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Sr Mgr Regulatory Labeling

Employer
Regeneron Pharmaceuticals, Inc.
Location
Tarrytown, New York
Start date
Aug 25, 2021

Job Details

Manages the development, review, approval, and maintenance of the Company Core Data Sheet (CCDS), USPI, EU SmPC and Rest of World (ROW) labeling. Provides labeling expertise to the Labeling Working Group and other relevant stakeholders, typically carrying out responsibilities with minimal guidance. Leads the development of labeling strategies and is responsible for the management of marketed or pipeline products, across the product lifecycle.

- Manages the Regulatory labeling process throughout the product lifecycle.

- Leads the Labeling Working Group and manages development, review, approval, and maintenance  of labeling  for CCDS, USPI, EU SmPC, and ROW labeling. Manages complex programs with minimal guidance from the Labeling Director. 

- Leads development of labeling strategies through interpretation of labeling regulations, guidelines and competitor analyses, and application to product situation.

- Leads development of target labeling documents to support the design and analysis plan for clinical trials, with guidance from the Labeling Director. 

- Leads or contributes to discussions on labeling topics at relevant management interactions.

- Effectively communicates labeling rationales to various levels of management to enable decision making.

- Provides labeling expertise on complex issues to stakeholders. Anticipates Health Authority perspectives and broader implications of strategies, proposing alternatives and providing advice to mitigate risk. Communicates consequences for product or portfolio.

- Prepares submission ready labeling documents. Maintains labeling documents in the electronic document management system and and relevant labeling trackers as appropriate.

- Contributes to the development of the Regulatory Labeling Group through active knowledge sharing and mentoring of junior staff members to build labeling expertise.

- Monitors worldwide regulation changes pertaining to Labeling regulations and maintains the labeling SOP and work instructions. May be responsible for leading or contributing to various continuous improvement projects.

Company

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to seven FDA-approved treatments and numerous product candidates in development, all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye disease, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, infectious diseases, pain and rare diseases.
 
Regeneron is accelerating and improving the traditional drug development process through our proprietary VelociSuite® technologies, such as VelocImmune® which produces optimized fully-human antibodies, and ambitious research initiatives such as the Regeneron Genetics Center, which is conducting one of the largest genetics sequencing efforts in the world.

Stock Symbol: REGN

Stock Exchange: NASDAQ

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Company info
Website
Phone
914-847-7000
Location
Corporate Headquarters
777 Old Saw Mill River Road
Tarrytown
New York
10591
United States

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