayne, IN.Pay and BenefitsThe pay range for this position is $24.00 - $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 Fort Wayne,IN.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/Blending TechnicianJob DescriptionThe Quality/Blending Technician plays a critical role in ensuring product integrity and compliance with customer requirements. This position supports both internal operations and customer-facing initiatives through rigorous testing, documentation, and collaboration with technical and sales teams.Responsibilities<ul><li>Batch, mix, and blend products according to specifications for customer orders.</li><li>Measure, weigh, and load raw materials into machines.</li><li>Monitor mixtures for consistency and viscosity.</li><li>Sample, test, and approve incoming raw materials and finished products to meet specifications and customer requirements.</li><li>Provide support for manufacturing areas.</li><li>Perform routine and advanced quality tests, including appearance, specific gravity, pH, and refractive index measurements, coating weight, and adhesion testing.</li><li>Execute various panel tests for corrosion resistance and coating performance.</li><li>Prepare internal lab samples.</li><li>Maintain inventory of retained samples and manage rotation schedules.</li><li>Generate Certificates of Analysis and maintain accurate records of all testing activities.</li><li>Ensure compliance with quality standards and internal SOPs.</li><li>Assist chemists and technical staff with special projects under the direction of leadership.</li><li>Provide technical support for sales initiatives and customer projects.</li></ul>Essential Skills<ul><li>Quality control</li><li>Laboratory skills</li><li>Blending and mixing experience</li><li>Quality assurance</li><li>QC analysis</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma required</li><li>Associates or Bachelor’s degree in a scientific discipline preferred</li><li>1-3 years of experience in GMP quality operations environment</li><li>Experience with blending, mixing, or other related manufacturing preferred</li></ul>Work EnvironmentThis role operates in a manufacturing environment involving metal working fluids, lubricants, and coolants. The standard work schedule is Monday through Friday, from 7 am to 4 pm. The company is currently renovating a new facility for expansion, offering the opportunity to develop SOPs and implement quality functions. The work setting includes a small team where independent work is expected post-training.Job Type &amp; LocationThis is a Contract to Hire position based out of Huntington, IN.Pay and BenefitsThe pay range for this position is $24.00 - $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 Huntington,IN.Application DeadlineThis position is anticipated to close on Mar 2, 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/Blending TechnicianJob DescriptionThe Quality/Blending Technician plays a critical role in ensuring product integrity and compliance with customer requirements. This position supports both internal operations and customer-facing initiatives through rigorous testing, documentation, and collaboration with technical and sales teams.Responsibilities<ul><li>Batch, mix, and blend products per specifications for customer orders.</li><li>Measure, weigh, and load raw materials into machines.</li><li>Monitor mixtures for consistency and viscosity.</li><li>Sample, test, and approve incoming raw materials and finished products to meet specifications and customer requirements.</li><li>Provide support for manufacturing areas.</li><li>Perform routine and advanced quality tests, including appearance, specific gravity, pH, and refractive index measurements, coating weight, and adhesion testing.</li><li>Execute various panel tests for corrosion resistance and coating performance.</li><li>Prepare internal lab samples.</li><li>Maintain inventory of retained samples and manage rotation schedules.</li><li>Generate Certificates of Analysis and maintain accurate records of all testing activities.</li><li>Ensure compliance with quality standards and internal SOPs.</li><li>Assist chemists and technical staff with special projects under the direction of leadership.</li><li>Provide technical support for sales initiatives and customer projects.</li></ul>Essential Skills<ul><li>Quality control</li><li>Laboratory skills</li><li>Blending and mixing expertise</li><li>Quality assurance</li><li>QC analysis</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma required</li><li>Associate or Bachelor degree in a scientific discipline preferred</li><li>1-3 years of experience in a GMP quality operations environment</li><li>Experience with blending, mixing, or related manufacturing preferred</li></ul>Work EnvironmentThe position is based in a manufacturing environment dealing with metalworking fluids, lubricants, and coolants. The work schedule is Monday to Friday, from 7 am to 4 pm. The company is renovating a new facility for expansion, offering a small team setting where independent work is encouraged post-training.Job Type &amp; LocationThis is a Contract to Hire position based out of Huntington, IN.Pay and BenefitsThe pay range for this position is $24.00 - $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 Huntington,IN.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: Quoting SpecialistJob DescriptionThe Quoting Specialist is responsible for generating a bill of materials based on project plans and serves as the single point of contact for all project quotations. This role involves working closely with field sales representatives daily and occasionally engaging with external customers. The main communication methods include phone, email, and Salesforce interactions. Responsibilities include determining the proper material and supplies for projects, facilitating new project quotations, preparing quotation revisions, assisting in pricing approval, performing contact management, and distributing submittal packages or product information as requested. The Quoting Specialist will also communicate with other departments and perform administrative duties as needed.Responsibilities<ul><li>Review and assist with project layouts and plans while applying knowledge of ADS products.</li><li>Work closely with the sales team to determine the proper materials and supplies needed for jobs.</li><li>Build rapport with field sales representatives and provide Salesforce support.</li><li>Develop an understanding of individual territory dynamics, including customer relationships, pricing, and competition.</li><li>Review a Bill of Materials to extract products needed to generate a finished quote.</li><li>Produce and deliver all quotes for the assigned sales territory.</li><li>Prepare new projects and quotes within Salesforce, confirm accuracy with sales representatives, and send to customers.</li><li>Modify existing quotes with different quantities, products, and customer information.</li><li>Ensure product numbers used on Salesforce project quotes match what is requested by the sales rep or customer.</li><li>Edit pricing on Salesforce project quotes to match the requested quoting strategy.</li><li>Collaborate with other departments to obtain products and pricing for quotes.</li><li>Manage the Salesforce contact list for sales representatives by adding, deleting, or updating contacts.</li><li>Review existing quotations in Salesforce for pricing validity and update pricing through collaboration with market analysts and outside sales reps.</li><li>Maintain confidentiality of all trade secrets and other company/customer information.</li><li>Assist with the development of new team members.</li><li>Follow all company procedures and policies.</li><li>Create solutions and adhere to ADS guiding principles of honesty, professionalism, and core values.</li></ul>Essential Skills<ul><li>Estimation and quoting expertise.</li><li>Experience with bill of materials and material management.</li><li>Proficiency in CRM software, particularly Salesforce.</li><li>Strong skills in Microsoft Excel.</li><li>Understanding of civil engineering, AutoCAD, and Civil CAD.</li><li>Ability to read and interpret blueprints.</li><li>Construction estimating experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior quoting or estimating experience is required; civil or related experience is a plus.</li><li>Experience using Salesforce or other CRM software is required.</li><li>Strong organizational and time-management skills.</li><li>Strong communication skills.</li><li>Ability to work efficiently in a fast-paced environment.</li><li>Degree or equivalent experience in civil CAD design is a plus.</li></ul>Work EnvironmentThis position is fully remote with all necessary equipment provided. The role is fast-paced, requiring the completion of 20-60 quotes per day. Work hours are from 8:00 AM to 5:00 PM in the Eastern Time Zone or 7:00 AM to 4:00 PM in the Central Time Zone. Opportunities for career advancement and movement into different groups within the company are available, with training provided.Please direct any questions or inquiries to the recruiter, Sebastian Althoff, at 'salthoff@actalentservices'!Job Type &amp; LocationThis is a Contract to Hire position based out of Hilliard, OH.Pay and BenefitsThe pay range for this position is $21.00 - $25.00/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 remote position.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.

Quoting Specialist

Job Title: Quoting Specialist Job DescriptionThe quoting specialist is a crucial role responsible for generating a bill of materials based on project plans and serving as the single point of contact for all project quotations. This position requires daily collaboration with field sales representatives and occasional interaction with external customers. Communication is primarily conducted over the phone, via email, or through Salesforce. The Estimator will work to determine the necessary materials and supplies, facilitate new project quotations, prepare quotation revisions, assist in the pricing approval process, manage contacts, and distribute submittal packages upon request. Additionally, the Estimator will collaborate with other departments as necessary and perform various administrative duties.Responsibilities<ul><li>Review and assist with project layouts and plans, applying knowledge of ADS products.</li><li>Work closely with the sales team to determine the appropriate materials and supplies for projects.</li><li>Build rapport with field sales representatives and provide Salesforce support.</li><li>Develop an understanding of individual territory dynamics, including customer relationships, pricing, and competition.</li><li>Review a Bill of Materials to extract necessary products for a finished quote.</li><li>Produce and deliver all quotes for the assigned sales territory and prepare new projects/quotes within Salesforce.</li><li>Modify existing quotes with varying quantities, products, and customers as needed.</li><li>Ensure product numbers on Salesforce quotes match requests from sales representatives or customers.</li><li>Edit pricing on Salesforce project quotes to align with the requested quoting strategy.</li><li>Collaborate with other departments to obtain products and pricing for quote generation.</li><li>Manage and update the Salesforce contact list for the sales representative.</li><li>Review existing quotations in Salesforce to verify pricing validity and update as necessary in collaboration with market analysts and outside sales representatives.</li><li>Maintain confidentiality of all trade secrets and company/customer information.</li><li>Assist in the development of new team members.</li><li>Adhere to company procedures, policies, and guiding principles of honesty, professionalism, and core values.</li></ul>Essential Skills<ul><li>Experience in estimation, quoting, and material management.</li><li>Proficiency in CRM software, specifically Salesforce.</li><li>Microsoft Excel proficiency.</li><li>Strong organization and time-management skills.</li><li>Excellent communication skills.</li><li>Ability to work efficiently in a fast-paced environment.</li></ul>Skills &amp; Qualifications<ul><li>Prior quoting or estimating experience is required; civil or related experience is a plus.</li><li>Degree or equivalent experience in technical program. </li><li>Knowledge of blueprint reading.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Hilliard, OH.Pay and BenefitsThe pay range for this position is $21.00 - $25.00/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 remote position.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.

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