06 nov
|
Sin nombre
|
Tijuana
06 nov
Sin nombre
Tijuana
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 (Tijuana)
🏢 Sin nombre
📍 Tijuana