Senior Regulatory Affairs, CMC Biologics/Vaccines (Remote EU)
Job Description & Overview
Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance.
Responsibilities include developing post-approval CMC submission strategies for variations, renewals, market expansions, and annual reports; coordinating submission preparation with manufacturing, supply chain,
#J-18808-LjbffrReady to apply for this vacancy?
This driving opportunity is hosted on CV-Library. Click below to view the official posting and submit your application.
Key Details
- Date Posted: 23 Oct 2026
- Location: verona
- Employment Type: Permanent
- Category: General
Need an updated driver CV?
Build an ATS-optimised transport CV in 5 minutes with professional templates.
Build Free CV NowEmployer Information
Parexel
Verified Transport EmployerVerified transport and logistics firm operating commercial fleets across the UK network.
More Jobs at Parexel