Design Assurance Engineer - ISO 13485 - Cambridge

Newton Colmore Consulting ,
Gloucester, Gloucestershire
Job Type: Full-time

Overview

Design Assurance Engineer - ISO 13485 - Cambridge Due to the recent growth of a small medical devices company, based in Cambridgeshire, they are currently looking for an experienced Design Assurance or Quality Assurance specialist to help with the creation and auditing of risk management files, design history files and QMS systems. As you will be managing the quality assurance of medical devices creation you will need to have a strong understanding of ISO 13485 and FDA 21 CFR Parts 820. It would also be useful to have exposure to EN 60601 and ISO 14971. You will work closely with the design groups of the business, so if you have specific design assurance knowledge this will be ideal. The company, you will be joining, have been growing for a few years and the expansion they are going through has been assured for several years, meaning the job security on offer is unparalleled in the marketplace right now. Communication skills are vital in this role, meaning when you report your finding after an audit you will need to be clear and concise. You will also need to have the confidence to present to a group of junior and senior personnel. You will be rewarded with an excellent career path, salary, benefits package and pension scheme. So, if you have a strong knowledge as working as a Quality Assurance Engineer, Quality Engineer, Design Assurance Engineer or another quality assurance role please make an application now. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.