PHARMAFull-time
RAQA Intern
DELHI NCR (IN)HYBRIDPOSTED: 7/13/2026
PHARMAFull-time
HIRING ORGANIZATIONSTRYKERMedical Technology / Healthcare
ROLE DEFINITION & 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.
REQUIRED VERIFIED SKILLS
Medical Device Rules (MDR) 2017
Documentation
Regulatory Compliance
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Internship compensation for global medical technology firms in the NCR region is generally competitive and aligned with industry standards for high-caliber early-career talent.
ORGANIZATION CONTEXT & CULTURE
Stryker is one of the world's leading medical technology companies, offering a diverse range of innovative products and services. They specialize in Orthopaedics, Medical and Surgical (MedSurg), and Neurotechnology and Spine. The company works closely with medical professionals to deliver solutions that improve patient outcomes and hospital efficiency.
TEAM SIZE: 50,000+ employees
INDUSTRY: Medical Technology / Healthcare
EXPECTED CAREER ROADMAP
This internship at a global medical technology leader provides foundational experience in regulatory submissions and quality assurance, serving as a launchpad for a career in Medical Device Regulatory Affairs.
APPLICATION ADVISORY
Emphasize your understanding of MDR 2017 and any academic or project experience related to medical devices or quality assurance in your application.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.