🏢 Hiring: Regulatory Affairs Specialist – Medtronic, Hyderabad
📍 Location: Hyderabad, India
🕒 Experience Required: 1+ years
💼 Role Type: Full-Time
🎓 Eligibility / Qualifications:
- Educational Background: B.Pharm, M.Pharm, M.Sc, B.Sc, Life Sciences, Engineering, or related fields
- Experience: 1+ years in regulatory affairs or related functions
📝 Key Responsibilities:
- Support preparation, submission, and maintenance of regulatory filings to local and global health authorities
- Assist in ensuring compliance with regulatory requirements for medical devices, pharmaceuticals, or biotech products
- Collaborate with cross-functional teams including Quality, Clinical, and Manufacturing to ensure regulatory adherence
- Review product documentation to ensure regulatory compliance and accuracy
- Track regulatory updates and assist in the implementation of new guidelines
- Maintain documentation for audits, inspections, and approvals
💡 Skills & Competencies:
- Strong understanding of regulatory requirements for medical devices, pharma, or biotech products
- Good written and verbal communication skills
- Detail-oriented and capable of handling multiple projects simultaneously
- Familiarity with documentation management and submission processes
📨 How to Apply:
For more details and to apply, visit: Medtronic Careers
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