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| Job Location | Stoke-on-Trent |
| Education | Not Mentioned |
| Salary | 38,000 - 45,000 per annum |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent , full-time |
Title: Senior Quality Specialist Location: Stoke on Trent Contact: Do you want to work in a friendly company where you can get to know everyone Are you feeling limited in your tasks and your scope Are you an experienced Quality Specialist in the medical device industry If yes, look no further! The CompanyThis company are a business with a singular focus, on manufacturing and engineering products to improve patients lives. With over 25 years of experience in their market and having sold their product globally in over 40 countries, the success of the business goes from strength to strength. With manufacturing in the UK, you will be based at the core of the business.This a fantastic opportunity to join a company and a team with a close-knit working culture, a passion for quality and the support to inspire their employers to reach their full potential. The OpportunityIn this role as Quality Assurance Specialist, you will have the chance to work on the Quality Management System with a particular focus on assisting in notified body audits, as with three notified bodies across the business, these happen quite regularly!You will also have the opportunity to work on customer complaints, risk assessments and identifying root cause to help implement process improvements.If you are looking for a position where you can make a difference, develop existing skills and learn new skills whilst working collaboratively with other departments such as quality, validation, production etc, look no further. As a Quality Specialist you will (not an exhaustive list):Implement and maintain QA procedures.Work closely with Quality Assurance (QA),Purchasing and Production departments to ensure materials, product and processes meet specification. Ensure nonconformities relating to pre-production and production product quality are investigated and appropriate correction and/or corrective action is taken. Ensure data from relevant sources is analysed and corrective and preventive action (CAPA) taken where appropriate. Requirements*5+ years of Quality Assurance experience in the medical device industryPrevious experience running internal auditsFluent written and speaking skills in EnglishExperience working within a manufacturing environment Interested in a further conversation Please apply to this advert or also send your CV to to arrange a confidential career discussion.Spring acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Spring Group UK is an Equal Opportunities Employer.By applying for this role your details will be submitted to Spring. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
Keyskills :
CAPAauditquality assurancecomplaintISO13485medical deviceroot cause