Senior Analyst - Regulatory Affairs

As a Senior Analyst in Regulatory Affairs based in Chennai, with 2.5-5 years of experience, you will be responsible for various tasks related to development, including interacting with customers and internal teams to gather requirements. Your role will involve creating and enhancing documents for CMMi and client specifications, providing technical guidance to junior developers, and maintaining existing features. You should have experience in using proofreading tools and version comparison techniques, along with proficiency in Adobe Illustrator and Adobe InDesign. A strong understanding of medical device labeling standards, print production, regulatory symbols, UDI, IFU formatting, and compliance documentation is essential. Your excellent attention to detail and organizational skills will be crucial for this role. Your responsibilities will include troubleshooting bugs, resolving ad-hoc requests, and providing support for both major and minor enhancements/new developments based on business/client requirements and feedback from the HCL team. Additionally, you will be expected to provide client support by presenting data, information, resolving tickets, and ensuring timely delivery of assigned tasks while maintaining quality standards. The ideal candidate for this position should have a B-Tech qualification and possess domain competencies in Labeling Requirements within the ERS domain. This role offers a unique opportunity to work in a dynamic environment with a focus on regulatory affairs. This position has 1 opening, and the Auto req ID is 1590991BR.,