Post Market Surveillance & Vigilance Specialist (Regulatory Affairs| Medical Device) – Onsite
Sartorius(19 days ago)
About this role
This role involves overseeing post market surveillance and vigilance activities within the regulatory affairs function for Sartorius's core product portfolio, ensuring compliance with global standards. It offers the opportunity to collaborate with various departments, manage data and documents, and contribute to product safety and quality responsibilities.
Required Skills
- Regulatory Affairs
- Post Market Surveillance
- Vigilance
- Data Management
- Quality Assurance
- Risk Assessment
- ISO13485
- GxP
- Medical Devices
- Pharmaceuticals
About Sartorius
sartorius.comSartorius offers solutions for the biopharmaceutical industry and laboratories, from drug discovery and development to production platforms for biomanufacturing.
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