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Senior Regulatory Affairs Specialist Job Description Position Objective: The Senior Regulatory Specialist will join the Reulatory Affairs, clinical and Compliance Team based at one of our Grand Island, Frederick, or Carlsbad site. As a Senior Regulatory Specialist you will be responsible for managing In-Vitro Diagnostic (IVD) Medical Device regulatory submissions (CE marking), Cell Therapy Drug Master File submissions to FDA for regulated products and provide regulatory support on development cell. After registering you may be able to apply for this job directly (if still active) on (Thermo Fisher Scientific)'s site. Future job matches may be sent from Geebo approved job partners.
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