Job Description
Role Description
Nordic Regulatory Affairs Coordinator
Location: Copenhagen, Denmark | Office-based | Full-time Planned start date: October 1st, 2026
Reports to: Head of QA/RA/PV/MC Nordics
About the Role
Zoetis is seeking a Regulatory Affairs (RA) Coordinator to join our Nordic team, supporting Denmark, Sweden, Norway, and Finland.
This role is well suited for a structured, service-minded coordinator who enjoys working across teams, keeping documentation in order, and ensuring tasks are completed on time. Regulatory Affairs experience is an advantage, but not a requirement — we value strong coordination skills, attention to detail, and the ability to learn and work confidently in regulated processes. Limited travel may be required.
This role offers a solid platform to develop within regulatory affairs and the pharmaceutical industry, with close collaboration across QA, RA and Pharmacovigilance (PV).
Key Responsibilities
- Coordinate tasks related to marketing authorizations for medicinal products across the Nordic markets (DK, FI, NO & SE)
- Coordinate packaging material and artwork updates to ensure compliance (a central part of the role)
- Support variation applications and marketing authorization procedures, ensuring activities are delivered on time and documentation is complete
- Provide local regulatory support for centrally approved products by coordinating inputs, tracking actions, and maintaining records
- Coordinate communication and follow-up with suppliers, regulatory authorities, and internal colleagues
- Support daily business continuity across QA, RA, and PV by coordinating activities, tracking status, and addressing practical issues
- Maintain archiving, documentation, and administrative processes within QA/RA/PV (e.g., document control, filing, templates, trackers)
Qualifications & Requirements
Education & Background
- Relevant education (e.g., business administration, life sciences, or similar) or equivalent experience from a coordination/administrative role
- Experience from a regulated industry (e.g., pharma/medico/healthcare/food/cosmetics) is an advantage, but not required
- Regulatory Affairs experience is a plus, not a requirement
Skills & Attributes
- Strong coordination and communication skills; comfortable working with multiple contacts and following up to keep tasks moving
- Highly structured and detail-oriented, with good discipline in documentation and version control
- Service-minded and solution-oriented; able to prioritize and keep overview when deadlines overlap
- Proactive and pragmatic; comfortable taking ownership of tasks and driving them to completion
- Collaborative, positive, and willing to support across functions when needed
Why?
Zoetis has strong development potential and is an international company on a growth trajectory. You will have an opportunity to broaden your capabilities, take part in a dynamic and agile company, where your effort and attitude are of the essence.
You will become part of a strong, supportive team that helps each other succeed. The role is based at our office in Parken, Copenhagen.
Application
We look forward to receiving your CV and application. We review applications on an ongoing basis, so we encourage you to apply as soon as possible.
Full time
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