CMC Regulatory Affairs Consultant: Post-Approval Vaccines/Bio
Role Description & Technical Scope
Parexel is seeking an Regulatory Affairs Consultant - CMC for post-approval activities related to vaccines or biological products. The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely regulatory outcomes.
You will support worldwide regulatory activities, manage regulatory information systems, and identify risks to timelines and approvals in a dynamic, global team.
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Key Details
- Date Posted: 23 Oct 2026
- Location: bardi
- Employment: Permanent
- Workplace: Hybrid
- Domain: General
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Parexel
Verified Tech EmployerEnterprise technology firm or security consultancy operating across the UK digital defense ecosystem.
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