1 to 25 of 35 QA Jobs in Oxfordshire

factory and a dedicated Gluten Free factory. We operate over a range of shifts in our production facilities, have on site services including a QA team, Engineers, Supply Chain, Logistics, Payroll and HR and we also have a dedicated on-site R&D team. The Position This role is to more »

Part 145 audits as required by the MAA audit programme. Deliver the effective implementation and maintenance of the ATrS Part 145 and Part CAMO Quality Assurance processes to fulfil the obligations of UK National Requirements. Plan and conduct Licenced Aircraft Engineers B1/B2/A Authorisation boards to assess … Facilitate the resolution of intra-departmental processes that support the timely issue/reissue of Licenced Aircraft Engineers Licences and Authorisations. Conduct Safety and Quality Assurance Audits in line with the audit plan throughout the Fleet Engineering Department and when required in other departments. Audits include preparation, in-brief of … list of responsibilities, please refer to the role profile attached. Skills, Knowledge & Expertise Extensive demonstrable experience in commercial aviation. Appropriate previous experience in a Quality Assurance and/or Safety Management role. Formal aeronautical maintenance training. Appropriate demonstrable ability to conduct audits and produce accurate reports. Extensive understanding of CAA more »

Food Manufacturing Quality Assurance Manager Oxfordshire/Hybrid Circa £45k per annum Benefits Performance related bonus scheme 25 days holiday + bank holidays Company pension Personal Development and Training opportunities Quality Assurance Manager for Oxfordshire based Free From Food Manufacturer, leading the overall Quality standards of the company and its more »

of opportunities for our engineers to develop professionally. We are recruiting a Quality Engineer who will be responsible for the planning and execution of quality assurance activities within operations and the supply chain to contribute to delivery of new product and programs, whilst sustaining and continually improving current programs and more »

in-class systems solutions within an Agile SCRUM/DevOps working framework to support key areas of the business such as R&D, Operations, Quality Assurance, and Third-Party Manufacturing groups. The team delivers end-to-end solutions from bespoke embedded firmware to database design and data analytics/reporting more »

company is at the forefront of driving transformational change across their services. Responsibilities: Implementation: Design, code, and test enhancements and bug fixes as needed. Quality Assurance: Collaborate with Product Quality Control to ensure solutions are robust, dependable, and highly usable. Documentation: Produce comprehensive product documentation to meet both internal and more »

troubleshooting and data analysis. Supervise the work of Assay Development Scientists or Technicians. Represent Analytical Development in cross-functional meetings/projects with manufacturing, Quality Assurance, Regulatory Affairs and external partners. Review and approve SOPs, risk assessments, protocols and reports. Provide regular updates of group activities to senior management. Skills more »

customize Salesforce features and functionalities to meet business needs. - Collaborate with developers and administrators to implement and deploy Salesforce solutions. - Conduct thorough testing and quality assurance to ensure successful solution delivery. - Provide ongoing support and training to end users to maximize adoption and effectiveness of Salesforce solutions. - Stay current with more »

definition of commissioning plan for GNC hardware) Contribute to current development-focused GNC activities as well as future production-focused GNC activities e.g. QA (Quality Assurance) processes. Contribute to system level activities, such as defining FMECA (Failure Mode, Effects, and Criticality Analysis) and FDIR (Fault/Failure Detection, Isolation, and more »

A Biotech is seeking a software development engineer (SDET)/QA engineer to join them in a permanent role. Their company has been built by a long-established world-leading pathogen genomics team from the University of Oxford, supported by the cloud computing scale and security of Oracle Inc, and … testing processes. Primary Responsibilities: Designing, developing, and executing automated test scripts for both front-end and back-end applications. Collaborating with software developers and quality assurance engineers to identify and resolve any issues or bugs in the software. Writing and maintaining test documentation, including test plans, test cases, and test more »

Junior QA Tester, Oxford, Hybrid 2/3 days a week in office, Up to £25,000 Note: this role do not offer sponsorship Are you passionate about ensuring quality in software development? We are currently seeking a Junior QA Tester to join a dynamic and growing team in Oxford … working closely within the team of product and developer specialists. As a Junior QA Tester, you will be responsible for testing software applications, identifying bugs and issues, and helping to ensure that our products meet high-quality standards. You will work closely with developers and other team members to ensure … aspects of our software are thoroughly tested and ready for release. Responsibilites Continuous Improvement: Identify opportunities for process improvement and efficiency gains within the QA, application support, and product operations functions Training and Development Provide training and support to team members to enhance their skills and knowledge in QA practices more »

with a very exciting and growing Biotechnology company based in Oxford and am assisting them in a search for an Associate DIrector of Clinical Quality Assurance (GCP). The successful candidate will be reporting directly to the Head of QA and spearhead all activities related to GCP. Main Duties and … preparation of material and delivery of training. To include onboarding/induction training and refresher training To take a lead role on behalf of QA on all GCP investigations including serious breaches and Urgent Safety Measures and to communicate these effectively within the organisation and escalation to the senior leadership … team To represent Quality on the clinical projects undertaken and be the main QA contact for CROs and GCP Laboratories Perform internal audits. These to include document audits such as Protocols, Investigator Brochure, Clinical Study Reports and regular audits on Trial Master File and Sponsor Oversight Files. Support the maintenance more »

at all levels, internally and externally in relation to critical quality concerns. Provide support to Production by elimination of rejects from stock identified by QA or Shop Floor personnel. Inspection and testing of material at Goods Inwards, manage inspection team on critical parts. Ensure that all in-house systems and more »

Forums and general briefings Quality Be responsible for managing and producing ITPs and ensure they are signed off by relevant parties Ensure that the QA File is produced and maintained Close out any technical queries Ensure as-builts and O&M manuals are submitted to the client on completion Key more »

into technical specifications and project plans. Partner with IT teams to prioritise and execute projects that align with business objectives. Conduct thorough testing and quality assurance for IT projects and system changes. Ensure that IT solutions are efficiently aligned with business needs and priorities. Monitor and report on project progress more »

way to design, build and run elite competition cars on the track and off-road across the globe. We are looking for a Supplier Quality Assurance Engineer to join our Motorsport team who will ensure that all supplied components meet expectations with regards to Quality Assurance and delivery schedules. Key more »

Your new company Our client, a leading Life Sciences Research company, is looking for a strategic Quality Assurance Manager to join their team to develop the company's Quality Management System and ensure consistent compliance. By joining this company, you will be at the forefront of innovative technological development that … Quality Associate. What you'll need to succeed To be considered for the role of Quality Manager, you will need to have demonstrated strategic QA leadership experience within a biotechnology, scientific or laboratory setting.Other key deliverables include: A proven track record of successfully designing and implementing a QMS within a more »

understand project requirements and integrate software components seamlessly. Testing and Code Review: Conduct unit testing and participate in code reviews to maintain code quality. Quality Assurance: Ensure software meets quality standards. Documentation: Create and maintain technical documentation for software components and systems, keeping it up to date with any changes more »

brighter future in tech. Key Responsibilities: Are you a meticulous and experienced Test Engineer looking to make a significant impact in the world of quality assurance? We are committed to delivering exceptional products to our customers. We pride ourselves on innovation, teamwork, and a relentless pursuit of excellence. As a more »

translate design mock-ups into functional web interfaces. Cross-Functional Collaboration: Collaborate with cross-functional teams to understand project requirements and deliver effective solutions. Quality Assurance: Conduct thorough testing of web applications to ensure functionality and performance meet specifications. Code Reviews: Participate in code reviews to maintain code quality and more »

can come in and build relationships with key stakeholders in order to keep the quality team moving forward. The ideal person will have strong QA experience within pharma and GCP, someone who is willing to be hands-on and into the detail expected when operating within a startup environment. This … business Assessing and updating RAG statuses and documentation best practices Liaising with key stakeholders across the business Report up to senior leadership and represent QA in reporting What you will bring: Previous project management experience within pharma/biotech or similar Outstanding knowledge of GCP, TFA and FDA regulations Strong more »

and test plans. Maintain accurate records of design iterations, changes, and approvals. Collaboration and Project Management: Work closely with cross-functional teams, including manufacturing, quality assurance, and project management, to ensure seamless integration of composite designs. Participate in project planning, timeline management, and milestone tracking. Provide technical support and guidance more »

/Inspector (PC-DMIS) We are seeking a skilled and experienced Metallic CMM Programmer proficient in PC-DMIS software to join a leading Motorsport Quality Assurance team. The ideal candidate will be responsible for programming, operating, and maintaining CMM equipment to ensure precise and accurate measurement of metallic components in … of metallic parts and assemblies. Interpret and understand technical drawings, GD&T (Geometric Dimensioning and Tolerancing), and CAD models to create accurate CMM programs. Quality Assurance and Inspection: Conduct first article, in-process, and final inspections to ensure components meet specified tolerances and quality standards. Analyse measurement data and provide more »

and creating systems to process huge amounts of data Designing APIs and plugins for integration with software and hardware systems. Building tools to aid QA and data visualisation. Researching, designing, and presenting new technologies and approaches. What you'll need to succeed Required: Expert knowledge of C++ (11-20) Strong more »

equivalent assessor qualifications. IT proficient in Microsoft office suite of software packages including Outlook and TEAMs Desirable: A Recognised Training/Teaching Qualification. Internal Quality Assurance qualifications. IOSH Health and Safety qualification. The use of Smart Assessor E-portfolio and Pro Monitor software packages Please view the job description attached more »