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Join our team at Cambridge University Press & Assessment and utilise your skills to make a real difference! As a full-stack web developer, you'll be adept and thrive in creating cutting-edge eLearning solutions with Typescript and ReactJS. Closely work within a cross-functional team including design

You'll have: Proven experience in technical delivery management, project management, or agile coaching within a software development environment. Experience leading cross-functional teams, including developers, testers, and DevOps engineers, without direct line management authority. A data-driven mi

Nuclera is a venture-backed biotech company headquartered in Cambridge, UK with significant operations in Boston, USA.Nuclera’s mission is to accelerate discovery by enabling rapid, easy access to functional proteins essential for drug discovery research.Our eProtein Discovery™ benchtop system a

Graduate R&D Engineer / Physicist Location: Cambridge, UK Salary: £30,000 – £40,000 Benefits: Comprehensive package including profit-related bonus, company performance bonus, private medical insurance, life insurance, pension scheme, and free lunch Contact: Adam Mayne – | 01234 823373 About the Role We are seeking a talented and motivated Graduate Physicist or R&D Engineer to join a cutting-edge product development team in Cambridge. This is an exceptional opportunity to contribute to the design and development of next-generation fluid control technologies that are transforming the medical, life sciences, environmental, and industrial sectors. As part of the multidisciplinary R&D team, you will be part of team exploring and applying advanced physical principles, such as piezoelectricity, non-linear acoustics, and resonant mechanics to develop innovative and disruptive products. As you progress you’ll be involved in every stage of the development cycle, from concept generation and prototyping to design refinement and commercial launch. This role is ideal for recent graduates (BSc, MSc, or PhD) in Physics or Engineering who have hands-on experience in applied physics through academic projects, internships, or industry placements. Key Responsibilities • Research and develop novel fluid control technologies using applied physics., • Design and execute experiments to validate concepts and prototypes., • Collaborate with cross-functional teams to bring products from concept to market., • Apply analytical and experimental techniques in mechanics, fluidics, and acoustics., • Contribute to the automation of laboratory testing using tools such as Python, LabVIEW, or MATLAB. Candidate Profile • A 1st or 2:1 degree in Physics or Engineering (MSc or PhD advantageous)., • Demonstrated experience in applied physics and concept development., • Strong analytical and experimental skills, especially in mechanics, fluidics, and acoustics., • Practical lab skills and the ability to design and run experiments independently., • Creative, curious, and imaginative approach to problem-solving., • Experience with simple electronic circuit design is a plus., • Familiarity with Python, MATLAB, or LabVIEW for data analysis and test automation is beneficial. Location Based in Cambridge, this role is easily commutable from Newmarket, Huntingdon, St Neots, Royston, Bury St Edmunds, Stevenage, and surrounding areas.

Surgical Robotics Software Lead Engineer - Cambridge - Perm Salary: £40,000 - £70,000 pa Location: Cambridge 5 days a week on site My client can provide Sponsorship for the right candidate Our client is a global advisory and product development company are looking for a Surgical Robotics Software Lead Engineer in the Cambridge area. Your expertise in surgical robotics, software coding, and technical project management will be crucial for this role. You will be responsible for the implementation of advanced surgical robotic software control systems. You will lead a project team of software engineers and collaborate with cross-functional teams to ensure the successful delivery of projects. Surgical Robotics Software Lead Engineer Responsibilities: • Lead the design and development of surgical robotic software systems for client projects., • Design and develop software applications and control algorithms for surgical robotics systems using Object Oriented languages (C# and C++) and/or Embedded code (C), • Proven experience in leading surgical robotic software development as a product following medical development processes., • Experience designing software for Real Time Operating Systems (RTOS)., • Proficiency in modern Object Oriented languages (C#, C++) and Embedded code (C)., • Solid understanding of robotics principles, including kinematics, dynamics, and control theory with robotics frameworks, communications Middleware and digital position controllers. Due to the volume of applications received for positions, it will not be possible to respond to all applications and only applicants who are considered suitable for interview will be contacted. Proactive Appointments Limited operates as an employment agency and employment business and is an equal opportunities organisation We take our obligations to protect your personal data very seriously. Any information provided to us will be processed as detailed in our Privacy Notice, a copy of which can be found on our website

We’re supporting a pioneering technology company in Cambridge that’s building cutting-edge control infrastructure for distributed, ultra-low latency systems. As they scale their platform, they’re now seeking a Principal FPGA Engineer to take a key role in developing high-performance digital control and networking subsystems on advanced Xilinx platforms. This is a senior, hands-on position with influence across architecture, verification, and system integration. You'll be working on time-critical applications involving 10G/25G networking, real-time packet processing, and precision timing—supporting a wider mission that combines hardware, software, and optical systems in a truly novel way. Key responsibilities: • Lead FPGA development for timing-critical control systems on Zynq and Ultrascale platforms, • Design and implement low-latency packet processing pipelines and digital interfaces, • Support system-level integration, debug, and performance tuning, • Define and contribute to verification strategies, automation flows, and CI pipelines, • Collaborate with cross-functional teams on architecture and system co-design Ideal profile: • Extensive RTL design experience (SystemVerilog/VHDL) with a focus on performance and timing closure, • Hands-on with Vivado, Xilinx SoCs, and high-speed interface protocols (AXI, PCIe, SPI, I2C), • Strong background in FPGA-based networking or hardware acceleration, • Proficient in Python for scripting, modelling, or tooling, • Comfortable working in a lab with oscilloscopes, logic analysers, and debuggers This is a high-impact role at the intersection of digital design, hardware-software integration, and precision systems engineering—ideal for a technically strong engineer ready to lead from the front. If you're interested in the position of Principal FPGA Engineer, please apply or contact Sam Cruse.

Senior Regulatory Affairs Associate - Pharmaceutical Artwork and Labelling Cambridge Permanent £ Competitive Scope of role: With a core focus on the artwork and labelling aspect, this role offers a unique mix of creative and analytical duties which enable the business to meet its objectives around compliance, safety and maintaining up-to-date information for a portfolio of pharmaceutical products. Role requirements: • Taking the lead on labelling and artwork for the US portfolio of products – ensuring timely production, accurate presentation and compliance of regulatory information., • Coordination of labelling changes – working with a variety of teams internally to identify risks and propose solutions., • Preparation, review and approval of labelling documents, artwork files and print proofs., • Contribute to and lead the preparation of ANDA/NDA submissions. Perform reference product PI checks and take ownership of the labelling database to ensure ongoing compliance., • Lead the promotional material submission process to the FDA, prepare labelling for sections of the regulatory dossiers and submissions., • Create, revise and finalise cartons, labels and leaflets for both new product launches and existing products which ensure that all standards pertaining to quality, regulatory and branding standards are met., • Work with third parties to coordinate artwork that reflect the business branding elements., • Use of Adobe Illustrator and InDesign tools to produce ready to print artwork of a high quality. Your background: • BSc in a Life Science subject, or equivalent., • Approx. 3-4 years of experience within regulatory affairs for Pharmaceutical products with a proven focus on artwork and labelling., • Good working knowledge of US-FDA regulations will be highly advantageous., • Strong command of Adobe Illustrator or InDesign will be a benefit, or a similar package on another platform which produces regulatory-compliant artwork., • Demonstrable ability to convey scientifically complex technical information with clarity and accuracy., • Comfortable working to stringent deadlines, adaptable and agile in your approach to a dynamic environment with changing demands., • Excellent written and verbal communication skills, capable of forming strong business relations through collaboration in cross-functional settings. Does this look like the next move for you? Do you have a proven regulatory affairs background from within the Pharmaceutical space, and want to bring your creative side into play too? Please apply here or contact for more information or a confidential conversation about this exciting new role.

Technical Business Analyst Infomedia, Hybrid, four days per month in the office, Cambridge, United Kingdom Infomedia are the global leader in retail automotive technology, providing solutions from our large suite of products in pursuit of creating efficiencies, best-in-class customer experience and sales empowerment for our Automaker and Dealership clients. Our team get to build, implement and support some of the coolest products on the market, using the latest tech in an environment where ideas are nurtured, curiosity is rewarded, and collaboration is key to our success. We are evolving fast, and so we are on the lookout for those who thrive in fast-paced and ever-changing environments where innovation and continual improvement are the norm. As an agile Business Analyst, you will be involved with projects related to our Data Analytics product. You will interact with internal teams and external partners to answer questions and support development & technical integrations. You will be working in an Agile squad, writing user stories and helping design solutions to technical problems. This role is suitable for someone passionate about learning and able to adapt to frequent change in a fast-paced environment. What you’ll do • Work with customers, application developers, architects, project management and team members to understand business requirements that drive the analysis and design of quality Data Analytics solutions. Involved in aspects and/or full systems development lifecycle and responsible for the creation and maintenance of project lifecycle documents/deliverables., • Aid application development project deliverables. Obtain an appropriate level of sign-off as appropriate throughout the project lifecycle., • Manage job and project requirements so that projects are completed on time, in scope, within budget, with minimal defects. May help to maintain documentation such as design documents, acceptance criteria and flow diagrams., • Assure compliance with required standards and that all necessary approvals have been obtained throughout the project lifecycle., • Interfaces with the business areas, customers, partners, vendors, technical staff and project teams to drive value and innovative solutions., • Accountable for all aspects of requirements testing to ensure minimal production UAT defects are realised, and completing analysis of the results, tying back to customer impacts. Will interface closely with the business and technical staff on the team during all phases of the project, including unit and system testing, integration and UAT testing, culminating with implementation checkout and post-implementation support. What you’ll bring • Strong ability to analyse and break complex problems into manageable parts, • Minimum 7 years BA experience - no graduatesplease, • Exposure to Data Analytics product development, • Strong written and verbal communication skills; strong ability to articulate complex situations and information clearly, • Ability to communicate and work effectively with technical resources, • Ability to identify and document solutions to complex business problems with accuracy., • Technical Writing - customer documentation that meets the requirements of functional and system design specifications (desirable), • Experience of working within an agile organisation (desirable), • Attention to detail; thorough, • Able to work collaboratively and effectively at all levels in an organisation., • Exposure to application/system testing, • Knowledge of JIRA and Confluence (nice to have). Why Choose Us As a global leader in our industry, we develop innovatively crafted, data-driven cloud software solutions for some of the best and most well-known automotive brands worldwide. The day-to-day varied work coupled with our relaxed, informal, yet high-performing environment are the key things that make our team happy. Culture and Benefits We take our team members and service very seriously. We live by our core values of: Accelerating Performance, Driving Innovation & Service, Navigating Global, Steering Locals and Having Fun in the Fast Lane. We work hard but we play hard too. We offer a robust benefits package including paid parental leave, flexible working arrangements, health perks, growth and career development and recognition. About Infomedia Infomedia offers its Microcat® EPC, Superservice™ Quoting software, Data & Analytics, and various Data Services as ‘turn-key’ solutions to our OEM customers and their dealership networks. • 30 years industry experience, • Established global operations throughout 186 countries in 34 languages, • Our software is used by over 220,000 automotive industry professionals around the world

We are looking for a Project Manager to join our team. As a Project Manager at CRFS, you will play a key role in planning, coordinating, and delivering projects across our engineering and product teams. You will work closely with stakeholders to ensure that projects are delivered on time, within scope, and to the highest quality standards. This role involves managing schedules, resources, and risks while keeping clear communication with colleagues and customers. Duties and responsibilities • Plan and manage projects from initiation through to completion., • Coordinate cross-functional teams to achieve project objectives., • Track progress, manage risks, and escalate issues where required., • Support the preparation of project documentation, reports, and updates., • Facilitate meetings with internal and external stakeholders., • Ensure project deliverables meet agreed timelines, budgets, and quality standards., • Contribute to the continuous improvement of project management processes. Experience and Qualifications Required • Previous experience in project management or coordination., • Strong organizational and time management skills., • Good communication and stakeholder engagement abilities., • Ability to manage multiple priorities in a fast-paced environment., • A proactive approach to problem-solving and delivery. Desirable • Experience working in a technical or engineering environment., • Familiarity with project management tools and methods., • Professional certification such as PRINCE2 or PMP.

An ambitious, deep-tech organisation at the forefront of biotechnology and artificial intelligence is seeking a visionary Head of AI to lead the development of next-generation biological foundation models. The client has two site locations, Cambridge, UK & Paris, France, and hybrid working from either office is required. Underpinned by the world’s most comprehensive and ethically sourced database of natural biodiversity, our platform enables cutting-edge research and discovery across academia and industry. Following a successful Series B funding round (£45 million), we are expanding our AI capabilities to develop state-of-the-art models and algorithms that will shape the future of biology and bioengineering. This is a unique opportunity to lead a high-performing AI team, influence partnerships with global technology leaders, and build on an exceptional data infrastructure that is entirely new to science. Key responsibilities • Lead and manage a team of AI and machine learning researchers/engineers, providing technical direction and fostering a culture of creativity and excellence, • Design and implement novel AI/ML models and algorithms, balancing exploratory research with robust, scalable solutions, • Collaborate closely with interdisciplinary teams of biologists, bioinformaticians, and engineers to translate research objectives into applied outcomes, • Oversee multiple concurrent research streams, ensuring strategic alignment with organisational goals, • Contribute to the overall AI systems architecture, supporting the transition from research prototypes to production-level tools, • Represent the company’s AI leadership through academic and industry collaborations, conferences, and publications, • Provide mentorship and guidance to junior and senior members of the AI team, • Shape and execute a long-term AI strategy rooted in novel biological data and real-world application. Essential requirements • Postgraduate degree (PhD or MSc) in Computer Science, Machine Learning, Computational Biology, or a related field, • At least 5 years of industry experience in AI/ML research or engineering, with a minimum of 4 years in a technical leadership role or 3 years in people management, • Strong publication record or equivalent practical expertise in areas such as generative AI, deep learning, or computational biology, • Proven experience applying AI techniques to biological challenges, particularly in areas like protein design or genomics, • Demonstrated success in leading high-impact AI projects and delivering real-world solutions, • Exceptional communication skills, capable of engaging with both technical and non-technical stakeholders, • Experience training large generative models, including distributed training across GPU clusters or cloud platforms (e.g., AWS, Azure), • Strong critical thinking, strategic planning, and problem-solving abilities. Desirable • Experience in protein or DNA bioinformatics, • Proficiency in MLOps and machine learning infrastructure, • Background in software engineering and data pipelines (e.g., using Airflow or similar tools), • Familiarity with cloud-based model deployment, • Exposure to Agile project management methodologies. This is a rare opportunity to shape the future of AI-driven biotechnology from both a strategic and technical perspective, working with a uniquely rich dataset and an ambitious cross-functional team.

Managing Director – Photonics & Scientific Technology (UK Based) Location: UK (Cambridge area) Sector: Scientific Imaging and optics Technology Position: Full-time, Permanent We are partnering with an established manufacturer at the forefront of imaging technologies, into markets including medical imaging, industrial security, aerospace, and scientific research. The business is entering an exciting new chapter and is now seeking a Managing Director to lead the organisation into its next phase of growth. The Role The Managing Director will provide strategic and operational leadership across all areas of the business, with responsibility for: • Defining and executing the company’s long-term growth strategy, • Full P&L ownership and delivery of revenue and profitability targets, • Leading and developing the senior management team across sales, operations, R&D, and finance, • Driving commercial excellence, with a strong focus on international growth and new market development, • Ensuring operational efficiency and maintaining the highest standards of quality, compliance, and customer satisfaction, • Acting as the external face of the business with key customers, partners, and stakeholders The Candidate We are seeking a commercially driven and strategically minded leader with: • Proven senior leadership experience, ideally as Managing Director, General Manager, or Business Unit Director, • A strong track record in photonics, optics, scientific instrumentation, spectroscopy, imaging technologies, or advanced manufacturing, • P&L responsibility and demonstrable success in growing a technology-driven business, • Excellent leadership skills, with the ability to inspire and manage cross-functional teams, • Strategic vision combined with hands-on operational oversight, • Strong communication and stakeholder management skills Why Apply? This is a unique opportunity to take the helm of a highly respected UK technology company and lead its growth journey in global scientific and commercial markets.

Description Nuclera is a venture-backed biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Nuclera’s mission is to accelerate discovery by enabling rapid, easy access to functional proteins essential for drug discovery research. Our eProtein Discovery™ benchtop system accelerates protein expression and purification optimization in research labs. Nuclera is seeking a strategic, hands-on Product Strategy Manager - Antibody Applications to own the antibody applications roadmap on our eProtein Discovery system. This high-impact role will drive adoption among antibody discovery and reagent developers by translating market needs into differentiated product strategy, offerings, and go-to-market plans. You’ll serve as the antibody domain expert within the product organization—partnering closely with R&D, commercial, and customer-facing teams to accelerate growth in this core application area. The ideal candidate will be a seasoned antibody scientist with proven commercial experience—deeply familiar with the pain points, challenges, and opportunities in antibody discovery workflows. They will be skilled at translating deep domain knowledge and voice-of-customer insights into compelling product strategies that drive adoption and success of Nuclera’s eProtein Discovery System. This role requires approximately 20% travel, including domestic and international trips, to attend customer meetings, industry events, and visits to UK office as needed. About the role: Product Strategy & Roadmap • Define and drive the antibody application strategy, identifying key workflows and unmet customer needs, • Develop a sequenced roadmap to guide productization of antibody-relevant workflows, • Champion market-fit, pricing models, and routes to scale adoption Go-to-Market & Commercialization • Collaborate with commercial and marketing teams to launch and scale antibody-focused solutions, • Support market messaging, product positioning, and customer segmentation, • Enable pilot-to-revenue transition through collaborations, validated use cases and scalable offerings Customer & Market Insights • Lead rigorous, ongoing market research and VOC programs (surveys, in-depth interviews, advisory boards) to surface unmet needs in protein science., • Translate these insights into prioritized feature investments and clear business cases that inform the product roadmap., • Spend significant time in the field with customers to understand pain points and validate fit, • Distill voice-of-customer insights into clear product needs and roadmap clarity, • Track competitive landscape to ensure differentiation and sharpen value proposition Cross-Functional Leadership & Stakeholder Management: • Serve as the senior liaison between external stakeholders (customers, KOLs, sales, marketing) and internal teams (R&D, operations, quality, finance)., • Champion product requirements, secure executive buy-in, and ensure transparent communication on priorities, timelines, and metrics., • Support onboarding, training, and internal enablement for antibody use cases, • Contribute to strategic planning and resource prioritization for antibody and adjacent applications Cultivate Strategic Partnerships with Thought Leaders: • Build and steer high-impact relationships with Key Opinion Leaders (KOLs), academic and industry collaborators, and channel partners—co-developing new applications and pioneering use cases that expand and differentiate our eProtein Discovery platform Requirements • 5+ years of experience in product strategy or product management, • Advanced degree (PhD, MS) in related field required and/or or application development in the antibody discovery or life sciences tools space, • Extensive knowledge of recombinant antibodies and downstream uses, • Proven track record building roadmaps, aligning cross-functional teams, and launching successful solutions, • Significant experience with customer engagement, market validation, and commercial translation, • Ability to think both strategically and tactically in a fast-paced, startup environment UK Benefits What we offer: In addition to competitive salaries, we offer a range of benefits including: • Company bonus scheme of 5%, • Life insurance, • Private medical insurance and cash plan, • 25 days' annual leave + Bank Holidays, • Enhanced employer's pension contributions, • Enhanced maternity and paternity Leave, • Investment in professional development and learning, • Access to amenities on Vision Park and in Histon, • Fresh fruit, tea, coffee, and snacks in the office, • Organised team events

Location: Cambridge, UK Job Type: Full-Time Salary: Competitive, based on experience Antibodies.com is a fast-growing, innovative company that supplies high-quality protein research tools to life scientists. These tools enable researchers to analyze components of living cells at the molecular level — essential for disease and therapeutics research. Headquartered in Cambridge (UK), with regional hubs in the USA and Sweden, we are experiencing remarkable year-on-year growth, and this is an exciting opportunity to join our team and help us achieve our mission: enabling researchers to discover more, for less. 🔗 Learn more at ___ 🔗 Learn more at About the Role Do you have a background in life sciences and a flair for writing? We’re looking for a talented Life Science Content Marketing Writer to help us communicate our products and vision to researchers around the world. This is a hands-on role suited to a dynamic, detail-oriented individual who is excited by the opportunity to work in a fast-paced, high-growth start-up. You’ll be responsible for creating engaging and scientifically accurate content across digital and print platforms to drive awareness, engagement, and sales. Key Responsibilities As a Life Science Content Marketing Writer, your responsibilities will include: • Writing scientific and marketing content for web, email, print, and social media., • Drafting flyers, brochures, and other marketing materials, and overseeing their visual design., • Creating and maintaining product landing pages and other website content., • Planning and writing newsletters for curated email campaigns and automated workflows., • Developing and executing multi-channel marketing campaigns to promote our products., • Collaborating with cross-functional teams to align messaging and branding., • Monitoring campaign performance and refining strategies for improved outcomes., • Implementing lead generation and nurturing strategies., • Using marketing automation tools to segment and manage customer workflows. Note: This is a varied role, and responsibilities may evolve as the company grows. Qualifications & Skills The ideal candidate will have: • A PhD in a life science field., • 5+ years of scientific writing and/or marketing experience., • Excellent written and verbal communication skills., • Strong attention to detail and accuracy in all tasks., • Experience with basic HTML and web editing., • Familiarity with SEO principles and keyword research., • Ability to work independently and manage multiple tasks effectively., • Marketing experience in a life science or biotech company (preferred but not essential). If you meet most of the criteria but not all, we still encourage you to apply. Remuneration We offer a competitive salary and benefits package, commensurate with experience. How to Apply To apply, please send your CV and a brief cover letter to .

Functional Assessor Nurse for Work Capability Assessments (WCA) – HYBRID WORKING Starting Salary: £40,000 - £42,000/pa + benefits + 10% yearly bonus Nurses: RGN, RMN, RNLD Why go with us? As healthcare professionals we understand the challenges presented by the current healthcar

Key Responsibilities: Act as the primary contact for customer enquiries, troubleshooting, and guidance Build strong relationships with both internal teams and external clients Track and report on customer satisfaction and feedback Work with cross-functional teams to improve processes and customer w

Functional Assessment Roles, 9-5 Monday to Friday all UK Bank Holidays off, Immediate Starts available.Do you want a role where your RGN/RMN/RNLD or Physiotherapy, Occupational Therapy and Paramedic skills and curiosity are at the core of the role? Are you seeking a role where you can combine your c

Collaborate with cross-functional IT, development, and infrastructure teams to keep configuration data current and reliable. Act as the go-to expert for CI discovery and ServiceNow CMDB, managing integrations and troubleshooting with precision. Deliver clear, actionable reports to monitor CMDB perfo

DXC continues to significantly expand our SAP business in the UK and in Europe and are looking for a SAP PP Functional Consultant to be part of our team.Our SAP Functional Consultants work directly with both clients and internal teams in a project environment to gather and analyse business requireme

The Role: Due to sustained continued expansion they now require a driven Device Engineer to lead the management of cross functional project activities within a multi-disciplined engineering team to meet specified project objectives / deliverables. Position: Device Engineer (Hybrid) Location: Cambrid

QAProven experience as a Test Engineer / QA Engineer in a similar role with strong experience to AI/ML projects. Develop automated testing frameworks for data pipelines, model training, and inference. Perform functional, integration, regression, and performance testing on AI systems.

About Summit: Ivonescimab, known as SMT112, is a novel, potential first-in-class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule. Ivonescimab displays unique cooperative binding to each of its intended targets with multifold higher affinity when in the presence of both PD-1 and VEGF. Summit has begun its clinical development of ivonescimab in non-small cell lung cancer (NSCLC), with three active Phase III trials: • HARMONi is a Phase III clinical trial which intends to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who have progressed after treatment with a 3rd generation EGFR TKI (e.g., osimertinib)., • HARMONi-3 is a Phase III clinical trial which is designed to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC. Overview of Role: The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Responsible for study start up and maintenance through study close out. Coordinates, leads and drives leads Summit cross functional team members, CROs and vendors to successfully deliver clinical studies. Responsible for all performance metrics and quality of deliverables in the clinical trial. Role and Responsibilities: • Oversees study scope, quality, timelines, and budget with the internal Summit functional leads, CRO and vendors to ensure that overall project objectives are met, • Initiates and builds solid professional relationships with key opinion leaders and clinical site staff, • Partners with the CRO to ensure robust patient enrollment strategies are developed and carried out effectively to ensure patient enrollment is completed on time, • Partners with the CRO to ensure robust ongoing data monitoring strategies are developed and carried out effectively to ensure delivery of high-quality data, • Proactive identification and management of study related risks, • Responsible for the development and management of clinical trial documents including (but not limited to) protocols, Case Report Forms (CRFs), consent documents, confidentiality agreements, • Responsible for reviewing and managing study related plans, processes including, • Investigator agreements (CTA), CRFs, CRF guidelines, statistical / pharmacokinetic analysis plans, monitoring plan, data management, safety monitoring, • Responsible for reviewing CRO and vendor contracts/work orders and specifications to enable study objectives to be met, • Reviews and approves essential document packages to enable timely site activations, • Reviews pre-study, study initiation, interim monitoring visit and at study closeout visit report, • Provides close oversight on the findings on the monitoring reports and loops back with broader team to provide updates, • Directs investigator performance and adherence to protocol, and proactively addresses conduct issues and enrollment problems, as necessary, • Responsible for oversight on the maintenance of the TMF and completeness at the end of the study, • Perform periodic QC of the TMF, • Oversee the creation and execution of clinical trial activities in accordance with Good Clinical Practices. Ensure compliance of clinical trials with national and international regulatory requirements and co-monitoring the assigned clinical trial following company SOPs, • Ensures the study is “inspection ready” always, • Responsible for oversight and coaching of the functional activities of Clinical Trial Associates allocated to the project, • All other duties as assigned Experience, Education and Specialized Knowledge and Skills: • Bachelor’s degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical related area preferred, • 5+ years of clinical project management experience in conducting international clinical trials in sponsor Pharma/Biotech organization, • Prior phase II and III experience required, • A solid understanding of the drug development process, ICH guidelines/GCP and specifically, each step within the clinical trial process, • Experience with budget forecasting and management, • Experience with clinical studies in oncology, • Ability to travel internationally to visit clinical sites and for study meetings. Amount will vary upon project needs (up to 20%), • Proven proficiency in overseeing large complex studies being managed in house and by a CRO, • Demonstrated ability to lead teams and work in a fast-paced team environment, • Experienced and enjoys building relationships with KOLs and site personnel, • Ability to successfully engage and work collaboratively with overseas clinical operations team members/colleagues, • Demonstrated ability to build and deliver on patient enrollment strategies, • Excellent interpersonal and decision-making skills. Demonstrates innovation, possesses drive, energy, and enthusiasm to deliver the program objectives, • Demonstrated ability to comprehend complex scientific concepts and data, • Proficient in reviewing and assessing clinical data, • Possesses excellent planning, time management & coordination skills, • Demonstrated ability to problem solve and use clear judgment in relation to regulatory requirements, interactions with external parties, timelines, and complex clinical programs, • Experience in working in a small organization, • Excellent written and oral communication skills Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit’s Talent Acquisition team at to obtain prior written authorization before referring any candidates to Summit.

My client seeking a reliable and skilled Fabric Technician/Handyperson to join our team on a 3-month contract based in Peterborough.The role involves carrying out planned, preventative, and reactive maintenance of the building fabric to ensure the site remains safe, functional, and well-maintained.Y

Functional Assessment Roles, 9-5 Monday to Friday all UK Bank Holidays off, Immediate Starts available.

Proactively coordinate and promote event-based marketing campaigns, ensuring effective audience engagement. Support cross-functional marketing projects, including product launches and new initiatives. Minimum 5 years’ experience in marketing communications or a related field.

Collaborate with the communications team on public relations, corporate communications, and event marketing. Proactively coordinate and promote event-based marketing campaigns, ensuring effective audience engagement. Support cross-functional marketing projects, including product launches and new ini

Development Programme Manager 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 are excited to be looking for a talented Development Programme Manager to join our team in Cambridge. As Development Programme Manager at Endomag, a Hologic company, your role will be to ensure our new implantable products align with Endomag’s strategic goals, are completed on time and within budget, and meet regulatory requirements, including actively contributing to the submission review process. You will manage relationships across the organization and with external partners, ensure compliance with ISO and FDA quality systems regulations, and facilitate effective project execution. We are looking for individuals with technical expertise, a solid background in project management and experience with product lifecycle development. Excellent communication and stakeholder management skills are a must, along with the ability to lead and motivate teams. KEY RESPONSIBILITIES Ensure timely delivery of programme milestones, supporting projects across the group in line with agreed budgets and resources Manage the engineering design and development of new medical device products at various stages of development leading cross functional teams Develop and document design requirements; lead design reviews and ensure Design History and Technical Files comply with Endomag’s ISO13485 Quality Management System including our ISO14971 compliant risk management process Actively contribute to the regulatory submission processes to ensure compliance and regulatory approval to ensure successful product launch KNOWLEDGE, SKILLS & EXPERIENCE Background in physics/chemistry/engineering or closely related field NPD project management experience in the medical device industry, ideally including implantable devices Experience in planning, organizing and executing projects, including budgeting, scheduling and resource management Knowledge of EU and FDA medical devices regulations and standards with experience in supporting devices during the regulatory submission processes Proven project management, organisational and time management skills Ability to analyse complex situations, identify potential problems and develop effective solutions Excellent presentation skills communicating technical and project requirements Well-organised with the ability to work with critical attention to detail and high levels of accuracy 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 mid-seniorlevel

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

Join the Central Engineering Software Operations team as a Project Manager where you will lead delivery of software projects that help our partners’ build energy efficient Arm powered products. Work closely with adjacent functional groups such as Engineering, Product Management, Legal and Operatio

Familiarity with computer/SoC architecture, as well as a solid understanding of system architecture and system software, is highly desirable. University degree in Engineering or higher or equivalent experience is preferred. C++ functional models that enable pre-silicon development of firmware, syste

Lead the creation, communication, and management of the CRM Product Roadmap, ensuring a prioritised and well-maintained product backlog. Serve as a Subject Matter Expert on CRM products, understanding both their functional use and underlying technology. Job Title: CRM Product Owner (maternity cover)

Represents Regulatory Affairs and may serve as Regional Lead or Global Regulatory Lead on cross-functional/cross-regional Regulatory Submission Teams. You will lead Regulatory Submissions Teams or other Regulatory Project Teams and represent Global TA Regulatory on cross-functional core and sub-team

Senior / Principal Scientist, Functional Materials.Lila Sciences is the world’s first scientific superintelligence platform and autonomous lab for life, chemistry, and materials science.We are pioneering a new age of boundless discovery by building the capabilities to apply AI to every aspect of t

Work in a flexible, inclusive, and innovation-driven environment. You’ll be part of a collaborative, cross-functional team developing and optimising synthetic routes for some of the most challenging molecules in drug development. Proficiency in tools like ChemDraw, Microsoft Office, and electronic

AI experience is a must and LLM testing knowledge will really set you apart. Functional, performance, and security testing of services on Azure. Support threat modelling and API security testing.

You will work closely with a lead data engineer and a multi-functional team of analysts and collaborators, dealing with diverse datasets from technical resource logs to user entered spreadsheets. Work with semi-structured and unstructured data ensuring robust data handling strategies. In this role,

Nuclera is a venture-backed biotech company headquartered in Cambridge, UK with significant operations in Boston, USA.Nuclera’s mission is to accelerate discovery by enabling rapid, easy access to functional proteins essential for drug discovery research.Our eProtein Discovery benchtop system acce

Research Associate - Mechanisms of G protein-coupled receptor (GPCR) activation (Fixed Term).Research Associate position in the group of Prof.Daniel Nietlispach at the Department of Biochemistry, University of Cambridge.The project studies functional aspects of GPCR activation.The position is funded

Nuclera’s mission is to accelerate discovery by enabling rapid, easy access to functional proteins essential for drug discovery research. Our eProtein Discovery benchtop system accelerates protein expression and purification optimization in research labs.

Cross-Functional Work: Collaborate with the Learning and Development and Technology teams to ensure comprehensive support and training for lawyers while staying current on technology advances and available tools, ensuring alignment with the firm's overall data and technology strategy. Technology Int

The recruitment team will provide further detail as you progress through the recruitment process or you can contact the Independence team upon request. Program/project management and team leadership. Proven experience managing cross-functional teams and large-scale technology or cybersecurity progra

Biology Laboratory Technician Apprentice (Level 3) - Precision for Medicine. Laboratory Technician - Genetic Toxicology. Laboratory Technician (Functional Genomics).

We are looking for an enthusiastic and driven Senior Web Application Engineer to join our team.Responsible for all aspects of the full software development life cycle, including requirements analysis, design, development, testing, documentation, and training.Creation of functional designs, specifica

Laboratory Technician (Functional Genomics). Sign in to set job alerts for “Laboratory Technician” roles. Biology Laboratory Technician Apprentice (Level 3) - Precision for Medicine.

This hands-on role supports low-volume, electro-mechanical batch production, ensuring quality, efficiency, and cross-functional collaboration.

Studying a Bachelors in Organic Chemistry, Polymer Chemistry, Materials Chemistry, Electrochemistry or a related discipline. Polymer / Organic Chemist Intern (12 months) - Starting Summer 2026. Project Title: Functional Materials: Molecular and Polymeric Chemistry for Electrochemical Devices.

In this role, you will work collaboratively as part of a cross-functional team of other Product Designers, User Experience Researchers, Content Designers, Product Managers, and Software Engineers to create digital products that have a real impact for young people and educators who are engaged with d

Role Details: Job Role: Oracle Functional Consultant (Fusion) Contract: 6 months initially (with high potential for extension) Location: Hybrid ? 3 days per week onsite (Midlands) Rate: £600 - £650 Outside IR35 pending SDS report Apply now for the Oracle Functional Consultant role to speak w

Job Description (Brief Summary of the role) Our SAP Functional Consultants work directly with both clients and internal teams in a project environment (ECC and S/4) to gather and analyse business requirements for the support and configuration of their specific SAP module(s). Works with business use