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Senior Quality Engineer Oxford Days Up to £60,000 A leading engineering and manufacturing company is looking for a Senior Quality Engineer to ensure high standards of product quality across all operations. This role includes quality assurance, process improvement, and compliance management, reporting directly to the Quality Manager. Skills / Duties • Lead quality assurance processes and audits, • Support continuous improvement initiatives, • Analyse production data to identify trends and issues, • Proven experience as a Quality Engineer in a manufacturing environment, • Strong understanding of QA/QC standards and procedures

BioTalent have partnered with a global pharmaceutical organization specializing in the development, manufacturing, and distribution of innovative diagnostic and therapeutic products used in highly regulated healthcare environments. With operations across multiple international markets, they are committed to delivering safe, high-quality medicines that support critical patient care pathways. The organization operates complex manufacturing facilities and maintains rigorous quality standards to ensure compliance with international regulatory requirements and industry best practices. They are looking to welcome a Senior QA specialist on a permanent basis-this will also include shift work. Position Summary The Senior QA Specialist is responsible for maintaining and improving the Quality Management System (QMS) to ensure full compliance with GMP regulations and internal quality standards. This role supports manufacturing, laboratory, and distribution activities, ensuring the highest standards of product quality and patient safety. Key Responsibilities • Maintain and oversee Quality Systems (CAPA, deviations, change control, complaints, document control) in compliance with GMP and regulatory requirements., • Review and approve batch records, validation documentation, protocols, and quality-related reports to ensure product release meets regulatory standards., • Lead internal audits and support regulatory inspections, ensuring inspection readiness at all times., • Investigate deviations and quality events, perform root cause analysis, and implement effective corrective and preventive actions., • Collaborate cross-functionally with Manufacturing, QC, Regulatory Affairs, and Supply Chain to drive continuous improvement and ensure product quality and compliance. Qualifications & Requirements • Degree in Pharmacy, Chemistry, Pharmaceutical Chemistry, or Biology (required)., • Minimum of 2 years of experience in Quality Systems within the pharmaceutical industry., • Strong knowledge of GMP regulations and quality management systems., • Experience in sterile manufacturing or highly regulated production environments is an asset., • Excellent analytical skills, strong attention to detail, and effective communication abilities. Reach out for more information to:

Our client is partnering with an organisation that's creating a transformative digital experience for students entering the world of work. They're building a scalable platform to support career readiness and connect young talent with meaningful opportunities. As an Automation QA Engineer, you’ll play a vital role in ensuring the quality and reliability of this platform as part of a dynamic, cross-functional tech team working at the forefront of modern software development. Why You’ll Want This Role • Be part of a team developing tools that impact hundreds of thousands of students across the UK, • Work within a modern engineering environment using cloud technologies and the latest testing frameworks, • Collaborate with product, design, and development to build a high-quality platform that truly makes a difference, • Influence the quality standards of a business committed to agile delivery, continuous improvement, and technical excellence Key Responsibilities • Collaborate within an Agile squad to support development and delivery of new product features, • Conduct thorough exploratory testing alongside automated test execution, • Build, maintain, and enhance automated testing pipelines using industry-leading tools, • Define and validate acceptance criteria for user stories, • Help identify technical debt and contribute to backlog refinement and prioritisation, • Support non-functional testing efforts, including performance and accessibility testing, • Contribute to documentation and peer review processes, • Share QA expertise with the wider engineering community to promote best practices Tech Stack You'll Work With • Test Automation: Cypress, Selenium, Cucumber/Gherkin, Postman, • DevOps & CI/CD: GitLab, Jenkins (or similar), Git, BrowserStack, • Performance & Accessibility Testing: K6, JMeter, • Collaboration Tools: Jira, Confluence, Snagit, • AI Tools: Exposure to GitHub Copilot or similar GenAI testing support tools About You • Strong background in full-stack web application testing (manual and automated), • Practical experience in Agile software development environments, • Proficient with modern automation frameworks and tools, • Knowledge of QA methodologies, accessibility, and performance testing, • Comfortable with REST API testing, • Strong communication skills and attention to detail, • Eager to mentor others and promote a culture of quality across the team, • A quick learner who stays up-to-date with emerging tools and trends Desirable: • Bachelor’s degree in Computer Science or similar, • Interest in applying AI tools to support automation, • Passionate about improving developer workflows and delivery pipelines Working Environment • Full-time, permanent role (37.5 hours/week), • Hybrid working options based in the UK, • Background screening required as part of the recruitment process

About the Role: I'm partnered with an innovative, fast-paced, global medical device company with a mission to save lives by making every donated organ count. A commercial-stage business committed to improving transplantation outcomes throughout the world, their first product has been used to support more than 5,000 transplant operations globally, and they are growing fast. They are now looking for a highly motivated and detail-oriented Quality Auditor to join their dynamic Quality team. In this pivotal role, you will lead and execute internal audits across their sites and conduct supplier audits to ensure products are safe and effective, verify full alignment with their Quality Management System, regulatory requirements, and industry best practices. This is a business that takes quality seriously because what they make genuinely matters — and they're looking for someone who understands that distinction. If you think beyond checklists, see audits as an opportunity to strengthen a business rather than just verify it, and want to work somewhere where the work has real meaning, this is worth a conversation. Key Responsibilities • Plan and conduct internal and supplier product and manufacturing audits in accordance with quality agreements and regulatory requirements including ISO 13485:2016, FDA 21 CFR Part 820, and EU MDR, • Identify areas for improvement within the QMS and supplier systems, and support the implementation and verification of corrective actions, • Develop and deliver audit reports, communicate findings to management, and monitor the effectiveness of corrective measures, • Support the development and implementation of action plans based on audit outcomes, • Support supplier qualification activities through audits for approval and periodic re-evaluation, ensuring adherence to quality agreement requirements and managing updates or revisions as necessary, • Partner with Procurement and Product Quality teams, providing audit data to support supplier qualification and re-evaluation processes, and collaborating to monitor supplier performance, • Foster strong working relationships with suppliers to drive continuous improvement and compliance, • Participate in and support external inspections and audits including BSI Notified Body and FDA, • Stay current with changes in applicable quality regulations and standards, providing training and guidance to internal teams as needed Skills & Experience • Audit Experience: Minimum 3 years in ISO 13485 QA-focused roles, including at least 1 year of hands-on practical auditing. Lead Auditor certification in ISO 13485, MDR or MDSAP desirable, • Interpersonal Skills: The ideal candidate is able to build rapport with auditees, anticipate reactions, and deal professionally with all situations. This role requires emotional intelligence and the ability to communicate the value of audits, making stakeholders feel at ease while encouraging open dialogue and genuine collaboration., • Critical Thinking & Continuous Improvement Mindset: We're looking for someone who thinks beyond checklists, someone who can look at processes end-to-end, ask the right questions, and spot practical ways to improve efficiency, compliance and overall performance, benefiting both quality and business outcomes., • Analytical Abilities: Strong attention to detail and demonstrable experience with process improvement, • Technical Proficiency: Proficient in Microsoft Office applications including Excel, PowerPoint, Visio and Word. Knowledge of MasterControl and Power BI is advantageous., • Organisational Skills: Organised, detail-oriented, and able to multitask and prioritise responsibilities in a fast-paced environment Qualifications • University or college degree, preferably in life sciences, quality, or regulatory affairs, or an equivalent combination of education and experience, • Minimum 3 years of experience in medical device quality system auditing or equivalent Location: Oxford-based, 3 days on-site with 2 days work from home per week. Ideally within a 50-mile / 1-hour commute of Oxford. Travel: 10–15% across Europe and the US for supplier audits

Quality Manager Advanced Technology / Engineering Environment PLEASE NOTE - THIS IS NOT A SOFTWARE QA ROLE Are you a Quality Manager who enjoys building robust quality systems within innovative engineering environments? Do you thrive on strengthening processes, driving continuous improvement, and ensuring complex products meet the highest standards? Looking for a role where your expertise in quality management can directly influence how advanced technology reaches global markets? If this sounds like you, this could be an exciting next career move. Our client is a growing technology organisation developing advanced hardware platforms used by international customers. With continued investment and increasing demand for their products, the business is entering an important stage of operational growth. To support this expansion, they are looking for an experienced Quality Manager to lead quality systems, drive operational improvements, and ensure products are delivered to exceptional standards. This is a highly visible role where quality leadership will play a critical part in enabling the organisation’s continued growth. Why This Role is Great This position offers the opportunity to own and evolve the quality framework of a growing engineering-led business. Working closely with operations, engineering, and supply chain teams, you will ensure quality processes support both innovation and reliable product delivery. In this role you will get to: • Lead and develop the organisation’s quality management systems, ensuring strong governance, traceability, and audit readiness, • Champion continuous improvement initiatives, driving structured problem-solving and root cause analysis across operations, • Strengthen product quality processes, including incoming inspection, in-process controls, and final testing frameworks, • Investigate and resolve quality challenges, using recognised problem-solving approaches and corrective action processes, • Collaborate with suppliers and internal teams to improve quality standards across the supply chain, • Support new product introduction activities, ensuring quality systems are embedded from development through to production, • Develop quality documentation, procedures, and operational standards, • Introduce and monitor key quality metrics, helping drive visibility and improvement across the business, • Promote safe and compliant operational practices within a complex engineering environment You will play a central role in ensuring the company’s products consistently meet the highest standards as the organisation scales. About You You are an experienced Quality Manager or Senior Quality Engineer who enjoys building strong systems, improving processes, and working closely with technical teams. You may currently work in advanced manufacturing, engineering-led organisations, precision hardware environments, or complex supply chain industries. You may bring experience in areas such as: • Quality management systems aligned with international quality standards (such as ISO frameworks), • Leading internal and external audits, • Root cause analysis and structured problem-solving approaches, • Quality processes across incoming inspection, production, and final product testing, • Continuous improvement methodologies such as Lean, Six Sigma, or operational excellence frameworks, • Supplier quality management within technical supply chains, • Working closely with engineering and operations teams to improve product and process quality Experience supporting new product introduction or manufacturing scale-up environments would be beneficial, though not essential. Candidates with strong transferable quality leadership experience are encouraged to apply. What You’ll Gain This role offers the opportunity to join a company where quality and operational excellence are fundamental to long-term success. Benefits include: • Competitive salary around £62,500 – £65,000, • Flexible and hybrid working arrangements where appropriate, • Performance-based bonus opportunity, • Equity or share participation scheme, • Private medical insurance, • Life assurance and income protection, • Enhanced family leave policies, • Employer pension contributions, • 25 days annual leave plus bank holidays, • Cycle to Work scheme, • Wellbeing initiatives and support programmes, • Professional development and training support, • Opportunities to participate in volunteering initiatives Diversity & Inclusion Our client and our agency are committed to creating inclusive workplaces where diverse perspectives are valued and respected. Applications are welcomed from candidates of all backgrounds and experiences. Adjustments can be made throughout the recruitment process to support accessibility. Interested? If you’re excited by the opportunity to lead quality excellence within an innovative technology organisation, we would love to hear from you. Apply today to explore how your expertise could contribute to the next stage of this organisation’s growth.

Info about the company An innovative and industry-leading organisation specialising in the development of high-end navigation and positioning systems for the Autonomous vehicles, Aerospace Drones, Geo Mapping and Robotics sectors. Info about what the x2 Support Engineer role entails X 2 brand new Support Engineer/ Test & Diagnosis Engineer roles as our client splits their Customer Support and a Test/QA team into 2 functions and creates a new support team, focused on the UK, Europe and Latin America markets. You will be happy to travel globally (all expenses paid), with a can-do approach and a desire to provide an excellent customer experience. Essential Requirements for the x2 Senior Support Engineer / Test & Diagnosis Engineer roles * Technical degree in engineering or equivalent experience (Electronics, Electrical, Telecommunications or Mathematics would also be good). * Experience with technical troubleshooting & fault diagnostics for complex hardware/software/electronics. * A methodical fault-finding approach * Technical support / fault finding experience within products in industry sectors such as Autonomous vehicles, Aerospace (Drones), Telecoms (antenna, aerials etc), Surveying or Robotics * Able to work in a customer facing environment - working under pressure, liaising with internal and external stakeholders. * Happy to travel within the UK, Europe and Latin America sometimes at fairly short notice ...

Senior Structural Engineer Oxford Up to £55,000 + bonus With a diverse work-stream that covers a wide range of disciplines in property and construction, you’ll get the chance to practice in various fields of structural engineering across many different construction sectors, playing a vital role in shaping the built environment across the UK. You’ll be responsible for providing a broad range of structural engineering services. You’ll be expected to work independently, with the guidance and support of the senior management team, and you’ll have plenty of opportunities to develop your managerial skills and advance your career. What you'll be doing; * Act as lead or sole designer as appropriate to the size and complexity of the project, responsible for everything from outline schemes to detailed design and the production of technical deliverables. * Carry out structural analysis and design in line with the Eurocode suite of design codes, ensuring designs are economical, sustainable, efficient, and buildable. * Oversee the production of detailed design drawings. * Check calculation packages, drawings, specifications, reports, and other project deliverables, ensuring compliance with our QA procedures. * Supervise and mentor junior engineers, technicians, and apprentices within the team, actively contributing to their future development. * Conduct surveys/inspections and produce hig...

Embedded Software & Hardware Q&A TEST ENGINEER Location: Oxfordshire, UK site (3 days in office - Hybrid) Compensation: DOE (£50-60k) Employment Type: Permanent – Full Time Department: Engineering (Reporting to CTO) PLEASE NOTE: this role requires a combination of Software and Hardware experience, with a background in embedded systems for physical electronic products in sectors like aerospace, defence, automotive. (If you are a Q&A tester for tech apps used in sectors like banking or finance, this would likely not be a fit for you.) Our client working in the Autonomous space, building the Trust Layer for Physical AI and Autonomous Systems. The next generation of safety-tech that will unlock the true benefits of AI. The current project is working on these systems for Drone and UAV tech. Working Culture Our client is a fast-growing start-up with ambitious goals and the culture reflects that. building something meaningful, they’re looking for people who are genuinely energised by that journey. You’ll thrive if you enjoy taking ownership, wearing multiple hats, learning quickly and are comfortable working beyond core hours when the work demands it - not because it’s expected day-to-day, but because seeing progress matters. The team is driven by the satisfaction of building, solving hard problems and moving fast together, embracing collaboration and change as part of start-up life. They are looking for people who want to be part of something being built from the ground up, who enjoy the momentum and responsibility that comes with it and who bring commitment, curiosity and teamwork to everything they do. The Role Looking for an exceptional QA Test Engineer to join our team building cutting-edge Runtime Assurance systems for AI and robotics applications. You will play a vital role in developing the safety-critical embedded software components that ensure the safe and reliable operation of solutions. Our client offers a competitive compensation package, benefits, and the chance to work on cutting-edge technologies like UAV and Drone tech that will help shape the future of AI and robotics safety in these fields. Responsibilities • Lead the design, development, and implementation of embedded software for the business, Runtime Assurance platform across various hardware architectures and real-time operating systems., • Ensure compliance with industry standards, regulations, and best practices for safety-critical software development, such as DO-178C, ISO 26262, and IEC 61508., • Build configuration and pipeline management, • Software-in-the-Loop and Hardware-in-the-Loop including automated deployment across multiple platforms., • Integration of different performance testing techniques across multiple types of simulation (gazebo sim, rosbag)., • Collaborate with cross-functional teams, including hardware engineers, systems architects, and AI/ML experts, to integrate embedded software components seamlessly into the overall system., • Participate in code reviews, performance optimisations, and thorough testing (unit, integration, and system-level) to maintain the highest quality standards., • Contribute to the continuous improvement of the team's software development processes, tooling, and methodologies. Key Skills and Experience • Bachelor's or Master's degree in Computer Science, Electrical Engineering, or a related field, or equivalent experience, with a strong focus on embedded systems QA, and software development and/or testing., • Experience with one or more CICD pipeline services (Jenkins, CloudBuild, AWS CodePipeline, etc), • Experience with infrastructure/Automation techniques (bash, python), • Knowledge of source control (git), • Experience with at least one test framework (pytest, gtest), • Hands-on experience in embedded software testing and QA, with a proven track record in delivering safety-critical systems., • Solid understanding of software development methodologies, such as Agile, Continuous Integration, and Test-Driven Development., • Develop, implement, and execute test strategies and verification activities for safety-critical software., • Perform static and dynamic code analysis using industry tools (e.g., Rapita RVS, LDRA, VectorCAST, Polyspace)., • Support compliance with safety standards (e.g., DO-178C, ISO 26262, IEC 61508, DEF STAN 00-55) through rigorous testing and documentation., • Define and maintain test cases, procedures, and automation frameworks to ensure consistency and repeatability., • Collaborate closely with software engineers, systems engineers, and safety teams to ensure test coverage against requirements., • Lead defect reporting, tracking, and resolution through structured QA processes., • Contribute to continuous improvement of verification and validation processes, tools, and best practices., • Prepare and present test results, coverage metrics, and assurance evidence for internal and external reviews., • Strong problem-solving, analytical, and debugging skills., • Excellent communication and collaboration abilities, with the ability to work effectively in cross-functional teams. Benefits • Salary sacrifice pension with a 5% matched company contribution., • Generous Holiday allowance, • EV Car Scheme., • Cycle to Work Scheme., • More exciting benefits to come as they grow. About the client Their software enables assured, trustworthy deployment of both traditional deterministic autonomy and AI or novel control methods, in any application, for the first time. They do this with no need for data or communications links, and begin the journey by applying their tech to autonomous systems in the aerospace and land domains. Their products are future-focused, compliance-ready & built for safety-critical environments.

PSR Solutions are recruiting for multiple Site Engineers on a freelance basis on a project in Oxfordshire. My client are a leading civil engineering sub-contractor, currently recruiting 3x Site Engineers to work on a large Groundworks project in Oxfordshire. Project is at cut + fill stage. Responsibilities include: * Setting out all aspects using Leica kit. * QA * Reporting and working with the Project Manager and General foreman. * Site set up and compliance with health and safety. Successful candidate will require their own Laptop + AutoCAD software. This is a long term role, and there is an opportunity to move on to their next project following this. If you are interested in the role, please apply or get in touch with Maayon at PSR for more information...

Info about the company An innovative and industry-leading organisation specialising in the development of high-end navigation and positioning systems for the Autonomous vehicles, Aerospace Drones, Geo Mapping and Robotics sectors. Info about what the x2 Support Engineer role entails X 2 brand new Support Engineer/ Test & Diagnosis Engineer roles as our client splits their Customer Support and a Test/QA team into 2 functions and creates a new support team, focused on the UK, Europe and Latin America markets. You will be happy to travel globally (all expenses paid), with a can-do approach and a desire to provide an excellent customer experience. Essential Requirements for the x2 Senior Support Engineer / Test & Diagnosis Engineer roles Technical degree in engineering or equivalent experience (Electronics, Electrical, Telecommunications or Mathematics would also be good). Experience with technical troubleshooting & fault diagnostics for complex hardware/software/electronics. A methodical fault-finding approach Technical support / fault finding experience within products in industry sectors such as Autonomous vehicles, Aerospace (Drones), Telecoms...

An innovative and growing medical technology company are recruiting a pro-active and experienced Quality Manager to implement a QMS and ensure compliance with ISO standards, GLP/GMP principles and regulatory requirements while overseeing audit readiness and operational quality across a growing start up business. Quality Manager Key Responsibilities: • Implement, maintain and optimize the company QMS (BPA or other)., • Ensure compliance with ISO 13485, ISO 900, GMP/GLP/GCP principles and ICH guidelines, • Draft, review, and approve SOPs, work instructions, and validation protocols., • Manage document control and ensure Good Documentation Practices (GDP)., • Deliver SOP and quality training for all employees and across all departments; maintain training records., • Coordinate internal, supplier, and external audits., • Support regulatory inspections and certification processes., • Track and ensure timely closure of audit findings and CAPAs., • Oversee laboratory and cleanroom quality compliance., • Participate in deviations, change controls, CAPA, complaints, and recalls., • Conduct risk assessments and root cause analyses.

A medical technology company in Oxford is seeking a Software Quality Manual Test Analyst to ensure the safety and quality of digital health solutions.

A leading video game development studio is seeking a passionate QA Analyst to test games across platforms. This role involves documenting bugs, creating test cases, and collaborating with the QA team.

As an experienced QA Analyst, you will work closely with Senior Analysts & Leads, and other team members. We’re seeking a passionate, enthusiastic and technically proficient QA Analyst to help shape our next wave of exciting projects. The QA Analyst position is focused on testing games and applica

As an experienced QA Analyst, you will work closely with Senior Analysts & Leads, and other team members. We're seeking a passionate, enthusiastic and technically proficient QA Analyst to help shape our next wave of exciting projects. The QA Analyst position is focused on testing games and applicati

You will undertake the full range of radiotherapy physicist duties, including treatment planning, checking, brachytherapy, equipment commissioning and QA, training staff and advising clinicians.

A leading independent game studio in the UK is seeking a passionate QA Analyst to test games across various platforms.

A leading healthcare institution in Oxford is seeking a Radiotherapy Physicist to undertake a wide range of duties including treatment planning and brachytherapy procedures.

A leading gaming company is looking for a Senior QA Analyst to join their team in Oxford.

Environmental Health and Safety (EHS) Officers. Collaborate closely with QA, Facilities, Manufacturing, R&D, and HR to embed safety into all business operations and projects. Support the management of biological, chemical, radiological, and ergonomic hazards commonly encountered in pharmaceutical an

We’relooking for Senior QA Analysts - players who are alsomasters of game quality. As a Senior QA Analyst, youdon’tjust click buttons, you see the whole map,anticipateevery trap, and make sure the team ships games that run smoothly for every player. Has proven QA experience in the world of games

As a Senior QA Analyst, you don't just click buttons, you see the whole map, anticipate every trap, and make sure the team ships games that run smoothly for every player. We're looking for Senior QA Analysts – players who are also masters of game quality. Has proven QA experience in the world of g

We are looking for an Independent Reviewing Officer (IRO) Service Manager who has relevant experience at management level and can support the delivery of high‑quality services to ensure the best outcomes for Oxfordshire children. Work closely with the Senior Service Manager and the two other Servi

Vacancy for QA Automation Engineer at Preservica.

A leading nuclear medicine company based in the United Kingdom is seeking a Senior QA Officer to ensure compliance with GMP standards and international legislation.

A clinical-stage biopharmaceutical company located in Oxford is seeking a full-time QA GCP Associate Director/Senior Manager.The successful candidate will oversee Clinical Quality Assurance activities, ensuring compliance with Good Clinical Practice (GCP) standards and managing audits.Candidates sho

Extended experience across QA which includes GDP activities (Responsible Person) would be preferred but not essential if you are a Qualified Person. We are currently searching for a Senior Compliance & Quality Assurance Consultant – ATMP – Qualified Person to join the team in the UK to support a

Blue Earth Therapeutics is a clinical‑stage radiopharmaceutical company developing the next generation of precision radioligand therapies for cancer. With a strong leadership team, cutting‑edge science, and an exciting growth trajectory, we are expanding our CMC & Supply Chain function with the addition of a highly organised and proactive CMC & Supply Chain Associate initially on a 6 month FTC. This is an excellent opportunity for someone looking to develop within radiopharmaceuticals, clinical supply, and logistics while playing a crucial role in delivering therapies to patients across Europe and the USA. The Opportunity As our CMC & Supply Chain Associate, you will support the end‑to‑end supply of therapeutic radiopharmaceuticals for multiple clinical studies. Working closely with the Supply Chain Manager, cross‑functional teams, and key external partners, you will help ensure the seamless flow of materials, documentation, and operational processes. Your work will directly contribute to ensuring patients receive high‑quality therapeutic doses on time — a pivotal role in our mission to deliver targeted radiotherapies that make a genuine difference. Key Responsibilities Support the full supply chain process, ensuring documentation and critical steps are completed accurately and on schedule Manage inventory, including retest/expiry oversight, and coordinate shipment of key materials (e.g., isotope, precursor) Raise quality‑related issues with QA and Supply Chain teams Maintain accurate records of supply, expenses, and clinical product usage Become an SAP user for PO raising, goods receipting, and invoice processing Keep organised, compliant, contemporaneous records of manufacturing and supply Conduct batch data trending and assist with operational metrics Organise internal and external meetings, vendor calls, and take minutes Support preparation of presentations and project materials Ensure compliance with the company Quality System and pharmacovigilance expectations Participate in ongoing professional development About You A scientific degree or relevant experience in a similar role Experience with radiopharmaceuticals or supply chain/logistics (desirable) Experience or understanding of EU GMP principles (desirable) Strong organisational and prioritisation skills Thrives in a dynamic, fast‑paced environment Proficiency in Microsoft Excel, Word, and PowerPoint A proactive, flexible team player with excellent attention to detail Good verbal and written communication skillsWhy Join Blue Earth Therapeutics? At Blue Earth Therapeutics, you'll be part of an ambitious, fast‑growing company at the forefront of radioligand therapy. We offer: A highly collaborative, supportive culture Opportunities for personal and professional growth A clear link between your work and real patient impact Competitive salary and benefits A team that celebrates milestones and innovates togetherIf you're driven, motivated, and excited by meaningful work in a rapidly advancing field — this role is for you

Embedded Software QA+Test Engineer Oxford (3 days a week) £55,000-£65,000 The Role My client is seeking a talented QA + Test Engineer with expertise in Embedded Software to join their team building cutting-edge assurance systems for AI and UAS/UAV/Drone applications. You will play a crucial role in developing software components that enable safe and reliable operation of AI-enabled robotics and autonomous systems within their product line. Responsibilities Lead the design, development, and implementation of embedded software for SAIF Systems' Runtime Assurance platform across various hardware architectures and real-time operating systems. Ensure compliance with industry standards, regulations, and best practices for safety-critical software development, such as DO-178C, ISO 26262, and IEC 61508. Build configuration and pipeline management Software-in-the-Loop and Hardware-in-the-Loop including automated deployment across multiple platform Integration of different performance testing techniques across multiple types of simulation (gazebo sim, rosbag) Key Skills and Experience Bachelor's or Master's degree in Computer Science, Electrical Engineering, or a related field, or equivalent experience, with a strong focus on embedded systems QA, and software development and/or testing. Experience with one or more CICD pipeline services (Jenkins, CloudBuild, AWS CodePipeline, etc) Experience with infrastructure/Automation techniques (bash, python) Knowledge of source control (git) Experience with at least one test framework (pytest, gtest) Hands-on experience in embedded software testing and QA, with a proven track record in delivering safety-critical systems. The role comes with generous benefits, is 3 days a week onsite and you must be eligible for UK SC clearance. No sponsorship is offered for this role. Please get in touch immediately to be considered

Your new company You will be joining a global biopharmaceutical organisation. Known for its innovation, high‑quality manufacturing, and patient‑focused culture, operating within state‑of‑the‑art GMP facilities supporting sterile manufacturing, biologics production, and advanced therapy programmes.The QC function plays a critical role in ensuring products meet regulatory, safety, and quality standards. You will be part of a collaborative, well‑established team working alongside experienced QC, QA, and manufacturing professionals. Your new role As a QC Analyst, you will be responsible for performing routine and non‑routine analytical and/or microbiological testing to support raw materials release, in‑process control, environmental monitoring, utilities testing, and finished product batches. Conducting analysis using HPLC, GC, UV-Vis, FTIR, and wet chemistry. Performing bioburden, endotoxin, EM, water testing, and sterility testing in line with GMP. Completing environmental monitoring of Grade A-D cleanrooms. Supporting microbial identification. Completing equipment calibration checks, lab housekeeping, and logbook entries. Participating in investigations (OOS/OOT/deviations) and contributing to root‑cause analysis. Supporting audits, CAPA implementation, and QC continuous improvement initiatives. Working in compliance with GMP, GLP, Annex 1, and site standards.What you'll need to succeed Essential A B.Sc./M.Sc. in Scientific or relevant experience. Good understanding of laboratory best practice and ability to follow SOPs precisely. Strong organisational skills and attention to detail. Ability to work on site in a regulated environment.Desirable Previous experience within a GMP QC laboratory. Experience in analytical techniques (HPLC/GC/UV) or microbiological methods (EM, bioburden, sterility).What you'll get in return Opportunity to work within a global biopharmaceutical organisation. Hands on training and development across QC testing, instrumentation, GMP, and data integrity. Competitive hourly/day rates, depending on experience. Potential for long term contract extension due to pipeline and ongoing site growth. Exposure to large scale manufacturing, sterile processing, and cutting edge technologies. Supportive team environment with strong emphasis on continuous improvement and collaboration.What you need to do now If you're interested in exploring this QC Analyst opportunity, please apply with your CV or contact me directly for a confidential discussion. We are currently shortlisting and would be happy to talk through the role, your experience, and next steps. If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career

Join us as we bring QA / Testing in house and be part of that in house team that sets the methodologies, best practices, and standards for our testing. Then continue to identify and implement improvements. You will be experienced in software testing in Agile environments and will design, execute, and maintain functional and non-functional test cases. You will understand functional, regression and exploratory testing. You will also be familiar with automation tools and frameworks, along with test management and defect tracking tools such as Jira, Zephyr. The role will involve and require demonstrated ability to understand and test APIs, UI, and back-end systems. Be a contributor with input into story-level test planning, highlight testing related risks and investigate issues to put in place mitigations while working closely with developers to support resolutions. There is great scope to really get involved and apply your experience and knowledge and make a real positive difference. You would likely bring an ISTQB certification. Gigaclear is a growing Fibre Broadband (FTTP / FTTH) company, developing our fibre-to-the-premises broadband infrastructure to some of the most difficult to reach areas of the UK, empowering those communities with broadband to rival any city. Staff rewards, benefits and opportunities We foster a collaborative, engaging culture that empowers staff to grow and maximise their skills. We want to challenge our people in a fair environment where hard work is rewarded and a path for progression is open to all. Generous employer pension; up to 8% matched contribution Income protection & life assurance 25 days holiday (plus bank holidays), holiday purchase scheme and Yay Days! Health cash plan, 24/7 remote GP access and Employee Assistance Programme including counselling & legal advice Unlimited access to online training and development content via our Learning Management System Long service benefits and monthly employee recognition Enhanced maternity and paternity provisions Flexible working environment Health & Wellbeing initiatives and company funded social events Our approach is to work guided by our mission, vision and values. Our Mission - Empowering communities with brilliant broadband Our Vision - Connected Communities Our Values - Own it, Find the Right Way, Work Together, Win Together

Environmental Engineer - Stack Monitoring Culham, Oxfordshire (2 days on site, 3 days flexible) 6-month contract | Full-time | Start ASAP £56-61/hour Inside IR35 Are you an Environmental Engineer with experience in emissions monitoring, radiological assessment, or air quality compliance? This is a unique opportunity to lead critical environmental studies supporting the safe and compliant operation of advanced engineering and research facilities. This role will focus on evaluating stack monitoring arrangements and assessing the feasibility of developing in-house monitoring capabilities. You'll play a key role in ensuring compliance with environmental and radiological regulations while helping shape future monitoring strategies. The Opportunity You'll lead two important technical studies: Stack Monitoring Feasibility Study - analysing historical emissions data, compliance requirements, and monitoring effectiveness In-House Monitoring Capability Study - evaluating the feasibility, requirements, and roadmap for internalising stack monitoring capabilityYour work will directly influence environmental compliance, regulatory engagement, and long-term monitoring strategy. Key Responsibilities Environmental & Radiological Assessment Review historical stack monitoring data, including tritium, radiological, and hazardous material emissions Analyse operational trends, contamination patterns, and measurement accuracy Evaluate compliance with UK environmental regulations, including EPR and IRR17 Assess Safety Case requirements and Best Available Techniques (BAT) obligations Define monitoring data requirements for regulatory submissionsMonitoring Strategy & Capability Development Audit existing stack monitoring systems, technologies, and processes Assess feasibility of developing in-house monitoring capability Identify required equipment, analytical tools, and competencies Develop recommendations for improved monitoring frequencies and methodologies Produce a roadmap for capability development, including cost and resource planningTechnical Reporting & Stakeholder Engagement Produce detailed technical reports and recommendations Apply QA/QC standards to data analysis and reporting Engage with internal stakeholders across environmental, safety, and operational teams Present findings and recommendations to senior management and technical committees What We're Looking For Essential Degree in Environmental Engineering, Environmental Science, Chemical Engineering, or related discipline Experience in emissions monitoring, environmental compliance, or stack monitoring Strong data analysis and technical reporting skills Knowledge of UK environmental and radiological regulatory frameworks Experience interpreting environmental or radiological monitoring dataHighly Desirable Experience with radiological monitoring, particularly tritium emissions MCERTS certification or emissions monitoring experience Knowledge of Environment Agency regulatory requirements Understanding of BAT, EPR, IRR17, or COMAH regulations Experience with stack sampling, CEMS, or laboratory analysisPersonal Attributes Strong analytical and problem-solving skills Excellent written and verbal communication abilities Ability to work independently and deliver technical studies Effective stakeholder engagement skills Why Apply? Lead critical environmental compliance and monitoring studies Influence the future strategy of emissions monitoring capability Work within a highly regulated, technically advanced environment Flexible hybrid working arrangement Immediate start with strong potential for extension Apply Now If you have experience in environmental engineering, emissions monitoring, or radiological compliance and want to contribute to a high-impact technical programme, we'd love to hear from you

Senior Quality Engineer Oxford Days Up to £60,000 A leading engineering and manufacturing company is looking for a Senior Quality Engineer to ensure high standards of product quality across all operations. This role includes quality assurance, process improvement, and compliance management, reporting directly to the Quality Manager. Skills / Duties Lead quality assurance processes and audits Support continuous improvement initiatives Analyse production data to identify trends and issues Collaborate with production and engineering teamsQualifications / Experience Proven experience as a Quality Engineer in a manufacturing environment Strong understanding of QA/QC standards and procedures Excellent analytical and problem-solving skillsTo apply, send your CV to Cameron Stevens or call (phone number removed) for a confidential discussion

Senior QA Officer Oxford Full time and permanent position Excellent salary and benefits An exciting opportunity has arisen for an experienced Senior QA Officer to join a leading radiopharmaceutical manufacturing site. This full-time, onsite role supports the delivery of high-quality products through robust Quality Assurance, GMP compliance, and continuous improvement across operations. You'll play a crucial part in maintaining high standards, supporting audits, and ensuring the effective running of the Quality Management System. Key Responsibilities Ensure site operations comply with GMP guidelines, pharmaceutical legislation, and internal quality standards Review and maintain documentation, including SOPs, quality records, deviations, CAPAs, investigations and change controls Support QC activities including review of test results, management of OOS, and environmental monitoring oversight Assist with inspection readiness, internal audits, and responses to regulatory findings Contribute to batch review activities, ensuring documentation meets licence requirements and supports QP releaseSkills & Experience Required Degree in Pharmacy, Chemistry, Pharmaceutical Science, Biology or a related field Minimum 2 years' experience working within Quality Systems in a GMP-regulated environment Strong understanding of GMP compliance and operation of pharmaceutical manufacturing facilities Excellent communication skills, attention to detail, and ability to work effectively under pressure Knowledge of radiation or radiopharmaceuticals (desirable) and a strategic mindset for long-term quality improvementIf this looks like an opportunity of interest, and you possess the required skills and experience, then please follow the link to apply

We are currently looking for an experienced Site Engineer to join a major earthworks project based in Oxford. This is a fantastic long-term opportunity for a Site Engineer to work on a substantial earthworks package with a well-established civil engineering contractor. The successful Site Engineer will be responsible for supporting the delivery of a large earthworks programme, including setting out, quality assurance, and coordination with site teams to ensure the earthworks activities are delivered safely and efficiently. This role is ideal for a Site Engineer with proven experience delivering heavy earthworks on civil engineering or infrastructure projects. The Site Engineer will play a key role in managing day-to-day engineering duties across the earthworks package while ensuring works are completed in line with drawings and specifications. Role Details Position: Site Engineer Location: Oxford Start Date: 30th March Duration: 18 months Rate: £300 – £375 per day Key Responsibilities Setting out and surveying for the earthworks package QA documentation and record keeping Working closely with the Site Engineer team and site management Monitoring progress of earthworks operations Ensuring works are delivered safely and to specification If you are a Site Engineer with strong earthworks experience and are available for a long-term contract starting 30th March, we would like to hear from you. Apply now or get in touch to discuss this Site Engineer opportunity further

Overview: I am working on behalf of a tier-one contractor recruiting a Site Engineer to join long-term water and wastewater frameworks across the Thames Valley (including Aylesbury, Banbury and Reading). You’ll provide technical, hands-on engineering support on-site from setup and setting-out through to commissioning and close-out, delivering projects such as treatment works upgrades, pumping station improvements, sewer rehabilitation and nature-based solutions that enhance biodiversity and resilience. Key Responsibilities: Perform setting-out, level checks and setting-out verification to design tolerances; produce and maintain accurate survey records and as-built information. Carry out quality inspections and testing to ensure works meet drawings, specifications and client requirements; raise and manage NCRs/defects and support remedial works. Support site setup and the Site Manager with implementation of company systems, method statements, RAMS and permit processes. Prepare, update and issue daily/weekly site engineering reports, progress records, site diaries and material/plant logs to support commercial and delivery teams. Coordinate with subcontractors, plant operators and operatives to sequence works and maintain programme progress; supervise and mentor junior technical staff. Assist with temporary works checks and handover of temporary installations to the Temporary Works Coordinator; ensure compliance with design and inspection regimes. Support commissioning activities and operational handover, including witnessing tests, assisting with SCADA/telemetry handover and liaising on water quality sampling where required. Contribute to cost control by logging materials, tracking plant usage and providing input to quantity surveying/estimating teams. Implement environmental controls and pollution prevention measures on site; follow ecological protection requirements and permit conditions. Use digital engineering tools (CAD, BIM viewers, survey/GNSS equipment) to produce and manage technical drawings and site records. Qualifications & Experience: HNC/HND, Foundation degree or Degree in Civil Engineering, Construction Management or equivalent practical/site experience. CSCS card and SSSTS (or SMSTS) certification. Practical experience on water/wastewater projects (treatment works, pumping stations, sewer rehabilitation, river/culvert works) or framework delivery is highly desirable. Competence in setting-out, site surveying (total station/GNSS) and producing as-built records. Familiarity with construction drawing interpretation, QA inspection/testing regimes and site safety practices. Desirable additional qualifications: Confined Space, First Aid at Work, NRSWA/Streetworks, AutoCAD/CAD skills, CPCS plant tickets. Strong organisation, communication and problem-solving skills; ability to work under direction and take initiative on technical matters. Full UK driving licence and willingness to travel across the operational region. Benefits: Structured training and development package with support towards professional chartership. Tailored health & wellbeing offering and private medical insurance. 26 days’ annual leave with option to buy additional days. Enhanced pension scheme and 4x life assurance. Clear career progression within major frameworks and opportunity to develop technical and site leadership skills. Competitive salary and additional site allowances where applicable. If you’re ready to develop your technical career as a Site Engineer in the UK water sector and work on long-term, secure frameworks with a tier-one contractor, apply now with your CV to be considered

You’re confident in manual and API testing, comfortable with basic SQL, and have a solid understanding of QA processes within modern software delivery environments. We’re now looking for a detail-driven QA Analyst who’s passionate about ensuring that what ships actually. In-depth understanding

Strong background in QA Operations within pharmaceutical manufacturing. AssureBio is partnering with a UK-based pharmaceutical manufacturer to appoint an experienced Qualified Person (QP) who can also lead QA Operations at site level. Provide senior QA oversight across manufacturing, testing, storag

QA Engineer — £45k–£50k — Join the Fintech Powering Superyachts & Artists Worldwide.

Are you someone who instinctively sees where a sales organisation could be sharper, more disciplined and more effective?.This is a high-impact, independent role focused on defining and elevating institutional sales standards.Reporting to the Head of Strategy & Execution — with direct Board exposur

QA Manager-Supply Chain Location: Grantham or CraigavonThe primary focus will be to assist, as a member of a small team, in the continued development of a strong internal and external supply chain, acting as the first ‘technical' point of call for suppliers, internal sites and support in any custo

Job Description Join Our Team: QA Auditor Position: QA AuditorLocation: Rotherham, S64 8ABSalary: £14.

About The RoleJoin the Samworth Brothers Team and become part of our dynamic family!At Samworth Brothers, we genuinely care about our colleagues and strive to create an engaging environment that values your unique contributions.We are committed to your success and offer a range of exceptional benefi

A food manufacturer is looking for a QA Manager to lead a 16-person QA team, support operations on the factory floor, and strengthen a quality culture that already takes food safety seriously. You'd be responsible for: Leading and developing the QA team Supporting production.

Job Description QA Release Officer We are currently recruiting for a QA Release Officer to support quality assurance and batch release activities within a regulated pharmaceutical manufacturing environment.

Mechanical & Electrical QA/QC Engineer This position would suit a meticulous QA/QC professional with strong experience in MEP building services across both mechanical and electrical installations.

Job Description Job Title: QA SupervisorLocation:BedfordWorking Hours: 40 hours per week, Monday to Friday, 6:00am 3:00pmPay: £13. Job Overview We are looking for a QA Supervisor to join our client in Bedford area.