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Roles & Responsibilities:
• Prepare summary reports for medical devices
• Perform trend analysis on customer complaints and product performance
• Conduct monthly and ad-hoc data analysis from complaints, sales, and trending databases
• Carry out literature searches and review clinical, scientific, and medical references
• Identify, interpret, and evaluate data from medical literature, clinical studies, and post-market sources
• Compile and submit clinical and post-market surveillance (PMS) documents
• Support international regulatory submissions in line with global medical device regulations
• Contribute to PMS plans and safety reports for assigned device portfolios
Qualification:
• Relevant degree in Life Sciences, Biomedical Engineering, Pharmacy (B.Pharm, D.Pharm, M.Pharm) , or related discipline
Experience:
• 3-6 years of experience in Medical Devices domain
• Hands-on experience in medical review and post-market surveillance
Skills:
• Strong knowledge of medical device regulations and PMS requirements
• Experience in complaint trending and safety data analysis
• Expertise in literature search and regulatory documentation
• Excellent analytical, documentation, and communication skills
• Ability to work in a fast-paced, office-based environment
• Immediate joiners preferred
About the Company:
ANRI Solutions is a leading recruitment partner connecting skilled professionals with top pharmaceutical, medical device, and healthcare organizations across India and globally.