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A rare job share opportunity for a Marketing Manager to work in the UK office of an international company with offices located within easy reach of Surrey/North Hampshire/London. \n The role requires the successful candidate to work 22.5 hours per week, flexible over full days or part days. \n Marketing Manager Benefits and Package: \n\n • Working 22.5 hours per week\n, • Free Parking\n, • Discretionary Bonus Scheme\n, • Company Pension Scheme\n, • Salary Sacrifice Car Scheme\n, • Death In Service\n, • Mobile\n, • Laptop\n\n Marketing Manager Key Responsibilities and Accountabilities: \n\n • Responsible for writing & implementing annual marketing plan which aligns the UK and HO business strategy.\n, • Managing the UK Marketing Budget and ensuring effective delivery of the marketing plan including monitoring ROI.\n, • B2C & B2B promotional activities with aim of developing sales and brand awareness in key markets.\n, • Manage relationships with 2-3 key marketing agencies supporting B2B and B2C activity.\n, • Regular liaison with HO marketing function in Germany\n, • Plan and deliver participation at national and international conferences and exhibitions.\n, • Support Bid & Tender process.\n, • Co-ordinate production of all B2C advertising - online & print.\n, • On an as required basis to co-ordinate, track & register sponsorship payments with the ABPI\n, • With support from colleagues ensure the UK office is aware of & adheres to compliance standards relevant to the pharma/medical device industries.\n, • Oversee UK website and ensure relevant content is maintained and updated.\n, • Ensure digital agency delivery for Google Ads, Meta Ads & Amazon Ads to maximise traffic to UK webshop & UK Amazon listings\n, • Proof translated documents to ensure good standard of Plain English to their respective audiences.\n, • Competitor analysis for key products..\n, • Support relationships with partners and other key stakeholders.\n, • Collaborate and share workload effectively with job share marketing manager.\n, • As part of the Senior Leadership Team, actively participate Marketing & Sales meetings and Monthly Operations Team Meetings\n\n Marketing Manager Qualities: \n\n • Level 4 CIM or equivalent Marketing Qualification\n, • Experience of medical device or pharma industry highly desirable\n, • Strong B2C and B2B marketing experience (Digital and offline).\n, • ABPI qualification or willingness to take qualification within 12 months of joining\n, • IT knowledge e.g. Microsoft Office (essential), SAP, databases, Shopify\n, • Amazon Vendor or Seller experience\n, • Proven content writing and editing experience.\n, • Excellent communications skills\n, • Strong team player who has the flexibility and ability to work in a small UK operation (12 people) and support tasks outside of marketing.\n, • Must be able to work in the office (occasional flexibility possible)\n\n Thank you for your application however due to the high volume of candidates applying, if you have not heard back from us within 5 days please assume that you have not been successful on this occasion.

Electrical Shift Engineer – Permanent Position Join a leading Facilities Maintenance team at the prestigious global headquarters of a luxury automotive brand in Woking, Surrey. This is an outstanding opportunity to work in a high-profile, technically varied environment where your expertise will make a visible difference every day. Salary: £45,000 per annum, plus on-call payments and excellent overtime rates of x1.5 and x2—giving you real scope to increase your overall earnings. You'll also enjoy a comprehensive company benefits package. Hours and Shift Pattern : 40 hours per week, Monday to Friday A rotating shift pattern offers variety across the working week: Early shift: 6:00am–2:30pm Day shift: 8:00am–5:00pm Late shift: 1:30pm–10:00pm On -call: A shared rota of just one week in nine, with additional payments available. About the Role This varied, hands-on position will see you delivering planned preventative maintenance, reactive repairs, additional works and emergency response across electrical and mechanical systems. You'll help keep a prestigious site operating safely, efficiently and to the highest standards. What You'll Bring to the Team You'll be a valued member of a collaborative shift technician team, providing flexible cover when needed and helping to deliver a reliable, responsive service. The role offers genuine variety, technical challenge and the opportunity to work across disciplines in a supportive environment. Key Responsibilities Deliver planned preventative maintenance in line with agreed schedules and procedures, maintaining high engineering standards and maximising the reliability of plant and associated electrical and mechanical systems. Work safely and consistently in accordance with the Health and Safety at Work etc. Act and all relevant site procedures. Maintain accurate records and documentation for planned and reactive electrical and mechanical maintenance. Respond promptly and effectively to reactive maintenance issues and helpdesk requests. Coordinate initial responses to client requests and keep stakeholders informed. Coordinate specialist subcontractors supporting electrical and mechanical maintenance schedules. Attend call-outs, breakdowns and emergencies relating to electrical and mechanical services when required. Diagnose faults and complete effective repairs during both planned and reactive maintenance. Repair and maintain lighting and electrical distribution systems. Support other trades and work flexibly across disciplines where required. Produce clear reports on completed work, equipment condition and follow-up actions. Undertake other reasonable duties requested by the client to support effective site operations. Work collaboratively with the wider team to complete tasks safely and efficiently. Develop and maintain a sound understanding of site-based systems and how they interact. Carry out LSP duties in line with L8 requirements when needed. Work primarily at the client's main campus in Woking, with occasional travel to other local buildings and, where business-critical, further afield. About You Essential Skills and Experience City & Guilds Level 3 Electrical Installation (2360), or a recognised equivalent qualification. Health and safety training, including a working knowledge of risk assessments and method statements. Experience in a similar maintenance role, including fault diagnosis and rectification. Experience delivering electrical elements of general building PPM schedules. Practical experience in electrical installation, testing and inspection. A good understanding of critical and non-critical building systems. Experience using a CAFM/PPM management system, ideally Concept, via a handheld device. Desirable City & Guilds Electrical Inspection and Testing, or equivalent. 18th Edition IET Wiring Regulations. Knowledge and understanding of Building Management Systems. A good basic understanding of mechanical systems. Knowledge of COSHH and the safe handling of substances. Benefits and Rewards Generous holiday allowance: 25 days, increasing with service, plus bank holidays and your birthday off—with the option to purchase up to five additional days. Enhanced financial protection: Life assurance, company sick pay and an enhanced employer pension contribution. Health and wellbeing: Private medical insurance after one year's service, wellbeing programmes and free, confidential 24/7 Employee Assistance Programme support. Recognition and referrals: Employee recognition programmes and generous referral bonuses. Flexible benefits: Eye-care vouchers, major retailer discounts, an electric vehicle salary-sacrifice lease scheme, personal IT equipment loans and impartial financial guidance. Community impact: One paid working day each year to volunteer in the local community. Everything you need to succeed: Full induction and training, plus a smartphone, tablet or laptop, uniform and PPE where applicable. To apply: If this sounds like the right opportunity for you, please submit your updated CV outlining your relevant experience — we'd be pleased to hear from you. TPBN1_UKTJ

Locations: Guildford, Surrey, United Kingdom Role ID 216019 Worker Type Regular Employee Studio/Department CT - Frostbite Work Model Hybrid Electronic Arts creates next-level entertainment experiences that inspire players and fans around the world. Here, everyone is part of the story. Part of a community that connects across the globe. A place where creativity thrives, new perspectives are invited, and ideas matter. A team where everyone makes play happen. Frostbite is EA's proprietary game engine. Its versatile tools and the latest technology power creation on some of the world's most iconic games, including titles from EA SPORTS and Battlefield. We are looking for a Software Engineer with expertise in developing and integrating runtime machine learning solutions to join our team. You will report to a Leader of Engine Development and collaborate with game teams, central technology engineers, and researchers to bring ML models into the hands of our players by deploying them directly within EA games. Responsibilities: Evaluate, adapt, extend, and improve existing machine learning runtime technologies, while designing and implementing new solutions from the ground up when needed. Partner with ML experts across EA to assess, apply, and scale models and architectures for on-device performance. Translate ML concepts, tradeoffs, risks, and technical constraints into clear language for different audiences. Build end-to-end solutions for running machine learning models across a variety of devices. Write clean, well-documented, and well-tested code that integrates smoothly with existing systems. Stay current with advancements in Deep Learning, Reinforcement Learning, Generative AI, and related fields by exploring industry developments, identifying relevant research, and proposing ways to apply it. Contribute to Frostbite's and EA's ML/AI communities by sharing knowledge, collaborating with partners, and mentoring teammates. Qualifications: 5+ years of hands‑on software engineering experience with C++, including a understanding of multithreading and performance optimization. Experience profiling and optimising real‑time software. Practical experience with software engineering fundamentals, including version control, code reviews, documentation, automated testing, coding standards, CI/CD, issue tracking, and Agile development. Knowledge of ML frameworks such as PyTorch or TensorFlow. Experience building and shipping end‑to‑end ML systems in real‑world production environments. A BSc or MSc in Computer Science, Engineering, Mathematics, or equivalent professional experience. Knowledge of GPU programming. Experience with game programming. Knowledge of ONNX or other intermediate representations for ML model graphs.. About Electronic Arts We’re proud to have an extensive portfolio of games and experiences, locations around the world, and opportunities across EA. We value adaptability, resilience, creativity, and curiosity. From leadership that brings out your potential, to creating space for learning and experimenting, we empower you to do great work and pursue opportunities for growth. We adopt a holistic approach to our benefits programs, emphasizing physical, emotional, financial, career, and community wellness to support a balanced life. Our packages are tailored to meet local needs and may include healthcare coverage, mental well‑being support, retirement savings, paid time off, family leaves, complimentary games, and more. We nurture environments where our teams can always bring their best to what they do. Electronic Arts is an equal opportunity employer. All employment decisions are made without regard to race, color, national origin, ancestry, sex, gender, gender identity or expression, sexual orientation, age, genetic information, religion, disability, medical condition, pregnancy, marital status, family status, veteran status, or any other characteristic protected by law. We will also consider employment qualified applicants with criminal records in accordance with applicable law. EA also makes workplace accommodations for qualified individuals with disabilities as required by applicable law. #J-18808-Ljbffr

Building an AI‑first organisation is central to Clinisys’ purpose and the impact we deliver. As a global provider of intelligent diagnostic informatics solutions, we build AI‑enabled, cloud‑based platforms to enhance diagnostic workflows across healthcare, life sciences, and public health. By applying intelligent technology thoughtfully and responsibly, we help laboratories and testing environments operate more effectively, generate meaningful insights at scale, and ultimately support healthier and safer communities. Operating across more than 30 countries, Clinisys expects all colleagues—regardless of role or function — to work confidently with AI‑enabled tools, apply digital and analytical thinking, and continuously adapt as technologies evolve, must drive an AI first sense of purpose and urgency. Clinisys has built an unrivalled reputation for deploying complex diagnostic networks and academic centres – and is the only provider to repetitively deliver to all disciplines end-to-end – at scale. Fostering healthier communities. The Complaints & Clinical Risk Quality Analyst is responsible for the investigation, analysis, trending, and resolution of customer complaints, clinical safety issues, and product‑related risks across the Clinisys product portfolio. The role supports complaint handling, post‑market surveillance, and clinical risk management activities to ensure compliance with applicable regulatory requirements while driving improvements in patient safety, product quality, and risk management practices. • Manage and support complaint handling activities throughout the complaint lifecycle, including intake, triage, investigation, root cause analysis, corrective actions, and closure., • Support post‑market surveillance activities through the collection, analysis, and interpretation of complaint, service, customer feedback, and product performance data., • Participate in clinical risk management activities, including hazard identification, risk assessment, risk evaluation, verification of risk control effectiveness, and maintenance of hazard logs., • Collaborate with Clinical Safety Officers, Product Management, R&D, and Customer Support teams to investigate complex clinical safety and product quality issues., • Utilize AI‑enabled tools and data analytics to improve complaint trending, signal detection, root cause analysis, and identification of recurring issues., • Bachelor's degree in Life Sciences, Healthcare, Nursing, Biomedical Engineering, Clinical Laboratory Science, Quality, Regulatory Affairs, Information Technology, or a related discipline., • 4-7 years' experience in Quality, Clinical Safety, Complaint Handling, Post‑Market Surveillance, Regulatory Affairs, or Risk Management within a regulated industry., • Minimum 5 years' experience working with DCB0129 (preferred) and/or DCB0160., • Experience investigating customer complaints, incidents, adverse events, and product quality issues., • Experience applying risk management principles in accordance with ISO 14971 or equivalent risk management frameworks., • Experience with CAPA processes, root cause analysis methodologies, and effectiveness verification activities., • Working knowledge of UK MDR, EU MDR/IVDR, FDA 21 CFR Part 820/QMSR, and ISO 13485., • Experience supporting medical devices, diagnostics, healthcare software, laboratory systems, or Software as a Medical Device (SaMD) products., • Experience with electronic Quality Management Systems (eQMS), complaint management systems, risk management tools, and data analysis platforms., • Experience using AI‑enabled tools to support complaint trending, signal detection, and investigation activities., • Experience with Laboratory Information Systems (LIS) or Laboratory Information Management Systems (LIMS)., • Knowledge of statistical analysis and trend monitoring methodologies., • Experience supporting internal audits, external audits, customer assessments, or regulatory inspections., • Experience across the full product lifecycle, including development, post‑market surveillance, complaint handling, and risk management. This role requires a working knowledge of Artificial Intelligence (AI) technologies and the ability to leverage them to improve processes and outcomes. A core understanding of AI concepts is required and must be able to demonstrate the use of AI tools in a professional setting. Onboarding As part of our onboarding process, all new employees will be required to attend / travel to the office on their first day of employment. This requirement is essential for onboarding activities, including the identity verification, completion of necessary documentation, receiving your IT equipment, introductions to key team members, and orientation to Clinisys policies and procedures. #LI-AD #LI-HYBRID #J-18808-Ljbffr

Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. We partner with leading pharmaceutical, biotechnology, and medical device companies, delivering end-to-end regulatory operations support and regulatory strategy with precision, speed, and global expertise. Job Title: Global Labeling Lead Location : Poland, UK , Romania, Hungary, Croatia, Czech Republic • Appropriately escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products following global labeling communication guidance and proposes risk mitigation., • Strategically develop and cultivate strong relationships among functions represented at the Labeling cross functional teams including clinical, safety, medical affairs, and commercial, to ensure the highest level of communication effectiveness for labeling strategy and content., • Precedent Search and Labeling Trends - Conducts precedent, analyzes relevant competitor labeling, health authority labeling requests for Client products, labeling guidance and trends; and develops strategies and labeling language for assigned product labels (TLP, CCDS, USPI, EU SmPC, others as appropriate) to ensure consistency with the overall product strategy, product claims and information in the CCDS and to ensure that Client products have the most competitive labeling possible; while maintaining awareness of recent in-class approvals., • Working within Labeling Team and GRA - Represents Global Labeling at Global Regulatory Team (GRT) - Liaises with US Labeling Operations, EU Labeling Operations, Labeling Devices Lead and Labeling Compliance to ensure labeling objectives and timelines are met., • Represents global labeling in departmental and cross-functional task-forces and initiatives., • Supports Health Authority Inspections (US, EU, and Global) by providing labeling information requests related to assigned products and overall labeling processes., • Vendor Management - Oversight and accountability for labeling activities managed by external vendor(s) for assigned products, ensuring seamless coordination, timely delivery, and adherence to quality standards., • Continuous Improvement - Actively contributes to the continuous improvement of labeling processes, identifying opportunities for optimization and implementing effective strategies to enhance agility, efficiency and accuracy., • BSc degree, preferred; BA accepted., • Advanced scientific degree (MSc, PhD, or PharmD) preferred., • 8+ years of pharmaceutical industry experience. This is inclusive of 6 years of labeling experience or combination of 5+ years regulatory and/or related experience., • Strategic Thinking - Ability to develop & execute clear and practical regulatory strategies based on regulatory requirements, competitive landscape, key priorities and risk management., • Demonstrates an understanding of core business aspect., • Communication - Ability to effectively collaborate with global cross-functional teams., • Ability to use communication skills to transfer knowledge, convey complex regulatory information in a clear and concise manner in written, verbal and group presentation formats., • Ability to promote regulatory decisions across global cross-functional teams. #J-18808-Ljbffr

Department: IT & Innovation Employment Type: Permanent - Full Time Location: Woking Office Menzies is an equal opportunities employer which means that we recruit, employ, train, pay, and promote regardless of race, religion, national origin, gender, sexual orientation, disability or age. We are building a first-class team and, to do so, we know that we need a diverse mix of talented people doing their best work. If you’re ready to make an impact, lead with purpose, and work in a place where your voice truly matters, keep reading! We have a great opportunity for an IT Security Analyst to join our team in either Woking (Surrey area) or Manchester office. This is an opportunity to support the work of the IT Security Operation team, responding to security alerts from our external SoC, monitoring and investigating alerts from internal security platforms. Seeking improvements to configurations and settings to improve security. Working with the operations and ServiceDesk teams to resolve Security related issues such as staff reported issues and system reported vulnerabilities. You would need to be organised, have a professional curiosity, be used to following processes and enforcing them. Alongside this, you would also need to be able to investigate events and to present findings in a concise and reasoned manner to support their conclusions. You will need to have enough confidence to challenge more senior staff when they are requesting tasks that are contrary to company policies or to inform staff, of all grades, when activities are detected that are contrary to policies. Why Menzies? At Menzies, our culture is our cornerstone. We blend technical excellence with genuine care for our people and clients. With over 1100 colleagues in the UK, we’ve built a culture based on shared values and mutual respect. Here’s why you’ll love working with us: • People First: Our work-life balance isn’t just talk. From agile working to generous leave, we create space for what matters to you and this is why we were recognised as one of the Best Places to Work 2024, 2025 and now also 2026, • Work with Inspiring Clients: You’ll be working with a range of clients so no two days will be the same., • Collaborate Across The Firm: Working with various people across the firm to raise the profile of Menzies Academy, • Innovate with Purpose: We’re always looking for better ways to work—leveraging tech, simplifying complexities, and delivering value., • Empathy at Our Core: We don’t just serve our clients; we build trusted relationships that stand the test of time., • Certified B Corp™: Part of a global community of over 10,000 businesses recognised for meeting high standards of social and environmental responsibility, accountability, and governance., • Perform initial triage and investigation of security incidents., • Monitor security alerts and events from SIEM and other security tools., • Participate in vulnerability management and patching., • Maintain and update security documentation and procedures., • Monitor Sec ops mailbox for alerts and triage them., • Work with the ServiceDesk team to assist with tickets that may be the result of a conflict or misconfiguration in the security stack., • Assist with reviews of vendor platforms and websites for compliance checks., • Assist with client questionaries related to IT Security., • Assist with CASB and web filtering change request reviews., • Assist with administration of security stack applications., • Assist with investigations of incidents logged by the SoC., • Provide cover for Security Manager., • Basic understanding of IT infrastructure components including networks, servers, operating systems, and cloud services., • Familiarity with IT service management principles (ITIL) and incident/problem/change management processes., • Ability to troubleshoot common IT issues and elevate complex problems appropriately., • Understanding of IT security principles, data protection, and access management., • Experience using IT service desk or ticketing systems (e.g., ServiceNow, Jira, or similar)., • Basic knowledge of Microsoft 365 environment including Exchange, Teams, SharePoint, and endpoint management., • Awareness of hardware support, device configuration, and software deployment processes., • Ability to document procedures, incidents, and resolutions clearly., • Strong customer service mindset with the ability to support non-technical users. Why Join Us? At Menzies, we know that success starts with our people. That’s why we offer: • Career Development: From learning opportunities to career coaching, we’ll help you achieve your goals., • Competitive Benefits: Private medical cover, pension matching, and enhanced parental leave, to name a few., • Flexibility That Works for You: Agile working is embedded in our culture., • Perks That Go Beyond: From volunteering days to wellbeing initiatives, we care about your whole self. To find out more about our benefits please read here #J-18808-Ljbffr

Cosmic Equipment UK are a growing company in an exciting high technology area at the forefront of new developments powering the green revolution. Cosmic Equipment UK are a dedicated, engineering-based organisation with the skills to meet the demanding needs of our expanding customer base of global device manufacturers around the world. At our base in the UK, we focus on developing solutions for testing challenging new technologies such as GaN and SiC as well as for the latest generation of mosfets, IGBT’s, diodes, SCR’s and bipolars. We have a track record of investing in our people and work hard to ensure that all our staff are well informed, well trained and well-motivated to be completely responsive to our customer needs. Product development is core to our existence, and we have introduced a significant new product nearly every year since our origins in the early 80's; our Mostrak test system has been through constant cycles of renewal, whilst always retaining compatibility. We operate seamlessly between our Engineering, Manufacture and Test, Customer Support and Technical Sales groups. Our success also lies in investing in and working closely with our external manufacturing base to ensure we are as responsive and nimble as possible whilst drawing on the experience and production efficiency of our family of dedicated CEM partners and OEM manufacturers. Above all, Cosmic Equipment UK is responsive. Reporting to the Production Engineer, the Junior Quality Inspector will support day-to-day quality assurance and inspection activities across Cosmic Equipment UK. The role is responsible for carrying out incoming inspection activities, supporting quality investigations, maintaining quality records and assisting in the continual improvement of the Quality Management System. The role works closely with Manufacturing, Engineering, Test, Support and external suppliers to ensure products, components, materials and processes meet defined quality standards, specifications and customer requirements. The role provides an excellent opportunity to develop practical quality inspection, quality assurance and quality engineering capability within a high-technology manufacturing environment. • Carry out Goods In inspection of incoming materials, components and products against engineering drawings, specifications, purchase orders and acceptance criteria, • Record inspection results accurately and identify, contain and escalation non-conforming materials where required, • Support goods inward activities, inventory management, kitting and order packing where necessary, • Monitor product quality, defect rates, scrap levels and inspection performance, highlighting trends and emerging quality concerns, • Coordinate the segregation, quarantine and administration of non-conforming materials and products, • Support containment activities relating to suspect or defective materials and components, • Assist with Non-Conforming Material management activities and participate in Material Review Board processes where required, • Support root cause investigations using structured problem-solving methodologies, • Assist with corrective and preventive action activities, including action tracking and effectiveness verification, • Support customer quality investigations and complaint resolution activities by gathering data, maintaining records and assisting with investigation activities, • Support supplier quality investigations and supplier corrective action activities by collecting inspection evidence and maintaining quality records, • Conduct routine process compliance checks to verify adherence to documented procedures, work instructions and quality requirements, • Support internal quality audits by preparing records, gathering evidence, recording findings and tracking corrective actions, • Assist with external audit preparation and ensure quality records remain audit ready, • Maintain accurate, organised and traceable quality documentation, records and inspection reports, • Support the administration and maintenance of the ISO 9001 Quality Management System, • Review and update quality documentation, procedures, forms and work instructions as directed, • Assist with updating calibration records for inspection, measurement and test equipment and assist in ensuring calibration activities remain current, • Assist in producing quality KPIs, quality reports and trend analysis to support management reviews and continuous improvement initiatives, • Support continuous improvement projects designed to improve product quality, process capability and operational performance, • Undertake other reasonable duties associated with quality assurance and inspection activities, • Ability to complete Goods In inspection checks, record inspection outcomes accurately and identify defects or non-conforming incoming materials, • Ability to read and interpret engineering drawings, specifications and acceptance criteria, • Understanding of quality records, document control, audit preparation and corrective action processes, • Knowledge of non-conformance management, containment activity and material review processes, • Understanding of calibration control and measurement system management, • Ability to use inspection equipment, including callipers, micrometres, gauges and measuring devices where applicable, • Working knowledge of ISO 9001 and quality management system requirements, • Ability to analyse quality data, identify trends and support practical improvement activity, • Familiarity with Microsoft Excel for quality reporting and trend analysis, • Awareness of quality tools such as 8D, 5 Why analysis, Cause and Effect, FMEA, Control Plans, MSA or Gauge R&R, • Excellent attention to detail and a right-first-time approach, • Structured and organised approach to managing records, priorities and follow-up actions, • Strong verbal and written communication skills, • Analytical and problem-solving mindset, • Strong interpersonal skills with the ability to build positive cross‑functional working relationships, • Confident working collaboratively in an engineering‑led manufacturing environment, • Willingness to learn and develop within quality inspection, quality assurance and quality engineering, • Experience within a manufacturing, engineering, inspection or quality environment, • Experience carrying out inspection, testing, quality checking or quality verification activities, • Experience maintaining quality records, inspection reports or quality documentation, • Strong attention to detail and ability to work accurately with documented requirements, • Good knowledge of Microsoft Office and ability to maintain accurate records and reports, • Previous experience in electronics, semiconductor, high‑technology manufacturing or engineering environment, • Experience supporting internal or external audits, • Experience with non‑conformance management, containment activity or corrective action processes, • Familiarity with structured quality tools, including 8D, 5 Why, FMEA, APQP, MSA, Gauge R&R or Process Control Plans, • ISO 9001 awareness or internal auditor training, • HNC, HND or equivalent qualification in Engineering, Manufacturing, Quality or a related technical discipline, • Experience using quality, compliance or QEHS systems, such as Mango, or reporting tools such as Excel or Power BI, • Lean manufacturing, continuous improvement or root cause analysis training, • This is a full‑time position with competitive salary and excellent benefits., • Comprehensive private medical cover including optical and dental support, giving you complete peace of mind., • 26 days of annual leave plus all UK bank holidays., • Convenient onsite parking for all employees, making your commute simple and stress‑free., • Regular social events, team activities, and company gatherings that help build a supportive, friendly workplace culture., • A competitive pension scheme to support your long‑term financial wellbeing. #J-18808-Ljbffr

Change people’s lives and love what you do! Cochlear develops world-leading medical devices that help people hear and be heard. As a top 100 medical device company and market‑leader in implantable hearing devices, more people choose a Cochlear‑branded cochlear or acoustic implant system than any other. Our employees tell us that the number one reason they enjoy working for Cochlear is the opportunity to make a difference to people’s lives. • Develop local business and brand plans for the Connected Care portfolio, aligned with country and EMEA priorities and informed by customer, partner and market insights, • Lead the introduction and lifecycle management of new products and services across the UK and Ireland, including pilots, controlled market releases and ongoing portfolio updates, • Develop go-to-market strategies covering pricing, positioning, messaging and launch plans in collaboration with local and EMEA teams, • Provide local market input into early-stage development and build evidence-based business cases for new service technologies and portfolio opportunities, • Act as the local subject matter expert for Connected Care solutions, providing product knowledge, training and current communication materials to internal and external stakeholders, • Generate market and competitor insight to strengthen digital product positioning, customer communications and objection handling, • Partner with Customer Experience, Implementation and Sales teams to improve clinic pathways, support sustainable adoption, customer visits and tender submissions, • Set and monitor performance measures that support adoption, clinic capacity and growth, while managing projects, budgets and stakeholders across a global matrix organisation, • Spend approximately 70% of your time supporting in-country activities and 30% supporting EMEA priorities., • You combine strong commercial awareness with a clear understanding of customer needs and can assess investment opportunities to maximise outcomes, • You are a confident Product Manager who can translate strategy into practical plans and successful delivery, • You build strong relationships across functions and are comfortable influencing stakeholders in local, regional and global teams, • You can manage multiple projects, priorities and product groups while maintaining attention to quality, timelines and budget, • You communicate complex information clearly and are confident delivering presentations, training and product guidance, • You bring a creative, proactive and solutions-focused mindset, with the agility to respond to changing market needs, • Approximately 3-5 years of marketing experience, ideally within medical devices, • Proven Product Management experience within a global matrix organisation, • Experience developing processes and supporting change management, • Strong commercial, analytical, project management and stakeholder management skills, • Excellent written and verbal communication and presentation skills, • Strong Microsoft Office skills; experience with CRM platforms such as Salesforce and ERP systems is desirable, • Bachelor's degree or equivalent in Marketing, Life Sciences or a related field, • Fluent English, • Knowledge or experience of audiology, hearing implants or the wider hearing care environment, • Experience within healthcare and an understanding of issues associated with hearing loss, • Experience with Software as a Service (SaaS), connected health, digital health products or managed services, • Experience supporting regulatory or reimbursement considerations relevant to a healthcare product portfolio For 40 years, Cochlear has been creating reliable products that continue to keep people connected to the world and to each other. We help people of all ages to hear in more than 180 countries around the world. Our technology connects people to life's possibilities and to the people who matter most. We have over 4000 employees globally dedicated to improving people's lives. To date, we have Invested over $2billion AUD in research and development. • Competitive salary, • 25 days holidays (plus UK Bank Holidays), • company pension, • flexible working patterns and the possibility to work remotely up to 40% per week yearly salary review, • Pension scheme, • Group Life Insurance, • Group Income Protection, • Employee Referral Bonus, • Service Anniversary Reward, • Cycle to work scheme Cochlear is committed to providing equal opportunities to avoid unlawful discrimination on the grounds of race, sex, disability, sexual orientation, religion/belief or age. In line with our corporate ethics and statutory obligations we strive to ensure that the work environment is free of harassment and bullying and that everyone is treated with dignity and respect - this is an important aspect of ensuring equal opportunities in employment. We are the global leader in implantable hearing solutions. We have provided more than 600,000 implantable devices, helping people of all ages to lead full and active lives. We help people hear and be heard. We empower people to connect with others and live a full life. We help transform the way people understand and treat hearing loss. We innovate and bring to market a range of implantable hearing solutions that deliver a lifetime of hearing outcomes. #J-18808-Ljbffr

Linux Configuration, Integration & Test (CIT) Engineer Location: Guildford, Surrey GU1 4QU Salary: Circa £50k £85k depending on experience plus benefits and bonus Contract: Full time, Permanent Benefits: Annual bonus, Private medical insurance, 8% employer pension contribution, Relocation assistance, Annual salary and development appraisal and 25 days annual leave + all bank holidays! Kaon is a small, dynamic company located in Guildford, Surrey. We are an industry leading organisation providing solutions for the defence sector, specialising in cutting edge bespoke sonar processing systems, including: DSP and image processing systems; high data rate networks and high-rate data recorders. Our size makes us dynamic and flexible and we maintain an open attitude to embracing emerging technologies. Our size also means we have a fast development cycle from early research and initial concepts through to implementation and deployment in real-world situations. We work closely with our customers and the technology we develop is designed to fit their specific needs. We take pride in our products and Kaon s success is a result of the skills and effort of our engineering team which is made up of signal processing, acoustic, software and systems engineers. Due to our continued success, we are looking to expand our highly skilled engineering team. We are seeking a Linux Configuration, Integration & Test (CIT) Engineer to support the development and delivery of Linux-based embedded systems. Acting as a technical specialist who bridges the gap between software development, hardware/embedded platforms, and system deployment. You will configure, merge, and validate Linux-based operating systems, kernels, drivers, and application stacks to ensure everything works reliably on target hardware and pay meticulous attention to testing and validation. Working as part of the engineering team, you will help deliver recording systems and advanced sonar solutions for deployment on Royal Navy ships and submarines. At Kaon, you'll have the opportunity to work across the full product lifecycle, from proposals and customer engagement through to system design, implementation, testing, delivery and in-service support within the UK and overseas. This role is ideal for someone with strong Linux expertise and an interest in hardware, looking to apply their skills across the development, production and testing of specialist embedded systems. This role will include: • Responsibility for configuration, integration and testing of real-time systems and software components;, • Installing optimising and testing Kaon bespoke software onto embedded Linux systems;, • Working within the Kaon Linux DevOps environment to integrate optimal setting configurations;, • Network configuration and optimisation and testing;, • Linux device driver installation, optimisation and testing;, • Linux kernel configuration, compilation, optimisation and testing;, • Configuring operating systems for security and optimal network and resource performance;, • Providing support and basic training to systems in the field;, • Assembling and configuring systems utilising server grade hardware;, • Undertaking testing, acceptance and accreditation processes on production systems;, • Coordinating with software engineers to specify operating system requirements and create OS images;, • Specifying hardware requirements and identifying suitable hardware components; Please note that due to the nature of Kaon s work this post is office-based and only open to UK Nationals who are willing and able to satisfy UK Government / MoD security vetting procedures. In order to be successful in this role you must have: • At least 8 years of experience working with Linux systems;, • In depth knowledge and familiarity with the Linux operating system and adept in its usage;, • Linux shell script development;, • Understanding of programming with C/C++;, • Understanding of programming python;, • Experience and interest in working with server grade hardware;, • Linux command line for OS and network configuration, resource optimisation and software installation;, • Understanding of Linux device drivers;, • Understanding of Linux security and configuration;, • Familiarity of the differences between Debian and Red Hat based distributions, • Understanding of common networking protocols;, • Appropriate higher or further education technical qualification in computer systems. Any of the following additional skills would be advantageous: Network design; Managed switch configuration; Knowledge and experience of kernel compilation; Experience in High Performance Computing HPC or NUMA architectures; Familiarity with IP multicast; Linux and IP security settings and configuration; Network qualifications, e.g. CCNA; Understanding of hardware level aspects associated with controlling and writing/using Linux driver interfaces; No agencies please. #J-18808-Ljbffr

Job title – Support Engineer Cosmic Equipment UK are a growing company in an exciting high technology area at the forefront of new developments powering the green revolution. Cosmic Equipment UK are a dedicated, engineering-based organisation with the skills to meet the demanding needs of our expanding customer base of global device manufacturers around the world. At our base in the UK, we focus on developing solutions for testing challenging new technologies such as GaN and SiC as well as for the latest generation of MOSFETs, IGBTs, diodes, SCRs and bipolar devices. We have a track record of investing in our people and work hard to ensure that all our staff are well informed, well trained and well motivated to be completely responsive to our customer needs. Product development is core to our existence, and we have introduced a significant new product nearly every year since our origins in the early 1980s. Our Mostrak test system has been through constant cycles of renewal, whilst always retaining compatibility. We operate seamlessly between our Engineering, Manufacture and Test, Customer Support and Technical Sales groups. Our success also lies in investing in and working closely with our external manufacturing base to ensure we are as responsive and nimble as possible whilst drawing on the experience and production efficiency of our family of dedicated CEM partners and OEM manufacturers. Above all, Cosmic Equipment UK is responsive. Reporting within the Customer Support function, the Support Engineer will install, commission, maintain and support Cosmic Equipment UK products at our Guildford facility and at customer sites worldwide. The role provides technical support through online meetings, telephone and email, as well as practical fault finding, repair and product training. The role works closely with customers and colleagues across Engineering, Manufacture and Test, Technical Sales and Customer Support to resolve technical issues, maintain accurate support documentation and communicate customer feedback that contributes to product and service improvement. The position is based in Guildford and requires regular international travel, including travel to Europe, North America, North Africa and Asia, occasionally at short notice. • Travel to customer sites worldwide to perform system installation, commissioning, set-to-work, repairs and planned or reactive maintenance, • Provide responsive technical support to customers through online meetings, telephone and email, • Diagnose faults and repair complex electronic circuits to component level, including through-hole and surface-mount devices, using circuit diagrams and schematics, • Use electronic test equipment, including oscilloscopes and digital voltmeters, safely and effectively during diagnostic and repair activities, • Investigate customer-reported issues, document findings and communicate clear recommendations or next steps, • Work with the Technical Author to maintain customer and support documentation, including manuals, guides, FAQs and troubleshooting notes, • Deliver product and system training to customers and colleagues, • Gather, record and communicate customer feedback to relevant internal teams to support product and service improvement, • Maintain accurate service, installation, repair and customer-support records, • Coordinate effectively with Engineering, Manufacture and Test, Technical Sales and other colleagues to resolve technical issues, • Follow applicable health and safety, quality, customer-site and company procedures when working in the UK and overseas, • Support continuous improvement activities relating to product reliability, serviceability, documentation and customer experience, • Undertake other reasonable duties associated with customer and product support activities, • Ability to diagnose and repair complex electronic circuits to component level using circuit diagrams and schematics, • Practical experience repairing both through-hole and surface-mount components, • Competence using electronic test equipment, including oscilloscopes and digital voltmeters, • Ability to install, commission, set to work, maintain and repair electronic systems, • Understanding of electrical and electronic engineering principles, • Ability to analyse technical information, identify root causes and develop practical solutions, • Ability to produce and maintain clear technical and service documentation, • Confidence delivering technical product training to customers and colleagues, • Good working knowledge of Microsoft Office and online meeting tools, • Excellent written and verbal communication skills, with the ability to explain technical information clearly, • Strong customer focus and a professional approach when representing Cosmic Equipment UK, • Structured and organised approach to managing support issues, priorities, travel and follow-up actions, • Ability to work independently and use sound judgement when supporting customers on site, • Strong analytical, fault-finding and problem-solving mindset, • Collaborative approach and ability to build positive working relationships across functions and cultures, • Adaptability, resilience and willingness to travel internationally, occasionally at short notice, • Commitment to continuous learning and product knowledge development, • Degree in Electronics or Electrical Engineering, or equivalent relevant technical experience, • Practical experience of component-level electronic fault finding and repair, • Experience repairing through-hole and surface-mount electronic assemblies, • Experience using circuit diagrams, schematics and electronic test equipment, • Experience managing technical support issues independently and communicating effectively with customers, • Willingness and ability to travel internationally as required, • Experience installing, commissioning, maintaining or supporting complex electronic test systems at customer sites, • Experience with power-conversion topologies, including inverters, DC-DC converters or power factor correction, • Knowledge of IGBT, SiC or GaN devices and high-voltage systems, • Experience using Linux operating systems, • Background in renewable energy, electric vehicle charging or industrial drives, • Experience delivering technical training or producing customer-facing technical documentation, • Project management or team-leadership experience, • This is a full-time position with competitive salary and excellent benefits., • Comprehensive private medical cover including optical and dental support, giving you complete peace of mind., • 26 days of annual leave plus all UK bank holidays., • Convenient onsite parking for all employees, making your commute simple and stress-free., • Regular social events, team activities and company gatherings that help build a supportive, friendly workplace culture., • A competitive pension scheme to support your long-term financial wellbeing., • International travel and the opportunity to work directly with customers and colleagues across global locations., • Work as part of a close-knit, collaborative team, supporting one another to achieve shared goals., • A culture of learning and development in a fast-evolving industry., • A wide variety of day-to-day activities. #J-18808-Ljbffr

Cosmic Equipment UK are a growing company in an exciting high technology area at the forefront of new developments powering the green revolution. Cosmic Equipment UK are a dedicated, engineering-based organisation with the skills to meet the demanding needs of our expanding customer base of global device manufacturers around the world. At our base in the UK, we focus on developing solutions for testing challenging new technologies such as GaN and SiC as well as for the latest generation of mosfets, IGBT’s, diodes, SCR’s and bipolars. We have a track record of investing in our people and work hard to ensure that all our staff are well informed, well trained and well-motivated to be completely responsive to our customer needs. Product development is core to our existence, and we have introduced a significant new product nearly every year since our origins in the early 80's; our Mostrak test system has been through constant cycles of renewal, whilst always retaining compatibility. We operate seamlessly between our Engineering, Manufacture and Test, Customer Support and Technical Sales groups. Our success also lies in investing in and working closely with our external manufacturing base to ensure we are as responsive and nimble as possible whilst drawing on the experience and production efficiency of our family of dedicated CEM partners and OEM manufacturers. Above all, Cosmic Equipment UK is responsive. Reporting to the Production Engineer, the Junior Quality Inspector will support day-to-day quality assurance and inspection activities across Cosmic Equipment UK. The role is responsible for carrying out incoming inspection activities, supporting quality investigations, maintaining quality records and assisting in the continual improvement of the Quality Management System. The role works closely with Manufacturing, Engineering, Test, Support and external suppliers to ensure products, components, materials and processes meet defined quality standards, specifications and customer requirements. The role provides an excellent opportunity to develop practical quality inspection, quality assurance and quality engineering capability within a high-technology manufacturing environment. • Carry out Goods In inspection of incoming materials, components and products against engineering drawings, specifications, purchase orders and acceptance criteria, • Record inspection results accurately and identify, contain and escalate non-conforming materials where required, • Support goods inward activities, inventory management, kitting and order packing where necessary, • Monitor product quality, defect rates, scrap levels and inspection performance, highlighting trends and emerging quality concerns, • Coordinate the segregation, quarantine and administration of non-conforming materials and products, • Support containment activities relating to suspect or defective materials and components, • Assist with Non-Conforming Material management activities and participate in Material Review Board processes where required, • Support root cause investigations using structured problem-solving methodologies, • Assist with corrective and preventive action activities, including action tracking and effectiveness verification, • Support customer quality investigations and complaint resolution activities by gathering data, maintaining records and assisting with investigation activities, • Support supplier quality investigations and supplier corrective action activities by collecting inspection evidence and maintaining quality records, • Conduct routine process compliance checks to verify adherence to documented procedures, work instructions and quality requirements, • Support internal quality audits by preparing records, gathering evidence, recording findings and tracking corrective actions, • Assist with external audit preparation and ensure quality records remain audit ready, • Maintain accurate, organised and traceable quality documentation, records and inspection reports, • Support the administration and maintenance of the ISO 9001 Quality Management System, • Review and update quality documentation, procedures, forms and work instructions as directed, • Assist with updating calibration records for inspection, measurement and test equipment and assist in ensuring calibration activities remain current, • Assist in producing quality KPIs, quality reports and trend analysis to support management reviews and continuous improvement initiatives, • Support continuous improvement projects designed to improve product quality, process capability and operational performance, • Undertake other reasonable duties associated with quality assurance and inspection activities, • Ability to complete Goods In inspection checks, record inspection outcomes accurately and identify defects or non-conforming incoming materials, • Ability to read and interpret engineering drawings, specifications and acceptance criteria, • Understanding of quality records, document control, audit preparation and corrective action processes, • Knowledge of non-conformance management, containment activity and material review processes, • Understanding of calibration control and measurement system management, • Ability to use inspection equipment, including callipers, micrometres, gauges and measuring devices where applicable, • Working knowledge of ISO 9001 and quality management system requirements, • Ability to analyse quality data, identify trends and support practical improvement activity, • Familiarity with Microsoft Excel for quality reporting and trend analysis, • Awareness of quality tools such as 8D, 5 Why analysis, Cause and Effect, FMEA, Control Plans, MSA or Gauge R&R, • Excellent attention to detail and a right-first-time approach, • Structured and organised approach to managing records, priorities and follow-up actions, • Strong verbal and written communication skills, • Analytical and problem-solving mindset, • Strong interpersonal skills with the ability to build positive cross-functional working relationships, • Confident working collaboratively in an engineering-led manufacturing environment, • Willingness to learn and develop within quality inspection, quality assurance and quality engineering, • Experience within a manufacturing, engineering, inspection or quality environment, • Experience carrying out inspection, testing, quality checking or quality verification activities, • Experience maintaining quality records, inspection reports or quality documentation, • Strong attention to detail and ability to work accurately with documented requirements, • Good knowledge of Microsoft Office and ability to maintain accurate records and reports, • Previous experience in electronics, semiconductor, high-technology manufacturing or engineering environment, • Experience supporting internal or external audits, • Experience with non-conformance management, containment activity or corrective action processes, • Familiarity with structured quality tools, including 8D, 5 Why, FMEA, APQP, MSA, Gauge R&R or Process Control Plans, • ISO 9001 awareness or internal auditor training, • HNC, HND or equivalent qualification in Engineering, Manufacturing, Quality or a related technical discipline, • Experience using quality, compliance or QEHS systems, such as Mango, or reporting tools such as Excel or Power BI, • Lean manufacturing, continuous improvement or root cause analysis training, • This is a full-time position with competitive salary and excellent benefits., • Comprehensive private medical cover including optical and dental support, giving you complete peace of mind., • 26 days of annual leave plus all UK bank holidays., • Convenient onsite parking for all employees, making your commute simple and stress-free., • Regular social events, team activities, and company gatherings that help build a supportive, friendly workplace culture., • A competitive pension scheme to support your long-term financial wellbeing. #J-18808-Ljbffr

• Workshop based - Unit 10, Epsom Downs Metro Centre, Waterfield, Tadworth, Surrey, KT20 5LR, • 35 hours per week (09.00 - 17.00 Monday to Friday), • £40,935 per annum, • 29 days' annual leave days (plus Bank Holidays), • Pension - matched company contribution up to 6%, • Company sick pay The Opportunity The Quality Assurance Engineer is responsible for the technical leadership, quality management, and regulatory compliance of all products manufactured, refurbished and supported by the Tadworth operation. Please note, this role involves working with medical certificated devices. Therefore, candidates will need to have demonstrable experience in working with such devices. This role will lead the safe and effective delivery of the Bugzi powered wheelchair loan service whilst also providing technical oversight across the wider product portfolio. This includes responsibility for product compliance, quality systems, production support, technical problem solving, product improvement, and workshop operations. The role combines technical leadership with practical hands-on engineering and manufacturing responsibilities. Purpose of the Role The Quality Assurance Engineer is responsible for the technical leadership, quality management, and regulatory compliance of all products manufactured, refurbished and supported by the Tadworth operation. This role will lead the safe and effective delivery of the Bugzi powered wheelchair loan service whilst also providing technical oversight across the wider product portfolio. This includes responsibility for product compliance, quality systems, production support, technical problem solving, product improvement, and workshop operations. Working closely with operational and service colleagues, the postholder will ensure products are manufactured, refurbished and maintained to the required standards, whilst identifying opportunities to improve product performance, reliability, sustainability and impact for the families Cerebra supports. The role combines technical leadership with practical hands-on engineering and manufacturing responsibilities. The postholder will be expected to actively participate in the manufacture, refurbishment, modification, testing and validation of products, whilst also leading quality, compliance, and continuous improvement activities. Key Areas of Responsibility 1. Technical Leadership • Act as the technical lead and engineering authority for all products manufactured, refurbished and supported by the Tadworth operation., • Provide day-to-day technical guidance, problem-solving, and decision-making support to workshop and operational staff., • Maintain oversight of technical documentation, specifications, product records, and engineering change activities., • Liaise with suppliers, manufacturers, and external technical partners to support service delivery and product development., • Contribute technical expertise to strategic planning, service improvement, and the introduction of new products, technologies and manufacturing processes. 2.Quality and Medical Device Compliance • Lead the implementation, maintenance, and continuous improvement of the Quality Management System (QMS)., • Ensure products are manufactured, refurbished, and maintained in accordance with applicable quality procedures, medical device regulations and relevant standards., • Maintain technical files, risk assessments, compliance documentation, and product records., • Lead investigations into complaints, incidents, non-conformances and corrective actions, ensuring lessons learned are implemented., • Act as the lead for audits, regulatory compliance, and quality-related activities across the service. 3.Refurbishment, Production & Workshop Operations • Lead and actively participate in the manufacture, refurbishment, servicing, modification, testing and validation of Bugzi wheelchairs and other products supported by the Tadworth operation., • Coordinate workshop activities, production planning and resource allocation to ensure products are delivered safely, efficiently and to the required quality standards., • Act as the senior technical resource within the workshop, providing practical support, fault diagnosis and technical sign-off where required., • Manage workshop equipment, tooling, materials and technical suppliers to support service delivery., • Lead, line manage and develop workshop technical staff, ensuring work is delivered safely, efficiently and to the required quality standards. 4.Product Support and Continuous Improvement • Lead field issue investigations, monitor product performance, and identify opportunities to improve safety, reliability, usability, and manufacturability., • Capture learning from service delivery, refurbishment activities, and family feedback to inform future product development., • Work closely with the Cerebra Innovation Centre (CIC) Design Team to identify, evaluate and implement product improvements, ensuring operational experience and technical learning are incorporated into future designs., • Evaluate and support the introduction of new products, technologies, materials and manufacturing processes., • Contribute to the ongoing development of Bugzi and the wider product portfolio. 5.Team Leadership and Service Development • Lead, line manage and develop workshop technical staff, ensuring work is delivered safely, efficiently and to the required quality standards., • Provide day-to-day leadership, coaching, performance management and technical support to team members, fostering a positive, collaborative and safety-focused working environment., • Support the recruitment, induction, training and ongoing professional development of technical staff, volunteers and students where appropriate., • Work collaboratively across Cerebra to support service delivery, continuous improvement activities, service planning, reporting and organisational objectives., • Maintain professional knowledge through continuing professional development and undertake additional duties appropriate to the role, acting at all times in accordance with Cerebra's policies, procedures and values. Person Specification Essential Criteria • Degree in Product Design Engineering, Mechanical Engineering, Product Design or a related engineering/technical discipline, or equivalent relevant industry experience, • Experience working with Class I Medical Devices, assistive technology, powered mobility products or rehabilitation engineering services, • Experience working in a technical, engineering, manufacturing or product development role, including responsibility for delivering projects independently, • Experience of hands-on product manufacture, assembly, refurbishment, testing, fault finding or workshop-based engineering activities, • Strong understanding of engineering principles, materials, manufacturing processes and technical documentation, including the ability to interpret technical drawings and specifications, • Experience working within a Quality Management System (QMS), maintaining technical documentation and supporting quality and compliance activities, • Knowledge and understanding of medical device regulations, standards, risk management and product compliance requirements, • Experience investigating technical issues, carrying out root cause analysis and implementing corrective actions, • Experience coordinating production, refurbishment or technical service activities and supporting others through technical leadership or supervision, • Excellent project management, organisational, communication and IT skills, with the ability to prioritise workload and meet deadlines, • Ability to work collaboratively within multidisciplinary teams and communicate effectively with technical and non-technical stakeholders, • Practical, proactive and hands-on approach, with a commitment to continuous improvement, quality and safety, • Willingness to undertake practical workshop activities as a significant part of the role, • Experience of line management, supervision or mentoring of technical, manufacturing or workshop-based staff Desirable Criteria • Experience of quality auditing, ISO 9001, 13485, or similar, supplier management, line management or regulated manufacturing environments, • Experience of CAD, rapid prototyping, product development and collaboration with design and innovation teams Personal Attributes • Strong problem-solving skills and sound technical judgement., • Ability to motivate, develop and support others to achieve high standards of performance and quality., • Confident leading small teams and managing competing priorities in a practical working environment., • Flexible and adaptable approach within a developing service., • Committed to Cerebra's values and improving outcomes for children and families. JBRP1_UKTJ

Territory: South West & Wales Company Overview Our client is a global leader in hearing healthcare and medical technology, with an established international presence and a strong reputation for innovation, clinical excellence and customer-focused solutions. The organisation works closely with healthcare professionals across the NHS and private healthcare sectors, providing specialist medical solutions designed to improve patient outcomes and access to care. Our clients are looking to appoint a commercially driven Regional Account Manager to develop customer relationships and drive growth across an assigned territory. Role Overview Working across an assigned territory, you will be responsible for driving sales growth, developing new and existing accounts, identifying commercial opportunities and building strong relationships with healthcare professionals. You will work closely with clinical and commercial stakeholders across the NHS and private healthcare sectors, providing product, clinical and technical support while identifying opportunities to develop the territory and improve patient pathways. The portfolio includes hearing implants and you will be selling to surgeons, audiologists, nurses and administrative teams. Key Responsibilities • Manage and develop an assigned territory, delivering agreed sales and growth targets., • Develop new accounts and maximise opportunities within existing customers., • Build strong relationships with clinical and non-clinical healthcare professionals., • Identify new business opportunities and develop effective account plans., • Develop referral networks and identify opportunities to improve patient pathways., • Provide product, clinical and technical support and training to customers., • Support relevant procedures, customer events, exhibitions and product launches., • Monitor sales activity, market developments and competitor activity., • Maintain accurate CRM records and provide regular performance reporting., • Work closely with internal teams to deliver excellent customer service., • Share customer feedback and market intelligence to support wider commercial strategy., • Identify emerging customer needs and opportunities for sustainable business growth. Person Specification The ideal candidate will have: • Experience in medical device, healthcare or B2B technical sales., • A proven track record of achieving commercial targets., • Strong account management and business development skills., • Experience working with NHS or healthcare organisations., • Excellent communication, influencing and relationship-building skills., • A proactive, commercially driven and customer-focused approach., • Experience in ENT, Audiology or medical devices would be advantageous. JBRP1_UKTJ

CDMO and Vendor - Delivering recruitment solutions across the UK and Europe. Operations Manager Location: Woking, Surrey Employment Type: Full-time, Site-Based Industry: GMP Pharmaceutical / Medical Device / Healthcare About the Role: We are seeking a highly experienced and driven Operations Manager to lead operations at a Woking pharmaceutical production site. This is a fully site-based role, ideal for a strategic leader with a strong engineering understanding and proven management experience in a GMP-regulated environment - whether pharmaceutical, medical device, or healthcare. • Oversee day-to-day site operations, ensuring compliance with GMP standards., • Direct line management of the Production Manager and Quality Control Manager., • Indirect leadership of a wider cross-functional team of around 30 site-based staff across production, quality, and engineering., • Drive operational excellence, continuous improvement, and site performance., • Collaborate with senior leadership to align site goals with broader business objectives., • Ensure robust engineering practices are embedded across the site., • Demonstrated leadership experience in a GMP-regulated setting., • Background in pharmaceutical, medical device, or healthcare manufacturing., • Strong understanding of engineering principles and their application in a regulated production environment., • Proven ability to manage and develop teams, both directly and indirectly., • Excellent communication, problem-solving, and decision-making skills., • Comfortable working in a fully site-based role., • Competitive salary and benefits package., • Opportunity to lead a high-performing team in a dynamic and growing organisation., • A collaborative and quality-focused work environment. Site manager, management, general manager, engineering, operations, operational, GMP, good manufacturing practice, production, project, validation, SOP, ISO, healthcare, pharma, pharmaceutical, medical device. #J-18808-Ljbffr

A leading recruitment firm in the UK seeks an experienced Operations Manager to lead operations at a Woking pharmaceutical production site. The ideal candidate will have a strong background in GMP-regulated environments, exceptional leadership skills, and a solid understanding of engineering principles. This is a site-based role promising a competitive salary and benefits, with opportunities for professional growth in a dynamic organisation. #J-18808-Ljbffr

Manage NHS and private hospital accounts for medical devices, focusing on sales strategy, relationship building, and achieving targets. Requires experience in medical device sales and NHS engagement.