6 of 6 Permanent CAPA Jobs in the North of England

working knowledge of ISO 13485, ISO 14971 and 21 CFR Part 820/QMSR requirements. Demonstrable experience in non-conformance investigation, root cause analysis, CAPA, risk management and validation. Strong understanding of process capability, inspection, measurement systems and process improvement methodologies. Proven ability to use data to influence technical and ...

manufacturing industry regulations (e.g. ISO 9001, GAMP 5, ISO 27001, 21 CFR Part 11) and data integrity guidelines. Lead root cause analysis (RCA) and CAPA for IT system outages, data synchronization failures, or automated line disruptions. Collaborate with OT, Automation, and Systems Engineering teams to validate software updates, digital twin ...

projects, as required. Work collaboratively with business process owners, technical system owners, and QA validation as needed. Experience with Quality systems like Change control, CAPA, and deviations. Qualifications What makes you remarkable? At Wood, we are committed to equal opportunities and welcome all talented individuals to consider joining our team. ...

and manufacturing software across our automated manufacturing facilities. You will validate shop-floor systems (MES, ERP, SCADA) and IoT devices, lead RCA and CAPA for outages, and design automated and manual test plans. Work is hybrid with flexible hours, strong career progression, and a culture focused on quality and continuous ...

with relevant quality standards and customer requirements. Leading internal and external audits and supporting corrective actions. Driving root cause analysis, corrective and preventive actions (CAPA). Monitoring quality performance, trends and key quality metrics. Supporting non-conformance, defect and customer complaint processes. Working with manufacturing and engineering teams to improve … Quality Management Systems, ideally ISO 9001 and/or other relevant industry standards. Internal and external audits. Root cause analysis and structured problem solving. CAPA, non-conformance and corrective action processes. Continuous improvement methodologies. Quality assurance and process control within an electronic manufacturing environment. Supplier quality and customer quality requirements. ...

times to be agreed with QM; SPECIFIC RESPONSIBILITIES Facilitate and support investigations for internal and external non -conformance with a RC and CAPA Support audits/visits by auditors and customers Contact customers/suppliers Act as first point of contact from the production area regarding quality matters. Promoting and … manufacturing environment (ideally food, print and/or packaging) essential. Experience in internal and/or external auditing is essential. Experience with RCA and CAPA essential. Knowledge of the global standards is essential. Computer skills including the use of Microsoft Excel, Outlook and Word to be in position to prepare ...