Quality Officer

Job Advertisement: Quality Officer Overview We are seeking a dedicated and detail-oriented Quality Officer to join our quality team at a leading pharmaceutical manufacturing organisation. This is a great opportunity for a QC analyst / QA officer to start / progress their career as a Quality Officer to contribute to the delivery of pharmaceutical products that meet both customer and regulatory requirements. Responsibilities As a Quality Officer, your key responsibilities will include: * Preparing quality documentation to support site operations, including works orders, specifications, bills of materials, and batch documentation. * Performing environmental monitoring of the facility in accordance with schedules and procedures. * Producing and maintaining administrative quality reports and documents. * Managing document administration for the Quality team, including issuing, retaining, and archiving documents, and maintaining records within the electronic Quality Management System (eQMS). * Providing quality support across key business areas. * Assisting with deviation investigations, corrective and preventive actions (CAPAs), change controls, and liaising with customers and suppliers on issues, investigations, and projects. * Participating in inspection readiness activities and the internal audit program. * Taking opportunities to develop within the QA Operations team and deputising as appropriate. Qualifications The ideal candidate will possess: * A strong understanding of quality principles and practices, preferably within a pharmaceutical or manufacturing environment. * Excellent organisational and documentation skills. * The ability to work collaboratively across teams and communicate effectively with internal and external stakeholders. * A proactive approach to problem-solving and a commitment to continuous improvement. * Familiarity with eQMS systems and regulatory requirements is desirable. Day-to-Day Your day-to-day activities will involve: * Preparing and reviewing quality documentation to ensure compliance with regulatory standards. * Conducting routine testing and environmental monitoring to maintain product and facility quality. * Collaborating with cross-functional teams to address quality-related issues and support operational excellence. * Managing and maintaining accurate records within the eQMS. * Participating in audits and readiness activities to uphold the organisation’s high standards. Benefits * Competitive salary up to £30,000. * Opportunity to work in a dynamic and innovative pharmaceutical manufacturing environment. * Professional development and growth opportunities within the Quality Assurance team. * A supportive and collaborative workplace culture. Note: We are unable to provide VISA sponsorship for this position