Novo Nordisk A/S
A Senior Regulatory Affairs Specialist at Novo Nordisk drives global regulatory strategies for drug-device combination products, ensuring timely approvals and compliance across diverse markets. The role involves leading health authority interactions, managing complex projects, and providing scientific input to cross-functional teams to secure market access.
Headquarters
Alle, Central Jutland, Denmark
Company Size
10001+ employees
Founded
1923
Novo Nordisk is a leading global healthcare company founded in 1923 and headquartered in Denmark, with the stated purpose of driving change to defeat diabetes and other serious chronic diseases. It researches, develops, manufactures and markets pharmaceutical products and medical devices across diabetes care, obesity, haemophilia, growth disorders and other endocrine conditions, and is widely known for its insulin and GLP‑1 therapies. Combining extensive R&D, large‑scale manufacturing and global commercial reach, Novo Nordisk emphasizes patient‑centred care, access programs and sustainability in its work to improve outcomes for people with chronic disease.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
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
View leadership team, funding history,
and employee contacts for Novo Nordisk A/S.
294% above the average for this role
Director, Regulatory Affairs - Pharmaceuticals
Stryker
Senior Manager, Regulatory Affairs
Avalyn Pharma
Sr. Principal Scientist/Sr. Director, Regulatory Affairs
MSD
Director, Regulatory Affairs
bauschlomb.com
Regulatory Professional - Regulatory Affairs
State of Indiana
Regulatory Affairs Specialist
State of Indiana