PHARMAFull-time
Regulatory Affairs Specialist
BANGALORE (IN)HYBRIDPOSTED: 8/13/2026
PHARMAFull-time
HIRING ORGANIZATIONSTRYKERMedical Technology / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Support regulatory compliance and submission activities for Orthopedic Instruments across global markets.
Monitor global regulatory requirements, guidance documents, and industry standards for medical devices.
Research and compile regulatory pathways, approval requirements, dossiers, and pre-submission packages.
Track submissions under review, organize technical/clinical documentation, and maintain regulatory records and intelligence files.
Coordinate meeting logistics and prepare supporting materials for internal teams and regulatory authority interactions.
REQUIRED VERIFIED SKILLS
Regulatory Affairs
Regulatory Dossiers
Medical Device Compliance
Technical Documentation
Regulatory Intelligence
Submission Tracking
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
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
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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