Manager, Global Labeling Product Leader

Johnson & Johnson Innovative Medicine is recruiting for a Manager, Global Labeling Product Leader. The position can be based at any of the following R&D sites: US (Titusville, NJ; Raritan, NJ; or Spring House, PA), Canada (Toronto, Ontario), UK (High Wycombe), Netherlands (Leiden), Belgium (Beerse), or Switzerland (Allschwil, Bern, Zug). 

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges. 

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential. 

At Johnson & Johnson, we all belong.

In this role, you will:

• Have responsibility for the development and maintenance of primary and derived labeling documents for assigned compounds in assigned portfolio.


• Participate in creation of, and maintain primary labeling documents – the Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, EU Product Information (EUPI) – and derived documents (labeling text for EU, US).


• Coordinate the development, revision, review and approval of primary and derived labeling documents, including the Labeling Working Group (LWG) and Labeling Committee (LC) activities related to these documents.


• Ensure the dissemination of internally approved CCDS, USPI, EUPI and derived labeling documents and supporting documentation; work with other functions to ensure quality of labeling deliverables (e.g., alignment of labeling text with data, regulatory requirements, consistency between labeling documents).


• Contribute to and participate in the global labeling strategy including the development of target labeling.


• Contribute to the continuous improvement of the end-to-end labeling process.