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Medtronics
Regulatory Affairs Specialist | Medtronic | Hyderabad
Apply for Regulatory Affairs Specialist role at Medtronic, Hyderabad. Hybrid work, full-time, 4–7 years’ RA experience required. Apply now.
Medtronic, a global leader in medical devices and healthcare innovation, is hiring for the role of Regulatory Affairs Specialist at its Hyderabad office (Nanakramguda location). This is a hybrid, full-time opportunity designed for experienced professionals in the regulatory affairs domain who want to contribute to healthcare access and equity while advancing their career with one of the world’s most trusted healthcare technology companies.
Company Overview
Medtronic is at the forefront of medical technology, therapies, and services, with a mission to alleviate pain, restore health, and extend life. With a culture of innovation and compassion, Medtronic challenges the limits of science and technology to transform healthcare. The company offers diverse opportunities for career development, global exposure, and impactful work in improving patient lives.
Job Role & Responsibilities
As a Regulatory Affairs Specialist, you will:
- Liaise with Operating Unit (OU) Regulatory teams for accurate process application and data assignment.
- Convert technical documents into Global Submission Summary Documentation (GSSD).
- Create e-BOM structures in CAP Agile for GSSD.
- Streamline regulatory processes using Artificial Intelligence tools.
- Ensure compliance with multiple Quality Management Systems (QMS).
- Stay updated with evolving global and US regulatory procedures.
- Collaborate with cross-functional teams to meet project milestones.
- Support project management activities, problem-solving, and process enhancements.
Eligibility / Qualifications
- Educational Requirement: Bachelor’s degree in Medical, Mechanical, Life Science, or related healthcare disciplines.
- Experience: 4–7 years in regulatory affairs within medical devices and/or pharmaceutical industries.
- Skills & Competencies:
- Ability to work independently under general supervision on moderately complex projects.
- Strong problem-solving and process improvement skills.
- Effective communication skills for internal and external collaboration.
- Flexibility to work in US EST time zone.
Nice to Have
- Knowledge of US and global regulatory frameworks.
- Experience in cross-functional team environments.
- Strong organizational, project management, and multitasking skills.
- RAPS Regulatory Affairs Certification (RAC).
- Excellent interpersonal, influencing, and negotiation abilities.
- Proven ability to thrive under pressure in dynamic environments.
Location & Work Type
- Location: Nanakramguda, Hyderabad, India
- Work Type: Hybrid, full-time
- Work Hours: Flexibility required for US EST time zone collaborations
Compensation & Benefits
- Competitive salary and performance-linked benefits.
- Flexible benefits package tailored to employee needs.
- Recognition of employee contributions with opportunities to share in organizational success.
- Comprehensive resources supporting career and personal growth.
About Medtronic
At Medtronic, employees are encouraged to pursue a career of exploration and innovation. With a focus on equity, access, and breakthrough technologies, Medtronic fosters a culture where professionals thrive while making a global impact. This role offers you the chance to shape the future of healthcare while building long-term career growth.
Application Process
Interested candidates can apply directly via the official Medtronic careers portal:
Apply Here
Apply soon to take the next step in your career with Medtronic, a trusted global healthcare innovator!
FAQs
1. What experience level is required for this role?
Candidates should have 4–7 years of regulatory affairs experience in medical device and/or pharmaceutical industries.
2. Is this a remote position?
It is a hybrid role, based in Nanakramguda, Hyderabad, with flexibility for remote work.
3. What qualifications are required?
A bachelor’s degree in Medical, Mechanical, Life Sciences, or related healthcare field is required.
4. Does Medtronic offer global exposure?
Yes, the role involves working with US EST time zone teams and staying updated with international regulatory frameworks.
5. What benefits does Medtronic provide?
Medtronic offers competitive salaries, flexible benefits, career development programs, and recognition-based rewards.
Quick Summary Table
| Company | Medtronic |
|---|---|
| Vacancy | Regulatory Affairs Specialist |
| Location | Nanakramguda, Hyderabad, India |
| Work Type | Hybrid, Full-time |
| Education | Bachelor’s in Medical, Mechanical, Life Sciences, or related fields |
| Experience | 4–7 years in Regulatory Affairs |
| Desirable | US/global RA knowledge, RAPS RAC Certification |
| Salary & Benefits | Competitive salary + flexible benefits package |
| Apply Link | Medtronic Careers Portal |