About the Role
A global biomanufacturing company in Hamilton, Ontario is seeking an Associate II for Commissioning, Qualification, and Validation. In this role, you'll support the development of validation plans and ensure compliance with GMP standards. Candidates should have 3+ years of experience in a biopharma environment and knowledge of regulatory guidance. The company values flexibility and adaptability, and offers a dynamic work environment with a focus on advanced cell and gene therapies.
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