Global CMC Regulatory Affairs Consultant Vaccines/Bio

06 ott - Firenze
Parexel

Parexel is seeking a Regulatory Affairs Consultant

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- 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. xlwpduy

Fluent English is required, and experience with Veeva Vault is valued.

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