26 to 50 of 84 CAPA Jobs in the UK

running of the QA department and the oversight of the Quality Management System. Manage investigations, including root cause, product impact and CAPA Handle customer complaints and customer regulatory questions Take part in the internal audit programme and support regulatory inspections Approve suppliers and starting materials using a risk-based approach ...

firmware introduction and development would be desirable. Experience of leading problem-solving teams using industry standard tools such as 8D, Ishikawa, 5 why, and CAPA is essential. Skills, Special Competencies IT Literate – Microsoft packages, SAP experience preferred but not essential. Must be self- motivated with the ability to work without ...

anomaliesReview and own test coverage, test limits, and guard-band decisionsLead failure analysis and root cause investigations for field returns and RMA cases; drive CAPA development and closurePartner with foundry process and packaging engineering teams to resolve issues during wafer fabrication, packaging, die sort, and final package testIdentify and implement ...

Understanding of asset management and reliability principles. Experience supporting CMMS implementations, upgrades, or data migrations. Familiarity with quality systems including change control, deviations, and CAPA processes. Experience supporting continuous improvement initiatives. What we offer in return Eisai offers a competitive salary and excellent wider benefits package that includes, Electric charging ...

and fixtures. -Support FAT/SAT activities and production readiness. Continuous Improvement & Quality -Drive Lean, Six Sigma, SPC and root cause analysis activities. -Support CAPA, non-conformance investigations and process compliance. -Deliver improvements in productivity, quality, cost and delivery. Data Analysis & Reporting Analyse manufacturing data (OEE, yield, scrap, rework) using ...

quality engineering or management). Knowledge of aerospace quality standards and regulatory requirements. Trained in quality tools and methodologies with certificate (e.g., SPC, PPAP, CAPA). Trained AS9100 Internal auditor with certificate (will consider automotive or with good demonstrable experience). Chartered Quality Engineer (CQE) by professional body. Experience with ...

initiatives. Coordinate BOM reviews, component qualification and supplier readiness activities. Ensure compliance with relevant standards including CE, UL, FCC, RoHS and REACH. Lead corrective and preventive action activities to improve quality and reliability. What We Are Looking For Required Degree or equivalent qualification in Electronic Engineering, Mechanical Engineering, Manufacturing Engineering ...

analog circuit design, signal integrity, high-speed amplifiers, bias circuits, and current sources. Extensive experience with quality systems and tools including ISO 9001, CAPA, NCMR, SPC, FMEA, Control Plans, 8D, and statistical analysis. Proven customer and supplier quality experience across wafer fabrication, assembly, testing, and optical module manufacturing. #J ...

analog circuit design, signal integrity, high-speed amplifiers, bias circuits, and current sources. Extensive experience with quality systems and tools including ISO 9001, CAPA, NCMR, SPC, FMEA, Control Plans, 8D, and statistical analysis. Proven customer and supplier quality experience across wafer fabrication, assembly, testing, and optical module manufacturing. #J ...

analog circuit design, signal integrity, high-speed amplifiers, bias circuits, and current sources. Extensive experience with quality systems and tools including ISO 9001, CAPA, NCMR, SPC, FMEA, Control Plans, 8D, and statistical analysis. Proven customer and supplier quality experience across wafer fabrication, assembly, testing, and optical module manufacturing. #J ...

/PCBA manufacturing knowledge IPC-A-610 and/or J-STD-001 experience AS9100 and/or ISO 9001 experience Root Cause/CAPA/8D/FMEA experience ERP/MRP experience Hands-on measurement, inspection and test equipment knowledge These requirements closely reflect the essential experience identified ...

Identify yield-loss drivers and implement corrective actions Quality & Failure Analysis Monitor manufacturing yield and quality metrics Support failure analysis, root-cause investigations, and CAPA activities Work with foundries and OSAT partners to resolve production issues Drive continuous improvement and cost-reduction initiatives Required Qualifications Good experience in semiconductor product ...

Management of Quality Reviews – Monthly Compilation and presentation of KPIs for Key business functions required supporting Management reviews. Raise, monitor, and verify CAPA/8D, working with relevant stake holders to drive robust RCCA. Compilation and maintenance of company documentation Maintenance of training material and deployment of training Drive ...

and continuous improvement initiatives.Coordinate BOM reviews, component qualification and supplier readiness activities.Ensure compliance with relevant standards including CE, UL, FCC, RoHS and REACH.Lead corrective and preventive action activities to improve quality and reliability.What We Are Looking ForRequiredDegree or equivalent qualification in Electronic Engineering, Mechanical Engineering, Manufacturing Engineering, Computer Engineering ...

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 ...

Technical Lead to support the Technical Team in ensuring Food Safety, Quality and Legal compliance across the site. You will manage QMS, audit readiness, CAPA, HACCP and allergen controls, working with cross-functional teams. You will drive internal GMP/QMS audits, supplier and customer standards alignment, and maintain documentation. ...

Holdings Inc is seeking a GCP Auditor to join our team. The role focuses on regulatory compliance, quality systems, and independent CAPA development in a CRO environment. Travel up to 30% within the UK/EU is expected. Strong knowledge of 21 CFR Part 11, FDA, and GxP is required ...

continuous compliance with accreditation standards. Maintain documentation, validation records, and equipment files in line with accreditation requirements. Participate in internal audits, external assessments, and CAPA processes. Support competency assessments and training related to new instruments and assays. Contribute to compliance efforts across ISO 27001 (information security), ISO 9001 (quality management ...

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 adequate resources are available to work safely. Monitor and review health and safety performance, observe safety behaviours in the workplace, taking appropriate corrective and preventive action as necessary and suggesting and implementing improvement activities. Key Stakeholders: Lead Back End Engineer Product Owners QA DevOps/Platform Head of Development ...

MHRA Software and AI as a Medical Device programme, MDCG guidance, FDA guidance, IMDRF) and assess impact on products and the QMS. Support CAPA and internal audit follow-ups where regulatory root causes are identified. What We’re Looking For 3 to 6 years' Regulatory Affairs experience in Medical Devices ...

ensure robust processes for volume production. The role emphasizes hands-on quality leadership in prototype and pre-production builds, supplier collaboration, and rigorous CAPA/DMAIC problem-solving to deliver compliant, high-quality #J-18808-Ljbffr ...

quality support to US Commercial Operations as required. Support Product Technical Complaint (PTC) activities for the US market. Support Global Change Control, Deviation, and CAPA processes across assigned regions. Support and perform product release activities for the US market and Kankakee-manufactured export products, collaborating with manufacturing site representatives … global teams. Strong organizational, communication, influencing, and stakeholder management skills. Ability to identify process improvement opportunities and implement practical, innovative solutions. Working knowledge of CAPA development and quality system methodologies is preferred. Experience supporting or implementing electronic quality systems and digital quality tools is advantageous. Strong computer skills, including Microsoft ...

and adequate resources are available to work safely. Monitor and review health and safety performance, observe safety behaviours in the workplace, taking appropriate corrective and preventive action as necessary and suggesting and implementing improvement activities. Key Stakeholders:Lead Back End EngineerProduct OwnersEngineering TeamArchitectureQADevOps/PlatformHead of DevelopmentSecurityBusiness Stakeholders including product ...

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 ...