Debiopharm is looking for a Pharmaceutical Quality (pQM) Specialist to join our Quality Management – R&D team in Lausanne, Switzerland. The role entails overseeing quality documentation, managing GMP support for development projects, and ensuring compliance with EU GMP and ICH guidelines. Ideal candidates will have a university degree in Pharmaceutical Sciences or a related field, and 3-5 years of GMP operations experience. Strong analytical skills, fluency in English and French, and the ability to work collaboratively are essential. Join us to make a significant impact in the field of oncology and anti-infective development.
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