Regulatory Affairs Specialist
Medtronic • Nanakramguda, India • Posted June 13, 2026
About the Role
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
**Responsibilities may include the following and other duties may be assigned:**
+ Prepare, review, file, and support premarket documents for global registrations for assigned projects.
+ Collaborate with business unit and international regulatory affairs personnel to support marketing authorizations for assigned projects.
+ Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects.
+ Develop Regulatory Strategies for new or modified products for assigned projects.
+ Monitor and provide information pertaining to impact of changes in the regulatory environment.
+ Document, consolidate, and maintain oral and written communication ...
**A Day in the Life**
**Responsibilities may include the following and other duties may be assigned:**
+ Prepare, review, file, and support premarket documents for global registrations for assigned projects.
+ Collaborate with business unit and international regulatory affairs personnel to support marketing authorizations for assigned projects.
+ Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects.
+ Develop Regulatory Strategies for new or modified products for assigned projects.
+ Monitor and provide information pertaining to impact of changes in the regulatory environment.
+ Document, consolidate, and maintain oral and written communication ...