21 of 21 Quality Management Jobs in Cambridgeshire

Location: Cambridge, UK Type: Permanent, Full-time Team: Quality, Engineering & Manufacturing Environment: Precision Manufacturing/High Technology About the Company Our client is an innovative technology business operating within a precision manufacturing environment, developing high-performance products for the communications industry. The business is currently going through an exciting … period of transformation and is looking to strengthen its quality capability. It has an entrepreneurial and collaborative culture, with employee development and continuous improvement at the heart of the organisation. The Opportunity This is an excellent opportunity for a Quality Engineer to have a genuine influence on product ...

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 ...

Quality Assurance Program Lead Title: Quality Assurance Program Lead Location: Boston (Hybrid) with travel to project or vendor sites as required Help build the quality program that lets utilities and regulators trust every component behind 10 gigawatts of new nuclear capacity We are seeking a Quality Assurance Program Lead to drive day-to-day execution of the quality program behind Alva's power uprate programs. As our first dedicated quality hire, you'll work alongside our quality consultant to stand up an integrated quality program that meets NQA-1 and achieves ...

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 ...

Description: The Associate Director, Central Monitoring leads Jazz's central monitoring capability within Global Clinical Development Operations, reporting into the Senior Director, Trial Risk Management & Monitoring. This role is accountable for defining, generating, and interpreting centralized data outputs – including Jazz portfolio level key risk indicators (KRIs) and statistical/… insights into concrete, risk-proportionate changes in monitoring strategy at the site, study, and CRA level. The Associate Director partners closely with Trial Risk Management, Site Monitoring, Data Management, and study teams to ensure that centralized monitoring is a driving force behind how, where, and how often monitoring ...

company solving some of the most challenging biological and medical problems that remain unmet. Our goal is to develop technologies that significantly increase the quality and length of life for those with debilitating and deadly cancers in the brain and body. We are backed by the best global venture … workflows, and how we select, roll out, use, and govern software across the company. As a medical device company operating under an ISO 13485 quality management system, how we structure, secure, and control access to our data matters enormously, and you will work closely with both ...

exciting opportunity for a highly capable and enthusiastic HCPC registered Biomedical Scientist to join our dedicated team in a modern department, providing a high-quality Haematology and Blood Transfusion service. Current experience in a UK NHS haematology and blood transfusion laboratory is essential for the Band 6 role … desirable for the Band 5 role. Our busy UKAS and MHRA accredited department is fully computerised (Winpath) and utilises the Q-Pulse quality management system. Equipment includes Sysmex XN track, Beckman Navios and Aquious Flow Cytometers, IL TOPs coagulation analysers, BioRad Variant II and twin Ortho Visions. Main ...

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 ...

culture, continuous learning mindset, and a shared mission to help biopharma run faster, smarter trials. At Qureight, we're building a company where data management is treated as a core capability, not an afterthought. Data management supports every imaging endpoint and biomarker we work with, in respiratory … love to meet you. About the role We are looking for a Clinical Data Manager to deliver compliant clinical data and image management activities for commercial (clinical study) projects. Bringing experience of clinical data management from clinical trials or imaging CROs, you will be responsible for image quality ...

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 ...

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 ...

other software languages and technologies. This may also extend to electronics and PCB design. About the role Software Development Full lifecycle development and release management for prototypes, products and support tools. Project Management Planning: Providing plans covering tasks, dependencies, effort, cost and resource allocation. Risk Management: Supporting … priorities and plans. Devise appropriate responses to problems and issues. Track and report own progress (deliverables, adherence to schedules, actual spend vs budget, etc.) Quality Management Progress according to agreed priorities and plans. Devise appropriate responses to problems and issues. Track and report own progress (deliverables, adherence ...

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 ...

within calibration schedules. Assemble major and minor mechanical assemblies. To carry out electrical sub-assemblies. To read engineering drawings and assemble products to quality requirements. To perform soldering to IPC standards. To promote and support continuous improvements and assist with A3, 8D and other process improvements. To promote best … practices to ensure ease of manufacture and testability. To ensure that processes are adhered to as prescribed within the Company Quality Management System. To help create and maintain a safe working environment and observe the published Health and Safety procedures. Responsible for ensuring a high standard of housekeeping ...

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 ...

excellence in patient care and innovative research. As a Specialist Biomedical Scientist, you will play a pivotal role in the delivery of high-quality diagnostic services within our Haematology team. You must have a relevant IBMS Specialist diploma or equivalent qualifications or equivalent experience. Applications may be accepted from … delivery of a 24/7 laboratory service. To perform the initial screening and further investigation of specialist diagnostic tests producing complex quality diagnostic results in order to aid patient treatment and care and authorise the results as directed by departmental procedures and guidelines. To use knowledge, interpretive skills ...

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 ...

points of failure. In addition, the role involves performing stock check and ensuring efficient use where appropriate. The post holder is responsible for processing quality control material, recording and interpreting results and clear communication of findings to the clinical scientists. If corrective actions are needed, these should be carried … 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 ...

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 ...