CMC Regulatory Lead – Biologics & Vaccines (Remote)
Clinical Role Overview
Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines. You will collaborate with manufacturing, QA, QC and regulatory teams to shape submission strategies and support variations, renewals and market expansions, with remote options across Europe.
Responsibilities include developing post-approval CMC submissions, assessing regulatory impact of changes, coordinating with cross-functional teams, reviewing study reports, and writing/
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Key Details
- Date Posted: 23 Oct 2026
- Location: bardi
- Employment Type: Permanent
- Workplace: Remote
- Category: General
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Parexel
Verified Healthcare EmployerVerified NHS trust or certified UK healthcare facility offering professional development and clinical governance.
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