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Senior Specialist, QA Operations Investigations
Bristol Myers Squibb
Leiden · On-siteMid level (2–5 years)Full-timePosted 19 days ago
About the job
What you'll do
The Senior Specialist is responsible for the quality review and approval of manufacturing and laboratory investigations to ensure compliance with cGMP policies. They will also manage CAPAs, perform root cause analysis, and support internal and external inspections.
What they're looking for
Candidates should have a bachelor's degree in a relevant science or engineering field and at least 4 years of experience in a regulated industry. Proficiency in deviation management, root cause analysis tools, and regulatory guidelines like FDA/EMA is required.
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