Medtronic, a global leader in healthcare technology, is seeking a Regulatory Affairs Specialist to join its team in Hyderabad. This hybrid role offers an exciting opportunity to contribute to life-changing medical innovations while ensuring compliance with global regulatory standards.
Key Responsibilities:
- Prepare and coordinate regulatory submissions, including license renewals and annual registrations.
- Ensure compliance with labeling, manufacturing, and clinical protocols.
- Monitor and enhance regulatory tracking and control systems.
- Stay updated on regulatory changes and recommend strategies for timely approvals.
- Interact with regulatory agencies as needed.
- Support internal audits and inspections.
Qualifications & Experience:
- Education: Bachelor’s degree (or equivalent as per U.S. immigration standards for foreign degrees).
- Experience: Minimum 2 years in regulatory affairs (or advanced degree with 0 years of experience).
- Skills: Strong project management, attention to detail, and knowledge of global regulatory guidelines.
Why Join Medtronic?
- Mission-Driven Work: Contribute to Medtronic’s goal of alleviating pain, restoring health, and extending life.
- Career Growth: Opportunities for mentorship and leadership development.
- Flexible Benefits: Competitive salary, health benefits, and work-life balance initiatives.
About Medtronic
Medtronic is a global healthcare technology leader with 95,000+ employees dedicated to solving the world’s most critical medical challenges. From R&D to manufacturing, Medtronic engineers life-saving solutions for patients worldwide.
