Job Reference: J5634735
Updated On: 27/04/2021
Status: Open to Applications
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Role OverviewWe are currently looking for a QA Analyst to join a leading Biopharmaceutical company based in the Central belt area. As the QA Analyst you will be responsible for ensuring procedures and standards are adhered to and GMP regulation compliance is maintained upon completion of documentation, by performing quality assurance review of completed documentation, and reviewing new and updated SOPs/policies.
Key Duties and ResponsibilitiesYour duties as the QA Analyst will be varied however the key duties and responsibilities are as follows:
1.Completing various document control functions when required, such as issuance of documentation and GMP compliance reviews.
2.Quality review of documentation such as workbooks, forms and other documentation contained within batch manufacturing records, Quality management system (QMS) records such as CAPAs and change controls.
3.To identify and contribute to areas for improvement within the quality management systems to ensure compliant and efficient systems.
4. To aid the rest of the QA team and assist with the actions necesarry for maintenance of the QMS.
To be successful in your application to this exciting opportunity as the QA Analyst we are looking to identify the following on your profile and past history:
1. Great organisational and communication skills, as well as being able to work affectively in a team.
2. Proven industry experience in Quality Assurance in a GMP regulated environment
3. Demonstrable experience and sound knowledge of GMP regulations
Key Words:Pharmaceuticals | GMP | cGMP | Quality Assurance | Sterile | Licensed Medicines | Quality Management System | Change Control | CAPA's | Deviations | Document control | Compliance | Audits | Specialist | Associate | Quality | QA | Batch Release | Documentation | KPI | Manufacturing | Specialist | Senior QA Officer | CAPAs | SOPs | QMS
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