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Job Location | Surrey |
Education | Not Mentioned |
Salary | Salary negotiable |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Contract, full-time |
QA, Quality, GMP, 13485 Your new companyThis Biotech specialise on the design, manufacture and supply of a growing portfolio of oncology and infectious disease diagnostic products. They started in the early 2000s and have rapidly expanded since. Their areas of expertise include molecular real-time kits, liquid Based Cytology, Infectious and Oncology Diagnostic reagents. They are looking to recruit a contract Quality Specialist.Your new roleAs Quality Specialist you will be assisting the maintenance of quality system documents and assisting the QA release of and filing of the subcontractor manufacturing records. You will participate in QMS and audit activities. You will also support the registration activities and regulatory submissions and participate in QA/RA meetings.What youll need to succeedIn order to be considered for this Quality Specialist role you will have previous experience of working with QMS. Previous experience of working in an ISO 9001/ISO 13485 environment is also necessary. You will have strong organisational skills and be able to work well independently as well as in a team.What you need to do nowIf youre interested in this role, click apply now to forward an up-to-date copy of your CV, or call us now.If this job isnt quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.