Senior Manager, Global Labeling Product Leader (2 Positions)

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 breakthroughs of tomorrow and profoundly impact health for humanity.

Job Function : Regulatory Affairs Group

Job Sub Function : Regulatory Affairs

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. You are encouraged to apply to the specific country(s) that align with your preferred location(s).

• United States - Requisition Number : R-007626
• Belgium, Poland - Requisition Number : R-008149
• United Kingdom - Requisition Number : R-008251

Your application to one or all postings will be considered as a single submission.

Position Overview

Johnson & Johnson Innovative Medicine R&D is recruiting for a Senior Manager, Global Labeling Product Leader . This hybrid role is based in Allschwil, Switzerland. The Associate Director will be a leading expert, managing large projects or processes, and developing methods for planning, directing, coordinating, and controlling regulatory affairs activities related to new and modified products worldwide, ensuring compliance with regulations and corporate policies.

Key Responsibilities

• Lead the development, revision, review, and maintenance of primary labeling (e.g., CCDS, USPI, EUPI) for assigned compounds.
• Provide guidance on labeling content, processes, timelines, and scientific integrity; coordinate resolution of labeling issues and collaborate with external partners as needed.
• Contribute to and implement global labeling strategies, understanding competitor activities and therapeutic area developments.
• Improve the end-to-end labeling process continuously.

Qualifications

• Bachelor’s degree in a scientific discipline required; advanced degrees preferred.
• At least 8 years of professional experience, with 6+ years in regulatory labeling content development for pharmaceuticals.
• Relevant experience in the pharmaceutical industry, understanding of drug development, and regulatory guidelines.
• Strong communication, organizational, negotiation, and project management skills.
• Ability to work independently and manage complex labeling projects.

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