Regulatory Affairs - Specialist/Senior Specialist/Assistant Manager
People First Consultants
- New Delhi
- Permanent
- Full-time
Microbiology, Pharmacy, pharmacology, Biotechnology, engineering, or medical technology.
- Minimum 5 years of experience in Medical devices regulatory affairs and 7-8 years of working
- Good working knowledge of MS-EXCEL and PowerPoint will be preferred.
- Association or working experience in Central/State regulatory authority will be preferred.
- Working experience of Regulatory document management system (Agile, RIMS, Livelink etc.)
- Working knowledge on requirements of India Drugs and Cosmetics Act, 1940 and Medical
and Japan.
- Individuals having a Regulatory Certification will be a plus.