Newton Colmore Consulting is seeking a Regulatory Affairs Specialist for a MedTech client in Cambridgeshire. You will ensure compliance with UK/European standards, drive regulatory strategy, and support audits across multiple product ranges.
Ideal candidates have 2–5 years of experience in regulatory affairs or QA for medical devices, with a background in engineering or biomedical fields. The role is based in the office and offers a strong benefits package.
#J-18808-LjbffrMedTech Regulatory Affairs Specialist – On-Site, Bonus in Cambridge employer: Newton Colmore Consulting
Join a dynamic mechanical engineering services company that prioritises employee growth and development, offering clear progression pathways and a supportive work culture. With a focus on building long-term relationships and delivering exceptional service, you'll thrive in an environment that values your expertise and encourages innovation. Located centrally in Hampshire, this role provides the unique advantage of engaging with diverse industrial sectors across the South Coast, ensuring your contributions have a meaningful impact on the business's success.
