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Senior Specialist, Quality Assurance
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Full-time
- The Sr Specialist Quality Assurance will be responsible for quality review of production and testing of clinical trial materials at external manufacturing site.
- Minimum of 3 years of relevant work experience in a pharmaceutical/biotech environment
- GMP quality assurance experience in the pharmaceutical or biotechnology industry
- Understanding of GMP regulatory requirements and implementation (FDA, ICH, EMA, etc
- Experience with Veeva preferred
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