Regulatory Affairs (RA) Associate – Medical Devices Salary: £30,000 – £40,000 per annum Benefits include: Monthly paid bonuses, 25 days holiday (plus bank holidays), pension scheme, training and progression Location: Aston Clinton (Aylesbury), Buckinghamshire Regulatory affairs associate overview This is a great opportunity for a junior regulatory affairs associate to join a growing medical engineering business based in Buckinghamshire. The company is a small part of a larger 300 employee business. The group designs and manufactures leading-edge electro-surgical tools, alongside the creative development of future surgical systems. The business are looking for either a graduate in a STEM field looking to move into regulatory affairs and quality assurance, or someone with 1-3 years of commercial experience. The regulatory affairs specialist will need to come from an engineering background, ideally medical devices, as opposed to a drug development / pharma background. You will join a small RA/QA team, comprised of two other RA/QA specialists. You will aid in the compliance certifications of new products, file technical documentation for MDR/FDA regs and be involved in biocompatibility reports, clinical evaluations, risk assessments and post-market surveillance (and more!). Regulatory Affairs Associate Requirements * Degree qualified within a relevant STEM field * Experience in regulatory affairs is desirable, specifically on medical devices or similar * 1 – 3 years of commercial experience (might take a graduate with no experience) * Knowledge of MDR and FPA compliance * A good team-player with excellent communication skills * A desire to join a high-performing team within a growing organisation If you are interested in discussing this regulatory affairs associate role, please apply now and we’ll be in touch
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CV-Library Recruiting Team