Global Labeling Product Leader

Title: Contractor Global Labeling Product Leader
Duration: Long term contract
Location: 100% remote


An opportunity has arisen for a Contractor Global Labeling Product Leader ( GLPL ) to support the products in Janssen R&D within the Global Labeling Centre of Excellence (GL CoE).

Responsibilities include development of target labeling, managing the development of updates to Company Core Data Sheets ( CCDSs ), Centralized/MRP EUPIs, and USPIs in accordance with GL CoE and GRA end-to-end labeling processes. System and business process training will be provided to the Contractor.

Qualifications, experience and skills

  • Minimum of Bachelor's degree in a scientific discipline. Advanced degree (MS, PharmD, Ph.D., or MD) desirable. Candidates without a scientific degree but with relevant labeling experience will be considered
  • At least 6 years experience in the pharmaceutical industry or health authority, with at least 5 years experience in regulatory affairs with direct experience associated with product labeling (prescribing and patient information) is preferred. Candidates with fewer years' experience will be considered.
  • · Product labeling experience should include authoring text for inclusion in CCDSs , in addition to EUPIs, and/or USPIs, including drafting text based on scientific source data, supporting rationale, regulatory requirements, standards, and templates, and liaison with subject matter experts and regulatory professionals.
  • Advanced Microsoft Word skills. Experience working in a Documentum-based document management system. Basic Excel and PowerPoint skills. Excellent project management, verbal, and written communication skills.

Job Requirements:
  • Responsibilities

    • Facilitation of Labeling Negotiations with Health Authorities for EUPI and USPI for the Assigned product(s); facilitating LWG review and LC endorsement of labeling documents; preparation and finalization of submission-ready EUPI and USPI
    • Processing Local Labeling Deviation requests for assigned products for ex-US and ex-EU markets, including facilitating LWG review and LC
    • Preparing updates to the CCDS, EUPI, and USPI for products in additional therapeutic areas (for new indications, safety updates, CMC revisions), including facilitating LWG review and LC endorsement of the CCDS and finalizing/releasing the CCDS
Raritan, NJ 08869, US