Job Reference: J5633992
Updated On: 17/12/2020
Status: Open to Applications
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Role OverviewI’m currently recruiting for a Quality Specialist to join a leading drug development and manufacturing business within the operational team, based in the Newport area. As the Quality Specialist you will be responsible for the following:
Key Duties and ResponsibilitiesYour duties as the Quality Specialist will be varied however the key duties and responsibilities are as follows:
1.Provide QA guidance across the manufacturing and packaging departments to assist in the resolution of any quality issues.
2.Perform process and departmental audits against the relevant GMP standards
3.Ensure timely release of product by the review of the critical process parameters of batch documentation, assessing the quality, safety and efficacy prior to QP certification.
4.Train others in batch documentation review of critical process parameters.
Role RequirementsTo be successful in your application to this exciting opportunity as the Quality Specialist we are looking to identify the following on your profile and past history:
1. Minimum of 5 GCSE’s/ a degree in higher education e.g. BTEC
2. Experience within the pharmaceutical industry; ideally of various dosage forms
3. A working knowledge and practical experience within a Pharmaceutical GMP environment.
Key Words: Quality Officer, Quality Assurance, GMP, Pharmaceutical
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