Satyajit Singha

Background

About Satyajit Singha

I’m a Medical Device Safety professional with over 2 years of experience in Wipro, currently working in Pharmacovigilance at IQVIA.My career began in medical device associate at Wipro, where I supported post-market surveillance, complaint handling, and safety documentation. That hands-on experience helped me understand how real-world device issues translate into regulatory actions and patient safety outcomes.Today, in my role at IQVIA, I work in pharmacovigilance operations, supporting drug safety case processing and regulatory compliance activities.My core areas include:• Medical device complaint management & PMS• Individual Case Safety Report (ICSR) processing• Safety data review and quality checks• Regulatory documentation support•Compliance with FDA, ISO : 13485 standard of data for Post MarketingSurveillance (PMS) of Medical devices.• Salesforce trackwise workflows• Oracle Argus and safety workflowsI also hold an M.Pharm in Pharmaceutics, with academic research experience in ophthalmic in-situ drug delivery systems — giving me a strong foundation across formulation, devices, and safety operations.I focus on accuracy, consistency, and making safety processes easier for busy teams.Always open to connecting with professionals working in pharmacovigilance, medical devices, or healthcare safety.