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.
#J-18808-LjbffrSenior QA Supervisor – CDMO Product Development & Compliance in madison at Unknown Company
This position is listed as full time and onsite.