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Nordic Regulatory Consultant
3 days ago
Your key responsibilities will include:
* Working with Regulatory Affairs, primarily on a local level, with focus on the Nordic countries (Sweden, Denmark, Norway, Finland, and Iceland)
* New registrations/variations/MAH-transfer applications
* Regular contact with health authorities
* Regulatory intelligence
* Local regulatory advice
* Launch preparations
* Strategic and operational regulatory support to clients and colleagues
* Regular follow-ups with clients
Qualifications
To be successful in this role, you will need:
* Understanding of registration procedures and requirements as well as product life cycle management from a regulatory affairs perspective
* Ability to work to deadlines and solve issues in a pragmatic and proactive way
* Excellent communication skills (oral and written) in Swedish & English language. Another Nordic language is a benefit but not a must
* 5+ years of experience in Regulatory Affairs, primarily focused on Nordic regulations
* MSc in Pharmacy, or equivalent
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