Senior QA Supervisor – CDMO Product Development & Compliance
Listed on 2026-10-01
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Business
Regulatory Compliance Specialist
Germer International
- Pharmaceutical Recruiting is seeking a CMDO QA Supervisor to develop, implement, and maintain the Quality System ensuring data integrity for process development, engineering batches, and clinical trials. The role focuses on regulatory compliance and customer inquiries across CDMO projects, with 100% onsite work.
Responsibilities include release of materials and products, procedure maintenance, regulatory dossier support, and audits.
The Senior QA Supervisor – CDMO Product Development & Compliance role at Germer International
- Pharmaceutical Recruiting is now open for applications in Madison, WI, United States.
The Senior QA Supervisor – CDMO Product Development & Compliance position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
We have an opening for a Senior QA Supervisor – CDMO Product Development & Compliance in Madison, WI, United States within Bio & Pharmacology & Health, Management & Operations.
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