Looking to start your career in Regulatory Affairs (RA) and Medical Device Regulatory Compliance? Stryker, one of the world’s leading medical technology companies, is hiring RAQA Interns for its Gurugram, India office. This hybrid internship offers an excellent opportunity for fresh graduates and early-career professionals to gain practical exposure to Medical Device Rules (MDR) 2017, regulatory submissions, complaint handling, adverse event reporting, BIS registration, and regulatory documentation.
If you are passionate about medical devices, regulatory compliance, and quality assurance, this Stryker RAQA Intern Jobs 2026 opportunity can be a strong foundation for your career in Regulatory Affairs.
Job Overview
| Particular | Details |
|---|---|
| Company | Stryker |
| Position | RAQA Intern |
| Department | Regulatory Affairs & Quality Assurance |
| Location | Gurugram, Haryana |
| Work Mode | Hybrid |
| Job Type | Full-Time Internship |
| Travel Requirement | Up to 10% |
| Experience | Freshers / Entry-Level |
| Industry | Medical Devices |
Key Responsibilities
As an RAQA Intern at Stryker, you will:
- Assist in preparing regulatory documentation for new product registrations and renewals.
- Support regulatory submission remediation activities.
- Maintain regulatory databases, trackers, and filing systems.
- Conduct research on Medical Device Rules, 2017 and regulatory updates.
- Track submission timelines and monitor regulatory approvals.
- Coordinate with cross-functional teams for regulatory documentation.
- Support Regulatory Affairs administrative activities.
- Learn complaint handling and adverse event reporting requirements.
- Assist with regulatory reporting to competent authorities.
- Understand BIS registration requirements and documentation.
Qualifications
Candidates with the following educational backgrounds are encouraged to apply:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Biomedical Sciences
- Biomedical Engineering
- B.Tech (Biomedical/Medical Devices)
- Other relevant Life Sciences degrees
Preferred Skills
- Basic understanding of Medical Device Rules (MDR) 2017.
- Knowledge of the Drugs & Cosmetics Act.
- Strong documentation and organizational skills.
- Excellent written and verbal communication.
- Good attention to detail.
- Ability to work collaboratively in a hybrid environment.
- Basic MS Office proficiency.
Why Join Stryker?
- Opportunity to work with a global medical technology leader.
- Hands-on experience in Regulatory Affairs and Quality Assurance.
- Exposure to medical device regulatory submissions.
- Learn complaint handling and adverse event reporting.
- Hybrid work flexibility.
- Excellent learning and career development opportunities.
- Exposure to international regulatory processes.
How to Apply
