Actalent
Quality Technician
We are seeking a dedicated and detail-oriented Quality Technician to join our team. The ideal candidate will have strong experience in quality assurance and validation within a regulated industry. This role offers an exciting opportunity to contribute to process improvements and support our growing team with multiple projects on the horizon. Responsibilities
Develop and execute validation protocols, including IQ, OQ, PQ, and TMV. Maintain detailed validation documentation such as VMPs, reports, and SOPs. Conduct risk assessments and manage change controls. Ensure compliance with regulatory standards, including GMP, GLP, CSV, and data integrity. Collaborate cross-functionally to support validation strategy and training initiatives. Monitor system performance and lead requalification activities. Qualify suppliers and vendors. Contribute to process improvements and continuous improvement initiatives. Essential Skills
3+ years of experience in validation or quality within a regulated industry. Knowledge of FDA regulations, including 21 CFR Part 820 standards. Proficiency in Microsoft Suite and experience with validation software. Strong communication, documentation, and analytical skills. Additional Skills & Qualifications
Preferred: Lean/Six Sigma certification. Experience with Learning Management Systems (LMS). Familiarity with inspection tools such as calipers and micrometers. Experience with OGP Smart Scopes. Work Environment
This position requires spending 70% of the time on the floor and 30% at a computer. The role is part of a tenured team with growth opportunities due to upcoming retirements and a variety of projects currently in development. Pay and Benefits
The 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 & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan
Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Two Rivers, WI. Application Deadline
This position is anticipated to close on Aug 28, 2025. About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 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.
We are seeking a dedicated and detail-oriented Quality Technician to join our team. The ideal candidate will have strong experience in quality assurance and validation within a regulated industry. This role offers an exciting opportunity to contribute to process improvements and support our growing team with multiple projects on the horizon. Responsibilities
Develop and execute validation protocols, including IQ, OQ, PQ, and TMV. Maintain detailed validation documentation such as VMPs, reports, and SOPs. Conduct risk assessments and manage change controls. Ensure compliance with regulatory standards, including GMP, GLP, CSV, and data integrity. Collaborate cross-functionally to support validation strategy and training initiatives. Monitor system performance and lead requalification activities. Qualify suppliers and vendors. Contribute to process improvements and continuous improvement initiatives. Essential Skills
3+ years of experience in validation or quality within a regulated industry. Knowledge of FDA regulations, including 21 CFR Part 820 standards. Proficiency in Microsoft Suite and experience with validation software. Strong communication, documentation, and analytical skills. Additional Skills & Qualifications
Preferred: Lean/Six Sigma certification. Experience with Learning Management Systems (LMS). Familiarity with inspection tools such as calipers and micrometers. Experience with OGP Smart Scopes. Work Environment
This position requires spending 70% of the time on the floor and 30% at a computer. The role is part of a tenured team with growth opportunities due to upcoming retirements and a variety of projects currently in development. Pay and Benefits
The 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 & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan
Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&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 Type
This is a fully onsite position in Two Rivers, WI. Application Deadline
This position is anticipated to close on Aug 28, 2025. About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 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.