1 to 25 of 56 QMS Jobs in the UK

our team and help ensure our sites meet the highest standards in quality, safety, and customer satisfaction. What Youll Do: Works cross functionally to manage and maintain the Quality Management System across the MYD sites. Ensure audit readiness for BRC, legal, and customer standards. Develop, deploy and maintain governance of the site HACCP/TACCP/VACCP plans. Accountable for More ❯

of everyday life and will be part of your working reality. We have built a representative and welcoming environment, for everyone. Your Profile • Strong understanding of Quality Management Systems (QMS) and aerospace industry standards (e.g., AS/EN 9100). • Proficiency in quality core tools (e.g., APQP, FAI, 8D analysis, IPCA+, CCP tools). • Knowledge of lean manufacturing, Six Sigma More ❯

Lean tools, supporting improvement activities and events. Stay up to date with quality management best practices, methodologies, and regulations. Essential Skills Minimum 3 year's experience in a Quality Management System role within an ISO9001/AS9100 certified manufacturing environment. Trained AS9100 Auditor. Strong documentation management and configuration control experience. Skilled in APQP, PPAP, FAIR, and other quality methodologies. Proficient More ❯

Lean tools, supporting improvement activities and events. Stay up to date with quality management best practices, methodologies, and regulations. Essential Skills Minimum 3 year's experience in a Quality Management System role within an ISO9001/AS9100 certified manufacturing environment. Trained AS9100 Auditor. Strong documentation management and configuration control experience. Skilled in APQP, PPAP, FAIR, and other quality methodologies. Proficient More ❯

This approach is fully embraced throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its obligations to act responsibly, ethically More ❯

Review and sign off all direct reports' timecards and expenses. Authorise Holiday requests of direct reports. Maintain register and carry out technical audits on projects as required. Ensure Quality Management System ISO 9001and 14001. Preferred Skills and Experience Excellent presentation and communication skills. Extensive experience, especially in designing and managing projects, minimum 10 years' experience within a design consultancy working More ❯

science, engineering or other relevant data-oriented discipline (or equivalent industrial experience) Experience working with medical devices that include a software or firmware component Experience working within a quality management system (ISO 13485 or ISO 9001), or in a regulated industry Industrial experience as Tier 2 or 3 Technical Support Engineer or similar role Experience in an early-stage company More ❯

and managing all Customer complaints and warranty, dealing with them effectively and in time. Embed a culture of continuous improvement throughout the company. Lead the Business to achieve quality management system targets for customers and business goals (KPIs). Responsibilities: Strategy and Development Contribute to the creation and implementation of best practice, strategy, policies, processes and procedures to aid and More ❯

within food manufacturing, ideally across multiple sites. Strong understanding of quality systems, continuous improvement, and data-driven decision-making. Excellent stakeholder engagement and communication skills. Experience with SAP, digital QMS tools, and project management. A proactive, collaborative mindset with a passion for driving change. What's in it for you? A competitive salary 10% Bonus paid annually Progression routes and More ❯

Systems : To complete all admin on time and accurately and ensure that all relevant paperwork is filed and archived to support due diligence Document Control : Administration of site Quality Management System and associated control documents including relevant factory paperwork Customer Management : Administration of customer complaints including login of data, investigation of issues, trending and reporting of data Customer Management : General More ❯

independent audits as required by the audit schedule to ensure that the Company remains in compliance with the requirements of relevant regulations and standards and to ensure the quality management system has been implemented and is being maintained. Evaluation of product specific issues and product realisation processes investigation (8D process), ensuring prevention of recurrence. Provide feedback on quality performance and More ❯

be reported to HS2. It is an SCSJV requirement that all employees, Design House, and Supply Chains must implement and comply with the requirements of ISO 9001:2015 Quality Management System, ISO 14001:2015 Environmental Management System with guidance for use", OHSAS 18001:2017 Occupational Health and Safety Management Systems and ISO/IEC 27001:2013 Information Security Management System More ❯

will be working under minimal supervision follows process instructions, drawing, test and repair schedules, to assemble, test and repair product and customer returns, to the requirements of the quality management system, and to achieve company and customer requirements. Location: Christchurch UK Benefits: Paid Time Off | Retirement with Employer Match | Health and Wellness Benefits | Learning and Development Opportunities | Competitive Pay | Bonus More ❯

procedures. Maintain accurate inspection records and quality documentation . Collaborate with production, engineering, and quality teams to support continuous improvement initiatives. Participate in internal audits and contribute to maintaining QMS compliance. Skills & Experience Required: Experience in quality inspection within an electrical or electro-mechanical manufacturing environment. Strong understanding of electrical principles , wiring practices, and circuit verification. Ability to interpret and More ❯

all functions. You will support the administrative aspect of the Technical Department taking responsibility for the day-to-day management and maintenance of some or all of the following: QMS, HACCP, Technical Reports, Non Conformance Logs, complaints, microbiological & nutritional surveillance; this work includes data entry, trending, information requests, co-ordination of actions, change management procedure and communicating to relevant parties. More ❯

Microsoft Office Desirable Criteria: Experience of applying RED, Marine-D, FCC, ISEDC, MCS rules Experience of cybersecurity legislative requirements for the RED and upcoming CRA requirements Knowledge of quality management system processes and procedures for example ISO 9001:2015 auditing Knowledge of ISO 17065 Certification requirement Ability to evaluate, and when required, communicate to others new developing technologies Willingness to More ❯

and associated documentation are implemented effectively and maintained through the lifecycle of the project. Promotion of zero defects and stop the line culture. Ensure compliance and assist with the QMS (ISO9000:2015). Participate in cross-functional teams to aid the development and identification of risk on new projects/processes inclusive of using an FMEA approach. What you'll More ❯

plays a crucial role in ensuring that project quality requirements and compliance standards across the organisation are met and managed effectively. Key Responsibilities: Develop, implement, and maintain a quality management system demonstrating regulatory compliance. Lead continuous improvement activities to enhance business and project processes. Conduct and manage audits on projects and processes, implementing necessary improvements. Coordinate and monitor quality policies More ❯

Programmers in UK and Europe on FSP. Job Responsibilities (But not limited to) Carry out all activities according to Tech Observer SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines. Implement and follow the latest versions of CDISC, FDA Guidelines, GCP and other industry standards; Participate in More ❯

precise specification requirements. Provide hands-on manufacturing support, including basic mechanical assembly, component installation, and production assistance. Complete test reports and documentation in line with customer requirements and Quality Management System standards. Carry out product upgrades and modifications to assemblies and finished products. Interpret and implement engineering changes from documentation. Identify product quality or performance issues and raise non-conformances More ❯

PPE, equipment and stock levels within the vehicle. Report any damage or shortages to the office to enable replacements to be arranged as necessary. Be aware of the Quality Management System which includes policies in place to support the business and its aims including but not limited to Health & Safety, Environmental, Data Protection, Anti-bribery & equality. Further information can be More ❯

PPE, equipment and stock levels within the vehicle. Report any damage or shortages to the office to enable replacements to be arranged as necessary. Be aware of the Quality Management System which includes policies in place to support the business and its aims including but not limited to Health & Safety, Environmental, Data Protection, Anti-bribery & equality. Further information can be More ❯

levels of customer satisfaction is maintained Preparation of Service Reports and customer presentations Organise regular Customer Service Reviews and meetings Retain accurate documentation in adherence to the Sword Quality Management System Act as customer point of contact for designated accounts Support Event Management requirements when required Support the Incident Manager role for all major Incidents impacting the allocated customer base More ❯

Some of what you will do! IFS Consultancy Assist with key aspects of IFS implementations, upgrades, business as usual activities and business improvements. Document relevant activities within the companys QMS (ISO 9001 Quality procedures) to ensure a high level of quality and repeatability. Responsibility for ensuring that quality control activities (including testing) are carried out satisfactorily. What you need! Experience More ❯

both Biomedical Science and IT. They will contribute to the development, implementation, and maintenance of digital information management systems within Pathology. Additionally, they will work within the Pathology Quality Management System to ensure and demonstrate the laboratory's compliance with ISO 15189 standards. Main duties of the job Act as the digital systems specialist within the Pathology department, providing expert … supporting, and developing the Laboratory Information Management System (LIMS) and other digital tools used in pathology workflows. Take a lead role in further developing the Pathology Quality Management System (QMS) within Pathology IT to ensure compliance with ISO 15189 standards and support laboratory accreditation. Support digital change management within the laboratory, including upgrades, configuration changes, and new system implementations. Assist … Participate in digital project groups, acting as the technical and scientific voice for system users. Support the maintenance and continual improvement of the digital aspects of the departments Quality Management System, ensuring that systems, processes, and documentation meet the requirements of ISO 15189 and are audit-ready. Work collaboratively with the Quality Manager and IT team to ensure audit trails More ❯