Internship - Site regulatory compliance and inspections (m/f/d)
Updated: May 13, 2024 07:47 PM GMT
Merck KGaA, Darmstadt, Germany
AubonneStart date : SeptemberDuration : 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... More Detail
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