Regulatory Affairs Specialist
Zentiva(2 months ago)
About this role
A Regulatory Affairs & Medical Affairs Specialist based in Portugal covering regulatory, medical, and market access functions for pharmaceutical products. The role supports regulatory compliance and product lifecycle activities across EU and national levels and liaises with internal and external stakeholders to enable successful product launches and market access.
Required Skills
- Regulatory Affairs
- Medical Affairs
- Market Access
- DCP
- MRP
- Labeling Compliance
- Submission Preparation
- Stakeholder Engagement
- Inspection Readiness
- Portuguese
+1 more
Qualifications
- Degree in Pharmacy
- Degree in Life Sciences
About Zentiva
zentiva.comWe develop, produce, and deliver high-quality, affordable medicines to more than 100 million people across Europe.
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