17 of 17 Quality Management Jobs in Cambridgeshire

Contract Quality Management Systems Engineers Aerospace & Defence Cambridge Hybrid Contract We are supporting a fast-growing defence technology organisation in Cambridge with the appointment of a number of experienced Quality Management Systems Engineers on a contract basis. These are exciting opportunities for experienced Quality professionals … come into a rapidly developing engineering and manufacturing environment, quickly understand the existing Quality Management System and help drive the improvements required to support ISO 9001/EN 9100 compliance. With several positions available, we are particularly interested in speaking with contractors who have strong backgrounds in Quality ...

Quality Manager Location: Cambridge, UK Team: Operations Job Type: Full-Time, Permanent About Us Forefront RF is a fabless semiconductor company developing breakthrough RF technology that radically simplifies RF front-end architectures for mobile and connected devices. Our long-term vision is to empower anyone to treat global connectivity … lifecycles and reduce waste. Role Overview As we continue to scale towards commercial deployment, this new role is key in establishing robust and scalable quality processes as we transition from development into production. You will lead the development, implementation, and continuous improvement of Forefront RF’s Quality Management ...

operating within the digital health and medical technology sector, developing advanced healthcare solutions that improve patient outcomes worldwide. They are seeking a highly organised Quality & Regulatory Coordinator to support the day-to-day operation of Quality Management Systems (QMS), Regulatory Affairs activities, compliance programmes, and information security … initiatives within a highly regulated environment. Responsibilities: Coordinate day-to-day Quality Management System (QMS) activities. Manage document control, version management, and review schedules. Maintain quality records, document registers, and compliance trackers. Coordinate training records and mandatory training requirements. Support the implementation and maintenance of electronic ...

firmware organization in executing compliant medical firmware development. It is not a general embedded firmware role. Working closely with the Head of Medical Devices, Quality, Systems, and Hardware teams, you will play a central role in the development of firmware for our insulin pump platform. You will … firmware architecture, requirements definition, and design from early concept through product release. Ensure firmware development is executed in accordance with a certified ISO 13485 Quality Management System, with practical application of IEC 62304 and ISO 14971. Act as the firmware compliance leader, guiding the team on requirements management ...

Responsibilities: Drive continuous improvement across the organisation to achieve high standards. Be the focal point for process standardisation and compliance with the organisations quality management system. Be the focal point to Saab UK functions for critical compliance areas including export control, health & safety and security. Develop and track … Excellence throughout the organisation. Co-ordinate all internal and external audit activity. Act as Risk and Opportunity Co-ordinator and lead all business continuity management activities. Co-ordinate compliance activity such as export control ensuring sufficient resources and processes are in place. Co-ordinate the implementation of new compliance ...

Quality Engineer £40,000–£55,000 | Cambridge | Onsite My client is looking for a Quality Engineer to join their growing manufacturing team in Cambridge. This is an excellent opportunity to play a key role in maintaining and improving quality systems for high-precision products used across … communications, defence, space and transportation sectors. The Role Manage and improve quality management systems and processes Lead non-conformance investigations, change control and corrective actions Conduct internal ISO9001 and ISO27001 audits Analyse manufacturing data to drive continuous improvement Support new product introduction (NPI) and Lean manufacturing initiatives Work ...

summary Join theCambridge Genomics Laboratory, lead provider for the East NHS Genomic Medicine Service, and play a pivotal role in delivering high-quality rare disease diagnostics and improve patient care. As a Principal Clinical Scientist, you will lead and manage a team of scientists, oversee the interpretation of complex … genomic data, authorise clinical reports, and provide specialist scientific expertise across a diverse test repertoire. You will contribute to service leadership, quality management, accreditation activities, staff development, and the implementation of innovative genomic technologies. Working closely with clinicians and multidisciplinary teams, you will help ensure an efficient, accurate ...

technology processes, and ensures suitable evidence is maintained to demonstrate compliance and control effectiveness. Role and Responsibilities Lead the end-to-end IT risk management practice, ensuring legal obligations are met and enterprise risks are detailed, owned, mitigated, and clearly communicated to leadership. AI Governance & Risk Management - Establish … enterprise governance goals. Manage and administer IT governance, security, and policy training programs across IT and the wider business via the Global Learning Management System (LMS). Support the development of engaging training content and deliver regular compliance reporting against key performance indicators. Maintain macro- and micro-level risk ...

technology processes, and ensures suitable evidence is maintained to demonstrate compliance and control effectiveness.****Role and Responsibilities***** Lead the end-to-end IT risk management practice, ensuring legal obligations are met and enterprise risks are detailed, owned, mitigated, and clearly communicated to leadership.* AI Governance & Risk Management - Establish … enterprise governance goals.* Manage and administer IT governance, security, and policy training programs across IT and the wider business via the Global Learning Management System (LMS).* Support the development of engaging training content and deliver regular compliance reporting against key performance indicators.* Maintain macro- and micro-level risk ...

complex bioinformatics issues by specialist examination of input & output data, and associated bioinformatics processes; includes communication with technical, scientific and clinical staff Planning and management of bioinformatics development projects; includes interfacing with technical, scientific and clinical functions of the genomic laboratory Contribution to and facilitation of appropriate local … Hospital and the Rosie Hospital in Cambridge. With over 13,000 staff and over 1100 beds the priorities of the Trust focus on a quality service which is all about people - patients, staff and partners. Recognised as providing 'outstanding' care to our patients and rated 'Good' overall ...

immediate start opportunity is available at our client's busy fruit and vegetable production site. Staffline is recruiting Quality Assurance to work in Chatteris. The rate of pay is £13.27 per hour up to 48 hours, with overtime paid at £16.59 per hour for all hours worked over 48. … candidates must have access to their own vehicle or reliable transport to travel to and from the workplace. Your Time at Work As a Quality Assurance, your duties include inspecting and reporting on all aspects of product quality from goods-in arrivals through to final release. You will ...

advantage in the role but is not essential. Responsibilities: All software and firmware development is carried out in accordance with the Flusso quality management system (QMS) and specifically the Software Development and Release Management Process. General software and firmware development Collaboration with colleagues in Test and Applications … Data Science to define cost-effective sensing Solution Architectures for target applications. Requirements capture/analysis, specification, design, implementation (with rigorous source code management), design reviews, code reviews, unit-testing and debug. Creation of internal releases for the Test Engineering team and investigation and resolution of issues uncovered during ...

outputs meet commercial agreements and project timelines Track timelines, dependencies, and risks Work with technical teams to define good data, ensure usable formats, resolve quality and completeness issues, and support standardisation and annotation workflows Bridge external data providers and internal data/ML teams Support senior leaders in identifying … transfer offices Develop repeatable processes for contracting, partner onboarding, data ingestion, and project delivery Help scale Qureight’s data partnerships function Requirements Proven project management experience overseeing complex, data-rich projects Proven experience supporting commercial data projects with external partners, including pharma/biotech, hospitals/healthcare providers ...

support sales objectives* Ensuring Health and Safety requirements for all activities are met* Ensuring all activities are carried out in accordance with the CRFS Quality Management System* Ensuring FAE Task Plans/Technical Reports are completed accurately and in accordance with agreed sales objectives* Ensuring Customer Training materials ...

treatment of all staff and customers within the scope of the post To support and participate in the formulation of standards and procedures for quality management and customer care expectations CORPORATE ACCOUNTABILITIES (applicable to all employees) 1. Equality, Diversity and Inclusion & Safeguarding Support and promote the Service ...

following activities: Digital Collection Analysis (e.g., lead a review of the digitisation workflow to inform its future state, focusing on day-to-day data management, preservation, and storage). Business change (e.g., determine and plan new processes and procedures for digital preservation, metadata improvement, and quality management ...

seeking a Regulatory Affairs Specialist. The role involves providing regulatory support across various teams, ensuring compliance with international regulations, and leading initiatives to optimize quality management systems. Ideal candidates will have a track record in regulatory strategy development, strong leadership skills, and knowledge of medical device compliance. This ...