Associate Director, Regulatory Affairs CMC - Hybrid Onsite
AbbVie
About this role
The Associate Director of Regulatory Affairs, CMC at AbbVie specializes in small molecule development, focusing on peptides and sterile injectables. The role involves strategic planning for regulatory submissions, coordinating with regulatory agencies, and leading internal initiatives to ensure product approval and compliance in a complex, matrix environment.
Skills
About AbbVie
abbvie.comAbbVie is a global, research-driven biopharmaceutical company that was spun off from Abbott Laboratories in 2013. It develops and commercializes specialty medicines across immunology, oncology, neuroscience, eye care and virology — with Humira historically its flagship product — and has broadened its portfolio through acquisitions (notably Allergan) and strategic collaborations. AbbVie emphasizes a robust R&D pipeline, targeted therapies, and global commercial and manufacturing capabilities. The company focuses on delivering long-term treatment options for complex, chronic and serious diseases.
About AbbVie
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
Unlock Company Insights
View leadership team, funding history,
and employee contacts for AbbVie.
Salary
$158k – $211k
per year
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