GMP QA Specialist

ScreenedFull Time
Livingston, Scotland
Posted 3 days ago
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About the role

TieTalent Livingston, Scotland, United Kingdom

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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.

Follow VRS Recruitment on LinkedIn to view all our latest vacancies!

Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.

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

Seniority level

  • Seniority level

    Entry level

Employment type

  • Employment type

    Full-time

Job function

  • Job function

    Quality Assurance
  • Industries

    Technology, Information and Internet

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