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GMP QA Specialist

Job Description

Location: Livingston, Scotland

Hours: 39 hours/week, Monday–Friday (flexible start/end times available)

Contract Type: Permanent, Full-Time

Visa Sponsorship: Not available

Seeking an accomplished GMP QA professional to join a successful biopharmaceutical CRO in Livingston.

Job Title: Quality Assurance Specialist

Administration and development of LIMS and other IT systems
Review and approval of procedures, protocols, reports, and certificates of analysis
Management of quality KPIs and metrics
Support for internal audits, client audits, and regulatory inspections
Coordination of quality documentation and controlled substances processes
Delivery of QMS and eLIMS training to staff
Lead or support continuous improvement initiatives in the QMS
Deputising for QA Management where required

Minimum of 12 months working within a GMP/GLP regulated laboratory
Experience within quality assurance would be a distinct advantage
Exemplary attention to detail and ability to liaise across multiple departments and externally

Enhanced Annual Leave (including sell-back options and service-linked increases)
Free On-site Parking
Enhanced Maternity, Adoption & Paternity Schemes
Global career progression opportunities
Access to Employee Assistance and Health & Wellbeing Programmes
Recognition for service, special achievements, and life events

Interested? Apply now to take the next step in your Quality Assurance career within a supportive and forward-thinking organisation.

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