Internship - Site regulatory compliance and inspections (m / f / d)

Start date : February 2025Duration :  6 monthsLocation :  Aubonne, Switzerland :  Participation to the Quality and Regulatory documentation practices related to the manufactured and tested products such as Site registration, Health Authority Paper inspection Support to the Regulatory Product Experts. Follow-up on regulatory submissions and health authority approvals of changes. Participation on Site Regulatory improvement projects.Coordinating the provision of regulatory deliverables to support regulatory submissionsUpdate the Site Master File, a document summarizing all ongoing activities in Aubonne, in close collaboration with the different departments on siteKPIs for SRC and Inspection team, Work on inspection preparation, if needed. Your profile :  A relevant diploma in Life-science (Pharmacy, Engeneering degree, Master Science, Chemistry or other related topic)Knowledge in Biotechnological sciences is a plusFluently spoken and written English and French Good editorial and communication skillsAutonomous