Senior Associate Quality Assurance
Amgen · Thousand Oaks, CA
QualityFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Senior Associate Quality Assurance position supporting drug product manufacturing operations at a biopharmaceutical facility. The role provides daily oversight of manufacturing areas, ensuring compliance with regulatory requirements and GMP standards in a Grade 8 cleanroom environment.
What they're looking for
- High school diploma/GED plus 4 years of GMP experience, or equivalent education-experience combination
- Demonstrated knowledge of GMP operations, SOPs, and documentation practices
- Ability to work flexible shift rotations including weekends in a 24/7 production environment
- Strong organizational and multitasking capabilities with effective written and verbal communication
- Experience evaluating documentation and operations against company procedures
- Preferred: Bachelor's degree in biochemistry, biology, chemistry, or related science field
What you'll be doing
- Provide daily oversight and quality support in drug product manufacturing areas with cleanroom gowning
- Perform manual visual inspection and review electronic batch records for GMP compliance
- Review and approve GMP documents, maintenance work orders, and minor quality deviations
- Evaluate compliance issues, provide recommendations, and ensure completion of quality records
- Support 24/7 production operations with flexible shift schedules across multiple rotating shifts
Privacy & handoff
This role links to Amgen's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.