Job Reference: J5632826
Updated On: 29/01/2020
Status: Open to Applications
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Role OverviewWe are currently looking for a QA Specialist to join a leading pharmaceutical company based in the South East area. As the QA Specialist you will be responsible for managing Pharmaceutical Quality System non-conformances, change controls, CAPAs and OOS system documentation.
Key Duties and ResponsibilitiesYour duties as the QA Specialist will be varied however the key duties and responsibilities are as follows:
1. As the QA Specialist, you will participate in the design of e-QMS workflows.
2. In your role as the QA Specialist, you will ensure that all systems used to monitor the progress of non-conformances, change controls, CAPAs and OOSs system documentation are kept up to date.
3. You will work closely with the QA Manager to deliver training for non-conformance, change controls, CAPA and OOS system documentation as required.
4. As the QA Specialist, you will provide advice and guidance to personnel on appropriate CAPAs and verify completion of CAPA actions.
Role RequirementsTo be successful in your application to this exciting opportunity as the QA Specialist we are looking to identify the following on your profile and past history:
1. Relevant degree in a related scientific subject.
2. Proven industry experience in Quality Assurance within the pharmaceutical industry.
3. A working knowledge and practical experience with QA principles, in particular non-conformance, change control and CAPA systems.
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