Medtronic Hiring Regulatory Affairs Specialist - Degree in Life Sciences Apply

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. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives.

Post : Regulatory Affairs Specialist

Job Description
Responsibilities include but are not limited to the following :
• Liason with OU Regulatory to ensure accurate application of processes and assignment of data attributes
• Conversion of Technical Documents to Global Submission Summary Documentation (GSSD).
• Creation of e-BOM structure in CAP Agile for GSSD.
• Streamline Processes through use of Artificial Intelligence.
• Monitors and remains in compliance with multiple Quality Management Systems.
• Keeps abreast of regulatory procedures and changes.

Candidate Profile
• Bachelor’s degree in Medical, Mechanical, Life Science or other healthcare related major.
• 4-7 years experiences for RA role in medical device and or pharmaceutical industry.
• Works independently with general supervision on larger, moderately complex projects / assignments.
• Contributes to the completion of project milestones.
• Adjusts or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.
• Communicates primarily and frequently with internal contacts. Contacts others to share information, status, needs and issues to inform, gain input, and support decision making.
• Flexible working hours – Times will be required to be work in US EST time zone.

Nice to Have
• US and global regulatory affairs knowledge and experience.
• Experience working with cross-functional teams.
• Effective verbal and written communication skills both internally and externally.
• Experience with solving problems and concerns.
• Experience with project management and adherence to time schedules.
• Work well under pressure in a dynamic environment.
• Highly organized, detail-oriented, and efficient.
• Team player who seeks to help and learn from colleagues seeing the department success as their own
• Ability to manage projects to completion within and outside of the direct department and company.
• Strong interpersonal and negotiation/influencing skills while maintaining a high level of professionalism
• Proactively seeks to develop and become well-versed within the regulatory landscape.
• RAPS Regulatory Affairs Certification (RAC).

Additional Information
Experience : 4-7 years
Qualification : Bachelor’s degree in Medical, Mechanical, Life Science
Location : Nanakramguda, Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 20th October 2025