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| Job Location | Warwickshire |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
QA ManagerQA Manager Medical Device | WarwickYour new companyThis is a very exciting opportunity to join a busy medical device regulatory consultancy in their UK based office. They are well established in UK & Europe and provide regulatory and quality expertise to medical device manufacturers and distributors.Your New roleYou will be joining the highly skilled UK based team as a QA Manager (Consultant). You will be responsible for providing expert quality management medical device advice for current and potential clients. You will be responsible for conducting internal audits to ISO13485, and ISO9001. You will be responsible for implementing/maintaining QMS documentation for clients that adhere to ISO 13485 requirements. You will be visiting clients and conducting quality/regulatory meetings and audits. As a consultant, you will be responsible for continuous contact with clients to provide ongoing advice on regulatory and quality changes, so strong communication skills are required.What youll need to succeedTo be successful in this role you will be highly experienced within the medical device industry, including knowledge of the practical uses, application, design and manufacturing, and regulatory affairs of med devices. You will have previous experience as a QA Manager or QA Consultant for a Medical Device Company, and will have extensive QMS ISO 13485 compliance and risk management ISO 14971 experience. You will have a degree or certificate in a science related, medical, or engineering field. Ideally, you will have the relevant qualifications, or 5+ years working experience in a similar role.What youll get in returnThis position is based in their UK office in the Warwick region. There is a Competitive salary on offer, with the opportunity to join and develop within this organisation. The company is very busy and is expanding to a third office within the upcoming years. What youll need to do nowIf youre interested in this role, click apply now to forward an up-to-date copy of your CV, or call me now.If this job isnt quite right for you but you are looking for a new position, please contact me for a confidential discussion on your career. Required skills
Keyskills :
GMP QA ISO13485 REGULATORY LEAD AUDITOR AUDITING MEDICAL DEVICE