Nordic Regulatory Specialist

Ferring Pharmaceuticals

Kastrup, Denmark
Onsite
Nordic pharmaceutical industry experience
Regulatory affairs management
Marketing authorizations maintenance
Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with extensive experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory tasks across the Nordic countries, ensuring compliance, and supporting quality assurance and pharmacovigilance processes. The position is based in Kastrup, Denmark, and requires fluency in English and at least one Nordic language

Job Summary

  • You will be responsible for managing RA work in the Nordics, with support from and in partnership with, Regulatory Managers in the Nordics with accountability for QA and PV.
  • Our International Pharma Science Center (IPC) in Kastrup, Denmark, is a state-of-the-art waterfront building with stunning views of Sweden and easy access to Copenhagen Airport.
  • You will be part of a dedicated team of three Regulatory experts working within the Nordics Cluster (Denmark, Finland, Iceland, Norway and Sweden), reporting to the Head of RQS – Nordics.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with extensive experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory tasks across the Nordic countries, ensuring compliance, and supporting quality assurance and pharmacovigilance processes. The position is based in Kastrup, Denmark, and requires fluency in English and at least one Nordic language.

Skills & Requirements

Must-have

  • Nordic pharmaceutical industry experience
  • Regulatory Affairs management
  • Marketing Authorizations maintenance
  • Promotional compliance and GDPR
  • Nordic regulatory compliance

Nice-to-have

  • Collaborating with cross-functional teams
  • Agility in navigating ambiguity
  • Strong digital proficiency
  • Creative and practical solutions

Key Requirements

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

Work Rights

Candidates must be located in the Øresund region

Tailored Resume

Cover Letter