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Regulatory Affairs Principal, Pharmaceutical and Combination Products

Remote · Norway Full-time

Job Description:

  • Provide strategic regulatory leadership to support the development, approval, and lifecycle management of pharmaceutical and combination drug-device products
  • Serve as a key regulatory partner to cross-functional teams, with a primary focus on FDA CDER interactions, IND/NDA submissions, and global regulatory strategy
  • Author and review INDs, NDAs, supplements, and other global regulatory submissions
  • Develop and deliver high-quality briefing documents, responses, and regulatory communications
  • Provide regulatory guidance on clinical, nonclinical, and CMC development activities
  • Drive combination product regulatory strategy, including coordination with FDA’s Office of Combination Products (OCP)
  • Advise on labeling strategy, including prescribing information and device components of combination products
  • Assess regulatory impact of development and post-approval changes and define appropriate regulatory pathways
  • Support global regulatory activities, including submissions and interactions with ex-U.S. health authorities (e.g., EMA)
  • Stay current on evolving regulatory requirements and translate them into actionable guidance for teams
  • Mentor and provide guidance to junior regulatory team members

Requirements:

  • 7+ years of regulatory affairs experience in pharmaceuticals, biotechnology, or combination products
  • Proven experience with FDA CDER submissions, including INDs, NDAs, and/or supplements
  • Demonstrated success interacting with FDA, including meeting preparation and regulatory strategy execution
  • Experience with combination products (drug-device) strongly preferred
  • Working knowledge of U.S. regulatory requirements (21 CFR 210/211, Part 4) and relevant FDA guidance
  • Exposure to global regulatory environments (e.g., EMA, ICH) preferred
  • Bachelor's degree in a scientific discipline required
  • Advanced degree (MS, PhD, PharmD) preferred
  • Certification RAC (US or Drugs) preferred
  • Travel 0-10%

Benefits:

  • Competitive salary
  • Flexible working hours
  • Professional development budget
  • Home office setup allowance
  • Global team events

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