Newton Colmore is seeking a Regulatory Affairs Specialist in Cambridge to support a broad range of innovative projects across medical and non-medical sectors. You will work within a shared QA/RA function embedded in product development, guiding teams to align with global regulatory expectations while enabling innovation.
The role involves interpreting ISO 9001/13485 and FDA 21 CFR 820 requirements, monitoring regulatory changes, and contributing to regulatory strategies throughout product
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Medical Devices Regulatory Affairs Specialist (Cambridge) employer: Newton Colmore
Newton Colmore is an exceptional employer, fostering a collaborative and innovative work culture where every team member's input is valued. Located in a dynamic environment, the company offers tailored benefits packages, monetary bonuses, and ample opportunities for professional growth, making it an ideal place for engineers passionate about pushing the boundaries of technology in high-performance computing.
