Quality Assurance Associate, Biopharma; JP

Location: Thousand Oaks, CA
Employment Type: Contract
Business Unit: Plant Quality Assurance Incoming and Packaging
Duration: 3 years with possible conversion to FTE
Posting Date: 03/15/2022

3 Key Consulting is hiring a Quality Assurance Associate for a consulting engagement with our client, a leading global biopharmaceutical company.

Primary responsibilities include inspecting raw materials, components, and labels; sampling raw materials, labels, and utilities; generating and compiling quality data and reports (e.g., lot track/trace, incidents). The role also involves assisting with document review, initiating incidents, and overseeing room clearance inspections.

• Experience in quality assurance or manufacturing within the pharmaceutical or medical device industry.
• Experience with GMP processes and documentation.
• Ability to methodically inspect printed materials for print quality defects, clinical product components (e.g., syringes and vials) for physical defects, and batch record documentation for accuracy and completeness.
• Strong teamwork skills with the ability to adapt to shifting priorities and responsibilities, and communicate effectively.
• Bachelor’s degree is preferred but not required.

Perform incoming inspection of raw materials, ensuring quality standards are met.

Opportunity for career growth and development.

• Candidate cannot be color blind.
• Lack of willingness to learn; candidate should be proactive and motivated.

Phone screening followed by a virtual 1:1 interview with a panel (45-60 minutes).

Qualified candidates are invited to send their resume to  For other opportunities, visit our website at  Feel free to share this opportunity with interested contacts.