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Manager, Global Labeling Product Leader

jj · Allschwil

Nouveau
Senior 🇬🇧 English
Document management systems Regulatory affairs Product labeling

Description du poste

About the role

Johnson & Johnson is looking for a Manager, Global Labeling Product Leader to be based in Allschwil, Switzerland, or alternatively in Berne or Zug. The role sits in the Regulatory Affairs group, within Global Labeling, which is responsible for the strategic development and lifecycle management of product labeling across therapeutic areas, established products, regions and affiliates. It covers the end-to-end labeling process, from target labeling through the Company Core Data Sheet (CCDS).

Key responsibilities

  • Lead the development, revision, review, agreement and maintenance of primary labeling (CCDS, USPI and associated patient labeling, EUPI) and derived labeling documents for assigned compounds.
  • Advise on labeling content, processes, timelines and scientific integrity, and coordinate the resolution of labeling issues that could affect primary or derived labeling.
  • Ensure labeling documents are high quality and compliant.
  • Contribute to the global labeling strategy, including understanding competitors' development plans and labeling aspects.
  • Contribute to continuous improvement of the end-to-end labeling process.

Required profile

  • Bachelor's degree in a scientific discipline; an advanced degree (MS, PhD, MD or PharmD) is preferred.
  • Minimum 4 years of relevant experience in the pharmaceutical industry (e.g. Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance).
  • Minimum 3 years of Regulatory Affairs with product labeling or labeling regulation experience, or equivalent, preferred.
  • Experience leading project teams in a matrix environment, with the ability to work largely independently with limited supervision.
  • Proactive approach, continuous improvement experience, and strong verbal and written communication, organizational, negotiation and partnering skills.

Required skills

  • Understanding of pharmaceutical drug development and basic knowledge of worldwide regulatory guidelines for labeling.
  • Experience with document management systems.
  • Ability to prioritize and manage multiple products and projects simultaneously (preferred).

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Source : ats:workday

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jj

Allschwil