Trabajos international business degree en CambridgeCrear alertas

Ecologist, Senior Ecologist, Environmental Planning, UK, COR7459The RoleThis is an excellent opportunity for an Ecologist / Senior Ecologist to join a growing environmental planning team within a well-established sustainability and environmental consultancy. The Senior Ecologist will take ownership of ecological inputs on a range of development and infrastructure projects, managing surveys, advising clients, and planning teams, and delivering high-quality ecological reporting.The CompanyThe Senior Ecologist will join a respected, international environmental and sustainability consultancy operating across the UK and globally. Despite its global reach, the business maintains a close-knit and collaborative team culture, with strong support for professional development and progression. The role sits within a growing UK environmental planning team, offering the chance to help shape services as the team expands.BenefitsGenerous holiday allowance plus bank holidaysPension schemeOngoing professional development and support toward higher professional membershipWhat's Required?The ideal candidate for the Senior Ecologist role will have some of the following:A degree in ecology or a related subject, or equivalent professional experienceExperience working as an ecological consultantAssociate CIEEM membership or working toward thisStrong ecological field skills across habitats and legally protected speciesA Natural England survey licence (Level 1 or above)A full UK driving licence and willingness to travel to sitesThe list above is important, but not as important as hiring the right person! So if you don't meet all of the criteria but feel this role could be a good fit, please apply or get in touch to discuss further.So What's Next?If you are a Senior Ecologist or an experienced Ecological Consultant looking to take the next step in your career within a growing and supportive environmental planning team, apply now for immediate consideration.Ecologist, Senior Ecologist, Environmental Planning, UKCorriculo Ltd acts as an employment agency and an employment business. #INDSCI #ChannelC #MRTPBN1_UKTJ

\n Introduction to role:\n Are you ready to harness AI to accelerate cell therapy trials and improve outcomes for people facing cancer and immune-mediated disease? AstraZeneca is building a world-class capability in AI for Clinical Development to transform how we design, run and analyze trials across our pipeline. As Director, Cell Therapy AI Business Partner, you will be the senior scientific and business link between our enterprise cell therapy leaders and the AI for Clinical Development team, turning unmet needs into a clear, high-value portfolio of AI solutions that deliver measurable impact. \n Based in Cambridge, UK, you will sit between clinical and scientific experts in cell therapy and AI scientists and engineers. You will frame rigorous clinical questions, shape them into tractable AI problems, guide development and validation, and drive adoption so solutions are trusted at the point of decision. In a fast-moving field, you will bring clarity, build credibility with senior stakeholders, demonstrate value early and scale what works. \n Do you thrive where cutting-edge science meets machine intelligence and enjoy leading through ambiguity to deliver evidence that changes decisions? This is your chance to shape the roadmap for AI in cell therapy clinical development across a diverse enterprise portfolio. Accountabilities:\n Demand shaping, prioritization, and value: Provide scientific leadership to identify and scope the highest-value clinical development questions in cell therapy that AI can address; translate function needs into a prioritized pipeline; build business cases with success metrics; track adoption and benefits after delivery; champion change so solutions are used in practice; guide buy-versus-build and vendor evaluations for cell therapy use cases. \n Strategy and forward look: Align cell therapy-focused AI efforts with the broader AI for Clinical Development portfolio; anticipate scientific and clinical nuances unique to cell therapy that shape design and validation; monitor the state of the art and co-create the forward roadmap; identify methodological requirements, evidence gaps and advocacy opportunities to safely advance clinical AI. \n Business partnering and relationship management: Serve as the primary, trusted partner between AI for Clinical Development and the enterprise cell therapy organization spanning hematology, oncology, autoimmune and rare diseases; act as a core member of cell therapy project teams while coordinating with AI delivery functions; develop a deep understanding of priorities, workflows and decision points; represent the voice of cell therapy to AI teams and the capabilities and constraints of AI to clinical teams; build credibility with senior leaders and provide structured decision support when priorities compete. \n Data, standards, and validation: Bring the clinical and scientific context—endpoints, reference standards and constraints—that AI teams need; work side by side with AI scientists and engineers from scoping through development, evaluation and clinical validation; define and guide clinical and scientific validation against the right reference standards to meet the evidentiary bar required in clinical development. Essential Skills/Experience:\n \n • \n Master’s degree in AI/ML with experience applying these methods to clinical and/or biomedical data. We welcome strong candidates from adjacent computational or scientific fields whose expertise maps to the role. \n • \n 5+ years experience developing AI/ML for clinical, biomedical, healthcare, or other life-sciences problems. \n • \n Applicable experience in drug development, clinical development, or the life sciences, sufficient to engage credibly with clinical and scientific teams. \n • \n Experience with the clinical and scientific validation of AI, predictive, or digital tools in a clinical or healthcare context. \n • \n Familiarity with generative AI and agentic systems applied to clinical development or the life sciences. \n • \n Demonstrated ability to define and frame scientific or clinical questions and to bridge between clinical, scientific, and technical teams. \n • \n Demonstrated partnering and stakeholder-management ability, including building credibility with and influencing senior clinical and scientific leaders. \n • \n Excellent grasp of how AI solutions are evaluated and validated, and what it takes for an AI solution to be trusted and adopted in a clinical development setting. \n • \n Excellent interpersonal, verbal, and written communication skills, with the ability to operate in an international matrix environment and bring structure and clarity to ambiguous problems. \n • \n Comfort with ambiguity and a bias for action in a fast-moving, build-from-the-ground-up environment. \n Desirable Skills/Experience:\n \n • \n Scientific or clinical experience in cell therapy (e.g., CAR-T and other engineered cell therapies). \n • \n Hands-on experience designing or running cell therapy clinical trials. \n • \n Familiarity with cell therapy-specific endpoints and measurements. \n • \n A record of scientific contribution (e.g., peer-reviewed publications), ideally including AI/ML or clinical AI venues, that establishes credibility with technical, clinical, and scientific audiences. \n \n When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Why AstraZeneca:\n Join a company where scientific curiosity meets purposeful delivery. You will collaborate with clinicians, data scientists and engineers who turn experiments into enterprise-grade solutions that reach global trials and, ultimately, patients. With a deep, innovative pipeline and sustained investment in R&D, we back teams to push scientific boundaries, publish at the highest levels and translate insights into medicines that change the practice of medicine. We bring diverse experts together to move fast and learn faster, and we value kindness alongside ambition so you can do your best work while contributing to a bold mission. Date Posted\n 23-Jul-2026 Closing Date\n 30-Jul-2026 \n Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form. \n #J-18808-Ljbffr

\n Qureight’s mission is to accelerate clinical trials and ensure breakthroughs in lung and heart disease reach patients without delay. Our AI-powered data and imaging curation platform enables the analysis of clinical imaging and other healthcare data, helping our customers bring treatments to market, faster. \n We’re looking for talented people who want their work to matter. With offices in Cambridge and London, you’ll join our multidisciplinary team of clinicians, scientists, and engineers. What unites us is our open culture, continuous learning mindset, and a shared mission to help biopharma run faster, smarter trials. About the role\n Qureight is seeking a visionary, transformational leader to serve as our Head of Quality Assurance and Regulatory Affairs. This role is pivotal in shaping the future of our clinical imaging and AI-enabled services, ensuring that our quality systems, processes, and regulatory strategies not only meet but exceed the highest standards of compliance and operational excellence. \n As the organisation’s strategic and operational lead for all quality and regulatory matters, you will drive innovation, compliance, and transformation across Qureight. Your expertise will ensure that our clinical trial activities, SaMD/AIaMD clearances, biomarker validations, and interactions with regulatory authorities are executed with precision, integrity, and a forward-thinking approach. \n You will act as the go-to subject-matter expert for all aspects of software regulation, including ISO 62304, ISO 82304, ISO 14971, ISO 34971, ISO 13485, ISO 27001, and AI-specific guidance such as ISO 42001. Your leadership will embed a culture of quality, efficiency, and continuous improvement, enabling Qureight to maintain its reputation as a leader in imaging core lab services and AI-driven clinical solutions. \n This role demands a proactive, results-driven individual who can balance rigorous compliance with pragmatism, speed, and operational excellence. If you are passionate about revolutionising quality processes, leading regulatory strategy, and shaping the future of AI in clinical trials, we want to hear from you. Key Responsibilities Regulatory Leadership & Strategy\n \n • Lead the development and execution of Qureight’s regulatory strategy, ensuring alignment with global standards and business objectives.\n, • Drive regulatory submissions and clearances for SaMD, AIaMD, and biomarker validations, acting as the primary liaison with regulatory authorities (e.g., FDA, MHRA, etc) and notified bodies.\n, • Design and execute Qureight’s digital biomarker validation strategy in the US and EU markets.\n, • Provide expert guidance on software regulation, including ISO 62304, ISO 82304, ISO 14971, ISO 34971, ISO 13485, ISO 27001, and ISO 42001, ensuring all systems and processes are compliant.\n, • Stay ahead of emerging regulations and AI guidance, proactively adapting Qureight’s strategies to maintain a competitive edge.\n Quality Transformation & Compliance\n \n, • Revolutionise Qureight’s quality processes and systems, implementing best-in-class frameworks to enhance efficiency, compliance, and scalability.\n, • Ensure all clinical operations adhere to ICH-GCP guidelines (R2/R3), applicable regulations, and internal quality standards.\n, • Lead the implementation, improvement and validation of new processes, procedures, and IT systems (e.g., eQMS, eTMF) to support GxP compliance and operational excellence.\n, • Oversee internal and external audits, including regulatory inspections, ensuring findings are addressed promptly and effectively\n Cross-Functional Collaboration & Leadership\n \n, • Partner with Clinical Operations, IT, Engineering, and Science Teams to integrate quality and regulatory requirements into digital platforms, AI-enabled solutions, and GxP-relevant systems.\n, • Embed a culture of quality awareness through training, workshops, and mentoring, ensuring all staff are competent and compliant with GCP, ISO standards, and internal policies.\n, • Support the Quality Manager in maintaining the Business Management System (BMS) as it relates to GCP and clinical operations.\n, • Develop and track quality objectives and performance metrics, aligning them with organisational goals and regulatory expectations.\n Risk Management & Continuous Improvement\n \n, • Oversee a robust risk management framework that ensures proactive identification, assessment, and mitigation of quality and compliance risks across all operations.\n, • Drive a data-informed approach to continuous improvement, leveraging quality metrics, trends, and industry benchmarks to shape strategic priorities and operational excellence.\n, • Champion a risk-based quality culture, ensuring accountability, transparency, and resilience in all processes, systems, and teams.\n, • Ensure the organisation anticipates and adapts to evolving regulatory and quality challenges, maintaining agility and compliance in a dynamic environment\n \n \n, • Demonstrable experience in regulatory affairs and quality assurance, with a strong focus on software/AI regulation (SaMD/AIaMD) and clinical trial compliance.\n, • Deep expertise in ICH-GCP (R2/R3), ISO 62304, ISO 82304, ISO 14971, ISO 34971, ISO 13485, ISO 27001, and ISO 42001, with a proven track record of successful regulatory submissions and clearances.\n, • Experience of biomarker validation pathways,\n, • Extensive experience in leading quality transformations, including the design and implementation of QMS, SOPs, and IT systems (e.g., eQMS, eTMF).\n, • Strong background in risk-based quality management, with the ability to balance compliance with operational efficiency.\n, • Experience in interacting with regulatory authorities (e.FDA, MHRA, IMDRF) and leading audits/inspections.\n, • Proven ability to develop and deliver training programs on GCP, ISO standards, and regulatory requirements.\n, • Excellent problem-solving, analytical, and project management skills, with a strategic mindset and execution-focused approach.\n, • Superb communication, collaboration, and stakeholder management abilities, with the gravitas to influence at all levels.\n It’s a bonus if you have the following:\n \n, • Experience of digital biomarker validation, especially in medical imaging.\n, • Experience with clinical imaging technologies, workflows, or core lab operations.\n, • Familiarity with DICOM standards, imaging protocols, or clinical data management systems.\n Qualifications & Education\n \n, • Educated to Bachelor's degree level or equivalent in a relevant scientific, technical, or regulatory discipline.\n, • Certified to Practitioner level or above as a quality professional (e.g., PCQI, RAC, or equivalent).\n It’s a bonus if you have the following:\n \n, • Training and experience as an Internal Auditor\n, • Are a member of international standards setting committees or regulatory trade bodies.\n What can you expect from us\n \n, • A comprehensive benefits package that includes an annual bonus plan, private medical insurance, life insurance, and a contributory pension scheme\n, • 25 days annual leave, plus bank holidays and enhanced maternity leave\n, • A diverse work environment that brings together experts in many fields, including software engineering, devops, data science, machine learning, quality assurance, regulatory affairs, and clinical operations.\n \n If you have any queries, please contact Careers@qureight.com. Everyone is welcome at Qureight. We are an equal opportunities employer and encourage applications from all suitably qualified candidates regardless of age, disability, ethnicity, sex, gender reassignment, religion or belief, sexual orientation, marriage and civil partnership, or pregnancy and maternity. \n Women and other underrepresented groups may be less likely to apply for a role unless they meet all or nearly all of the requirements. If this applies to you, we still encourage you to apply – you may be a great fit, even if you don’t meet every qualification. We’d love to hear from you. \n If you require any adjustments to the application or selection process, please let us know. We will be happy to support you. \n #J-18808-Ljbffr

An exciting opportunity has arisen for a Principal Electronics & Software Product Engineer to join a specialist product design consultancy focused on developing innovative technologies for multinational clients across the medical industry. The business has expanded its global capability while maintaining a reputation for exceptional engineering, strong project leadership, and delivery within regulated and safety-critical markets. This role sits within a rapidly growing technical team developing complex electromechanical products from concept through to manufacture. This position is ideal for an experienced electronics or electromechanical product development engineer looking to step into a principal-level role, lead multidisciplinary teams, and take ownership of full product architectures while contributing to business growth and client development. Main Responsibilities of the Principal Electronics & Software Product Engineer (Cambridge): • Develop electronics and embedded software (C/C++) for diverse and technically complex new products, • Lead the integration of electromechanical product designs through to manufacture and production transfer, • Take technical ownership of product architecture from concept generation through to launch, • Deliver technical progress to clients and, over time, lead multidisciplinary project teams, • Contribute to requirements definition, specification development, schematic capture, PCB layout, hardware bring-up, debugging, and product validation, • Support project planning, resourcing, and leadership activities, • Build strong client relationships and support the conversion of new opportunities into commercial contracts Requirements of the Principal Electronics & Software Product Engineer (Cambridge): • Proven industry experience designing, prototyping, and testing electronic circuits and systems, including embedded software development in C/C++, • Strong practical electronics skills including soldering, PCB rework/modification, wiring, and use of common laboratory test equipment, • Experience across the electronic product development lifecycle from concept through to prototype and manufacture, • Ability to work effectively within cross-disciplinary teams, with strong written, verbal, and presentation skills, • A First or 2:1 degree in Engineering from a leading university (UK top 10 or equivalent), • Eligibility to work in the UK (visa sponsorship not available), • Experience in project planning, leadership, or team coordination would be advantageous Working Pattern & Benefits: • Full-time, permanent role, • Competitive salary and performance-based bonus structure, • Career development support including mentoring and personal training budgets, • Opportunity to work on innovative, safety-critical products in regulated international markets, • Exposure to multinational clients and potential travel opportunities, • Ethical working environment focused on improving lives through engineering excellence To apply please send your CV to clam@redlinegroup.com, or for more information contact Chuck Lam on 01582 878868.

_ is a fast-growing medical device software company headquartered in Bern, Switzerland. Our mission is to enable the right decisions sooner in healthcare, through transformative AI & data management solutions for disease screening and monitoring. Join our diverse team of entrepreneurs, developers, researchers, and commercial experts who are collectively shaping the future of healthcare. We are looking for a Cloud Engineer to join our team, where you will play a critical role in optimizing our cloud infrastructure to meet our customers’ needs. This position is pivotal to our mission of providing a seamless, secure, and scalable experience on our platform • Enhance and maintain highly available, secure, and scalable AWS cloud environments and services., • Manage and prioritize tasks in the cloud infrastructure backlog to address immediate needs and plan long-term improvements., • Set up infrastructure monitoring and observability solutions, proactively addressing availability, performance or security issues., • Learn the current infrastructure and take ownership of day to day cloud operational tasks and activities., • Assess new technologies, systems, and services for production readiness, ensuring seamless and stable integration., • Prepare and maintain documentation on cloud processes, procedures, and architectures to ensure clear understanding and team-wide knowledge., • Apply AWS Well-Architected Framework principles to evaluate and optimize our current infrastructure., • Contribute in out of office hour cloud deployments once or twice a month, • Conduct POCs (proof of concepts) on new AWS services, third-party tools, and technologies to drive continuous improvement in our infrastructure., • A demonstrated entrepreneurial and collaborative mindset with a proactive approach to problem-solving., • A university degree in Computer Science, Information Technology, or a related field., • 3-5 years of hands-on experience with AWS cloud services in a professional setting., • Proficiency with core AWS services, including IAM, S3, KMS, RDS, VPC, ECS, EC2, and more., • Experience working with multi-account and multi-region AWS production environment setups and using IaaC to manage them., • Strong hands-on experience with Infrastructure as Code (IaC) tools, preferably Terraform., • Scripting experience with one or more languages, such as Python, Bash, or Node.js., • Good knowledge of cloud security principles and services, such as AWS WAF, GuardDuty, Config and CloudTrail., • Familiarity with CI/CD pipelines and tools preferably GitLab, • Experience with software version control and Git., • Strong understanding of cloud networking concepts, including VPC, VPC Peering, Subnets, and Load Balancing., • Familiarity with monitoring and observability tools for cloud environments, such as Grafana, Prometheus, OpenSearch, and the ELK stack., • Strong analytical and problem-solving skills, with a proactive approach to challenges., • A genuine interest in staying updated with new AWS services and features, integrating advancements into the cloud environment., • Ability to work well in a flexible, startup environment, taking initiative to establish new processes when necessary., • Excellent verbal and written English communication skills., • Good listening skills., • Familiarity with industry best practices in cloud architecture principles., • Ability to work independently and collaboratively within a team setting., • Availability to work during Central European Time (CET) business hours. What We Offer • A chance to be part of an exceptional team driving innovation in healthcare., • A competitive salary in a supportive work environment that fosters work-life balance., • Opportunities for professional growth and development in an international setting., • A culture of collaboration and inclusion, which is fundamental to our ethos., • Occasional travel to our HQ in Switzerland, immersing you in our core operations and company culture.

This job is with AstraZeneca, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Job Title: Regulatory Affairs Intelligence Director Location: Cambridge Salary: competitive Introduction to role: Are you ready to turn regulatory intelligence into decisive advantage that accelerates medicines to patients? This role sits at the intersection of competitive insight, regulatory science, and portfolio strategy translating emerging signals into clear regulatory choices for our pipeline and marketed assets. You will partner closely with senior regulatory leaders and cross-functional intelligence groups to anticipate shifts in guidance, identify precedent that unlocks smarter development pathways, and shape responses that influence external policy. In an agile, collaborative environment, you will help convert complex data into action that shortens timelines, strengthens labels, and improves patient outcomes. Accountabilities: Conduct analysis and impact assessment of Regulatory Intelligence across the portfolio in a given therapeutic area (TA) and communicate findings to key stakeholders and senior leaders within the assigned therapeutic area. Work closely with other Intelligence groups within the company (PIRS, GIACE, Clinical Information Science, etc) to provide the disease area/scientific platform specific Regulatory interpretation and impact. Serve as the central point person within TA in leading bespoke Regulatory research for RADs including project level Regulatory strategy, due diligence, disease area strategy, initiatives etc. Partner with International, China, and Japan Regulatory Affairs Directors to align on TA-specific guidance and regulatory intelligence across regions; contribute to the holistic regulatory landscape by disease/scientific platform and coordinate with PIRS to gather input and provide feedback on draft guidance and policies.Proactively Conduct analysis of new drug development and regulatory approaches on e.g. novel clinical trial concepts, RWE, early regulatory access, adaptive/conditional licensing as it relates to the TA Research and analyze Regulatory guidance, precedence, and other asset-specific research projects to support our products and development pipeline per market/region Review relevant regulatory assessment documents from agencies to extract key insights in supporting Regulatory landscaping and strategy Perform research and analysis of relevant Regulatory hearings providing pre-meeting briefings and post-meeting impact analysis to key stakeholders and senior leaders within the Company In coordination with functions in the TA, liaise with Reg Ex/PIRS to support their development and deployment of new technologies, including artificial intelligence, to facilitate regulatory intelligence. Essential Skills/Experience: An advanced degree in a science related field and/or other appropriate knowledge/experience. Demonstrate competencies of strategic thinking, data and impact analysis, and excellent oral and written communication skills. In-depth knowledge of the designated therapeutic area. Ability to evaluate the impact of key Regulatory Intelligence on disease area and project strategy. Ability to critically distinguish between "noise" and meaningful news to key stakeholders and senior leaders. Have a working knowledge about Regulatory Intelligence tools and stay current with regulatory news regarding key competitors and the disease area. Have a solid knowledge of US and European Regulatory Affairs. Have a good understanding of drug development. Desirable Skills/Experience: A good understanding of the commercial aspects of drug development. Broad background of experience working in the pharmaceutical business and prior experience in several areas within regulatory affairs; experience in the relevant therapy area (small molecules and biologics) is preferred. Critical thinking on current global regulatory science trends and questions, with a good understanding of the corresponding scientific and clinical components. Why AstraZeneca: Here, regulatory intelligence directly shapes strategy from the earliest stages through approval and beyond-bringing life-changing medicines to patients faster. You will work in a fast-moving, collaborative setting where diverse experts come together to challenge assumptions, influence external regulators on new technologies, and design progressive solutions. Expect unexpected teams in the same room unleashing bold thinking, backed by leaders who remove barriers and value kindness alongside ambition. With a strong focus on analytics, technology adoption, and continuous learning, you will broaden your impact across modalities and stages of development while honing your craft through clear development paths and a culture that shares, tests, and improves ideas together. What is next: Ready to make a positive impact? Apply now to join our journey towards operational excellence! So, what's next? Complete your application before the below closing date 8th August 2026 Where can I find out more? Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/ Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/ Follow AstraZeneca on Instagram https://www.instagram.com/astrazeneca_careers/?hl=en Salary: Negotiable

ROLE OVERVIEW We are currently looking for a Regional Business Specialist to join a leading provider of scientific and analytical solutions based in the UK. This exciting opportunity allows you to work at the forefront of cutting-edge technology, supporting customers with innovative instrumentation and driving growth across your designated territory. If you’re passionate about scientific solutions, customer service, and strategic sales, this role offers a fantastic platform to develop your career within a forward-thinking company committed to societal impact. As a key member of our client’s sales team, you will play a pivotal role in expanding the reach and success of their analytical instrumentation portfolio. Your technical expertise, combined with your commercial acumen, will enable you to deliver tailored solutions that meet customer needs and uphold the company’s values of professionalism, integrity, and innovation. KEY DUTIES AND RESPONSIBILITIES Your duties as the Regional Business Specialist will be varied however the key duties and responsibilities are as follows: • Drive the growth of our client’s analytical and material testing product range within your designated territory through proactive sales and strategic planning., • Engage in pre-sales technical discussions, assess customer requirements, and recommend appropriate solutions to ensure customer satisfaction and successful sales closures., • Conduct product demonstrations and presentations to showcase the capabilities and applications of the company’s technology to potential and existing customers., • Collaborate closely with internal teams including service, product specialists, and marketing to deliver exceptional support and ensure alignment with customer objectives., • As the Regional Business Specialist, you will maintain accurate records of customer interactions and sales activities, utilizing CRM (SAP) effectively for forecasting and reporting. ROLE REQUIREMENTS To be successful in your application to this exciting role as the Regional Business Specialist, we are looking to identify the following on your profile and past history: • A Degree or higher level in scientific disciplines such as chemistry, analytical chemistry, pharmacy, biochemistry, or related fields., • Proven experience in solution selling, ideally with chromatography systems, spectroscopy, and mass spectrometry, coupled with hands-on laboratory experience., • Strong understanding of mass spectrometry and chromatography theory, with the ability to learn new systems quickly., • Willingness to travel regularly within the territory, including occasional international travel for training and events, and a valid driver’s license. WHAT’S IN IT FOR YOU? Joining our client offers the opportunity to work with a global leader in scientific innovation, supporting the development of advanced analytical techniques. You will be part of a collaborative, supportive team that values continuous learning and professional growth. Your work will contribute to societal benefits including healthcare advancements and environmental initiatives, making a positive impact through science and technology. Key Words: scientific solutions / analytical instrumentation / chromatography / mass spectrometry / customer support / sales / technical expertise / territory management / innovation / professional development “Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career

An exciting opportunity has arisen for a Principal Electronics & Embedded Software Engineer to join a team developing innovative medical and technology products, taking ideas from concept through to manufacture for some of the world's leading companies. The business has expanded its global capability while maintaining a reputation for exceptional engineering, strong project leadership, and delivery within regulated and safety-critical markets. This role sits within a rapidly growing technical team developing complex electromechanical products from concept through to manufacture. This position is ideal for an experienced Principal Electronics & Embedded Software Engineer looking to step into a principal-level role, lead multidisciplinary teams, and take ownership of full product architectures while contributing to business growth and client development. Main Responsibilities of the Principal Electronics & Embedded Software Engineer (Cambridge): Develop electronics and embedded software(C/C++) for diverse and technically complex new products Lead the integration of electromechanical product designs through to manufacture and production transfer Take technical ownership of product architecture from concept generation through to launch Deliver technical progress to clients and, over time, lead multidisciplinary project teams Contribute to requirements definition, specification development, schematic capture, PCB layout, hardware bring-up, debugging, and product validation Support project planning, resourcing, and leadership activities Build strong client relationships and support the conversion of new opportunities into commercial contracts Requirements of the Principal Electronics & Embedded Software Engineer(Cambridge): Proven industry experience designing, prototyping, and testing electronic circuits and systems, including embedded software development in C/C++ Strong practical electronics skills including soldering, PCB rework/modification, wiring, and use of common laboratory test equipment Experience across the electronic product development lifecycle from concept through to prototype and manufacture Ability to work effectively within cross-disciplinary teams, with strong written, verbal, and presentation skills A First or 2:1 degree in Engineering from a leading university (UK top 10 or equivalent) Eligibility to work in the UK (visa sponsorship not available) Experience in project planning, leadership, or team coordination would be advantageous Working Pattern & Benefits: Full-time, permanent role Competitive salary and performance-based bonus structure Career development support including mentoring and personal training budgets Opportunity to work on innovative, safety-critical products in regulated international markets Exposure to multinational clients and potential travel opportunities Ethical working environment focused on improving lives through engineering excellence To apply please send your CV to (url removed), or for more information contact Mike Belmar on (phone number removed)

Why join Marshall Land Systems in this role? As the Independent Design Assurance Lead / Systems Design Authority within Marshall Land Systems, you will act as the independent technical representative supporting the Chief Engineer. The role provides objective oversight, governance, and assurance across Land Systems programmes and products, ensuring engineering solutions are technically sound, compliant, safe, and fit for purpose throughout the product lifecycle. Operating independently from programme delivery teams, you will provide authoritative technical challenge, assess design maturity and technical risk, and maintain confidence that engineering decisions align with customer requirements, business objectives, regulatory obligations, and engineering best practice. Your responsibilities include: Independent Design Assurance Act as the independent authority for technical design assurance across Land Systems programmes Provide objective assessment of engineering solutions throughout the system lifecycle, from concept development through design, integration, verification, validation, and in-service support Conduct independent reviews of system architectures, design solutions, requirements compliance, and technical evidence Assess the adequacy of engineering processes, methodologies, and technical decision-making Verify that designs meet contractual, regulatory, safety, quality, and operational requirements Ensure appropriate technical risks are identified, managed, and escalated Systems Design Authority Maintain oversight of system-level technical integrity across programmes and product lines Provide authoritative guidance on systems engineering principles, architecture development, requirements management, integration, and verification strategies Review and endorse key technical baselines and system design decisions Ensure consistency between customer requirements, system architecture, subsystem designs, and verification activities Challenge technical assumptions and decisions where evidence is insufficient or risks remain unacceptable Support the management of technical debt, concessions, and design deviations Engineering Governance Support the Chief Engineer in establishing and maintaining effective engineering governance arrangements Chair or participate in independent design reviews, technical gate reviews, and assurance boards Review engineering deviations, waivers, concessions, and non-conformances Ensure engineering decisions are supported by appropriate evidence and documented rationale Monitor adherence to engineering lifecycle processes, standards, and procedures Provide assurance input into engineering policy, standards, and continuous improvement initiatives Technical Risk and Compliance Assess programme technical risks and the effectiveness of mitigation strategies Review safety cases, hazard analyses, and certification evidence as appropriate Ensure compliance with applicable defence standards, legislation, customer specifications, and internal governance requirements Support technical investigations and root cause analysis activities Provide independent assessment of design maturity and readiness at key programme milestones Stakeholder Engagement Act as a trusted advisor to the Chief Engineer and Engineering Leadership Team Engage with Programme Managers, Technical Authorities, Systems Engineers, Design Engineers, Quality Assurance, Safety, and Integrated Logistics Support functions Interface with customers, regulators, suppliers, and external technical authorities as required Support customer design reviews, technical audits, and assurance activities Provide confidence to stakeholders through clear, evidence-based assurance reporting Undertake additional activities as required by line management Apply if you have most of the following: Significant experience delivering complex engineering systems within defence or aerospace Extensive experience in systems engineering, technical risk management or engineering governance Proven track record of leading independent design reviews and providing authoritative technical assurance across the system lifecycle Experience assessing system architectures, requirements management, integration, verification, and validation activities Strong track record of influencing senior stakeholders and providing independent technical judgement Experience operating within matrix-managed, multi-disciplinary engineering environments Desirable: Experience operating as a Design Authority, Systems Design Authority, Chief Engineer representative, or Independent Technical Authority Experience with military vehicle, defence platform, or land systems development programmes Knowledge of defence acquisition, certification, and assurance frameworks Technical Skills & Qualifications: Degree-qualified in Engineering, Systems Engineering, or a related technical discipline Strong understanding of systems engineering lifecycle processes and associated standards Excellent technical report writing, presentation, and communication skills Ability to assess complex technical issues and provide independent, evidence-based judgement Strong stakeholder management, influencing, and leadership skills Desirable Chartered Engineer (CEng) status Lead Auditor qualification or recognised assurance certification Knowledge and practical application of ISO 9001, ISO 15288, DEF STAN standards, NATO standards and functional Safety standards (where applicable) Familiarity with engineering governance frameworks and assurance methodologies Additional local needs: Hybrid working offered Occasional UK and international travel Successful candidate will need to be eligible to hold UK SC Clearance Ability to operate effectively across complex stakeholder and programme environments Benefits of this role include: Influence the technical direction and integrity of complex defence and land systems programmes while working closely with senior engineering leadership Develop expertise in independent design assurance, systems engineering governance, and technical risk management across the full product lifecycle Build credibility as a trusted technical authority, engaging with customers, regulators, suppliers, and senior stakeholders Shape engineering excellence and continuous improvement initiatives that drive quality, compliance, and operational effectiveness across the organisation Marshall Land Systems is a Canadian-owned global company with an unrivalled pedigree of British engineering excellence. From its origins in Cambridge, UK, through more than a century of innovation, pioneering advances from the nose of Concorde to the early Hydrogen fuel cell technology that ultimately powered the moon landings, Marshall engineers now continue to innovate specialist vehicles and infrastructure for NATO forces across the world. From bomb disposal vehicles to deployed shelters, from command and control to CT scanners on the battlefield, Marshall Land Systems protects people in critical situations with the very best in engineering. It employs 600 people with major facilities the UK, Canada, and the Netherlands. #LI-DS1

Assist in reviewing contract month-end P&L’s with the Chief Financial Officer, Management Accountant, and Business Unit Management Team.

Due to exceptional growth across the business, our client is looking for a General Commercial Solicitor to play an integral role within their high‑performing Commercial Legal Team. You’ll be a key partner to the business, leading on major commercial contracts, managing legal and regulatory risk,

We are looking for a Data Protection Expert to join the Office of the Data Protection Officer (“ODPO”).The ODPO is part of the Digital Regulatory Compliance team sitting within the wider Legal Department.This is a fantastic opportunity for a privacy professional to further develop their career i

Personal Injury Solicitor / Legal Executive – Cambridgeshire.Legal 500-ranked regional law firm.Oculus Legal Group is working in partnership with a highly regarded, Legal 500-ranked regional law firm that is continuing to invest heavily in the growth of its Personal Injury department.This is an ex

William James Recruitment is a specialist legal recruitment consultancy, partnering with leading law firms across the UK and internationally, including Legal 500-ranked practices. This is an excellent opportunity for a Private Client Solicitor to join a Tier 1-ranked Private Client practice, advisin

Based in East London (on the district line), they have grown substantially over the last 10 years to a turnover of £11m and over 65 fee earners and are now a Top 200 UK Law firm with a strong business plan of a further 30% growth and development in the next five years.

Mechanical & Electrical Supervisor required for a Data Centre project in Surrey.Data Centre experience required.Experience in Supervising installers and contractors.

If you enjoy managing complex projects, influencing stakeholders, and delivering measurable business outcomes, we'd love to hear from you. Prepare business updates and presentations for senior leadership. Lead strategic projects with real business impact.

Level 3 Rope Access Technicians | Liverpool Bay Decommissioning Project | August & September 2026.Copius Group is mobilising two experienced offshore teams for a major decommissioning project in Liverpool Bay, and we’re looking to connect with skilled professionals ready for upcoming trips in Augu

You are someone who easily grasps what makes a purpose-led business special and knows how to protect that essence while building structure. Adaptable, hands-on, and experienced in fast-moving, owner-managed businesses where priorities evolve, and authentic leadership is key. Note: With the current C

NET MAUI, GitHub Copilot, Docker, Kubernetes, Microservices architecture, Angular 21, Vue.TypeScript, Programmer, Full Stack Engineer, Architect,.We have several fantastic new roles for.NET Developer to join an ambitious Fintech start-up.This is your chance to work with the sharpest minds in private

This is a broad disputes-focused role advising senior stakeholders on a range of contentious and potentially contentious matters across the business. Working closely with senior business stakeholders across multiple jurisdictions.

A growing, premium food manufacturing business is seeking an Operations Director to lead and optimise its end-to-end manufacturing function during an exciting period of expansion. Operating within the ambient food category and supplying major retail and foodservice customers through branded and thir

Collaborate across the business to develop purchasing systems and business process, understand individual departmental needs. Represent the business in contract negotiations, creating robust contracts and protecting the interests of the organisation. Develop and maintain business wide end to end spe

Join Syner-Med: Where Innovation Meets Impact.At Syner-Med, we're a growing UK healthcare company on a mission to solve problems that matter — in.Women's Health, Vascular Medicine, and Infectious Disease.From established specialist medicines to next-generation diagnostics, we bring genuinely usefu

We are establishing Swapetech’s UK IC design centre and are looking for a Founding Chief SerDes Architect to lead our in-house SerDes R&D capability.This is a senior technical leadership role for someone who wants to define architecture, build a high-calibre design team, and take ownership of next

Opportunity to join a highly innovative and internationally recognised business. With operations spanning multiple international markets, the organisation is recognised for driving innovation across digital infrastructure, connectivity, and next-generation technology solutions. Despite its global sc

Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems.Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced tr

With more than 1,000 completed projects using a range of molecular formats and 20 clinical-stage molecules, we are internationally recognised for tackling novel and challenging discovery programs. You will work with a high degree of scientific independence, designing and executing experiments, troub

A successful track record of growing business units, developing new markets and leading operational teams. Grow the renewables pipeline and successfully convert new business opportunities. This is an excellent opportunity for an ambitious senior leader looking to take ownership of a growing renewabl

You'll have genuine autonomy to develop relationships, negotiate acquisitions and establish the foundations of a growing development business, supported by an established construction business capable of delivering the schemes. An exciting opportunity has arisen to join an ambitious, privately-owned

Successful experience of enabling business change working with business leaders to drive proactive People and Culture Strategy in support of business objectives. Proven ability to understand business goals and then design & implement new approaches, policies, programmes to affect continual improveme

If you are an ambitious estimator looking to progress your career within a forward-thinking business that values quality, innovation, and professional development, we would like to hear from you. As an Electrical Estimator, you will play a key role in securing new business by preparing accurate and

Working across our international e-commerce business, you'll play a key role in delivering exceptional customer journeys, executing CRM campaigns, and supporting the continued growth of our global online and boutique channels. Bachelor’s degree in Marketing, CRM, Business, or a related field. Expo

Competitive Salary - Open to discuss.We are seeking an experienced and strategic Director of Education to join an established specialist education provider supporting a diverse portfolio of SEN schools across the UK.This is a high-profile leadership position, responsible for driving educational exce

Providing pragmatic legal advice across business, investment and operational activities.

You'll join a business that is investing heavily in AI and be trusted to define how AI tools are selected, governed, adopted, and scaled across the organisation. This established international organisation is building its AI capabilities and creating the foundations needed to support responsible, la

We’re partnering with a growing logistics business in Portland that is looking to bring on. Business Development Executives. Clear progression path as the business scales.

Slick Gorilla began in the UK and has grown into a global men’s hair care brand, known for launching the first Men’s Hair Powder in 2016.The company now operates in over 60 countries and sells on average one bottle of hair powder every minute.With an industry-leading social media presence, best

Microsoft 365 Technical Specialist.We're looking for an experienced.Microsoft 365 Technical Specialist.Microsoft Partner delivering cloud transformation projects for customers across the UK.This is a customer-facing Professional Services role where you'll design, implement, migrate and optimise Micr

Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems.Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced tr

You’ll play a key role in evolving the brand aesthetic while ensuring collections remain commercially successful, inclusive, and exciting for a growing international customer base. Ensuring collections align with business strategy, growth plans, and customer demand. Maintaining awareness of compet

They are regularly engaged on domestic and international deals, including matters in emerging markets.

You will act for mid tier businesses, household name PLCs and other major international groups.

This is a fantastic opportunity for an operational leader to shape the future of a growing UK manufacturing business. Managing the operational P&L and contributing to business growth. Degree qualified in Engineering, Manufacturing, Operations, MBA or equivalent advantageous.

Partner closely with HR, Communications, Legal and business leaders to drive positive employee relations outcomes. You could currently be an Industrial Relations Manager, Employee Relations Manager, HR Business Partner with a strong IR focus, or a specialist Industrial Relations professional looking

Long-established, privately-owned business. The business will support and fund the qualification through its internal development programme for the right candidate. We're partnering with one of the UK's most respected privately-owned lift businesses to recruit a Project Supervisor covering the Midla

If you have built and grown a commercial grounds, arb or winter services business, keep read. The Estates Division is the largest part of that business, bringing together grounds maintenance, arboriculture and winter services under one leadership. EBITDABuild the operating model and leadership team

A newly created role with real influence over how projects are delivered across the business. The opportunity to work closely with the Chief Operating Officer on strategic business initiatives. Join a Business That Invests in You.