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Regulatory Release Specialist

vor 1 Woche


Luzern, Luzern, Schweiz MSD Switzerland Vollzeit

The Clinical Supplies Quality team plays a crucial role at MSD Switzerland, ensuring the release of packaged and labeled drugs for usage in clinical studies. This team is responsible for overseeing the release of clinical and commercial drugs, including packaging, incoming label stock, and primary packaging components to the release of clinical finished goods.

Key Responsibilities:

  • Review and approval of incoming label stock
  • Release of clinical finished goods, involving review of printed and applied labels
  • GMP review of batch records and regulatory filings, culminating in final release authorization

Requirements and Qualifications:

  • Minimum 2 years of experience in a regulated environment, preferably within the pharmaceutical or medical technology sectors
  • Prior experience in a similar role is highly valued
  • A university degree (bachelor's or higher) is preferred

This is a temporary position; further details will be provided upon application.