MDR Stability Advisor

This job has now expired please search on the home page to find live IT Jobs.

A requirement has arisen for an MDR Stability Advisor to join the MDR team at a multi-national manufacturer of Medical Device and Health care products.The role is a 12 month initial contract (LTD Company / Umbrella) with the possibility of extension.Based full-time on-site at their facility in Cheshire, North-West England.The MDR Stability Advisor will be working within a strictly maintained ISO13485 & ISO9001 QMS to GMP/GLP standards.Role / responsibilitiesProduce shelf-life plans, stability processes, technical reports and other documentation for Medical Device productsEnsure compliance with Stability Study guidelines (ICH)Provide assurance that QMS and GLP/GMP standards are metContribute to the definition/requirements for stability studies for medical device productsMaintain technical files relating to the products stability requirementsSkills / Knowledge required:Qualified to Degree Level (or equivalent) in a STEM related subject and 4-5 years experience working in an Quality, NPD, or R&D role within the Medical Device or Pharma sector.Knowledge of FDA and European regulations in relation to Stability Testing, Quality Standards (such as ISO13485:2003, ISO9001 and 21 CFR Part 820)Understand the function of Stability Testing within the product development process of Medical DevicesAbility to analyse data gathered from several sourcesStrong research abilityRate up to £45 per hour dependant on experience.Highly experienced team, great company and experience to add to your CV!Please apply if interested and we will be in touch to discuss in more detail. To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales