Onsite QA Specialist — Day Shift, COA & CAPA Expert

ACTalent; Eden Prairie (MN); On-site; USD 36,000 - 41,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability insurance

Health Savings Account

Transportation benefits

Employee Assistance Program

Paid time off

Job summary

Actalent is hiring a Quality Assurance Specialist for a fully onsite, long-term contract-to-hire role in Eden Prairie, MN. You will review batch records, verify COAs, and manage deviations, CAPAs, and change controls while supporting investigations and continuous improvement initiatives.

The position requires 3+ years in a cGMP manufacturing environment and a Bachelor's degree in a scientific field. Day shift with standard benefits and on-site facility exposure to personal care products.

Qualifications

• 3+ years of quality experience in a cGMP manufacturing environment.
• Strong knowledge of cGMP, GDP, and quality documentation requirements.
• Bachelor's degree in a scientific discipline or related field, or equivalent education and experience.
• Hands-on experience with quality systems, including deviations, CAPAs, investigations, change controls, and batch record review.

Responsibilities

• Review batch records and supporting documentation for accuracy and compliance.
• Prepare and verify Certificates of Analysis (COAs) and other quality documentation.
• Manage deviations, CAPAs, change orders, quality alerts, and customer complaints.
• Support investigations related to deviations and other quality events.
• Apply Lean principles and 5S to drive continuous improvement.
• Assist with writing deviations, investigations, and quality documentation.

Skills

Quality Assurance

cGMP knowledge

Documentation review

CAPA investigations

Education

Bachelor's degree in science

Tools

Deviations management

Change controls

Job description

Actalent is hiring a Quality Assurance Specialist for a fully onsite, long-term contract-to-hire role in Eden Prairie, MN. You will review batch records, verify COAs, and manage deviations, CAPAs, and change controls while supporting investigations and continuous improvement initiatives.

The position requires 3+ years in a cGMP manufacturing environment and a Bachelor's degree in a scientific field. Day shift with standard benefits and on-site facility exposure to personal care products.