Offer summary
Qualifications:
Experience in Medical Devices Regulatory Affairs, Knowledge of UK MDR 2022 compliance, Familiarity with EU MDD and MDR regulations, Expertise in ISO 13485 QMS, Understanding of patents and trademarks.Key responsabilities:
- Create and update technical files and reports
- Compile vigilance PMS and PSUR reports
- Assist with regulatory submissions and registrations
- Liaise with departments for documentation updates
- Manage patents, trademarks, and standards database