Regulatory Affairs Specialist
Zentiva(10 days ago)
About this role
Join Zentiva as a Regulatory Affairs Specialist and contribute to the approval and regulation of pharmaceutical products across various markets. The role involves managing product registration, ensuring compliance, and collaborating with internal and external teams in a dynamic international environment.
Required Skills
- Regulatory Affairs
- Dossier Preparation
- Regulatory Submissions
- Compliance Monitoring
- Pharmacovigilance
- EU Legislation
- Coordination
- Communication
- Data Management
About Zentiva
zentiva.comWe develop, produce, and deliver high-quality, affordable medicines to more than 100 million people across Europe.
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