CMC Regulatory Strategy Lead – Biopharma Development
Listed on 2026-10-08
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Healthcare
GSK is seeking a CMC Regulatory Lead to drive regulatory strategy across development to early commercial products. You will coordinate cross-functionally to prepare, review, and submit CMC content, while assessing risks and implementing mitigation plans.
You may mentor teams and collaborate with internal/external partners to align regulatory expectations. The role requires extensive experience with global CMC regulations, strong leadership, and a track record of influencing regulators.
We are currently recruiting a CMC Regulatory Strategy Lead – Biopharma Development for our team in Waltham, MA, United States.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Waltham, MA, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 144..
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