Remote CMC Regulatory Affairs Associate — Submissions (Centro)

Remote CMC Regulatory Affairs Associate — Submissions (Centro)

06 nov
|
Importante empresa
|
Centro

06 nov

Importante empresa

Centro

Parexel is seeking a Senior Regulatory Associate to author integral CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs. You will prepare CMC packages, support GMP submissions, manage change control assessments, and ensure regulatory compliance across regions.

Ideal candidates have at least 5 years in biotech/pharma regulatory affairs, strong M3 authoring experience, and solid cross-regional regulatory knowledge. Remote work options are available.

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📌 Remote CMC Regulatory Affairs Associate — Submissions (Centro)
🏢 Importante empresa
📍 Centro

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