AbbVie

Manager, RA TA Group, Regulatory Affairs(Oncology)

AbbVie

1 month ago
Minato City, Tokyo, Japan
Onsite
Full Time
Senior
0 applicants
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AbbVie
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About this role

The Regulatory Affairs TA at AbbVie is responsible for ensuring the timely approval of new products and indications by developing strategic regulatory plans, leading submissions, and managing interactions with regulatory authorities. The role involves coordinating global and local teams, maintaining regulatory records, and supporting product commercialization.

Skills

AbbVie

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.

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

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