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Job Location | Cambridge |
Education | Not Mentioned |
Salary | 27,500 per annum |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent, full-time |
An opportunity has arisen within our Cambridge-based Regulatory, Medical and Quality Affairs Department which is responsible for regulatory compliance, generating technical evidence and maintaining the quality systems required for in vitro device manufactureand sales.Reporting to the QC/QA Manager, your role will predominantly focus on Quality Assurance activities responsible for the management and maintenance of the Quality Management System, ensuring compliance with established processes and assisting in process improvement.You will also support the QC Team Leader with document auditing, batch release of final products and manufacturing/test equipment maintenance.This is a key role in the roll-out of OGTs new electronic Quality Management System (eQMS). Your role will be pivotal in the establishment of a number of core processes to support the new eQMS functionality and in the review and continual improvement of existingprocesses as they are transferred to the new system.Quality Assurance duties will include: