Nordic Regulatory Specialist

Ferring Pharmaceuticals

Kastrup, Denmark
**
Nordic pharmaceutical industry experience
Regulatory affairs in nordics
Marketing authorizations lifecycle management
** Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with over five years of experience in Regulatory Affairs within the Nordic pharmaceutical industry. This on-site role in Kastrup, Denmark, involves managing regulatory activities, ensuring compliance, and collaborating with cross-functional teams across 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.
  • Maintain regulatory systems and documentation, including product information, regulatory databases (e.g., DKMAnet, Farmalogg, LiiV, VnrExtranet), Ferring electronic files, and implement changes.
  • 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: 75

** Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with over five years of experience in Regulatory Affairs within the Nordic pharmaceutical industry. This on-site role in Kastrup, Denmark, involves managing regulatory activities, ensuring compliance, and collaborating with cross-functional teams across Nordic countries. **

Skills & Requirements

Must-have

  • Nordic pharmaceutical industry experience
  • Regulatory Affairs in Nordics
  • Marketing Authorizations lifecycle management
  • Promotional compliance and GDPR
  • Maintain regulatory systems and documentation

Nice-to-have

  • Collaborating with cross-functional teams
  • Navigating ambiguity with agility
  • Strong digital proficiency
  • International, dynamic, and collaborative environment

Key Requirements

  • 5+ years' experience in pharmaceutical industry
  • Strong expertise in Regulatory Affairs
  • Experience in Pharmacovigilance
  • Experience in Quality Assurance
  • Experience in promotional compliance
  • Fluent in English and at least one Nordic language

Work Rights

Must be located in the Øresund region

Tailored Resume

Cover Letter