Regulatory Affairs Medical Devices Jobs in New Delhi

Zoot Systems - Delhi

Lead the preparation and maintenance of regulatory submissions,technical files,design dossiers,and other documentation required for product approvals advanced degree preferred Not disclosed INR

from: naukri.com - 25 days ago

Delhi, India

the medical device industry. In-depth knowledge and experience with EUMDR 2017, USFDA regulations (including 21 CFR Part 820), and ISO 13485 standards. Proven track record of successful regulatory submissions Not Mentioned

from: Monsterindia.com - 4 days ago

Delhi

in Medical devices regulatory affairs and 7-8 years of working experience in a Medical devices/Pharmaceutical company. Good working knowledge of MS-EXCEL and PowerPoint will be preferred. Working experience Not Mentioned

from: Monsterindia.com - More than 30 days ago

Delhi, India

Are you a seasoned professional in the medical device industry, ready to embark on a unique opportunity to drive real impact We are seeking a Regulatory Affairs Consultant to join ideally as soon as possible a dynamic Not Mentioned

from: Monsterindia.com - 16 days ago

Gurgaon / Gurugram, India

a minimum of 5 or more years' regulatory or equivalent experience within a pharmaceutical and/or medical device company, or similar organization. RAC certification or Advanced Degree (Masters in Regulatory Not Mentioned

from: Monsterindia.com - More than 30 days ago