GMP QA Specialist

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.

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

#J-18808-Ljbffr

Full job description from WhatJobs. Apply for this role →