01 Oct
|
Novumgen
|
Vadodara
Role & responsibilities
Support preparation of NDS, ANDS, DIN applications, amendments, and other applicable regulatory submissions for Canada market.
Compile and review regulatory documentation and ensure submission content is complete, accurate, and consistent.
Provide regulatory support to cross-functional teams.
Handling of deficiency responses of Marketing Authorization Applications
Communicate with partners for timely information availability
Ensure timely submission of variation and commercial urgency requests to relevant regulatory authorities
Maintenance of different project trackers
Renewals and other applicable lifecycle activities
Preferred candidate profile
2 to 7 years of experience in Regulatory Affairs (RA), specifically in the Canadian market.
Experience in pharmaceutical formulations.
B.Pharm, M.Pharm, or any other relevant degree in Life Sciences or a related field.
📌 Regulatory Executive Canada Vadodara
🏢 Novumgen
📍 Vadodara