15 oct
|
Parexel
|
México
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 (México)
🏢 Parexel
📍 México