Manager, Global Labeling Product Leader

Johnson & Johnson Johnson & Johnson · Pharma · Raritan, NJ +4

Manager, Global Labeling Product Leader for Johnson & Johnson's Innovative Medicine R&D. Responsible for the development, revision, review, and maintenance of primary labeling documents (CCDS, USPI, EUPI) and derived labeling for assigned compounds. Requires a scientific degree, 4+ years in pharma, and 3+ years in regulatory affairs/labeling. Must understand drug development and worldwide regulatory guidelines for labeling.

What you'd actually do

  1. Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
  2. Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation. Ensure high quality and compliant labeling documents.
  3. Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeling and target labeling.
  4. Contribute to the continuous improvement of the end-to-end labeling process.

Skills

Required

  • Bachelor's degree in a scientific discipline
  • 4 years of relevant experience in the pharmaceutical industry
  • Understanding of pharmaceutical drug development
  • Experience in discussing and communicating scientific concepts
  • Basic understanding of worldwide regulatory guidelines and their applications for guidance for labeling
  • Experience leading project teams in a matrix environment
  • Experience participating in continuous improvement projects
  • Experience working with document management systems
  • Exceptional verbal and written communication skills
  • Strong organizational, negotiation, and partnering skills
  • Ability to work independently

Nice to have

  • Advanced degree (Master’s PhD, PharmD) in a scientific discipline
  • 3 years of Regulatory Affairs experience in product labeling/labeling regulations, or equivalent
  • Experience effectively/appropriately prioritizing and managing multiple products and projects simultaneously
  • Ability to drive a collaborative, customer-focused, learning culture

What the JD emphasized

  • scientific discipline
  • pharmaceutical industry
  • product labeling
  • labeling regulations
  • pharmaceutical drug development
  • scientific concepts
  • worldwide regulatory guidelines
  • labeling
  • project teams
  • continuous improvement projects
  • document management systems
  • verbal and written communication skills
  • organizational, negotiation, and partnering skills