Job:Regulatory Affairs Specialist/Senior Specialist/Assistant Manager

Experience:1012 Years

Skills:

The ideal candidate would have a diploma/degree in a scientific discipline such as Biology
Microbiology Pharmacy pharmacology Biotechnology engineering or medical technology.
• Minimum 5 years of experience in Medical devices regulatory affairs and 78 years of working
experience in a Medical devices/Pharmaceutical company.
• Good working knowledge of MSEXCEL 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
Device Rules 2017 and/or regulations of advanced markets like US/EU/Australia/Singapore
and Japan.
• Individuals having a Regulatory Certification will be a plus.