GMP QA Specialist – Gene Therapy | Impact & Growth

A global CDMO in Switzerland is seeking an experienced Quality Assurance professional to support its GMP facility. The role involves implementing quality systems, reviewing quality documents, and managing CAPA processes. Candidates should possess a Master’s or PhD in relevant fields, with a minimum of 5 years of experience in a GMP-regulated biopharmaceutical environment. The position offers competitive compensation, flexible working hours, and opportunities for personal and professional development.
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