Part-Time VP, Regulatory Affairs — FDA Submissions
Listed on 2026-10-15
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Pharmaceutical
Regulatory Compliance Specialist, Medical Science Liaison, Healthcare Compliance
Pro Pharma is seeking an Interim VP, Regulatory Affairs to provide senior strategic and hands‑on support across development programs. You will help set regulatory priorities, lead preparation for FDA interactions and key submissions, and advise cross‑functional teams on regulatory decisions.
The role supports the organization through a period of limited capacity, with a 20‑hour workweek and a four‑month duration in a hybrid schedule in the United States.
This is a great opening to take on the Part-Time VP, Regulatory Affairs — FDA Submissions role at PPG US Pro Pharma Group, LLC.
We are looking to fill the Part-Time VP, Regulatory Affairs — FDA Submissions position at PPG US Pro Pharma Group, LLC in Raleigh, NC, United States.
The Part-Time VP, Regulatory Affairs — FDA Submissions role at PPG US Pro Pharma Group, LLC is now open for applications in Raleigh, NC, United States.
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