Quality Assurance Coordinator
Vor 7 Tagen
MSD Switzerland requires a dedicated Regulatory Release Specialist to join their Clinical Supplies Quality team. In this role, you will play a vital part in releasing packaged and labeled drugs for use in clinical studies. Your responsibilities will include reviewing and releasing incoming label stock, as well as overseeing the release of clinical and commercial drugs.
Main Responsibilities:
- Review and approve incoming label stock to ensure compliance with regulations
- Release of clinical finished goods, including review of printed and applied labels
- Conduct GMP reviews of batch records and regulatory filings to authorize final releases
Requirements:
- At least 2 years of experience working in a regulated environment, ideally within the pharma or medtech industries
- Prior experience in a similar role is highly beneficial
- A university degree (bachelor's or higher) is desirable
This position is temporary; more information will be provided after applying.
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