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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