Sterility Assurance Lead — GMP Manufacturing Excellence
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Quality Assurance - QA/QC
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Pharmaceutical
Job Description & How to Apply Below
Bio-Techne Corp. is seeking a Sterility Assurance Program Manager to lead the sterility program in a GMP manufacturing environment. You will own policies, validations, testing, and contamination control while guiding cross‑functional teams to mitigate sterility risks.
The role requires deep knowledge of aseptic processing, sterile dosing, and regulatory requirements (FDA/EMA/ISO). Onsite work in a bio/pharma manufacturing setting with strong emphasis on quality and continuous improvement.
This role, Sterility Assurance Lead — GMP Manufacturing Excellence at Bio-Techne Corp., could be your next career step.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Sterility Assurance Lead — GMP Manufacturing Excellence role in the description above.
We appreciate your interest in this position.
Join Bio-Techne Corp. and contribute to our ongoing work.
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