This is a fantastic opportunity for someone that would enjoy working across Quality Assurance and Regulatory Affairs within a Medical Device company who design, develop and manufacture under one roof, based at their state of the art facility in Buckinghamshire. The projects that you will be working on are complex and critical to ensure compliance with local and international regulations. The role is varied and includes the following: ? Technical file documentation, to ensure compliance with MDR and FDA; for example biocompatibility reports, clinical evaluations, risk assessments, and post market surveillance ? Quality system management, to ensure compliance with MDR and FDA; for example internal auditing, non-conformance reporting, data analysis ? Technical/sales support The ideal candidate will: ? Be organised and enjoy technical documentation ? Be required to collaborate with a team of electronic and mechanical engineers ? Be enthusiastic with a can do attitude Experience: ? Graduate to 3 years commercial experience, with a science/engineering degree Job benefits: A competitive salary and great benefits including monthly bonus scheme. In addition, youll be joining a company which is ambitious, creative, and centred around teamwork. ADZN1_UKTJ