QA Specialist - GMP/CDMO in Gene Therapy, Flexible Hours

A leading CDMO in Switzerland is seeking a QA Specialist to implement quality systems and oversee operational excellence in its GMP facility. The ideal candidate will have a strong background in biotechnology, with at least 5 years of experience in a GMP-regulated environment. Responsibilities include reviewing quality documents, conducting root cause analysis, and ensuring compliance with industry regulations. This role offers competitive compensation and opportunities to work on innovative gene therapy projects.
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