GMP QA Specialist

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 with in 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

• Seniority level: Associate
• Employment type: Full-time
• Job function: Quality Assurance
• Industries: Pharmaceutical Manufacturing

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

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