Quality Assurance Specialist

35000 - 45000 per annum + competitive
13 Nov 2017
15 Nov 2017
Contract Type
Full Time
An innovative medical device company is recruiting for a Quality Specialist to join their growing team based in Oxford. This role provides the opportunity to report directly to the CEO and work closely with an external Quality Consultant. This position will enable you to maintain the ISO 13485 Quality Management System and design quality control protocols and SOPs. You will also be required to compile quality documents including certificates of analysis, technical files and batch records. This role will allow you to take responsibility for the organisational quality assurance, working closely with other departments to ensure compliance, maintain document control, and ensure changes are documented and trained out. You will benefit from working for a fast growing innovative company allowing you to make a real difference in its development and progression into a multinational organisation. You will have scope to build your own team as the business grows allowing you to advance your own career with the satisfaction of also bringing life changing medical devices to patients. To apply for this role you will need: Bachelor's degree in a relevant scientific or life sciences discipline; Experience with QMS ISO 13485, FDA 21 CFR 820 and Medical Device Directives 93/42/EEC; At least 2 years experience working in a quality control environment in a medical related industry. The opportunity to work with this medical device organisation would provide a highly competitive salary plus benefits including 25 days holiday per year, excellent pension scheme and much more. If you believe you have the experience and capabilities to fulfil this Quality Specialist role then please reply immediately or call Claire on 0117 938 8088. Sthree UK is acting as an Employment Agency in relation to this vacancy. - provided by Dice DEGREE, QUALITY MANAGEMENT