Quality Assurance Specialist (QMS)
30 Days Old
As a Quality Assurance Specialist, you will be responsible for:
* Supporting day-to-day QA activities, including review and approval of GMP documentation, batch-related records, and QMS deliverables.
* Contributing to core QMS processes such as deviations, CAPAs, change controls, and document control to ensure compliance with internal and regulatory standards.
* Assisting with the implementation and testing of the new eQMS, supporting data migration, user coordination, and quality documentation updates.
* Collaborating with QA, production, supply chain, and IT teams to drive continuous improvement and ensure robust quality practices across the organisation.
To be successful as a Quality Assurance Specialist, you will have:
* Experience working within a GMP-regulated pharmaceutical QA environment with strong exposure to QMS activities.
* Good understanding of core quality processes, compliance expectations, and documentation requirements within pharmaceutical operations.
* Strong organisational and communication skills with the ability to work effectively with cross-functional teams and manage multiple priorities.
* A proactive, detail-driven approach with enthusiasm to support digital quality initiatives.
Quality Assurance Specialist | QA | QMS | eQMS |Pharmaceutical | GMP | CAPA | Deviations | Change Control | Document Control | Quality Systems | Compliance | QA Operations | Continuous Improvement | Quality Documentation
- Location:
- Clerkenwell
- Salary:
- £35,000 - £45,000 /annum
- Job Type:
- FullTime
- Category:
- Medical/Pharmaceutical/Scientific
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