A leading global healthcare company, Medtronic, is hiring for the position of Regulatory Affairs Specialist in Hyderabad, India. This is an excellent opportunity for professionals with experience in regulatory affairs within the pharmaceutical or medical device industry. If you are looking to grow your career in regulatory strategy, compliance, and global submissions, this role offers strong exposure and career advancement.
Medtronic is known for innovation in healthcare technology and a strong commitment to improving patient outcomes worldwide. This Regulatory Affairs Specialist job in Hyderabad provides a chance to work in a collaborative environment with global regulatory teams.
Job Overview
Job Title: Regulatory Affairs Specialist
Company: Medtronic
Location: Nanakramguda, Hyderabad, India
Employment Type: Full-Time
Work Mode: Flexible Work Arrangement
Experience Required: 4–7 Years
Industry: Pharmaceutical / Medical Devices
Key Responsibilities
As a Regulatory Affairs Specialist at Medtronic, you will play a critical role in ensuring regulatory compliance and supporting product approvals across global markets.
- Prepare, review, and submit regulatory documents for global product registrations
- Develop regulatory strategies for new and modified products
- Collaborate with cross-functional and international regulatory teams
- Review clinical and pre-clinical data for submission readiness
- Monitor changes in global regulatory requirements (India, US FDA, EU)
- Maintain communication with health authorities and regulatory agencies
- Support audits, inspections, and regulatory assessments
- Review labeling, promotional materials, and change control documents
- Maintain regulatory documentation systems and records
- Ensure compliance with product approvals and regulatory standards
Required Qualifications
- Bachelor’s degree in Life Sciences, Medical, Mechanical, Electrical, or related field
- 4–7 years of regulatory affairs experience in pharmaceutical or medical device industry
- Strong knowledge of global regulatory frameworks (India, US FDA, EU)
- Excellent written and verbal communication skills
- Strong attention to detail and ability to manage multiple tasks
- Good planning, organizational, and teamwork skills
- Proficiency in English (reading, writing, speaking)
Preferred Skills
- Experience in global regulatory submissions
- Knowledge of RAPS Regulatory Affairs Certification (RAC)
- Strong project management and problem-solving skills
- Ability to work in dynamic and cross-functional environments
Benefits
Medtronic offers a competitive salary along with a flexible benefits package designed to support employees at every stage of their career.
- Attractive salary package (₹8,00,000 – ₹15,00,000 per annum estimated)
- Performance-based incentives (Medtronic Incentive Plan – MIP)
- Health and wellness benefits
- Career growth and global exposure
- Supportive and inclusive work environment
How to Apply