Senior QA Specialist II - GMP & Regulatory Compliance
Bachem Holding AG
Bachem Americas is seeking a QA Specialist II to perform day-to-day QA activities ensuring drug substances meet FDA and international regulations across R&D to commercial stages. The role reviews GMP documents, provides cGMP guidance, and supports audits. You will manage GMP records, coordinate QA reviews, train new hires, drive continuous improvement, implement the Quality Management System, and archive GMP records using electronic systems such as MasterControl. #J-18808-Ljbffr Bachem Holding AG
Vacancy posted 3 hours ago
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