Nordic Regulatory Specialist

Ferring Pharmaceuticals

Kastrup, Denmark
**
Nordic pharmaceutical industry experience
Regulatory affairs management
Promotional compliance and gdpr
** Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with over five years of experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory work across Nordic countries, ensuring compliance, and collaborating with various stakeholders in a dynamic, international environment. **

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: 75

** Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with over five years of experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory work across Nordic countries, ensuring compliance, and collaborating with various stakeholders in a dynamic, international environment. **

Skills & Requirements

Must-have

  • Nordic pharmaceutical industry experience
  • Regulatory Affairs management
  • Promotional compliance and GDPR
  • Maintenance of Marketing Authorizations
  • Nordic regulatory systems and documentation

Nice-to-have

  • Collaborating with cross-functional teams
  • Navigating ambiguity with agility
  • Delivering clear presentations
  • Digital proficiency with MS Office and Teams

Key Requirements

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

Work Rights

Candidates must be located in the Øresund region

Tailored Resume

Cover Letter