Regulatory Affairs Job at Medtronic | Apply Now
Looking for a regulatory affairs job in a leading healthcare company? Medtronic is offering an exciting opportunity for professionals in Hyderabad. This role is perfect for candidates with experience in medical devices or pharmaceuticals who want to grow in global regulatory environments. If you are exploring Medtronic careers or a rewarding medical job, this could be your next big move.
Job Details
- Job Position: Regulatory Affairs Specialist
- Location: Nanakramguda, Hyderabad, India
- Job ID: R62391
- Job Type: Full Time
About the Company
Medtronic is a global leader in healthcare technology with a mission to alleviate pain, restore health, and extend life. With over 95,000 employees worldwide, the company focuses on innovation and improving healthcare access and equity. Choosing Medtronic careers means being part of a team that works on real-world healthcare challenges and builds life-changing solutions.
Job Description
This regulatory affairs job involves supporting design and development control activities while ensuring compliance with global regulatory requirements. The role requires working closely with cross-functional teams to develop regulatory strategies, manage submissions, and support product approvals in international markets.
Qualifications
Required:
- Bachelor’s degree in Medical or related field
- 4–7 years of experience in regulatory affairs (medical device or pharma industry)
- Strong understanding of India, US FDA, and EU regulations
- Excellent communication and organizational skills
- Strong attention to detail and ability to multitask
Nice to Have:
- Global regulatory affairs experience
- Experience with cross-functional teams
- Project management skills
- RAPS Regulatory Affairs Certification (RAC)
- Strong problem-solving and interpersonal skills
Key Responsibilities
- Prepare, review, and file premarket documents for global registrations
- Collaborate with international regulatory teams for marketing authorizations
- Review pre-clinical and clinical protocols for submissions
- Develop regulatory strategies for new or modified products
- Monitor regulatory environment changes and assess their impact
- Maintain communication with health authorities
- Compile submission materials, license renewals, and registrations
- Participate in inspections and audits
- Review promotional and labeling materials for compliance
- Support regulatory documentation and reporting systems
