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 ..... full job details .....