Regulatory Affairs Associate
Allergan
AbbVie in Irvine, CA is seeking a Senior Associate, RA CMC to lead post-approval CMC changes and support regulatory filings. You will author and assemble CMC sections for marketed products, coordinate with RA CMC leads, and work across diverse teams to ensure timely submission readiness. The role requires 4 years of pharma experience with knowledge of CTD structure and electronic document management; strong communication is essential. #J-18808-Ljbffr
Vacancy posted 5 days ago
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