- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …and providing reasonable accommodation to individuals with disabilities. **Brief Job Overview** This ** Senior Verification GMP Auditor ** is a ... manufacturing (QCM) documentation for products submitted into the USP Verification Program **Remote employees must reside in one of...here at USP?** The incumbent will serve as a GMP auditor as well as the primary… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …tools to promote engaged, collaborative, and results-driven work environments. _The Senior Manager, Verification Programs has the following responsibilities:_ * ... Overview** This is a direct supervisory position in the Verification team of USP's Global Laboratory and Technical Operations...supplements and/or pharmaceuticals. * Knowledge of and experience with GMP audits using 21 CFR parts 111 and 117… more
- Integra LifeSciences (Princeton, NJ)
- …members, and ExM/Contract manufacturing leadership and maintains knowledge of current GMP expectations to define and drive Commercial QA objectives, strategies, and ... position. + DMAIC experience + Certified Quality Engineer (CQE) + Certified Quality Auditor (CQA) + Proficient with Minitab. + Coaching and mentoring skills. +… more
- West Pharmaceutical Services (Exton, PA)
- …through our sustainability efforts. **Job Summary** In this role, the Senior Quality Engineer provides quality direction, governance, and Quality Management System ... documentation and design manufacturing documentation (eg, product specifications, design verification & validation activities, FMEA risk documents, test methods,… more