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von: NonStop Consulting
MSAT is your playground? Do you have experience in all areas of pharmaceutical production (Upstream, Downstream, DxP, Quality Control...) and are ready to manage them holistically? Then get in touch!
Our client is looking for an experienced expert to oversee the technical and analytical aspects of pharmaceutical manufacturing processes.
Your Responsibilities:
- Technical leadership and supervision of pharmaceutical production, including technology transfer, manufacturing processes, and quality control.
- Drafting, reviewing, and approving GxP and quality documents to ensure regulatory compliance.
- Managing Change Controls within the MSAT area.
- Acting as a key interface for Quality Assurance, Regulatory Affairs, and external partners (CMOs, laboratories, API suppliers).
- Providing expertise on analytical methods (HPLC, endotoxins, sterility, etc.).
- Supporting regulatory inquiries and GMP compliance.
- Overseeing stability studies and managing reference standards.
Your Profile:
- Master's degree in Life Sciences (Pharmacy, Chemistry, Biotechnology, etc.).
- At least 5 years of experience in GMP environments, with a focus on manufacturing (e.g., oral forms, injectables) and analytical processes.
- Strong knowledge of quality management (CCs, CAPAs, deviations).
- Excellent organizational skills, initiative, and intercultural competence.
- Proficiency in IT tools (MS Office, project management software).
- Fluent in English; French is an advantage.
Interested? Apply now!
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