Senior Regulatory Affairs Lead — Drug-Device Combos (US NDA)

Planet Pharma is seeking a Regulatory Affairs specialist with end-to-end experience in IND/CTA to NDA/MAA submissions for drug-device combination products. The role emphasizes DMF submissions, device regulations, and US NDA support within a fast-paced sponsor-side environment.

The successful candidate will drive regulatory strategies, collaborate across functions, and manage complex submissions to tight deadlines in the Greater London area.

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