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Senior Electronics Engineer | £60-80k | Cambridge Are you a creative and determined Electronics Engineer ready to lead projects that deliver world-leading, cutting-edge solutions across diverse industries? My client is a highly successful R&D consultancy developing completely cutting-edge solutions for some of the most stable and fastest-growing markets on Earth. You will be innovating on customer re... ZIPC1_UKTJ

We are recruiting on behalf of an established main contractor with a strong regional presence who are seeking an Experienced Estimator to join their expanding team in Cambridge. This is an excellent opportunity to become part of a respected, financially secure business delivering a wide range of projects across sectors such as healthcare, education, defence, R&D, life sciences, commercial, industr... ZIPC1_UKTJ

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Brief Description: The Associate Director, Medical Writing, is responsible for the efficient preparation of high-quality, strategically aligned medical writing deliverables within one or more program. S/he will work directly with cross functional teams to author regulatory documents (eg, protocols, clinical study reports, briefing books, submission documents, investigator brochures). For programs with multiple deliverables, s/he may be responsible for managing writers. The incumbent will ensure that strategically aligned communication points are conveyed in medical writing deliverables and that the communication points are consistent across program documentation. S/He will mitigate risk associated with medical writing and disclosure processes by contributing to Best Practices and SOPs. This role has global responsibilities, including participation in global teams and interaction with regulatory agencies in multiple regions. This role may have line management responsibilities. Essential Functions/Responsibilities Works with the cross functional team to ensure effective communication of data in the respective documents. Works with the cross functional team to ensure that communication needs for the clinical data are considered early in the development program to enable consistency of data presentation and messaging throughout the clinical program lifecycle. Analyzes study level documents for their ability to deliver the information required by the target audience (eg, health authorities). Communicates proactively and efficiently within the MW team and across R&D. Ensures quality of medical writing deliverables and that work on assigned projects adheres to departmental procedures / practices, and industry / international standards. Possible oversight of contract medical writers to ensure efficient preparation of medical writing deliverables for assigned clinical program(s) according to budget and timelines. Collaboration and strategic partnership with cross functional team members to ensure understanding of program strategy and the nature of medical writing services required to deliver on company objectives. Required Knowledge, Skills, and Abilities Exceptional English language skills and ability to write and edit complex material to ensure accuracy, clarity, and effectiveness. Clear understanding of lean authoring for clinical regulatory documents. A solid understanding of the clinical development process, including the documents that are required at each stage. For early development: knowledge of pre-clinical and nonclinical regulatory requirements and reporting is required. Prior contribution to, and an understanding of, global submissions. Expert MS Office skills with a special focus on word processing, tables, spreadsheets, presentations, graphics and templates. Excellent written and oral communication skills and demonstrated coaching and problem-solving abilities. Knowledge of ICH and CTD guidelines for clinical and regulatory submission documents Ability to think strategically; demonstrated negotiating skills and resourcefulness. Demonstrated ability to manage several projects simultaneously. Ability to critically analyze and synthesize complex scientific information. High degree of influencing skills in shaping and developing content and wording. Demonstrated ability to work collaboratively; multicultural sensitivity, builds positive and productive relationships, seeks input and demonstrates an appreciation for diverse views by incorporating them into decisions / proposals. Successful track record of leading complex clinical / regulatory writing projects. Demonstrated ability to make decisions even in the absence of complete information. An excellent understanding of all aspect of ICH-GCP; keen insight on external clinical publication practices and standards (ICMJE, AMA, GPP). Excellent organizational and time management skills and attention to detail. Required/Preferred Education and Licenses BA/BS with at least 8 years (or advanced degree with at least 5 years) writing experience in the pharmaceutical industry across therapeutic areas required. Advanced degree preferred. LI-DM1 Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $154,400.00 - $231,600.00 Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Location: This role can be based either in Cambridge or Kent Science Park, Sittingbourne Job Role: We are looking for dynamic, creative, and talented computational chemist to join our expanding Discovery & Medicinal Chemistry Department. Reporting to the Director of Medicinal Chemistry, you will apply your expertise, leadership and guidance to discover and develop novel small-molecule therapeutic agents. You will be working within a patient-focused, science-driven, and multi-disciplinary biopharmaceutical environment, covering all stages of the drug discovery process. You will collaborate with scientists from other disciplines within Jazz Pharmaceuticals and with external collaborators to build an innovative portfolio of therapeutics across our exciting and growing oncology and neuroscience pipelines. Working at the forefront of drug discovery you will advance projects from target selection to preclinical drug candidates and FiH trials, and contribute to the growth of the medicinal chemistry team. Key Responsibilities: Utilize modern molecular modelling methods to support different stages of R&D programs. Collaborate effectively with other departments and functions to advance research discovery projects expeditiously from hit identification to high quality preclinical candidates. Design, lead and drive computational studies on projects throughout the several discovery phases and ensure execution on agreed deliverables. Opportunities to lead or co-lead projects in addition to drive discipline-specific endeavours. Set the vision and strategy for computational chemistry. Foster innovative thinking in all areas of departmental activities, with a particular focus on computational and medicinal chemistry. Manage CRO compchem activities, providing expertise and guidance. Present plans and results internally, including at board level, and externally at conferences. Contribute to the writing of patent applications, scientific publications, and internal reports. Develop and mentor less experienced staff. Keep up to date with the latest scientific advances and trends in drug discovery to deliver the next-generation therapies. Undertake ongoing professional development by attending relevant training and conferences. Requirements & Qualifications: MSc/PhD in a relevant scientific discipline (Pharmaceutical Sciences, Chemistry, Computational Chemistry) with a solid foundation in molecular modelling built in a pharma/biotech/CRO setting. Expert knowledge in CADD software packages and modern molecular modelling techniques. Sound knowledge in cutting-edge cheminformatic tools, AI/ML-enabled technologies, and in silico drug design, including both structure- and ligand-based methodologies. Passion for drug discovery with a deep entrepreneurial and problem-solving attitude. Mastery of all the theoretical and practical principles of medicinal chemistry and drug design. Broad knowledge of biophysical, biochemical, and cell-based assays used in the early stages of the drug discovery process. In depth understanding of multi-parameter optimization and ability to integrate disease biology, ADME/DMPK and toxicology data to solve complex drug discovery problems. Excellent leadership, management, organizational and team-working skills, and a talent to deliver project milestones within the expected time frame. Demonstrated track record of scientific publications. Exceptional oral, written, and interpersonal communication skills, and ability to develop and grow strong cross-functional collaborations. LI-onsite LI-SM1 Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .

Socode are working with a global high-tech engineering business developing complex precision systems used in advanced industrial applications. As their next-generation products move through critical development phases, they’re now looking to add a Principal Mechanical Engineer to their R&D team. This is a senior, hands-on role where you’ll take ownership of major mechanical systems on complex electromechanical products — not just small sub-assemblies. What will you be doing? • Leading mechanical development on new product programmes from technical specification through to production, • Defining mechanical requirements around performance, reliability, cost, and serviceability, • Producing detailed CAD, drawings, tolerances, and full bills of materials, • Leading the build, integration, and testing of complex mechanical and electromechanical sub-systems, • Selecting and validating cost-effective manufacturing methods and mitigating technical risks, • Working closely with suppliers to source and manufacture components, • Supporting product integration, system testing, and early-life issue resolution, • Ensuring designs meet relevant standards and internal quality requirements, • Contributing to technical documentation, training material, and customer support, • A Mechanical Engineering degree (or closely related discipline), • Extensive experience delivering products in high-technology R&D and manufacturing settings, • Advanced 3D CAD capability in SolidWorks with working knowledge of simulation and analysis, • A track record of owning products through the full development cycle, from early concept to production support, • Strong practical understanding of a wide range of manufacturing methods, including CNC machining, sheet metal, moulded parts, castings, and additive methods, • Solid background in designing and packaging electromechanical systems, • Proven experience with motion and drive systems such as mechanisms, motors, linear rails, and bearings, • Good working knowledge of materials selection, tolerancing, and mechanical reliability, • Hands-on experience designing jigs, fixtures, and supporting manufacturing processes, • A structured, analytical engineer who is comfortable with risk assessment and design reviews, • Someone who can lead technically while remaining hands-on with detailed design Nice to have: • Previous exposure to fluid-based precision systems, • Understanding of pneumatics, fluid handling, or safe machinery design

Socode are working with a fast-growing medical robotics company developing next-generation robotic systems for minimally invasive surgery. As their core platform moves through critical development phases, they’re now looking to add a Mechanical Engineer to their R&D team. This is a true product-development role where you’ll own real mechanisms on a complex electromechanical system — not just small sub-assemblies. What will you be doing? • Designing and developing precision mechanical systems from concept through to production, • Working hands-on with prototypes, testing, and iterative design improvements, • Integrating mechanisms with sensors, actuators, and electronics, • Using analysis and simulation tools to validate your designs, • Selecting materials and manufacturing routes for both prototypes and scale-up, • Supporting design reviews with clinical, manufacturing, quality, and regulatory teams, • Working with external suppliers and supporting verification and validation testing, • Designing simple fixtures to support test and validation work We’re looking for: • A Mechanical Engineering (or similar) degree, • 5+ years of experience in a hands-on R&D or startup-style environment, • Strong experience designing precision mechanical systems, • Confident with tolerance analysis, FEA, and solid engineering fundamentals, • Strong 3D CAD skills, ideally SolidWorks, • Comfortable building and testing your own designs in a lab, • Someone who takes ownership, spots problems early, and follows them through, • A practical engineer who cares about product quality and robustness, • Experience across the entire product life-cycle Nice to have: • ISO 13485, FDA 21 CFR Part 820, • Good understanding of design for manufacture and reliability

DSP Engineer | Cambridge, Cambridgeshire I’m currently supporting a long-standing client in their search for a DSP Engineer to join their growing R&D team, based on-site in Cambridge, Cambridgeshire. This is a permanent DSP Engineer job offering the opportunity to work at the forefront of high-performance audio technology, contributing to both existing platforms and future product innovations. The role sits within a multidisciplinary team responsible for the design, development, and optimisation of advanced digital signal processing systems for world-class audio products. It’s an excellent opportunity for a hands-on DSP specialist who enjoys both coding and problem-solving in a collaborative and technically rich environment. Essential Skills & Experience for the DSP Engineer job: • Degree (2:1 or above) in a relevant field (e.g. Audio Engineering, DSP, Electronics, Physics)., • Hands of DSP experience, • Working knowledge of C / C++ or python This is a fantastic opportunity for an experienced DSP Engineer to join a world-class engineering team in Cambridge, Cambridgeshire and contribute to the development of cutting-edge audio technology. They can also offer a hybrid working model with 3 days working in the office and 2 days from home. APPLY HERE for the DSP Engineer job in Cambridge, Cambridgeshire by sending a copy of your CV to For more information you can call Scott Newcomen on 01525 659123.

Optical Design Engineer | Cambridge | Hybrid | Are you an Optical Design Engineer with experience in Lens Design and Modelling? Do you want to work on the cutting edge of display technology? Then this might just be the role for you! We are looking for an Optical Design Engineer with experience in lens design, birefringence, and optical modelling to join an established and experienced team directly contributing to the development of groundbreaking optical systems. Role responsibilities: • Design and simulate advanced optical components using tools like Zemax, Lumerical, DIMOS, or Techwiz., • Perform hands-on optical experiments and metrology, including interferometry., • Analyse sample performance and feed back into new product designs., • Collaborate with R&D, engineering, and customer teams to drive innovation., • Support customer and partner engagements through technical meetings and site visits. Skills, Qualifications & Experience: • MSc or higher in Physics, Mathematics, or a relevant Engineering discipline PhD would be preferable., • Excellent understanding of optical physics, birefringence, and polarisation., • Proficient in optical modelling tools (Zemax, Lumerical, DIMOS, Techwiz)., • Experience with liquid crystals is a strong plus., • Ability to independently design and run interferometry experiments., • Some programming experience with Python or MATLAB is desirable., • Able to adapt and thrive in a dynamic, evolving environment., • Strong communication and interpersonal skills., • Comfortable working independently or as part of a multi-disciplinary team. What’s in it for you? • Competitive salary, • Hybrid working., • 25 days annual leave + public holidays (increasing to 30 with length of service)., • Pension (6% on employer side)., • Death in Service (4X salary)., • Private medical insurance (family option available)., • Health cash plan (optical, dental, chiropody, chiropractic and others)., • Prescription safety glasses., • Official learning and development support., • Share incentive plan., • Cycle to work scheme., • Free onsite parking.

Our exciting new client is now searching for a III-V Device Engineering Manager with deep expertise in III-V semiconductor device design, development and volume manufacturing. The candidate will play a pivotal role in leading the scaling the production of the first product range and developing the new product range for optical communication systems. This role will sit at the intersection of R&D, Operations, Engineering and external foundry partners. Ensuring that new epi layers, process flows, tests are scalable from prototyping using in-house facilities through to volume manufacturing at foundry partners. Required skills will include: • Strong semiconductor device manufacturing knowledge with a focus on III-V technologies, • Strong background in design, test, and volume production of high-speed photodetectors (APDs or photodiodes preferred), • Proven experience transferring products to high-volume manufacturing and working closely with foundries, • Excellent communication and management skills, • Degree in Electrical Engineering, Physics, Materials Science, or a related field Please contact Rachel Anderson for further details.

About the Company This is an initial 6-month FTC, with a salary ranging between £30,000-£35,000 with a great set of benefits including Bupa healthcare, 5% employer pension & much more! Our client’s technical teams work at the forefront of materials science and electrochemical innovation, contributing to a rapidly evolving programme focused on next-generation energy solutions. They are seeking a Laboratory Technician to join the team, this role supports a wide range of laboratory activities, contributing to material preparation, cell assembly, testing programmes and day-to-day laboratory operations. You will work closely with scientists, engineers and technical leaders. The ideal candidate for this role will have experience with wet chemistry techniques in the lab. Key Responsibilities • Support laboratory activities assigned by the Head of Lab Operations, • Prepare and cure polymer membrane materials in line with defined SOPs, • Assemble electrochemical cells and cell stacks, from small-scale units to mechanically assembled stacks, • Conduct testing of electrochemical cells using battery and cell-testing equipment following set protocols, • Maintain high standards of health & safety and laboratory housekeeping, contributing to a positive safety culture, • Check, calibrate and maintain laboratory equipment, reporting issues promptly, • Monitor laboratory stock levels, assist with ordering and receive materials into the inventory system, • Ensure safe and efficient operation of laboratory processes and equipment, including maintenance and fault reporting Person Specification • Level 3 qualification (A-Level, NVQ) or higher in a science or engineering discipline; Level 2 with strong laboratory experience considered, • Experience with wet chemistry techniques and/or analytical equipment (FTIR, UV-Vis, TGA) is desirable, • Experience calibrating or validating laboratory equipment or materials, • Methodical approach to assembly, materials preparation and testing, • Willingness to learn new techniques and a good understanding of scientific principles, • Understanding of laboratory health & safety, 5S, and continuous improvement principles, • Experience in a project-based R&D environment is advantageous Sounds good, how do I apply? • Option 1: Click the apply button, don't worry if you don't have an up-to-date CV, we can discuss whatever you have to hand., • Option 2: Find Alexander Donnelly on LinkedIn and drop me a message or connection request

Novogene is a leading global provider of genomic services and solutions. Leveraging the latest next-generation sequencing (NGS), bioinformatics expertise, and the largest sequencing capacity in the world, Novogene provides unsurpassed data quality and fast turnaround time to all our customers. We are seeking a proactive and data-driven Project Analysis Coordinator to join our Cambridge Team. This role is highly collaborative and requires drive, organisation, and foundational analysis skills. You will work closely with different business sectors and deliver project data analysis to support business growth. You are expected to support pipline optimisation to support the team achieve higher goals. The successful candidate must be willing to communite Cambridge office when required. Job description: • Responsible for data analysis and result delivery of projects related to the research services in Novogene European laboratories and the clinical services, ensuring accurate and efficient execution and delivery of projects and after-sales analysis., • Responsible for the maintenance and continuous optimization and upgrading of data analysis pipelines and processes, ensuring stable and efficient workflows that meet diverse requirements., • Responsible for ensuring that project operations comply with relevant compliance requirements,continuously improving and cooperating with relevant quality assurance work., • Responsible for pipeline development and pipeline module R&D tasks., • Assist in addressing analysis-related issues encountered by customers during after-sales support to ensure customer satisfaction., • Possible webinar/conferences opportunities to promote service or share knowledge. Skills required: • Experience in bioinformatics analysis or bioinformatics software development in human genome high-throughput sequencing techniques., • Familiar with the common bioinformatics analysis software, especially for variant calling, annotation, gene expression quantification and differential expression, among others., • Capable to establish NGS data analysis process., • Master Perl python R, C / C programming languages, proficient in the use of linux operating system, familiar with basic mathematical statistics knowledge and tools;, • Project and time management skills., • Good communication and presentation skills., • Excellent English. Chinese knowledge is valued., • Experience in clinical/biopharma environment is preferred. All employment decisions at Novogene are based on business requirements on its positions and skill sets on applicants. The business is committed to providing an inclusive and accessible recruiting experience for candidates with disabilities, or other physical or mental conditions. Our privacy policy:

• Job title: R&D Technologist, • Location: Cambridge, • Contract Length: 12 months, • Working Hours: 37.5 hours/week, • Pay Rate: £15.88 About the Role Opportunity to work in the cutting edge of R&D in the biopharmaceutical industry at a globally leading CDMO. Role involves helping develop novel molecular and synthetic biology constructs, culturing mammalian cells in flasks and small-scale bioreactors, high throughput DNA assembly and analytical methodologies, whilst also ensuring the good maintenance of the laboratories. Key Responsibilities • 90-100% lab-based position focusing on the generation of new plasmids for the expression of complex biological molecules., • DNA sequencing processing and assessment., • Culture mammalian cell lines in flasks and small-scale bioreactors and perform analytical procedures such as high throughput protein quantification, and others, as required by the project. - Prepare media and feeds from basal components., • Write high-quality reports about the project and present the findings to R&D team., • Keep electronic laboratory notebooks to a high standard and contribute to the routine maintenance of the laboratory space and equipment., • Confident with computers and willing to learn automation., • Perform other duties as assigned. Education-Required: • BSc or MSc in Biological/Biomedical Sciences, Biotechnology, Biochemistry or other Biology based course Work Experience: • Entry Level: Biological/Biomedical Sciences, Biotechnology, Biochemistry key focus on molecular biology and mammalian cell culture., • Basic working knowledge of core molecular biology techniques required, • Practical experience in molecular biology and mammalian cell culture techniques is preferable.

About 52North 52North is a medical technology company on a mission to make emergency care safer and more effective. Awarded breakthrough status for its first product Neutrocheck® by the UK Government in 2024, we build innovative diagnostic and digital solutions to transform patients’ journeys in emergency care. Our mission-driven team of scientists, engineers, clinicians, and designers is backed by leading UK and US hospital venture funds, including Meridian Health Ventures and Cedars-Sinai Intellectual Property company, alongside partners such as the University of Cambridge and Macmillan Cancer Support. About the Opportunity This is an exciting opportunity for an experienced Senior Programme Manager to take ownership of 52North’s flagship Neutrocheck® programme through late-stage development, verification & validation, and regulatory submission. You will lead a complex, multidisciplinary programme spanning hardware and software development, analytical and clinical V&V, regulatory readiness, and commercial preparation for a breakthrough, first-in-class IVD product. You will take over a well-defined programme with established functional leads, external partners and transition plans in place, ensuring continuity and momentum during this critical phase. Working closely with functional leads, the leadership team and external partners, you will be responsible for programme planning, risk management and delivery timelines. Neutrocheck is built on 52North’s proprietary Aster™ technology, which uses lateral flow technology to enable the measurement of both cell-based and soluble biomarkers from a single sample, in a rapid, easy-to-use and portable format. Leveraging the expertise you build through managing Neutrocheck®, you will also be responsible for planning and managing Aster Platform pipeline R&D projects. As a relatively small start-up company, you will also have the opportunity to contribute to wider business objectives and activities, such as supporting funding applications and developing programme management processes. This role offers a rare opportunity to lead a breakthrough diagnostic programme at a pivotal moment, with real potential to improve outcomes for patients. If you are an experienced senior programme manager who relishes complex multidisciplinary programmes, who has a strong technical background in life sciences or engineering and who has significant experience managing design and development programmes in the IVD or medical device industries, this is an ideal role for you. Note that this is a hybrid position requiring you to be in our Cambridge office at least two days a week, with Tuesday as the company’s anchor day. The role is a fixed-term 1-year contract, providing maternity cover. Position Overview What you will do • Work with experienced Functional Leads and External partners, you will own and deliver the Neutrocheck® programme through late development, design freeze, V&V, and regulatory submission readiness., • Work with Functional Leads to develop, deliver and maintain integrated programme plans, covering hardware, software, analytical, clinical, regulatory, and commercial projects., • Proactively identify, manage, and mitigate programme risks, dependencies, and resource constraints., • Lead cross-functional programme teams and coordinate external partners including CROs and CMOs., • Plan and manage proof-of-principle, feasibility, and D&D projects within the Aster™ platform pipeline., • Provide programme insights and recommendations to the leadership team to support informed decision-making and prioritisation., • Contribute to wider business activities, such as funding applications and the development of programme management processes. What we need • Degree in life sciences or engineering, • 5+ years' experience managing IVD or medical device design and development programmes, • Managed IVD or medical device programmes through late development, design freeze and V&V, • Managed a complex cross-functional programme, involving hardware & software D&D, analytical V&V, clinical trial, regulatory and commercial projects, • Multidisciplinary systems thinker, able to engage with and proactively manage hardware, software, clinical, regulatory and commercial aspects and interdependencies of the programme., • Excellent verbal and written communication skills., • Excellent teamwork and leadership skills, evidenced by successful delivery of cross-functional programmes/projects., • Excellent problem-solving and proactive risk-management skills., • Experience managing internal programme teams, CROs/CMOs and diverse internal and external stakeholders (e.g. leadership teams/board), • Comfortable managing and planning multiple projects in parallel., • Proactive, can-do attitude. Able to work in a fast-paced environment, with significant uncertainty and programme risk., • Experience working within ISO13485-compliant quality systems., • Willing to contribute to wider business objectives and tasks. Even better if… • Experience with lateral flow technology, • Managed/supported IVD or medical device programmes through a regulatory submission (E.g. UKCA, CE and/or FDA), • Managed proof-of-principle and feasibility projects, • Experience working in a start-up company, or small business What can you expect from us • 28 days annual leave plus bank holidays., • A diverse and inclusive work environment that brings together multidisciplinary experts in many fields, including scientists, engineers, clinicians and designers. How to apply Please upload a CV and covering letter by clicking 'Apply Now', or by emailing your CV and covering letter to . Your covering letter should explain why you are applying for the job and what skills and experience you can bring to the role. We review CVs as we receive them and interview as soon as we have applications that look like a good match (usually within one week). We do not use closing dates. So, please apply as soon as possible to avoid missing out on this role. We advertised this role on 19 December 2025. If you have any queries, please contact Everyone is welcome at 52North. We are an equal opportunities employer and encourage applications from eligible and suitably qualified candidates regardless of age, disability, ethnicity, gender, gender reassignment, religion or belief, sexual orientation, marital or civil partnership status, or pregnancy and maternity/paternity. Studies have shown that some groups tend to apply to jobs if they meet all or almost all of the requirements while others apply even if they meet only some of the requirements. If that sounds like you then please apply – we are happy to review your application and let you know if we think you might be a good match. If you need any adjustments made to the application or selection process so you can do your best, please let us know. We are happy to help.

PE Global is currently recruiting for an Observational Research Manager role for a leading multi-national BioPharma client. This is an initial 12 months contract position. The pay rate is £32.35ph PAYE or £43.83 ph Umbrella. Would be ideal to have someone willing to be onsite 1-2 days per week (Uxbridge or Cambridge), and the role will become mostly remote, with the requirement to come onsite when needed to. Duties of the role/Responsibilities • Responsible for writing of SAPs, • Contributes to projects using real-world healthcare data assets, • Guiding the analysts to explore RWD, • Contributes to research strategy within the product team and epidemiology TA, • Provides input into epidemiology department meetings, • Stays abreast of the latest developments in the field of epidemiology and drug development, healthcare RWD and contributes to the field, • Promotes epidemiologic awareness, • Promotes understanding and use of RWD and epidemiologic methods, • Communicate significant scientific information to a variety of audiences. Education/Experience • PhD in Epidemiology, Statistics, Genetic Epidemiology or other subject with high quantitative content, • Experience in CPRD and HES and/or UK Biobank, • Experience in epidemiologic research, • Experience in working with observational data, • Experience communicating epidemiological information (written and oral), • Experience in the design, execution, and analysis of epidemiology studies within Pharmaceutical or Public Health setting, • Experience in research to support drug development, • Experience with other large databases, • Experience in epidemiological project planning and management, • Experience working in multi-disciplinary teams, • Record of publication in peer-reviewed journals. Interested candidates should submit an updated CV. Please click the link below to apply, alternatively send an up to date CV to

Requirements: * Background in mechanical or manufacturing engineering with relevant industry experience in NPI / project engineering. As they take further steps into optimised production, they are looking to have a dedicated NPI Project Engineer to be the nexus between their R&D teams and their m

Activity Instructor - October Holiday Camp - Cambridge, Cambridgeshire.Making school holidays extraordinary.Seasonal work in school holidays.Full season or part season roles available, and additional hours available for staff that hold a paediatric first aid qualification (usually 8am – 6pm).The r

Regulatory Manager / Medical Devices (UK, Hybrid) This one’s for the regulatory people who actually enjoy being close to the product. I’m working with a UK-based medtech company building a connected medical device that’s already in use and heading into its next regulatory phase. They’re looking for a Regulatory Manager who’s comfortable sitting at the intersection of Regulatory and Quality shaping strategy, owning submissions, and being the calm, credible voice when auditors, engineers and founders all want answers. What you’d actually be doing • Owning regulatory strategy across the product lifecycle, • Leading and coordinating submissions 510(k) experience essential and MDR desirable as this will be next), • Being the go-to person for auditors, notified bodies and regulators, • Keeping the QMS tight, usable, and fit-for-purpose (ISO 13485, CAPA, risk, design controls), • Working closely with R&D, software, clinical and leadership, not sat in a silo, • Helping shape how Quality & Regulatory scales as the product and business grow The experience that matters • Solid medical device regulatory background (5+ years is the right ballpark), • FDA experience (successfully submitted a 510(k) submission, • Software / connected device exposure is useful, not a blocker if you’ve worked closely with software teams, • Confident communicator, you don’t disappear when questions get uncomfortable A few important bits • Hybrid working - One day a week on-site (Mondays), • Seniority and scope to grow with the business, • Open to permanent — and potentially contract, • Salary flexible for someone who genuinely fits the brief, • UK candidates only - No sponsorship offered.

I am working with an exceptional management and technology consultancy who are growing! Cambridgeshire based. This is your chance to become an important part of their innovative Energy Transition team as a Managing Consultant. In this role you will focus on assisting clients in the Energy Transition sector, accelerating scientific and engineering solutions to market. You will have the opportunity to: • Active involvement in managing client relationships, managing sales process and supporting engagement with clients., • Lead medium to large-scale complex technical multi-disciplinary assignments., • Initiate, lead and win sales, • Grow, manage and develop a high performing team on energy transition focussed scientist and engineers, You are likely to have: • A network of senior industry contacts and potential buyers across the Energy Transition sector., • Consulting and commercial experience, • Experience within technology innovation - managing and delivering R&D projects, • An understanding and ability to sell the technology and services, • Previous research and development/scientific background What’s in it for you: • Private medical insurance, • Annual performance based bonus, • Profit share options, • Transport allowance If you are an Energy Transition professional interested in this opportunity, please contact me on for further details

Software Engineer Near Cambridge My client, a fast-growing AI company based near Cambridge, is seeking talented Software Engineers to join a small but rapidly expanding development team. This is an opportunity to work on a wide variety of projectsfrom early-stage prototypes to fully developed products- helping to create new technologies that solve complex, real-world challenges. This is a hands-on role offering autonomy, responsibility, and exposure to diverse technical domains across the full R&D lifecycle. Key Responsibilities Designing and developing software for both prototype systems and production-ready products Working across multiple projects concurrently and adapting to varied technical challenges Collaborating with multidisciplinary engineers to integrate software with hardware and wider system components Rapidly learning and applying new technologies Contributing to problem-solving throughout the development process Supporting software used to control hardware platforms, sensors, or custom devices Requirements Strong academic background (2:1 or above) in a STEM discipline (Computer Science, Mathematics, Physics, Engineering, etc.) Demonstrated ability to tackle difficult or ambiguous technical problems Ability to work independently with minimal supervision Willingness and ability to learn new tools, languages, and technologies quickly Working knowledge of Python Desirable (Not Essential) Experience interfacing software with hardware or embedded systems Familiarity with computer networking Experience with deep-learning frameworks (TensorFlow, PyTorch) Understanding of machine learning, statistics, optimisation, or algorithm development Experience developing mobile applications (iOS and/or Android) Suitable for both graduates and experienced engineers with strong problem-solving skills and a desire to learn. Role Details Location:Near Cambridge Working Pattern: Onsite, 5 days a week Eligibility: Full UK work rights required (no sponsorship available) Opportunity: Work across the entire prototype-to-product lifecycle in a fast-paced R&D environment Interested? Please Click Apply Now!Software Engineer - Near Cambridge TPBN1_UKTJ

Stock Condition and Energy Surveyor.Cambourne, Cambridgeshire - 4 day working week.Proposed Start Date: February 2026.Application Deadline: 17/02/2026 - may close early due to interest.Are you passionate about improving housing standards and energy efficiency?.Sellick Partnership is working with a r

About the RoleWe're seeking a dynamic and driven M&E Quantity Surveyor to join our growing commercial team in either Cambridge or Norwich.This is a fantastic opportunity for an experienced QS or for professionals currently working as Contract Managers, Project Managers, or Site Supervisors who are r

Holding an Engineering related Degree / HNC/HND and a Project Management qualification, the ideal Project Manager will bring proven experience of project or programme management within a technical engineering or a R&D environment; being a strong leader with excellent interpersonal skills as well as

R&V is looking for a Class 1 drivers for well known and respected company. Essential Requirements:- Minimum of 2 years experience in Class 1 driving- National Insurance Number- Right to work in the UK- Full UK driving licence- Good level of English- Flexibility in starting times.

Role: Community Host Salary £30K Location: Cambridge Hours: Shift pattern, Monday to Saturday, 40 hours per week Join a Groundbreaking Rental Revolution as a Community Host! Step into an exciting opportunity to be part of the single-family rental community, redefining what it means to r

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)! The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to ensure successfu

Holding an Engineering related Degree / HNC / HND and a Project Management qualification, the ideal Project Manager will bring proven experience of project or programme management within a technical engineering or a R&D environment; being a strong leader with excellent interpersonal skills as well a

PV Engineer/ Technician Solar Farm.Salary: £45,000 £50,000 per year (DOE).Job Type: Full-time, permanent.Location: Sites across the UK (region-based).Schedule: MondayFriday with a paid weekend rota (approx.Why this is a great opportunity.Our client is one of Europes leading solar-energy firms, r

I'm currently working with a pioneering life sciences company that focused on revolutionising the development and manufacturing RNA-based medicines, vaccines, and therapeutics.They are searching for an R&D Engineer to join their ranks, please see JD: Job Title: R&D Engineer Department: Researc

Senior Electronics Engineer | £60-80k | Cambridge.Are you a creative and determined Electronics Engineer ready to lead projects that deliver world-leading, cutting-edge solutions across diverse industries?.My client is a highly successful R&D consultancy developing completely cutting-edge solutions

Introduction Saab UK is part of Scandinavia's largest defence company, bringing together the best of Swedish and British innovation. Saab offers world-leading solutions and services in defence, aviation, space, and civil security to keep people and society safe. Our UK presence has been growing at pace, meaning we can offer a wide range of opportunities for personal fulfilment and career growth. We currently employ over 600 people across eight sites in the UK, and our specialisations include software engineering, underwater robotics, radars, AI, and armed forces training. The Role: This role is part of our BlueBear Business in Bedfordshire. You will be required to support a mixture of R&D and product development activities within a leading autonomy and unmanned systems company. Blue Bear continuously innovate within core areas such as UAV autopilots, mission systems, ground control stations, and all supporting systems and infrastructure. You will be keen to get involved in all development areas and have a good track history/proven track record in both problem solving and quality software development. Working as part of a team in a multidisciplinary team you will have good communication skills. A can-do attitude and a genuine passion for innovative technology will be advantageous. Develop low-level drivers for UAV for control of effectors, reading instrumentation and integration of novel sensors. Key Responsibilities: * Primarily, your role will be to lead in the design, implementation and test of real time embedded software to support both experimental activities and product development, ensuring real-time safety, security and redundancy considerations are met. * Develop, own and execute firmware roadmaps working closely with Software and Electronics department leads. * Lead a skilled team in the delivery of firmware for high-paced projects. * The opportunity will enable the successful candidate to gain knowledge of cutting-edge autonomous systems. * You will be responsible for delivery, reporting and presentation of technical work and writing and submitting any necessary documentation. * Delivery and maintenance of the embedded systems software within the UAV specifically. * Support development of automated HWIL test environments. Qualifications and Experience: * Minimum 5+ years experience of embedded Linux * Experience leading a team of low-level software engineers. * Sound understanding of Linux kernel configuration and tuning * Experienced user of Linux OS build toolchains such as Yocto and Buildroot * Programming languages: C, C++, Python, Scripting (including Bash) * Ability to work from application code right down to bare metal * Experience of working with core communication interfaces such as UART, Ethernet, SPI, I2C, CAN * Experienced at hardware level debugging and fault finding * Experience of Electronics design, development and testing. * Awareness of FPGAs and VHDL. * Able to interpret relevant data from electronic schematics and component datasheets and application notes for the purposes code writing * RTOS coding and debugging * Awareness of assurance frameworks (DO-178C etc.) and secure by design. * Conducting code reviews * Familiar with use of version control tools such as Git Other Duties and Responsibilities: * To undertake such other duties and responsibilities as may be reasonably required within the grade and level of the post. * You will be expected to perform different tasks as necessitated by your evolving role within the company and the overall business objectives of the company. By submitting an application to Saab UK you consent to undertaking workforce screening activities that may include but are not limited to: Baseline Personnel Security checks, National Security Vetting, reference checks, verification of working rights and in all circumstances preferred candidates will be placed through a security interview.

Linux Systems Administrator High-Growth AI Company (Near Cambridge) My client is a fast-growing AI company near Cambridge, seeking a Linux Systems Administrator to manage, optimise, and secure their Linux-based systems while supporting cross-platform environments. This hands-on role is ideal for someone who thrives in dynamic, fast-paced environments and enjoys building robust, scalable infrastructure for R&D teams. Key Responsibilities Build, maintain, and optimise Linux server environments to ensure high availability and performance Implement security best practices across Linux, Windows, and macOS systems Conduct regular system audits, updates, and patch management Support Windows and macOS devices to ensure smooth integration with company infrastructure Establish centralised administration processes for consistent system management Automate workflows using scripting and configuration management tools (e.g., Bash, Python, Ansible) Collaborate with developers and R&D teams to deploy, monitor, and manage applications and services Maintain clear documentation and ensure standardised system configurations Requirements Strong experience managing Linux servers and system environments Familiarity with Windows and macOS device administration Proficiency in scripting (e.g., Bash, Python) and automation tools Good understanding of networking fundamentals and security protocols Proactive, detail-oriented problem solver with strong communication skills Comfortable working independently and collaboratively in an engineering environment Whats on Offer Full-time, hands-on role supporting core R&D infrastructure Opportunity to shape processes, automation, and system architecture in a scaling environment Exposure to cutting-edge AI technologies in a high-growth company Work onsite near Cambridge, collaborating closely with engineering and R&D teams Direct impact on infrastructure reliability, security, and performance Interested? Please Click Apply Now!Linux Systems Administrator High-Growth AI Company (Near Cambridge) TPBN1_UKTJ

Title: Estimator (Cambridge)Location: Cambridge, Cambridgeshire, East Anglia, UKCompany: One Way Resourcing LimitedWe are recruiting on behalf of an established main contractor with a strong regional presence who are seeking an Experienced Estimator to join their expanding team in Cambridge. This is an excellent opportunity to become part of a respected, financially secure business delivering a wide range of projects across sectors such as healthcare, education, defence, R&D, life sciences, commercial, industrial and residential.The role is office-based in Cambridge, working closely with an experienced Estimating Team while benefiting from flexibility to work from other regional offices when required.Estimator Suitability:This position suits either:An intermediate Estimator looking to progress within a large and stable organisation,orAn experienced Estimator seeking to contribute their expertise to a forward-thinking contractor known for promoting from within.Estimator Key Responsibilities:Produce cost plans including first-principles pricingTake off quantities using Autodesk Design ReviewLead tender enquiries and prepare detailed work package allocationsAssess subcontractor quotes, identify scope gaps and propose value-engineering solutionsPrice preliminaries and competitive tenders under guidance of senior teamBenchmark using data and forecasting toolsReview commercial and contract informationAttend client meetings and present tender informationPrepare risk and opportunity registersConduct site visits and liaise with internal departments for material and labour pricingEstimator Required Skills & Experience:Proven estimating experience within construction (experience in Commercial, MOD, Education or Healthcare sectors advantageous but not essential)Familiarity with a range of procurement routes including D&B, Traditional and 2-StageStrong numeracy, commercial awareness and attention to detailExcellent communication skills written, verbal and client-facingProficient in Microsoft Office; experience with Causeway/Excel-based estimating tools desirableHighly organised, proactive and able to meet tight deadlinesFull UK driving licenceEstimator Benefits:Competitive salary (negotiable DOE)Company car or car allowance25 days holiday + bank holidays (increasing with service)Contributory pension schemeFree parkingReward and discount platform accessSupport for professional development and further trainingStandard hours: 8:15am 5:00pm, Monday to FridayTPBN1_UKTJ

Senior Product Engineer Role location: Cambridge, UK Discover a career with real meaning. One that offers the opportunity to showcase your talents, achieve measurable success and gain immense satisfaction by shaping the future of cancer care. At Endomag, a Hologic company, we’re redefining cancer treatment and empowering clinicians worldwide with innovative medical solutions. We’re now looking for a Senior Product Engineer to join our dynamic team in Cambridge —someone who thrives on solving complex challenges, driving excellence, and making an impact that truly matters. As Senior Product Engineer at Endomag, a Hologic company, you will play a critical role in supporting released products and managing the transition of new innovations from R&D to our manufacturing partners, collaborating closely with QA/RA teams and suppliers. You will be responsible for investigating customer feedback, monitoring product performance, and identifying opportunities for improvement in design, manufacturing, and usage. Additionally, you will actively participate in post-market surveillance and work to address emergent failure modes, ensuring that products consistently meet highest quality standards and deliver optimal outcomes for customers and patients. Due to the nature of the role, UK and international travel will be required - around 25% KEY RESPONSIBILITIES • Act as technical lead for sustaining activities on current surgical guidance and implantable products. Manage and resolve product issues related to manufacturing, quality, or field performance in collaboration with suppliers., • Drive improvements to design for manufacturability, serviceability, and cost-efficiency. Work with the Endomag Repair Centre to develop and improve repair processes for existing and new products., • Support change control processes and documentation in alignment with quality system requirements., • Support the transfer of new products to manufacturing partners ensuring quality standards are met., • Collaborate with cross-functional teams including Quality, Regulatory, Operations, and R&D., • Participate in supplier audits, validations, and technical reviews. Work with supply chain to ensure product is supplied to stringent quality levels., • Ensure compliance with all applicable medical device regulations, including ISO 13485, FDA 21 CFR Part 820, and MDR., • Support regulatory submissions through compilation of Design History Files (particularly later stages), device manufacturing records and regulatory documentation. KNOWLEDGE, SKILLS & EXPERIENCE • A technical or scientific background in engineering., • Experience in high-tech engineering to exacting standards, ideally within medical device industry., • Understanding of quality and regulatory requirements, including ISO 13485, MDSAP, MDD/MDR, and 21 CFR., • Experience working with international manufacturing or supply partners., • Excellent problem-solving skills and a detail-oriented approach., • Excellent written and verbal communication skills., • Skilled in leading process & continuous improvement projects, ensuring successful implementation within set timelines., • Comfortable working in a high-compliance, fast-paced environment., • Experience in Statistical Process Control (SPC) techniques for monitoring and improving manufacturing processes. Ready to Make an Impact? If you have the right skills and experience and want to join our team, apply today. We can’t wait to hear from you! Innovate with Purpose: Work at the forefront of life-changing medical technology. Collaborative Culture: Join a friendly, supportive team where your contributions matter. Personal Growth: Expand your skills in a fast-growing, global company. #LI-KP1 #associate

Title: Senior FPGA Engineer (Cambridge)Location: Cambridge, Cambridgeshire, East Anglia, CB4 0DS, UKCompany: Platform Recruitment LimitedSenior FPGA Engineer | £100-180k | CambridgeThis is an opportunity to join a global team developing ultra-low latency technology.You will oversee all aspects of FPGA system design, driving advancements to ensure my client maintains its technological advantage by building the next generation of infrastructure.Responsibilities as aSenior FPGA Engineer:Architecting and implementing RTL designs on high-end FPGAs (Xilinx / Intel).Performing simulation, synthesis, P&R, and timing analysis for ultra-low-latency systems.Leading the definition of micro-architectures and verification environments.Driving technical excellence across the FPGA team through mentorship and code reviews.Collaborating with firmware, software and infrastructure teams to optimise full-stack performance.Requirements:7+ years FPGA / RTL design experience in timing-critical systems.Strong background in SystemVerilog, synthesis, timing closure and verification.Hands-on with Vivado / Quartus or equivalent toolchains.Familiarity with AXI, PCIe, Ethernet or custom high-speed interfaces.Bonus skills for aSenior FPGA Engineer:Exposure to high-performance computing, networking or real-time data systems.Knowledge of C/C++ or Python for tooling, verification or firmware collaboration.Appreciation for hardwaresoftware co-design and system-level optimisation.Apply now to join a global leader in an extremely high growth market!Platform Recruitment: Platform recruitment covers a wide range of IT and Engineering positions, including C++, Embedded, Electronics, Mechanical, DevOps, Cloud, Support, Project Management, Technical Sales, and more.TPBN1_UKTJ

Title: Soft Goods Development Designer (Cambridge)Location: Cambridge, Cambridgeshire, East Anglia, UKCompany: Coates Recruitment LtdJob Title:Soft Goods Development DesignerSalary:£30,000 £45,000 (Depending on experience)Craft. Create. Shape Products That Change Lives.Are you skilled in sewing, textiles, and pattern development?Do you enjoy hands-on creative work, turning fabric ideas into functional prototypes?Would you like to apply your craft to meaningful products that support comfort, mobility and independence?If yes, keep reading.The OpportunityWe're looking for aSoft Goods Development Designerto join an innovative product development team!My client design and manufacture assistive medical equipment, from seating to pressure-care products that enhance comfort, safety, and independence for people who need extra support.This is acreative, practical, design-driven rolewhere youll develop soft-material prototypes, experiment with fabrics, and collaborate with R&D to bring new product concepts to life.What Youll Be DoingCreating patterns, sewing prototypes, and developing soft-goods components for assistive medical productsCollaborating closely with R&D and designers to translate concepts into fully functional samplesSelecting and testing textiles, foams, and other soft materials to meet comfort, durability, and regulatory standardsIterating on designs through prototyping, evaluation, and refinementMaintaining excellent craftsmanship accurate stitching, clean finishing, precise patterningContributing to continuous improvement and innovation in materials and manufacturing processesWhat Youll NeedStrong background in textiles, garment construction, or upholstery, or soft-goods product makingExcellent sewing, pattern cutting, and prototyping skills with a high attention to detailAbility to interpret sketches, design ideas, or technical drawings and turn them into working samplesCreative problem solver with a hands-on approachGood communication skills and ability to work with designers, engineers, and production teamsOrganised, self-motivated, and able to prioritise in a dynamic environmentCommitment to quality, comfort, safety, and user-centred designThe OfferCompetitive salary (£30,000 £45,000)Company laptop25 days annual leave + public holidaysPrivate medical healthcareTraining and development opportunitiesAboutMy client is a dynamic and forward-thinking company creating assistive medical equipment that improves peoples lives. Comfort, quality, and user-centred design are at the heart of everything we do.Ready to apply your craft in a role where creativity truly matters?TPBN1_UKTJ

Senior RF Data Scientist / Research Engineer Near Cambridge My client, a fast-growing AI company based near Cambridge, is seeking a Senior RF Data Scientist / Research Engineer to work at the intersection of RF hardware, digital signal processing, and machine learning.This hands-on R&D role involve

Title: Senior Electronics Design Engineer (Cambridge)Location: Cambridge, Cambridgeshire, East Anglia, CB22 5LS, UKCompany: Platform Recruitment LimitedSenior Electronics Engineer | £60-80k | CambridgeAre you a creative and determined Electronics Engineer ready to lead projects that deliver world-leading, cutting-edge solutions across diverse industries?My client is a highly successful R&D consultancy developing completely cutting-edge solutions for some of the most stable and fastest-growing markets on Earth.You will be innovating on customer requirements, not just following a spec, so you have the opportunity to be creative.Responsibilities as aSenior Electronics Engineer:Design high-quality analogue and digital circuits for client projects across the full product development lifecycleLead electronics hardware development, collaborating with multi-disciplinary teamsArchitect and lead integration, issue resolution, and verification activities at both the hardware and system levelsInteract directly with clients to plan projects, formalise design requirements, implement, test, and hand over finished designsRequirements:Proven track record of managing the full product development lifecycle of multiple electronics designs.A strong hands-on passion for designing both analogue and digital circuits, coupled with a strong academic background in electronics or engineering.Comfortable operating in a fast-paced environment with excellent communication and detailed project planning/execution experienceBonus skills for aSenior Electronics Engineer:FPGA hardware design experience including VHDL/Verilog programmingRF design, test and compliance to 6GHzExperience with circuit simulation using SPICEApply now to lead multi-disciplinary project teams and deliver cutting-edge solutions that improve people's lives!Platform Recruitment: Platform recruitment covers a wide range of IT and Engineering positions, including C++, Embedded, Electronics, Mechanical, DevOps, Cloud, Support, Project Management, Technical Sales, and more.TPBN1_UKTJ

Job Description C++ Engineer - Robotics Location: Cambridge, Cambridgeshire Salary: £45,000 - £55,000 plus benefits and share options We are partnered with a robotics business in the Cambridge area who are developing next-generation autonomous platforms. They are looking for a C++ Engineer - R

Job Description Senior Electronics Engineer | £60-80k | Cambridge Are you a creative and determined Electronics Engineer ready to lead projects that deliver world-leading, cutting-edge solutions across diverse industries? My client is a highly successful R&D consultancy developing completely cut

A leading recruitment firm is seeking an experienced Head of R&D to lead innovation and manage a multidisciplinary team in developing regulatory-compliant products.The ideal candidate will have extensive R&D leadership experience, ideally in a regulated healthcare setting, and an advanced degree, pr

We are building a next-generation.Unity-based desktop application to a collaborative, browser-based platform.The goal is to enable real-time 3D visualisation, customisation, and streamlined data workflows for clinical users.Lead architectural decisions and R&D phases of a browser-native 3D platform

A leading biotechnology company in Cambridge is seeking a Technical Product Marketing Manager, Flow Cytometry.This on-site role involves executing product strategy and collaborating with R&D and Sales teams to ensure successful product launches.Ideal candidates will have a PhD in life sciences and e

A leading gastrointestinal health company is seeking a Molecular Assay Development Scientist to support the development and validation of molecular assays in Cambridge.You will work closely with the R&D and QA teams, ensuring high standards in laboratory practices.The ideal candidate has a BSc or MS

Ideal Requirements for the Head of Research and Development. We're partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!. Job Stability - Thrive in one of the industry's most resilient and future-proof markets.

A biotechnology company in Cambridge is seeking a Scientist / Principal Research Associate to join their Beta Islet Team.This role involves performing and optimizing pluripotent stem cell differentiation and collaborating with R&D to advance innovative therapies.Ideal candidates should possess a PhD

A biotechnology start-up is seeking a scientifically credentialed strategist to manage the post-sales journey for pharmaceutical partners.This role involves leading integration of AI models, consulting R&D teams on drug development challenges, and expanding partnerships.Candidates should have a PhD

A leading R&D consultancy in the UK seeks a Senior Electronics Design Engineer to innovate and deliver high-quality electronic circuits. The ideal candidate has a solid background in electronics or engineering and thrives in a collaborative, fast-paced environment. This role involves leading project

An ability to learn new technologies quickly and work effectively both independently and as part of a team. A full-time, permanent position in our modern open-plan R&D Center near Cambridge. Our engineers have a great passion and work ethic, have a broad set of technical skills and are ready to mast