GMP Quality Specialist – R&D (Lausanne)

Debiopharm is seeking a Pharmaceutical Quality Specialist in Lausanne, Switzerland. This permanent role focuses on ensuring robust oversight of quality documentation and vendor activities, driving compliance with quality standards. The ideal candidate will have a relevant degree and 3-5 years of GMP experience, with strong analytical and organizational skills. Fluency in English and French is essential. Join a team committed to oncology and anti-infective development, fostering an innovative work environment.
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