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Medtronic, a global leader in healthcare technology, is inviting applications for the position of Associate Regulatory Affairs Specialist in Nanakramguda, Hyderabad, India.
This hybrid role is perfect for candidates with 2–4 years of regulatory experience who are eager to build a rewarding career in medical devices, regulatory documentation, and labeling compliance. If you’re passionate about regulatory sciences and healthcare innovation, this opportunity is designed for you.
📝 Key Responsibilities
As an Associate Regulatory Affairs Specialist, you will:
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- Collect, maintain, archive, and retrieve regulatory and clinical source documents.
- Support leadership in audits and submission-related activities (CAP Agile, Veeva upload/review).
- Assist in developing and executing cross-functional meetings.
- Track and report metrics related to regulatory writing and deliverables.
- Create, review, and reproduce product labeling content.
- Ensure labeling compliance with medical, legal, and regulatory requirements.
- Monitor and recommend improvements to labeling processes, tools, and systems.
- Review promotional materials for compliance with scientific and regulatory data.
🎓 Qualifications
To be successful in this role, you must have:
- Education: Bachelor’s degree in life sciences, pharmacy, or related discipline.
- Experience: 2–4 years in regulatory affairs, medical writing, or clinical documentation.
- Strong organizational and problem-solving skills.
- Ability to communicate effectively with internal teams.
💼 Benefits & Compensation
Medtronic offers:
- Competitive salary (estimated range: ₹7,00,000 – ₹12,00,000 per annum, depending on experience).
- Flexible benefits package to support employees at every career and life stage.
- Global exposure in a collaborative and innovation-driven environment.
- Career growth opportunities within the world’s largest medical device company.
📍 Job Location
- Location: Nanakramguda, Hyderabad, India
- Work Type: Full-time | Hybrid
✅ How to Apply
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