We are seeking an experienced to be part of our small QA team reporting directly to the Quality Manager. This is a full time permanent role.  Based in Slough, although we can consider a hybrid working arrangement with a minimum of 3 days in the office.

 

Qualifications, skills and experience must include:

CAPA - Acting as CAPA lead, investigate and identify actions for improvement within the QMS. Create and review SOPs and Work Instructions In-depth working knowledge of ISO 13485:2016 and experience of auditing and assessing to medical device standards and regulations Suppliers – manage supplier selection and evaluation processes including re-evaluations and supplier complaints Maintain working knowledge of Regulatory and Quality System requirements eg (ISO 13485, MDR/MDD) Experience in implementation, management and improvement of Quality System processes Ideally, educated to degree level in LifeScience / Engineering, or equivalent through experience Your Benefits 34 days holiday (inclusive of public holidays)  Generous Pension  Private Medical  Medical cash back scheme  Company sick pay  Life Assurance  Critical illness and income protection (service requirements apply)  Perkbox benefits platform