Require Regulatory Affairs Manager at Medtronic

Medtronic Jobs in Hyderabad | Regulatory Affairs Manager – Medical Device

At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

Medtronic Hiring for Below Position

Post: Regulatory Affairs Manager

Job Description

This people leadership role is based in Nanakramguda, Hyderabad and is responsible for leading a Regulatory Affairs team supporting global medical device regulatory activities. The position oversees regulatory submission planning and execution, drives operational excellence, develops regulatory talent, and partners with cross-functional teams to ensure compliance and successful product lifecycle management. Limited domestic and international travel may be required.

Primary Responsibilities

• Lead and develop a Regulatory Affairs team responsible for global regulatory submissions, registrations, renewals, and compliance activities
• Oversee preparation, review, and coordination of regulatory documentation packages for product approvals and lifecycle management
• Develop and execute regulatory strategies that align with business objectives and global regulatory requirements
• Partner with Quality, Engineering, Clinical, Manufacturing, and Commercial teams to ensure regulatory compliance
• Monitor changes in global regulatory regulations, standards, and guidance documents and assess business impact
• Drive continuous improvement initiatives for regulatory processes, documentation quality, and compliance tracking
• Provide leadership during regulatory inspections, audits, agency interactions, and compliance activities
• Manage team performance, resource planning, talent development, and succession planning

Candidate Profile

• Education: Bachelor’s degree in Engineering, Biomedical Engineering, Life Sciences, or related scientific discipline
• Experience: 15+ years of regulatory affairs experience within medical device or pharmaceutical industry
• Leadership: Minimum 5 years of people leadership experience managing regulatory, quality, or compliance teams
• Skills: Experience supporting regulatory submissions, registrations, compliance activities, and lifecycle management
• Knowledge: Working knowledge of global medical device regulatory requirements and regulatory agency interactions
• Communication: Effective verbal and written communication skills for global cross-functional collaboration

Preferred Qualifications

• Advanced degree in Engineering, Biomedical Engineering, Life Sciences, or Regulatory Affairs
• Experience leading global Regulatory Affairs teams within a multinational medical device organization
• Demonstrated success driving process improvements and operational excellence programs
• Experience supporting regulatory inspections and interactions with international regulatory authorities
• Strong analytical skills with experience using technology and reporting tools for regulatory metrics

How To Apply for Medtronic Regulatory Affairs Manager Job

Interested and eligible candidates can apply online through the official Medtronic careers portal.

Regulatory Affairs Manager : Apply Online

About Medtronic

Medtronic is a global leader in medical technology, services and solutions. The company is committed to improving patients’ lives through innovation in medical devices and healthcare solutions.

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