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A fantastic opportunity has arisen for a Microfluidics Engineer to join a Cambridge based biotech company. This is a full-time permanent position.Key Responsibilities:Provide technical leadership and expertise across the company's microfluidic activities, driving the development, integration and application of microfluidic technologies across multidisciplinary projects.Lead the experimental validation and iterative optimisation of microfluidic performance, including droplet generation, flow control and droplet sorting.Maintain and develop the microfluidic platform, introducing innovative approaches to improve its capabilities and performance.Design and develop microfluidic devices and technologies for the high-throughput screening of plastic-depolymerising enzymes.Lead microfluidic device fabrication, testing and optimisation.Develop and integrate optical and optofluidic systems for the detection, measurement and sorting of droplets.Analyse and interpret experimental data to support the development and optimisation of screening technologies.Work proactively with researchers across multiple disciplines, including biochemists, chemists, bioinformaticians and other scientific specialists.Maintain accurate and comprehensive records of experimental work, results and development activities.The ideal candidate must have:Strong practical experience in microfluidic technology development and experimental optimisation.Proficiency with CAD tools used for microfluidic device design, such as AutoCAD.A Master's degree or PhD in Mechanical Engineering, Chemical Engineering, Biomedical Engineering or a related discipline.A methodical and data-driven approach to experimental work and problem solving.Experience with programming for instrument control, such as LabVIEW.We endeavour to reply to every candidate, every time but if you haven't heard back within 10 days, please understand that you have unfortunately been unsuccessful for this position, or the position has been filled.Please call the office or send an email to discuss other potential positions.TPBN1_UKTJ

PhD‑Level Ultrasound Technology Consultant - Cambridge A prominent medical technology innovator in Cambridge is seeking a PhD‑level ultrasound specialist to help drive the development of next‑generation surgical and interventional devices.The organisation has a long-standing reputation for transforming complex scientific challenges into commercially successful products and works extensively across healthcare, life sciences and the wider physical sciences. You would be joining a culture that values curiosity, open collaboration and entrepreneurial thinking.It is an environment where scientific creativity is encouraged, ideas are shared freely and individuals are given the space to shape projects and influence technical direction. This position is ideal for someone who wants to play a central role in advancing surgical technology.The work spans the development of sophisticated medical systems, including robotic surgical platforms and intelligent instruments with integrated sensing, all designed to support clinicians in delivering safer and more effective procedures.You will take responsibility for high‑impact technical programmes, combining scientific depth with commercial awareness, and you will apply your ultrasound expertise across the full innovation pathway, from early feasibility studies through to preparing products for market. A key part of the role involves working closely with partner organisations to define technical strategy, strengthen long‑term relationships and deliver meaningful outcomes.As you progress, you will have opportunities to build your profile within the surgical technology community and contribute to shaping future industry direction.Each project offers the chance to broaden your scientific knowledge, develop leadership capability and see your work translate into real clinical benefit.Candidates previously placed with this organisation have consistently advanced their careers and expanded their responsibilities. You will thrive in this role if you enjoy working within multidisciplinary teams and value an environment where rigorous thinking and open discussion are central to the way problems are solved.A strong foundation in ultrasound is essential, gained through a PhD, postdoctoral research or relevant industrial experience.The organisation welcomes applications from recent PhD graduates as well as individuals with early‑career industry experience.Knowledge in areas such as transducer design, ultrasound signal processing, high‑speed electronics, image segmentation, regulatory standards like EN 60601 and metrology techniques including scanning hydrophones will be particularly valuable. The company operates from a purpose‑built, award‑winning campus surrounded by green space and designed to support creative and collaborative work.Employees benefit from a comprehensive package that includes an annual bonus, enhanced pension contributions, private medical cover, free meals, life assurance and a range of additional perks typically associated with a leading technology employer. Interest in this opportunity is expected to be high.If the role aligns with your experience and ambitions, early application is strongly recommended. To discuss the position further, contact Andrew Welsh, Director of Medical Devices, Biotech and DeepTech Recruitment at Newton Colmore, on .You may also submit your CV, and a member of the team will be in touch to guide you through the next steps. #J-18808-Ljbffr

Nuclera, a Cambridge-based biotech company behind the eProtein Discovery platform, is seeking an experienced software engineer to join a small, driven engineering team. You will contribute to the next growth phase by delivering full lifecycle software for prototypes, products and support tools within a cross-functional environment. Over 6–12 months, your role will broaden to include other languages and technologies, potentially extending to electronics and PCB design, while maintaining strong #J-18808-Ljbffr

Lila is hiring a Staff IT Systems Engineer, Identity to own the architecture and roadmap for identity and access management across the company. This is a senior individual-contributor role with company-wide scope, focused on how employees, services, and AI agents authenticate, receive access, and operate securely. You’ll join the IT & Security team and partner closely with Security, People, Engineering, and Lab Operations. You’ll modernize Lila’s identity foundation across cloud IAM, SSO, SaaS administration, machine identity, and identity governance while mentoring engineers and raising the bar for identity engineering practice. This role is especially important as Lila scales its workforce, physical footprint, autonomous labs, and AI-native operating model. The right person will make identity systems more secure, automated, auditable, and easier for employees to use. • Own the architecture and roadmap for Lila’s identity platform across Okta, Entra ID, AWS IAM, GCP IAM, SSO, and directory services., • Drive Lila’s Zero Trust roadmap, including phishing-resistant MFA, continuous access evaluation, device trust, and endpoint integration., • Build a machine identity and AI-agent identity program for service accounts, API keys, workload identities, OAuth/OIDC grants, MCP servers, and autonomous lab systems., • Design identity governance capabilities, including access certification, entitlement reviews, and automated joiner, mover, and leaver workflows., • Set standards for SaaS identity integrations across Google Workspace, Slack, Atlassian, Microsoft 365, and the broader application portfolio., • Build production-grade automation using Python or Go, Terraform, workflow platforms, and AI-assisted engineering tools., • Partner with Security on identity threat modeling, incident response, access audits, and compliance readiness., • Serve as the technical escalation point for complex identity issues and mentor engineers across IT and Security., • Document architecture decisions, processes, and runbooks that improve identity operations at scale., • Deep experience in IT systems engineering, infrastructure, or identity engineering, with significant ownership of identity and access management systems., • Strong Okta experience, including SSO, SAML, OIDC, SCIM, authorization policies, and workflow automation., • Experience designing and scaling IAM, Zero Trust, or identity governance programs in a complex technical environment., • Strong understanding of cloud IAM concepts across providers such as AWS, GCP, Entra ID, or similar platforms., • Ability to build and operate automation using Python or Go, APIs, event-driven workflows, and infrastructure-as-code., • Working knowledge of machine identity concepts, including workload identity federation, secrets management, and service account governance., • Strong technical judgment, troubleshooting ability, and written communication skills., • Track record mentoring engineers and leading cross-functional technical initiatives without relying on formal authority., • Experience in biotech, pharma, life sciences, R&D, or another regulated technical environment., • Familiarity with SOC 2, ISO 27001, HIPAA, GxP, or similar compliance frameworks., • Experience securing lab instrumentation, robotics, IoT, scientific computing, or autonomous systems., • Experience designing or operating identity systems for AI agents or agentic workflows., • Experience with endpoint management or MDM platforms such as Jamf, JumpCloud, or Kandji., • Experience building Slack apps, Slackbots, internal developer tooling, or identity self-service workflows., • Experience supporting M&A integration or rapid headcount scaling from an identity perspective. We offer competitive base compensation with bonus potential and generous early-stage equity. Your final offer will reflect your background, expertise, and expected impact. Full-time U.S. employees receive a comprehensive benefits program including medical, dental, and vision coverage; employer-paid life and disability insurance; flexible time off with generous company wide holidays; paid parental leave; an educational assistance program; commuter benefits, including bike share memberships for office based employees; and a company subsidized lunch program. Full-time employees outside the U.S. receive a comprehensive benefits program tailored to their region. USD salary ranges apply only to U.S.-based positions; international salaries are set to local market. $163,400 — $199,500 USD Lila Sciences is building Scientific Superintelligence to solve humankind's greatest challenges. We believe science is the most inspiring frontier for AI. Rather than hard-coding expert knowledge into tools, LILA builds systems that can learn for themselves. LILA combines advanced AI models with proprietary AI Science Factory instruments into an operating system for science that executes the entire scientific method autonomously, accelerating discovery at unprecedented speed, scale, and impact across medicine, materials, and energy. Learn more at www.lila.ai. Guided by our core values of truth, trust, curiosity, grit, and velocity, we move with startup speed while tackling problems of historic importance. If this sounds like an environment you’d love to work in, even if you don’t meet every qualification listed above, we encourage you to apply. Lila Sciences iscommitted to equal employment opportunityregardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Information you provide during your application process will be handled in accordance with our Candidate Privacy Policy. #J-18808-Ljbffr

At Biocair, our specialist temperature-controlled logistics solutions support pharmaceutical, biotech, research and healthcare organisations around the world. We are looking for a Business Development Manager to help grow our UK healthcare and life-sciences business. You will develop new customer relationships, grow existing partnerships and help expand our presence across markets including pharmaceutical, biotechnology, Cell & Gene Therapy, R&D and laboratory organisations. Reporting to the Global Accounts and UKI Sales Director, you will have ownership of your commercial territory while working closely with colleagues across Operations, Customer Service, Finance, Project Management, Sales and Marketing. This is a field-based role with a minimum of one day per week in the Cambridge office. Travel across the territory, including occasional overnight stays, forms part of the role. We welcome people who have built their skills through different career paths. Relevant commercial experience might come from logistics, transportation, healthcare, life sciences or another environment where you have sold complex services and built lasting B2B customer relationships. You will take ownership of developing a healthy sales pipeline and converting opportunities into sustainable, profitable customer relationships. You will identify new prospects, respond to incoming opportunities and grow established accounts by understanding customer needs and identifying appropriate Biocair services and solutions. A particular focus will be helping develop and execute our UK Cell & Gene Therapy growth strategy, identifying opportunities and strengthening Biocair's position as a specialist logistics partner. You will: • build, qualify and progress a sustainable pipeline of opportunities;, • develop new customer relationships and expand existing accounts;, • lead customer discovery conversations and translate requirements into appropriate commercial solutions;, • prepare proposals, quotations and pricing solutions;, • lead and coordinate responses to tenders, RFPs and RFQs;, • negotiate commercial agreements in partnership with relevant internal teams;, • own revenue, growth and profitability outcomes within your territory;, • conduct effective customer business reviews and follow through on opportunities, risks and agreed actions;, • collaborate with Operations, Customer Service, Finance and Project Management so proposed solutions are commercially viable and operationally deliverable;, • monitor customers, competitors and market developments to identify opportunities and risks;, • maintain accurate pipeline, opportunity and customer information in Salesforce;, • contribute forecasts, business planning and commercial insight; and, • represent Biocair appropriately at customer meetings, industry conferences, exhibitions and networking activities. We are interested in what you have achieved and how you work, rather than a particular career route. You will bring evidence of: • delivering B2B commercial growth and working towards sales or growth targets in logistics, transportation, healthcare, life sciences or a related environment;, • developing prospects into new customer relationships and growing established accounts;, • understanding customer challenges and translating them into commercially viable propositions;, • managing a pipeline and using CRM technology such as Salesforce;, • commercial negotiation and working with contracts or customer agreements;, • analysing customer, market or commercial information to make sound decisions;, • communicating commercial ideas clearly in writing, conversation and presentations;, • collaborating across operational, finance and customer-facing teams;, • organising competing priorities and progressing opportunities through to an outcome; and, • taking ownership of commercial activity within an assigned market or territory The role also requires the ability to use standard Microsoft Office applications to create effective reports, business cases and customer presentations. Experience of pharmaceutical, biotech, Cell & Gene Therapy, clinical/research, healthcare or specialist logistics environments could help you get up to speed, but candidates should not screen themselves out solely because their background uses different terminology. • Pension, Life Assurance & Group Income Protection, • Private Medical Insurance & Healthcare Cash Plan, • Enhanced Primary & Secondary Caregiver Leave, • 25 days holiday + Birthday Leave + Volunteering Leave, • Cycle to Work Scheme & Discount Shopping Scheme, • Specsavers Vouchers & Employee Assistance Programme, • Car Allowance + Eligible for Sales Commission Scheme, • Full-time, Monday to Friday, 08:30 to 17:30, • Field based with one working day per week spent working with the team at our Cambridge office in Sawston (CB22 3EG), • Travel will be required as needed To learn more about Biocair, please visit us at: Biocair is committed to building an inclusive workplace where everyone feels welcome, included, valued and respected. We are an equal opportunity employer and welcome applications from all backgrounds. If you require adjustments during the recruitment process, please contact: Biocair provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. • Applicants must have the right to work in the United Kingdom., • Visa sponsorship is not available for this opportunity. Once we have received your application, our Talent Acquisition (TA) team aims to respond within 3 working days. The process typically includes: • First-stage interview (Teams), • Second-stage interview (onsite) This gives you the opportunity to meet key stakeholders and experience the team and environment first hand. • Applications close on: Monday 12 October 2026 (we reserve the right to close early should we receive a high volume of strong applications). #J-18808-Ljbffr

Linkzill in Cambridge is seeking a Biotechnology Intern for a flexible 3-month internship.

Do you want to use your engineering skills to build agentic workflows that help find treatments for rare disease patients? Healx is an AI-powered tech bio company that is redesigning drug discovery. With 10,000 rare diseases affecting 400 million people globally, 90% of which have no approved treatment, Healx is on a mission to pioneer the next generation of drug discovery to help rare disease patients in need. We combine data, artificial intelligence and deep pharmacology expertise to develop treatments more quickly and cheaply than traditional drug discovery. Diversity and inclusion sits at the heart of our mission to help people with rare diseases, and we believe that attracting and empowering a diverse team is critical to achieving this goal. We welcome applications from people from all backgrounds and walks of life. Below we have included the qualities that we feel are required for you to excel in this role; however we appreciate that people can apply transferable skills and experience. If you think you have what it takes, love our mission and resonate with our values but are worried you don't tick every box – we still want to hear from you and encourage you to apply! • Care for Rare – Rare disease patients are at the heart of what we do, • Grow as individuals – We are learners always seeking to enhance our expertise, • Win as a team – We strive to remain inclusive and diverse and we celebrate successes and lessons together, • Innovate and deliver – Our mission requires rapid innovation and calculated risks that won't compromise our high standards Healx is looking for an Agentic AI Engineer to build LLM-agentic workflows that power our drug discovery platform. Reporting to our Director of Tech Strategy, you'll design and build agents that solve real drug discovery problems. Working closely with scientists across the company, you'll understand the questions that matter most to their work, then design and refine agents that reason over our knowledge graph, proprietary methods, scientific literature and other sources to generate, triage and rationalise testable therapeutic hypotheses for rare diseases. You won't be starting from scratch. We've adopted an agentic framework (our stack currently includes Python, ADK and AgentSpace) and built workflows already delivering impact across our drug discovery platform. But this is a fast-moving field, so a big part of the role is helping us adapt as the landscape shifts. You'll work alongside the technical lead who owns our agentic infrastructure, with scope to take ownership of specific workflows and grow your influence as you do. You'll join a cross-functional team of machine learning engineers, software engineers, bioinformaticians, drug discovery scientists and clinicians, all working to sharpen how Healx makes better decisions in drug discovery. • Build and refine AI-agentic workflows on our internal framework to help drug discovery scientists generate the best testable therapeutic hypotheses to progress., • Translate discovery problems into agent designs, working out where an agentic approach genuinely adds value, and where it doesn't, • Integrate agents with our knowledge graph, proprietary methods, scientific literature and other sources so they reason over the right evidence for each problem, • Expand and maintain our existing GenAI tools so they keep pace with the team’s needs and a fast-moving ecosystem, • Contribute to how we evaluate agentic workflows, helping shape sensible evals, testing and quality standards as the practice matures, • Write clear, maintainable, well-documented code that others on the team can build on In 3 months, you have: • Got to grips with our agentic framework and the discovery problems it serves, and made your first contributions land in the codebase, • Built working relationships with the scientists and engineers you partner with, and started turning their feedback into concrete improvements In 6 months you have: • Taken at least one agentic workflow from idea to a production tool scientists use in our drug discovery pipeline - built on our framework, with sensible evaluation and documentation, • Operating with real independence - owning agentic workflows end to end, proposing improvements. We'd love to hear from you if • You've built and shipped LLM-agentic systems that deliver real value - agents that use tools, orchestrate multi-step workflows and behave reliably in production., • You have at least 2 years of software engineer or ML engineer working experience. And you have strong software engineering fundamentals - you write clear, tested, maintainable Python code that others can build on, • Fluency with the modern LLM/agent toolkit - model APIs, prompting, tool use, RAG, and the patterns this fast-moving ecosystem is converging on (MCP, agent frameworks, evals)., • You enjoy working closely with non-engineers - you are the kind of person who'll sit with a scientist to understand what they actually need. It’s a bonus if you have: • Experience in drug discovery, biology, or another life science domain, • Familiarity with knowledge graphs or reasoning over structured or heterogeneous data, • Experience building evaluation harnesses or testing strategies for LLM systems, • A track record of picking up unfamiliar domains quickly and becoming useful fast, • Interest in or experience with biotech / techbio and its impact on patient outcomes. Healx works from a modern accessible office in the centre of Cambridge within easy reach of the train station. We offer a flexible, diverse and inclusive working environment that considers your individual needs and believes in maintaining a sustainable work-life balance and we are open to discussing flexible working arrangements. We are a hybrid team operating on a highly collaborative model that values synchronization and pair programming. You will be welcomed by a team of colleagues with decades of accumulated experience in their areas of expertise, happy to help you develop your own skills in a highly collaborative environment and who are keen to provide guidance and support in your personal and career development plans. Healx will provide you with support and guidance to help you do your best work and make an impact. We offer flexible working and believe in maintaining a sustainable work-life balance. If you require any reasonable adjustments during the recruitment process, please let us know — we’re happy to accommodate. Financial - Competitive salary, share options, 7% employer pension contributions, life insurance of 4x base salary. Health and Wellbeing - Private medical insurance, 25 days annual leave (plus bank holidays) with the option to purchase additional days to support a healthy work-life balance, wellbeing support via Spill and our Employee Assistance Programme. Hybrid Working - We will only consider UK-based applicants for this position. We offer flexible and remote working options, home office set-up allowance, periodic in-person team days for company-wide collaboration and celebration. Family Friendly - Enhanced family leave policies, miscarriage and fertility leave, flexible working practices. Personal Development and Growth - Personal learning and development budgets, regular personal development conversations and career support. Community Engagement and Support - One paid day off per year to volunteer for a cause aligned with our mission of supporting patients living with rare diseases; the opportunity to hear from and engage with patient groups and communities who offer us valuable insights into the experiences of those affected by rare diseases. For more information about Healx and how we use your data please go to privacy/ #J-18808-Ljbffr

Quotient is seeking a Senior Engineer in our Data Infrastructure team to design and evolve our cloud, data and AI infrastructure underpinning our genomics-first drug discovery platform. Working within the Data Infrastructure team, you will lead complex initiatives spanning AWS platform engineering, scientific data systems and AI/ML workloads. You will collaborate closely with cloud engineers, data engineers, bioinformaticians, AI scientists, computational biologists, and experimental scientists to turn evolving scientific needs into secure, reliable and scalable engineering solutions. This is a senior individual-contributor role with substantial technical autonomy. You will make cross-system architecture and operational trade-offs, establish reusable engineering patterns, and mentor our Cloud Engineers and Data Engineers through design reviews, delivery and troubleshooting. The role does not require formal line management, but it does require clear technical leadership and accountability for platform outcomes. This hybrid role is based at the Chesterford Research Campus, near Cambridge, and reports to the Head of Data Infrastructure. The successful candidate will normally work from the campus at least three days per week, participate in operational support and incident escalation, and must have permission to work in the UK. • Lead the architecture and evolution of our AWS-based infrastructure across cloud services, scientific data platforms and AI/ML workloads, balancing delivery speed, reliability, security and cost., • Design and implement reusable infrastructure-as-code, CI/CD and environment-management patterns that make production systems easier to build, test, deploy and operate., • Own cross-cutting engineering decisions for observability, identity and access management, networking, resilience, capacity, data movement and lifecycle management., • Partner with Cloud Engineers and Data Engineers to deliver integrated solutions, providing practical mentoring through technical design, code review, incident response and operational improvement., • Work with AI scientists, computational biologists and scientific teams to translate model development, training, evaluation, inference and data requirements into secure, reproducible platform capabilities., • Diagnose and resolve complex failures spanning infrastructure, data pipelines, applications and AI workloads; lead incident reviews and ensure corrective actions improve the wider system., • Establish and reinforce engineering standards for testing, documentation, release management, operational readiness, security and cost visibility across the Data Infrastructure team., • Evaluate new technologies and shape the infrastructure roadmap with the Head of Data Infrastructure, making pragmatic build-versus-buy and sequencing decisions for an early-stage biotech., • Substantial experience designing, building and operating production cloud or data infrastructure, typically gained through seven or more years of relevant work or equivalent demonstrated capability., • Advanced hands‑on experience with AWS and ownership of multiple interdependent production systems, including the ability to troubleshoot failures across service boundaries., • Strong experience with infrastructure‑as‑code, CI/CD, containerised workloads, cloud networking, identity and access management, and production observability., • Strong software engineering skills in Python and Linux, including automated testing, version control, code review and maintainable automation or platform tooling., • Experience supporting data‑intensive life‑science systems or workflows, with enough domain understanding to reason about large scientific datasets, reproducibility, provenance and scientific user needs., • Experience enabling AI/ML workloads in cloud environments, such as data preparation, model training, evaluation, inference, orchestration or production deployment., • A track record of leading complex technical initiatives under ambiguity, making explicit trade‑offs and remaining accountable for reliable operational outcomes., • Demonstrated ability to mentor engineers and communicate architecture, risk and delivery choices clearly to both technical and scientific stakeholders., • Genomics, digital pathology, structural biology or other high‑volume scientific data modalities and formats., • AWS CDK, Batch, ECS, EKS, S3, RDS or Postgres, Athena, SageMaker, Bedrock, or equivalent services., • Scientific workflow and data orchestration frameworks such as Nextflow, Dagster, Airflow or similar., • Platform security, privacy or governance controls for sensitive biomedical or clinical data., • Identity platforms and federation technologies such as Entra ID, SSO or role‑based access patterns., • Working in an early‑stage biotech, research‑intensive startup or another fast‑changing environment with a small engineering team., • Encourage respectful disagreement and cultivate open‑minded, ego‑free interactions to continuously push each other towards excellence, • Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source, • Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions, • Use a company‑first mindset to guide decision‑making; prioritize team over individual success, • Take calculated risks and challenge convention in the quest for exceptional outcomes Quotient Therapeutics is a privately‑held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first‑in‑category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS). Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. #J-18808-Ljbffr

This is a hybrid role, with requirements to be on-site in Sittingbourne, Kent with occasional travel to Cambridge. The Zifo Lab Computing Analyst provides technical IT laboratory services, including multivendor instrument, information technology and validation/compliance services when applicable. The individual will provide the consulting skills required to analyze customer needs and gaps to propose solutions for the desired state. He or she will work with business users and managers of customers in conjunction with the internal Zifo support team. • Provides technical support of customer laboratory environments, typically for computers that are integrated with instrumentation, • Manages lab computing aspects of installing new, retirement and relocation of equipment, • Implements Windows based security, • Ensures adherence to client’s corporate policies through periodic reporting and compliance programs, • Acts as the technical support contact for field service engineers and external vendors, • Provides technical subject matter expertise for new system validation and change management efforts, • Document procedures, policies, troubleshooting and best practices, • Create and maintain a physical inventory of lab equipment, PC’s, software, and any other information pertinent to the environment if applicable, • Perform system preventative maintenances based on client’s schedule, if applicable, • Excellent customer service skills complemented by an ability to listen to and interpret client requests, • Ability to troubleshoot complex instrument and technology issues, • Strong oral and written communication skills, • Ability to identify, track and complete tasks for multiple projects, • Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code, • Independent, self-motivated & results driven individual, • Willingness & ability to acquire quickly new technical skills & business principles, • Ability for Critical Thinking and Logical Reasoning, • Experienced in ticketing systems, • Good understanding of pharmaceutical research and drug Discovery & development processes and biologics workflows (preferred, not required), • Preferred to hold a Bachelor of Science in computer science, life science or equivalent industry experience, • 2+ years of relevant technical experience including (but not limited to); Windows technologies, networking, remote computing and backup systems, • Experience with virtual machine support (preferred)Experience with scientific instrumentation (preferred), • Experience with Ignition automation software a plus but not mandatory, training will be provided Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies. A passion to learn and a spirit of teamwork characterizes us. We revere excellence and the value everyone brings. At Zifo, our culture is one where we debate, challenge ourselves and interact with all alike. We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability. #J-18808-Ljbffr

Nuclera is a venture-backed, founder-driven biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Our purpose is to improve human health by making proteins accessible to life science researchers around the world. In 2024, we launched eProtein Discovery - a breakthrough protein expression, characterization, and purification platform, consisting of cloud-based software and a lab-based instrument (with proprietary cartridges and consumables). Since then, we have established a growing installed base in North America, Europe and Asia, receiving numerous awards and customer accolades. We are looking for an experienced full-stack software engineer to work on our customer-facing cloud and instrument software as well as the internal tools that support our in-house protein screening services. You’ll be involved in the full software development lifecycle, including working closely with biologists and other stakeholders to define use-cases and requirements, translating those requirements into technical designs, implementing those designs in code and writing tests to verify its correctness. No prior knowledge of biology is necessary, but curiosity and an eagerness to learn is critical. This role is for you if you: • Have at least 5 years industry experience as a software engineer., • Are confident working across backend, frontend, dev-ops and QA., • Have a product mindset, with a track record of gathering requirements, owning features end to end, and working directly with key stakeholders to deliver the right outcome., • Are ready to take ownership of code and keep it up-to-date with the latest best-practices., • Java and Python, • REST and Websocket APIs, • A backend web framework (e.g. Micronaut, Spring), • Google Cloud or an equivalent cloud service provider (e.g. AWS, Azure), • HTML, CSS and TypeScript or JavaScript, • React or an equivalent frontend technology (e.g. Angular), • Containerisation (e.g. Docker, Podman), • Automated testing (e.g. JUnit, Mockito, pytest), • Automated build and deployment pipelines, • Version control in Git, • Java Reactive Streams, • Asynchronous Python, • PostgreSQL, • Kubernetes, Helm, Flux, Terraform, • Figma, Balsamiq, • GitLab CI, • Claude Code or an equivalent AI coding assistant, • Experience with bioinformatics data processing pipelines In addition to competitive salaries, we offer a range of benefits including: • Company bonus scheme of 5%, • Share option incentive scheme, • 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, • Fresh fruit, tea, coffee, and snacks in the office, • Organised summer events for staff #J-18808-Ljbffr

STEMCELL Technologies, Canada’s largest biotech company is looking for a Senior Quality Engineer to join our team out of our Cambridge, Waterbeach site! As the Senior Quality Engineer, you will support the development and manufacture of innovative instrumentation and single-use consumables for GMP cell and gene therapy manufacturing, as well as research use only (RUO) applications. Working closely with Engineering, Manufacturing, and the broader Quality team, you will provide quality expertise throughout the product lifecycle, ensuring products meet applicable regulatory and quality requirements. • Lead Design Control and risk management activities, including Hazard Analysis and Design and Process FMEA, to identify and control risks and ensure compliance with ISO 13485, 21 CFR Part 820, cGMP, ISO 14971, IEC 60601-1, IEC 61010-1, RoHS and WEEE and other applicable requirements, • Evaluate and approve technical documentation, Design input documents, verification and validation reports, vendor qualification and design transfer activities and overall independent quality support for the project, • Develop and implement risk-based inspection plans and in-process and final inspection procedures, including appropriate sampling strategies for instrumentation components, • Performs quality inspection/processing of incoming raw materials and final inspection testing, • Builds and maintains quality metrics and supports all QMS activities such as document management, non conformance investigations (NCRs/SCARs), CCRs, CAPAs, internal and external audits and factory inspections, • Bachelor’s degree in Mechanical, Electrical, Software, or Biomedical Engineering with 6–10 years of relevant experience, or a Master’s degree with 4+ years of experience; an advanced degree is preferred, • Experience in an instrumentation or manufacturing environment is preferred, • Strong systems knowledge, including experience with Enterprise Resource Planning, Product Life Cycle Management, and Requirements Management Systems, is considered an asset, • Strong knowledge across mechanical, electrical, and software engineering disciplines, with extensive understanding of applicable regulatory and quality standards, • Demonstrated ability to review complex designs, develop risk management documentation, and establish processes that support manufacturing in alignment with design specifications STEMCELL Technologies is a privately owned, Vancouver-based biotechnology company that helps power leading-edge life science research around the world. Driven by our love of science and passion for quality, we are a company of Scientists Helping Scientists—standing by our customers to provide the outstanding products, technical support, and training they need to advance their research. Scientists performing stem cell, immunology, cancer, regenerative medicine, and cellular therapy research are among those who rely on our cell culture media, cell separation products, instruments, accessory products, and services. Through our many regional offices, as well as our distribution centers in Vancouver, Seattle, Grenoble, and Singapore, we deliver our innovative, specialized products to more than 100 countries. With over 1,800 employees globally, most with scientific or engineering degrees, STEMCELL is proud to be the largest biotechnology employer in Canada. This is an opportunity to work with highly motivated colleagues in a science-oriented, creative, and dynamic environment. We offer a competitive salary, excellent benefits, and meaningful career development opportunities. STEMCELL is well recognized for exceptional leadership and business practices. We are one of Canada’s Best Managed Companies and operate an ISO 14001-certified environmental management system to measure and reduce our environmental impact. As an equal opportunity employer, STEMCELL is dedicated to ensuring that every employee feels safe, valued, and respected for who they are. We know that scientific progress and innovation occur when diverse, creative minds come together and we are committed to nurturing a culture of inclusivity and belonging. STEMCELL enforces a zero-tolerance policy for any form of discrimination. Selection decisions are solely based on job-related factors. The annual salary for this job ranges from: £46,100.00 - £69,100.00 STEMCELL determines an individual’s pay within the range based on multiple factors including experience, education, job-related skills, and equity within the team or organization. For jobs that are eligible for sales incentives, the range noted above is inclusive of target incentives; actual incentives are based on individual performance results in accordance with company policy. In addition to base salary, STEMCELL offers a comprehensive total rewards package that may include health benefits, retirement savings, and more (depending on region). #J-18808-Ljbffr

Nuclera is a venture-backed, founder-driven biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Our purpose is to improve human health by making proteins accessible to life science researchers around the world. In 2024, we launched eProtein Discovery™ - a breakthrough protein expression, characterization, and purification platform, consisting of cloud-based software and a lab-based instrument (with proprietary cartridges and consumables). Since then, we have established a growing installed base in North America, Europe and Asia, receiving numerous awards and customer accolades. We are looking for an experienced full-stack software engineer to work on our customer-facing cloud and instrument software as well as the internal tools that support our in-house protein screening services. You’ll be involved in the full software development lifecycle, including working closely with biologists and other stakeholders to define use-cases and requirements, translating those requirements into technical designs, implementing those designs in code and writing tests to verify its correctness. No prior knowledge of biology is necessary, but curiosity and an eagerness to learn is critical. This role is for you if you: • Have at least 5 years industry experience as a software engineer., • Are confident working across backend, frontend, dev-ops and QA., • Have a product mindset, with a track record of gathering requirements, owning features end to end, and working directly with key stakeholders to deliver the right outcome., • Are ready to take ownership of code and keep it up-to-date with the latest best-practices., • Java and Python, • REST and Websocket APIs, • A backend web framework (e.g. Micronaut, Spring), • Google Cloud or an equivalent cloud service provider (e.g. AWS, Azure), • HTML, CSS and TypeScript or JavaScript, • React or an equivalent frontend technology (e.g. Angular), • Containerisation (e.g. Docker, Podman), • Automated testing (e.g. JUnit, Mockito, pytest), • Automated build and deployment pipelines, • Version control in Git, • Java Reactive Streams, • Asynchronous Python, • PostgreSQL, • Kubernetes, Helm, Flux, Terraform, • Figma, Balsamiq, • GitLab CI, • Claude Code or an equivalent AI coding assistant, • Experience with bioinformatics data processing pipelines In addition to competitive salaries, we offer a range of benefits including: • Company bonus scheme of 5%, • Share option incentive scheme, • 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, • Fresh fruit, tea, coffee, and snacks in the office, • Organised summer events for staff #J-18808-Ljbffr

Are you already an experienced bioanalyst looking for your next role? Do you have refined skills in LC-MS maintenance and troubleshooting? Are you proficient in bespoke method development within small molecules? If you answered yes to any, or all of those questions then good news, our Cambridge site have a vacancy for a Senior Technical Specilaist - DMPK! A highly experienced lab and office based bioanalyst providing wide in-depth scientific and technical expertise to both multidisciplinary integrated Drug Discovery projects and standalone DMPK projects. This role combines hands-on bioanalytical expertise with project leadership, mentoring, and continuous improvement responsibilities to support small and large molecule drug discovery programmes. Offering you opportunities across varied DMPK and broader scientific projects and development across multiple scientiic and technical areas. • Developing, optimising and executing the bioanalysis of samples from in vivo DMPK studies for small and large molecule drug discovery projects in an early discovery setting., • Extensive knowledge of modern UPLC-MS systems and software including chromatographic method development., • Demonstrated ability to perform routine and complex troubleshooting, maintenance, and optimisation of mass spectrometry and LC equipment, ensuring reliable operation and rapid resolution of technical issues., • Experience in the analysis of different sample types such as plasma, blood, brain, lung, bile, faeces, urine., • Demonstrated experience of pharmacokinetic parameter determination and an understanding of the underlying principles., • Comprehensive troubleshooting and problem-solving skills using both technical and scientific expertise., • Strong organisation and time management skills alongside an inbuilt flexibility to adapt to change., • Excellent communication skills and be an effective team player; these will be essential to successful execution of projects whilst working in a matrix and multi-skilled environment., • Lead scientific and technical projects, ensuring delivery of high-quality data to agreed timelines., • Drive innovation through the development of novel assays, protocols and analytical approaches., • Mentor, coach and develop colleagues, acting as a technical role model and recognised subject matter expert., • BSc or equivalent in relevant scientific area., • Industry experience in pharma, biotech or other commercial organisations., • Expert user of Mass Spectrometry instrumentation., • Experience in the bioanalytical method development of challenging analytes, in complex matrices., • Accurate & diligent experimental planning, execution and troubleshooting., • Good communication skills (verbal/written) internally and externally., • Excellent team player., • Positive ‘can do’ attitude., • Creative problem solving., • Ability to plan & execute work independently., • Project management., • Strong organisation and time management skills alongside an inbuilt flexibility to adapt to change., • Experience of guiding/mentoring junior colleagues., • LC-MS/MS maintenance and troubleshooting., • Bespoke method development for small molecules., • We offer a comprehensive benefits package from day one including generous pension, bonus and health cover. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. #J-18808-Ljbffr

As a Senior Product Designer II / Staff Product Designer on the Software Product team, you will shape core Lila App experiences that help scientists, ResOps, and LAS users plan, execute, and learn from scientific workflows. You will translate complex scientific workflows and AI-native product capabilities into intuitive, trustworthy, and scalable software experiences. You will partner closely with product, engineering, scientists, and operations teams to design workflows that support product externalization and high-quality user experiences across the Lila App. Your work will influence how users interact with Lila's scientific superintelligence platform and autonomous lab systems. • Design end-to-end Lila App workflows for scientists, ResOps, and LAS users., • Translate scientific and operational complexity into clear, intuitive product experiences., • Partner with product, engineering, science, and operations to define user problems and tradeoffs., • Prototype AI-native interactions that help users understand and act on system recommendations., • Conduct lightweight research, workflow mapping, and usability testing with internal users., • Contribute scalable design patterns that improve consistency across the Lila App., • Use AI-enabled design tools to accelerate exploration, iteration, and communication., • 5+ years of product design, UX design, or interaction design experience., • Strong portfolio showing end-to-end product design and shipped product impact., • Experience designing complex, data-rich, technical, or operational software products., • Ability to simplify ambiguous technical workflows into clear product experiences., • Strong interaction design, information architecture, and systems thinking skills., • Experience partnering with product managers, engineers, and domain experts., • Comfort using modern AI tools for design exploration, prototyping, and synthesis., • Experience designing for scientists, lab operations, biotech, or AI-enabled technical users., • Experience designing AI-native workflows, trust calibration, explainability, or review flows., • Familiarity with data visualization, workflow orchestration, LIMS, or scientific data management., • Experience contributing to or scaling a design system., • Comfort working in ambiguous, early-stage product areas. We offer competitive base compensation with bonus potential and generous early-stage equity. Your final offer will reflect your background, expertise, and expected impact. Full-time U.S. employees receive a comprehensive benefits program including medical, dental, and vision coverage; employer-paid life and disability insurance; flexible time off with generous company wide holidays; paid parental leave; an educational assistance program; commuter benefits, including bike share memberships for office based employees; and a company subsidized lunch program. Full-time employees outside the U.S. receive a comprehensive benefits program tailored to their region. USD salary ranges apply only to U.S.-based positions; international salaries are set to local market. $180,000 - $256,000 USD Lila Sciences is building Scientific Superintelligence™ to solve humankind's greatest challenges. We believe science is the most inspiring frontier for AI. Rather than hard-coding expert knowledge into tools, LILA builds systems that can learn for themselves. LILA combines advanced AI models with proprietary AI Science Factory™ instruments into an operating system for science that executes the entire scientific method autonomously, accelerating discovery at unprecedented speed, scale, and impact across medicine, materials, and energy. Learn more at www.lila.ai. Guided by our core values of truth, trust, curiosity, grit, and velocity, we move with startup speed while tackling problems of historic importance. If this sounds like an environment you'd love to work in, even if you don't meet every qualification listed above, we encourage you to apply. Lila Sciences is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Information you provide during your application process will be handled in accordance with our Candidate Privacy Policy. Lila Sciences does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Lila Sciences or its employees is strictly prohibited unless contacted directly by Lila Science's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Lila Sciences, and Lila Sciences will not owe any referral or other fees #J-18808-Ljbffr

A pioneering biotechnology company in Cambridge seeks either a qualified lawyer or an experienced contracts manager to oversee commercial legal contracting and broader legal issues. This role involves negotiating and maintaining various contracts while collaborating with R&D and clinical operations teams. Ideal candidates possess relevant biotech or life sciences experience. The position offers a hybrid working model with full or part-time options. #J-18808-Ljbffr

Ethos is looking for experienced medical affairs professionals and MSLs from pharma/biotech to train our language model on professional presentations and slide deck tasks. This fully remote role offers flexible hours and a chance to work with cutting-edge AI in a scientific context. Contract is 5–20 hours per week at USD 100 per hour, with ASAP start. Requirements include PharmD/MD/PhD with 4+ years in medical affairs, proven ability to produce compliant presentations, and expert PowerPoint #J-18808-Ljbffr

We have an opportunity for a Senior Engineer in our AI & Algorithms team, working with a particular focus on our defence and security clients. You'll join a team of talented engineers and scientists designing, building and testing intelligent systems that solve hard, real-world problems, such as signal processing (sensor data, radar), vision, and information processing (transformers, edge AI). We have an opportunity for a Senior Engineer in our AI & Algorithms team, working with a particular focus on our defence and security clients. You'll join a team of talented engineers and scientists designing, building and testing intelligent systems that solve hard, real-world problems, such as signal processing (sensor data, radar), vision, and information processing (transformers, edge AI). As an AI Engineer, you'll take the technical lead on parts of our projects, mentor more junior colleagues, and play an active part in shaping and winning new work. With well-equipped labs and substantial computing resources behind you, you'll turn state-of-the-art research into systems our clients can depend on. Much of our defence and security work requires security clearance, so we ask for it up front. You won't work exclusively in that sector, but a genuine interest in it matters to us. Some examples of the projects we do can be found here. We offer a flexible approach to hybrid working, although some of the projects you will be working on will require full-time working in the office. • Applying data-driven software development in machine learning/AI, applied statistics, and sensor processing, alongside mathematical computing techniques such as digital signal processing, simulation, and numerical optimisation., • Taking technical ownership of significant parts of client projects, delivering quality work to budget and schedule with little supervision., • Acting as technical authority or technical lead on smaller projects and contributing to the technical direction of larger ones., • Mentoring and supporting less experienced engineers and helping them develop as technical consultants., • Working directly with clients to understand their problems, show what's possible, and build their confidence in our work., • Contributing to proposals and helping scope new work, translating client needs into credible technical approaches., • Building demonstrators and internal capability that showcase our expertise in defence, security and adjacent markets., • 3+ years' experience delivering applied AI and machine learning solutions, and the judgement that comes with it., • Strong Python programming skills and a solid grasp of modern software development practice., • A strong undergraduate degree in a relevant technical subject, such as AI/machine learning, computer science, mathematics, physics or theoretical physics., • A track record of delivering quality technical work in a team., • The ability to lead and mentor others., • An interest in working with clients and getting involved in proposals and sales conversations., • A genuine affinity for working in the defence and security sector. While not essential requirements, we would also be very interested if you have experience with any of the following: • Previous experience working on defence or security projects., • Technical experience with any of: signal processing, edge computing, statistical modelling, numerical optimisation, or simulation., • A PhD or published research in a data-driven field., • Experience leading or mentoring a small technical team. Because of where this role sits, holding (or being able to obtain) UK security clearance is essential. You must be eligible to obtain Security Check (SC) level security clearance (guidance/united-kingdom-security-vetting-applicant). You must be able to work in the UK without restrictions in accordance with UK National Law and be prepared to successfully undertake an appropriate level of UK National Security Vetting according to UK Government criteria. Cambridge Consultants creates exciting and novel breakthroughs in technology and products. Our work on intelligent systems area has helped create world-first and market-changing technologies including real-time AI-enhanced medical imaging, autonomous defence systems against cyberattacks, and edge algorithms to help visually impaired people navigate indoor spaces. We combine our research output with engineering rigour to create innovative and robust solutions to solve complex problems presented to us by our clients. We help clients across a diverse range of markets, including defence/security, healthcare, biotech, industrial and energy, so there is no shortage of variety. At the heart of what we do are talented and motivated multi-disciplinary teams empowered to create cutting edge technologies and systems to solve difficult problems for our clients. We offer a diverse, fun, and challenging work environment where you'll have the chance to work on a wide variety of projects that deliver real value using technology. We recognise and celebrate individual talent and we understand the importance of letting individuals be just that. Our people are here to do the best work of their lives and our job is to provide the platform for them to do it. #J-18808-Ljbffr

The Bradfield Centre, 184 Cambridge Science Park, Milton Road, Cambridge CB4 OGA, UK As a Biotechnology Intern, you will support the development of biotechnological products and work on business development projects related to our technologies, including gene libraries and microarrays. • Assisting in the development and testing of Oligo Pools, microarray chips, and gene libraries., • Supporting business development by identifying new opportunities in the biotech market., • Assisting with client interactions and helping communicate product capabilities., • Preparing technical reports and business proposals., • Conducting research on market trends and competitor products., • Strong understanding of biotech techniques and technologies., • Interest in business development within the biotech industry., • Good analytical skills and proficiency with data analysis tools., • Ability to work collaboratively and communicate effectively. #J-18808-Ljbffr

The Chemical Biology Resources Team at the European Bioinformatics Institute (EMBL-EBI) is looking for a talented Scientist with a flair for data curation to be responsible for the quality of bioactivity and drug discovery data in the ChEMBL database. The Chemical Biology Resources Team at the European Bioinformatics Institute (EMBL-EBI) is looking for a talented Scientist with a flair for data curation to be responsible for the quality of bioactivity and drug discovery data in the ChEMBL database. ChEMBL is a world-leading chemogenomics resource, providing open bioactivity data and associated tools to the scientific community. ChEMBL is widely used through both academia and industry to support drug discovery. You will work in a team-oriented environment, collaborating closely with fellow scientists and technical experts, chemo- and bio-informaticians and software engineers across EMBL-EBI and with our many external partners from the UK and internationally. In this role you will be responsible for the curation of biological data in the ChEMBL database. Reporting to the ChEMBL Team Coordinator, you will: • work together with the other members of the ChEMBL data team to curate bioactivity data in the ChEMBL database ensuring the delivery of high quality data, • map measured bioactivity data from the scientific literature to other biological entities (proteins, cell-lines etc) using a variety of bioinformatics resources and ontologies, • work collaboratively with other EMBL-EBI teams to integrate ChEMBL data into their resources and vice versa, • proactively identify new data types and additional annotations that address the needs of the community, • identify and validate the potential therapeutic targets of drug molecules and compounds in clinical development from a variety of sources, • work with data depositors to help them format and curate their data to the standards required for deposition into ChEMBL, • manually check and annotate data by reference to the original data sources such as the scientific literature, Pharma Company pipelines and prescribing information, • develop semi-automated processes for identifying and correcting erroneous data, • be actively involved in training and external user support, • work with other team members to publish project outcomes in scientific articles in the peer-reviewed literature, • You will have excellent attention to details, strong communication skills and be able to interact with technical experts as well as scientists seeking solutions to their "real world" problems., • A PhD (or equivalent) in a biological or biomedical science, • Excellent knowledge of pharmacology, potential biological targets and mechanisms of drug action, • Good knowledge of the various experimental techniques used to determine the activity of compounds in different in vitro and in vivo assay systems, • Ability to work accurately and quickly to deadlines, • Able to work both as part of a team and independently, • Good communication skills (both verbal and presentational), • Prior experience of biological data curation and knowledge of bioinformatics databases, • Some knowledge of biological ontologies, • Experience of working in a drug discovery environment, • Experience of working with and manipulating file formats such as FASTA, Excel, XML, OBO and familiarity with regular expressions and text matching, • Experience of querying relational databases using SQL would also be advantageous, • Open mindset – welcoming diverse ideas and perspectives., • Professional outlook - ensuring meticulous attention to quality and detail., • Teamwork – working together for shared success., • Respect – treating all colleagues with professionalism and kindness, • Inclusivity – allowing everyone space to shine in their own way. Contract length: 3 years, renewable to a maximum of 9 years Salary: Grade 5, salary from £3,452.02 after tax, plus generous financial benefits and allowances based on family circumstances. Excluding personal pension and insurance contributions. Do something meaningful At EMBL-EBI you can apply your talent and passion to accelerate science and tackle some of humankind's greatest challenges. EMBL-EBI, part of the European Molecular Biology Laboratory, is a worldwide leader in the storage, analysis and dissemination of large biological datasets. We provide the global research community with access to publicly available databases and tools which are crucial for the advancement of healthcare, food security, and biodiversity. We are located on the Wellcome Genome Campus, alongside other prominent research and biotech organisations, and surrounded by beautiful Cambridgeshire countryside. This is a highly collaborative and inclusive community where our employees enjoy a relaxed atmosphere. We are committed to ensuring our employees feel valued, supported and empowered to reach their professional potential. Watch this video to see how EMBL-EBI makes an impact. • Financial incentives: Monthly family, child and non-resident allowances, annual salary review, pension scheme, death benefit, long-term care, accident-at-work and unemployment insurances, • Flexible working arrangements - including hybrid working patterns, • Private medical insurance for you and your immediate family (including all prescriptions and generous dental & optical cover), • Generous time off: 30 days annual leave per year, in addition public holidays, • Relocation package including installation grant (if required), • Campus life: Free shuttle bus to and from work, on-site library, subsidised on-site gym and cafeteria, casual dress code, extensive sports and social club activities (on campus and remotely), • Family benefits: On-site nursery, 10 days of child sick leave, generous parental leave, holiday clubs on campus and monthly family and child allowances, • Benefits for non-UK residents: Visa exemption, education grant for private schooling, financial support to travel back to your home country every second year and a monthly non-resident allowance. For detailed information please visit our employee benefits page here. • International applicants: We recruit internationally and successful candidates are offered visa exemptions. Please take a look at our International Applicants page for further information., • EMBL is a signatory of DORA. Find out how we apply DORA principles to our recruitment and performance assessment processes here., • Diversity and inclusion: At EMBL, we believe that diverse teams drive innovation and scientific excellence. We encourage applications from candidates of all genders, identities, nationalities and/or any other diverse backgrounds. 05/10/2026 #J-18808-Ljbffr

Do you bring deep experience in IVD or companion diagnostic product development and a track record of leading complex programs through regulatory approval or pivotal clinical trials? Can you align cross‑functional teams and biopharma partners around the scientific, regulatory, operational, and commercial milestones needed to deliver diagnostic solutions? If this sounds like you and you are driven by purpose, join the SOPHiA GENETICS Diagnostics Solutions team as a Program Leader and enable us to make a positive impact on the outcomes for cancer and rare disease patients worldwide. This role is attached to our Corporate HQ in Switzerland. For any individuals not based in Switzerland, this would require international relocation but this can be support for suitably qualified individuals. This role cannot be done remotely from outside of Switzerland. We believe there is a smarter, more data‑driven way to make decisions in healthcare and our cloud‑native AI powered SOPHiA DDM Platform makes that vision a reality on a daily basis. You will have direct input to our mission to democratise data‑driven medicine for the ultimate benefit of cancer and rare disease patients across the globe. As Program Leader, you will be accountable for the end‑to‑end strategic and operational leadership of one or more in‑vitro diagnostic development programs, including Clinical Trial Assays, tumour profiling tests, Companion Diagnostics, and software as a medical device. You will ensure programs are co‑developed, validated, and submitted on time and in alignment with each biopharma partner’s drug development timeline. This role requires deep knowledge of IVD and CDx development, strong biopharma customer management skills, and the ability to orchestrate cross‑functional teams across development, verification and validation, clinical, regulatory, and commercial workstreams. • Define and own the design and development strategy for IVD, CTA, tumour profiling, CDx, and/or SaMD programs, aligning analytical and clinical validation and regulatory timelines with biopharma drug development milestones, including IND, Phase I/II/III, BLA, NDA, and MAA., • Build trusted biopharma partnerships as the primary project contact, maintaining transparency on status, risks, decisions, co‑development agreements, technical feasibility scopes, and joint development plans in collaboration with Biopharma Business and Legal., • Lead internal and joint governance—including portfolio reviews, business stage gates, design reviews, Joint Steering Committees, and Joint Development Teams—to drive aligned, timely decision‑making., • Integrate Bioinformatics and Assay Development, Verification and Validation, Clinical Operations, Regulatory Affairs, Quality Assurance, Manufacturing, Product Management, and Biopharma teams around a coherent program strategy, milestones, resources, and shared accountability., • Deliver diagnostic programs from requirements definition through product development, verification and validation, regulatory submission, and commercial launch while managing timelines, budgets, risks, resources, and contingency plans. We know that every background is different, but to be best set for success we see you bringing: • 8+ years of experience in diagnostic product development or program/project ownership across IVD, CDx, or clinical laboratory assays, including at least 3 years in cross‑functional project or program leadership., • A demonstrated track record of delivering an IVD or CDx program through FDA approval or CE marking, or a CTA through a pivotal clinical trial., • Deep knowledge of IVD and CDx development, including assay and bioinformatics development, analytical and clinical validation, design controls, regulatory interactions, and global regulatory strategy., • Experience managing budgets, resource planning, technical and regulatory risks, and complex external biopharma partnerships in a matrixed, multi‑partner environment., • The ability to move between high‑level business strategy and tactical daily program operations, supported by strong technical communication, influencing, negotiation, and conflict‑resolution skills., • A solid understanding of drug‑diagnostic co‑development and the regulatory interdependencies between CDx and drug approval; familiarity with EU IVDR and FDA requirements is preferred., • Oncology therapeutic area experience and a hands‑on technical background in one or more diagnostic platforms are preferred., • A B.S. degree or equivalent is required; a PhD, MSc, or equivalent degree in molecular biology, biochemistry, analytical chemistry, genomics, pathology, or a related life sciences discipline is preferred. You will be joining an organization with the patient at the heart of every decision and action, driven by purpose as we pursue exponential growth. Business recognition and accolades include: • World's most innovative companies (Top 10), • World's smartest companies (Top 50), • 100 Best Places to Work in Boston, • Top 10 European Tech Startup, • Top 10 European biotechs startup to watch, • Top 25 East‑Coast Biotech to watch Our benefits package is comprehensive, but varies internationally in‑line with local standards and laws. You can discuss a full breakdown with us, but as a brief overview: • Sickness and Accident coverage through Helsana, • Meal Vouchers at 90CHF PM with our partner cafeteria, • A fun and engaging work environment, with Rest & Entertainment space, full stocked free coffee machine and free fruit/snacks, • Free parking in an easy to access location, • A strong social committee whose purpose is to make SOPHiA GENETICs both enjoyable as well as rewarding, • As our global HQ, you’ll have direct interaction and exposure to senior leadership and our executive team locally Like the strands of DNA itself, SOPHiA GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient & Nimble and Fearlessly Adventurous At SOPHiA GENETICS we established our 7 Virtues to clarify how our principles show up each day through action. We Decide; We Do; We Collaborate; We Innovate; We Empower; We Adapt and We Learn. At the centre of our Virtues is our Mantra, We Care, which provides a constant reminder of the compassionate, benevolent, and hopeful nature of our mission and how it should be threaded through each of our Virtues and everything we do. Learn more about our DNA and Virtues on our Careers portal We use the power of AI to help our partners make decisions. If you’re utilising AI in your search and application process, why not use some of these prompts, or read our AI guide. ‘What impact can I expect to have on the world by working at SOPHiA GENETICS?’ ‘I have an interview with SOPHiA GENETICS. What should I know before I meet with them?’ ‘I am a job title - What can SOPHiA GENETICS offer my career?’ Starting Date: As suitable Location: Rolle, CH (Hybrid) - International Relocation welcome Contract: Permanent #J-18808-Ljbffr

Abiologics, Inc. is seeking a motivated co-op to join the Pharmacology team for a 6-month term in Watertown, MA. You will perform biochemical and cell-based assays under mentorship and lead an independent project to advance Abiologics’ platform. You will collaborate cross-functionally with a design-make-test team and gain hands-on exposure to discovery science in a Flagship Pioneering environment. This role offers real ownership and mentorship within a fast-paced biotech setting. #J-18808-Ljbffr

At Cambridge Consultants, we believe the future of technology isn't just smart, it has agency. We're moving past passive tools and building human-centred digital services and products: systems that reason, plan, and act around the people who use them. Our work spans autonomous systems at the frontier of biology, sensing, and AI. We hire self-motivated builders, not ticket-takers. If you thrive in highly agile environments, can cut through ambiguity with first-principles thinking, and want to ship things that matter, this is the kind of place where you'll feel at home. You’ll be working on systems that haven't existed before. Think of an Agentic Coach that navigates the unpredictability of human biology, or the software architecture behind a fully automated Dark Lab. These aren't chatbots waiting for questions. They're proactive systems that maintain world models, interpret human intent, and intervene before the user knows to ask. These systems create genuine impact for clients tackling problems no one else can solve. Building them means designing and wiring agent harnesses: layered architectures that span from sensor‑edge reasoning to high‑level planning, backed by stateful multi‑turn reasoning, persistent per‑user memory, and robust evaluation pipelines. You’ll work in two directions at once. Internally, you’ll use the latest AI tools to sharpen how we build, prototype, and ship. Externally, you’ll deliver the breakthrough systems our clients deploy, designed to move from prototype to production at pace. There’s no single technology stack. You’ll work with agents, multi‑agent systems, and the latest generative AI tools, but your work will always be grounded in solid software engineering. Expect to build scalable distributed systems in core languages like Python and TypeScript, leveraging frameworks such as NextJS and Pydantic, agent orchestration tools (LangGraph, CrewAI), and protocols like MCP. You’ll deploy on cloud platforms (AWS, GCP, Azure) using Docker, Kubernetes, and infrastructure‑as‑code, backed by rigorous CI/CD and observability (OpenTelemetry, Prometheus). Due to the clients we work with, you must be eligible for UK security clearance. • AI System Architecture: Designing and implementing the logic for autonomous systems, including maintaining world models, integrating multimodal sensing, and building real‑time human‑machine interaction loops., • Infrastructure & Production Engineering: Designing the underlying software for scalable, secure, and observable cloud deployments. You will apply the engineering rigor required to take experimental AI from concept to robust live launch., • Rapid Client Prototyping: Driving a demo‑first delivery model. You will focus on fast experimentation to actively show tangible value and working software to clients, rather than describing it in slide decks., • Domain Translation & Integration: Partnering directly with deep‑tech subject matter experts (like biologists and roboticists) to apply software solutions to complex physical constraints., • Applied AI Expertise: You have hands‑on experience utilising multi‑agent frameworks, long‑term memory systems, RAG pipelines, vector/graph databases, and reasoning‑loop patterns (such as ReAct and Chain‑of‑Thought)., • Core Software Fluency: You possess strong programming skills in Python and TypeScript, coupled with practical experience in cloud engineering, containerisation, and modern DevOps. You know that great agents still require rock‑solid software foundations., • High Tolerance for Ambiguity: You are energised by uncertainty and shifting targets. You treat shifting requirements as normal, and you know exactly when to ship a rough prototype to learn quickly versus when to slow down for architectural rigour., • Cross‑Disciplinary Communication: You can seamlessly navigate the gap between code and reality, collaborating with clients, roboticists, and scientists to clearly deliver the "art of the possible.", • Variety of work: Projects spanning biotech, finance, robotics, and beyond. No two engagements look alike., • Continuous learning: A mentoring and learning package shaped by your goals, backed by squad‑based knowledge sharing across the company., • Engineering autonomy: A free hand in choosing the right tools and processes. We trust your engineering judgement., • Access to world‑class experts: You'll share a building with biologists, roboticists, electronics engineers, and mathematicians. Few places let you tap that range of expertise on a single project., • Hybrid working environment: We're flexible about where you work on a day‑to‑day basis. We also love the energy of collaborating in person, so we'd love you to be in Cambridge for key meetings. By submitting an application to Cambridge Consultants, you confirm that the information provided in this application, together with any supporting documentation, is true, complete, and accurate to the best of your knowledge and belief. You understand that any false statement, misleading information, or material omission may render you liable to disqualification from the recruitment process, withdrawal of any offer of employment, or dismissal without notice if discovered following appointment. You acknowledge that the organisation reserves the right to verify the information supplied. #J-18808-Ljbffr

3 weeks ago Be among the first 25 applicants We're looking for a skilled Frontend Developer with expertise in TypeScript and React to build and enhance the cutting-edge design and analysis tools behind our revolutionary eProtein Discovery platform. Join us in shaping the future of protein prototyping technology! Nuclera is a venture-backed, founder-driven biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. The company's mission is to improve human health by making proteins accessible. We are beginning this mission through the launch of our eProtein Discovery platform. eProtein Discovery is a breakthrough protein expression, characterization, and purification technology, consisting of a lab-based benchtop instrument, cloud-based software and proprietary cartridges and consumables. The goal is to enable rapid protein access to life science researchers around the world. We are looking for an experienced frontend or full-stack software engineer to join our team of engineers working on both the cloud-based and on-instrument software used by our customers to design and execute experiments on the eProtein Discovery platform. You'll be involved in the full software development lifecycle, including gathering requirements from biologists and other stakeholders, translating those requirements into UI designs and working with backend engineers to implement those designs in code. No prior knowledge of biology is necessary, but curiosity and an eagerness to learn is critical. The culture in the software team supports in-office and hybrid working. About the role: • Have at least 3 years industry experience as a software engineer., • Be ready to take ownership of code and keep it up-to-date with the latest best-practices, • Have a passion for translating complex requirements into simple, easy-to-understand user interfaces, • Have a strong interest in backend development, • Be curious about protein synthesis Requirements Essential You should have experience with the following languages, tools and methodologies: • React with state management libraries such as Redux, • Typescript or Flow typing and modern ES6 javascript, • HTML and CSS, • Webpack, • Version control with Git, • Unit testing with Jest, React testing library or similar framework, • Java and Python, • Knowledge of CI/CD pipelines, • Agile software development and code reviews Desirable It would be beneficial for you to have some experience with: • Data visualisation libraries e.g. D3, websockets and storybook, • Design tools such as Figma and Balsamiq, • Cloud technologies such as Kubernetes and Google Cloud Platform 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, • Mid-Senior level, • Full-time, • Engineering and Information Technology, • IT Services and IT Consulting Referrals increase your chances of interviewing at Nuclera by 2x Get notified about new Software Engineer jobs in Cambridge, England, United Kingdom. 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Nuclera is a Cambridge-based biotech company building eProtein Discovery software and instruments. You will join a cross-functional team to develop cloud and instrument software, collaborating with biologists and stakeholders to translate use-cases into robust features. The role covers backend and frontend work, dev-ops and QA, with a product mindset and ownership of features from design to delivery. Curiosity and learning are encouraged. #J-18808-Ljbffr

Quotient is seeking a highly strategic, intellectually agile, and clinically minded leader to serve as Vice President of Translational Medicine. This is a senior clinical leadership role responsible for integrating clinical insights across scientific, drug discovery and corporate teams to support prioritization of disease areas, drug targets, medicine profiles, and leading early translational planning into clinical development strategies with a high probability of clinical and regulatory success. The role will provide both strategic and scientific leadership opportunities and the opportunity to work across a broad span of functional areas including human genetics, human target validation, translational biology, biomarker discovery, clinical pharmacology, and clinical development and commercial strategy. This individual will have a strong influence on the shape and direction of Quotient’s drug discovery pipeline strategy, applying deep clinical insight to evaluate and prioritize somatic genomics-discovered drug targets, assets, and development plans across a wide range of disease areas. This role would suit an MD or MD/PhD with a background in early clinical development within a pharma, biotech, or translational research setting who is comfortable working in a scientifically rich environment to help shape drug development programs from the earliest stages of discovery. As Quotient’s drug discovery pipeline expands, this individual will be expected to assume clinical leadership of Quotient’s Phase 1/2 clinical trials; working with CROs and a growing internal clinical development team. • Provide expert clinical insight into disease area strategy assessments, target selection, and translational biology planning across a range of discovery projects., • Apply structured clinical reasoning across a broad range of therapeutic areas — evaluating unmet need, current/future standard of care, patient/treatment/diagnostic barriers, clinical feasibility, and early clinical signals, • Identify transformational medicine opportunities where Quotient’s platform could be used to develop new medicines in ways not possible with existing approaches., • Gather and support the integration of inputs from across disciplines (scientific, clinical, commercial, regulatory) to support the development of early target medicine profiles (TMP), • Adopt and test agentic AI algorithms to support clinical indication ideation and clinical trial prediction to support pipeline decision-making, • Actively develop novel clinical development strategies and detailed plans, study protocols, and associated documents across all phases of development, reflecting internal and external stakeholder input (e.g., patients, evidence generation, regulators, payors, pharmacovigilance)., • Bring clinical expertise to regulatory interactions and documents including briefing documents, presentations, IND/CTA submissions, • Provide medical monitoring and oversight of the safety of study participants in Quotient’s clinical trials., • Establish and nurture a network of external clinical experts and advisors to pressure-test hypotheses, support indication selection, and refine development strategies., • Serve as a clinical strategy partner in investor discussions and partnering conversations, • At least 4+ years in clinical drug development within early-stage biotech, pharmaceutical industry, and/or translational research settings., • MD, MD/PhD, or equivalent clinical training; ideal candidate will have spent meaningful time in patient-facing roles, • Demonstrated success in translating scientific ideas/drug targets into novel clinical development strategies and/or experimental medicine strategies., • Demonstrated experience in driving disease area and drug discovery project strategy development across multiple disease and therapy areas, • Intellectually agile, curious and confident in offering perspectives outside their domain expertise. The incumbent should be able to go deep quickly in new therapeutic areas despite limited prior experience, • Comfortable working in a scientifically rich, early discovery-stage setting and ability to thrive in a fast-paced, dynamic environment. The right person will be energized by the potential to help shape and build Quotient’s future drug development aspirations., • Encourage respectful disagreement and cultivate open-minded, ego-free interactions to continuously push each other towards excellence, • Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source, • Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions, • Use a company-first mindset to guide decision-making; prioritize team over individual success, • Take calculated risks and challenge convention in the quest for exceptional outcomes Quotient Therapeutics is a privately-held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS). Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Quotient Therapeutics (“Quotient”) and Flagship Pioneering (“FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Quotient, FSP or their employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto. The salary range for this role is $0 - $0. Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. • Quotient Therapeutics, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. When you apply for a role at Flagship Pioneering or one of its portfolio companies, we collect and use personal information you provide (such as your name, contact details, work history, and application materials) to evaluate your application, communicate with you, and comply with legal obligations. Your application data is processed through Greenhouse, our applicant tracking system, and may also be reviewed using AI-assisted screening tools. We do not sell your personal information. California residents have rights under the CCPA/CPRA including to know, delete, and opt out of the sharing of their personal information. If you are located in the EU or UK, we process your data under GDPR and you have rights to access, rectify, and erase your data. To exercise your rights or for questions, contact . Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. #J-18808-Ljbffr

Abselion is a life science tools company headquartered in Cambridge, UK, working on the next generation of analytical technologies. We have developed a benchtop analytical instrument, called Amperia, which uses proprietary Redox Electrochemical Detection (RED) technology to quantify proteins and viral vectors directly from crude samples in minutes, without purification, and without specialist training. We work with teams across protein expression, process development and in academia, biotech and pharma across the globe who are tired of waiting days for analytical results that should take minutes. We are a team who care deeply about the science, move quickly, and believe that the best outcomes come from genuinely understanding and helping customers solve real problems. At Abselion we are looking for a Software Engineer to contribute to the development of the software powering our Amperia analytical instrument, with a strong focus on machine control and hardware integration. You will work across the software stack, with particular emphasis on controlling and interfacing with instrumentation, firmware, and experimental workflows. Frontend and UI work is part of the role but not the primary focus. You will collaborate closely with lab scientists, electronics engineers, and mechanical engineers to translate experimental and hardware requirements into reliable, maintainable software. This includes working on real-time control, device communication, and ensuring robust operation of the system. This role is well suited to someone who enjoys working close to physical systems and hardware, and contributing to complex, evolving products in a multidisciplinary environment. • Contribute to development of software controlling instrumentation and experimental workflows, • Interface with firmware and hardware components (e.g. microcontrollers, sensors, actuators), • Support implementation of reliable communication between software and devices, • Help diagnose and resolve issues across hardware-software boundaries, • Contribute to development of backend systems, data handling, and experiment execution, • Support rapid prototyping and iteration of new hardware and experimental features, • Assist in integrating new capabilities into the existing software platform, • MEng or equivalent in; Computer Science/Software Engineering, Physics or engineering, • 2-5 years experience in software development in in instrumentation or hardware-related environments, • Strong programming skills in python, C++, TypeScript, • Experience in machine control, embedded systems, or hardware integration, • A demonstrated ability to rapidly pick up new skills in context and apply them at a high level., • Good understanding of git, automated build processes, and software development lifecycle (SDLC), • Strong communication skills and ability to collaborate across disciplines, • Dynamic and fast-paced work environment in a rapidly expanding company, • Be part of a step-change in life science instrumentation, • Working on cutting-edge technology at the intersection of biology, engineering, and data science, • Share option scheme, • Base salary between £40,000 - £55,000 per annum, • Most important of all, join a great team! Immediate The role is full timeon-site located in Cambridge, UK. First stage: Remote; Second stage: Remote; Third stage: In person #J-18808-Ljbffr

ProFound Therapeutics is seeking an innovative and highly motivated Co-Op/Intern with experience in cell biology and/or oncology to support the Oncology team. You will contribute scientific and technical expertise to a multidisciplinary group, focusing on conceptualization, experimentation, data analysis, and strategic planning. The role is a full-time, 40 hours/week co-op from January 2027 to June 2027 with five days in office, offering hands-on experience in a fast-paced biotech environment #J-18808-Ljbffr

At IQVIA Discovery Sciences , we are accelerating scientific innovation through advanced cellular models and cutting-edge research technologies. We are seeking a highly experienced Senior Technical Specialist - Stem Cells to join our talented scientific team and play a pivotal role in supporting innovative drug discovery programmes. This is an exciting opportunity for a stem cell specialist who combines deep technical expertise with scientific curiosity and enjoys working in a fast-paced, collaborative environment where their work directly contributes to ground-breaking therapeutic research. As a Senior Technical Specialist II, you will be the subject matter expert for stem cell culture technologies, supporting the development, maintenance, optimisation, and delivery of high-quality cellular systems for a range of discovery projects. You will work closely with multidisciplinary teams across sites, helping to solve complex technical challenges while ensuring the consistent supply of robust cellular models for research programmes. • Lead the development, optimisation, and implementation of stem cell culture technologies., • Culture, maintain, expand, and troubleshoot a wide variety of stem cell, primary, and recombinant cell lines., • Manage multiple cell culture programmes simultaneously, ensuring delivery against critical project timelines., • Generate and supply high-quality cell batches to support high-throughput screening and ongoing discovery activities., • Apply contemporary cryopreservation techniques to ensure consistency, reproducibility, and long-term cell line integrity., • Provide technical leadership in troubleshooting cellular assays and culture-related challenges., • Drive best practice across cell culture workflows, sharing knowledge and expertise with colleagues., • Ensure compliance with biological safety requirements and contamination control procedures., • Collaborate with scientists, project teams, and stakeholders across departments and global locations., • Engage with external suppliers, research partners, and occasionally clients to support scientific objectives., • Bachelor's degree in Cell Biology, Stem Cell Biology, Life Sciences, Biotechnology, or a related scientific discipline., • Significant experience working within a stem cell or advanced cell culture environment., • Extensive hands-on experience culturing, maintaining, and troubleshooting stem cell lines., • Strong understanding of cell culture technologies, cellular assays, and cryopreservation methodologies., • Proven scientific problem-solving and technical troubleshooting skills., • Experience managing multiple priorities within a deadline-driven environment., • Excellent organisational and time management skills., • A collaborative mindset with strong communication skills and the ability to build effective relationships across teams., • Advanced practical experience with pluripotent stem cells (iPSC or ESC) and differentiation workflows., • Experience with automated liquid handling platforms and high-throughput technologies., • Knowledge of molecular biology techniques and cell line engineering., • Experience supporting cell line generation and characterisation programmes., • Exposure to client-facing scientific projects within a CRO, biotech, or pharmaceutical environment., • Be part of a globally recognised organisation at the forefront of healthcare and drug discovery., • Work alongside an exceptional scientific leadership team and subject matter experts., • Contribute to innovative programmes that have the potential to transform patient outcomes., • Access advanced technologies, modern laboratory facilities, and diverse scientific challenges., • Collaborate with colleagues across the UK, Europe, and global research networks., • Enjoy ongoing development opportunities and the chance to further establish yourself as a leader in stem cell science. If you're passionate about stem cell biology, thrive on solving complex scientific challenges, and want to contribute to the next generation of therapeutic innovation, we'd love to hear from you. Join IQVIA Discovery Sciences and help advance the science that changes lives. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. #J-18808-Ljbffr

Do you want to use your engineering skills to build agentic workflows that help find treatments for rare disease patients? Healx is an AI-powered tech bio company that is redesigning drug discovery. With 10,000 rare diseases affecting 400 million people globally, 90% of which have no approved treatment, Healx is on a mission to pioneer the next generation of drug discovery to help rare disease patients in need. We combine data, artificial intelligence and deep pharmacology expertise to develop treatments more quickly and cheaply than traditional drug discovery. Diversity and inclusion sits at the heart of our mission to help people with rare diseases, and we believe that attracting and empowering a diverse team is critical to achieving this goal. We welcome applications from people from all backgrounds and walks of life. Below we have included the qualities that we feel are required for you to excel in this role; however we appreciate that people can apply transferable skills and experience. If you think you have what it takes, love our mission and resonate with our values but are worried you don't tick every box – we still want to hear from you and encourage you to apply! Care for Rare – Rare disease patients are at the heart of what we do Grow as individuals – We are learners always seeking to enhance our expertise Win as a team – We strive to remain inclusive and diverse and we celebrate successes and lessons together Innovate and deliver – Our mission requires rapid innovation and calculated risks that won’t compromise our high standards Healx is looking for an Agentic AI Engineer to build LLM-agentic workflows that power our drug discovery platform. Reporting to our Director of Tech Strategy, you'll design and build agents that solve real drug discovery problems. Working closely with scientists across the company, you'll understand the questions that matter most to their work, then design and refine agents that reason over our knowledge graph, proprietary methods, scientific literature and other sources to generate, triage and rationalise testable therapeutic hypotheses for rare diseases. You won't be starting from scratch. We've adopted an agentic framework (our stack currently includes Python, ADK and AgentSpace) and built workflows already delivering impact across our drug discovery platform. But this is a fast-moving field, so a big part of the role is helping us adapt as the landscape shifts. You'll work alongside the technical lead who owns our agentic infrastructure, with scope to take ownership of specific workflows and grow your influence as you do. You'll join a cross-functional team of machine learning engineers, software engineers, bioinformaticians, drug discovery scientists and clinicians, all working to sharpen how Healx makes better decisions in drug discovery. Build and refine AI-agentic workflows on our internal framework to help drug discovery scientists generate the best testable therapeutic hypotheses to progress. Translate discovery problems into agent designs, working out where an agentic approach genuinely adds value, and where it doesn’t Integrate agents with our knowledge graph, proprietary methods, scientific literature and other sources so they reason over the right evidence for each problem Expand and maintain our existing GenAI tools so they keep pace with the team’s needs and a fast-moving ecosystem Contribute to how we evaluate agentic workflows, helping shape sensible evals, testing and quality standards as the practice matures Write clear, maintainable, well-documented code that others on the team can build on In 3 months, you have: Got to grips with our agentic framework and the discovery problems it serves, and made your first contributions land in the codebase Built working relationships with the scientists and engineers you partner with, and started turning their feedback into concrete improvements In 6 months you have: Taken at least one agentic workflow from idea to a production tool scientists use in our drug discovery pipeline — built on our framework, with sensible evaluation and documentation Operating with real independence — owning agentic workflows end to end, proposing improvements. We’d love to hear from you if You have built and shipped LLM‑agentic systems that deliver real value — agents that use tools, orchestrate multi‑step workflows and behave reliably in production. You have at least 2 years of software engineer or ML engineer working experience. And you have strong software engineering fundamentals — you write clear, tested, maintainable Python code that others can build on Fluency with the modern LLM/agent toolkit — model APIs, prompting, tool use, RAG, and the patterns this fast‑moving ecosystem is converging on (MCP, agent frameworks, evals). You enjoy working closely with non‑engineers — you are the kind of person who'll sit with a scientist to understand what they actually need. It’s a bonus if you have: Experience in drug discovery, biology, or another life science domain Familiarity with knowledge graphs or reasoning over structured or heterogeneous data Experience building evaluation harnesses or testing strategies for LLM systems A track record of picking up unfamiliar domains quickly and becoming useful fast Interest in or experience with biotech / techbio and its impact on patient outcomes. Healx works from a modern accessible office in the centre of Cambridge within easy reach of the train station. We offer a flexible, diverse and inclusive working environment that considers your individual needs and believes in maintaining a sustainable work-life balance and we are open to discussing flexible working arrangements. We are a hybrid team operating on a highly collaborative model that values synchronization and pair programming. You will be welcomed by a team of colleagues with decades of accumulated experience in their areas of expertise, happy to help you develop your own skills in a highly collaborative environment and who are keen to provide guidance and support in your personal and career development plans. Healx will provide you with support and guidance to help you do your best work and make an impact. We offer flexible working and believe in maintaining a sustainable work-life balance. If you require any reasonable adjustments during the recruitment process, please let us know — we’re happy to accommodate. Financial – Competitive salary, share options, 7% employer pension contributions, life insurance of 4x base salary. Health and Wellbeing – Private medical insurance, 25 days annual leave (plus bank holidays) with the option to purchase additional days to support a healthy work-life balance, wellbeing support via Spill and our Employee Assistance Programme. Hybrid Working – We will only consider UK-based applicants for this position. We offer flexible and remote working options, home office set-up allowance, periodic in-person team days for company-wide collaboration and celebration. Family Friendly – Enhanced family leave policies, miscarriage and fertility leave, flexible working practices. Personal Development and Growth – Personal learning and development budgets, regular personal development conversations and career support. Community Engagement and Support – One paid day off per year to volunteer for a cause aligned with our mission of supporting patients living with rare diseases; the opportunity to hear from and engage with patient groups and communities who offer us valuable insights into the experiences of those affected by rare diseases. For more information about Healx and how we use your data please go to privacy/ #J-18808-Ljbffr

Quotient is seeking a Senior Engineer in our Data Infrastructure team to design and evolve our cloud, data and AI infrastructure underpinning our genomics-first drug discovery platform. Working within the Data Infrastructure team, you will lead complex initiatives spanning AWS platform engineering, scientific data systems and AI/ML workloads. You will collaborate closely with cloud engineers, data engineers, bioinformaticians, AI scientists, computational biologists, and experimental scientists to turn evolving scientific needs into secure, reliable and scalable engineering solutions. This is a senior individual-contributor role with substantial technical autonomy. You will make cross-system architecture and operational trade-offs, establish reusable engineering patterns, and mentor our Cloud Engineers and Data Engineers through design reviews, delivery and troubleshooting. The role does not require formal line management, but it does require clear technical leadership and accountability for platform outcomes. This hybrid role is based at the Chesterford Research Campus, near Cambridge, and reports to the Head of Data Infrastructure. The successful candidate will normally work from the campus at least three days per week, participate in operational support and incident escalation, and must have permission to work in the UK. • Lead the architecture and evolution of our AWS-based infrastructure across cloud services, scientific data platforms and AI/ML workloads, balancing delivery speed, reliability, security and cost., • Design and implement reusable infrastructure-as-code, CI/CD and environment-management patterns that make production systems easier to build, test, deploy and operate., • Own cross-cutting engineering decisions for observability, identity and access management, networking, resilience, capacity, data movement and lifecycle management., • Partner with Cloud Engineers and Data Engineers to deliver integrated solutions, providing practical mentoring through technical design, code review, incident response and operational improvement., • Work with AI scientists, computational biologists and scientific teams to translate model development, training, evaluation, inference and data requirements into secure, reproducible platform capabilities., • Diagnose and resolve complex failures spanning infrastructure, data pipelines, applications and AI workloads; lead incident reviews and ensure corrective actions improve the wider system., • Establish and reinforce engineering standards for testing, documentation, release management, operational readiness, security and cost visibility across the Data Infrastructure team., • Evaluate new technologies and shape the infrastructure roadmap with the Head of Data Infrastructure, making pragmatic build-versus-buy and sequencing decisions for an early-stage biotech., • Substantial experience designing, building and operating production cloud or data infrastructure, typically gained through seven or more years of relevant work or equivalent demonstrated capability., • Advanced hands‑on experience with AWS and ownership of multiple interdependent production systems, including the ability to troubleshoot failures across service boundaries., • Strong experience with infrastructure‑as‑code, CI/CD, containerised workloads, cloud networking, identity and access management, and production observability., • Strong software engineering skills in Python and Linux, including automated testing, version control, code review and maintainable automation or platform tooling., • Experience supporting data‑intensive life‑science systems or workflows, with enough domain understanding to reason about large scientific datasets, reproducibility, provenance and scientific user needs., • Experience enabling AI/ML workloads in cloud environments, such as data preparation, model training, evaluation, inference, orchestration or production deployment., • A track record of leading complex technical initiatives under ambiguity, making explicit trade‑offs and remaining accountable for reliable operational outcomes., • Demonstrated ability to mentor engineers and communicate architecture, risk and delivery choices clearly to both technical and scientific stakeholders., • Genomics, digital pathology, structural biology or other high‑volume scientific data modalities and formats., • AWS CDK, Batch, ECS, EKS, S3, RDS or Postgres, Athena, SageMaker, Bedrock, or equivalent services., • Scientific workflow and data orchestration frameworks such as Nextflow, Dagster, Airflow or similar., • Platform security, privacy or governance controls for sensitive biomedical or clinical data., • Identity platforms and federation technologies such as Entra ID, SSO or role‑based access patterns., • Working in an early‑stage biotech, research‑intensive startup or another fast‑changing environment with a small engineering team., • Encourage respectful disagreement and cultivate open‑minded, ego‑free interactions to continuously push each other towards excellence, • Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source, • Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions, • Use a company‑first mindset to guide decision‑making; prioritize team over individual success, • Take calculated risks and challenge convention in the quest for exceptional outcomes Quotient Therapeutics is a privately‑held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first‑in‑category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS). Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Quotient Therapeutics (“Quotient”) and Flagship Pioneering (“FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Quotient, FSP or their employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto. When you apply for a role at Flagship Pioneering or one of its portfolio companies, we collect and use personal information you provide (such as your name, contact details, work history, and application materials) to evaluate your application, communicate with you, and comply with legal obligations. Your application data is processed through Greenhouse, our applicant tracking system, and may also be reviewed using AI‑assisted screening tools. We do not sell your personal information. California residents have rights under the CCPA/CPRA including to know, delete, and opt out of the sharing of your personal information. If you are located in the EU or UK, we process your data under GDPR and you have rights to access, rectify, and erase your data. To exercise your rights or for questions, contact . #J-18808-Ljbffr

Quotient is seeking a Senior Engineer in our Data Infrastructure team to design and evolve our cloud, data and AI infrastructure underpinning our genomics-first drug discovery platform. Working within the Data Infrastructure team, you will lead complex initiatives spanning AWS platform engineering, scientific data systems and AI/ML workloads. You will collaborate closely with cloud engineers, data engineers, bioinformaticians, AI scientists, computational biologists, and experimental scientists to turn evolving scientific needs into secure, reliable and scalable engineering solutions. This is a senior individual-contributor role with substantial technical autonomy. You will make cross-system architecture and operational trade-offs, establish reusable engineering patterns, and mentor our Cloud Engineers and Data Engineers through design reviews, delivery and troubleshooting. The role does not require formal line management, but it does require clear technical leadership and accountability for platform outcomes. This hybrid role is based at the Chesterford Research Campus, near Cambridge, and reports to the Head of Data Infrastructure. The successful candidate will normally work from the campus at least three days per week, participate in operational support and incident escalation, and must have permission to work in the UK. Responsibilities: • Lead the architecture and evolution of our AWS-based infrastructure across cloud services, scientific data platforms and AI/ML workloads, balancing delivery speed, reliability, security and cost., • Design and implement reusable infrastructure-as-code, CI/CD and environment-management patterns that make production systems easier to build, test, deploy and operate., • Own cross-cutting engineering decisions for observability, identity and access management, networking, resilience, capacity, data movement and lifecycle management., • Partner with Cloud Engineers and Data Engineers to deliver integrated solutions, providing practical mentoring through technical design, code review, incident response and operational improvement., • Work with AI scientists, computational biologists and scientific teams to translate model development, training, evaluation, inference and data requirements into secure, reproducible platform capabilities., • Diagnose and resolve complex failures spanning infrastructure, data pipelines, applications and AI workloads; lead incident reviews and ensure corrective actions improve the wider system., • Establish and reinforce engineering standards for testing, documentation, release management, operational readiness, security and cost visibility across the Data Infrastructure team., • Evaluate new technologies and shape the infrastructure roadmap with the Head of Data Infrastructure, making pragmatic build-versus-buy and sequencing decisions for an early-stage biotech. Qualifications: • Substantial experience designing, building and operating production cloud or data infrastructure, typically gained through seven or more years of relevant work or equivalent demonstrated capability., • Advanced hands-on experience with AWS and ownership of multiple interdependent production systems, including the ability to troubleshoot failures across service boundaries., • Strong experience with infrastructure-as-code, CI/CD, containerised workloads, cloud networking, identity and access management, and production observability., • Strong software engineering skills in Python and Linux, including automated testing, version control, code review and maintainable automation or platform tooling., • Experience supporting data-intensive life-science systems or workflows, with enough domain understanding to reason about large scientific datasets, reproducibility, provenance and scientific user needs., • Experience enabling AI/ML workloads in cloud environments, such as data preparation, model training, evaluation, inference, orchestration or production deployment., • A track record of leading complex technical initiatives under ambiguity, making explicit trade-offs and remaining accountable for reliable operational outcomes., • Demonstrated ability to mentor engineers and communicate architecture, risk and delivery choices clearly to both technical and scientific stakeholders., • Genomics, digital pathology, structural biology or other high-volume scientific data modalities and formats., • AWS CDK, Batch, ECS, EKS, S3, RDS or Postgres, Athena, SageMaker, Bedrock, or equivalent services., • Scientific workflow and data orchestration frameworks such as Nextflow, Dagster, Airflow or similar., • Platform security, privacy or governance controls for sensitive biomedical or clinical data., • Identity platforms and federation technologies such as Entra ID, SSO or role-based access patterns., • Working in an early-stage biotech, research-intensive startup or another fast-changing environment with a small engineering team. Values and Behaviors: • Encourage respectful disagreement and cultivate open-minded, ego-free interactions to continuously push each other towards excellence, • Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source, • Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions, • Use a company-first mindset to guide decision-making; prioritize team over individual success, • Take calculated risks and challenge convention in the quest for exceptional outcomes About Quotient: Quotient Therapeutics is a privately-held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS). Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Recruitment & Staffing Agencies: Quotient Therapeutics ("Quotient") and Flagship Pioneering ("FSP") do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Quotient, FSP or their employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto. Privacy Notice for Applicants:When you apply for a role at Flagship Pioneering or one of its portfolio companies, we collect and use personal information you provide (such as your name, contact details, work history, and application materials) to evaluate your application, communicate with you, and comply with legal obligations. Your application data is processed through Greenhouse, our applicant tracking system, and may also be reviewed using AI-assisted screening tools. We do not sell your personal information. California residents have rights under the CCPA/CPRA including to know, delete, and opt out of the sharing of their personal information. If you are located in the EU or UK, we process your data under GDPR and you have rights to access, rectify, and erase your data. To exercise your rights or for questions, contact . #J-18808-Ljbffr

Cambridge, United Kingdom Quotient is seeking a Senior Engineer in our Data Infrastructure team to design and evolve our cloud, data and AI infrastructure underpinning our genomics-first drug discovery platform. Working within the Data Infrastructure team, you will lead complex initiatives spanning AWS platform engineering, scientific data systems and AI/ML workloads. You will collaborate closely with cloud engineers, data engineers, bioinformaticians, AI scientists, computational biologists, and experimental scientists to turn evolving scientific needs into secure, reliable and scalable engineering solutions. This is a senior individual-contributor role with substantial technical autonomy. You will make cross-system architecture and operational trade-offs, establish reusable engineering patterns, and mentor our Cloud Engineers and Data Engineers through design reviews, delivery and troubleshooting. The role does not require formal line management, but it does require clear technical leadership and accountability for platform outcomes. This hybrid role is based at the Chesterford Research Campus, near Cambridge, and reports to the Head of Data Infrastructure. The successful candidate will normally work from the campus at least three days per week, participate in operational support and incident escalation, and must have permission to work in the UK. • Lead the architecture and evolution of our AWS-based infrastructure across cloud services, scientific data platforms and AI/ML workloads, balancing delivery speed, reliability, security and cost., • Design and implement reusable infrastructure-as-code, CI/CD and environment-management patterns that make production systems easier to build, test, deploy and operate., • Own cross-cutting engineering decisions for observability, identity and access management, networking, resilience, capacity, data movement and lifecycle management., • Partner with Cloud Engineers and Data Engineers to deliver integrated solutions, providing practical mentoring through technical design, code review, incident response and operational improvement., • Work with AI scientists, computational biologists and scientific teams to translate model development, training, evaluation, inference and data requirements into secure, reproducible platform capabilities., • Diagnose and resolve complex failures spanning infrastructure, data pipelines, applications and AI workloads; lead incident reviews and ensure corrective actions improve the wider system., • Establish and reinforce engineering standards for testing, documentation, release management, operational readiness, security and cost visibility across the Data Infrastructure team., • Evaluate new technologies and shape the infrastructure roadmap with the Head of Data Infrastructure, making pragmatic build-versus-buy and sequencing decisions for an early-stage biotech., • Substantial experience designing, building and operating production cloud or data infrastructure, typically gained through seven or more years of relevant work or equivalent demonstrated capability., • Advanced hands‑on experience with AWS and ownership of multiple interdependent production systems, including the ability to troubleshoot failures across service boundaries., • Strong experience with infrastructure‑as‑code, CI/CD, containerised workloads, cloud networking, identity and access management, and production observability., • Strong software engineering skills in Python and Linux, including automated testing, version control, code review and maintainable automation or platform tooling., • Experience supporting data‑intensive life‑science systems or workflows, with enough domain understanding to reason about large scientific datasets, reproducibility, provenance and scientific user needs., • Experience enabling AI/ML workloads in cloud environments, such as data preparation, model training, evaluation, inference, orchestration or production deployment., • A track record of leading complex technical initiatives under ambiguity, making explicit trade‑offs and remaining accountable for reliable operational outcomes., • Demonstrated ability to mentor engineers and communicate architecture, risk and delivery choices clearly to both technical and scientific stakeholders., • Genomics, digital pathology, structural biology or other high‑volume scientific data modalities and formats., • AWS CDK, Batch, ECS, EKS, S3, RDS or Postgres, Athena, SageMaker, Bedrock, or equivalent services., • Scientific workflow and data orchestration frameworks such as Nextflow, Dagster, Airflow or similar., • Platform security, privacy or governance controls for sensitive biomedical or clinical data., • Identity platforms and federation technologies such as Entra ID, SSO or role‑based access patterns., • Working in an early‑stage biotech, research‑intensive startup or another fast‑changing environment with a small engineering team., • Encourage respectful disagreement and cultivate open‑minded, ego‑free interactions to continuously push each other towards excellence, • Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source, • Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions, • Use a company‑first mindset to guide decision‑making; prioritize team over individual success, • Take calculated risks and challenge convention in the quest for exceptional outcomes Quotient Therapeutics is a privately‑held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first‑in‑category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS). Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. #J-18808-Ljbffr

Are you already an experienced bioanalyst looking for your next role? Do you have refined skills in LC-MS maintenance and troubleshooting? Are you proficient in bespoke method development within small molecules? If you answered yes to any, or all of those questions then good news, our Cambridge site have a vacancy for a Senior Technical Specilaist - DMPK! A highly experienced lab and office based bioanalyst providing wide in-depth scientific and technical expertise to both multidisciplinary integrated Drug Discovery projects and standalone DMPK projects. This role combines hands-on bioanalytical expertise with project leadership, mentoring, and continuous improvement responsibilities to support small and large molecule drug discovery programmes. Offering you opportunities across varied DMPK and broader scientific projects and development across multiple scientiic and technical areas. Developing, optimising and executing the bioanalysis of samples from in vivo DMPK studies for small and large molecule drug discovery projects in an early discovery setting. Extensive knowledge of modern UPLC-MS systems and software including chromatographic method development. Demonstrated ability to perform routine and complex troubleshooting, maintenance, and optimisation of mass spectrometry and LC equipment, ensuring reliable operation and rapid resolution of technical issues. Experience in the analysis of different sample types such as plasma, blood, brain, lung, bile, faeces, urine. Demonstrated experience of pharmacokinetic parameter determination and an understanding of the underlying principles. Comprehensive troubleshooting and problem-solving skills using both technical and scientific expertise. Strong organisation and time management skills alongside an inbuilt flexibility to adapt to change. Excellent communication skills and be an effective team player; these will be essential to successful execution of projects whilst working in a matrix and multi-skilled environment. Lead scientific and technical projects, ensuring delivery of high-quality data to agreed timelines. Drive innovation through the development of novel assays, protocols and analytical approaches. Mentor, coach and develop colleagues, acting as a technical role model and recognised subject matter expert. BSc or equivalent in relevant scientific area. Industry experience in pharma, biotech or other commercial organisations. Expert user of Mass Spectrometry instrumentation. Experience in the bioanalytical method development of challenging analytes, in complex matrices. Accurate & diligent experimental planning, execution and troubleshooting. Good communication skills (verbal/written) internally and externally. Excellent team player. Positive ‘can do’ attitude. Creative problem solving. Ability to plan & execute work independently. Project management. Strong organisation and time management skills alongside an inbuilt flexibility to adapt to change. Experience of guiding/mentoring junior colleagues. LC-MS/MS maintenance and troubleshooting. Bespoke method development for small molecules. What We Offer You We offer a comprehensive benefits package from day one including generous pension, bonus and health cover. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. #J-18808-Ljbffr

Optical Systems Engineer - Medical Devices - Cambridge We are working with a leading Medical Devices company in Cambridge to recruit an Optical Systems Engineer who will play a key role in the development of industry disrupting and lifesaving/improving Medical Technologies. This is a hands-on engineering role where you'll be designing and integrating optical systems into complex medical technologies.From early feasibility through to product launch, you'll be involved in every stage of development, helping to shape devices that improve diagnostics, treatment, and patient outcomes across a range of clinical applications. You'll be joining a multidisciplinary team of engineers and scientists, collaborating on projects that demand precision, creativity, and a deep understanding of how optics interact with mechanical, electronic, and biological systems.Your work will span simulation, prototyping, testing, and refinement, with a strong emphasis on regulatory compliance and real-world usability. We're looking for someone with a solid academic foundation in physics, engineering, or a related discipline, and hands-on experience in optical design and analysis.You should be confident using industry-standard tools and have a track record of delivering robust solutions in regulated environments.Experience in medical devices is highly desirable, but not essential if you bring strong transferable skills and a passion for healthcare innovation. This role is ideal for someone who enjoys solving technical challenges, mentoring junior colleagues, and working closely with clients to bring ideas to life.You'll be encouraged to explore new approaches, contribute to system-level thinking, and help shape the future of medical technology. In return, you'll receive a competitive salary, annual bonus, private healthcare, generous pension contributions, and access to a wide range of lifestyle and professional development benefits. For more information, please contact Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery Recruitment at Newton Colmore, on .Alternatively, submit your application and a member of our team will be in touch.Please note that without a CV, we can only provide limited information. #J-18808-Ljbffr

Ipsen is seeking a Senior Manager to lead programming on multiple compounds and studies within Statistical Programming. This role combines hands-on SAS programming with managerial responsibilities to ensure timely, high-quality deliverables, either in house or via CROs. The position requires 8+ years of programming experience in pharmaceutical/biotech/CRO environments, SAS proficiency, and CDISC knowledge. English is essential; French is a plus. #J-18808-Ljbffr

Slough, UK The actual location of this job is in Slough, United Kingdom. Join Lonza’s Biologics R&D team and play a pivotal role in shaping the digital future of laboratory science. This role sits at the intersection of science, data, and engineering, with a strong focus on owning and delivering laboratory informatics solutions (ELN, SDMS) that enable scalable, high-quality scientific workflows. This is a unique opportunity to take ownership of lab informatics systems and play a key role in Lonza’s digital transformation. You will work in a highly collaborative environment, bridging science and technology to enable next-generation R&D. What you will get: • An agile career and dynamic working culture., • An inclusive and ethical workplace., • Compensation programs that recognize high performance., • A variety of benefits dependent on role and location. The full list of our global benefits can be found here: careers/benefits What you will do: • Lead the end-to-end implementation, configuration, and optimization of laboratory informatics systems (ELN, SDMS) across R&D, • Act as a subject matter expert, driving adoption and continuous improvement of lab informatics platforms, • Partner closely with R&D scientists to translate experimental workflows into structured, scalable digital solutions, • Design and implement data models, templates, metadata structures, and workflows aligned with FAIR data principles, • Build and maintain integrations between lab systems, automation platforms, analytics tools, and cloud environments using APIs and middleware, • Develop robust data flows to improve interoperability, reduce manual effort, and ensure high-quality data capture, • Provide user training, documentation, and ongoing support to ensure successful system adoption, • Contribute to digital architecture discussions and help shape the evolution of Lonza’s R&D data ecosystem What we are looking for: • MSc (or equivalent) in Bioinformatics, Biology, Chemistry, Engineering, or a related field, • Proven hands-on experience implementing or owning ELN or SDMS platforms in a pharma/biotech R&D environment, • Alternatively, significant experience as a power user/end user of ELN/ systems, with involvement in system configuration, optimization, or rollout, • Strong understanding of scientific workflows and experimental data lifecycle management, • Experience with data modelling, metadata standards, and FAIR data principles, • Programming/scripting experience (Python, R, SQL) and experience integrating systems via APIs (REST, GraphQL), • Strong communication skills with the ability to work across scientific and technical teams About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. #J-18808-Ljbffr

Nuclera is a venture-backed, founder-driven biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Our purpose is to improve human health by making proteins accessible to life science researchers around the world. In 2024, we launched eProtein Discovery™ - a breakthrough protein expression, characterization, and purification platform, consisting of cloud-based software and a lab-based instrument (with proprietary cartridges and consumables). Since then, we have established a growing installed base in North America, Europe and Asia, receiving numerous awards and customer accolades. As a key player in a small engineering team, you will support the next stage of Nuclera’s growth through: • New Products - Contributing to development of a new product platform and its support tools., • Installed Base Support - Sustaining and being the internal expert and primary point of contact for manufacturing and field support issues relating to current generation Instrument. Over time (6-12 months), your skills and responsibilities will broaden to include other software languages and technologies. This may also extend to electronics and PCB design. • Full lifecycle development and release management for prototypes, products and support tools., • Planning: Providing plans covering tasks, dependencies, effort, cost and resource allocation., • Risk Management: Supporting risk identification, evaluation and choice of risk response strategies., • Execution & Self-Monitoring: Progress according to agreed priorities and plans. Devise appropriate responses to problems and issues. Track and report own progress (deliverables, adherence to schedules, actual spend vs budget, etc.), • Progress according to agreed priorities and plans. Devise appropriate responses to problems and issues. Track and report own progress (deliverables, adherence to schedules, actual spend vs budget, etc.), • Bachelors’ Degree in Software Engineering, Computer Science or similar., • 5+ years of full lifecycle development for multi-technology products developed to rigorous standards. Life science equipment / medical device equipment experience desired., • Programming Languages: C for STM32 and Raspberry Pi Pico 2, python 3, Bash, • Operating Systems / Frameworks: Embedded Linux / Yocto, Docker, • Development Environment: Git / Gitlab / CI/CD, Jira, • Software Quality: coding standards/static analysis, code/design review, testing - unit, integration, hardware-in-the-loop, • Technologies: real-time control & monitoring (motion / mechanism functions & temperature control) embedded systems / electronics, LAN networking, • Strong initiative, problem-solving, task prioritization, and end-to-end execution / completion., • Effective relationship management, cross-functional teamwork, clear documentation, and presentation skills., • Current UK driving licence. Willing and able to occasionally travel nationally / internationally on business as required., • Programming Languages: C for SAM 4S / SAM D20, Java, Javascript / React, • Operating Systems / Frameworks: Torizon, PyQt 6, RTOS, • Development Environment: VS Code, Claude AI, • Software Quality: Software Architecture / UML, Design Controls, Stage-Gate Development, Problem solving (DMAIC, 8D), • Technologies: Microfluidics, Optics / Image Processing, Machine Learning / Neural Networks, Cybersecurity, PCB Design (Altium), GUI Design In addition to competitive salaries, we offer a range of benefits including: • Company bonus scheme of 5%, • Share option incentive scheme, • 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, • Fresh fruit, tea, coffee, and snacks in the office, • Organised summer events for staff #J-18808-Ljbffr

Nuclera is a venture-backed, founder-driven biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Our purpose is to improve human health by making proteins accessible to life science researchers around the world. In 2024, we launched eProtein Discovery™ - a breakthrough protein expression, characterization, and purification platform, consisting of cloud-based software and a lab-based instrument (with proprietary cartridges and consumables). Since then, we have established a growing installed base in North America, Europe and Asia, receiving numerous awards and customer accolades. As a key player in a small engineering team, you will support the next stage of Nuclera’s growth through: • New Products - Contributing to development of a new product platform and its support tools., • Installed Base Support - Sustaining and being the internal expert and primary point of contact for manufacturing and field support issues relating to current generation Instrument. Over time (6-12 months), your skills and responsibilities will broaden to include other software languages and technologies. This may also extend to electronics and PCB design. • Full lifecycle development and release management for prototypes, products and support tools., • Planning: Providing plans covering tasks, dependencies, effort, cost and resource allocation., • Risk Management: Supporting risk identification, evaluation and choice of risk response strategies., • Execution & Self-Monitoring: Progress according to agreed priorities and plans. Devise appropriate responses to problems and issues. Track and report own progress (deliverables, adherence to schedules, actual spend vs budget, etc.), • Progress according to agreed priorities and plans. Devise appropriate responses to problems and issues. Track and report own progress (deliverables, adherence to schedules, actual spend vs budget, etc.), • Bachelors’ Degree in Software Engineering, Computer Science or similar., • 5+ years of full lifecycle development for multi-technology products developed to rigorous standards. Life science equipment / medical device equipment experience desired., • Programming Languages: C for STM32 and Raspberry Pi Pico 2, python 3, Bash, • Operating Systems / Frameworks: Embedded Linux / Yocto, Docker, • Development Environment: Git / Gitlab / CI/CD, Jira, • Software Quality: coding standards/static analysis, code/design review, testing - unit, integration, hardware-in-the-loop, • Technologies: real-time control & monitoring (motion / mechanism functions & temperature control) embedded systems / electronics, LAN networking, • Strong initiative, problem-solving, task prioritization, and end-to-end execution / completion., • Effective relationship management, cross-functional teamwork, clear documentation, and presentation skills., • Current UK driving licence. Willing and able to occasionally travel nationally / internationally on business as required., • Programming Languages: C for SAM 4S / SAM D20, Java, Javascript / React, • Operating Systems / Frameworks: Torizon, PyQt 6, RTOS, • Development Environment: VS Code, Claude AI, • Software Quality: Software Architecture / UML, Design Controls, Stage-Gate Development, Problem solving (DMAIC, 8D), • Technologies: Microfluidics, Optics / Image Processing, Machine Learning / Neural Networks, Cybersecurity, PCB Design (Altium), GUI Design In addition to competitive salaries, we offer a range of benefits including: • Company bonus scheme of 5%, • Share option incentive scheme, • 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, • Fresh fruit, tea, coffee, and snacks in the office, • Organised summer events for staff #J-18808-Ljbffr

Flagship Pioneering is seeking a motivated co-op in Cambridge, MA to explore corporate communications, media relations, and public affairs. You will monitor media, help craft executive communications, and contribute creative content for social channels, internal channels, and events. You are an undergraduate student from Northeastern University approved for spring 2027, with strong English skills and proficiency in Canva, Microsoft Office, and Adobe Creative Suite. #J-18808-Ljbffr

Are you looking to develop your career in laboratory automation and drug discovery? IQVIA Discovery Sciences in Cambridge is seeking an Associate Technical Specialist to support our Sample Management team, helping to deliver critical laboratory operations that accelerate research programmes. • Operate and maintain automated laboratory platforms, including Echo, Tecan, Janus, Beckman, HighRes, Mosquito, SmartCell and Hamilton Tube Store systems., • Support liquid handling protocol development and routine sample management activities., • Complete SAP transactions and laboratory documentation accurately and on time., • Troubleshoot technical issues and contribute to continuous improvement initiatives., • Ensure all work is performed safely and in compliance with quality standards., • BSc in a scientific discipline., • Laboratory experience gained through academia or industry., • Strong problem-solving, communication and data handling skills., • Good IT literacy and interest in automation technologies., • Experience within Pharma, Biotech or CRO environments and knowledge of liquid handling automation would be advantageous., • Work with industry-leading automation technologies., • Build expertise in sample management and drug discovery., • Join a collaborative team that values innovation, development and continuous improvement., • Contribute to research that helps improve patient outcomes worldwide. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. #J-18808-Ljbffr

Svitla Systems Inc. is looking for a Middle Data and AI Support Engineer for a full-time position (40 hours per week) in Mexico. Our client is a global, science-led biopharmaceutical company specializing in discovering, developing, and commercializing prescription medicines. The company operates in several therapeutic areas, including oncology, cardiovascular, renal, metabolic, respiratory, immunology, and rare diseases. They work alongside the world's leading academic and biotech research institutions to stimulate innovation and evaluate emerging technologies. The client operates in over 100 countries, and its innovative medicines are used by millions of patients worldwide. The headquarters is located in Cambridge, United Kingdom. This location aligns with the focus on science and innovation, providing proximity to leading academic and research institutions. The Critical Operations team is responsible for keeping US Market data accurate, reliable, and available to business users across areas such as samples, calls, medications, products, and sales. As a Data Support Engineer, you will provide production support for data pipelines, monitoring Airflow DAGs, SnapLogic pipelines, and Databricks jobs, investigating data issues, and managing incidents, service requests, and problem records. The role focuses on hands-on data investigation, SQL-based validation, documented recovery procedures, and effective issue escalation within defined SLAs. • 3+ years of experience providing production support for data pipelines or ETL processes, working within SLAs in a shift-based or follow-the-sun support model., • Hands-on experience investigating data issues end-to-end, from source or vendor files through ingestion, transformation, and loading to published tables or reports., • Advanced SQL skills for data analysis and reconciliation, including joins, CTEs, window functions, row-count reconciliation, and identifying missing or duplicate loads., • Production experience with Apache Airflow, including monitoring DAG runs, reading task logs, and interpreting Python tracebacks., • Hands-on experience with a cloud data platform, preferably Databricks or Snowflake; experience with Amazon Redshift or an equivalent platform is also considered., • Experience handling incidents, service requests, and problem records within an ITIL-based process and defined SLAs., • Ability to document investigation findings clearly, identify the appropriate resolver team, and provide evidence to support escalation., • Ability to work independently within documented recovery procedures and elevate issues that require further technical intervention., • Working English, with the ability to communicate effectively during daily handovers with the team in India., • Experience with Databricks, including job runs, Delta tables, and Databricks SQL., • Experience with Snowflake and Amazon Redshift., • Experience with SnapLogic or a similar ETL tool., • Experience working with AWS S3., • Proactive use of AI tools for troubleshooting, SQL analysis, and technical documentation., • Basic Python skills for troubleshooting data pipelines., • Experience with ServiceNow., • Pharmaceutical industry experience, ideally involving US commercial data such as IQVIA data, CRM calls, and samples., • Monitor Airflow DAG runs, SnapLogic pipelines, and Databricks jobs during the assigned shift., • Investigate pipeline failures by identifying the failing step in logs, checking source file availability in S3, and validating data freshness using SQL., • Prioritize incidents based on business impact when multiple pipelines fail simultaneously., • Execute documented recovery procedures from established runbooks without making code changes., • Escalate issues that cannot be resolved through documented recovery procedures to the appropriate resolver group, providing the relevant evidence and investigation findings., • Validate data loads using SQL in Databricks, Amazon Redshift, and Snowflake, including row counts by period, missing periods, and duplicate records., • Manage incidents, service requests, and problem records in ServiceNow within defined SLAs., • Keep requesters informed throughout the resolution process and document resolution details according to team standards., • Provide written handovers to the team in India, including open issues, actions taken, and pending decisions., • Document new failure patterns in the relevant runbook or knowledge base and flag recurring issues for further investigation., • Work with #1 winner of the ‘Best Place to Work’ award!, • US and EU projects based on advanced technologies., • Legal IMSS contract and competitive compensation., • Regular performance appraisals to support your growth., • Flexibility in workspace, either remote or in our welcoming office., • Remote work financial support., • Comprehensive medical insurance including family., • Life insurance, maternity policy, family days off., • Christmas Bonus in the amount of 30 days' payment., • Bonuses for recommendations of new employees., • Bonuses for article writing, public talks, other activities., • 15 vacation days, 25% vacations bonus, 11 national holidays., • Personalized learning program tailored to your interests and skill development., • Free tech webinars and meetups organized by Svitla., • Monthly Pantry Vouchers, free office snacks, and drinks., • Fun corporate online\offline celebrations and activities., • Awesome team, friendly and supportive community! #J-18808-Ljbffr

Our client is a pioneering and rapidly developing biotechnology company based in Cambridge, who now seek a lawyer or experienced contracts manager to oversee their commercial legal contracting and broader legal issues. Reporting to the Head of Intellectual Property and based at their head office in Cambridge, the role will oversee, prepare, negotiate, execute and maintain all commercial contracting and risk working alongside R & D, clinical operations and legal functions covering contracts such as MSAs, MTAs, CDAs, research and collaboration, clinical trial, manufacturing, quality and supply agreements as well as others. You will either be a qualified lawyer or experienced contracts manager, preferably with existing experience of working for or with a similar biotech, academic tech transfer office, pharmaceutical or life sciences company (although other relevant candidates may be considered). You will also need to be a team oriented, proactive self starter who can operate in a smaller fast moving organisation and communicate and work effectively across all levels of a business. The role can be worked on a full or part time basis and will operate a hybrid office working model (which may depend on the number of days worked). For more information about this key and exciting opportunity please contact Rob Baron of Baron Crawford. #J-18808-Ljbffr

We are seeking a skilled and highly motivated Bioinformatics Developer to join the Human Genomics Team at EMBL-EBI and contribute to the maintenance and development of the DECIPHER platform. DECIPHER is a global data sharing platform that fuels rare disease discovery and enables patient diagnosis. This is an exciting opportunity to join an innovative multi-disciplinary team dedicated to providing tools to assist in the interpretation of genetic variation and the responsible sharing of clinical data for patient benefit. DECIPHER aggregates information from open data resources such as gnomAD and UniProt and utilizes bioinformatics tools such as the Ensembl Variant Effect Predictor (VEP) to create detailed variant annotations. These are presented in user friendly visualisations to help clinical experts interpret likely disease-associated variants identified in their patients. Clinical centres can share variants and summary phenotype information from their patients through DECIPHER, enabling matching with other patients with similar conditions and collaboration between clinicians for patient benefit. With the help of DECIPHER, many thousands of patients now have a diagnosis and hundreds of papers are published every year improving understanding of rare diseases. By joining this project you will be playing an important role in advancing rare disease research, diagnosis, and discovery for genomic health. As the Bioinformatics Developer in the DECIPHER team, you will work alongside two software developers, a support specialist and the project leader to make the latest research data available for use in clinical settings. You will utilize your bioinformatics knowledge in assessment of resources, discussions with data producers and data analysis, reformatting, and integration tasks. This role offers the exciting opportunity to gain knowledge of clinical genomics and improved web development skills while creating tools to facilitate genomic medicine. You will see the real world impact of your work through interactions with our clinical collaborators and other DECIPHER stakeholders. This role can be offered on a full-time or a part-time basis at 80% of full-time hours. • Investigating, assessing and integrating molecular biology and phenotypic data in varying formats from public resources, • Deploying bioinformatics tools in the DECIPHER environment and analysing genomic data, • Designing, testing, implementing data structures and user interfaces to represent information relating to the human genome and genetic disorders., • Supporting DECIPHER users by responding to bug reports and requests for support or new features, • Working with stakeholders to understand and translate their requirements into feature specifications, • Performing ad hoc analyses to investigate potential data issues and support decision making, • Liaising with other groups at EMBL-EBI and external collaborators to understand the resources they have created and how they could integrate with DECIPHER, • Bringing bioinformatics expertise to the DECIPHER team and representing the DECIPHER project at internal and external meetings, • Bachelors (or equivalent) degree in biological, clinical or computational sciences, • Higher degree or equivalent experience in bioinformatics, software engineering or computational sciences, • Experience of bioinformatics standards, tools and resources, preferably those relevant to variant annotation, • Experience of creating methods to manage and process genomics data, • Experience designing and utilising large-scale relational databases, preferably with PostgreSQL., • Proficiency in a language used for data manipulation and analysis such as R and Python., • Familiarity with software development in JavaScript (preferably Node.js or browser-based)., • Proficiency working in a UNIX/Linux environment., • Excellent attention to detail and the ability to deliver a high-quality product to agreed deadlines., • Good communication and interpersonal skills and the ability to work closely with colleagues, giving and receiving constructive feedback, • A professional and helpful manner when responding to support requests, • Experience of collaborating on development projects and working with colleagues from different disciplines., • Experience of working with and interpreting genomic/ molecular biology datasets, • Experience in developing reactive, data-driven web applications in JavaScript frameworks such as Vue, React, or Angular., • Proficiency working in a HPC bioinformatics environment., • Experience of working with clinical data and/or ontologies, • Experience of training people to use web tools or supporting users seeking assistance through a helpdesk system At EMBL-EBI, we are pleased to offer hybrid working options for all our employees, with an expectation that you will be on site at least two days a week, with Thursday being our "team day". Contract length: 2 years grant based contract Salary: Grade 5 or 6 monthly salary from £3,452.05 or £3,861.91 after tax plus generous benefits and financial allowances based on personal circumstances. Excluding personal pension and insurance contributions. Do something meaningful At EMBL-EBI you can apply your talent and passion to accelerate science and tackle some of humankind's greatest challenges. EMBL-EBI, part of the European Molecular Biology Laboratory, is a worldwide leader in the storage, analysis and dissemination of large biological datasets. We provide the global research community with access to publicly available databases and tools which are crucial for the advancement of healthcare, food security, and biodiversity. Join a culture of innovation We are located on the Wellcome Genome Campus, alongside other prominent research and biotech organisations, and surrounded by beautiful Cambridgeshire countryside. This is a highly collaborative and inclusive community where our employees enjoy a relaxed atmosphere. We are committed to ensuring our employees feel valued, supported and empowered to reach their professional potential. Watch this video to see how EMBL-EBI makes an impact. • Financial incentives: Monthly family, child and non-resident allowances, annual salary review, pension scheme, death benefit, long-term care, accident-at-work and unemployment insurances, • Flexible working arrangements - including hybrid working patterns, • Private medical insurance for you and your immediate family (including all prescriptions and generous dental & optical cover), • Generous time off: 30 days annual leave per year, in addition public holidays, • Relocation package including installation grant (if required), • Campus life: Free shuttle bus to and from work, on-site library, subsidised on-site gym and cafeteria, casual dress code, extensive sports and social club activities (on campus and remotely), • Family benefits: On-site nursery, 10 days of child sick leave, generous parental leave, holiday clubs on campus and monthly family and child allowances, • Benefits for non-UK residents: Visa exemption, education grant for private schooling, financial support to travel back to your home country every second year and a monthly non-resident allowance., • International applicants: We recruit internationally and successful candidates are offered visa exemptions. Please take a look at our International Applicants page for further information., • EMBL is a signatory of DORA. Find out how we apply DORA principles to our recruitment and performance assessment processes here., • Diversity and inclusion: At EMBL, we believe that diverse teams drive innovation and scientific excellence. We encourage applications from candidates of all genders, identities, nationalities and/or any other diverse backgrounds. #J-18808-Ljbffr

Cambridge, UK. Full-time, permanent. Office-based, 5 days per week at 93 Lawrence Weaver Road, Cambridge. Abselion is a life science tools company headquartered in Cambridge, UK, working on the next generation of analytical technologies. We have developed a benchtop analytical instrument, called Amperia, which uses proprietary Redox Electrochemical Detection (RED) technology to quantify proteins and viral vectors directly from crude samples in minutes, without purification, and without specialist training. We work with teams across protein expression, process development and in academia, biotech and pharma across the globe who are tired of waiting days for analytical results that should take minutes. We are a team who care deeply about the science, move quickly, and believe that the best outcomes come from genuinely understanding and helping customers solve real problems. We are looking for a GTM Engineer to join our Sales & Marketing team. The focus of the role is lead generation, while also providing support to our social media marketing and engaging in ongoing improvement of the tools and workflows to empower the wider team day to day, that means running structured outbound campaigns: pre-conference prospecting ahead of major industry conferences, and trigger-based LinkedIn prospecting, to build a steady pipeline of qualified meetings. Selling a scientific instrument is a long, consultative process. Your job is not to mass outbound blindly; it's to make sure every lead is well-targeted, every conversation is logged, and the sales efforts are focused on the most promising leads. • Run structured outbound prospecting campaigns to generate qualified leads Execute trigger-based prospecting: identifying relevant signals (funding, hires, publications, role changes) and reaching out with targeted, credible messaging., • Work alongside the Sales team to hand off warm leads and keep the top-of-funnel moving without relying on a single point of failure., • Track and report on outbound response and conversion rates, feeding learnings back into messaging and targeting., • Support the Marketing function with content and scheduling across our social channels (primarily LinkedIn), helping build Abselion's presence with the scientific and biotech community., • Help translate customer wins, conference activity, and product updates into engaging social content, working with the wider Sales & Marketing team on messaging., • Help maintain and improve the CRM (HubSpot) and the wider GTM tool stack: flagging friction, fixing broken workflows, and suggesting practical automations., • Support lead enrichment and data hygiene so the sales team starts every conversation informed., • Document processes so the tools and workflows you improve are adopted, not abandoned., • 2-5 years in a role combining sales/marketing operations with hands-on technical building, e.g. GTM Engineer, RevOps, Sales Operations, Marketing Operations, Growth Engineer., • Comfort writing code: Python, JavaScript, or similar; SQL; familiarity with APIs, webhooks, and no-code/low-code automation tools (Clay, n8n, Zapier, Make)., • Practical experience using LLMs and AI tools in production workflows, not just chat, but building automations that call models, parse outputs, and act on them., • Deep, hands-on expertise with HubSpot, not just using it, but configuring, automating, and integrating it., • Strong analytical mindset, able to define metrics, build dashboards, and tell the story behind the numbers., • Some exposure to social media content or scheduling for a brand or organisation., • Strong written communication: this role does a lot of outbound messaging and content, so clarity and tone matter., • Experience prospecting into scientific or technical buyers (biotech, pharma, life sciences, deep-tech, hardware)., • Comfort with no-code/low-code automation tools or basic scripting, useful for the tools-improvement side of the role but not essential., • Some scientific literacy: enough to read a protein-research paper abstract and understand what a prospect is working on., • Dynamic and fast-paced work environment in a growing Series A biotech., • The chance to shape how we approach lead generation and social presence ahead of our biggest events of the year., • Share option scheme., • Competitive base salary (£40,000 to £55,000 depending on experience)., • Visa sponsorship available., • Be part of a great team working at the intersection of biology, engineering, and data science. Immediate. First stage: Video call; Second stage: Face to face interview at the Cambridge office (including a short prospecting/messaging exercise). #J-18808-Ljbffr

About the teamWe are seeking a skilled and highly motivated Bioinformatics Developer to join the Human Genomics Team at EMBL-EBI and contribute to the maintenance and development of the DECIPHER platform. DECIPHER is a global data sharing platform that fuels rare disease discovery and enables patient diagnosis. This is an exciting opportunity to join an innovative multi-disciplinary team dedicated to providing tools to assist in the interpretation of genetic variation and the responsible sharing of clinical data for patient benefit.DECIPHER aggregates information from open data resources such as gnomAD and UniProt and utilises bioinformatics tools such as the Ensembl Variant Effect Predictor (VEP) to create detailed variant annotations. These are presented in user friendly visualisations to help clinical experts interpret likely disease-associated variants identified in their patients. Clinical centres can share variants and summary phenotype information from their patients through DECIPHER, enabling matching with other patients with similar conditions and collaboration between clinicians for patient benefit. With the help of DECIPHER, many thousands of patients now have a diagnosis and hundreds of papers are published every year improving understanding of rare diseases. By joining this project you will be playing an important role in advancing rare disease research, diagnosis, and discovery for genomic health.Your roleAs the Bioinformatics Developer in the DECIPHER team, you will work alongside two software developers, a support specialist and the project leader to make the latest research data available for use in clinical settings. You will utilise your bioinformatics knowledge in assessment of resources, discussions with data producers and data analysis, reformatting, and integration tasks. This role offers the exciting opportunity to gain knowledge of clinical genomics and improved web development skills while creating tools to facilitate genomic medicine. You will see the real world impact of your work through interactions with our clinical collaborators and other DECIPHER stakeholders.This role can be offered on a full-time or a part-time basis at 80% of full-time hours.Your primary responsibilities will include:• Investigating, assessing and integrating molecular biology and phenotypic data in varying formats from public resources• Deploying bioinformatics tools in the DECIPHER environment and analysing genomic data• Designing, testing, implementing data structures and user interfaces to represent information relating to the human genome and genetic disorders.• Supporting DECIPHER users by responding to bug reports and requests for support or new features• Working with stakeholders to understand and translate their requirements into feature specifications• Performing ad hoc analyses to investigate potential data issues and support decision making• Liaising with other groups at EMBL-EBI and external collaborators to understand the resources they have created and how they could integrate with DECIPHER• Bringing bioinformatics expertise to the DECIPHER team and representing the DECIPHER project at internal and external meetingsYou have• Bachelors (or equivalent) degree in biological, clinical or computational sciences• Higher degree or equivalent experience in bioinformatics, software engineering or computational sciences• Experience of bioinformatics standards, tools and resources, preferably those relevant to variant annotation• Experience of creating methods to manage and process genomics data• Experience designing and utilising large-scale relational databases, preferably with PostgreSQL.• Proficiency in a language used for data manipulation and analysis such as R and Python.• Familiarity with software development in JavaScript (preferably Node.js or browser-based).• Proficiency working in a UNIX/Linux environment.• Excellent attention to detail and the ability to deliver a high-quality product to agreed deadlines.• Good communication and interpersonal skills and the ability to work closely with colleagues, giving and receiving constructive feedback• A professional and helpful manner when responding to support requestsYou may also have• Experience of collaborating on development projects and working with colleagues from different disciplines.• Experience of working with and interpreting genomic/ molecular biology datasets• Experience in developing reactive, data-driven web applications in JavaScript frameworks such as Vue, React, or Angular.• Proficiency working in a HPC bioinformatics environment.• Experience of working with clinical data and/or ontologies• Experience of training people to use web tools or supporting users seeking assistance through a helpdesk systemHybrid Working: At EMBL-EBI, we are pleased to offer hybrid working options for all our employees, with an expectation that you will be on site at least two days a week, with Thursday being our “team day”Contract length: 2 years grant based contractSalary: Grade 5 or 6 monthly salary from £3,452.05 or £3,861.91 after tax plus generous benefits and financial allowances based on personal circumstances. Excluding personal pension and insurance contributions.Why join usDo something meaningful At EMBL-EBI you can apply your talent and passion to accelerate science and tackle some of humankind's greatest challenges. EMBL-EBI, part of the European Molecular Biology Laboratory, is a worldwide leader in the storage, analysis and dissemination of large biological datasets. We provide the global research community with access to publicly available databases and tools which are crucial for the advancement of healthcare, food security, and biodiversity.Join a culture of innovation We are located on the Wellcome Genome Campus, alongside other prominent research and biotech organisations, and surrounded by beautiful Cambridgeshire countryside. This is a highly collaborative and inclusive community where our employees enjoy a relaxed atmosphere. We are committed to ensuring our employees feel valued, supported and empowered to reach their professional potential. Watch this video to see how EMBL-EBI makes an impact.Enjoy lots of benefits:• Financial incentives: Monthly family, child and non-resident allowances, annual salary review, pension scheme, death benefit, long-term care, accident-at-work and unemployment insurances• Flexible working arrangements - including hybrid working patterns• Private medical insurance for you and your immediate family (including all prescriptions and generous dental & optical cover)• Generous time off: 30 days annual leave per year, in addition public holidays• Relocation package including installation grant (if required)• Campus life: Free shuttle bus to and from work, on-site library, subsidised on-site gym and cafeteria, casual dress code, extensive sports and social club activities (on campus and remotely)• Family benefits: On-site nursery, 10 days of child sick leave, generous parental leave, holiday clubs on campus and monthly family and child allowances• Benefits for non-UK residents: Visa exemption, education grant for private schooling, financial support to travel back to your home country every second year and a monthly non-resident allowance.For detailed information please visit our employee benefits page here.What else you need to know• International applicants: We recruit internationally and successful candidates are offered visa exemptions. Please take a look at our International Applicants page for further information.• EMBL is a signatory of DORA. Find out how we apply DORA principles to our recruitment and performance assessment processes here.• Diversity and inclusion: At EMBL, we believe that diverse teams drive innovation and scientific excellence. We encourage applications from candidates of all genders, identities, nationalities and/or any other diverse backgrounds.• How to apply: To apply please submit a cover letter and a CV through our online system. Applications will close at 23:59 CET on the date shown below. We aim to provide a response within two weeks after the closing date.Closing Date 08/10/2026 #J-18808-Ljbffr

1 week ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Who We Are TetraScience is the Scientific Data and AI Cloud company. We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data management solutions, scientific use cases, and AI-enabled outcomes. In connection with your candidacy, you will be asked to carefully review the Tetra Way letter, authored directly by Patrick Grady, our co-founder and CEO. This letter is designed to assist you in better understanding whether TetraScience is the right fit for you from a values and ethos perspective. It is impossible to overstate the importance of this document and you are encouraged to take it literally and reflect on whether you are aligned with our unique approach to company and team building. If you join us, you will be expected to embody its contents each day. What You Will Do Providing a strategic technical partnership with Customers, you will bridge the gap between the business objectives and technical execution. You will be the primary technical leader for scientific end-users to design, architect, and deliver highly impactful solutions to pharmaceutical and biotech customers. You will work to understand scientists' and R&D IT analysts' needs, analyze their data environment, assist in the design and implementation of our solutions and enable customers to achieve faster ROI, reduced risk, smoother scaling, accelerated product adoption and ensure the long-term success of projects. • Primary technical point of contact across strategic accounts, • Lifecycle engagement & adoption acceleration from presales to delivery, • Technical health & risk management, • Strategic planning and stakeholder management across sales, product management and engineering teams, • Sales enablement & growth support, • Deep and wide technical and science senior relationships, • Deeply understand Customer scientific data and AI architecture & goals, • Provide proactive, prescriptive technical guidance, • Act as a trusted advisor aligned to Customer outcomes, • Drive adoption & success plan execution, • Conduct regular technical reviews, • Identify risks & recommend optimizations, • Lead technical strategy for expansions, • Support POCs & co-innovation, • Manage resolution for escalated issues, • Accelerate time to value, • Improve stability & uptime, • Strategic roadmap alignment, • Prioritized support & faster resolutions, • Support growth through hands on sessions and enablement presentations, • Showcase tailored demonstrations to prospects, to both small and large audiences, • Solution Mapping: Map business requirements to technical solutions, • ROI Calculation: Determine potential return on investment for proposed solutions, • Relationship Building: Cultivate relationships with clients, sales teams, and technical teams, • Working with the science and technology Partners such as Databricks and Google, • Negotiation Skills: Collaborate with clients and sales teams to reach beneficial agreements, • Product Knowledge: Develop a deep understanding of the company's product or service offerings, • Demo Development: Design and showcase tailored demonstrations to prospects, • Proposal Writing: Contribute to RFPs/RFIs with detailed technical specifications and solutions, • Timeline Management: Ensure projects are kept on track and within scope, • Stakeholder Management: Coordinate with various stakeholders to ensure the smooth flow of presales activities, • Scientific background academic and/or 5+ years professional experience in Life Sciences, • Senior Technical Architecture experience 5+ years, • Commercial tech sales support, • R&D IT OR Data & Informatics, • Data Modeling: Understand logical, physical, and conceptual data models, • Database Systems: Proficiency in cloud RDBMS (like Snowflake) and NoSQL databases (like Redshift and Databricks), • Big Data Technologies: Familiarity with tools like Spark, and data warehousing solutions, • Cloud Platforms: Experience with cloud providers mainly AWS especially their data services, but also Azure, Google Cloud, • Data Governance and Quality: Understanding of data lineage, metadata management, and data quality processes and tools, • Analytics and BI Tools: Familiarity with tools such as Tableau, Power BI, QlikView, and their backend requirements, • Competitive Salary and equity in a fast-growing company, • Supportive, team-oriented culture of continuous improvement, • Generous paid time off (PTO), • Flexible working arrangements - Remote work We are not currently providing visa sponsorship for this position #J-18808-Ljbffr

Flagship Pioneering is seeking a motivated co-op to join the Technical Operations team in Cambridge, MA. You will build dashboards, automate workflows, and connect data across systems to accelerate medicine development. You’ll own projects end-to-end, choose tools, and work with senior leaders across CMC to turn challenges into working software. This role emphasizes hands-on development and real ownership in a fast-paced biotech environment. #J-18808-Ljbffr

Quotient Therapeutics in Cambridge seeks a Vice President of Translational Medicine to lead clinical strategy across discovery and development, integrating genetic, biomarker, pharmacology, and regulatory insights to shape early program choices. The role demands strategic decision making and cross-functional influence in a fast-paced biotech setting. MD or MD/PhD with early clinical development experience is preferred; the candidate will oversee Phase 1/2 activities, collaborate with CROs, and #J-18808-Ljbffr