Nikhilesh Gajbhiye

As a Drug Safety Associate at IQVIA, I ensure the safety and quality of drugs by processing adverse event cases according to regulatory guidelines and project requirements. I create, maintain, and track the cases using various databases and software tools, and collaborate with internal and external stakeholders to provide accurate and timely reports. Before joining IQVIA, I worked as a Junior Regulatory Affairs Specialist at Sciformix, where I was involved in the qualification of raw and packaging materials for global markets (US and EMEA). I also created regulatory specifications and documents for different products and clients, and supported the regulatory compliance and audit activities. I have a Master of Pharmacy degree in Pharmaceutics and Drug Design from Bharati Vidyapeeth, where I learned the fundamentals and applications of drug development and delivery. I am passionate about enhancing my knowledge and skills in the fields of drug safety and regulatory affairs, and I am always eager to learn from new challenges and opportunities. I have a strong attention to detail, analytical thinking, and problem-solving skills, which enable me to deliver high-quality and reliable results. I also value teamwork, communication, and customer satisfaction, and I strive to contribute to the success and growth of the organization.