Quality Assurance Analyst
Responsibilities
- Verify alignment between approved documentation and LIMS configuration.
- Support data integrity assessments and documentation reviews.
- Execute QA review and approval activities related to implementation deliverables.
- Participate in User Acceptance Testing (UAT), protocol execution, and deviation resolution.
- Support SOP creation, review, and implementation activities.
- Collaborate with QC, project teams, and stakeholders during rollout activities.
- Ensure implementation activities align with regulatory expectations and company quality standards.
Requirements
- 3+ years of QA experience within a GMP-regulated environment.
- Prior participation in a LIMS implementation.
- Strong understanding of GMP documentation practices and data integrity principles.
- Exceptional attention to detail and organizational skills.
Qualifications
- Experience in veterinary pharmaceutical, pharmaceutical, biotechnology, or medical device industry.
- Experience supporting software validation or computerized system validation activities.
- Familiarity with ALCOA+ and FDA data integrity expectations.
Skills
- Experience in veterinary pharmaceutical, pharmaceutical, biotechnology, or medical device industry.
- Experience supporting software validation or computerized system validation activities.
- Familiarity with ALCOA+ and FDA data integrity expectations.
Benefits
- Medical, dental & vision coverage.
- Critical Illness, Accident, and Hospital coverage.
- 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 coverage.
- Health Spending Account (HSA).
- Transportation benefits.
- Employee Assistance Program.
- Time Off/Leave (PTO, Vacation or Sick Leave).
Pay and Schedule
The pay range for this position is $35.00 - $50.00/hr.
This is a Contract position based out of Bridgeton, MO.
About the Role
We are seeking a dedicated Quality Assurance Specialist to ensure system configuration and migrated data align with GMP compliance. This role involves verifying the alignment between approved documentation and LIMS configuration, supporting data integrity assessments, and participating in various QA activities.
Work Environment
The Quality Assurance Specialist will work in a QA workspace and cubicle, collaborating with over five project team members and interacting with analysts and QA personnel and leadership. The role operates Monday through Friday, 8:00 - 4:30, with a flexible, hybrid work schedule available.
Company Information
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
About Actalent
Actalent 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.