26 to 34 of 34 CAPA Jobs in England

Quality Engineer to drive quality across warehouse and logistics automation projects, covering manufacturing, assembly, installation and commissioning activities. You will lead inspections, audits and CAPA, investigate root causes with 8D/5 Why/Ishikawa, manage supplier quality, and monitor KPIs using Excel and BI tools while collaborating with engineering ...

with flexible working policies and opportunities for training and progression. You will work with cross-functional teams, ensure compliance with OT security standards, support CAPA and maintenance, and help drive continuous improvement initiatives to optimise packaging and manufacturing processes. #J-18808-Ljbffr ...

software release pipelines and hardware manufacturing runs, facilitating strict "Go/No-Go" readiness reviews prior to customer delivery. Continuous Improvement & Root Cause Analysis (CAPA): Implement robust Corrective and Preventive Action (CAPA) processes, analyzing field performance data, warranty claims, and customer defect tickets to drive iterative product and process enhancements. … quality control gates. Proven process excellence capabilities , with deep familiarity or certification in Six Sigma, Lean, or ISO quality methodologies, using defect analytics and CAPA processes to eliminate repeat failure modes and achieve strict SLA metrics (e.g., 99.99%+ uptime, MTBF targets). This position is based in London and ...

write the procedure as you learn the repair Experience writing technical documentation in a regulated environment - service procedures, work instructions, SOPs - and participating in CAPA and nonconformance processes Working knowledge of ISO 13485 quality system requirements as they apply to service and repair Systems thinker: you see a pile ...

Product and Marketing teams. This is a broad, hands-on position where you will take ownership of quality improvement activities, non-conformances, CAPA, root-cause investigations, risk management, complaint handling and process improvement. You will also support design controls, new product introduction, supplier quality, change control and the maintenance and … experience within medical devices or another highly regulated manufacturing environment Strong knowledge of ISO 13485 and medical device quality systems Experience managing non-conformances, CAPA and root-cause investigations Knowledge of quality tools such as 8D, 5 Why, Fishbone, FMEA and structured problem-solving Experience supporting manufacturing process controls, change ...

excellent opportunity for someone with a strong background in manufacturing who enjoys working across the full quality lifecycle, from internal auditing and CAPA management to validation, supplier quality and continuous improvement. Key responsibilities include: Maintaining and improving the Quality Management System (QMS) Planning and conducting ISO 13485 internal audits and … role within a manufacturing environment Strong working knowledge of ISO 13485:2016 Qualified ISO 13485 Internal Auditor with hands-on auditing experience Experience with CAPA, non-conformance management, root cause analysis, change control and continuous improvement Excellent communication, analytical and problem-solving skills Benefits : 25 days annual leave plus Bank ...

inspections, process audits and compliance checks Non-Conformances: Investigate issues and lead root cause analysis using 8D, 5 Why and Ishikawa Corrective Actions: Manage CAPA and ensure issues are resolved effectively Supplier Quality: Support supplier audits, quality issues and performance improvement Project Support: Work with engineering and project teams through … material handling, engineering or manufacturing Strong knowledge of ISO 9001 Experience with internal and supplier auditing Good understanding of 8D, 5 Why, Fishbone and CAPA Experience with quality inspections and non-conformance management Strong analytical and problem-solving skills Good knowledge of Microsoft Excel ; Power BI and ERP experience would ...

and standards, and review supplier performance on costs, compliance, and milestone delivery. Provide technical expertise to engineering technicians, including assisting with complex equipment failures, CAPA implementation and improvement activities. Act as the point of contact for production automation support, focusing on equipment performance, with flexibility in working hours as required. … Participate in Continuous Improvement activities, including DMAIC, RCA, and CAPA processes and input into deviations as automation SME. About You This role is suited to a motivated person with good influencing, communication, and teamworking skills. A successful candidate will have a passion for understanding and mastering a variety of complex ...

site, helping diagnose faults and guiding safe recovery of M&E systems. Own Root Cause Analysis (RCA) creation and closure, and drive Corrective and Preventive Actions (CAPA) through to completion. Lead structured problem solving on complex and recurring faults, using trend, alarm and maintenance data to resolve underlying causes rather … operational risk of works on live M&E systems. Experience leading or contributing to Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) following M&E system incidents, with a structured approach to problem solving. Confident supporting site teams under pressure during live incidents, and comfortable coaching and training ...