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Regulatory Compliance Expert

vor 1 Woche


Luzern, Luzern, Schweiz Merck Gruppe - MSD Sharp & Dohme Vollzeit
Job Requirements

To be successful in this role, you will need:

  • 3 years' experience in pharmaceutical industry in a QA function.

  • A strong background in Current Good Manufacturing Practice (cGMP), risk management, investigations, and problem-solving.

  • Strong written and verbal communication skills.

  • An ability to think logically and be proactive under pressure.

  • An ability to work as part of a team and on your own initiative in a constructive manner.

  • Strong attention to detail and precision in preparing and reviewing GMP documentation.

  • Experience interacting with regulatory officials would be a plus.

  • Experience in quality management systems such as Veeva, SAP, PAS-X etc. would be a plus.