GMP QA Specialist

VRS Recruitment; Livingston; On-site; GBP 30,000 - 40,000; Full time

Benefits offered by this job

Enhanced Annual Leave

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

Job summary

A leading biopharmaceutical CRO in Livingston is seeking a Quality Assurance Specialist. The role involves managing quality systems, auditing, and training. Ideal candidates will have GMP/GLP experience and excellent attention to detail. This position offers enhanced benefits and career progression opportunities within a supportive environment.

Qualifications

• Minimum of 12 months working within a GMP/GLP regulated laboratory.
• Experience within quality assurance would be a distinct advantage.

Responsibilities

• 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.

Skills

Attention to detail

Cross-department communication

Job description

Overview

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.

Role

Job Title: Quality Assurance Specialist

Responsibilities

• 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

Qualifications

• 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

Benefits

• 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

Details

• 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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