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Job Location | Plymouth |
Education | Not Mentioned |
Salary | £40,000 per annum |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent , full-time |
Quality Engineer Validation Specialist Medical Devices Plymouth Permanent Contract Focus of the roleReporting to the Quality Manager you will be responsible for quality compliance, technical documentation, project management and co-ordination of projects with other departments.This job will aid in the maintenance of compliance to relevant cGMP, FDA QSR 21 CFR 820, ISO13485 & European Medical Devices Directive MDD94/42/EEC.Role Responsibilities