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CBSbutler Holdings Limited trading as CBSbutler is seeking a Trainee Medical Field Service Engineer to support hospital-based equipment across Central and Greater London. The role offers structured training, field visits to clinical environments and a clear path into medical device engineering. You will install, service and maintain electromechanical medical devices, work with clinical teams, and develop fault-finding and repair skills through hands-on experience. #J-18808-Ljbffr

Location: London / Central & Greater London Salary: Up to £30,000 + £2k Bonus + £5/d lunch allowance + Company Vehicle + Benefits Are you looking to build a career in medical field service engineering, or already have field service experience and want to develop your skills within the medical sector? An exciting opportunity is available for a Trainee Medical Field Service Engineer to join a specialist healthcare engineering team, supporting customers across London. This is a field service opportunity with full product and technical training provided. We're open to candidates at different stages of their technical career - from a school or college leaver at entry-level, through to an experienced electro-mechanical field service engineer looking to move into medical devices. You’ll be field based and spend your days visiting hospitals and healthcare sites across Central and Greater London, supporting a range of medical and electromechanical equipment. • Installing, servicing and maintaining medical and electromechanical equipment, • Carrying out planned preventative maintenance and routine safety and performance checks, • Supporting electrical, mechanical and electromechanical fault-finding, • Completing straightforward repairs and component replacements following training, • Assisting experienced engineers with installations and more complex technical work, • Ensuring equipment is safe, operational and ready for clinical use, • Building professional relationships with customers and clinical teams, • Completing accurate service reports and digital records, • Managing tools, spare parts and test equipment, • Escalating more complex or unfamiliar faults appropriately The equipment you'll support initially includes garment management systems, operating and procedure tables, X-ray chairs and other low-risk medical equipment. As your skills and experience develop, you'll have the opportunity to broaden your technical knowledge across the wider product portfolio. You’ll regularly work within hospital environments, including areas around operating theatres, so you’ll need to be comfortable working in a clinical setting and remain calm and professional when equipment issues arise. Monday-Friday, 40 hours per week Typically 8:30am-5:30pm The role will predominantly involve travel to hospitals in Central and Greater London, with some travel nationally when required. We're interested in candidates with a practical technical background, whether you've gained your experience through education, an apprenticeship, employment or an existing field service engineering role. This could suit: • A school/college leaver with level 2 qualifications (GCSE's) and hands-on experience, • An apprentice or junior engineer looking to take the next step, • A technician with experience in electrical, mechanical or electromechanical equipment, • An experienced field service engineer looking to move into the medical device sector You’ll ideally have: • Some hands-on experience with electrical, mechanical or electromechanical equipment, • A practical approach to fault-finding and problem-solving, • Good customer-facing and communication skills, • The ability to think on your feet and work calmly under pressure, • Flexibility to travel as required, • A willingness to learn and develop your technical skills, • A Level 2 technical qualification, GCSE equivalent or relevant practical experience, • A full UK driving licence, • Indefinite right to work in the UK - sponsorship is not available Previous experience in medical devices, field service, maintenance, electromechanical equipment, or similar environments would be advantageous, but is not essential. • Salary up to £30,000, • Company vehicle, • £5 daily lunch allowance, • Annual Engineer Bonus of up to £2,000, • Full technical and product training, • Long-term career development within medical engineering, • Private pension, • Other benefits Interested in medical engineering? Whether you're starting your engineering career or looking to bring existing field service experience into the medical sector, this is an opportunity to develop your technical skills through structured training and hands-on experience. Medical engineering experience isn't essential - we're looking for practical ability, a customer-focused approach and the willingness to learn. #J-18808-Ljbffr

£45,000–£55,000 + Company Van + Bonus & Incentives Field Based | Southern UK Are you an experienced field salesperson looking for greater autonomy — or an opportunity to move into medical device sales? We’re recruiting for a growing specialist medical device manufacturer supplying high-quality patient handling and transport equipment into NHS and private healthcare organisations across the UK. This is a genuinely autonomous territory role. You’ll take ownership of the Southern UK region, developing existing accounts, winning new business and demonstrating a premium range of equipment directly to healthcare customers. Previous medical device experience isn’t essential. We’re equally interested in strong B2B field salespeople from capital equipment, technical products or other solution-led sales environments who can demonstrate a track record of developing a territory. • Proven B2B field sales experience, • Strong new business and account development skills, • Confident presenting and demonstrating products, • Commercial, self-motivated and comfortable managing your own territory, • Medical device, healthcare or capital equipment experience is advantageous, but not essential, • Full UK driving licence The territory covers Southern UK, from South Wales across to Kent, including Wiltshire, Surrey and Sussex. The package £45,000–£55,000 basic salary depending on experience, plus company van, pension and quarterly/annual performance-related bonuses and incentives. A strong opportunity for an experienced salesperson who wants autonomy, a quality product range and the chance to build a career within the medical device sector. #J-18808-Ljbffr

Get AI-powered advice on this job and more exclusive features. Direct message the job poster from VRS Recruitment Our client is a global leader in laboratory services, committed to delivering excellence in technical solutions and customer experience working within highly regulated sectors such as life sciences, diagnostics, pharmaceutical, and environmental analysis. We’re looking for a dynamic Laboratory & Operations Manager to take ownership of one of their major accounts, shaping the service delivery model and driving operational excellence. Key responsibilities will include: • Leading and developing a diverse team of engineers and administrators to deliver exceptional service every day, • Building strong relationships with clients, become the trusted point of contact for partners, and drive operational performance, compliance, and continuous improvement, • Identify, monitor and manage site performance, identifying service improvement opportunities, guiding process changes, and support the expansion of the services provided onsite, • Present operational reports, lead governance meetings, and communicate effectively with key internal & external stakeholders We seek a passionate leader who thrives on empowering people, building structure, and delivering results in a client-focused environment. Successful candidates will possess: • Proven leadership experience managing teams, engineering or laboratory operations, ideally in a regulated environment (GMP), • Laboratory or technical operations experience within the pharmaceutical, biotech or medical device sectors, • Excellent communicator with strong relationship-building skills, capable of influencing across teams and driving continuous improvement, • Experience managing budgets, KPIs, and compliance frameworks (e.g., safety, audit readiness) In this role you’ll be working in a supportive setting where your contributions shape both client success and internal performance. A competitive salary and benefits package is provided, along with ongoing development opportunities and an opportunity to lead a significant client account. This is a key leadership role, combining technical oversight, strategic planning, and cross-functional collaboration to ensure laboratory services support the broader program goals. If you are a strategic laboratory leader with a passion for driving operational excellence and client success, we would like to hear from you. Apply now to find out more! Keyword Summary: Site Lead, Laboratory Services, Team Leadership, Client Account Management, OneSource, Service Delivery, KPIs & SLAs, Technical Service, Laboratory Operations, Engineering Management, Life Sciences, Pharmaceuticals, Compliance, Continuous Improvement, Southeast, Surrey, Reading, London, Slough, Berkshire, VRS9183PC • Mid-Senior level, • Full-time, • Science, Management, and Engineering, • Pharmaceutical Manufacturing and Staffing and Recruiting #J-18808-Ljbffr

Your new company We are seeking an experienced Regulatory Affairs Specialist to join the Technical Documentation team on a contract basis.This is an excellent opportunity for a regulatory professional with strong IVD/IVDR expertise to play a key role in the preparation, remediation, and maintenance of technical documentation supporting a complex product portfolio. You will work within a global regulatory environment, collaborating with cross-functional stakeholders to ensure compliance with evolving regulatory requirements. Your new role Compile, review and maintain IVD/IVDR Technical Documentation in line with EU regulatory requirements. Author and update technical files and associated regulatory documentation. Support technical documentation activities related to a strategic divestment project. Review existing documentation for compliance gaps and support remediation activities. Develop and maintain regulatory content including: Technical Files / Technical Documentation Summary Technical Documentation (where applicable) Labelling and regulatory content Instructions for Use (IFUs) Collaborate with Regulatory Affairs, Quality, R&D, Clinical, Manufacturing and Product Management teams. Ensure documentation meets regulatory requirements and supports product registrations and life cycle management activities. Participate in internal reviews and regulatory inspections/audits as required. Essential Experience Proven experience working in Regulatory Affairs within the Medical Device or In Vitro Diagnostics (IVD) industry. Strong understanding of EU IVDR (2017/746) requirements. Hands-on experience compiling Technical Documentation / Technical Files for IVD products. Experience authoring and reviewing technical regulatory documents. Knowledge of design control, risk management and regulatory submission documentation. Ability to work independently within a fast-paced project environment. Desirable Experience Experience writing or managing Instructions for Use (IFUs). Previous involvement in regulatory remediation, compliance or divestment projects. Experience working within large global life sciences, diagnostics or medical device organisations. Familiarity with document management systems and electronic quality management systems. What you'll need to succeed We're looking for a proactive and detail-oriented regulatory professional who can quickly integrate into an established team and deliver high-quality documentation with minimal supervision. You will be comfortable managing multiple priorities, engaging with stakeholders across different functions, and driving documentation activities to meet critical project timelines. What you'll get in return Remote working What you need to do now If you have strong IVD/IVDR technical documentation experience, have authored technical files and regulatory documents, and are looking for your next contract opportunity with a global leader in diagnostics and life sciences, we'd love to hear from you. TPBN1_UKTJ

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s Corporate headquarters are located in Ontario Canada and US headquarters in New Jersey USA, with additional physical offices in Asia and Europe. Everest is known in the industry for its high-quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success. Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest. To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Biostatistician, working remotely in the United Kingdom. • Lead efforts in resolving day to day work related issues and problems, securing quality, improving efficiency and productivity of statistical and programming operations., • Lead assigned projects by applying project management skills, statistical and programming techniques; achieve quality and on time delivery of deliverables, earn client’s trust and repeat business., • Provide statistical expertise for design, analysis and reporting of clinical trials and research projects., • Contribute to the writing of statistical sections of study protocols, perform sample size calculation, develop randomization specifications, and generate randomization codes., • Write Statistical Analysis Plans (SAPs) and properly address Peer Statistician review comments., • Create and maintain Statistical and Programming Quality Control (QC) and QA Plans for assigned projects., • Provide input to unblinded data management plan when required., • Assist in research and development of statistical methodologies and processes., • Develop and/or review ADaM dataset specifications. Review and provide input to SDTM dataset specifications when required., • Perform QC validation of analysis datasets and TLGs., • Perform third level review of dry runs and final run., • Lead statistical dry runs and final run by actively participating or contributing to project and resources management, addressing statistical and programming questions and interacting with data management to follow up and resolve data issues., • Review and provide input to the Analysis Data Reviewer’s Guide, discuss and incorporate Data Standards Reviewer’s review comments to ensure quality of the document., • Perform statistical analysis as per SAP, and address peer/QC review comments and findings., • Perform statistical validation of core results, address additional QC validation comments and findings on the core results., • Plan and conduct or contribute to the trial results reporting/dissemination meetings., • Under supervision contribute to the contents describing any deviation from the planned analysis and deviation from study conduct for the Clinical Study Report (CSR). Review CSR to ensure accuracy, completeness and appropriateness of the interpretation of the statistical results., • Write statistical report or statistical sections of the CSR., • Perform statistical analyses for publications, including but not limited to abstracts, manuscripts, presentations and posters., • Provide statistical input to Case Report Forms (CRF) design and database/variable structure., • Provide statistical input to non-CRF data collection and acquisition methods and approaches., • Review Data Management Plan sections relating to critical data collection and cleaning. Provide statistical input to Data Validation Specification., • Specify and/or program database quality acceptance checks, assess and report data quality issues, and follow through until resolution., • Perform ongoing assessment and communication of data quality issues, including protocol deviations., • Assist data management and trial management team in preparing for database lock. A Ph.D. degree in statistical science, mathematical analysis or related fields plus 2 years highly relevant experience or a Master’s degree plus 4 years highly relevant experience, with demonstrated ability and sustained performance. Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process. #J-18808-Ljbffr

PDD is seeking a mid-to-senior consultant to help clients create products, services and experiences that are safe, intuitive, relevant and desirable. Working within multi-disciplinary teams of researchers, designers and engineers, you will plan and deliver people-centred research and human factors activities, translate evidence into clear design and business direction, and build trusted client relationships. The role can flex toward human factors and usability, qualitative and contextual research, or a blend of both, depending on the successful candidate’s strengths. At senior level, the role includes greater ownership of complex global projects, commercial performance, client development, service development and mentoring. International travel will form part of some activities. • Plan, scope and deliver research, human factors and usability work across the project lifecycle, from proposal and study design through fieldwork, analysis, reporting and presentation., • Select and apply appropriate methods, which may include contextual inquiry, ethnographic research, interviews, formative and validation usability studies, task or heuristic analysis, expert review, co-creation workshops, or journey mapping., • Moderate research and usability sessions and facilitate workshops in the UK and internationally, adapting approaches to different participants, cultures, products and project contexts., • Analyse and synthesise qualitative and usability evidence, translating findings into actionable insights, design requirements, risk controls, opportunity areas and strategic recommendations., • Produce clear, accurate and engaging deliverables, including proposals, research plans, protocols, technical reports and client presentations, tailored to the audience and purpose., • Lead or contribute to multi-disciplinary project teams; manage scope, schedules, budgets, resources, quality and project risks in line with agreed client expectations and PDD processes., • Build trusted client relationships throughout delivery, identify and resolve issues early, and help generate repeat and new work through high-quality consulting and sound commercial judgement., • Collaborate with business development, sales and marketing colleagues to shape proposals, estimates, campaigns and a compelling service offering., • Contribute to the evolution of PDD’s human sciences capabilities, methods, procedures and knowledge sharing, including awareness of changing client needs, market practice and relevant regulation., • At senior level, provide day-to-day direction, coaching and constructive feedback to colleagues and support the development of junior team members., • Maintain professional knowledge and undertake continuing development relevant to the role., • Practical experience applying human-centred research, human factors, ergonomics, usability or user-centred design methods in commercial, consultancy, academic or other applied settings., • Ability to plan and deliver qualitative research or usability activities, including participant-facing fieldwork, analysis and synthesis., • Strong analytical judgement and the ability to turn complex evidence into clear, useful recommendations for products, services, experiences or business strategy., • Excellent written, verbal and presentation skills, with the ability to communicate technical or complex material clearly to clients and multi-disciplinary teams., • Confidence working directly with clients and collaborating effectively with researchers, designers, engineers and commercial colleagues., • Strong organisation and self-management, including the flexibility to balance priorities and deliver high-quality work across concurrent projects, deadlines and budgets., • Experience preparing high-quality study protocols, reports or other technical documentation., • Experience in healthcare or medical-device development, including applying relevant human factors regulatory expectations across one or more markets., • Ability to learn unfamiliar sectors, technologies and evidence bases quickly and apply that knowledge responsibly., • Willingness and practical ability to travel internationally when projects require it., • Experience working in a consultancy or another client-facing environment, including contributing to proposals, estimates or business development., • Experience leading complex, multi-site or international research or usability programmes and maintaining strong client relationships., • Experience with drug-delivery devices or other safety-critical products and with use-related risk management, such as hazard identification, use-related FMEA, use-related risk analysis or residual-risk evaluation., • Experience designing and evaluating instructions for use, quick-reference guides, training content or other instructional materials., • Breadth across methods such as ethnography, contextual research, co-creation, journey mapping, persona development, task analysis, heuristic review and usability evaluation., • Information or visual design capability that helps make complex findings accessible and persuasive., • Experience mentoring colleagues, guiding project teams or contributing to the development of a research or human factors service offering., • A degree or postgraduate qualification in human factors, ergonomics, psychology, anthropology, product design, usability engineering, cultural studies, another human or social science, or a related discipline would be relevant. Equivalent applied experience and evidence of strong professional practice will also be considered. Chartered status, or progress toward it, is welcome but not required. #J-18808-Ljbffr

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Quay Recruitment Group Ltd is recruiting a Territory Sales Manager for the Southern UK region in a growing medical device manufacturer.