Vahima. P
Biomedical Engineer| Regulatory Affairs Specialist | Medical Devices | EU MDR & IVDR | Gap & Trend Analysis | PMS & Complaints Handling | ISO 13485| ISO 14971| Cybersecurity Documentation | Medical device Labeling
- Role
- Senior Executive at Quest Global
- Location
- Madurai South, TN, IN
- LinkedIn followers
- 500 followers
About Vahima. P
Biomedical engineer with four years 10 months of progressive experience in regulatory affairs of medical device. Skilled in technical documentation as per EU IVDR regulation, Microsoft tools. Certified in Advanced lean six sigma yellow belt, Mini-course MDR 2017/745. Knowledge in Medical device regulation 2017/745 and IVDR regulation 2017/746. Navigates high stress situations and achieve goals on time and under budget.
Experience
Senior Executive
Aug 2024 — Present · Trivandrum, IN
Education
PSNA College of Engineering and Technology
Bachelor of Engineering - BE, Biomedical/Medical Engineering
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