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Job Description & How to Apply Below
A biotech company is seeking a Sr. Specialist in Quality Operations in Toronto. The role requires ensuring the quality of cGMP activities at external contract organizations for investigational cell and gene therapy products. Candidates should have at least 5 years of experience in QA within the pharma or biotech industry, with strong knowledge of cGMP regulations and the ability to work with diverse teams.
This position offers an opportunity to engage with external partners and enhance compliance practices.
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