Associate Regulatory Affairs Specialist

Careers that Change Lives

A Day in the Life

Responsibilities may include the following and other duties may be assigned.

• Coordination and preparation of registration packages required for regulatory submissions (new registrations, renewals, and variations).
• Compiling regulatory documentation required for supporting tenders & importation activities in the region.
• Following-up with distributors and service providers to ensure on time submission / approvals.
• Conducting and coordinating Field Actions activities as required in the region.
• Developing and updating regulatory tracking / control systems.
• Keeping abreast of regulatory procedures.
• Monitoring regulatory changes on country level and highlighting impact on company products.
• Interaction with regulatory agencies.

Must Have : Minimum Requirements

Pharmaceutical / Science Bachelor's Degree or any medical field.

Nice to Have

About Medtronic

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.