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Senior QA Lead, External Quality Ops; cGMP
Job Description & How to Apply Below
A leading biotech firm in Toronto is seeking a Sr. Specialist in Quality Assurance to ensure quality of cGMP activities at external contract organizations for investigational cell and gene therapy products. The role entails leading compliance activities, overseeing technology transfer, and supporting investigations. Candidates should possess a Life Sciences degree and at least 5 years of relevant experience in a GMP-regulated environment.
Strong knowledge of cGMP regulations and cooperation with CxOs are essential. A proactive attitude and adaptability to alternate time zones are preferred.
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Position Requirements
10+ Years
work experience
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