Center Quality Manager — QA & Compliance Lead
Listed on 2026-10-15
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Octapharma Plasma, Inc. is seeking a Center Quality Manager I to ensure compliance with FDA, EMA, and local regulations while safeguarding donor safety. This role operates independently from center Operations and collaborates with the Operations team to uphold product quality and regulatory standards.
You will lead QA activities, manage audits, training, and CAPA processes, and contribute to continuous improvement in a fast‑growing plasma donation network across the United States.
We have an opening for a Center Quality Manager I — QA & Compliance Lead in Grand Rapids, MI, United States within Bio & Pharmacology & Health, IT & Technology.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Grand Rapids, MI, United States.
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