Keval Patel Email & Phone Number

Welcome to my LinkedIn profile! I'm Keval Patel, a dedicated Quality Assurance Specialist specializing in ensuring product excellence and regulatory compliance in medical device manufacturing environments.With over four years of experience in GMP-compliant environments, I've developed a keen eye for detail and a deep understanding of regulatory requirements. My primary focus has been on maintaining the highest standards of product quality while adhering to stringent regulatory guidelines.In my role as a Quality Assurance Specialist at Nobel Biocare (Envista Holdings Corporation), I provide essential site support for various quality-related functions. This includes training administration, document control, complaint handling, incident reporting, field action, recall coordination, and non-conformance management. I collaborate closely with cross-functional teams to ensure that all aspects of the quality management system are implemented effectively and maintained to regulatory standards.My expertise encompasses a comprehensive understanding of regulatory requirements, including HPFBI/FDA guidelines, ISO standards, cGMP regulations, and SOPs. I leverage this knowledge to support warehouse activities, manage inventory, and oversee product inspections and releases. Additionally, I contribute to controlled distribution processes, ensuring compliance with company policies and GMP requirements.Looking ahead, my next goal is to transition into a regulatory role within the medical device and pharmaceutical industry. I'm passionate about navigating complex regulatory landscapes and ensuring compliance with industry standards. I hold a degree in Chemical Laboratory Technology from Seneca Polytechnic and a Bachelor of Science in Chemistry from Gujarat University. Furthermore, I have completed certificates in Understanding How Medical Devices are Regulated in Canada and Medical Device Establishment Licensing and Post-market Regulation.I am deeply committed to driving excellence and continuous improvement in medical device manufacturing. I thrive in collaborative environments where I can contribute my skills and expertise to achieve organizational goals. Let's connect and explore opportunities to work together toward maintaining the highest standards of quality and compliance.