Newton Colmore Consulting is seeking a Regulatory Affairs and Quality Assurance Assistant for a Cambridge-based role in the medical devices sector. You will support the QA and Regulatory Affairs Manager and help drive compliance across product development and improvements.
You will gain exposure to ISO 13485, FDA 510(k) and FDA 21 CFR Part 820 standards, with chance to work with R&D teams and contribute to regulatory submissions while developing your expertise in quality systems and regulatory
#J-18808-LjbffrRegulatory & QA Assistant - Medical Devices (Cambridge) employer: Newton Colmore
Join a dynamic and innovative medical devices company in Cambridge, where your contributions will directly impact the development of life-changing technologies. With a strong focus on employee growth, this organisation offers excellent career progression opportunities, a competitive salary, and a comprehensive benefits package, all within a collaborative work culture that values your input in both regulatory affairs and quality assurance. Be part of a team that not only meets industry standards but also strives to improve lives globally.
