Entrust Resource Solutions is supporting a GMP-regulated analytical testing laboratory in search for an experienced QA Specialist to support and develop Quality Assurance activities across a growing QC testing environment.
This is an excellent opportunity for someone with GMP QA experience looking for a broad and hands‑on role across QA oversight, quality systems, audits, deviations, CAPAs, data integrity, equipment qualification, and Computer Systems Validation activities within a fast‑paced laboratory environment.
The successful individual will play a key role in ensuring laboratory operations, systems, and documentation remain compliant with GMP, GDP, regulatory expectations, and client quality requirements while supporting the continued development of GMP capability across the site.
Qualifications
* GMP QA experience within pharmaceutical or analytical laboratory environments
* Experience supporting deviations, CAPAs, change controls, and audits
* Knowledge of Data Integrity, Annex 11 & 21 CFR Part 11 requirements
* Experience with IQ/OQ/PQ and equipment qualification activities
* Exposure to Computer Systems Validation (CSV) activities
* Strong documentation review and QMS experience
* Excellent organisational and stakeholder management skills
Experience within QC testing laboratories, contract testing environments, or analytical services organisations would be highly beneficial.
For more information or a confidential discussion, please get in touch directly - lynsey@entrustrs.com
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