We are currently looking for a Quality Assurance Specialist to join a leading pharmaceutical company based in the London area. As the QA Specialist, you will be responsible for ensuring the highest standards of quality and compliance within the manufacturing and production processes.
Your duties as the Quality Assurance Specialist will be varied however the key duties and responsibilities are as follows:
1. Ensure batch records for biological drug substances are reviewed prior to Qualified Person (QP) certification.
2. Monitor compliance with the requirements of Good Manufacturing Practice (GMP).
3. Review and assess the quality impact of any deviations prior to review and certification of the product by QP or Quality Assurance (QA).
4. Prepare Key Performance Indicator (KPI) information, including analysis of trends.
To be successful in your application to this exciting role as the Quality Assurance Specialist, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Proven industry experience in quality assurance within the pharmaceutical sector.
3. A working knowledge and practical experience with Good Manufacturing Practice (GMP) and Quality Management Systems (QMS).
Key Words: | Quality Assurance Specialist | GMP | QMS | Pharmaceutical | Compliance | Batch records | KPI | Deviations | Internal audits | Quality culture | Biological | Drug Substances |
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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