Lundbeck
A Manager Regulatory Affairs Operations leads technical and operational strategies for global regulatory publishing and submissions to health authorities like the FDA. This role ensures high-quality, compliant submissions throughout the product lifecycle while driving process optimization and digital modernization within the regulatory team. The position involves mentoring staff, managing complex eCTD submissions, and collaborating with cross-functional partners to meet evolving Health Authority expectations.
Headquarters
Copenhagen, Hovedstaden, Denmark
Company Size
5001-10000 employees
Founded
1915
Lundbeck is a global biopharmaceutical company headquartered in Copenhagen, Denmark, focused on the research, development and commercialization of treatments for disorders of the brain. Its therapeutic areas include neurology and psychiatry—such as depression, schizophrenia, Alzheimer’s and Parkinson’s diseases, epilepsy and migraine—and it provides patient resources, awareness campaigns and community engagement. Lundbeck invests in neuroscience research and partnerships to advance innovative medicines and improve outcomes for people living with brain disorders worldwide. The company works with healthcare providers, payers and patient organizations to address unmet needs in brain health.
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 Lundbeck.
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