QC Validation Officer

QC Validation Officer Location: Wrexham Sector: Pharmaceutical Manufacturing An excellent opportunity has arisen for an experienced QC professional to join a well-established pharmaceutical manufacturer in Wrexham as a QC Validation Officer. This role offers the chance to support QC systems and laboratory instrumentation while contributing to compliance, operational excellence, and continuous improvement activities within a regulated environment. Key Responsibilities * Schedule and execute maintenance, calibration, and qualification activities for QC equipment. * Manage GMP-relevant QC computer systems and Chromatography Data Systems (CDS), including Empower. * Provide technical support for chromatography equipment and associated software systems. * Ensure compliance with Data Integrity and cGMP requirements. * Support Computer System Validation (CSV) activities for QC systems and equipment. * Lead investigations into equipment-related deviations and implement corrective and preventive actions (CAPAs). * Drive continuous improvement and quality enhancement initiatives. * Generate and maintain GMP documentation relating to QC operations, automated systems, and validation activities. Requirements * Bachelor's degree in a scientific discipline or equivalent experience. * Good understanding of cGMP and Data Integrity requirements within the pharmaceutical industry. * Experience with laboratory equipment maintenance, calibration, qualification, and validation. * Strong knowledge of chromatography equipment and Chromatography Data Systems (CDS), preferably Empower. * Experience supporting or participating in Computer System Validation (CSV) activities. * Understanding of automated QC systems within a pharmaceutical manufacturing environment. Benefits * 7% matched pension scheme * Generous holiday allowance * Employee rewards platform with retail and dining discounts * Salary sacrifice schemes * Sports and social club * Subsidised on-site canteen * Free on-site parking