26 to 50 of 58 CAPA Jobs in the UK

products, including PPAP activities. Assist with root cause analysis of production rejects, defects and process deviations. Develop and implement effective corrective and preventative actions (CAPA). Modify and develop PLC programmes to improve process capability, repeatability and line performance. Work collaboratively with Production, Quality and Engineering teams to prevent recurring ...

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. ...

Oversee phase‐appropriate clinical sample testing activities, ensuring rigorous quality control, quality assurance, data integrity, and operational excellence throughout assay execution. Lead deviation investigations, CAPA activities, and inspection‐readiness efforts to support compliance and audit preparedness. Serve as a scientific subject‐matter expert for molecular assay strategies across multiple clinical ...

Quality Systems Manager to lead our quality management system under ISO standards in the UK. You will own QMS governance, document control, and CAPA processes while coordinating with engineering and manufacturing to ensure product quality and regulatory compliance. The role emphasizes leadership, data-driven improvement, supplier/customer audits, and ...

seeking a Senior Product Quality Engineer for our international semiconductor client. The role drives customer quality improvements across development and manufacturing, leading RMAs, CAPA actions, and ISO 9001 compliant processes. You will guide NCMR handling, supplier quality, and continuous improvement initiatives, including Lean, Six Sigma, and 5S, to ensure product ...

exposure. This broad QA role sits within a lean biotech environment and works closely with Clinical Development and other functions across clinical quality, audits, CAPA, investigations, QMS and inspection readiness. As Director, you will lead GCP compliance, manage audit programmes, drive CAPAs and investigations, and provide QA input #J ...

stakeholder communications, and execution controls protect data center availability. The role leads incident response and post-incident reviews, directs root cause analysis and corrective and preventive action plans, validates commissioning and design deliverables, oversees site assessments and build activities, and establishes consistent operational policies and procedures. The Senior Manager holds ...

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 ...

/3D scanning as needed Make conformity, containment, and release decisions on complex quality issues Lead non-conformance investigations, MRRs, root cause analysis, and CAPA Support 8D problem-solving for customer returns or escapes Take part in third-party and regulatory audits (ISO, CAA, FAA), representing the business with customers ...

components Update and maintain stock reports with received deliveries and stock usage Assist in preparing documentation for internal and external audits. Support CAPA tracking and non-conformance documentation where required. Contribute to continuous improvement initiatives within operations. Competency requirements · A positive, pro-active can-do attitude. · Attempt to keep ...

electronic failure mechanisms Hands-on experience with oscilloscopes, multimeters, electronic loads, logic analyzers, X-ray, and thermal imaging Experience writing 8D reports and managing CAPA to closure Strong English technical writing; ability to collaborate with global teams Mandarin Chinese proficiency is required — this role involves close collaboration with ...

conformance reports (NCR's) and then undergoing root cause analysis (RCA's) with a view of advising and agreeing on corrective and preventative actions (CAPA's). Essential Requirements: Previous experience as a Quality Compliance Engineer or similar At least 3 years' experience conducting audits in a highly regulated environment ...

conformance reports (NCR's) and then undergoing root cause analysis (RCA's) with a view of advising and agreeing on corrective and preventative actions (CAPA's). Essential Requirements: * Previous experience as a Quality Compliance Engineer or similar * At least 3 years' experience conducting audits in a highly regulated environment ...

conformance reports (NCR's) and then undergoing root cause analysis (RCA's) with a view of advising and agreeing on corrective and preventative actions (CAPA's). Essential Requirements: * Previous experience as a Quality Compliance Engineer or similar * At least 3 years' experience conducting audits in a highly regulated environment ...

entails three days on-site at the Maidenhead office. You will own the quality and compliance infrastructure, provide expert GVP guidance, lead investigations and CAPA, coordinate health authority audits, monitor KPIs, and deliver PV training while shaping the #J-18808-Ljbffr ...

requires regular travel across Europe/Nordics, with focus on high-density AI cooling and power. You’ll perform design reviews, audits, RCA/CAPA, and coach site engineers to improve reliability and energy efficiency. #J-18808-Ljbffr ...

scale. Joining a newly established AI function at an exciting early stage, you will play a key role in shaping the future of AI capa click apply for full job details ...

chain operations; support external compliance audits. Engineering Change Control: Manage Engineering Change Notifications (ECNs/ECRs) and oversee controlled technical documentation. Root Cause Analysis & CAPA: Lead non-conformance investigations (NCR), customer returns (RMA), and implementation of CAPA using structured techniques (8D, 5-Why). Cross-Functional Quality Support: Collaborate directly … Requirements & Qualifications Essential Criteria: Proven experience working within an ISO 9001 certified Quality Management System. Strong background in Quality Assurance (QA), root cause analysis, CAPA, and non-conformance management. Excellent documentation, administrative, and Microsoft Office skills. Strong communication skills with experience working alongside Production and Engineering teams. Ability to work ...

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. ...

activities in line with ISO 14971 , including hazard analysis, risk evaluation and mitigation strategies. Supporting post‐market surveillance, vigilance and complaints investigations , ensuring robust CAPA and documentation. Working as part of, or leading, cross‐functional project teams , managing quality deliverables, tracking actions and supporting timely decision‐making. Qualifications … environments. A well‐developed understanding of risk management (ISO 14971) and exposure to human factors/usability engineering . Experience with supplier quality, audits, CAPA and document control . Excellent communication, organisational and project management skills, with the confidence to work with diverse stakeholders. We know the skill-gap and ...

within aerospace, defence, automotive or another regulated manufacturing environment Knowledge of regulated frameworks such as EASA Part 21 or equivalent Experience managing non-conformance, CAPA and root cause investigations Ability to interpret engineering drawings, specifications and manufacturing documentation Strong communication and stakeholder man agement skills Particularly desirable experience ISO/… AS9100 Lead Auditor certification AS9100 certification or recertification projects FMEA RCCA/8D CAPA SPC Lean/Six Sigma Multiple contract opportunities available This is a significant period of growth for the organisation, creating a number of opportunities for experienced Quality professionals to make an immediate impact. If you have ...

contact for external certification and customer audits Investigating non-conformities, customer complaints and internal quality issues using structured root cause analysis and CAPA methodologies Monitoring and reporting quality KPIs, analysing trends and identifying opportunities for continuous improvement Supporting New Product Introduction (NPI), verification and validation activities, process changes and customer … highly desirable Experience planning, leading or supporting internal and external audits Strong problem-solving capability using structured methodologies such as 8D, FTA, Ishikawa and CAPA Familiarity with quality tools including FMEA, Control Plans, SPC, MSA, 5S and Kaizen would be advantageous Knowledge of ESD control standards and electronics workmanship standards ...

take ownership of a broad range of quality and technical activities, work closely with the wider technical function and gain valuable experience across audits, CAPA, product quality, traceability, training and continuous improvement. Most importantly, this role has been created with career progression in mind. The plan is to develop … role, preferably within food manufacturing, FMCG or fresh produce A good understanding of GMP, HACCP, food safety and quality systems. Experience with non-conformance, CAPA and Root Cause Analysis. Experience supporting or completing audits. Strong attention to detail and excellent organisational skills. The ability to analyse information, identify trends and ...

related field. Minimum of 5 years' experience in industrial Quality. Proficiency in ISO 9001 and the process-based approach. Experience with audits, NC/CAPA, and continuous improvement. Solid experience in Health and Safety Key Skills: You will be accountable for the UK’s Quality Management System/ISO9001 … BI. Ability to work with ERP/integrated management systems and document management or Quality tools. Ability to manage the non-conformity (NC) and CAPA processes. Able to identify recurring issues and contribute to their sustainable resolution. Participate in monitoring supplier Quality performance. Support organisational and process changes. Safety/ ...

effective decision-making as the organisation scales. Working cross-functionally, the successful candidate will manage and improve quality activities including document control, SOPs, nonconformances, CAPA, change control and internal audits. They will also review existing processes, identify opportunities for improvement, maintain quality records and contribute to technical documentation. This … optimisation of workflows and quality processes. Review existing processes to identify gaps, inefficiencies and practical opportunities for improvement. Govern quality activities including nonconformances, CAPA, change control, internal audits and quality metrics. Generate, review and revise SOPs, technical documentation and associated quality records. Work cross-functionally to support compliance across software ...