ENGINEER QUALITY
On-siteSt. Louis, Missouri, United States
Job Summary
Quality Engineer to develop and monitor quality management systems to ensure FDA compliance; responsible for maintaining Process Variance Reports (PVR) and generating Annual Product Reviews (APR) for manufacturing and distribution locations; ensure GMP documentation and quality attributes are maintained, and drive investigation of customer complaints; utilize CAPAs, root-cause analysis, FMEA and HAZOP studies, and assist in GMP/GDP training; create or modify SOPs and work instructions, perform statistical process analysis, and monitor regulatory and quality documentation to support ongoing compliance; interact with multiple departments to implement improvements and maintain timely deliverables.
Required Qualifications
- Bachelor’s Degree in a related Science or Engineering field
- Knowledge of current GMPs and FDA regulations
- 2-5 years of experience in manufacturing of food, cosmetics or pharmaceutical products
- Ability to develop technical compliant documents and communicate effectively
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.