Associate Director, Regulatory Affairs CMC - Hybrid Onsite

AbbVie

2 months ago

North Chicago, IL

Onsite

Full Time

Senior

0 applicants

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About this role

The Associate Director of Regulatory Affairs in CMC at AbbVie is responsible for developing and managing regulatory strategies, preparing submissions, and serving as a liaison with regulatory agencies for small molecule, peptides, and sterile injectable products. The role involves leading initiatives to ensure successful product approvals and maintaining compliance across global regulatory environments.

Skills

About AbbVie

abbvie.ca

AbbVie is a global biopharmaceutical company (spun out of Abbott in 2013) that discovers, develops and commercializes specialty medicines across immunology, oncology, neuroscience, eye care and virology. It is best known for blockbuster brands such as Humira and a growing portfolio that includes targeted biologics and small molecules (and expanded capabilities after the Allergan acquisition). AbbVie emphasizes large-scale R&D, clinical development and strategic partnerships to advance its pipeline and bring therapies to patients worldwide. Headquartered in North Chicago, Illinois, the company operates globally with a focus on long-term innovation and patient outcomes.