Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist to manage regulatory affairs across the Nordic region, with a focus on compliance, pharmacovigilance, and quality assurance. The position is located in Kastrup, Denmark, and requires over five years of experience in the pharmaceutical industry, particularly in regulatory affairs
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 to manage regulatory affairs across the Nordic region, with a focus on compliance, pharmacovigilance, and quality assurance. The position is located in Kastrup, Denmark, and requires over five years of experience in the pharmaceutical industry, particularly in regulatory affairs.
Skills & Requirements
Must-have
Nordic pharmaceutical industry experience
Regulatory Affairs expertise
Marketing Authorizations maintenance
Variations preparation and submission
Nordic regulatory compliance
Promotional compliance and GDPR
Nice-to-have
Collaborating with cross-functional teams
Delivering clear presentations
Navigating ambiguity with agility
Strong digital proficiency
International, dynamic, and collaborative environment
Key Requirements
5+ years' experience in pharmaceutical industry
Experience in Pharmacovigilance
Experience in Quality Assurance
Experience in promotional compliance
Fluent in English and at least one Nordic language