GMP QA Specialist

Job Title: Quality Assurance Specialist

Location: Livingston, Scotland

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

Salary: Competitive + Excellent Benefits

Contract Type: Permanent, Full-Time

Visa Sponsorship: Unfortunately, not available for this role

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

The Role

As a Quality Assurance Specialist, you will play a key role in maintaining and improving the Quality Management System (QMS) in line with GMP and regulatory standards. You’ll support day-to-day quality operations, assist in audits, and ensure that quality metrics and systems are accurately maintained and reported.

Other key responsibilities will include:

• 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
  
  Applications are invited from candidates with a minimum of 12 months working within a GMP/GLP regulated laboratory. Experience within quality assurance would be a distinct advantage. You must have exemplary attention to detail and be confident liaising across multiple departments and externally.
  
  What’s in it for you?
  
  Join a company that genuinely cares about your growth and wellbeing. Employees benefit from:
  
  
• Enhanced Annual Leave (including sell-back options and service-linked increases)
  
  
• Company Pension Plan & Life Assurance (4x salary)
  
  
• Free On-site Parking
  
  
• Healthcare Cash Plan (after 6 months)
  
  
• 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 through VRS Recruitment to take the next step in your Quality Assurance career within a supportive and forward-thinking organisation.
  
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  Key words: QA, quality assurance, GMP, good manufacturing practice, laboratory, chemistry, analytical, microbiology, pharmaceutical, biopharmaceutical, quality management system, QMS, GLP, GxP, Livingston, Edinburgh, Glasgow, Stirling, VRS9121AW