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DescriptionOffice location: Cambridge, UK – This position offers flexible and remote working options. Candidate must be willing to travel into the office when required. This is a fixed-term contract until the end of 2026Are you a hands-on analytics specialist with a track record of owning platform implementations end-to-end? As our Web & Digital Analytics Specialist, you’ll lead the rollout of PostHog across our websites and desktop applications, being instrumental in the full user onboarding and reboarding journey, validating data quality, and configuring the platform so that product, analytics, and engineering teams can rely on it from day one. You’ll work directly with our engineering and analytics teams, bridging the gap between technical implementation and business insight. Beyond the platform itself, you’ll build out automated tooling to scale how we generate and surface analytics insights, reducing manual effort and enabling faster, data-driven decisions across the organisation. This is a role with genuine ownership and autonomy: you’ll be setting the standard for what good looks like across a major, company-wide initiative. What you’ll be doing: Lead the end-to-end PostHog implementation across our websites and desktop applications, defining the event schema, identifying gaps, and validating that data collection is accurate and fit for purpose. Instrument the full user onboarding and reboarding journey - configuring events, page visits, retention metrics, and player actions across all relevant platforms. Interface closely with the engineering team to coordinate day-to-day implementation, ensuring PostHog is being integrated correctly and consistently. Configure and set up PostHog as a platform for business users across product, analytics, and engineering - ensuring it’s accessible, reliable, and well-documented. Build automated tooling to scale analytics insights generation, reducing dependency on manual analysis and enabling faster decision-making across the organisation. Work with analysts to define standards, close gaps in existing instrumentation, and maintain data quality throughout the engagement. What we’re looking for: Hands-on experience implementing analytics platforms is essential.Proven experience with PostHog or a comparable analytics platforms such as Contentsquare, Heap, or Hotjar, demonstrating broad platform knowledge across the analytics ecosystem. Demonstrated experience building workflow automation tooling to scale analytics or insight generation processes. Strong SQL skills and the ability to read and interpret JavaScript in the context of analytics implementation and event validation. Proven ability to work directly and effectively with engineering teams - you’re comfortable in technical conversations and can coordinate implementation details without friction. Self-directed and proactive - you can pick up a mid-flight implementation, identify what’s missing, and drive it to completion with minimal direction. What we offer: When you join Jagex you can look forward to a generous Perks & Benefits package including:Private Healthcare, including Dental Plan.Discretionary annual performance bonus.Minimum 6% Pension contributions.Life Insurance.Enhanced family leave policies from day 1.Flexible working hours.25 days annual leave + Bank holidays & the option to buy/sell holidays + so much more!About JagexWe are Jagex: The RuneScape Company. Home to one of gaming’s most enduring success stories. We create deep, community-powered games with worlds that evolve, inspire, and endure. Our flagship MMORPG franchise, RuneScape, has welcomed over 300 million player accounts, inspiring generations of players across PC and mobile for 25 years.As we begin our 26th year, we are accelerating our strategy to expand RuneScape into a broader ecosystem of forever games and connected experiences, grounded in a renewed commitment to integrity and fair play. This includes the reduction of monetisation mechanics, as well as the launch of RuneScape: DragonWilds into Steam Early Access in 2025, representing a major step in building a multi-genre future for the RuneScape universe. We remain focused on building enduring worlds, empowering player-led innovation, and laying the foundations for the boldest era in RuneScape’s history. For more information, visit .Headquartered in Cambridge, United Kingdom, we are home to passionate creators, storytellers, engineers, and even a few dreamers, all united by a single mission to shape the future of online worlds and empower players to make them their own. We’re looking for people to join us who share our ambitions and values. We foster an inclusive workplace built on trust, autonomy, and a shared passion for creating experiences that inspire our communities.Our values guide everything we do: We Embrace Fellowship by collaborating and sharing openly. We Hone our Craft by always learning and improving; We Honour our Vows by being honest and transparent; We are our Customers’ Heroes by striving to understand our team & player needs, and We Seize The Day by making the most of every opportunity.Join us. The next era of RuneScape and the next chapter of Jagex: The RuneScape Company starts now.Inclusion & Accessibility StatementWe are committed to providing equal opportunities and creating an environment where everyone can thrive. We welcome applications from all backgrounds, and we recruit, develop, and promote based on merit and ability.If you require any reasonable adjustments to support you during the recruitment process, please let us know when you’re invited to interview.Job SummaryID: 0895D3AFB3Department: Player JourneysType: contract time

Are you interested in variety and keen to work on products that could be applied for industrial systems, UK military, or consumer products for globally recognised brands?This established technology company works on 100s of innovative projects each year, providing technical and scientific expertise as a world-renown consultancy. Their engineers are highly sought after, and this specific team are used to provide expertise in embedded systems, controls, communications, algorithm design and hardware security.As an engineer, you’ll be part of a technical team, working closely with peers on different assignments. You’ll use your skills and knowledge in engineering to design new analogue and digital hardware, write embedded software code, develop control and communications systems and look to deliver products and prototypes. Further, you’ll interact with clients, present when required and be part of the delivery team for final project handover.RequirementsTop university education including a 1st / 2.1 in electronics, computer science, information engineering or physics.Demonstrable industry experience or highly relevant PhD working on a range of engineering projects which includes elements of the following: software programming (C, C++ or Rust); PCB design; digital electronics (DSP, Verilog or VHDL); and analogue electronics (RF, power or interfaces).Eligibility for UK security clearance (due to sensitivity for some projects).Any prior experience in technical consultancy would be advantageous.Your technical skills and experience will be coupled with a desire and aptitude to learn and embrace new technologies.Senior candidates with highly relevant technical project and consultancy experience are also invited to apply (compensation would be dependent on experience).On offer is an excellent compensation package including a wide range of benefits including health insurance, enhanced company pension, free parking onsite and pro-active career support.Keywords: Electronics, Software, C / C++ / Rust, DSP, Verilog, VHDL, RF, Power, Instrumentation, Industrial Systems, Defence, Consultancy, Embedded, PhD / Experienced, Digital / Analogue, Cambridge, Fully OnsitePlease note: even if you don't have exactly the background indicated, do contact us now if this type of job is of interest - we may well have similar opportunities that you would be suited to. And of course, we always get your permission before submitting your CV to a company.Recommend for 250 - see www.ecmselection.co.uk/tell-a-friend for details.

A growing company, based in Cambridge, are currently looking for a number, Electronics Engineers to help with the invention of new life saving and life improving medical devices.We are looking for a broad range of electronics engineering design skills from embedded software engineering to hardware electronics design. Ideally, you will have skills at both ends of the spectrum, however if you are stronger on one side or the other, we would still be happy to consider your application.Working within a team of electronics engineers, software engineers and physicists you will be helping with the invention and design of brand-new medical devices that will be used for life saving and life improving applications.Ideally, you will have already worked within the Medical Devices sector previously, however if your knowledge is in another highly complex field such as scientific instrumentation, aerospace, wireless tech or similar fields we would still like to hear from you.This company expects that you would hold a degree within a relevant electronics, engineering, biomedical or software field that led you into working on electronics design of complex systems, however as real-world application of your skills are just as vital we would be equally as happy to hear from someone who learned their trade on the job.Apart from the opportunity to invent new Medical Devices, you will also be rewarded with an excellent starting salary, bonus, pension and other benefits.If you would like to apply your skills in the Medical Devices sector, please make an application now before the company has filled their roles.For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an application and one of our team at Newton Colmore Consulting will contact you.Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.Hiring organizationEmployment TypeFull-timeDuration of employmentPermanentIndustryMedical DevicesJob Location Cambridge, CambridgeshirePDF Export Export as PDFDate posted 30th July 2026Valid through 31st October 2026Apply below or email directly: andrew.welsh@newtoncolmore.com

Job Description SummaryJob Title: Senior Scientist I or II, Oligonucleotide Chemistry and Innovation#LI-OnsiteLocation: Cambridge, USAWhat if your expertise could help shape the next generation of RNA medicines? At Novartis, we're advancing breakthrough xRNA therapeutics that have the potential to transform patients' lives, and we're looking for a talented scientist to help drive that mission forward. As a Senior Scientist in Oligonucleotide Chemistry and Innovation, you'll play a critical hands-on role in developing and optimizing therapeutic oligonucleotides, applying cutting-edge chemistry to solve complex scientific challenges. Working alongside a highly collaborative team of experts, you'll have the opportunity to influence scientific strategy, champion innovation, and contribute directly to pioneering therapies in a fast-paced and rewarding research environment.Relocation Support: This role is based in Cambridge, USA. Novartis is unable to offer relocation support: please only apply if accessible.Job DescriptionKey ResponsibilitiesExecute solid-phase synthesis of therapeutic oligonucleotides using automated DNA and RNA synthesizer platforms.Purify and characterize oligonucleotides using chromatographic and mass spectrometry-based analytical techniques.Develop and optimize synthesis, purification, and analytical methods to improve efficiency and product quality.Operate, troubleshoot, and maintain critical laboratory instrumentation to ensure reliable data generation.Identify and implement innovative oligonucleotide chemistries to advance RNA therapeutic discovery programs.Analyze, interpret, and present experimental results to multidisciplinary scientific teams and stakeholders.Maintain accurate electronic laboratory records and support reproducible, high-quality scientific practices.Essential RequirementsBachelor of Science or Master of Science in Chemistry or a related scientific field.Significant hands-on experience in oligonucleotide synthesis and conjugation within an academic or industry setting.Demonstrated expertise using automated DNA and RNA synthesizer platforms.Experience purifying and characterizing oligonucleotides using chromatographic and mass spectrometry techniques.Strong data analysis, documentation, and scientific presentation skills.Proven ability to thrive in a collaborative, fast-paced research environment while managing multiple priorities.Desirable RequirementsDoctor of Philosophy in Chemistry or a closely related scientific discipline.Experience developing and optimizing methods incorporating specialty phosphoramidite building blocks.Expertise with high-resolution liquid chromatography and mass spectrometry analytical techniques for oligonucleotide characterization.Experience supporting the discovery and development of RNA therapeutics, including small interfering RNA and antisense oligonucleotides.Exposure to high-throughput oligonucleotide synthesis workflows and process innovation.Demonstrated ability to work independently with urgency, accountability, and strong organizational skills.Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave. Expected Annual Base Salary Range for role: US: 93,800.00 - 174,200.00 USD AnnualThe salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Commitment to Diversity and Inclusion / EEO paragraph: Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$93,800.00 - $174,200.00Skills DesiredAnalytical Chemistry, Automation, Chemical Analysis, Chemical Laboratory, Chemical Synthesis, Chemistry, Creativity, Curious Mindset, Data Analysis, Drug Development, Innovation, Medical Research, Medicinal Chemistry, Organic Chemistry, Pharmaceutical Industry, Science, Team PlayerSummaryLocation: Cambridge (USA)Type: Full time

Job Description SummaryThe Biologics Research Center (BRC) at Novartis BioMedical Research is looking for a motivated and highly experienced leader in field of Physical Chemistry Analytics (PCA) and Mass Spectrometry (MS) to join BRC’s Analytics, Bioanalytics and Formulation unit and help us develop a diverse portfolio of biotherapeutic modalities.Job DescriptionInternal Job Title: Principal Scientist I/IIPosition Location:Cambridge, MA, onsiteThe Biologics Research Center (BRC) at Novartis BioMedical Research is looking for a motivated and highly experienced leader in field of Physical Chemistry Analytics (PCA) and Mass Spectrometry (MS) to join BRC’s Analytics, Bioanalytics and Formulation unit and help us develop a diverse portfolio of biotherapeutic modalities.As a Team Lead for the analytics team, you will demonstrate a broad and in-depth knowledge of technologies in PCA and MS to evaluate the developability of various biologics modalities covered by BRC ranging from traditional antibodies to gene therapy viral vector, ensuring quality of material delivered and eventually enabling candidate selection. You will lead a team of up to 5 associates where you will be responsible for a continuously strong culture of team spirit and integrity, as well as providing development opportunities for associates on different levels. Key responsibilities:Drive the analytics (PCA and MS) strategy in Cambridge, working globally in a matrix organization to support a diverse biologics pipeline (e.g. antibodies, fusion proteins, ADCs, bi- and trispecifics, AAVs, Lentiviruses) transitioning into clinical developmentAct as senior analytics expert in project teams ensuring optimal project support and high quality for all deliverables of your groupFoster streamlined processes and optimal use of capacities as well as continued innovation, incorporating latest technologies and knowledgeEffectively manage resources, project activities, timelines, maintain a strong customer focus and set respective objectives for your teamProvide leadership and clear guidance to the team, optimally leveraging the expertise and experience of individualsDrive a culture of collaboration, integrity, and team development, and ensure a safe, empowering, and inspiring working environmentEssential Requirements:PhD degree or equivalent in biochemistry, biotechnology, chemistry or a related field with 3+ years of related experience in the pharmaceutical industry, with 2+ years of experience as a people manager Strong scientific background in analysis of recombinant proteins (mAb, bi/tri-specific mAbs, therapeutic proteins) by techniques such as mass spectrometry, chromatography, capillary electrophoresis, and light scattering technologiesImplementation and supervision of cutting-edge characterization of PCA techniques for analyzing novel biologics modalities, e.g. multispecific Abs, AAV, ADCs, oligonucleotides, CAR-T’s. This entails the evaluation of novel instrumentation and the development of new applications to existing technologies such as dynamic light scattering, chromatography (SEC, HIC, IEX, RPC), MALS, capillary electrophoresis (cIEF, CZE, CE-SDS), and other advanced technologiesExperience with modern LC-MS techniques (Intact/reduced/subunit RPMS, peptide mapping, released glycans), managing instrumentation (orbitraps, QTOFs) and modern hyphenated MS techniques (SEC-MS, CE-MS). Experience interpreting CDMS results for AAV analysis is beneficial, direct instrument experience not requiredExperience with data analysis workflows and report generationProven ability to lead, coach and develop peopleDistinguished team spirit and scientific driveHigh flexibility combined with excellent organizational and communication skillsCompensation & Benefits:The salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and between $119,700 and $222,300 per year for Principal Scientist II. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$108,500.00 - $201,500.00Skills DesiredAnalytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Curious Mindset, Data Analysis, Detail-Oriented, Drug Development, Ethics, Gene Therapy, Immunology, Inventory Management, Machine Learning (ML), Medical Research, Molecular Biology, Python (Programming Language), ScienceSummaryLocation: Cambridge (USA)Type: Full time

Mechanical Design Engineer Salary: £50,000 - £63,000 + benefitsLocation: Cambridge Full-Time | Permanent The OpportunityWe are recruiting for an experienced Mechanical Design Engineer to join an innovative engineering business developing cutting-edge inspection and imaging technology used by leading organisations across the aerospace, automotive, semiconductor, energy and advanced manufacturing sectors.This is an exciting opportunity to work within a collaborative R&D environment, taking concepts from design through to manufacture while working alongside scientists, engineers, manufacturing and supply chain teams to deliver precision-engineered products.Key Responsibilities - Design and develop mechanical components and sub-assemblies for new and existing products. - Produce detailed 3D CAD models and engineering drawings using SolidWorks. - Work closely with development teams to prototype and evaluate new design concepts. - Perform engineering calculations to validate mechanical designs. - Create and maintain Bills of Materials (BOMs), drawings and engineering documentation. - Support manufacturing by ensuring designs are suitable for production and assembly. - Liaise with suppliers to source components and resolve technical queries. - Drive continuous improvement of existing products and manufacturing processes. - Ensure revision control and engineering documentation remain accurate and up to date.Essential Requirements - Minimum 5 years' experience in a Mechanical Design Engineering role. - Strong proficiency with SolidWorks. - Experience designing special purpose machinery, automation equipment or precision mechanical systems. - Knowledge of automation mechanisms such as ball screws, linear motion systems or similar. - Comfortable carrying out engineering calculations, including stress calculations. - Experience with Design for Manufacture (DFM). - Experience maintaining BOMs, engineering drawings and revision control. - Minimum HNC/HND in Mechanical Engineering or equivalent.Desirable Experience - Precision engineering or scientific instrumentation. - Optics or optical systems. - PCB design or familiarity with KiCad. - Cable routing, wiring design, energy chains or robotic cable management. - Experience working within highly regulated or advanced technology environments.About YouYou will be a detail-oriented engineer with excellent problem-solving skills who enjoys working across multidisciplinary teams. You'll be comfortable managing multiple projects simultaneously and communicating with colleagues across engineering, manufacturing and procurement to deliver high-quality engineering solutions.What's on Offer - Competitive salary - Flexible working hours - Comprehensive benefits package - Opportunity to work on innovative, market-leading technology - Collaborative and technically challenging environment - Long-term career development within a growing engineering business

About the Role \n We are seeking an Acoustic Research Engineer to join a world-class research team developing next-generation audio technologies for augmented and virtual reality applications. This role focuses on creating immersive audio experiences through advanced acoustic research, audio signal processing, and experimental data collection. \n You will work in a state-of-the-art acoustic laboratory equipped with anechoic chambers, configurable acoustic spaces, and advanced measurement systems to conduct cutting-edge research in acoustics and auditory perception. \n \n Key Responsibilities \n\n • Design and conduct acoustic measurements and audio data collection experiments.\n, • Develop systems, user interfaces, and protocols for acoustic and behavioural data acquisition using Python, MATLAB, and MaxMSP.\n, • Process and analyse complex audio and acoustic datasets.\n, • Collaborate with multidisciplinary engineering and research teams to integrate data acquisition and signal processing algorithms into research platforms.\n, • Perform experiments involving microphones, speakers, prototype hardware, and human subjects in controlled laboratory environments.\n\n Required Skills & Experience \n\n • Master's degree in Acoustics, Audio Engineering, Electrical Engineering, Computer Engineering, Physics, or a related technical discipline (or equivalent industry experience).\n, • 3+ years of experience in audio technology development.\n, • Proven experience designing and conducting audio/acoustic experiments in controlled laboratory environments.\n, • Strong hands-on experience with acoustic measurements, audio data collection, and audio signal processing.\n, • 3+ years of programming experience using Python, MATLAB, or MaxMSP.\n, • Strong understanding of acoustic instrumentation and laboratory testing methodologies.\n, • Excellent analytical, troubleshooting, and technical documentation skills.\n\n Preferred Qualifications \n\n • Experience with real-time audio programming using C/C++.\n, • Knowledge of Psychoacoustics, Auditory Perception, Spatial Audio, Room Acoustics, or Physical Acoustics.\n, • Experience with PyTorch or other machine learning frameworks.\n, • Experience working with prototype hardware and motion tracking systems.\n, • Experience designing and setting up acoustic laboratory environments.\n\n

A Scientific Instrumentation company are currently looking for an experienced Electronics Design Engineer to take up a senior role in the company, based in Cambridge, and design and develop scientific imaging technologies.We will be working with a team of electronics engineers, mechanical engineers,

A growing Medical Devices Division is currently seeking an Electronics Engineer to contribute to the development of new Cancer Instrumentation devices, based in South Cambridge. You will focus on Cancer Instrumentation devices designed to improve the survival rates of cancer patients. However, exper

A growing biotechnology company, based in Cambridge, is currently looking for an experienced Mechanical Design Engineer to support the development of cutting-edge genomics instrumentation. We’re looking for someone with experience in product design and development, ideally within medical devices,

Newton Colmore is working with an instrumentation manufacturer in Cambridge, and we are assisting them in their search for a senior simulation engineer.This is an exciting period of growth for this company, that work on several different product lines, from state-of-the-art airport scanning technology to top secret RADAR systems.You will be aiming to build and test physics-based models at the edge of what's possibleWhat you will be doing.You will model and analyse complex systems using MATLAB/Simulink, working alongside a multidisciplinary team of scientists, engineers, and designers. This isn't incremental work — you'll be applying deep engineering fundamentals to problems that directly impact people’s lives.What you can bring.You will need to have strong domain knowledge of MATALB and Simulink, ideally applied to systems engineering. This will need to include physics-based modelling and model-based systems engineering, with test bench development and code revision.You will need to be naturally curious, adaptable, and any knowledge of signal processing or Simulink HDL would be highly desirable.Why this roleThe company offer an environment that promotes pushing the boundaries of what is possible and trust their people to do great work. You will almost exclusively be working on new product development, and as well as autonomy, they make sure you have the right mentoring whenever you need it.They are offering tailored packages and can modify the seniority of the role to suit the right person. The package has a full suite of benefits including monetary bonuses and market-beating pension contributions.Interested?If you would like to find out more about this exciting role then make a confidential application now and a member of our team will be in touch with all the details.Hiring organizationEmployment TypeFull-timeBeginning of employmentASAPDuration of employmentPermanentIndustryIndustrial EngineeringJob Location Cambridge, UKWorking Hours Monday to FridayBase Salary60000-90000 Per yearDate posted 30th April 2026Valid through 27th May 2026PDF Export Export as PDFApply below or email directly: matthew.lowdon@newtoncolmore.com

Job Description:Role Overview As a Project Engineer at Huntsman, you will play a pivotal role in delivering engineering projects and supporting strategic investments at our Duxford site. Working closely with the Engineering & Maintenance team, you will ensure compliance with process safety standards, regulatory requirements, and Huntsman’s corporate CAPEX program. This is a dynamic position where you will contribute to continuous improvement, reliability, and innovation across site operations. Do you think you’re the right fit for this opportunity? Apply today! Role Responsibilities Act as the responsible Project Engineer for the site, ensuring compliance with regulatory requirements and maintaining engineering standards. Deliver site engineering systems that support EHS compliance. Contribute to strategic investment planning and provide project support for CAPEX and small projects within budget. Collaborate on preventive maintenance programs and continuous improvement initiatives. Plan and cost site-managed projects, ensuring timely submission of documentation for approvals. Maintain site drawings and technical information, and provide updates on analytics and automation tools. Support projects to ensure delivery on time, in full, and aligned with corporate engineering requirements. Drive EHS improvements and contribute to Huntsman’s Zero Harm objectives. Experience and Competencies Degree, HND, or HNC in Engineering (Electrical, Mechanical, Instrumentation, or Chemical). Experience in the chemical sector (pharma or biochemical or manufacturing considered). Strong background in engineering functions and project support. Knowledge of regulatory and statutory engineering requirements. Proficiency in MS Office (Microsoft Projects), AutoCAD, and data intelligence solutions. Knowledge of SAP is nice to have Familiarity with LEAN tools (VSM, SMED, Kaizen) and continuous improvement. Key Competencies Team working and relationship building. Delivering valuable results and performance focus. Conceptual and innovative thinking. What next? If you would like to join an innovative, collaborative, and multicultural team, please apply now. Your application will be forwarded to a Talent Acquisition Partner, who will strive to get back to you as soon as they can. We understand that applying for a new job is a big decision, and we will work hard to keep you updated and support you along the way. About Us At Huntsman, we pride ourselves on being a people-oriented organization. Our family-like atmosphere is cultivated by our diverse groups of team members around the world. We welcome the talent, experience, and fresh ideas that employees at all stages of their careers bring to Huntsman. In return, we offer you the opportunity to become an integral part of a dynamic, industry-leading company, where safety and ethics always come first. Additional Locations:SummaryLocation: UK - DuxfordType: Full time

What you will be involved with:Designing, developing, maintaining and improving existing instrumentation framework and tools.

This small and multi-disciplinary group within a larger company develop diverse, groundbreaking electronics technologies. Explore new challenges, collaborate, and see your work come to fruition in months rather than years – and then onto the next challenge.You’ll get to co-develop systems which combine advanced sensors, imaging, EM, acoustics, fluidics and AI, with applications in edge computing, instrumentation and special projects. You may apply skills in digital electronics, FPGA, DSP, embedded code, analogue electronics and RF.Along with the innate perks of such work, the company offer a generous salary, strong pension contribution, catered lunches, social and leisure facilities, and family-friendly leave policies.Your CV will show your strong relevant degree and supporting qualifications, and additional experience, likely commercial, or through a master’s degree and/or PhD. In addition, your experience will include several of:Digital electronics design, schematics capture and PCB layoutFPGA design, RTL development in VHDL / Verilog / SystemVerilogDSP, signal processing and/or related algorithmsAnalogue electronics, which may include work with sensors, RF or microwave EMNetwork protocols design and communications generallyEmbedded software in C, C++ and/or RustIt is likely you will have collaborated with other engineers and scientists on past projects. Any additional experience in Python, C#, MATLAB or other software systems is a plus. Some projects may involve security clearance, hence you will need to be a British citizen with 5+ years’ UK residence.Please note: even if you don’t have exactly the background indicated, do contact us now if this type of job is of interest – we may well have similar opportunities that you would be suited to. And of course, we always get your permission before submitting your CV to a company.

A leading inventor of Medical Devices are looking for an experienced Physicist who has successfully developed a number of complex Medical Devices. Based in Cambridge, you will be working alongside other physicists, electronics engineers, mechanical engineers and other medical devices industry experts to invent lifesaving and life-improving technologies.The Medical Devices you will develop will be across different medical technologies, so past industry experience in any of the following will be useful – Medical Imaging, Surgical Systems, Electro-Medical, Medical Instrumentation, Robotics, Machine Learning, Medical Diagnostics and other complex Medical Devices. You do not need to have worked in all of these, but the more fields the better when you have successfully brought a product to market.Working in industry is essential with this role, so ideally you will have been within a commercial organisation for at least a couple of years since leaving University. The only exception would be if you were working as a consultant to Medical Devices Companies while you were completing a PhD or during a post-doc role.This company has a fantastic track record developing new technologies, winning multiple awards. For the right people, this company offers an excellent salary, career training & development, bonus, pension and other excellent benefits.Honestly, most people want to join this company for the continued involvement of inventing new technologies, meaning you will always be tested and never become bored.Due to the complex nature of this role, you will need to hold a degree within a Physics, Engineering, Scientific or other field that led you into a product focused Physicist role, on Medical Devices.If you are interested, please make an application now as I find this type of role tends to be snapped up quite quickly.For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore, on +44 121 268 2240 or make an application and one of our team at Newton Colmore will contact you.Newton Colmore is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.Hiring organizationEmployment TypeFull-timeDuration of employmentPermanentIndustryMedical DevicesJob Location Cambridge, CambridgeshirePDF Export Export as PDFDate posted 17th July 2026Valid through 31st October 2026Apply below or email directly: andrew.welsh@newtoncolmore.com

Job Description SummaryLI#-OnsiteLocation: CambridgeInternal Title: Senior Scientist ISupport discovery and development projects through the design, development, and execution of in-vitro ADME assays, while building next generation lab automation capabilities to deliver high-quality study data for informed decision-making.Job DescriptionKey Responsibilities:Plan, execute and report ADME assays such as metabolic stability and permeability to support PK Science’s strategies.Interpret in vitro ADME data and translate findings to support early discovery, compound optimization and selection.Contribute to novel ADME methodologies and expand assay capabilities.Advance automation strategies (e.g., liquid handling, assay miniaturization, assay multiplexing) to expand laboratory capacity, standardize execution to reduce manual effort, and strengthen discovery assay operations.Execute and/or contribute to fully automated, end-to-end ADME assay workflows integrated with AI-enabled analytics.Develop methods to support small and large molecule bio-analysis using LCMS-MS, HRMS, and ICP-MS techniques.Troubleshot lab instrumentation and automation platforms.Manage study timelines, objectives and budgets, ensure accuracy of project progress in company tracking tools. Under management supervision, work to effectively communicate data, strategy and results to the project teams. Contribute to internal ADME study reports and regulatory documents (IND, IMPD, NDA, etc.).Participate in cross-departmental teams, department-wide initiatives and work streams.Complete all required organizational trainings and requirements according to corporate timelines. Adhere in strict accord to the appropriate SOP, quality and HSE guidelines.Essential Requirements:BSc or MSc with relevant experience in drug metabolism and pharmacokinetics or related field.BSc: 7+ years; MSc: 4+ years of ADME/DMPK experience.Experience working in a drug discovery or development laboratory or relevant experience in a CRO, Pharma or Biotech is highly desirable. Experience in metabolic stability and permeability assays highly preferrable; cell culture experience is a plus.Experience with laboratory automation integrated with AI-enabled analytics is highly desirable.Knowledge of related disciplines (e.g., bioanalytical, toxicology, biomarker) in the drug discovery or development process.Ability to work as part of a cross-functional team in a highly dynamic, matrixed, project-team environment. Strong organizational and project skills with critical thinking and problem-solving skills. Fluent oral and written EnglishThe salary for this position is expected to range between $89,600 and $166,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$89,600.00 - $166,400.00Skills DesiredAdobe Photoshop, Chemistry, Collaboration, Compensations Management (Employees) (Inactive), Curious Mindset, Drug Development, Employee Recruitment, Flexibility (Inactive), Oscilloscope, Patient Care, Pipeline (Software) (Inactive), Sales, Small Businesses, TeamworkSummaryLocation: Cambridge (USA)Type: Full time

A Life-Science company, based in Cambridgeshire, are currently looking for an experienced Embedded Software Engineer to work on real-time software for embedded control systems.The technologies you will work on will range from new life-science instrumentation through to robotics projects.All the proj

Job Overview: As a Security Engineer – Fuzzing Specialist, you will own and evolve our coverage-guided fuzzing program. Your mission is to uncover hard-to-reach security flaws before attackers do, drive fixes to closure, and help product teams to embrace dynamic testing like fuzzing. You’ll scout for new attack surfaces, craft high-performance fuzzing harnesses, and design custom sanitisers that push the state of the art. Success means measurable coverage gains, actionable crash reports, and products that ship with provable resilience.Responsibilities:Map & prioritise fuzzing surfaces across services, libraries, APIs, and protocols; maintain a living risk-based roadmap.Design, build, and extend fuzzing harnesses (libFuzzer, AFL++, Honggfuzz, etc.) that improve code-path exploration and minimise false positives.Continuously improve coverage by growing seed corpus, deploying targeted mutation strategies, and integrating new instrumentation techniques.Automate crash triage & root-cause analysis; distinguish exploitable vulnerabilities from benign faults and drive CVE-level findings to remediation.Develop custom sanitisers to expose classes of bugs traditional fuzzing misses.Validate fixes & guard against regressions through differential fuzzing and regression corpora.Assess external disclosures (bug bounties, supply-chain advisories) to determine fuzzing detectability and refine harnesses when gaps are found.Document, report, and share insights — from coverage metrics to post-mortems to create data-driven security.Required Skills and Experience:1+ years in application or product security with a deep focus on coverage-guided fuzzing.Hands-on expertise with at least one modern fuzzing framework (e.g., libFuzzer, AFL++, Honggfuzz).Proficient in C/C++ plus strong scripting ability in Python for automation.Solid understanding of memory-safety vulnerabilities, undefined behaviour, sanitisers, and compiler instrumentation.Demonstrated ability to triage crashes using debuggers, profilers, and reverse-engineering tools (gdb/lldb, IDA/Ghidra).Excellent written communication for documenting findings and influencing engineering teams.“Nice To Have” Skills and Experience :Contributions to open-source fuzzing tools, sanitisers, or security research publications.Knowledge of distributed fuzzing at scale (GCP/AWS, Kubernetes, or bare-metal clusters).Familiarity with kernel, embedded, or firmware fuzzing (e.g., Syzkaller, QEMU-based harnesses).Background in reverse engineering, static analysis or symbolic execution.Experience integrating fuzzing into CI/CD pipelines and tracking coverage metrics.If you’re passionate about breaking software safely, love high-coverage charts, and want to make a measurable dent in product security, we’d love to hear from you!#LI-CI1Our 10x MindsetAt Arm, we believe progress happens when people are empowered to think bigger and push beyond what seems possible. Our 10x mindset is about curiosity, ambition and creating impact that will be used by millions. We learn fast, prioritise collaboration and turn bold ideas into real technology. We look for people who are inspired by this way of working and want to grow in an environment where bold ideas are welcomed. Discover how the 10x mindset shapes life at Arm: Use of AI in Your ApplicationAt Arm, we embrace the benefits AI can bring, including in recruitment. You may use AI to support your preparation, such as improving the clarity of written responses, practicing interview questions, or learning more about our industry. However, your application, and interview responses must reflect your own thinking, experience, and abilities. We want to understand your authentic perspective, creativity, and approach to problem solving. As such, you may not use AI to complete assigned tasks as part of any assessments. If you plan to use AI-supported or assistive technologies as part of a reasonable adjustment, please contact accommodations@arm.com so we can support you.Recruitment Adjustments and AccommodationsAt Arm, we want to build extraordinary teams. If you need an adjustment or an accommodation during the recruitment process, please email accommodations@arm.com. To note, by sending us the requested information, you consent to its use by Arm to arrange for appropriate accommodations. All accommodation or adjustment requests will be treated with confidentiality, and information concerning these requests will only be disclosed to the extent necessary to provide the accommodation. Although this is not an exhaustive list, examples of support include breaks between interviews, having documents read aloud, or office accessibility. Please email us about anything we can do to accommodate you during the recruitment process.Hybrid WorkingArm’s approach to hybrid working is designed to create a working environment that supports both high performance and personal wellbeing. We believe in bringing people together face to face to enable us to work at pace, whilst recognizing the value of flexibility. Within that framework, we empower groups/teams to determine their own hybrid working patterns, depending on the work and the team’s needs. Details of what this means for each role will be shared upon application. In some cases, the flexibility we can offer is limited by local legal, regulatory, tax, or other considerations, and where this is the case, we will collaborate with you to find the best solution. Please talk to us to find out more about what this could look like for you.Equal OpportunitiesArm is an equal opportunity employer, committed to providing an environment of mutual respect where equal opportunities are available to all applicants and colleagues. We are a diverse organization of dedicated and innovative individuals, and don’t discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Would you like to join a team working across the software technology components used by hundreds of millions of users across multiple platforms and market segments globally? As a Software Architect in the Software Organisation, you will work with our key software ecosystems to define software solutions to enable Arm technology and develop strategies to have those solutions adopted and enabled for users. Our Central Engineering Software group delivers support for Arm technologies across a wide variety of software projects and creates example software solutions to demonstrate real world applications. You will join a team of software solution architects addressing the growing demand for software to support Arm systems. The position will be based at Arm offices in Cambridge, Budapest, or Bangalore. Job Overview: As a member of a large software engineering team you will help evolve our software strategy across all computing segments, including data centre, automotive, mobile, robotics, networking, home, laptops, TVs, embedded and IoT. You will drive adoption of new features and trends in core processing, accelerators, and system hardware, focusing on improved security, reliability, and performance. Responsibilities: Understanding new Arm architecture and IP features, their implementation and what that means for existing software components and tools. Devising how to promote their benefits to software ecosystems and resolve issues that arise in their adoption. Analysis and deep understanding of software solutions currently deployed in products, in particular the major open-source software projects such as Linux. Delivering software improvements back to the relevant open-source projects as a reference for Arm customers to create their own systems from. Working with Arm’s OS, OEM and Silicon Partners to drive standards that enable the optimisation, differentiation, and fast evolution benefits of Arm’s Partner model Building new software paradigms onto Arm reference hardware designs Profiling the performance of the system and innovating ways to improve Leading validation of the functionality, security and safety You can expect to be working closely with some of the greatest household names in our industry to help develop, optimize, and deliver the software needed to support Arm's pioneering IP, as well as helping Arm grow its role in new market segments. Required Skills and Experience:Knowledge of Arm based computer Architecture and the range of SoCs and devices that are created using Arm hardware IP. Experience of software profiling, instrumentation, and optimization for real world applications and workloads such as AI stacks, run-time compilers and multimedia processing. Strong understanding of complex multi-component computing systems with demonstrable low-level OS/device driver development or integration experience Authoritative knowledge of C or C++ development with proficiency with optimizing applications, workloads, and compilers Understanding of how to rigorously test software and design software for test Experience of the software lifecycle: has taken complex software from concept to production and maintenance “Nice To Have” Skills and Experience : Experience with Android, ChromeOS or Windows software and systems Experience with Linux, Linux distributions, Cloud/Edge applications and networking software Knowledge of Artificial Intelligence software stacks, algorithms and tooling Knowledge of multimedia system designs involving GPUs, compositing display processors and image signal processing Familiarity with System-on-a-Chip architectures In Return: Our UK offices are outstanding places to collaborate. If you are interested but unsure whether you tick all the boxes, we still would love you to reach out! We are keen to welcome versatile people into Arm! Please note that no relocation package is available for this role. If skilled worker sponsorship is required, Arm will meet costs associated with sponsorship for the employer only. All fees associated with the individual’s application e.g. visa application fee and Immigration Health Surcharge, will be the responsibility of the successful candidate. #LI-CM1Our 10x MindsetAt Arm, we believe progress happens when people are empowered to think bigger and push beyond what seems possible. Our 10x mindset is about curiosity, ambition and creating impact that will be used by millions. We learn fast, prioritise collaboration and turn bold ideas into real technology. We look for people who are inspired by this way of working and want to grow in an environment where bold ideas are welcomed. Discover how the 10x mindset shapes life at Arm: Use of AI in Your ApplicationAt Arm, we embrace the benefits AI can bring, including in recruitment. You may use AI to support your preparation, such as improving the clarity of written responses, practicing interview questions, or learning more about our industry. However, your application, and interview responses must reflect your own thinking, experience, and abilities. We want to understand your authentic perspective, creativity, and approach to problem solving. As such, you may not use AI to complete assigned tasks as part of any assessments. If you plan to use AI-supported or assistive technologies as part of a reasonable adjustment, please contact accommodations@arm.com so we can support you.Recruitment Adjustments and AccommodationsAt Arm, we want to build extraordinary teams. If you need an adjustment or an accommodation during the recruitment process, please email accommodations@arm.com. To note, by sending us the requested information, you consent to its use by Arm to arrange for appropriate accommodations. All accommodation or adjustment requests will be treated with confidentiality, and information concerning these requests will only be disclosed to the extent necessary to provide the accommodation. Although this is not an exhaustive list, examples of support include breaks between interviews, having documents read aloud, or office accessibility. Please email us about anything we can do to accommodate you during the recruitment process.Hybrid WorkingArm’s approach to hybrid working is designed to create a working environment that supports both high performance and personal wellbeing. We believe in bringing people together face to face to enable us to work at pace, whilst recognizing the value of flexibility. Within that framework, we empower groups/teams to determine their own hybrid working patterns, depending on the work and the team’s needs. Details of what this means for each role will be shared upon application. In some cases, the flexibility we can offer is limited by local legal, regulatory, tax, or other considerations, and where this is the case, we will collaborate with you to find the best solution. Please talk to us to find out more about what this could look like for you.Equal OpportunitiesArm is an equal opportunity employer, committed to providing an environment of mutual respect where equal opportunities are available to all applicants and colleagues. We are a diverse organization of dedicated and innovative individuals, and don’t discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Hexcel is currently seeking an Electrical and Controls Project Engineer for our Duxford, UK location. Develop electrical and control system specifications for manufacturing equipment. Create and maintain electrical, instrumentation, and control documentation.

Controls and Instrumentation EngineerLocation: Slough, United KingdomThe actual location of this job is in Slough, United Kingdom. Relocation assistance is available for eligible candidates and their families, if needed.Join Lonza Biologics in Slough as a Controls and Instrumentation Engineer and play a key role in supporting the reliable operation and continuous improvement of our biopharmaceutical manufacturing facilities. You will use your expertise in automation, control systems, and instrumentation to help deliver safe, compliant, and high-quality processes that support the manufacture of life-changing medicines.This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.What you will get:An agile career and dynamic working culture where you can develop your technical expertise and grow your career.The opportunity to work with advanced automation and control technologies within a leading biopharmaceutical manufacturing environment.An inclusive and ethical workplace where collaboration and innovation are encouraged.Compensation programs that recognize high performance.A variety of benefits dependent on role and location.The full list of our global benefits can be found here: .What you will do:Design, develop, implement, and maintain control systems and instrumentation solutions that support biopharmaceutical manufacturing processes.Configure, troubleshoot, and optimise automation systems including PLCs, Distributed Control Systems (DCS), and SCADA platforms.Develop and maintain engineering documentation, including control strategies, functional specifications, control narratives, wiring diagrams, and technical drawings.Maintain, calibrate, and troubleshoot process instrumentation including sensors, transmitters, valves, and analytical equipment to ensure reliable operation.Lead and support commissioning, qualification, and validation activities for control systems and instrumentation.Collaborate with manufacturing, quality, engineering, IT teams, and external suppliers to deliver effective technical solutions.Drive continuous improvement initiatives, conduct root cause investigations, and provide technical support and training to operational teams.What we are looking for:A degree in Electrical Engineering, Automation, Chemical Engineering, or a related technical discipline, or equivalent relevant experience.Significant experience in controls and instrumentation engineering, ideally gained within a biopharmaceutical, pharmaceutical, or other regulated manufacturing environment.Strong experience with PLC programming and troubleshooting, including platforms such as Rockwell Automation or Siemens.Experience working with Distributed Control Systems (DCS), particularly Emerson DeltaV, and HMI/SCADA platforms.Strong knowledge of process instrumentation principles, calibration techniques, troubleshooting methodologies, and industrial communication protocols.Experience working in a GxP/cGMP regulated environment, with knowledge of computerized system validation (CSV) principles.Ability to interpret P&IDs, electrical schematics, and technical documentation, with excellent problem-solving and communication skills.About LonzaAt Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.Ready to shape the future of life sciences? Apply now.SummaryLocation: UK - Slough; UK - CambridgeType: Full time

This company is expanding its team dedicated to Medical Devices Instrumentation, primarily focusing on Cancer Instrumentation. A growing division within an established Medical Devices organisation in South Cambridge is currently seeking an experienced Medical Devices Mechanical Engineer to contribut

Job title: \n Research Scientist - Geothermal Multi-Phase Fluid Dynamic Experimentalist \n \n About Us: \n We are a global technology company, driving energy innovation for a balanced planet. \n \n At SLB we create amazing technology that unlocks access to energy for the benefit of all. That is our purpose. As innovators, that has been our mission for 100 years. We are facing the world’s greatest balancing act- how to simultaneously reduce emissions and meet the world’s growing energy demands. We’re working on that answer. Every day, a step closer. \n \n Our collective future depends on decarbonizing the fossil fuel industry, while innovating a new energy landscape. It’s what drives us. Ensuring progress for people and the planet, on the journey to net zero and beyond. For a balanced planet. \n \n Our purpose: Together, we create amazing technology that unlocks access to energy for the benefit of all. You can find out more about us on https://www.slb.com/who-we-are \n \n Location: \n Cambridge, UK \n \n SLB Cambridge Research (SCR) is part of SLB’s global network of research and engineering centres. SCR is a dynamic, multidisciplinary environment with state-of-the-art research and computing facilities. We work on applied research projects in the physical sciences to meet the current and future challenges of the industry. \n \n Job Summary: \n We are seeking a creative self-motivated Research Scientist to develop experiments for understanding the complex flow dynamics in geothermal systems. The initial focus will be on designing and leading experiments to validate mathematical models of fluid flow in enhanced geothermal systems. \n \n The focus will then expand to lead the experiments to improve design and optimization of geothermal systems. The job will require experience in mechanical design, building, and commissioning of experiments at temperature and pressure. \n \n The candidate will also need to work constructively and effectively in a multidisciplinary team with business and engineering teams to ensure their solutions have a significant impact. They will also present their work internally and externally. \n \n Responsibilities: \n\n • Work in designing and executing multiphase fluid flow experiments (gas, liquid, and solid phases) to contribute to our research of geothermal systems at SCR\n, • Work with modellers and geothermal domain experts to build and validate models and concepts\n, • Engage and collaborate with SLB technical community\n, • Ability to develop novel solutions to research and engineering problems, and articulate them to the technology team and management\n, • Publish scientific papers, write patent applications and attend conferences\n\n \n Qualifications: \n\n • PhD in Fluid mechanics or a related field\n, • Experience in design of experimental rigs and expertise in building, and commissioning of experiments is essential\n, • Experience in particle tracking techniques\n, • Experience in heat transfer (modelling or experiments)\n, • Experience in data acquisition, signal processing, and data interpretation including data science approaches is highly desirable\n, • Experience in advanced instrumentation for multiphase flow measurements including laser-optical (PLIF, PIV), electrical, ultrasonic, and nuclear techniques is desirable\n, • CFD modelling of multiphase flows (OpenFoam, COMSOL, Ansys) is desirable\n, • Relevant publications in reputable peer-reviewed journals are desirable\n, • Understanding of Geothermal Systems is desirable\n\n \n What we can offer you: \n Competitive base salary with bonus, private healthcare for employee & family, subsidised dental care, Health & Wellbeing programs such as the Employee Mental health support, health & wellness coaching, part employer and employee funded pension contribution, Income protection scheme, life insurance. \n \n Other benefits are also available through the SLB flexible benefits program. \n \n SLB is an equal employment opportunity employer. Qualified applicants are considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or other characteristics protected by law. \n \n The recruiting process and the position can be adapted to fit most disabilities, please do not hesitate to mention this when applying.

\n Job Title: Director of Pathology Location: Cambridge, UK Hybrid working: Minimum 3 days per week in the office Introduction to role:\n Are you ready to bring decisive medical leadership in pathology to accelerate personalised diagnostics that guide clinical trials and patient care? This is a chance to shape how novel biomarkers become trusted tests that identify the right patients for the right therapies, faster. \n You will join our internal accredited laboratory delivering in-house diagnostic testing for early-phase clinical studies and pioneering approaches in patient stratification. Your oversight will ensure assays are robust, validated and clinically meaningful, directly influencing how our medicines are developed and how patients are selected for studies. Working at the intersection of pathology, quality, and translational science, you will help advance companion and complementary diagnostics— including computational pathology and image analysis—across a biomarker-driven portfolio. \n At Director level, you will look beyond daily operations to set direction, influence governance, and represent the laboratory in internal and external forums. Will you help us lift diagnostic standards, bring new technologies into practice, and translate cutting-edge science into results that clinicians and patients can trust? Accountabilities:\n \n • Medical and Technical Oversight: Provide pathology oversight of assay performance, result review and reporting practices in an accredited environment supporting clinical and biomarker development.\n, • CAP/CLIA and GxP Compliance: Act in a role aligned to CAP/CLIA expectations; ensure testing and reporting practices meet regulatory and professional standards, including ISO 15189, GCP, IVDR and HTA requirements.\n, • Result Authorisation and Interpretation: Review, interpret and approve laboratory results and reports, ensuring outputs are scientifically valid, clinically appropriate and compliant with defined quality requirements; contribute to clinical and scientific interpretation of pathology and biomarker data.\n, • Method Evaluation and Approval: As technical lead, evaluate and approve novel test methods; ensure fitness for purpose and appropriate validation or verification before clinical use.\n, • Operational Partnership: Work closely with the Laboratory Director, QA/QC and operational leadership to evolve methods, procedures, instrumentation, staffing models and workflow design.\n, • Strategy and Companion Diagnostics: Provide scientific and medical input into assay and biomarker strategy, including companion diagnostic development and clinical implementation planning; align with broader clinical development objectives.\n, • Innovation and Digital Pathology: Drive continuous improvement and the introduction of emerging technologies, including digital pathology, image analysis and data-enabled diagnostic workflows.\n, • Clinical Trial Support: Provide medical and technical oversight for prospective patient testing in clinical studies, ensuring protocol-aligned reporting, documentation and quality standards.\n, • External Engagement and Governance: Represent the laboratory in governance forums; contribute to external regulatory interactions; lead capability-building in diagnostic pathology and companion diagnostics across matrix teams.\n Essential Skills/Experience:\n \n, • Medical degree recognised by the General Medical Council (GMC).\n, • Current Licence to Practice in the United Kingdom.\n, • Significant experience practising at consultant pathologist level, or equivalent senior medical pathology role, within a diagnostic or regulated laboratory environment.\n, • Experience providing medical and technical oversight for testing within an accredited or regulated laboratory environment.\n, • Strong working knowledge of CAP/CLIA, ISO 15189, GCP, IVDR, HTA and applicable standards governing laboratory quality systems, patient testing, and report issuance.\n, • Experience reviewing, authorising, or providing medical oversight of laboratory reports, ensuring outputs are scientifically valid, medically appropriate, and compliant with regulatory and quality requirements.\n, • Ability to provide clear clinical and scientific interpretation of pathology and biomarker data, integrating findings with other data streams where relevant.\n, • Strong leadership, communication, and stakeholder management skills, with the ability to work effectively across matrix teams and provide oversight to multidisciplinary laboratory activities.\n Desirable Skills/Experience:\n \n, • GMC Specialist Registration in an appropriate pathology specialty.\n, • FRCPath in Histopathology or another relevant pathology discipline, or equivalent specialist qualification.\n, • PhD, MD(Res), or equivalent higher research qualification in pathology, oncology, translational medicine, biomarker science, or a related discipline.\n, • Experience in companion diagnostic and predictive biomarker development within pharmaceutical, biotechnology, or accredited diagnostic laboratory settings, working in line with ISO 13485 and ISO 14971.\n, • Experience serving in a role aligned to CAP Technical Supervisor, General Supervisor, or Laboratory Director responsibilities for high-complexity testing.\n, • Familiarity with digital pathology, image analysis, and computational pathology approaches in a regulated environment.\n, • Experience with diagnostic methods, such as PCR, NGS, spatial omics, proteomics, mass spectrometry and other platforms relevant to precision medicine.\n, • Experience leading or supporting clinical trial assay governance, including oversight of testing strategies, report processes, and protocol-aligned patient testing.\n, • Experience overseeing or contributing to prospective patient testing in support of clinical trials, including understanding of protocol-driven testing, result reporting, and documentation requirements.\n Why AstraZeneca:\n Here, your expertise in diagnostic pathology fuels a bold mission: detecting disease earlier, matching patients to targeted treatments and tackling some of the toughest cancers through science and technology. With a deep, well-funded pipeline and teams empowered to make smart, fast decisions, we bring clinicians, data scientists and engineers together to turn breakthrough ideas into validated tests that shape studies and patient outcomes. You will find the ambition to push boundaries balanced with a culture that values collaboration and kindness—so you can lead, learn and see the real-world impact of your work every day. \n Lead the evolution of diagnostics that guide life-changing medicines—take the next step in your career and shape how patients are identified and treated. Date Posted\n 14-Aug-2026 Closing Date\n 27-Aug-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

Job Title: Director of Pathology Location: Cambridge, UKHybrid working: Minimum 3 days per week in the officeIntroduction to role: Are you ready to bring decisive medical leadership in pathology to accelerate personalised diagnostics that guide clinical trials and patient care? This is a chance to shape how novel biomarkers become trusted tests that identify the right patients for the right therapies, faster. You will join our internal accredited laboratory delivering in-house diagnostic testing for early-phase clinical studies and pioneering approaches in patient stratification. Your oversight will ensure assays are robust, validated and clinically meaningful, directly influencing how our medicines are developed and how patients are selected for studies. Working at the intersection of pathology, quality, and translational science, you will help advance companion and complementary diagnostics— including computational pathology and image analysis—across a biomarker-driven portfolio. At Director level, you will look beyond daily operations to set direction, influence governance, and represent the laboratory in internal and external forums. Will you help us lift diagnostic standards, bring new technologies into practice, and translate cutting-edge science into results that clinicians and patients can trust?Accountabilities: - Medical and Technical Oversight: Provide pathology oversight of assay performance, result review and reporting practices in an accredited environment supporting clinical and biomarker development. - CAP/CLIA and GxP Compliance: Act in a role aligned to CAP/CLIA expectations; ensure testing and reporting practices meet regulatory and professional standards, including ISO 15189, GCP, IVDR and HTA requirements. - Result Authorisation and Interpretation: Review, interpret and approve laboratory results and reports, ensuring outputs are scientifically valid, clinically appropriate and compliant with defined quality requirements; contribute to clinical and scientific interpretation of pathology and biomarker data. - Method Evaluation and Approval: As technical lead, evaluate and approve novel test methods; ensure fitness for purpose and appropriate validation or verification before clinical use. - Operational Partnership: Work closely with the Laboratory Director, QA/QC and operational leadership to evolve methods, procedures, instrumentation, staffing models and workflow design. - Strategy and Companion Diagnostics: Provide scientific and medical input into assay and biomarker strategy, including companion diagnostic development and clinical implementation planning; align with broader clinical development objectives. - Innovation and Digital Pathology: Drive continuous improvement and the introduction of emerging technologies, including digital pathology, image analysis and data-enabled diagnostic workflows. - Clinical Trial Support: Provide medical and technical oversight for prospective patient testing in clinical studies, ensuring protocol-aligned reporting, documentation and quality standards. - External Engagement and Governance: Represent the laboratory in governance forums; contribute to external regulatory interactions; lead capability-building in diagnostic pathology and companion diagnostics across matrix teams. Essential Skills/Experience: - Medical degree recognised by the General Medical Council (GMC). - Current Licence to Practice in the United Kingdom. - Significant experience practising at consultant pathologist level, or equivalent senior medical pathology role, within a diagnostic or regulated laboratory environment. - Experience providing medical and technical oversight for testing within an accredited or regulated laboratory environment. - Strong working knowledge of CAP/CLIA, ISO 15189, GCP, IVDR, HTA and applicable standards governing laboratory quality systems, patient testing, and report issuance. - Experience reviewing, authorising, or providing medical oversight of laboratory reports, ensuring outputs are scientifically valid, medically appropriate, and compliant with regulatory and quality requirements. - Ability to provide clear clinical and scientific interpretation of pathology and biomarker data, integrating findings with other data streams where relevant. - Strong leadership, communication, and stakeholder management skills, with the ability to work effectively across matrix teams and provide oversight to multidisciplinary laboratory activities. Desirable Skills/Experience: - GMC Specialist Registration in an appropriate pathology specialty. - FRCPath in Histopathology or another relevant pathology discipline, or equivalent specialist qualification. - PhD, MD(Res), or equivalent higher research qualification in pathology, oncology, translational medicine, biomarker science, or a related discipline. - Experience in companion diagnostic and predictive biomarker development within pharmaceutical, biotechnology, or accredited diagnostic laboratory settings, working in line with ISO 13485 and ISO 14971. - Experience serving in a role aligned to CAP Technical Supervisor, General Supervisor, or Laboratory Director responsibilities for high-complexity testing. - Familiarity with digital pathology, image analysis, and computational pathology approaches in a regulated environment. - Experience with diagnostic methods, such as PCR, NGS, spatial omics, proteomics, mass spectrometry and other platforms relevant to precision medicine. - Experience leading or supporting clinical trial assay governance, including oversight of testing strategies, report processes, and protocol-aligned patient testing. - Experience overseeing or contributing to prospective patient testing in support of clinical trials, including understanding of protocol-driven testing, result reporting, and documentation requirements. 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: Here, your expertise in diagnostic pathology fuels a bold mission: detecting disease earlier, matching patients to targeted treatments and tackling some of the toughest cancers through science and technology. With a deep, well-funded pipeline and teams empowered to make smart, fast decisions, we bring clinicians, data scientists and engineers together to turn breakthrough ideas into validated tests that shape studies and patient outcomes. You will find the ambition to push boundaries balanced with a culture that values collaboration and kindness—so you can lead, learn and see the real-world impact of your work every day. Lead the evolution of diagnostics that guide life-changing medicines—take the next step in your career and shape how patients are identified and treated.Date Posted14-Aug-2026Closing Date27-Aug-2026Our 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.SummaryLocation: UK - CambridgeType: Full time

A growing medical devices company, based in Cambridge, are currently looking for an experienced Mechanical Engineer to help with the development of complex instrumentation. You will be working within an established team of Mechanical Engineers, where your focus will be on complex instrumentation tha

Job Description SummaryThis role is responsible for designing, developing, implementing and maintaining laboratory robotics which support exploratory biology in an automated fashion. The work is hands-on and requires a broad range of engineering disciplines including project management, troubleshooting electrical and mechanical parts, developing protocols, liquid handling, and providing operating system validation/verification. The team's focus is to design, build, maintain, and improve large and small automated systems for high throughput screening and automated cell culture.Job DescriptionInternal Job Title: Senior Automation Engineer IPosition Location: Cambridge, MA onsiteThis role is responsible for designing, developing, implementing and maintaining laboratory robotics which support exploratory biology in an automated fashion. The work is hands-on and requires a broad range of engineering disciplines including project management, troubleshooting electrical and mechanical parts, developing protocols, liquid handling, and providing operating system validation/verification. The team's focus is to design, build, maintain, and improve large and small automated systems for high throughput screening and automated cell culture.Key Responsibilities:Act as a primary support engineer for laboratory automation and instrumentation within DSc in Cambridge, MA. Responsible for the setup, operation, and maintenance of state-of-the-art high throughput screening (HTS) systems.Working with scientists to adapt biological assays from the bench to fully automated assays using high throughput screening systems. Knowledge of Biosero Orchestrator and Green Button Go scheduling software is highly desirable.Act as project manager for small- and large-scale automation projects. The successful candidate will manage, plan, develop, and execute laboratory automation projects from start-up to completion.Work effectively with multi-disciplinary groups and individuals to implement solutions that reflect operational efficiencies in terms of throughput, delivery, costs, as well as health, safety and environmental considerations.Establish, monitor, and maintain a stable and productive automation environment through QC and preventative maintenance.Assist in the development of SOP’s, maintenance manuals, start-up procedures, and provide training to new users of equipment.Must be self-motivated with the ability to multitask and effectively manage timelines.Must be able to work independently and in team situations.Essential Requirements:B.S. in mechanical, electrical or bioengineering, or similar engineering discipline.3+ years experience servicing and implementing automated systems.Experience designing, building and deploying automated laboratory workflows in life sciences or clinical laboratories.Strong organizational, written, and verbal communications skills required to interact effectively between scientific staff, customers, key stakeholders, and vendors.Strong computer skills including MS Office and CAD (preferably SolidWorks).Strong troubleshooting and problem-solving skills.Desirable Requirements:In addition to the experience above, the ideal candidate would have familiarity with the following systems and associated software: Biosero Orchestrator / Green Button Go robotic platforms, HighRes BioSolutions (Staubli/Denso/Precise) / Cellario robotic platforms, CellTrio RoboCell, Beckman Echo, GNF Director robotic platforms, and a wide range of laboratory benchtop equipment.Basic understanding of C# or equivalent programming language.Interest in the evaluation, integration, and optimization of AI models and orchestration frameworks.Familiarity with data analysis platforms like Genedata Screener, Spotfire and AI agents.Experience working with engineers and scientists to develop new automated platforms.Create innovative solutions to support complex biological assays at scale.Experience integrating automated systems to LIMS and other scientific data systems, either in-house or commercially available, to support reliable data capture, transfer, traceability, and downstream analysis.The salary for this position is expected to range between $93,800 and $174,200 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$93,800.00 - $174,200.00Skills DesiredData Analysis, Problem Solving, Structural BiologySummaryLocation: Cambridge (USA)Type: Full time

An exciting and expanding Scientific Systems organisation, based in a walking distance from Cambridge City Centre, are currently looking for Senior Product Design Engineer to help and lead the Electro-Mechanical development of cutting-edge scientific instrumentation technologies.This company are still in a start-up phase, meaning if you join now you will gain access to equity in the business. The plans this company have in place make me think they will be nothing but a success.You will be working alongside scientists, physicists, engineers and other experts needed to develop this new technology. Due to working with these types of R&D experts, you will need to have been successful in this type of role previously, specifically within highly regulated environments like Medical Devices, Life Sciences, Aerospace and other field where you have applied your Product Design skills to scientific instrumentation technologies, specifically electro-mechanical technologies.As you will be in a senior role in the business, the future plan is that you would take on mentorship role straight away and due to this you will need to have expert CAD experience where you can help others with complex issues. I’d expect that in the future that you would get the opportunity to move into more of a management/team leader type role, however this will not be immediate.Specific industry backgrounds that would be useful include, but not limited to, medical devices instrumentation, diagnostics instrumentation, scientific instrumentation and fluidics instrumentation.It would be highly advantageous is you have been involved with new product introduction. As a start-up company, you would be expected to help with other areas of the business whenever needed, so wider knowledge and experience will be considered as they may help other areas of the business.Unlike many start-up companies, this organisation already has all of its funding secured so this means the job security is assured more than most companies in the current global market. Apart from career progression and job security, you will be rewarded with starting salary, benefits package (at a greater level than most start-up companies, in line with most established companies) and equity shares.I’m expecting a lot of interest in this role and they are still interviewing and making offers to candidates, despite the global issues with COVID-19, so if you are interested, I suggest making an application now or risk missing out. Interviews are being held via different video technology.For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore, on +44 121 268 2240 or make an application and one of our team at Newton Colmore will contact you.Newton Colmore is a specialist recruitment company within the Medical Devices, Scientific Engineering, Data Science, Machine Learning, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.Hiring organizationEmployment TypeFull-timeDuration of employmentPermanentIndustryMedical DevicesJob Location Cambridge, CambridgeshirePDF Export Export as PDFDate posted 25th July 2026Valid through 31st October 2026Apply below or email directly: andrew.welsh@newtoncolmore.com

MEICA and capital maintenance - Our Mechanical, Electrical, Instrumentation, Control & Automation (MEICA) experts offer a one-stop solution, including ongoing opera. Were problem solvers with over 140 years of combined experience in engineering and infrastructure. Our Mechanical, Electrical, Instrum

Exciting opportunity to join an innovative, industry leading laboratory equipment distributor to drive Sales in the South East. Our client is a leading provider of analytical instruments in the UK with products ranging from sample preparation systems to elemental analysis instrumentation. This opportunity calls for an ambitious scientist looking to drive sales whilst providing excellent service to customers. Within this role, you will support customers by identifying their key pain points and advising which products in your portfolio would best serve their requirements. Your position will focus on managing existing accounts and identifying new customers in academic, CRO, biotech and pharma laboratories. You will be based remotely and are expected to travel ~60% of your time to customer sites across the Southeast for instrument demonstrations, presentations and negotiation. To be considered for this position you will have: BSc minimum in Chemistry or related subject Eligibility to work in the UK without sponsorship UK driver’s license and willingness to travel Proven experience within scientific sales and understanding of the sales process is highly desirable For your work you will be provided with a competitive basic salary, commission scheme, car and additional employee benefits. Please apply below to receive more details! Keywords: chemistry equipment, laboratory equipment, consumables sales, ...

Astute's Power team is partnering with a leading Energy from Waste company in the UK to recruit an Electrical Controls and Instrumentation Technician for its site in Milton Keynes. The following information provides an overview of the skills, qualities, and qualifications needed for this role. The EC&I Technician role comes with a starting salary of up to £52,000 and a bonus. If you are an apprentice trained EC&I Technician with strong Controls and Instrumentation knowledge xsngvjr and experience on heavy industrial Please click on the apply button to read the full job description

The Opportunity: The Gas Service Technical Lead provides technical leadership and support for the safe, reliable, and efficient operation of Gas farm and onsite gas storage facilities. The role ensures the integrity, availability, and compliance of gas storage, handling, distribution, and associated control systems while driving operational excellence and continuous improvement. Technical Authority & Subject Matter Expertise Act as primary technical point of escalation and the technical authority for gas farm systems, equipment, and processes. Provide expert guidance on gas storage, transfer, distribution, pressure management, and associated utilities. Lead technical investigations, root cause analysis, and problem resolution for operational issues. Provide day-to-day technical support to gas farm operations and maintenance teams. Troubleshoot process, equipment, and control system issues to minimise operational disruption. Support the development of technical standards and best practices. Represent the gas farm during audits, inspections, and external technical reviews. Process Safety, Compliance & Risk Management Champion process safety, operational discipline, and adherence to relevant legislation, standards, and company procedures. Conduct technical auditing, regulatory compliance oversight Ensure gas farm operations comply with safety, environmental, and regulatory requirements. Support risk assessments, management of change (MOC), and safety reviews. Promote safe working practices and challenge unsafe conditions or behaviours. Asset Reliability & Maintenance Develop and maintain strategies to maximise equipment reliability and availability. Provide technical oversight for maintenance activities, inspection programmes, and equipment performance. Identify reliability risks and implement mitigation plans. Support lifecycle management of critical assets, including vessels, pipework, valves, compressors, pumps, instrumentation, and control systems. Operations Support Assist with operational planning, shutdowns, start-ups, and abnormal operating conditions. Ensure operating procedures and technical documentation remain accurate and effective. Engineering Projects & Continuous Improvement Support changes, modifications, and improvement projects from concept through implementation. Lead or support technical improvement initiatives to enhance safety, efficiency, capacity, and sustainability. Support commissioning, testing, and handover of new or modified equipment. Identify opportunities for optimisation and cost reduction. undefined Collaboration & Knowledge Sharing Act as a technical mentor to operational personnel. Share knowledge and promote technical excellence across the organisation. Collaborate with operations, maintenance, engineering, HSE, and project teams. QUALIFICATIONS (Education/Training, Experience and Certifications) IOSH or NEBOSH Gas Safe Certification/Qualification MediGas Certification/qualification, desirable COMPEX awareness award/certification ATEX awareness award/certification Pressure Systems Safety Regulations (PSSR) awareness A level, O Level, GCSE; associate degree or undergraduate degree in business or science related field is preferred Forklift Certification preferred but not essential Spill containment, ADR, IATA, DOT, IMDG training preferred but not essential GMP/GLP training preferred but not essential Valid Driver's License KNOWLEDGE, SKILLS, ABILITIES & COMPETENCIES (Those necessary to achieve conformity of products and services) Technical Experience & Industry Knowledge Extensive experience working with gas systems, gas storage, and distribution. Experience leading technical investigations and reliability improvement initiatives. Demonstrated experience supporting hazardous operations, gas systems, pressure equipment, and process safety principles. Knowledge of relevant industry standards, regulations, and asset integrity. undefined Leadership, Communication and Collaboration undefined Previous experience mentoring associates is required. Leadership and decision-making. Ability to influence across multidisciplinary teams. Effective communication and stakeholder management. Customer service focus and ability to work collaboratively. undefined Safety, Risk & Compliance undefined Strong safety and risk awareness. Commitment to operational excellence and continuous improvement. undefined Analytical & Technical Skills undefined Problem-solving and analytical capability. Excellent attention to detail. Proficient in data capture, analysis, and reporting, utilising various IT systems. Proficient in Microsoft Office tools including Word, Excel, and PowerPoint. Able to adapt to emerging best practices and industry innovations. undefined Sustainability & Environmental Responsibility undefined Identify opportunities to reduce gas losses and emissions. Support energy efficiency and sustainability initiatives. Promote environmentally responsible operating practices. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.comand let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. Privacy Policy: We will use the personal information that you have submitted to us in order to consider your application for the relevant role. Your privacy is important to us. Please click here for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests. 3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation. TPBN1_UKTJ

Redline has been retained by a leading instrumentation manufacturer who are looking for an Import & Export Coordinator Based in Cambridge. This Import & Export Coordinator based in Cambridge will control all imports and exports for various departments. They will be responsible for the timely, cost and effective shipping of all equipment whilst adhering to standard procedures and policies. The Import & Export Coordinator based in Cambridge will have responsibilities such as: Creation of Dispatch notes for equipment being shipped out. Creation of importation/ exportations commercial invoices. Obtain export and import entries in order to complete files to satisfy audit requirements. Communicate with the compliance team to ensure operations are in line with requirements. Check and validate all freight and packing invoices. Handle all IPR shipments. This is an exciting opportunity to join a growing company who can offer the opportunity for career progression and personal development. To apply for this Import & Export Coordinator job, based in Cambridge please send your CV to , or for more information contact Ricky Wilcocks on 01582 8788810

AVEVA is creating software trusted by over 90% of leading industrial companies.Job Title: Product Owner, Electrical Engineering SoftwareLocation: Cambridge, United Kingdom (Hybrid)Employment Type: Full-timeThe jobAs Product Owner for the Electrical application, you will work with colleagues across Engineering & Schematics, including testers, developers, scrum masters, product owners, and management, to improve and evolve product capabilities. You will help translate electrical engineering requirements into clear user stories, support backlog prioritisation, and ensure the product delivers high-quality, fit-for-purpose outcomes for customers working in industrial electrical design environments.Key ResponsibilitiesProduce detailed user stories that capture electrical engineering requirements and support high-quality product deliverablesManage and refine the product backlog so business and customer requirements are clearly documented and prioritisedEnsure user stories include enough detail to support accurate estimation, development, and comprehensive test scenariosEngage with internal and external reference groups, customer workshops, and Voice of Customer discussions to gather and validate requirementsParticipate in sprint ceremonies to communicate status, demonstrate deliverables, and support validation of the product visionEssential RequirementsDegree-qualified, or equivalent experience, in Electrical Engineering or a closely related disciplineProven industry experience in electrically intensive sectors such as process plant, power generation and distribution, marine, oil and gas, food and beverage, or similar regulated industrial environmentsProven experience in leading a team to deliver effective projects or programmes.Strong understanding of industrial electrical systems, including LV/MV/HV distribution, control systems, and instrumentation interfaces as they relate to CAD-based design workflowsExperience producing, reviewing, or issuing electrical design deliverables such as:Single-line diagramsSchematic and wiring diagramsCable schedulesEquipment layoutsPanel drawings and termination drawingsGood knowledge of electrical engineering standards, codes, and working practices, such as IEC, BS, IEEE, project standards, or client specificationsDesired Skills and CompetenciesPractical knowledge of design lifecycle management, including document control, revision management, and handover requirements within electrical projectsAbility to use electrical engineering expertise to deliver fit-for-purpose product capabilities that create customer impactKnowledge of ETAP or similar power system analysis and simulation tools is an advantage.Curiosity to learn from customers, industry practice, and internal teams to evolve electrical design workflows and product adoptionClear and reliable communication, with the ability to build trust and deliver standards-aligned outcomes across technical and non-technical stakeholdersR&D at AVEVAOur global team of 2000+ developers work on an incredibly diverse portfolio of over 75 industrial automation and engineering products, which cover everything from data management to 3D design. AI and cloud are at the centre of our strategy, and we have over 150 patents to our name.Our track record of innovation is no fluke – it’s the result of a structured and deliberate focus on learning, collaboration and inclusivity. If you want to build applications that solve big problems, join us.Find out more: aveva.com/en/about/careers/r-and-d-careers/UK Benefits include:Flexible benefits fund, emergency leave days, adoption leave, 28 days annual leave (plus bank holidays), pension, life cover, private medical insurance, parental leave, education assistance program.It’s possible we’re hiring for this position in multiple countries, in which case the above benefits apply to the primary location. Specific benefits vary by country, but our packages are similarly comprehensive.Find out more: aveva.com/en/about/careers/benefits/Hybrid workingWe work in a hybrid way at AVEVA. Most roles are based at a local AVEVA office, with an expectation of being on-site 50% of your working hours to support collaboration and connection. Some positions are fully office-based depending on the nature of the work, and certain roles that support specific customers or markets may be remote. The working arrangement for this position will be confirmed during the hiring process.Hiring processInterested? Great! Get started by submitting your cover letter and CV through our application portal. AVEVA is committed to recruiting and retaining people with disabilities. Please let us know in advance if you need reasonable support during your application process.Find out more: aveva.com/en/about/careers/hiring-processAbout AVEVAAVEVA is a global leader in industrial software with more than 6,500 employees in over 40 countries. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals, and minerals – safely, efficiently, and more sustainably.We are committed to embedding sustainability and inclusion into our operations, our culture, and our core business strategy. Learn more about how we are progressing against our ambitious 2030 targets: sustainability-report.aveva.com/Find out more: aveva.com/en/about/careers/AVEVA requires all successful applicants to undergo and pass a drug screening and comprehensive background check before they start employment. Background checks will be conducted in accordance with local laws and may, subject to those laws, include proof of educational attainment, employment history verification, proof of work authorization, criminal records, identity verification, credit check. Certain positions dealing with sensitive and/or third-party personal data may involve additional background check criteria.AVEVA is an Equal Opportunity Employer. We are committed to being an exemplary employer with an inclusive culture, developing a workplace environment where all our employees are treated with dignity and respect. We value diversity and the expertise that people from different backgrounds bring to our business. AVEVA provides reasonable accommodation to applicants with disabilities where appropriate. If you need reasonable accommodation for any part of the application and hiring process, please notify your recruiter. Determinations on requests for reasonable accommodation will be made on a case-by-case basis.SummaryLocation: Cambridge, United KingdomType: Full time

Job Description SummaryJob Title: Research Scientist I or II, Oligonucleotide Chemistry#LI-OnsiteLocation: Cambridge, USARelocation Support: This role is based in Cambridge, USA. Novartis is unable to offer relocation support: please only apply if accessible.Imagine helping shape the future of RNA-based medicines through hands-on scientific innovation. At Novartis, we're pushing the boundaries of xRNA therapeutics to address some of the world's most challenging diseases, and we're looking for a talented scientist to join us on that journey. As a Research Scientist in Oligonucleotide Chemistry, you'll play a key role in synthesizing, optimizing, and characterizing therapeutic oligonucleotides while collaborating with a diverse team of experts across discovery and development. This is an exciting opportunity to apply your scientific expertise, grow your technical skills, and contribute directly to groundbreaking therapies that have the potential to transform patients' lives.Job DescriptionKey ResponsibilitiesExecute solid-phase synthesis of research-scale oligonucleotides using advanced automated DNA and RNA synthesizers.Purify, desalt, and characterize oligonucleotides using chromatographic and mass spectrometry techniques.Develop and optimize synthesis, purification, and analytical methods to improve performance and reproducibility.Operate, maintain, and troubleshoot laboratory instrumentation supporting oligonucleotide production and analysis.Prepare and maintain standard operating procedures to support high-quality and consistent laboratory practices.Organize, analyze, and document experimental results using electronic laboratory notebook systems.Contribute effectively within a collaborative, fast-paced research environment focused on therapeutic innovation.Essential RequirementsBachelor of Science or Master of Science in Chemistry or a related scientific discipline.One to three years of laboratory experience in academic or industrial research environments.Hands-on experience with automated solid-phase synthesizers and therapeutic oligonucleotide synthesis workflows.Proficiency in oligonucleotide purification, characterization, and analysis using chromatography and mass spectrometry techniques.Understanding of RNA therapeutics and their application in biological systems.Strong collaboration, adaptability, and self-motivation in a fast-paced scientific environment.Desirable RequirementsExperience supporting oligonucleotide process development, optimization, or technology innovation initiatives.Excellent scientific communication skills with the ability to present findings to multidisciplinary teams.Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave. Expected Annual Base Salary Range for role: US:66,800.00 - 124,000.00 USD AnnualThe salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. Commitment to Diversity and Inclusion / EEO paragraph: Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$66,800.00 - $124,000.00Skills DesiredAlgorithms, Analytical Chemistry, Automation, Chemical Analysis, Chemical Biology, Chemical Laboratory, Chemical Synthesis, Chemistry, Collaboration, Creativity, Data Analysis, Drug Development, Innovation, Medicinal Chemistry, Organic Chemistry, Pharmaceutical Industry, Physics, Team PlayerSummaryLocation: Cambridge (USA)Type: Full time

British Antarctic Survey (BAS) in Cambridge is seeking an Instrumentation Engineer to design, test and optimise small-scale structures and enclosures for remote field instruments.

Williams Companies, through its Williams operations, seeks an Instrumentation & Electrical (I&E) Operations Technician III to maintain gas processing systems and ensure reliability.

Job Title: Technical Author Location: Cambridge Salary: £40,000 to £45,000 Employment Type: Permanent Working Arrangements: Onsite working We’re partnering with a highly respected engineering business in Cambridge to appoint a Technical Author with proven experience in optics, lasers or photonics. This role is ideal for someone who enjoys turning complex technical detail into clear, consistent product content that genuinely supports end‑users and internal teams. What You’ll Be Doing - Creating high‑quality documentation across product manuals, datasheets, user guides and application notes - Maintaining consistent tone, terminology and structure across all product content - Translating optical/photonics concepts into accessible, customer‑friendly language - Ensuring documentation aligns with quality, regulatory and compliance requirements - Supporting new product introductions with structured, accurate content packages What Our Client Is Looking For - Proven experience as a Technical Author within optics, lasers, photonics or a related engineering field - Strong ability to produce clear, concise and consistent technical content - Solid understanding of optical systems, laser technologies, photonics components or instrumentation - Confidence interpreting engineering drawings, specifications and test data - Excellent communication skills and the ability to collaborate with multidisciplinary teams - High attention to detail and a structured approach to documentation management Desirable Skills - Familiarity with ISO standards or regulated environments - Background in physics, engineering or a related technical discipline - Familiar with SEO Why This Role Stands Out - Opportunity to work with cutting‑edge optical and photonics technologies - Supportive, knowledge‑sharing engineering cultur - Genuine scope to influence documentation strategy and product communication For more information, please contact Cathy Swain. T: (phone number removed) E: (url removed)

Position: Senior Mechanical Engineer (Hybrid) Location: Cambridgeshire Salary: £50,000 - £75,000 + Excellent Benefits Shape the Future of Advanced Medical Technology Are you an experienced Mechanical Engineer looking to work on genuinely innovative products that improve lives? An exciting opportunity has arisen for a Senior Mechanical Engineer to join a highly successful engineering and technology business developing complex, next-generation electro-mechanical products for the healthcare sector. This is an opportunity to become part of a collaborative multidisciplinary engineering team, where you'll play a key role in taking innovative concepts through design, development and manufacture while working on technically challenging projects using the latest engineering technologies. The Role As a Senior Mechanical Engineer, you'll be responsible for the design and development of sophisticated electro-mechanical systems, working closely with engineering, manufacturing and quality teams throughout the complete product lifecycle. Key responsibilities include: • Designing and developing innovative electro-mechanical products and assemblies., • Creating creative engineering solutions to challenging technical problems., • Supporting product development from concept through to manufacture., • Collaborating with multidisciplinary engineering teams to deliver robust design solutions., • Producing and reviewing technical documentation, design reports and verification plans., • Supporting design verification, validation and manufacturing activities., • Ensuring designs comply with relevant quality and regulatory standards., • Driving continuous improvement throughout the product development process. About You We're looking for engineers who can demonstrate: • HND, Degree or equivalent experience in Mechanical Engineering or a related discipline., • Strong mechanical design experience within a complex engineering environment., • Excellent SolidWorks CAD skills., • Experience developing complex electro-mechanical systems., • A good understanding of Design for Manufacture (DFM) and Design for Assembly (DFA)., • Experience supporting products through transfer to manufacture., • Excellent problem-solving and communication skills., • The ability to work effectively within multidisciplinary engineering teams. Experience within Medical Devices, Life Sciences, Scientific Instrumentation, Robotics, Aerospace or another highly regulated engineering environment would be advantageous, although engineers from other precision engineering sectors will also be considered. What's on Offer • Salary between £50,000 and £75,000 depending on experience., • Excellent benefits package., • Genuine opportunities for technical and career progression., • Collaborative engineering culture., • Opportunity to work on cutting-edge products that make a real-world difference., • Modern facilities and an innovative working environment. If you're looking for a role where you can make a significant technical contribution whilst continuing to develop your career within a growing, technology-led organisation, we'd love to hear from you. Apply today for a confidential discussion

Technology development, proof of concept and prototyping with diverse applications Cambridge (south); to £80k DoE plus good benefits This small and multi-disciplinary group within a larger company develop diverse, groundbreaking electronics technologies. Explore new challenges, collaborate, and see your work come to fruition in months rather than years – and then onto the next challenge. You’ll get to co-develop systems which combine advanced sensors, imaging, EM, acoustics, fluidics and AI, with applications in edge computing, instrumentation and special projects. You may apply skills in digital electronics, FPGA, DSP, embedded code, analogue electronics and RF. Along with the innate perks of such work, the company offer a generous salary, strong pension contribution, catered lunches, social and leisure facilities, and family-friendly leave policies. Your CV will show your strong relevant degree and supporting qualifications, and additional experience, likely commercial, or through a master’s degree and/or PhD. In addition, your experience will include several of: • Digital electronics design, schematics capture and PCB layout, • FPGA design, RTL development in VHDL / Verilog / SystemVerilog, • DSP, signal processing and/or related algorithms, • Analogue electronics, which may include work with sensors, RF or microwave EM, • Network protocols design and communications generally, • Embedded software in C, C++ and/or Rust It is likely you will have collaborated with other engineers and scientists on past projects. Any additional experience in Python, C#, MATLAB or other software systems is a plus. Some projects may involve security clearance, hence you will need to be a British citizen with 5+ years’ UK residence. Another top job from ECM, the high-tech recruitment experts. Even if this job's not quite right, do contact us now - we may well have the ideal job for you. To discuss your requirements call (phone number removed) or email your CV. We will always ask before forwarding your CV. Please apply (quoting ref: CV27582) only if you are eligible to live and work in the UK. By submitting your details you certify that the information you provide is accurate

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

I'm currently recruiting for an Applications Support Engineer to join an innovative technology business developing advanced metrology and instrumentation solutions for the semiconductor industry. This is a highly technical, customer-facing role combining applications engineering, technical support, instrumentation, testing and troubleshooting, with the opportunity to work on some genuinely cutting-edge technology. The role will involve: Providing pre- and post-sales technical support to customers Processing customer samples and delivering product demonstrations and training Installation, setup, testing, debugging and development of scientific instrumentation Supporting customers with data interpretation and technical troubleshooting Working closely with engineering teams to feed customer requirements into future product development Attending trade shows, customer sites and technical events * International travel - potentially up to 50% of the role, sometimes at short notice We're looking for someone with a Masters degree and relevant industrial experience, or a PhD, ideally with experience working with scientific instrumentation, signal processing and waveform analysis. Experience within semiconductors, failure analysis, GHz TDR, Terahertz systems, lasers, optics or robotics would be advantageous, but isn't essential. Salary: Up to £45,000 DOE Location: Cambridge Travel: Up to 50% internationally - you need to be comfortable/eligible with short notice global travel. It's an excellent opportunity for someone who enjoys getting hands-on with complex technology, solving technical problems and working directly with customers across an international market. If this sounds like something you'd be interested in, drop me a CV

A well-established UK electronics design and manufacturing business is hiring a Senior Electronics Engineer to take technical ownership of hardware design within its R&D team. They develop advanced sensing and instrumentation products for professional and specialist markets, with design and manufacture kept entirely in-house. What the role involves This is a lead-from-the-bench role rather than a management one. You'd own electronic design across products from early concept to production release - analogue, digital, power, video, mixed-signal and embedded - producing schematics, calculations, layout guidance and BOMs, then reviewing and signing off designs against technical, cost, reliability and manufacturability requirements. Alongside your own design work you'd lead prototype bring-up, board-level debug, integration and verification, feed into architecture decisions on new products, and act as a technical sounding board for less experienced engineers. There's close collaboration with firmware, software, mechanical and production teams, plus involvement in component selection, obsolescence management and supplier engagement. What they're looking for Degree or equivalent experience in electronic or electrical engineering A substantial track record designing hardware for high-performance products - defence, aerospace, industrial, scientific or comparable Strong across analogue, digital, power and mixed-signal design Proven experience taking designs through concept, prototype, verification and production release Strong practical debug skills at board and system level Familiarity with embedded systems, microcontrollers, FPGA interfaces or sensor integration The judgement and communication skills to guide others and hold design standards Nice to have: Altium, ruggedised or portable product development, low-power design, EMC and environmental qualification, serial and high-speed interfaces

C++, Embedded , C#, Python / TypeScript, Scientific Instrumentation, Onsite (No Hybrid) Cambs - West; £50,000 to £65,000 DoE Based close to Cambridge, this biotech instrumentation company develops hardware platforms used for protein characterisation and cell line development. Their key technology is centred around proprietary microfluidic systems that enable quick and accurate scientific processes. The company’s main two product lines are well-received and require maintenance and iterative updates to keep them modern and abreast of new technology advancements. They are looking to hire a Software Engineer to take a lead role over one of these product lines and deliver new features. Requirements: • BSc / BEng in computer science, electronics or similar (ideally holding a Master’s), and demonstrable commercial software experience working on application-level software for hardware instruments (Windows and Linux)., • Strong programming skills with C++ including embedded. Experience with C# for instrumentation control and data analysis would be highly desirable. Any experience with Python or TypeScript would be advantageous., • Demonstrable experience taking ownership for software projects involving hardware. Experience with FDA 21 CFR Part 11 compliance would be a bonus. This is a hands-on role, requiring good software skills and experience for taking project responsibility and delivery. The position is fully onsite at their offices, which is close to road (A505) and train links. Note, no company sponsorship is available. Applicants should have full, unrestricted rights to work in the UK. Preference is for applicants who are based locally (Cambridge, Royston, Letchworth, Stevenage, Biggleswade, St Neots, Bishop’s Stortford). Another top job from ECM, the high-tech recruitment experts. Even if this job's not quite right, do contact us now - we may well have the ideal job for you. To discuss your requirements call ecm or email your CV. We will always ask before forwarding your CV. Please apply (quoting ref: CV27691) only if you are eligible to live and work in the UK. By submitting your details you certify that the information you provide is accurate

Exciting opportunity to join an innovative, industry leading laboratory equipment distributor to drive Sales in the South East. Our client is a leading provider of analytical instruments in the UK with products ranging from sample preparation systems to elemental analysis instrumentation. This opportunity calls for an ambitious scientist looking to drive sales whilst providing excellent service to customers. Within this role, you will support customers by identifying their key pain points and advising which products in your portfolio would best serve their requirements. Your position will focus on managing existing accounts and identifying new customers in academic, CRO, biotech and pharma laboratories. You will be based remotely and are expected to travel ~60% of your time to customer sites across the Southeast for instrument demonstrations, presentations and negotiation. To be considered for this position you will have: • BSc minimum in Chemistry or related subject, • Eligibility to work in the UK without sponsorship, • UK driver’s license and willingness to travel, • Proven experience within scientific sales and understanding of the sales process is highly desirable For your work you will be provided with a competitive basic salary, commission scheme, car and additional employee benefits. Please apply below to receive more details! Keywords: chemistry equipment, laboratory equipment, consumables sales, capital sales, business development, account management, sales, sales executive, technical sales, technical sales specialist, London, Cambridge, Oxford, Kent, Leicester, Northampton, Ipswich, St. Albans, Luton, Watford, VRS9389PC Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website

Electronics Engineer Location: Cambridge | Permanent | Full-time An innovative advanced technology company is seeking an experienced Electronics Engineer to join its close-knit engineering team. You will work on complex electronic systems spanning analogue signal processing, digital electronics and embedded FPGA/MCU platforms, collaborating with engineers across multiple disciplines. The Role Design, specify, verify and validate PCBs for advanced products. Design and document cables and wiring systems. Maintain version-controlled engineering data and coordinate PCB assembly with external suppliers. Integrate third-party electronic devices into wider systems. Cross functional collaboration with other engineering teams. Support hardware development, testing, integration and product release. Essential Experience 2.1 degree or above in Electronic Engineering or a related physical science. 4+ years' professional experience in electronics design, PCB layout, manufacture and testing. Experience using a distributed version-control system such as Git or Mercurial. Strong problem-solving skills and the ability to work effectively within a small multidisciplinary team. Genuine interest in instrumentation and electronic system development. Desirable Skills FPGA development, Verilog and FPGA development toolchains. Embedded C/C++ and Python. CE compliance, EMC testing and product safety. PCB design using KiCad or similar CAD packages. Experience with USB, CAN or similar communication interfaces. Hardware integration within multidisciplinary products

Workshop Engineer £32,000 - £36,000 + Product Training + Progression + Excellent Company Benefits Cambridge (Ideally located: St Neots, Stevenage, Bishop's Stortford, Bury St Edmunds) Do you have an hands on mechanical background? Are you looking to advance your career technically with a company offering industry-leading training where you will work on cutting-edge technology? This is an exciting opportunity to join a leading supplier and be part of a team that uses state-of-the-art equipment, supplying their products to a variety of specialist markets. This company is a market leader in their field, specializing in instrumentation and testing sectors. They have an excellent reputation within the industry and are currently in high demand for their services, which has led them to recruit like-minded engineers to assist with the additional workload. In this role, you will be part of a team that evaluates and develops powertrain control systems for future vehicles. This is a Monday-to-Friday role with an alternating shift pattern with full product training provided to the successful candidate. This role would suit a Engineer looking to join a rapidly-growing business that provides specialist training and progression opportunities. The role: Powertrains Operation of complex facilities 7am - 3pm then 3pm - 11pm alternating weekly The person: An interest in the Automotive industry Seeking additional training and career progression Commutable to Cambridge Reference Number: BBBH(phone number removed) To apply for this role or to be considered for further roles, please click "Apply Now" or contact Sam Claridge at Rise Technical Recruitment. Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles. The salary advertised is the bracket available for this position. The actual salary paid will be dependent on your level of experience, qualifications and skill set and will be decided by our client, the employer. Rise are not responsible or liable for any hiring decisions made by the end client. We are an equal opportunities company and welcome applications from all suitable candidates

Projects range from defence and security to robotics and consumer products Cambridge (fully onsite); to c£65,000 + Top Benefits Are you interested in variety and keen to work on products that could be applied for industrial systems, UK military, or consumer products for globally recognised brands? This established technology company works on 100s of innovative projects each year, providing technical and scientific expertise as a world-renown consultancy. Their engineers are highly sought after, and this specific team are used to provide expertise in embedded systems, controls, communications, algorithm design and hardware security. As an engineer, you’ll be part of a technical team, working closely with peers on different assignments. You’ll use your skills and knowledge in engineering to design new analogue and digital hardware, write embedded software code, develop control and communications systems and look to deliver products and prototypes. Further, you’ll interact with clients, present when required and be part of the delivery team for final project handover. Requirements Top university education including a 1st / 2.1 in electronics, computer science, information engineering or physics. Demonstrable industry experience or highly relevant PhD working on a range of engineering projects which includes elements of the following: software programming (C, C++ or Rust); PCB design; digital electronics (DSP, Verilog or VHDL); and analogue electronics (RF, power or interfaces). Eligibility for UK security clearance (due to sensitivity for some projects). Any prior experience in technical consultancy would be advantageous. Your technical skills and experience will be coupled with a desire and aptitude to learn and embrace new technologies. Senior candidates with highly relevant technical project and consultancy experience are also invited to apply (compensation would be dependent on experience). On offer is an excellent compensation package including a wide range of benefits including health insurance, enhanced company pension, free parking onsite and pro-active career support. Keywords: Electronics, Software, C / C++ / Rust, DSP, Verilog, VHDL, RF, Power, Instrumentation, Industrial Systems, Defence, Consultancy, Embedded, PhD / Experienced, Digital / Analogue, Cambridge, Fully Onsite Another top job from ECM, the high-tech recruitment experts. Even if this job's not quite right, do contact us now - we may well have the ideal job for you. To discuss your requirements call ecm or email your CV. We will always ask before forwarding your CV. Please apply (quoting ref: CV27673) only if you are eligible to live and work in the UK. By submitting your details you certify that the information you provide is accurate