Roles & Responsibilities
• Perform medical device complaint investigations in compliance with global regulatory standards
• Conduct risk assessments and support product safety evaluations
• Analyze device-related adverse events and technical complaints
• Prepare, review, and maintain investigation reports with high documentation accuracy
• Collaborate with cross-functional global teams for complaint resolution and root cause analysis
• Ensure adherence to medical device regulations, quality systems, and SOPs
Qualification
• B.Pharm / M.Pharm
• Biomedical Engineering / Mechanical Engineering
• B.Sc Medical Imaging & Radiology Technology
• Master’s in Molecular Biology
• B.Sc Nursing
• BDS (Bachelor of Dental Surgery)
Experience
• 0-5 years of experience in medical device investigation, complaint handling, or related safety/quality roles
• Prior exposure to medical device safety processes preferred
Skills
• Strong knowledge of medical devices, complaint investigation, and risk assessment
• Excellent verbal and written English communication skills
• Good analytical, documentation, and problem-solving abilities
• Willingness to work in rotational and night shifts
• Ability to collaborate with global stakeholders
Walk-In Details
• Dates: 15th & 16th January 2026
• Reporting Time: 10:00 AM – 12:00 PM
• Venue: Gate 1, Plot No. 8 & 9, Block DM, Sector V, Salt Lake, Kolkata, West Bengal – 700091
• Documents Required: Updated resume (CV) and original government ID proof
About the Company
Wipro is a global leader in IT, consulting, and healthcare & life sciences services, delivering end-to-end solutions across pharmacovigilance, medical devices, clinical research, and regulatory domains, with a strong focus on quality, compliance, and innovation.