Medical Device Complaint Investigators

Roles & Responsibilities
• Perform medical device complaint investigations in compliance with ISO 13485 and ISO 14971
• Conduct risk assessments, hazard analysis, and FMEA
• Support CAPA initiation, investigation, and closure activities
• Prepare, review, and maintain high-quality investigation and compliance documentation
• Ensure adherence to global regulatory and quality system requirements
• Collaborate with cross-functional and global teams for complaint resolution
• Support audit readiness and continuous quality improvement initiatives

Qualifications
• Any Life Science Graduate
• For Kolkata location: B.Pharm / M.Pharm, Biomedical / Mechanical Engineering / B.Sc Medical Imaging & Radiology / M.Sc Molecular Biology / B.Sc Nursing / BDS

Experience
• Pune & Hyderabad: 3-9 years (Immediate joiners preferred)
• Kolkata: 0-5 years (Relevant medical device investigation experience required)

Skills
• Medical Device Complaint Investigation
• ISO 14971 Risk Management
• ISO 13485 Quality Management Systems
• CAPA, Root Cause Analysis
• FMEA and Risk Assessment
• Excellent English communication skills
• Willingness to work rotational shifts and from office

Walk-In Interview Details
Hyderabad
Dates: 12, 15 & 16 January 2026
Venue: Wipro Limited, Manikonda STPI, Tower 6, 3rd Floor, Gachibowli, Hyderabad – 500032
Contact: Pavan

Pune
Dates: 12, 14 & 16 January 2026
Venue: Unit 2, Plot No. 31, Hinjewadi Phase 2, Rajiv Gandhi Infotech Park, Pune – 411057
Contact: Riya / Varsha

Kolkata
Dates: 13, 15 & 16 January 2026
Venue: Gate 1, Plot 8 & 9, Block DM, Sector V, Salt Lake, Kolkata – 700091
Contact: Sarita

Reporting Time: 10:00 AM – 12:30 PM

Documents to Carry
• Updated Resume
• Original Government ID Proof
• Mention source of walk-in information on top of CV

About the Company
Wipro Limited is a leading global information technology, consulting, and business services company with a strong presence in healthcare and medical devices. Wipro supports global clients with regulatory-compliant quality, safety, and post-market surveillance services, offering professionals exposure to international standards, advanced technologies, and long-term career growth opportunities.