Global CMC Regulatory Affairs Consultant Vaccines/Bio
Role Description & Overview
Parexel is seeking a Regulatory Affairs Consultant - CMC vax/bio in Caserta, Italy, offering home or office based work. You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products within a regulatory team.
You will collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely delivery. Fluent English is required, and experience with Veeva Vault is valued.
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Key Details
- Date Posted: 23 Oct 2026
- Location: roma
- Employment: Permanent
- Workplace: Hybrid
- Specialism: General
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