The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.

To evolve in this environment, we are looking for our next Process Validation Expert.

You will be responsible for:

• Technical transfer, process validation, IMP & commercial manufacturing campaign activities coordination
• Coordination of production troubleshooting/investigation and potential support, if required
• Coordination with Pharmaceutical Development entities
• Training of Aubonne site personnel
• Internal / External audits