Senior Regulatory Affairs Specialist - Global Approvals

A pharmaceutical company is seeking a Senior Specialist in Regulatory Affairs to manage and execute regulatory programs for product approvals. This role demands at least 5 years of relevant experience, including knowledge of US Regulatory Affairs. Responsibilities include strategy development, preparation of regulatory submissions, and assisting in product labeling. Candidates must have excellent organizational and communication skills, alongside a commitment to an inclusive workplace.

The position is full-time in Richmond, VA.
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