Nordic Regulatory Specialist

Ferring Pharmaceuticals

Kastrup, Denmark
On-site
Nordic pharmaceutical industry experience
Regulatory affairs in nordics
Marketing authorizations maintenance
Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist based in Kastrup, Denmark, who has extensive experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory activities, maintaining compliance, and supporting QA and PV processes across the Nordic countries

Job Summary

  • Lead Regulatory Affairs activities as the Nordic Subject Matter Expert, including maintenance of Marketing Authorizations, preparation and submission of variations, lifecycle management, and coordination with Global and Nordic Regulatory colleagues.
  • Ensure Nordic compliance through maintenance of local and regional SOPs in line with corporate policies and EU/EEA legislation.
  • By joining our International Pharma Science Center (IPC) in Kastrup, you become part of Ferring’s global network—collaborating across functions in a state-of-the-art waterfront building with stunning views of Sweden and easy access to Copenhagen Airport.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist based in Kastrup, Denmark, who has extensive experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory activities, maintaining compliance, and supporting QA and PV processes across the Nordic countries.

Skills & Requirements

Must-have

  • Nordic pharmaceutical industry experience
  • Regulatory Affairs in Nordics
  • Marketing Authorizations maintenance
  • Promotional compliance and GDPR
  • EU/EEA legislation understanding

Nice-to-have

  • Collaborating effectively with cross-functional teams
  • Delivering clear, confident presentations
  • Navigating ambiguity with agility
  • Strong digital proficiency
  • Communicating fluently in English and Nordic language

Key Requirements

  • 5+ years' experience in pharmaceutical industry
  • Strong expertise in Regulatory Affairs
  • Experience in Pharmacovigilance, Quality Assurance
  • Experience in promotional compliance
  • Current understanding of regulatory requirements for all Nordics countries

Work Rights

Candidates must be located in the Øresund region

Tailored Resume

Cover Letter