Regulatory Affairs Associate

Job Description

Company Description HMS Medical Systems, established in 1994, is a premier manufacturer, supplier, and exporter of physiotherapy and electrotherapy equipment. Known for our high-quality products, we serve a global market with a comprehensive range, including Interferential therapy, TENS, Ultrasound therapy, and more. Our products are widely utilized across physiotherapy units, hospitals, and healthcare sectors due to their durability, optimal performance, and high utility. We are ISO 13485:2016 and CE certified, reflecting our commitment to quality and customer satisfaction. Role Description This is a full-time on-site role located in Chennai for a Regulatory Affairs Associate. The Regulatory Affairs Associate will be responsible for preparing and managing regulatory documentation, ensuring compliance with regulatory requirements, and overseeing regulatory submissions. The role involves staying updated with regulatory affairs to ensure that the company's products meet all necessary regulations and standards. Qualifications Regulatory Documentation, Regulatory Compliance, and Regulatory Requirements skills Experience in Regulatory Submissions and Regulatory Affairs Excellent analytical and problem-solving skills Strong attention to detail and organizational skills Ability to work independently and within a team Bachelor's degree in a relevant field such as Health Sciences, Biomedical Engineering, or a related discipline Experience in the medical device industry is a plus Show more Show less