Quality Assurance Operations Supervisor, Pharmaceutical Manufacturing - 2nd Shift
Siegfried · Irvine, CA
QualityFull-time$90k–$110kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Siegfried seeks a Quality Assurance Operations Supervisor for second-shift leadership at its Irvine pharmaceutical manufacturing facility. The role involves supervising QA professionals, overseeing sterile and aseptic manufacturing operations, ensuring cGMP compliance, and driving quality culture across the production floor.
What they're looking for
- Bachelor's degree in Biology, Chemistry, Biochemistry, Engineering, or related scientific field
- 4-6 years Quality Assurance or Manufacturing experience in GMP-regulated environments
- Demonstrated supervisory or team leadership experience
- Strong knowledge of cGMP requirements and FDA regulations
- Excellent communication, coaching, and problem-solving skills
- Ability to make sound risk-based quality decisions in fast-paced settings
What you'll be doing
- Supervise and mentor QA Technicians and Associates; manage shift staffing and priorities
- Provide real-time quality oversight for formulation, filling, inspection, and packaging activities
- Perform in-process verifications, line clearances, and batch record reviews on manufacturing floor
- Support investigations, deviations, and CAPA activities; drive continuous improvement initiatives
- Represent Quality during client audits, customer visits, and regulatory inspections
Privacy & handoff
This role links to Siegfried'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.