TieTalent Livingston, Scotland, United Kingdom
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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.
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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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