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 assur...