Principal Scientist (Portfolio Generation) £50,400 - £64,400 plus benefits Department: Therapeutic Innovation, R&I Reports to: Vice President of Portfolio Generation Location : Babraham Research Campus, Cambridge (1-2 days per week on site) Contract type/hours: Permanent, Full time 35 hours per week (flexible working requests will be considered) Closing date: Sunday 8th March 23:55pm Interview Date: Approximately week commencing 23rd March Interview process: Competency based interview with task/presentation At Cancer Research UK, we exist to beat cancer. We are seeking an experienced Principal Scientist to join our Portfolio generation team at Cancer Research Horizons in Cambridge. As a Principal Scientist, you will identify and assess new therapeutic opportunities from academic sources and help evaluate advanced oncology assets suitable for acceleration through TI's capabilities. You will design and lead focused workplans to de risk promising concepts and guide them to clear entry decisions for the TI portfolio, working closely with drug discovery teams and key stakeholders. You will review Expressions of Interest for Therapeutic Catalyst schemes, recommend proposals for progression, and support academic PIs in developing costed proposals and high quality workplans. You will coordinate multiple Catalyst projects post approval, facilitating interactions with academic partners and determining potential routes for TI involvement. You will also contribute to assessment processes for wider CRUK/CRH initiatives such as C Further, ensuring rigorous scientific evaluation. Your attendance at relevant cancer conferences will support ongoing knowledge building, networking, and identification of new therapeutic opportunities. Every role at CRH is united by a single mission: beating cancer sooner. We carry out work that matters-impacting patients, families, and the future of science. About Cancer Research Horizons As the world's biggest medical research charity, we've helped bring eleven new cancer drugs to market. However, there is still an urgent need to bring more effective treatments to patients faster. We have recently developed a new approach to driving therapeutic innovation through the creation of Cancer Research Horizons (CRH). We have brought together Cancer Research UK's established drug discovery teams under one organisation and leadership team, combining our unique pipeline of cancer biology expertise and access to CRUK's world-class academic network, cutting edge technology platforms and clinical expertise to 1) Bring new treatments to patients faster and 2) Tackle the biggest challenges in discovering cancer drugs by seeking out more radical ideas and embracing risk in our bid to achieve success. Based at sites in Cambridge, the CRUK Scotland Institute in Glasgow, and Newcastle University, you'll be joining over 200 staff from both industrial and academic backgrounds, all dedicated to bringing forward the day we cure cancer. What will you be doing? Development of multiple new opportunities/ from concept review, through to evaluation and de-risk to a decision point on drug discovery portfolio entry (in collaboration with key drug discovery stakeholders). Lead on the development and delivery of workplans to agreed inflection points. Act as a primary point of contact between academic collaborators and CRH-TI within Portfolio Generation space as required. Assist the triage of Therapeutic Catalyst expressions of interest and the development of full proposals. Lead multiple Therapeutic catalyst projects to required/approved endpoints including option to accelerate via additional TI support. Matrix manage drug discovery activities and interactions with PIs in conjunction with key drug discovery stakeholders (Target Validation and Project Enabling leads). Make strategic recommendations to relevant review groups/leadership teams. What are we looking for? PhD or equivalent experience in relevant cancer field. Significant experience of early drug target discovery and the evaluation process (target selection, validation, technical feasibility etc), preferentially developed in a drug discovery environment. Previous experience of working with PI's and helping to deliver early translation projects in cancer discovery Excellent interpersonal skills with the ability to network and build strong working relationships. Strong scientific and strategic understanding of what it takes to drive exciting opportunities towards future drug discovery starts (biology and early drug discovery). An appreciation of the use of preclinical cancer models to support therapeutic discovery. Proven ability to contribute at a technical level to multiple programmes simultaneously. Evidence of strategic thinking and an ability to develop project plans. Collaborative team player, but also a highly self-motivated individual able to prioritise and manage time effectively with the highest levels of quality, productivity, and urgency in delivery. Maintenance of the highest standards of records, data and documentation. Ability to conceive and manage workplans across teams aimed at de-risking a therapeutic opportunity area progressing to drug discovery start decision points. Ability to embed across multiple scientific areas and act as a credible lead: Flexible, unafraid of failure, able to focus on the key experiments, comfortable with ambiguity and making judgement calls. Our organisation values are designed to guide all that we do. Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human : Act to have a positive impact on people Together: Act inclusively and collaboratively We're looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer. If you're interested in applying and excited about working with us but are unsure if you have the right skills and experience, we'd still love to hear from you. What will I gain? We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals. You can explore our benefits by visiting our careers web page. How do I apply? We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively. For more information on this career opportunity please visit our website or contact us. For more updates on our work and careers, follow us on: Linked In, Facebook, Instagram, X and YouTube.
Mar 04, 2026
Full time
Principal Scientist (Portfolio Generation) £50,400 - £64,400 plus benefits Department: Therapeutic Innovation, R&I Reports to: Vice President of Portfolio Generation Location : Babraham Research Campus, Cambridge (1-2 days per week on site) Contract type/hours: Permanent, Full time 35 hours per week (flexible working requests will be considered) Closing date: Sunday 8th March 23:55pm Interview Date: Approximately week commencing 23rd March Interview process: Competency based interview with task/presentation At Cancer Research UK, we exist to beat cancer. We are seeking an experienced Principal Scientist to join our Portfolio generation team at Cancer Research Horizons in Cambridge. As a Principal Scientist, you will identify and assess new therapeutic opportunities from academic sources and help evaluate advanced oncology assets suitable for acceleration through TI's capabilities. You will design and lead focused workplans to de risk promising concepts and guide them to clear entry decisions for the TI portfolio, working closely with drug discovery teams and key stakeholders. You will review Expressions of Interest for Therapeutic Catalyst schemes, recommend proposals for progression, and support academic PIs in developing costed proposals and high quality workplans. You will coordinate multiple Catalyst projects post approval, facilitating interactions with academic partners and determining potential routes for TI involvement. You will also contribute to assessment processes for wider CRUK/CRH initiatives such as C Further, ensuring rigorous scientific evaluation. Your attendance at relevant cancer conferences will support ongoing knowledge building, networking, and identification of new therapeutic opportunities. Every role at CRH is united by a single mission: beating cancer sooner. We carry out work that matters-impacting patients, families, and the future of science. About Cancer Research Horizons As the world's biggest medical research charity, we've helped bring eleven new cancer drugs to market. However, there is still an urgent need to bring more effective treatments to patients faster. We have recently developed a new approach to driving therapeutic innovation through the creation of Cancer Research Horizons (CRH). We have brought together Cancer Research UK's established drug discovery teams under one organisation and leadership team, combining our unique pipeline of cancer biology expertise and access to CRUK's world-class academic network, cutting edge technology platforms and clinical expertise to 1) Bring new treatments to patients faster and 2) Tackle the biggest challenges in discovering cancer drugs by seeking out more radical ideas and embracing risk in our bid to achieve success. Based at sites in Cambridge, the CRUK Scotland Institute in Glasgow, and Newcastle University, you'll be joining over 200 staff from both industrial and academic backgrounds, all dedicated to bringing forward the day we cure cancer. What will you be doing? Development of multiple new opportunities/ from concept review, through to evaluation and de-risk to a decision point on drug discovery portfolio entry (in collaboration with key drug discovery stakeholders). Lead on the development and delivery of workplans to agreed inflection points. Act as a primary point of contact between academic collaborators and CRH-TI within Portfolio Generation space as required. Assist the triage of Therapeutic Catalyst expressions of interest and the development of full proposals. Lead multiple Therapeutic catalyst projects to required/approved endpoints including option to accelerate via additional TI support. Matrix manage drug discovery activities and interactions with PIs in conjunction with key drug discovery stakeholders (Target Validation and Project Enabling leads). Make strategic recommendations to relevant review groups/leadership teams. What are we looking for? PhD or equivalent experience in relevant cancer field. Significant experience of early drug target discovery and the evaluation process (target selection, validation, technical feasibility etc), preferentially developed in a drug discovery environment. Previous experience of working with PI's and helping to deliver early translation projects in cancer discovery Excellent interpersonal skills with the ability to network and build strong working relationships. Strong scientific and strategic understanding of what it takes to drive exciting opportunities towards future drug discovery starts (biology and early drug discovery). An appreciation of the use of preclinical cancer models to support therapeutic discovery. Proven ability to contribute at a technical level to multiple programmes simultaneously. Evidence of strategic thinking and an ability to develop project plans. Collaborative team player, but also a highly self-motivated individual able to prioritise and manage time effectively with the highest levels of quality, productivity, and urgency in delivery. Maintenance of the highest standards of records, data and documentation. Ability to conceive and manage workplans across teams aimed at de-risking a therapeutic opportunity area progressing to drug discovery start decision points. Ability to embed across multiple scientific areas and act as a credible lead: Flexible, unafraid of failure, able to focus on the key experiments, comfortable with ambiguity and making judgement calls. Our organisation values are designed to guide all that we do. Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human : Act to have a positive impact on people Together: Act inclusively and collaboratively We're looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer. If you're interested in applying and excited about working with us but are unsure if you have the right skills and experience, we'd still love to hear from you. What will I gain? We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals. You can explore our benefits by visiting our careers web page. How do I apply? We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively. For more information on this career opportunity please visit our website or contact us. For more updates on our work and careers, follow us on: Linked In, Facebook, Instagram, X and YouTube.
Are you ready to lead the introduction of new drug substance manufacturing technologies that move breakthrough molecules into early clinical studies? Do you see yourself setting the standards that enable safe, compliant scale up while accelerating material to patients who need it most? This role sits at the heart of our Large Scale Lab in Macclesfield, where innovative science meets disciplined manufacturing to deliver clinical trial supply with precision and pace. You will join our Early Chemical Development team, working across a diverse portfolio of small molecules and emerging modalities. As a scientific leader in our Specials and Production section, you will establish and continuously improve the business processes that enable New Product Introduction and GMP operations at scale. Your impact will be tangible: every robust process you design, every training you deliver, and every technology you implement will help transform promising science into real world medicines. In this role, you will collaborate closely with analytical, process chemistry, engineering, and quality experts, as well as external partners and regulators. You will be empowered to think differently, bring forward new ways of working, and champion the adoption of novel technologies that increase speed, compliance, and reliability across our manufacturing capability. Accountabilities Manufacturing Technology Enablement: Establish and refine new manufacturing technologies within the Large Scale Lab to deliver high quality drug substance for early clinical studies, ensuring rapid and reliable supply. Process Ownership and Compliance: Maintain end to end oversight of core business processes (New Product Introduction, Materials Management, Production Standards, Cleaning, Process Risk Assessments) so that operations remain safe, efficient, and compliant. Documentation and Controls: Own the documentation and procedures that define and control manufacturing (batch records, product labels, waste labels), ensuring clarity, traceability, and audit readiness. SHE and GMP Leadership: Ensure all Safety, Health & Environment and GMP assessments are completed with actions implemented before execution; uphold and improve standards through visible leadership in the manufacturing asset. Training and Coaching: Promote, train, coach, and mentor colleagues on business processes and best practices, building capability and consistency across teams. Regulatory Engagement: Contribute as a Subject Matter Expert during internal and external regulatory inspections, demonstrating control, compliance, and continuous improvement. Technology Scouting and Adoption: Seek out, evaluate, and implement new technologies and novel product platforms; track and interpret evolving regulations and industry trends to future prove our capabilities. Cross Functional Collaboration: Partner with process chemistry, engineering, analytical sciences, and quality to integrate development learnings into scalable, GMP ready processes; align delivery to project timelines and scientific rigor. Continuous Improvement: Use risk based thinking and operational insights to optimise throughput, reduce variability, and enhance right first time performance across clinical manufacturing. Essential Skills/Experience Minimum BSc/BEng level education in a relevant discipline (for example Chemistry, or Chemical Engineering,) and a significant number of years' experience working within a CMC development and/or manufacturing organisation. Significant experience within a pharmaceutical drug substance or fine chemical manufacturing organisation. The role holder should have a thorough working knowledge of the pharmaceutical industry to ensure that industry standards are applied, as well as possess an understanding of other relevant developments in Industry. A strong understanding and practical experience of the principles and management of SHE and cGMP. Experience of technical supervision, coaching and mentoring or leading teams of people on scientific projects. Strong stakeholder management, collaboration and prioritisation skills. Excellent communication and strategic influencing skills across interfaces of discipline, culture and diverse individuals within our exciting department. Desirable Skills/Experience Demonstrated strong scientific leadership. Ability to analyse and interpret complex situations and provide clear strategic direction. Experience GMP Drug Substance Manufacturing for Early Clinical Study supply. Ability to think and operate across functional boundaries, challenge the status quo and seek opportunities for business improvement. Proven problem solver with in depth technical skills. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life changing medicines. In person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Join a company where curiosity meets action and science meets delivery. Here, you will collaborate with talented people across disciplines and with external partners, leveraging modern digital, data and automation tools to solve complex manufacturing challenges that directly impact patients. We bring unexpected teams together to spark ideas, value kindness alongside ambition, and back bold thinking with the resources to make it real. Your leadership in our Macclesfield campus will help turn rigorous chemistry and engineering into reliable clinical supply-advancing medicines that can change lives worldwide. Date Posted 02-Mar-2026 Closing Date 16-Mar-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.
Mar 04, 2026
Full time
Are you ready to lead the introduction of new drug substance manufacturing technologies that move breakthrough molecules into early clinical studies? Do you see yourself setting the standards that enable safe, compliant scale up while accelerating material to patients who need it most? This role sits at the heart of our Large Scale Lab in Macclesfield, where innovative science meets disciplined manufacturing to deliver clinical trial supply with precision and pace. You will join our Early Chemical Development team, working across a diverse portfolio of small molecules and emerging modalities. As a scientific leader in our Specials and Production section, you will establish and continuously improve the business processes that enable New Product Introduction and GMP operations at scale. Your impact will be tangible: every robust process you design, every training you deliver, and every technology you implement will help transform promising science into real world medicines. In this role, you will collaborate closely with analytical, process chemistry, engineering, and quality experts, as well as external partners and regulators. You will be empowered to think differently, bring forward new ways of working, and champion the adoption of novel technologies that increase speed, compliance, and reliability across our manufacturing capability. Accountabilities Manufacturing Technology Enablement: Establish and refine new manufacturing technologies within the Large Scale Lab to deliver high quality drug substance for early clinical studies, ensuring rapid and reliable supply. Process Ownership and Compliance: Maintain end to end oversight of core business processes (New Product Introduction, Materials Management, Production Standards, Cleaning, Process Risk Assessments) so that operations remain safe, efficient, and compliant. Documentation and Controls: Own the documentation and procedures that define and control manufacturing (batch records, product labels, waste labels), ensuring clarity, traceability, and audit readiness. SHE and GMP Leadership: Ensure all Safety, Health & Environment and GMP assessments are completed with actions implemented before execution; uphold and improve standards through visible leadership in the manufacturing asset. Training and Coaching: Promote, train, coach, and mentor colleagues on business processes and best practices, building capability and consistency across teams. Regulatory Engagement: Contribute as a Subject Matter Expert during internal and external regulatory inspections, demonstrating control, compliance, and continuous improvement. Technology Scouting and Adoption: Seek out, evaluate, and implement new technologies and novel product platforms; track and interpret evolving regulations and industry trends to future prove our capabilities. Cross Functional Collaboration: Partner with process chemistry, engineering, analytical sciences, and quality to integrate development learnings into scalable, GMP ready processes; align delivery to project timelines and scientific rigor. Continuous Improvement: Use risk based thinking and operational insights to optimise throughput, reduce variability, and enhance right first time performance across clinical manufacturing. Essential Skills/Experience Minimum BSc/BEng level education in a relevant discipline (for example Chemistry, or Chemical Engineering,) and a significant number of years' experience working within a CMC development and/or manufacturing organisation. Significant experience within a pharmaceutical drug substance or fine chemical manufacturing organisation. The role holder should have a thorough working knowledge of the pharmaceutical industry to ensure that industry standards are applied, as well as possess an understanding of other relevant developments in Industry. A strong understanding and practical experience of the principles and management of SHE and cGMP. Experience of technical supervision, coaching and mentoring or leading teams of people on scientific projects. Strong stakeholder management, collaboration and prioritisation skills. Excellent communication and strategic influencing skills across interfaces of discipline, culture and diverse individuals within our exciting department. Desirable Skills/Experience Demonstrated strong scientific leadership. Ability to analyse and interpret complex situations and provide clear strategic direction. Experience GMP Drug Substance Manufacturing for Early Clinical Study supply. Ability to think and operate across functional boundaries, challenge the status quo and seek opportunities for business improvement. Proven problem solver with in depth technical skills. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life changing medicines. In person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Join a company where curiosity meets action and science meets delivery. Here, you will collaborate with talented people across disciplines and with external partners, leveraging modern digital, data and automation tools to solve complex manufacturing challenges that directly impact patients. We bring unexpected teams together to spark ideas, value kindness alongside ambition, and back bold thinking with the resources to make it real. Your leadership in our Macclesfield campus will help turn rigorous chemistry and engineering into reliable clinical supply-advancing medicines that can change lives worldwide. Date Posted 02-Mar-2026 Closing Date 16-Mar-2026 Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.
Cambridge University Press & Assessment
Cambridge, Cambridgeshire
Job Title:Principal Data Scientist Salary: £74,200 - £99,250 Location: Cambridge/Hybrid with 2 day per week at the office Contract: Permanent Hours: Full time 35 hours per week Are you excited by the challenge of applying data science and AI to problems that genuinely matter? At Cambridge Assessment, we are transforming how assessments are designed, delivered and marked worldwide. As a Principal Data Scientist, you will play a pivotal role at the heart of this transformation - leading our data science capability for AI-enabled assessment products used by millions of learners globally. We are Cambridge University Press & Assessment, a world-leading academic publisher and assessment organisation and a proud part of the University of Cambridge. This is a senior, influential role where you will combine deep technical expertise with strategic leadership. You will shape our data strategy, lead and mentor a growing team, and work closely with researchers, engineers and product teams to turn complex data into insight, innovation and trusted solutions. About the role As Principal Data Scientist, you will lead the operational data science and analytics capability within our Assessment & Research Capabilities (ARC) function. You will be the data leader for automarking, representing ARC's data capability across Exam Technology and the wider organisation. You will: Set the direction for data science and analytics supporting automarking and AI-driven assessment Lead and grow a small, high-impact team of data scientists and engineers Curate high-quality data products used across research, machine learning and product teams Act as a trusted partner to senior stakeholders, influencing product and research decisions with evidence and insight Ensure sensitive exam and candidate data is handled responsibly and ethically Additional responsibilities and accountabilities include: Lead data science, data engineering and analytics activities within ARC Define and own the data strategy for automarking and related AI capabilities Design and oversee data warehouses, pipelines and integrations with the wider organisation Translate complex business and research needs into robust data solutions Provide expert input into product, research and architectural decisions, up to board level Build strong relationships with internal teams and external research partners Champion best practice in data quality, DataOps and analytics engineering This position has been classified as a hybrid role, requiring the selected candidate to typically spend 40-60% of their time collaborating and connecting face-to-face at their dedicated location. Aside from our hybrid principles, other flexible working requests will be considered from the first day of employment, including other work arrangements should you require adjustments due to a disability or long-term health condition. About You To be successful in this role, you will bring: Extensive experience in data science, analytics or analytics engineering in a complex environment Advanced SQL skills, including writing, analysing and optimising large analytical queries Strong experience with a data science programming language such as Python, R or Julia Hands-on experience with data transformation tools such as dbt, Dataform or SQLMesh Experience using BI and visualisation tools such as Metabase, Looker, Tableau or Power BI A strong understanding of data warehousing principles (e.g. Kimball methodology) Experience designing data models that enable self-service analytics Proven ability to translate business or research questions into data-driven insights Experience communicating complex technical concepts to non-technical and senior audiences Leadership experience, including mentoring and guiding other data professionals If you meet the above minimum requirements, we encourage you to apply. Your application will be even stronger if you can also demonstrate the following desirable criteria: Machine learning or AI product experience Exposure to automarking, assessment, or high-stakes data environments Skills in experimentation and statistical analysis (A/B testing, forecasting) Familiarity with DataOps (CI/CD, testing, orchestration, observability) For a detailed job description, please refer to the link at the bottom of the advert on our careers site. We are a Disability Confident (DC) employer that is committed to equality and inclusion ensuring our recruitment process is accessible to all. The DC scheme's Offer of an Interview commitment applies to applicants who opt in, and disclose a disability or a long-term health condition, and best meet the minimum criteria for the role. In instances where interviewing all qualifying candidates is not practicable, we prioritise those who best meet the minimum criteria, as we would for applicants who do not have a disability or long-term health condition. Cambridge University Press & Assessment is an approved UK employer for the sponsorship of eligible roles and applicants under the Skilled Worker visa route. Please refer to the gov.uk website for guidance to understand your own eligibility based on the role you are applying for. Rewards and benefits We will support you to be at your best in work and to live well outside of it. In addition to competitive salaries, we offer a world-class, flexible rewards package , featuring family-friendly and planet-friendly benefits including: 28 days annual leave plus bank holidays Private medical and Permanent Health Insurance Discretionary annual bonus Group personal pension scheme Life assurance up to 4 x annual salary Green travel schemes Ready to pursue your potential? Apply now. We aim to support candidates by making our interview process clear and transparent. The closing date for all applications will be 13 th March We will review applications on an ongoing basis, and shortlisted candidates can expect interviews to take place shortly after it closes. As part of the application process, you can expect: At application stage: four technical questions to answer when submitting your CV. Stage 1: 30-minute screening call with the hiring manager. Stage 2: 60-minute session includes questions about key skills as well as a code review or whiteboard exercise. Stage 3: 90-minute system design exercise with an assignment provided at least three days before the interview. During the interview, is where the designs are explained and discussed. Stage 4: Leadership and cultural 45-minute interview. If you require any reasonable adjustments during the recruitment process due to a disability or a long-term health condition, there will be an opportunity for you to inform us via the online application form. We will do our best to accommodate your needs. Please note that successful applicants will be subject to satisfactory background checks including DBS due to working in a regulated industry. We are committed to an equitable recruitment process. As such, applications must be submitted via our official online application procedure. Please refrain from sending your CV directly to our recruiters. If you experience technical difficulties or require additional support with submitting your online application, contact the Recruiter. Why join us Joining us is your opportunity to pursue potential. You will belong to a collaborative team that is exploring new and better ways to serve students, teachers and researchers across the globe - for the benefit of individuals, society and the world. Sharing our mission will inspire your own growth, development and progress, in an environment which embraces difference, change and aspiration. Cambridge University Press & Assessment is committed to being a place where anyone can enjoy a successful career, where it is safe to speak up, and where we learn continuously to improve together. We welcome applications from all candidates, regardless of demographic characteristics (age, disability, educational attainment, ethnicity, gender, marital status, neurodiversity, religion, sex, gender identity and sexual identity), cultural, or social class/background. We believe better outcomes come through diversity of thought, background and approach. We welcome applications from people from all backgrounds and communities, actively seeking to employ people from a wide range of different communities. Documents Principal Data Scientist.pdf (400.92 KB)
Mar 03, 2026
Full time
Job Title:Principal Data Scientist Salary: £74,200 - £99,250 Location: Cambridge/Hybrid with 2 day per week at the office Contract: Permanent Hours: Full time 35 hours per week Are you excited by the challenge of applying data science and AI to problems that genuinely matter? At Cambridge Assessment, we are transforming how assessments are designed, delivered and marked worldwide. As a Principal Data Scientist, you will play a pivotal role at the heart of this transformation - leading our data science capability for AI-enabled assessment products used by millions of learners globally. We are Cambridge University Press & Assessment, a world-leading academic publisher and assessment organisation and a proud part of the University of Cambridge. This is a senior, influential role where you will combine deep technical expertise with strategic leadership. You will shape our data strategy, lead and mentor a growing team, and work closely with researchers, engineers and product teams to turn complex data into insight, innovation and trusted solutions. About the role As Principal Data Scientist, you will lead the operational data science and analytics capability within our Assessment & Research Capabilities (ARC) function. You will be the data leader for automarking, representing ARC's data capability across Exam Technology and the wider organisation. You will: Set the direction for data science and analytics supporting automarking and AI-driven assessment Lead and grow a small, high-impact team of data scientists and engineers Curate high-quality data products used across research, machine learning and product teams Act as a trusted partner to senior stakeholders, influencing product and research decisions with evidence and insight Ensure sensitive exam and candidate data is handled responsibly and ethically Additional responsibilities and accountabilities include: Lead data science, data engineering and analytics activities within ARC Define and own the data strategy for automarking and related AI capabilities Design and oversee data warehouses, pipelines and integrations with the wider organisation Translate complex business and research needs into robust data solutions Provide expert input into product, research and architectural decisions, up to board level Build strong relationships with internal teams and external research partners Champion best practice in data quality, DataOps and analytics engineering This position has been classified as a hybrid role, requiring the selected candidate to typically spend 40-60% of their time collaborating and connecting face-to-face at their dedicated location. Aside from our hybrid principles, other flexible working requests will be considered from the first day of employment, including other work arrangements should you require adjustments due to a disability or long-term health condition. About You To be successful in this role, you will bring: Extensive experience in data science, analytics or analytics engineering in a complex environment Advanced SQL skills, including writing, analysing and optimising large analytical queries Strong experience with a data science programming language such as Python, R or Julia Hands-on experience with data transformation tools such as dbt, Dataform or SQLMesh Experience using BI and visualisation tools such as Metabase, Looker, Tableau or Power BI A strong understanding of data warehousing principles (e.g. Kimball methodology) Experience designing data models that enable self-service analytics Proven ability to translate business or research questions into data-driven insights Experience communicating complex technical concepts to non-technical and senior audiences Leadership experience, including mentoring and guiding other data professionals If you meet the above minimum requirements, we encourage you to apply. Your application will be even stronger if you can also demonstrate the following desirable criteria: Machine learning or AI product experience Exposure to automarking, assessment, or high-stakes data environments Skills in experimentation and statistical analysis (A/B testing, forecasting) Familiarity with DataOps (CI/CD, testing, orchestration, observability) For a detailed job description, please refer to the link at the bottom of the advert on our careers site. We are a Disability Confident (DC) employer that is committed to equality and inclusion ensuring our recruitment process is accessible to all. The DC scheme's Offer of an Interview commitment applies to applicants who opt in, and disclose a disability or a long-term health condition, and best meet the minimum criteria for the role. In instances where interviewing all qualifying candidates is not practicable, we prioritise those who best meet the minimum criteria, as we would for applicants who do not have a disability or long-term health condition. Cambridge University Press & Assessment is an approved UK employer for the sponsorship of eligible roles and applicants under the Skilled Worker visa route. Please refer to the gov.uk website for guidance to understand your own eligibility based on the role you are applying for. Rewards and benefits We will support you to be at your best in work and to live well outside of it. In addition to competitive salaries, we offer a world-class, flexible rewards package , featuring family-friendly and planet-friendly benefits including: 28 days annual leave plus bank holidays Private medical and Permanent Health Insurance Discretionary annual bonus Group personal pension scheme Life assurance up to 4 x annual salary Green travel schemes Ready to pursue your potential? Apply now. We aim to support candidates by making our interview process clear and transparent. The closing date for all applications will be 13 th March We will review applications on an ongoing basis, and shortlisted candidates can expect interviews to take place shortly after it closes. As part of the application process, you can expect: At application stage: four technical questions to answer when submitting your CV. Stage 1: 30-minute screening call with the hiring manager. Stage 2: 60-minute session includes questions about key skills as well as a code review or whiteboard exercise. Stage 3: 90-minute system design exercise with an assignment provided at least three days before the interview. During the interview, is where the designs are explained and discussed. Stage 4: Leadership and cultural 45-minute interview. If you require any reasonable adjustments during the recruitment process due to a disability or a long-term health condition, there will be an opportunity for you to inform us via the online application form. We will do our best to accommodate your needs. Please note that successful applicants will be subject to satisfactory background checks including DBS due to working in a regulated industry. We are committed to an equitable recruitment process. As such, applications must be submitted via our official online application procedure. Please refrain from sending your CV directly to our recruiters. If you experience technical difficulties or require additional support with submitting your online application, contact the Recruiter. Why join us Joining us is your opportunity to pursue potential. You will belong to a collaborative team that is exploring new and better ways to serve students, teachers and researchers across the globe - for the benefit of individuals, society and the world. Sharing our mission will inspire your own growth, development and progress, in an environment which embraces difference, change and aspiration. Cambridge University Press & Assessment is committed to being a place where anyone can enjoy a successful career, where it is safe to speak up, and where we learn continuously to improve together. We welcome applications from all candidates, regardless of demographic characteristics (age, disability, educational attainment, ethnicity, gender, marital status, neurodiversity, religion, sex, gender identity and sexual identity), cultural, or social class/background. We believe better outcomes come through diversity of thought, background and approach. We welcome applications from people from all backgrounds and communities, actively seeking to employ people from a wide range of different communities. Documents Principal Data Scientist.pdf (400.92 KB)
At QinetiQ, we're not just imagining tomorrow, we are creating it. From cutting edge defence technology to ground breaking innovations, our mission is to empower and protect lives. Join us as a Principal Scientist at our Malvern site, where you will have the opportunity to work with advanced RF sensing and Electronic Warfare technologies alongside some of the brightest minds in the industry. The Role As a Principal Scientist, you will provide technical leadership in radar and electronic warfare, helping to shape the development of next generation sensing systems that operate in complex and contested electromagnetic environments. Day to day, you'll lead and deliver complex research and development projects, guide multi disciplinary teams, work closely with defence customers, and drive innovation in RF sensing, signal processing and system performance. Responsibilities Providing technical leadership across radar and electronic warfare projects Leading research, development and delivery of advanced RF sensing and signal processing solutions Working directly with customers to understand requirements and deliver high impact outcomes Coaching and mentoring engineers and scientists within the team Driving innovation and maintaining high technical standards Supporting business development and future capability growth Essential Experience Deep expertise in radar, electronic warfare or RF sensing systems Strong background in signal processing and electronic surveillance techniques Experience developing and analysing algorithms using MATLAB and/or Python Knowledge of trials, data analysis and system performance assessment Ability to lead complex technical projects and multi disciplinary teams Experience working with defence customers or in regulated, mission critical environments Essential Qualifications Degree in Science or Engineering or a nationally recognised equivalent Significant post graduate industry or research experience (typically 9-12+ years) We value difference and we don't have a fixed idea when it comes to background or education, provided you can show the required level of experience and willingness to learn then we would like to hear from you. This role is 37 hours per week based at Malvern. Hybrid working patterns are available. Travel to other QinetiQ and customer sites will be expected. Malvern The Malvern facility is noted for its work in electronic warfare, surveillance and complex system integration, contributing significantly to the UK's defence capabilities. Developing technologies for military and civilian applications, including sensors, communications and cyber security. Why Join QinetiQ? As we continue to grow into new markets around the world, there's never been a more exciting time to join QinetiQ. The formula for success is our appetite for innovation and having the courage to take on a wide variety of complex challenges. As a QinetiQ employee, you'll experience a unique working environment where teams from different backgrounds, disciplines and experiences enjoy collaborating widely and openly as we undertake this exciting and rewarding journey. Through effective teamwork, and pulling together, you'll get to experience what happens when we all share different perspectives, blend disciplines, and link technologies; constantly discovering new ways of solving complex problems in a diverse and inclusive environment where you can be authentic, feel valued and realise your full potential. Visit our website to read more about our diverse and inclusive workplace culture . Benefits Matched contribution pension scheme, with life assurance Generous holiday allowance, with the option to purchase additional days Options to join Health Cash Plan, Private Medical Insurance and Dental Insurance Employee discount portal: Personal Accident Insurance, Travel Insurance, Restaurants, Cinema Tickets and much more We are proud to support the Armed Forces community by honouring the Armed Forces Covenant and maintaining our Gold Award standard in the Defence Employer Recognition Scheme Volunteering Opportunities - helping charities and local community Recruitment Process We want to make sure that our recruitment process is as inclusive as possible and we aspire to bring out the best in our candidates by creating an environment where everyone feels valued, heard and supported. If you have a disability or health condition that may affect your performance in certain assessment types, please speak to your Recruiter about potential reasonable adjustments. Many roles in QinetiQ are subject to national security vetting being completed, applicants who already hold the appropriate level of vetting may be able to transfer it upon appointment. A number of roles are also subject to additional restrictions, which means factors such as nationality or previous nationalities may affect the roles that you can be employed in. Please note that all applicants for this role must be eligible for SC clearance, as a minimum.
Mar 03, 2026
Full time
At QinetiQ, we're not just imagining tomorrow, we are creating it. From cutting edge defence technology to ground breaking innovations, our mission is to empower and protect lives. Join us as a Principal Scientist at our Malvern site, where you will have the opportunity to work with advanced RF sensing and Electronic Warfare technologies alongside some of the brightest minds in the industry. The Role As a Principal Scientist, you will provide technical leadership in radar and electronic warfare, helping to shape the development of next generation sensing systems that operate in complex and contested electromagnetic environments. Day to day, you'll lead and deliver complex research and development projects, guide multi disciplinary teams, work closely with defence customers, and drive innovation in RF sensing, signal processing and system performance. Responsibilities Providing technical leadership across radar and electronic warfare projects Leading research, development and delivery of advanced RF sensing and signal processing solutions Working directly with customers to understand requirements and deliver high impact outcomes Coaching and mentoring engineers and scientists within the team Driving innovation and maintaining high technical standards Supporting business development and future capability growth Essential Experience Deep expertise in radar, electronic warfare or RF sensing systems Strong background in signal processing and electronic surveillance techniques Experience developing and analysing algorithms using MATLAB and/or Python Knowledge of trials, data analysis and system performance assessment Ability to lead complex technical projects and multi disciplinary teams Experience working with defence customers or in regulated, mission critical environments Essential Qualifications Degree in Science or Engineering or a nationally recognised equivalent Significant post graduate industry or research experience (typically 9-12+ years) We value difference and we don't have a fixed idea when it comes to background or education, provided you can show the required level of experience and willingness to learn then we would like to hear from you. This role is 37 hours per week based at Malvern. Hybrid working patterns are available. Travel to other QinetiQ and customer sites will be expected. Malvern The Malvern facility is noted for its work in electronic warfare, surveillance and complex system integration, contributing significantly to the UK's defence capabilities. Developing technologies for military and civilian applications, including sensors, communications and cyber security. Why Join QinetiQ? As we continue to grow into new markets around the world, there's never been a more exciting time to join QinetiQ. The formula for success is our appetite for innovation and having the courage to take on a wide variety of complex challenges. As a QinetiQ employee, you'll experience a unique working environment where teams from different backgrounds, disciplines and experiences enjoy collaborating widely and openly as we undertake this exciting and rewarding journey. Through effective teamwork, and pulling together, you'll get to experience what happens when we all share different perspectives, blend disciplines, and link technologies; constantly discovering new ways of solving complex problems in a diverse and inclusive environment where you can be authentic, feel valued and realise your full potential. Visit our website to read more about our diverse and inclusive workplace culture . Benefits Matched contribution pension scheme, with life assurance Generous holiday allowance, with the option to purchase additional days Options to join Health Cash Plan, Private Medical Insurance and Dental Insurance Employee discount portal: Personal Accident Insurance, Travel Insurance, Restaurants, Cinema Tickets and much more We are proud to support the Armed Forces community by honouring the Armed Forces Covenant and maintaining our Gold Award standard in the Defence Employer Recognition Scheme Volunteering Opportunities - helping charities and local community Recruitment Process We want to make sure that our recruitment process is as inclusive as possible and we aspire to bring out the best in our candidates by creating an environment where everyone feels valued, heard and supported. If you have a disability or health condition that may affect your performance in certain assessment types, please speak to your Recruiter about potential reasonable adjustments. Many roles in QinetiQ are subject to national security vetting being completed, applicants who already hold the appropriate level of vetting may be able to transfer it upon appointment. A number of roles are also subject to additional restrictions, which means factors such as nationality or previous nationalities may affect the roles that you can be employed in. Please note that all applicants for this role must be eligible for SC clearance, as a minimum.
Senior or Principal Soil Scientist page is loaded Senior or Principal Soil Scientistlocations: GB.Bristol.The Hub: GB.London.Nova Northtime type: Full timeposted on: Posted Todayjob requisition id: R-145181 Job Description OverviewWe have a great opportunity for a dynamic and motivated Senior or Principal Soil Scientist (depending on experience) to join our Sustainable Land and Resource Management team in the UK to support with managing project delivery and driving technical delivery and business development.We are seeking an individual with a strong technical background and experience in the assessment and management of soil and agricultural land quality, with a focus on Agricultural Land Classification (ALC) and sustainable management of soils on infrastructure projects and construction sites. The successful applicant will be an important part of an innovative and technically excellent team of Soil Scientists helping deliver major projects. As a member of our team, you will be involved in a range of office and field-based work, engaging with our experienced staff to deliver excellence to our clients, and will work closely with a wide range of other professionals to deliver holistic solutions to environmental and engineering problems.The Sustainable Land and Resource Practice is a well-established, award winning, multi-disciplinary, environmental and engineering practice with an extensive portfolio of regeneration and development projects and a highly skilled team winning numerous industry awards over the years. The Practice is growing our soil and agricultural land quality service line, and the successful candidate will work on a number of large projects across a range of exciting markets, including the development of Cities, Transportation, Water, Defence and Energy infrastructure. Your Role Lead on the technical delivery of ALC, soil resource surveys and sustainable management of soils. Support and lead on client work development, preparation of proposals and input into bids for multi-disciplinary infrastructure projects. Liaison with clients, stakeholders, regulators, sub-contractors and other internal disciplines. Work effectively as part of a team and with other professionals (environmental scientists, engineers, planners) to provide a consistent and integrated service to our clients. Maintain excellent professional relationships which will lead to and secure repeat business. Compliance with Health and Safety policies and procedures, including preparing and reviewing health and safety plans and managing health and safety on site. Provide technical guidance, constructive support and mentoring to junior staff and supporting their technical development. Developing own competence and maintain CPD necessary to fulfil the responsibilities of the role, with support from the business on own training and development needs. About you Degree qualified in a relevant engineering or science subject (e.g. soil science, geology and environmental science ). Relevant post-graduate experience. Full or Chartered Membership of relevant professional body such as the British Society of Soil Science. If not Chartered, we would expect the candidate, with our support, to become chartered 6 to 12 months after joining. Demonstrate a proven track record of undertaking soil surveys including recording accurate descriptions of soil profiles, undertaking hand texturing, collecting soil samples and interpretating soil chemical and physical analyses. Detailed working knowledge and specialist understanding of ALC including interpretating soil properties and conditions. Working knowledge and demonstrable understanding of the relevant legislation, technical guidance, industry standards and best practice, especially in respect to agricultural soil assessment and the protection and sustainable management of soils. Experienced in preparing and reviewing technical reports ALC assessments, Soil Resources Plans, Soil Handling Management Plans and Aftercare Plans. Experience in writing EIA chapters is desirable but not essential. Demonstrate a proven track record of providing advice on earthworks related sustainable soils management and project management including managing project teams resulting in delivery to high standards. Excellent communication skills and proven ability to manage and mentor staff as well as managing time and work as part of a team as well as individual working. Flexible and prepared to take on new challenges. Full UK driving licence and the ability and willingness to travel throughout the UK and work on short term assignments. Reward & benefitsExplore the rewards and benefits that help you thrive - at every stage of your life and your career. Enjoy competitive salaries, employee rewards and a brilliant range of benefits you can tailor to suit your own health, wellbeing, financial and lifestyle choices. Make the most of a myriad of opportunities for training and professional development to grow your skills and expertise. And combine our hybrid working culture and flexible holiday allowances to balance a great job and fulfilling personal life. About AtkinsRéalisWe're , a world-class engineering services and nuclear organization. We connect people, data and technology to transform the world's infrastructure and energy systems. Together, with our industry partners and clients, and our global team of consultants, designers, engineers and project managers, we can change the world. We're committed to leading our clients across our various end markets to engineer a better future for our planet and its people. Additional information Security clearance This role may require security clearance and offers of employment will be dependent on obtaining the relevant level of clearance. If this is necessary, it will be discussed with you at interview. The vetting process is delivered by United Kingdom Security Vetting (UKSV) and may require candidates to provide proof of residency in the UK of 5 years or longer. If applying to this role please do not make reference to (in conversation) or include in your application or CV, details of any current or previously held security clearance.We are committed to creating a culture where everyone feels that they belong - a place where we can all be ourselves, thrive and develop to be the best we can be. So, we offer a range of family friendly, inclusive employment policies, flexible working arrangements and employee resource groups to support all employees. As an Equal Opportunities Employer, we value applications from all backgrounds, cultures and ability. Worker Type Employee Job Type Regular At AtkinsRéalis , we seek to hire individuals with diverse characteristics, backgrounds and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion or disability, but enriches itself through these differences.
Mar 03, 2026
Full time
Senior or Principal Soil Scientist page is loaded Senior or Principal Soil Scientistlocations: GB.Bristol.The Hub: GB.London.Nova Northtime type: Full timeposted on: Posted Todayjob requisition id: R-145181 Job Description OverviewWe have a great opportunity for a dynamic and motivated Senior or Principal Soil Scientist (depending on experience) to join our Sustainable Land and Resource Management team in the UK to support with managing project delivery and driving technical delivery and business development.We are seeking an individual with a strong technical background and experience in the assessment and management of soil and agricultural land quality, with a focus on Agricultural Land Classification (ALC) and sustainable management of soils on infrastructure projects and construction sites. The successful applicant will be an important part of an innovative and technically excellent team of Soil Scientists helping deliver major projects. As a member of our team, you will be involved in a range of office and field-based work, engaging with our experienced staff to deliver excellence to our clients, and will work closely with a wide range of other professionals to deliver holistic solutions to environmental and engineering problems.The Sustainable Land and Resource Practice is a well-established, award winning, multi-disciplinary, environmental and engineering practice with an extensive portfolio of regeneration and development projects and a highly skilled team winning numerous industry awards over the years. The Practice is growing our soil and agricultural land quality service line, and the successful candidate will work on a number of large projects across a range of exciting markets, including the development of Cities, Transportation, Water, Defence and Energy infrastructure. Your Role Lead on the technical delivery of ALC, soil resource surveys and sustainable management of soils. Support and lead on client work development, preparation of proposals and input into bids for multi-disciplinary infrastructure projects. Liaison with clients, stakeholders, regulators, sub-contractors and other internal disciplines. Work effectively as part of a team and with other professionals (environmental scientists, engineers, planners) to provide a consistent and integrated service to our clients. Maintain excellent professional relationships which will lead to and secure repeat business. Compliance with Health and Safety policies and procedures, including preparing and reviewing health and safety plans and managing health and safety on site. Provide technical guidance, constructive support and mentoring to junior staff and supporting their technical development. Developing own competence and maintain CPD necessary to fulfil the responsibilities of the role, with support from the business on own training and development needs. About you Degree qualified in a relevant engineering or science subject (e.g. soil science, geology and environmental science ). Relevant post-graduate experience. Full or Chartered Membership of relevant professional body such as the British Society of Soil Science. If not Chartered, we would expect the candidate, with our support, to become chartered 6 to 12 months after joining. Demonstrate a proven track record of undertaking soil surveys including recording accurate descriptions of soil profiles, undertaking hand texturing, collecting soil samples and interpretating soil chemical and physical analyses. Detailed working knowledge and specialist understanding of ALC including interpretating soil properties and conditions. Working knowledge and demonstrable understanding of the relevant legislation, technical guidance, industry standards and best practice, especially in respect to agricultural soil assessment and the protection and sustainable management of soils. Experienced in preparing and reviewing technical reports ALC assessments, Soil Resources Plans, Soil Handling Management Plans and Aftercare Plans. Experience in writing EIA chapters is desirable but not essential. Demonstrate a proven track record of providing advice on earthworks related sustainable soils management and project management including managing project teams resulting in delivery to high standards. Excellent communication skills and proven ability to manage and mentor staff as well as managing time and work as part of a team as well as individual working. Flexible and prepared to take on new challenges. Full UK driving licence and the ability and willingness to travel throughout the UK and work on short term assignments. Reward & benefitsExplore the rewards and benefits that help you thrive - at every stage of your life and your career. Enjoy competitive salaries, employee rewards and a brilliant range of benefits you can tailor to suit your own health, wellbeing, financial and lifestyle choices. Make the most of a myriad of opportunities for training and professional development to grow your skills and expertise. And combine our hybrid working culture and flexible holiday allowances to balance a great job and fulfilling personal life. About AtkinsRéalisWe're , a world-class engineering services and nuclear organization. We connect people, data and technology to transform the world's infrastructure and energy systems. Together, with our industry partners and clients, and our global team of consultants, designers, engineers and project managers, we can change the world. We're committed to leading our clients across our various end markets to engineer a better future for our planet and its people. Additional information Security clearance This role may require security clearance and offers of employment will be dependent on obtaining the relevant level of clearance. If this is necessary, it will be discussed with you at interview. The vetting process is delivered by United Kingdom Security Vetting (UKSV) and may require candidates to provide proof of residency in the UK of 5 years or longer. If applying to this role please do not make reference to (in conversation) or include in your application or CV, details of any current or previously held security clearance.We are committed to creating a culture where everyone feels that they belong - a place where we can all be ourselves, thrive and develop to be the best we can be. So, we offer a range of family friendly, inclusive employment policies, flexible working arrangements and employee resource groups to support all employees. As an Equal Opportunities Employer, we value applications from all backgrounds, cultures and ability. Worker Type Employee Job Type Regular At AtkinsRéalis , we seek to hire individuals with diverse characteristics, backgrounds and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion or disability, but enriches itself through these differences.
Principal MSAT Scientist Location: Edinburgh BioQuarter Who are we? We are RoslinCT, a world leading Cell and Gene Therapy Contract Development and Manufacturing Organisation creating cutting edge therapies that change people's lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life changing products utilising ground breaking science. Find out more about what we do here! Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package - we reward our people at the level they deserve. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover - you are automatically covered for three times your basic salary to give you and your family peace of mind. Flexible benefits such as retail discounts and access to the Cycle2Work scheme. Your new role The Principal Manufacturing Science and Technology (MSAT) Scientist will be responsible for providing in depth technical leadership and guidance on the commercial manufacturing of CASGEVY by managing complex changes associated with scale out, life cycle management, right first time and efficient operations with directly reporting to MSAT Manager. You will have direct contact with RoslinCT's client, supporting with long term process improvements and quality investigations. Create realistic, innovative solutions to complex technical and operational challenges, analysing data and presenting recommendations to both senior and executive management. Continuously drive process improvements to embed a right first time culture, ensuring best practices, efficient methodologies, and consistent quality standards are maintained. Support the resource allocation and timeline planning of new projects or demand. Lead, manage, and develop a team of MSAT Scientists and Associate MSAT Scientists, providing mentorship, technical guidance, and performance feedback to build capability and expertise within the team. Work closely with, and facilitate technical support, to wider departments within the business. Collaborate with the Business Development team on client engagement and development of new sales proposals. Ensure that all technical transfer activities are conducted in compliance with GMP, health and safety, and other relevant regulatory standard. About you Prior team leadership experience in a GMP manufacturing environment, preferably within Commercial sterile manufacturing. Working knowledge of cGMP systems and FDA/EU regulations within cell and gene therapy manufacturing. Experience working with stem cells, cellular therapies or cell banking. Exceptional communication skills - working closely with individuals at all levels including RoslinCT employees, stakeholders and suppliers. A desire to support continuous improvement, with a right first time approach. Ability to work under pressure to meet client demands and deadlines. Due to business critical needs, this role will require flexibility on working hours when required. Qualifications A Degree in Life Sciences, or related subject. Next Steps If this sounds like you, then please hit 'Apply' now. We will ask you to upload your CV and complete a short application form detailing why you are interested and why we should hire you. E EO & Accessibility At RoslinCT, we're all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they're valued and encouraged to be themselves, whether they're our employees, customers, or partners. We take pride in being an equal opportunity employer. We treat all applicants fairly and don't discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms. If you've got any specific needs or concerns regarding accessibility during the recruitment process, don't hesitate to reach out to us at . We're here to assist and make things as smooth as possible for you.
Mar 03, 2026
Full time
Principal MSAT Scientist Location: Edinburgh BioQuarter Who are we? We are RoslinCT, a world leading Cell and Gene Therapy Contract Development and Manufacturing Organisation creating cutting edge therapies that change people's lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life changing products utilising ground breaking science. Find out more about what we do here! Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package - we reward our people at the level they deserve. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover - you are automatically covered for three times your basic salary to give you and your family peace of mind. Flexible benefits such as retail discounts and access to the Cycle2Work scheme. Your new role The Principal Manufacturing Science and Technology (MSAT) Scientist will be responsible for providing in depth technical leadership and guidance on the commercial manufacturing of CASGEVY by managing complex changes associated with scale out, life cycle management, right first time and efficient operations with directly reporting to MSAT Manager. You will have direct contact with RoslinCT's client, supporting with long term process improvements and quality investigations. Create realistic, innovative solutions to complex technical and operational challenges, analysing data and presenting recommendations to both senior and executive management. Continuously drive process improvements to embed a right first time culture, ensuring best practices, efficient methodologies, and consistent quality standards are maintained. Support the resource allocation and timeline planning of new projects or demand. Lead, manage, and develop a team of MSAT Scientists and Associate MSAT Scientists, providing mentorship, technical guidance, and performance feedback to build capability and expertise within the team. Work closely with, and facilitate technical support, to wider departments within the business. Collaborate with the Business Development team on client engagement and development of new sales proposals. Ensure that all technical transfer activities are conducted in compliance with GMP, health and safety, and other relevant regulatory standard. About you Prior team leadership experience in a GMP manufacturing environment, preferably within Commercial sterile manufacturing. Working knowledge of cGMP systems and FDA/EU regulations within cell and gene therapy manufacturing. Experience working with stem cells, cellular therapies or cell banking. Exceptional communication skills - working closely with individuals at all levels including RoslinCT employees, stakeholders and suppliers. A desire to support continuous improvement, with a right first time approach. Ability to work under pressure to meet client demands and deadlines. Due to business critical needs, this role will require flexibility on working hours when required. Qualifications A Degree in Life Sciences, or related subject. Next Steps If this sounds like you, then please hit 'Apply' now. We will ask you to upload your CV and complete a short application form detailing why you are interested and why we should hire you. E EO & Accessibility At RoslinCT, we're all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they're valued and encouraged to be themselves, whether they're our employees, customers, or partners. We take pride in being an equal opportunity employer. We treat all applicants fairly and don't discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms. If you've got any specific needs or concerns regarding accessibility during the recruitment process, don't hesitate to reach out to us at . We're here to assist and make things as smooth as possible for you.
Life at UiPath The people at UiPath believes in the transformative power of automation to change how the world works. We're committed to creating category-leading enterprise software that unleashes that power. To make that happen, we need people who is curious, self propelled, generous, and genuine. People who loves being part of a fast moving, fast thinking growth company. And people who cares-about each other, about UiPath, and about our larger purpose. Could that be you? Your mission As a Principal Software Engineering Manager in the UiPath IXP organization, you will shape the technical direction of our intelligent document processing platform and the systems powering AI driven extraction at enterprise scale. You will also directly manage a team of engineers, combining hands on technical leadership with people management responsibility. You will provide technical leadership, architectural vision, and strategic ownership across multiple services - influencing how we design, build, and operate distributed AI systems globally. You will guide the evolution of backend services, real time pipelines, and platform infrastructure supporting specialized and generative AI models. A key part of this role is guiding the technical strategy for applied AI systems - helping the organization decide when to leverage external foundational models versus internally developed or self hosted models, balancing performance, cost, privacy, and long term platform differentiation. What you'll do at UiPath Technical Leadership & Vision Define and drive the long term architectural direction for core backend and platform systems supporting enterprise scale AI workloads. Identify systemic technical risks and opportunities, leading initiatives that improve scalability, reliability, and developer productivity across teams. Establish engineering standards, architectural principles, and best practices adopted across the organization. Partner with product and engineering leadership to translate business strategy into technical execution. AI Strategy & Applied Decision Making Collaborate with research teams to translate experimental models into reliable production systems. Drive architectural decisions around hybrid AI systems combining deterministic logic, classical ML, and generative AI. Define patterns for safe, observable, and scalable model deployment and inference. Ensure AI platform evolution aligns with enterprise customer expectations around security, privacy, and reliability. People Management Directly manage 5-10 engineers, owning their career development, performance reviews, goal setting, and day to day coaching. Foster a high performing, inclusive team culture grounded in psychological safety and engineering excellence. Drive hiring, onboarding, and retention for your team; participate in calibration and compensation planning. Remove blockers, balance workload, and ensure team health alongside delivery commitments. What you'll bring to the team 7+ years designing and operating large scale distributed commercial systems. 2+ years of experience directly managing software engineers, including performance management, career development, and team building. Demonstrated impact beyond a single team, influencing architecture or engineering direction across multiple groups. Deep expertise in backend systems, distributed architectures, concurrency, and performance optimization. Strong experience with cloud ecosystems (Azure, AWS, or GCP) and container orchestration (Docker, Kubernetes, Helm). Proficiency in Python or comparable backend languages; Rust or other systems languages a strong plus. Experience with distributed databases and data platforms (e.g., PostgreSQL, CockroachDB, Elasticsearch). Strong architectural judgment and ability to evaluate trade offs across scale, complexity, and delivery timelines. Excellent communication skills, with the ability to explain complex technical concepts to diverse audiences and coach engineers at varying levels of seniority. Maybe you don't tick all the boxes above-but still think you'd be great for the job? Go ahead, apply anyway. Please. Because we know that experience comes in all shapes and sizes-and passion can't be learned. Many of our roles allow for flexibility in when and where work gets done. Depending on the needs of the business and the role, the number of hybrid, office based, and remote workers will vary from team to team. Applications are assessed on a rolling basis and there is no fixed deadline for this requisition. The application window may change depending on the volume of applications received or may close immediately if a qualified candidate is selected. We value a range of diverse backgrounds, experiences and ideas. We pride ourselves on our diversity and inclusive workplace that provides equal opportunities to all persons regardless of age, race, color, religion, sex, sexual orientation, gender identity, and expression, national origin, disability, neuro diversity, military and/or veteran status, or any other protected classes. Additionally, UiPath provides reasonable accommodations for candidates on request and respects applicants' privacy rights. To review these and other legal disclosures, visit our privacy policy.
Mar 02, 2026
Full time
Life at UiPath The people at UiPath believes in the transformative power of automation to change how the world works. We're committed to creating category-leading enterprise software that unleashes that power. To make that happen, we need people who is curious, self propelled, generous, and genuine. People who loves being part of a fast moving, fast thinking growth company. And people who cares-about each other, about UiPath, and about our larger purpose. Could that be you? Your mission As a Principal Software Engineering Manager in the UiPath IXP organization, you will shape the technical direction of our intelligent document processing platform and the systems powering AI driven extraction at enterprise scale. You will also directly manage a team of engineers, combining hands on technical leadership with people management responsibility. You will provide technical leadership, architectural vision, and strategic ownership across multiple services - influencing how we design, build, and operate distributed AI systems globally. You will guide the evolution of backend services, real time pipelines, and platform infrastructure supporting specialized and generative AI models. A key part of this role is guiding the technical strategy for applied AI systems - helping the organization decide when to leverage external foundational models versus internally developed or self hosted models, balancing performance, cost, privacy, and long term platform differentiation. What you'll do at UiPath Technical Leadership & Vision Define and drive the long term architectural direction for core backend and platform systems supporting enterprise scale AI workloads. Identify systemic technical risks and opportunities, leading initiatives that improve scalability, reliability, and developer productivity across teams. Establish engineering standards, architectural principles, and best practices adopted across the organization. Partner with product and engineering leadership to translate business strategy into technical execution. AI Strategy & Applied Decision Making Collaborate with research teams to translate experimental models into reliable production systems. Drive architectural decisions around hybrid AI systems combining deterministic logic, classical ML, and generative AI. Define patterns for safe, observable, and scalable model deployment and inference. Ensure AI platform evolution aligns with enterprise customer expectations around security, privacy, and reliability. People Management Directly manage 5-10 engineers, owning their career development, performance reviews, goal setting, and day to day coaching. Foster a high performing, inclusive team culture grounded in psychological safety and engineering excellence. Drive hiring, onboarding, and retention for your team; participate in calibration and compensation planning. Remove blockers, balance workload, and ensure team health alongside delivery commitments. What you'll bring to the team 7+ years designing and operating large scale distributed commercial systems. 2+ years of experience directly managing software engineers, including performance management, career development, and team building. Demonstrated impact beyond a single team, influencing architecture or engineering direction across multiple groups. Deep expertise in backend systems, distributed architectures, concurrency, and performance optimization. Strong experience with cloud ecosystems (Azure, AWS, or GCP) and container orchestration (Docker, Kubernetes, Helm). Proficiency in Python or comparable backend languages; Rust or other systems languages a strong plus. Experience with distributed databases and data platforms (e.g., PostgreSQL, CockroachDB, Elasticsearch). Strong architectural judgment and ability to evaluate trade offs across scale, complexity, and delivery timelines. Excellent communication skills, with the ability to explain complex technical concepts to diverse audiences and coach engineers at varying levels of seniority. Maybe you don't tick all the boxes above-but still think you'd be great for the job? Go ahead, apply anyway. Please. Because we know that experience comes in all shapes and sizes-and passion can't be learned. Many of our roles allow for flexibility in when and where work gets done. Depending on the needs of the business and the role, the number of hybrid, office based, and remote workers will vary from team to team. Applications are assessed on a rolling basis and there is no fixed deadline for this requisition. The application window may change depending on the volume of applications received or may close immediately if a qualified candidate is selected. We value a range of diverse backgrounds, experiences and ideas. We pride ourselves on our diversity and inclusive workplace that provides equal opportunities to all persons regardless of age, race, color, religion, sex, sexual orientation, gender identity, and expression, national origin, disability, neuro diversity, military and/or veteran status, or any other protected classes. Additionally, UiPath provides reasonable accommodations for candidates on request and respects applicants' privacy rights. To review these and other legal disclosures, visit our privacy policy.
Cambridge University Press
Cambridge, Cambridgeshire
Job Title: Principal Data Scientist Salary: £74,200 - £99,250 Location: Cambridge/Hybrid with 2 day per week at the office Contract: Permanent Hours: Full time 35 hours per week Are you excited by the challenge of applying data science and AI to problems that genuinely matter? At Cambridge Assessment, we are transforming how assessments are designed, delivered and marked worldwide. As a Principal Data Scientist, you will play a pivotal role at the heart of this transformation - leading our data science capability for AI-enabled assessment products used by millions of learners globally. We are Cambridge University Press & Assessment, a world-leading academic publisher and assessment organisation and a proud part of the University of Cambridge. This is a senior, influential role where you will combine deep technical expertise with strategic leadership. You will shape our data strategy, lead and mentor a growing team, and work closely with researchers, engineers and product teams to turn complex data into insight, innovation and trusted solutions. About the Role As Principal Data Scientist, you will lead the operational data science and analytics capability within our Assessment & Research Capabilities (ARC) function. You will be the data leader for automarking, representing ARC's data capability across Exam Technology and the wider organisation. Set the direction for data science and analytics supporting automarking and AI-driven assessment Lead and grow a small, high-impact team of data scientists and engineers Curate high-quality data products used across research, machine learning and product teams Act as a trusted partner to senior stakeholders, influencing product and research decisions with evidence and insight Ensure sensitive exam and candidate data is handled responsibly and ethically Additional responsibilities and accountabilities Lead data science, data engineering and analytics activities within ARC Define and own the data strategy for automarking and related AI capabilities Design and oversee data warehouses, pipelines and integrations with the wider organisation Translate complex business and research needs into robust data solutions Provide expert input into product, research and architectural decisions, up to board level Build strong relationships with internal teams and external research partners Champion best practice in data quality, DataOps and analytics engineering This position has been classified as a hybrid role, requiring the selected candidate to typically spend 40-60% of their time collaborating and connecting face-to-face at their dedicated location. Aside from our hybrid principles, other flexible working requests will be considered from the first day of employment, including other work arrangements should you require adjustments due to a disability or long-term health condition. About You Extensive experience in data science, analytics or analytics engineering in a complex environment Advanced SQL skills, including writing, analysing and optimising large analytical queries Strong experience with a data science programming language such as Python, R or Julia Hands on experience with data transformation tools such as dbt, Dataform or SQLMesh Experience using BI and visualisation tools such as Metabase, Looker, Tableau or Power BI A strong understanding of data warehousing principles (e.g. Kimball methodology) Experience designing data models that enable self service analytics Proven ability to translate business or research questions into data driven insights Experience communicating complex technical concepts to non technical and senior audiences Leadership experience, including mentoring and guiding other data professionals If you meet the above minimum requirements, we encourage you to apply. Your application will be even stronger if you can also demonstrate the following desirable criteria: Machine learning or AI product experience Exposure to automarking, assessment, or high stakes data environments Skills in experimentation and statistical analysis (A/B testing, forecasting) Familiarity with DataOps (CI/CD, testing, orchestration, observability) For a detailed job description, please refer to the link at the bottom of the advert on our careers site. We are a Disability Confident (DC) employer that is committed to equality and inclusion ensuring our recruitment process is accessible to all. The DC scheme's Offer of an Interview commitment applies to applicants who opt in, and disclose a disability or a long term health condition, and best meet the minimum criteria for the role. In instances where interviewing all qualifying candidates is not practicable, we prioritise those who best meet the minimum criteria, as we would for applicants who do not have a disability or long term health condition. Cambridge University Press & Assessment is an approved UK employer for the sponsorship of eligible roles and applicants under the Skilled Worker visa route. Please refer to the gov.uk website for guidance to understand your own eligibility based on the role you are applying for. Rewards and Benefits We will support you to be at your best in work and to life well outside of it. In addition to competitive salaries, we offer a world class, flexible rewards package, featuring family friendly and planet friendly benefits including: 28 days annual leave plus bank holidays Private medical and Permanent Health Insurance Discretionary annual bonus Group personal pension scheme Life assurance up to 4 x annual salary Green travel schemes Ready to pursue your potential? Apply now. We aim to support candidates by making our interview process clear and transparent. The closing date for all applications will be 13th March. We will review applications on an ongoing basis, and shortlisted candidates can expect interviews to take place shortly after it closes. Application Process At application stage: four technical questions to answer when submitting your CV. Stage 1: 30 minute screening call with the hiring manager. Stage 2: 60 minute session includes questions about key skills as well as a code review or whiteboard exercise. Stage 3: 90 minute system design exercise with an assignment provided at least three days before the interview. During the interview is where the designs are explained and discussed. Stage 4: Leadership and cultural 45 minute interview. If you require any reasonable adjustments during the recruitment process due to a disability or a long term health condition, there will be an opportunity for you to inform us via the online application form. We will do our best to accommodate your needs. Please note that successful applicants will be subject to satisfactory background checks including DBS due to working in a regulated industry. We are committed to an equitable recruitment process. As such, applications must be submitted via our official online application procedure. Please refrain from sending your CV directly to our recruiters. If you experience technical difficulties or require additional support with submitting your online application, contact the Recruiter. Why join us Joining us is your opportunity to pursue potential. You will belong to a collaborative team that is exploring new and better ways to serve students, teachers and researchers across the globe - for the benefit of individuals, society and the world. Sharing our mission will inspire your own growth, development and progress, in an environment which embraces difference, change and aspiration. Cambridge University Press & Assessment is committed to being a place where anyone can enjoy a successful career, where it is safe to speak up, and where we learn continuously to improve together. We welcome applications from all candidates, regardless of demographic characteristics (age, disability, educational attainment, ethnicity, gender, marital status, neurodiversity, religion, sex, gender identity and sexual identity), cultural, or social class/background. We believe better outcomes come through diversity of thought, background and approach. We welcome applications from people from all backgrounds and communities, actively seeking to employ people from a wide range of different communities.
Mar 02, 2026
Full time
Job Title: Principal Data Scientist Salary: £74,200 - £99,250 Location: Cambridge/Hybrid with 2 day per week at the office Contract: Permanent Hours: Full time 35 hours per week Are you excited by the challenge of applying data science and AI to problems that genuinely matter? At Cambridge Assessment, we are transforming how assessments are designed, delivered and marked worldwide. As a Principal Data Scientist, you will play a pivotal role at the heart of this transformation - leading our data science capability for AI-enabled assessment products used by millions of learners globally. We are Cambridge University Press & Assessment, a world-leading academic publisher and assessment organisation and a proud part of the University of Cambridge. This is a senior, influential role where you will combine deep technical expertise with strategic leadership. You will shape our data strategy, lead and mentor a growing team, and work closely with researchers, engineers and product teams to turn complex data into insight, innovation and trusted solutions. About the Role As Principal Data Scientist, you will lead the operational data science and analytics capability within our Assessment & Research Capabilities (ARC) function. You will be the data leader for automarking, representing ARC's data capability across Exam Technology and the wider organisation. Set the direction for data science and analytics supporting automarking and AI-driven assessment Lead and grow a small, high-impact team of data scientists and engineers Curate high-quality data products used across research, machine learning and product teams Act as a trusted partner to senior stakeholders, influencing product and research decisions with evidence and insight Ensure sensitive exam and candidate data is handled responsibly and ethically Additional responsibilities and accountabilities Lead data science, data engineering and analytics activities within ARC Define and own the data strategy for automarking and related AI capabilities Design and oversee data warehouses, pipelines and integrations with the wider organisation Translate complex business and research needs into robust data solutions Provide expert input into product, research and architectural decisions, up to board level Build strong relationships with internal teams and external research partners Champion best practice in data quality, DataOps and analytics engineering This position has been classified as a hybrid role, requiring the selected candidate to typically spend 40-60% of their time collaborating and connecting face-to-face at their dedicated location. Aside from our hybrid principles, other flexible working requests will be considered from the first day of employment, including other work arrangements should you require adjustments due to a disability or long-term health condition. About You Extensive experience in data science, analytics or analytics engineering in a complex environment Advanced SQL skills, including writing, analysing and optimising large analytical queries Strong experience with a data science programming language such as Python, R or Julia Hands on experience with data transformation tools such as dbt, Dataform or SQLMesh Experience using BI and visualisation tools such as Metabase, Looker, Tableau or Power BI A strong understanding of data warehousing principles (e.g. Kimball methodology) Experience designing data models that enable self service analytics Proven ability to translate business or research questions into data driven insights Experience communicating complex technical concepts to non technical and senior audiences Leadership experience, including mentoring and guiding other data professionals If you meet the above minimum requirements, we encourage you to apply. Your application will be even stronger if you can also demonstrate the following desirable criteria: Machine learning or AI product experience Exposure to automarking, assessment, or high stakes data environments Skills in experimentation and statistical analysis (A/B testing, forecasting) Familiarity with DataOps (CI/CD, testing, orchestration, observability) For a detailed job description, please refer to the link at the bottom of the advert on our careers site. We are a Disability Confident (DC) employer that is committed to equality and inclusion ensuring our recruitment process is accessible to all. The DC scheme's Offer of an Interview commitment applies to applicants who opt in, and disclose a disability or a long term health condition, and best meet the minimum criteria for the role. In instances where interviewing all qualifying candidates is not practicable, we prioritise those who best meet the minimum criteria, as we would for applicants who do not have a disability or long term health condition. Cambridge University Press & Assessment is an approved UK employer for the sponsorship of eligible roles and applicants under the Skilled Worker visa route. Please refer to the gov.uk website for guidance to understand your own eligibility based on the role you are applying for. Rewards and Benefits We will support you to be at your best in work and to life well outside of it. In addition to competitive salaries, we offer a world class, flexible rewards package, featuring family friendly and planet friendly benefits including: 28 days annual leave plus bank holidays Private medical and Permanent Health Insurance Discretionary annual bonus Group personal pension scheme Life assurance up to 4 x annual salary Green travel schemes Ready to pursue your potential? Apply now. We aim to support candidates by making our interview process clear and transparent. The closing date for all applications will be 13th March. We will review applications on an ongoing basis, and shortlisted candidates can expect interviews to take place shortly after it closes. Application Process At application stage: four technical questions to answer when submitting your CV. Stage 1: 30 minute screening call with the hiring manager. Stage 2: 60 minute session includes questions about key skills as well as a code review or whiteboard exercise. Stage 3: 90 minute system design exercise with an assignment provided at least three days before the interview. During the interview is where the designs are explained and discussed. Stage 4: Leadership and cultural 45 minute interview. If you require any reasonable adjustments during the recruitment process due to a disability or a long term health condition, there will be an opportunity for you to inform us via the online application form. We will do our best to accommodate your needs. Please note that successful applicants will be subject to satisfactory background checks including DBS due to working in a regulated industry. We are committed to an equitable recruitment process. As such, applications must be submitted via our official online application procedure. Please refrain from sending your CV directly to our recruiters. If you experience technical difficulties or require additional support with submitting your online application, contact the Recruiter. Why join us Joining us is your opportunity to pursue potential. You will belong to a collaborative team that is exploring new and better ways to serve students, teachers and researchers across the globe - for the benefit of individuals, society and the world. Sharing our mission will inspire your own growth, development and progress, in an environment which embraces difference, change and aspiration. Cambridge University Press & Assessment is committed to being a place where anyone can enjoy a successful career, where it is safe to speak up, and where we learn continuously to improve together. We welcome applications from all candidates, regardless of demographic characteristics (age, disability, educational attainment, ethnicity, gender, marital status, neurodiversity, religion, sex, gender identity and sexual identity), cultural, or social class/background. We believe better outcomes come through diversity of thought, background and approach. We welcome applications from people from all backgrounds and communities, actively seeking to employ people from a wide range of different communities.
Overview Job description Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - Stevenage Posted Date: Feb 3 2026 At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together. Position Summary You will lead applied and translational omics analyses that turn complex biological data into clear decisions. You will work with experimental scientists, data engineers, and clinical teams to design analyses and integrate multi-omic and clinical data. We value clear communication, practical problem solving, curiosity, and collaboration. This role offers visible impact, career growth, and aligns with our mission of uniting science, technology and talent to get ahead of disease together. This role will provide you the opportunity to lead key activities to progress your career. These responsibilities include some of the following: Design and run reproducible analyses of genomic, transcriptomic, proteomic and other omics datasets. Integrate multi-omic and clinical data to prioritize targets, nominate biomarkers, and define patient subgroups. Build, validate and productionize analysis pipelines and tools that support cross-functional teams. Communicate results clearly and make practical recommendations to project teams and decision-makers. Collaborate with laboratory and clinical colleagues to design analyses that guide experiments and studies. Ensure data quality, metadata standards, documentation and reproducible research practices. Key Responsibilities: Lead hands-on analysis of large, diverse omics datasets, including bulk and single-cell data. Apply statistical methods, machine learning, and causal inference to answer translational questions. Develop scripts, workflows, and software artifacts that follow reproducible research and FAIR principles. Troubleshoot data issues, perform rigorous quality control and document analysis steps. Mentor junior scientists and contribute to a collaborative and respectful team culture. Monitor new methods and tools and evaluate them for adoption in projects. Impact the GSK drug development pipeline through development and application of innovative computational and statistical approaches to the analysis, integration and interpretation of spatial, single cell and other cutting edge high dimensional multi-omic data. Help drive the evaluation and development, and lead the application, of analytics methods for spatial and single cell omics in the context of clinical studies. Work within or lead cross-functional project teams with GSK scientists and external collaborators, focusing on impacting clinical study and biomarker decisions across respiratory, immunology, infectious disease, neurodegeneration or metabolic disease. Effectively communicate analysis findings and recommendations, with expert interpretation, to project teams. Work with focus and agility to deliver against objectives, demonstrating strong statistical, analytical and critical thinking skills. Additional responsibilities include advancing analytics in spatial and single-cell omics within clinical studies and collaborating across cross-functional teams to support biomarker decisions. Why You? Basic Qualifications: Advanced degree (Master's with relevant experience or PhD preferred) in computational biology, bioinformatics, genetics, biostatistics, or related field. Programming experience in R and/or Python for data analysis and scripting. Experience processing and analyzing large omics datasets, including quality control and normalization. Experience with common genomics file formats and tools (for example VCF, BAM/FASTQ, single-cell data structures). Experience reproducible analyses and use of version control (for example Git). 1+ years of experience with single-cell and spatial omics analysis workflows. Preferred Qualifications: Clear communication skills and experience working in multidisciplinary teams. Experience integrating omics with clinical or real-world data for translational analyses. Experience productionizing pipelines or contributing to shared analysis platforms. Evidence of influencing research through publications or major project contributions. Proven ability to derive and apply novel insights from these and other emerging genomic technologies. Ability to critically evaluate cutting-edge tools and frameworks for single-cell and spatial data analysis, integration, visualization, and interpretation, and their application to clinical development. Proven expertise in statistical modelling, hypothesis testing, and data-driven inference. Expertise in statistical approaches to the identification and assessment of predictive and prognostic biomarkers. Experience with clinical trial data analysis and working in a regulatory environment. Notes: This position requires on-site attendance in accordance with GSK's Performance with Choice policy. Salary and benefits: If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges from $121,275 to $202,125. The US salary ranges take into account factors including location, skills, experience, and market rate. This position offers an annual bonus and eligibility to participate in our share-based long-term incentive program. Available benefits include health care and other insurance benefits, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. Please visit the GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call. If your inquiry does not relate to adjustments, we will not be able to support you through these channels. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, pregnancy, gender identity, or sexual orientation, parental status, national origin, age, disability, or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
Mar 01, 2026
Full time
Overview Job description Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - Stevenage Posted Date: Feb 3 2026 At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together. Position Summary You will lead applied and translational omics analyses that turn complex biological data into clear decisions. You will work with experimental scientists, data engineers, and clinical teams to design analyses and integrate multi-omic and clinical data. We value clear communication, practical problem solving, curiosity, and collaboration. This role offers visible impact, career growth, and aligns with our mission of uniting science, technology and talent to get ahead of disease together. This role will provide you the opportunity to lead key activities to progress your career. These responsibilities include some of the following: Design and run reproducible analyses of genomic, transcriptomic, proteomic and other omics datasets. Integrate multi-omic and clinical data to prioritize targets, nominate biomarkers, and define patient subgroups. Build, validate and productionize analysis pipelines and tools that support cross-functional teams. Communicate results clearly and make practical recommendations to project teams and decision-makers. Collaborate with laboratory and clinical colleagues to design analyses that guide experiments and studies. Ensure data quality, metadata standards, documentation and reproducible research practices. Key Responsibilities: Lead hands-on analysis of large, diverse omics datasets, including bulk and single-cell data. Apply statistical methods, machine learning, and causal inference to answer translational questions. Develop scripts, workflows, and software artifacts that follow reproducible research and FAIR principles. Troubleshoot data issues, perform rigorous quality control and document analysis steps. Mentor junior scientists and contribute to a collaborative and respectful team culture. Monitor new methods and tools and evaluate them for adoption in projects. Impact the GSK drug development pipeline through development and application of innovative computational and statistical approaches to the analysis, integration and interpretation of spatial, single cell and other cutting edge high dimensional multi-omic data. Help drive the evaluation and development, and lead the application, of analytics methods for spatial and single cell omics in the context of clinical studies. Work within or lead cross-functional project teams with GSK scientists and external collaborators, focusing on impacting clinical study and biomarker decisions across respiratory, immunology, infectious disease, neurodegeneration or metabolic disease. Effectively communicate analysis findings and recommendations, with expert interpretation, to project teams. Work with focus and agility to deliver against objectives, demonstrating strong statistical, analytical and critical thinking skills. Additional responsibilities include advancing analytics in spatial and single-cell omics within clinical studies and collaborating across cross-functional teams to support biomarker decisions. Why You? Basic Qualifications: Advanced degree (Master's with relevant experience or PhD preferred) in computational biology, bioinformatics, genetics, biostatistics, or related field. Programming experience in R and/or Python for data analysis and scripting. Experience processing and analyzing large omics datasets, including quality control and normalization. Experience with common genomics file formats and tools (for example VCF, BAM/FASTQ, single-cell data structures). Experience reproducible analyses and use of version control (for example Git). 1+ years of experience with single-cell and spatial omics analysis workflows. Preferred Qualifications: Clear communication skills and experience working in multidisciplinary teams. Experience integrating omics with clinical or real-world data for translational analyses. Experience productionizing pipelines or contributing to shared analysis platforms. Evidence of influencing research through publications or major project contributions. Proven ability to derive and apply novel insights from these and other emerging genomic technologies. Ability to critically evaluate cutting-edge tools and frameworks for single-cell and spatial data analysis, integration, visualization, and interpretation, and their application to clinical development. Proven expertise in statistical modelling, hypothesis testing, and data-driven inference. Expertise in statistical approaches to the identification and assessment of predictive and prognostic biomarkers. Experience with clinical trial data analysis and working in a regulatory environment. Notes: This position requires on-site attendance in accordance with GSK's Performance with Choice policy. Salary and benefits: If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges from $121,275 to $202,125. The US salary ranges take into account factors including location, skills, experience, and market rate. This position offers an annual bonus and eligibility to participate in our share-based long-term incentive program. Available benefits include health care and other insurance benefits, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. Please visit the GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call. If your inquiry does not relate to adjustments, we will not be able to support you through these channels. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, pregnancy, gender identity, or sexual orientation, parental status, national origin, age, disability, or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
A leading biotech company in London is seeking a Senior/Principal Scientist to lead statistical and population genomics efforts. This role involves working with large-scale human genetics data, and applying statistical methodologies to accelerate target identification across various therapeutic areas. Candidates should possess a PhD in relevant fields and experience in statistical genetics. This is a unique opportunity to impact patient outcomes and advance drug discovery through cutting-edge research.
Feb 28, 2026
Full time
A leading biotech company in London is seeking a Senior/Principal Scientist to lead statistical and population genomics efforts. This role involves working with large-scale human genetics data, and applying statistical methodologies to accelerate target identification across various therapeutic areas. Candidates should possess a PhD in relevant fields and experience in statistical genetics. This is a unique opportunity to impact patient outcomes and advance drug discovery through cutting-edge research.
About Relation Relation is an end-to-end biotech company developing transformational medicines, with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life's most devastating diseases. We leverage single-cell multi-omics directly from patient tissue, functional assays, and machine learning to drive disease understanding-from cause to cure. This year, we embarked on an exciting dual collaboration with GSK to tackle fibrosis and osteoarthritis, while also advancing our own internal osteoporosis programme. By combining our cutting edge ML capabilities with GSK's deep expertise in drug discovery, this partnership underscores our commitment to pioneering science and delivering impactful therapies to patients. We are rapidly scaling our technology and discovery teams, offering a unique opportunity to join one of the most innovative TechBio companies. Be part of our dynamic, interdisciplinary teams, collaborating closely to redefine the boundaries of possibility in drug discovery. Our state of the art wet and dry laboratories, located in the heart of London, provide an exceptional environment to foster interdisciplinarity and turn groundbreaking ideas into impactful therapies for patients. We are committed to building diverse and inclusive teams. Relation is an equal opportunities employer and does not discriminate on the grounds of gender, sexual orientation, marital or civil partner status, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability, or age. We cultivate innovation through collaboration, empowering every team member to do their best work and reach their highest potential. By joining Relation, you will become part of an exceptionally talented team with extraordinary leverage to advance the field of drug discovery. Your work will shape our culture, strategic direction, and, most importantly, impact patients' lives. The Opportunity This is a unique opportunity for a Senior/Principal Scientist to lead and shape statistical and population genomics efforts to accelerate target identification and validation across multiple therapeutic areas. You will work with large-scale human genetics resources (e.g. biobanks and population cohorts) and apply cutting edge statistical genetics methodologies to generate actionable insights. As part of the Cross Indication team, you will operate at the interface of human genetics, computational biology, and machine learning, translating genetic evidence into target prioritisation frameworks and mechanistic hypotheses. You will play a key role in developing robust, scalable analysis pipelines and ensuring genetic insights are integrated into decision making across the organisation. Your responsibilities Lead statistical and population genomics analyses using large-scale datasets to support target discovery and validation. Design and implement statistical genetics methodologies for target prioritisation, including approaches leveraging GWAS, fine mapping, colocalisation, polygenic risk, rare variant analyses, and functional annotation. Develop scalable computational workflows for reproducible genetics analysis, enabling robust and efficient delivery across multiple programmes. Integrate human genetics evidence with multi omics datasets (e.g. transcriptomics, proteomics) to uncover disease mechanisms and prioritise actionable targets. Partner closely with experimental, translational, and ML teams to validate hypotheses, interpret findings, and guide downstream decision making. Communicate results clearly and confidently to internal stakeholders, including presenting methods, results, risks/limitations, and recommendations. Contribute to publications, scientific communications, and project documentation, supporting scientific excellence and external visibility. Professionally, you have PhD in statistical genetics, genomics, computational biology, bioinformatics, or a related quantitative field. Post PhD experience, ideally including time in an industry, biotech, or pharmaceutical environment. Deep expertise in statistical genetics and population genomics, including experience with large scale human genetic datasets and post GWAS analyses. High proficiency in Python (preferred) and R, with experience working in high performance computing environments. Ability to operate independently at a senior level, providing technical leadership and driving projects from concept through delivery. Desirable knowledge or experiences Familiarity with single cell transcriptomics or patient derived datasets. Experience working in interdisciplinary teams within biotech or pharma settings. Knowledge of machine learning techniques applied to biological data. Experience with causal inference frameworks (e.g. Mendelian randomisation) to strengthen target validation. Strong understanding of the end to end drug discovery process and how genetic evidence informs decision making. Personally, you are Inclusive leader and team player. Clear communicator. Driven by impact. Humble and hungry to learn. Motivated and curious. Impact driven and passionate about improving patient outcomes. Comfortable working in dynamic, fast paced environments. Join us in this exciting role, where your contributions will directly impact advancing our understanding of genetics and disease risk, supporting our mission to deliver transformative medicines to patients. Together, we're not just conducting research-we're setting new standards in the fields of machine learning and genetics. The patient is waiting! Relation is a committed equal opportunities employer. RECRUITMENT AGENCIES: Please note that Relation does not accept unsolicited resumes from agencies. Resumes should not be forwarded to our job aliases or employees. Relation will not be liable for any fees associated with unsolicited CVs.
Feb 28, 2026
Full time
About Relation Relation is an end-to-end biotech company developing transformational medicines, with technology at our core. Our ambition is to understand human biology in unprecedented ways, discovering therapies to treat some of life's most devastating diseases. We leverage single-cell multi-omics directly from patient tissue, functional assays, and machine learning to drive disease understanding-from cause to cure. This year, we embarked on an exciting dual collaboration with GSK to tackle fibrosis and osteoarthritis, while also advancing our own internal osteoporosis programme. By combining our cutting edge ML capabilities with GSK's deep expertise in drug discovery, this partnership underscores our commitment to pioneering science and delivering impactful therapies to patients. We are rapidly scaling our technology and discovery teams, offering a unique opportunity to join one of the most innovative TechBio companies. Be part of our dynamic, interdisciplinary teams, collaborating closely to redefine the boundaries of possibility in drug discovery. Our state of the art wet and dry laboratories, located in the heart of London, provide an exceptional environment to foster interdisciplinarity and turn groundbreaking ideas into impactful therapies for patients. We are committed to building diverse and inclusive teams. Relation is an equal opportunities employer and does not discriminate on the grounds of gender, sexual orientation, marital or civil partner status, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability, or age. We cultivate innovation through collaboration, empowering every team member to do their best work and reach their highest potential. By joining Relation, you will become part of an exceptionally talented team with extraordinary leverage to advance the field of drug discovery. Your work will shape our culture, strategic direction, and, most importantly, impact patients' lives. The Opportunity This is a unique opportunity for a Senior/Principal Scientist to lead and shape statistical and population genomics efforts to accelerate target identification and validation across multiple therapeutic areas. You will work with large-scale human genetics resources (e.g. biobanks and population cohorts) and apply cutting edge statistical genetics methodologies to generate actionable insights. As part of the Cross Indication team, you will operate at the interface of human genetics, computational biology, and machine learning, translating genetic evidence into target prioritisation frameworks and mechanistic hypotheses. You will play a key role in developing robust, scalable analysis pipelines and ensuring genetic insights are integrated into decision making across the organisation. Your responsibilities Lead statistical and population genomics analyses using large-scale datasets to support target discovery and validation. Design and implement statistical genetics methodologies for target prioritisation, including approaches leveraging GWAS, fine mapping, colocalisation, polygenic risk, rare variant analyses, and functional annotation. Develop scalable computational workflows for reproducible genetics analysis, enabling robust and efficient delivery across multiple programmes. Integrate human genetics evidence with multi omics datasets (e.g. transcriptomics, proteomics) to uncover disease mechanisms and prioritise actionable targets. Partner closely with experimental, translational, and ML teams to validate hypotheses, interpret findings, and guide downstream decision making. Communicate results clearly and confidently to internal stakeholders, including presenting methods, results, risks/limitations, and recommendations. Contribute to publications, scientific communications, and project documentation, supporting scientific excellence and external visibility. Professionally, you have PhD in statistical genetics, genomics, computational biology, bioinformatics, or a related quantitative field. Post PhD experience, ideally including time in an industry, biotech, or pharmaceutical environment. Deep expertise in statistical genetics and population genomics, including experience with large scale human genetic datasets and post GWAS analyses. High proficiency in Python (preferred) and R, with experience working in high performance computing environments. Ability to operate independently at a senior level, providing technical leadership and driving projects from concept through delivery. Desirable knowledge or experiences Familiarity with single cell transcriptomics or patient derived datasets. Experience working in interdisciplinary teams within biotech or pharma settings. Knowledge of machine learning techniques applied to biological data. Experience with causal inference frameworks (e.g. Mendelian randomisation) to strengthen target validation. Strong understanding of the end to end drug discovery process and how genetic evidence informs decision making. Personally, you are Inclusive leader and team player. Clear communicator. Driven by impact. Humble and hungry to learn. Motivated and curious. Impact driven and passionate about improving patient outcomes. Comfortable working in dynamic, fast paced environments. Join us in this exciting role, where your contributions will directly impact advancing our understanding of genetics and disease risk, supporting our mission to deliver transformative medicines to patients. Together, we're not just conducting research-we're setting new standards in the fields of machine learning and genetics. The patient is waiting! Relation is a committed equal opportunities employer. RECRUITMENT AGENCIES: Please note that Relation does not accept unsolicited resumes from agencies. Resumes should not be forwarded to our job aliases or employees. Relation will not be liable for any fees associated with unsolicited CVs.
Job Description Site Name: UK - Hertfordshire - Stevenage Posted Date: Feb We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK GSK. Principal Scientist, Genomic Translational Research In this role you will: Create protocols and perform the sample processing for genomic experiments (e.g. RNAseq, WES, scRNAseq). Prepare samples and libraries for sequencing. Run flow cytometry and FACS sorting experiments. Develop immunogenicity assays for product validation. Offer technical expertise and support to other team members, helping them troubleshoot and optimize their experimental protocols. Solve technical issues operate as part of a cross functional project team. Collaborate with King's College London scientists within the GSK KCL Translational Oncology Research Hub, an exclusive research collaboration between GSK and the Comprehensive Cancer Centre at KCL. Basic Qualifications & Skills We are looking for professionals with these required skills to achieve our goals: PhD (or equivalent experience) in Cancer Biology, Genomics, Immunology, or related field, with extensive experience in cancer genomics. Expertise with NGS, flow cytometry, single cell RNA sequencing and library preparation. Strong background in developing and applying cutting edge genomic technologies to study cancer biology. Strong understanding of immunology and cancer biology, including T cell biology and the molecular mechanisms underlying tumorigenesis and cancer progression. Ability to communicate with team members from different backgrounds by training/discipline, as well as senior members of the GSK stakeholders/research partner units. Ability to deliver high quality, consistent results in a timely fashion with a positive can do and result oriented attitude. Preferred Qualifications & Skills Please note the following skills are not necessary, just preferred, if you do not have them, please still apply: A track record of scientific publication. Experience in collaboration with biopharma. Strong strategic thinking and problem solving skills, with the ability to navigate complex scientific and business challenges. Experience in analysis of major next generation sequencing (sc TCR) techniques and generation of insights from such data. Closing Date for Applications: 9th March 2026 Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Feb 28, 2026
Full time
Job Description Site Name: UK - Hertfordshire - Stevenage Posted Date: Feb We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. Discover more about our company wide benefits and life at GSK on our webpage Life at GSK GSK. Principal Scientist, Genomic Translational Research In this role you will: Create protocols and perform the sample processing for genomic experiments (e.g. RNAseq, WES, scRNAseq). Prepare samples and libraries for sequencing. Run flow cytometry and FACS sorting experiments. Develop immunogenicity assays for product validation. Offer technical expertise and support to other team members, helping them troubleshoot and optimize their experimental protocols. Solve technical issues operate as part of a cross functional project team. Collaborate with King's College London scientists within the GSK KCL Translational Oncology Research Hub, an exclusive research collaboration between GSK and the Comprehensive Cancer Centre at KCL. Basic Qualifications & Skills We are looking for professionals with these required skills to achieve our goals: PhD (or equivalent experience) in Cancer Biology, Genomics, Immunology, or related field, with extensive experience in cancer genomics. Expertise with NGS, flow cytometry, single cell RNA sequencing and library preparation. Strong background in developing and applying cutting edge genomic technologies to study cancer biology. Strong understanding of immunology and cancer biology, including T cell biology and the molecular mechanisms underlying tumorigenesis and cancer progression. Ability to communicate with team members from different backgrounds by training/discipline, as well as senior members of the GSK stakeholders/research partner units. Ability to deliver high quality, consistent results in a timely fashion with a positive can do and result oriented attitude. Preferred Qualifications & Skills Please note the following skills are not necessary, just preferred, if you do not have them, please still apply: A track record of scientific publication. Experience in collaboration with biopharma. Strong strategic thinking and problem solving skills, with the ability to navigate complex scientific and business challenges. Experience in analysis of major next generation sequencing (sc TCR) techniques and generation of insights from such data. Closing Date for Applications: 9th March 2026 Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Job Title: Senior AI Scientist - Hit Discovery and Protein Sciences Location: Cambridge, UK Competitive salary and benefits Introduction to the role: Are you acuriousDataand AIScientist seeking a role where yourexpertisecan make an extraordinary impact? This is an opportunity to join a dynamic and enthusiastic environment and transform the way we discoverhitsand protein reagentsin drug discovery. Diverse Minds. Bold Disruptors. Meaningful Impactthrough Partnership. At AstraZenecawe'rededicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.There'sno better place to make a difference to medicine,patientsand society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning,growthand development. Join a place built on innovation and creativity. We harness digital, data science & AI to fast-forward our research. Your scientific vision would ensure that new small moleculesand peptidesdiscovered usingyour skillsandinpartnershipwith our technical platformscan serve as the seeds for future medicines and make a real difference in our mission to help patients. You will be basedin early drug discovery R&DwithinData Sciences & Quantitative Biologydepartmentin Discovery Sciencesand will work closely with our colleagues in the Hit Discoveryand Protein Sciencesdepartments.To learn more about our department and culture watch this video: A Life-changing day - Meet our Quantitative Biology team at AstraZeneca. What you will do You will develop data science, computational and AI solutions to enable the discovery of hits (small molecules and peptides) and protein reagents enhancing the output from our hit and ledatageneration platforms. This will involve close collaboration with screening scientists, chemists, biologists, informaticians and statisticians. Wetruly believethat everyone hasan important rolein drug discoveryandeach individualbringsaunique set of competencies. Your curiosity and passion for personal development combined with support from colleagues and leaders, will ensure you maximise your potential and contribution, building from your current skills and experience. Essential requirements: Our team is a highly collaborative group of scientists, working in an evolving technical and scientific landscape. Therefore, you will be comfortable workingin a dynamic and team-focussedenvironment. Critical will be tohave effective communication skills and a proactive and delivery-focused approach. Aligned to Hit Discoveryand Protein Sciencesactivities, you will bring analytical skills,innovationand your strategic mindsetto this excitingand evolvingarea. A PhD or equivalent numbers of years in industry/academia in bioinformatics, cheminformatics, computer science, AI/ML, statistics or related computational and data science subject areas applied to chemistry, biology or medicine. Experience in data science, AI/ML and/or modelling methods applied to the analysis of highly multidimensional or unstructured datasets in molecular, drug discovery or biomedical contexts. Programming in Python, R and/or Shell, and experience with querying and integrating data from disparate sources (e.g. SQL, NoSQL, Graph or file-based approaches). Experience in developing computational workflows applied to the analysis of experimental or AI-generated data (e.g. Nextflow or Snakemake), knowledge of version control systems (e.g. Git and GitHub) and high-performance computing infrastructure. Experiencereporting data analysis results, drawing conclusions and defining recommended actions in interdisciplinary and collaborative environments. Desirables: Experience in AI/ML and/or physics-based mathematical modelling methods applied to peptides, small molecules and/or proteins. Experience in data analysis of high-throughput assays (peptides /small molecule screens, virtual or high content screening, chemical profiling, mass spectrometry, recombinant protein expression and/or omics). Experience in developing software and packages. Track record of publishing relevant research as preprints, peer-reviewed journals, conferences, and other scientific proceedings. Ability to collaborate and build consensus across cross-functional teams. Ability to identify opportunities and synergies across projects. Experience in communicating chemistry and protein concepts within a data science context. Why AstraZeneca There are many opportunities to develop yourself and your career. From our diverse portfolio and collaboration to our ground-breaking innovations -it's a place for lifelong learning. You'll be based in our Discovery Centre placed in the heart of the Cambridge Biomedical Campus - an open, welcoming and vibrant centre that will encourage us and our partners to push the boundaries of scientific innovation. Next Steps: Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. Please apply via the link and one of our team members will be in touch as soon as possible. This is being actively recruited so early application is advised. Where can you find more? Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Follow AstraZeneca on Instagram
Feb 28, 2026
Full time
Job Title: Senior AI Scientist - Hit Discovery and Protein Sciences Location: Cambridge, UK Competitive salary and benefits Introduction to the role: Are you acuriousDataand AIScientist seeking a role where yourexpertisecan make an extraordinary impact? This is an opportunity to join a dynamic and enthusiastic environment and transform the way we discoverhitsand protein reagentsin drug discovery. Diverse Minds. Bold Disruptors. Meaningful Impactthrough Partnership. At AstraZenecawe'rededicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.There'sno better place to make a difference to medicine,patientsand society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning,growthand development. Join a place built on innovation and creativity. We harness digital, data science & AI to fast-forward our research. Your scientific vision would ensure that new small moleculesand peptidesdiscovered usingyour skillsandinpartnershipwith our technical platformscan serve as the seeds for future medicines and make a real difference in our mission to help patients. You will be basedin early drug discovery R&DwithinData Sciences & Quantitative Biologydepartmentin Discovery Sciencesand will work closely with our colleagues in the Hit Discoveryand Protein Sciencesdepartments.To learn more about our department and culture watch this video: A Life-changing day - Meet our Quantitative Biology team at AstraZeneca. What you will do You will develop data science, computational and AI solutions to enable the discovery of hits (small molecules and peptides) and protein reagents enhancing the output from our hit and ledatageneration platforms. This will involve close collaboration with screening scientists, chemists, biologists, informaticians and statisticians. Wetruly believethat everyone hasan important rolein drug discoveryandeach individualbringsaunique set of competencies. Your curiosity and passion for personal development combined with support from colleagues and leaders, will ensure you maximise your potential and contribution, building from your current skills and experience. Essential requirements: Our team is a highly collaborative group of scientists, working in an evolving technical and scientific landscape. Therefore, you will be comfortable workingin a dynamic and team-focussedenvironment. Critical will be tohave effective communication skills and a proactive and delivery-focused approach. Aligned to Hit Discoveryand Protein Sciencesactivities, you will bring analytical skills,innovationand your strategic mindsetto this excitingand evolvingarea. A PhD or equivalent numbers of years in industry/academia in bioinformatics, cheminformatics, computer science, AI/ML, statistics or related computational and data science subject areas applied to chemistry, biology or medicine. Experience in data science, AI/ML and/or modelling methods applied to the analysis of highly multidimensional or unstructured datasets in molecular, drug discovery or biomedical contexts. Programming in Python, R and/or Shell, and experience with querying and integrating data from disparate sources (e.g. SQL, NoSQL, Graph or file-based approaches). Experience in developing computational workflows applied to the analysis of experimental or AI-generated data (e.g. Nextflow or Snakemake), knowledge of version control systems (e.g. Git and GitHub) and high-performance computing infrastructure. Experiencereporting data analysis results, drawing conclusions and defining recommended actions in interdisciplinary and collaborative environments. Desirables: Experience in AI/ML and/or physics-based mathematical modelling methods applied to peptides, small molecules and/or proteins. Experience in data analysis of high-throughput assays (peptides /small molecule screens, virtual or high content screening, chemical profiling, mass spectrometry, recombinant protein expression and/or omics). Experience in developing software and packages. Track record of publishing relevant research as preprints, peer-reviewed journals, conferences, and other scientific proceedings. Ability to collaborate and build consensus across cross-functional teams. Ability to identify opportunities and synergies across projects. Experience in communicating chemistry and protein concepts within a data science context. Why AstraZeneca There are many opportunities to develop yourself and your career. From our diverse portfolio and collaboration to our ground-breaking innovations -it's a place for lifelong learning. You'll be based in our Discovery Centre placed in the heart of the Cambridge Biomedical Campus - an open, welcoming and vibrant centre that will encourage us and our partners to push the boundaries of scientific innovation. Next Steps: Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. Please apply via the link and one of our team members will be in touch as soon as possible. This is being actively recruited so early application is advised. Where can you find more? Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Follow AstraZeneca on Instagram
About Maxion Maxion Therapeutics is a biotechnology company developing antibody-based drugs for previously untreatable ion channel- and G protein-coupled receptor (GPCR)-driven diseases, including autoimmune conditions, chronic pain, and cardiovascular disease. Maxion is developing a pipeline of potentially first- and best-in-class therapeutics using its proprietary KnotBody technology to generate potent, selective, and long-acting therapeutics by combining naturally occurring mini-proteins ('knottins') with antibodies using state-of-the-art phage and mammalian display technologies. Maxion was founded in 2020 by Dr John McCafferty (CTO) and Dr Aneesh Karatt-Vellatt (CSO). Dr McCafferty previously co-invented antibody phage display, which was the subject of the 2018 Nobel Prize in Chemistry awarded to his co-inventor Sir Gregory Winter. The Company is based near Cambridge, UK and is backed by international blue-chip investors. For more information, please visit: About the Role We are seeking a highly skilled Senior AI Research Scientist with expertise in computational protein design and generative protein modelling to enable AI- and structure-guided approaches to therapeutic antibody and KnotBody design. The successful candidate will drive the development, implementation, deployment and adoption of generative AI/ML models to enable therapeutic protein design, engineering and optimisation, utilising Maxion's proprietary KnotBody technology. This is a unique opportunity for someone who is excited to roll up their sleeves, build new capabilities from the ground up, and drive forward discovery programmes. The successful candidate will bring strong technical skills, a collaborative mindset, and the ability to thrive in a fast-paced biotech environment. Key Responsibilities Develop the computational protein design platform through integration, adaptation and benchmarking of generative protein design & engineering tools (AlphaFold/OpenFold, RFDiffusion, ProteinMPNN, Boltz, FrameFlow, etc) into the drug discovery process. Build generative and predictive models for protein design by training and fine-tuning ML models (VAEs, diffusion models, transformers) focused on prediction of functional therapeutic proteins and their properties (affinity, stability, and developability). Enable computational optimisation of therapeutic proteins, leveraging various ML approaches (genetic algorithms, Bayesian optimisation, physics-based methods, etc.) and integrating experimental data. Build datasets, data pipelines, training workflows, and evaluation tools for model training, benchmarking, and continuous learning. Cross functional collaboration with internal R&D and discovery teams to translate predictive models into deployable tools and testable experimental hypotheses. Candidate Profile Ph.D. or MSc. in Computational Biology, Computer Science, Bioinformatics, Natural Sciences or a related subject. Essential skills/experience Strong programming skills in Python and experience with deep learning frameworks (PyTorch, JAX, TensorFlow in order of preference). Substantial experience of structural bioinformatics and computational protein design, for example: protein structure modelling & prediction, generative protein sequence & structure design, protein-protein docking, physics-based modelling & simulation, etc. Experience training and fine-tuning ML models for protein design or related tasks. Experience of integrating computational predictions with experimental validation data for property optimisation. Experience working with modern MLOps stacks (Docker, Kubernetes, CI/CD, GitHub, etc.) to deploy and monitor models. Experience working with antibody sequence and structure datasets, using in silico tools for predicting protein properties and guiding engineering campaigns. Desirable skills/experience Publication(s) in relevant peer-reviewed journals, ideally focused on antibody design, AI/ML based protein modelling, or non-standard scaffolds (e.g. knottins, minibinders, etc.). Experience applying generative or structure-based models to challenging target classes (e.g. ion channels, GPCRs). What can we offer you? A competitive salary based on experience A comprehensive benefits package including generous pension contribution, Private Life and Medical Insurance, Cycle to Work Scheme, participation in the company Share Option Scheme, on site parking and more. Significant opportunities for career progression within a dynamic company. Located in a state-of-the art Science Park with easy access to Cambridge by car, train and bus, and offering on-site gym, cafe, and a vibrant social community. Working alongside an innovative team of scientists, including the founders, who are Key Opinion Leaders in the field. A supportive work environment with a key focus on fostering collaborative working environment within a friendly team. To apply for this position, just click on the link to upload your CV and covering letter outlining your suitability for this role, including your salary expectations. Due to data safety, please do not email or apply via direct messaging. This is a permanent position. Agencies: We are recruiting this role with our selected recruitment partner - PIR International. If you need to get in touch regarding the role please reach out directly to the contact at PIR:
Feb 28, 2026
Full time
About Maxion Maxion Therapeutics is a biotechnology company developing antibody-based drugs for previously untreatable ion channel- and G protein-coupled receptor (GPCR)-driven diseases, including autoimmune conditions, chronic pain, and cardiovascular disease. Maxion is developing a pipeline of potentially first- and best-in-class therapeutics using its proprietary KnotBody technology to generate potent, selective, and long-acting therapeutics by combining naturally occurring mini-proteins ('knottins') with antibodies using state-of-the-art phage and mammalian display technologies. Maxion was founded in 2020 by Dr John McCafferty (CTO) and Dr Aneesh Karatt-Vellatt (CSO). Dr McCafferty previously co-invented antibody phage display, which was the subject of the 2018 Nobel Prize in Chemistry awarded to his co-inventor Sir Gregory Winter. The Company is based near Cambridge, UK and is backed by international blue-chip investors. For more information, please visit: About the Role We are seeking a highly skilled Senior AI Research Scientist with expertise in computational protein design and generative protein modelling to enable AI- and structure-guided approaches to therapeutic antibody and KnotBody design. The successful candidate will drive the development, implementation, deployment and adoption of generative AI/ML models to enable therapeutic protein design, engineering and optimisation, utilising Maxion's proprietary KnotBody technology. This is a unique opportunity for someone who is excited to roll up their sleeves, build new capabilities from the ground up, and drive forward discovery programmes. The successful candidate will bring strong technical skills, a collaborative mindset, and the ability to thrive in a fast-paced biotech environment. Key Responsibilities Develop the computational protein design platform through integration, adaptation and benchmarking of generative protein design & engineering tools (AlphaFold/OpenFold, RFDiffusion, ProteinMPNN, Boltz, FrameFlow, etc) into the drug discovery process. Build generative and predictive models for protein design by training and fine-tuning ML models (VAEs, diffusion models, transformers) focused on prediction of functional therapeutic proteins and their properties (affinity, stability, and developability). Enable computational optimisation of therapeutic proteins, leveraging various ML approaches (genetic algorithms, Bayesian optimisation, physics-based methods, etc.) and integrating experimental data. Build datasets, data pipelines, training workflows, and evaluation tools for model training, benchmarking, and continuous learning. Cross functional collaboration with internal R&D and discovery teams to translate predictive models into deployable tools and testable experimental hypotheses. Candidate Profile Ph.D. or MSc. in Computational Biology, Computer Science, Bioinformatics, Natural Sciences or a related subject. Essential skills/experience Strong programming skills in Python and experience with deep learning frameworks (PyTorch, JAX, TensorFlow in order of preference). Substantial experience of structural bioinformatics and computational protein design, for example: protein structure modelling & prediction, generative protein sequence & structure design, protein-protein docking, physics-based modelling & simulation, etc. Experience training and fine-tuning ML models for protein design or related tasks. Experience of integrating computational predictions with experimental validation data for property optimisation. Experience working with modern MLOps stacks (Docker, Kubernetes, CI/CD, GitHub, etc.) to deploy and monitor models. Experience working with antibody sequence and structure datasets, using in silico tools for predicting protein properties and guiding engineering campaigns. Desirable skills/experience Publication(s) in relevant peer-reviewed journals, ideally focused on antibody design, AI/ML based protein modelling, or non-standard scaffolds (e.g. knottins, minibinders, etc.). Experience applying generative or structure-based models to challenging target classes (e.g. ion channels, GPCRs). What can we offer you? A competitive salary based on experience A comprehensive benefits package including generous pension contribution, Private Life and Medical Insurance, Cycle to Work Scheme, participation in the company Share Option Scheme, on site parking and more. Significant opportunities for career progression within a dynamic company. Located in a state-of-the art Science Park with easy access to Cambridge by car, train and bus, and offering on-site gym, cafe, and a vibrant social community. Working alongside an innovative team of scientists, including the founders, who are Key Opinion Leaders in the field. A supportive work environment with a key focus on fostering collaborative working environment within a friendly team. To apply for this position, just click on the link to upload your CV and covering letter outlining your suitability for this role, including your salary expectations. Due to data safety, please do not email or apply via direct messaging. This is a permanent position. Agencies: We are recruiting this role with our selected recruitment partner - PIR International. If you need to get in touch regarding the role please reach out directly to the contact at PIR:
Principal Scientist, Genomic Translational Research We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We are seeking a highly motivated Principal Scientist with hands on expertise in molecular biology in the context of immuno oncology to join the Oncology Translational Research team within GSK Oncology TA. The successful candidate will work as part of a team that evaluates patient derived organoids through cutting edge cellular, genomic and molecular techniques, and partners with AI/ML and analytics experts to integrate data from these multimodal approaches to generate clinical insights. The goal of this is to improve cancer patient risk stratification, identify clinical biomarkers and predict future targeted and/or immuno therapy susceptibilities. In this role you will: Create protocols and perform the sample processing for genomic experiments (e.g. RNAseq, WES, scRNAseq). Prepare samples and libraries for sequencing. Run flow cytometry and FACS sorting experiments. Develop immunogenicity assays for product validation. Offer technical expertise and support to other team members, helping them troubleshoot and optimize their experimental protocols. Solve technical issues operate as part of a cross functional project team. Collaborate with King's College London scientists within the GSK KCL Translational Oncology Research Hub, an exclusive research collaboration between GSK and the Comprehensive Cancer Centre at KCL. Basic Qualifications & Skills PhD (or equivalent experience) in Cancer Biology, Genomics, Immunology, or related field, with extensive experience in cancer genomics. Expertise with NGS, flow cytometry, single cell RNA sequencing and library preparation. Strong background in developing and applying cutting edge genomic technologies to study cancer biology. Strong understanding of immunology and cancer biology, including T cell biology and the molecular mechanisms underlying tumorigenesis and cancer progression. Ability to communicate with team members from different backgrounds by training/discipline, as well as senior members of the GSK stakeholders/research partner units. Ability to deliver high quality, consistent results in a timely fashion with a positive can do and result oriented attitude. Preferred Qualifications & Skills A track record of scientific publication. Experience in collaboration with biopharma. Strong strategic thinking and problem solving skills, with the ability to navigate complex scientific and business challenges. Experience in analysis of major next generation sequencing (sc TCR) techniques and generation of insights from such data. Closing Date for Applications 9th March 2026 Adjustments to the Recruitment Process Please note, if you require any adjustments during our recruitment process to assist you in demonstrating your strengths and capabilities, contact us at . You can also request a call. Equal Opportunity Employer GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Feb 28, 2026
Full time
Principal Scientist, Genomic Translational Research We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We are seeking a highly motivated Principal Scientist with hands on expertise in molecular biology in the context of immuno oncology to join the Oncology Translational Research team within GSK Oncology TA. The successful candidate will work as part of a team that evaluates patient derived organoids through cutting edge cellular, genomic and molecular techniques, and partners with AI/ML and analytics experts to integrate data from these multimodal approaches to generate clinical insights. The goal of this is to improve cancer patient risk stratification, identify clinical biomarkers and predict future targeted and/or immuno therapy susceptibilities. In this role you will: Create protocols and perform the sample processing for genomic experiments (e.g. RNAseq, WES, scRNAseq). Prepare samples and libraries for sequencing. Run flow cytometry and FACS sorting experiments. Develop immunogenicity assays for product validation. Offer technical expertise and support to other team members, helping them troubleshoot and optimize their experimental protocols. Solve technical issues operate as part of a cross functional project team. Collaborate with King's College London scientists within the GSK KCL Translational Oncology Research Hub, an exclusive research collaboration between GSK and the Comprehensive Cancer Centre at KCL. Basic Qualifications & Skills PhD (or equivalent experience) in Cancer Biology, Genomics, Immunology, or related field, with extensive experience in cancer genomics. Expertise with NGS, flow cytometry, single cell RNA sequencing and library preparation. Strong background in developing and applying cutting edge genomic technologies to study cancer biology. Strong understanding of immunology and cancer biology, including T cell biology and the molecular mechanisms underlying tumorigenesis and cancer progression. Ability to communicate with team members from different backgrounds by training/discipline, as well as senior members of the GSK stakeholders/research partner units. Ability to deliver high quality, consistent results in a timely fashion with a positive can do and result oriented attitude. Preferred Qualifications & Skills A track record of scientific publication. Experience in collaboration with biopharma. Strong strategic thinking and problem solving skills, with the ability to navigate complex scientific and business challenges. Experience in analysis of major next generation sequencing (sc TCR) techniques and generation of insights from such data. Closing Date for Applications 9th March 2026 Adjustments to the Recruitment Process Please note, if you require any adjustments during our recruitment process to assist you in demonstrating your strengths and capabilities, contact us at . You can also request a call. Equal Opportunity Employer GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Location: Cheltenham Salary: Competitive Benefits: Bonus and commission scheme, comprehensive benefits package including private medical and pension, flexible hybrid working, clear progression with funded training, and enhanced long-term incentives including additional leave and retention bonuses. Work on analytics platforms that support highly sensitive, mission critical programmes within a secure environment. This is an opportunity to build and scale modern data platforms while contributing to projects of national significance, alongside some of the strongest engineers in the sector. The Client: We're partnering with a leading organisation in the secure government sector to support the growth of a key programme delivering advanced data and analytics capabilities. This is a critical hire within an expanding team, focused on building and scaling platforms that underpin mission critical solutions. Operating at the forefront of data, cloud, and AI driven innovation, they offer an environment where engineers can work on complex, high impact challenges with real world significance. The Candidate: This would suit a candidate with a strong background in data or analytics platform engineering, who is comfortable working across both software development and infrastructure. You'll enjoy solving complex technical challenges, working in dynamic environments, and collaborating closely with Data Scientists and MLOps teams. A pragmatic, adaptable mindset is key, along with a passion for building scalable, secure systems that enable data driven outcomes. You should also be comfortable working in secure, highly regulated environments. The Role: We are seeking Senior and Principal Analytics Platform Engineers to join a growing team delivering high impact solutions within a secure environment. You will play a key role in designing, building, and evolving a modern analytics platform, supporting the full lifecycle from development through to deployment and ongoing optimisation. This is a hands on role offering exposure to a broad and evolving technology landscape. Due to the nature of the work, you will be operating within a highly secure environment with specific access requirements. Key Duties: Design, build and evolve scalable analytics and data platforms. Contribute across the full software development lifecycle. Support cloud migration and data management initiatives. Develop, test and deploy new platform capabilities. Troubleshoot and enhance existing analytics services. Provide hands on support to Data Scientists and MLOps teams. Tackle complex engineering challenges across a varied tech stack. Requirements: Strong experience with Python. Experience with Kubernetes and Docker. Understanding of CI/CD pipelines (e.g. GitLab). Exposure to data platforms, MLOps or machine learning environments. Spark or Scala. AWS services (e.g. S3). Elasticsearch or graph databases. OIDC/OAuth. Node.js or React. To apply for this Analytics Platform Engineer permenent job, please click the button below and submit your latest CV. Curo Services endeavour to respond to all applications. However, this may not always be possible during periods of high volume. Thank you for your patience. Curo Resourcing Ltd acts as an Employment Business for contract and temporary recruitment as well as an Employment Agency in relation to permanent vacancies.
Feb 27, 2026
Full time
Location: Cheltenham Salary: Competitive Benefits: Bonus and commission scheme, comprehensive benefits package including private medical and pension, flexible hybrid working, clear progression with funded training, and enhanced long-term incentives including additional leave and retention bonuses. Work on analytics platforms that support highly sensitive, mission critical programmes within a secure environment. This is an opportunity to build and scale modern data platforms while contributing to projects of national significance, alongside some of the strongest engineers in the sector. The Client: We're partnering with a leading organisation in the secure government sector to support the growth of a key programme delivering advanced data and analytics capabilities. This is a critical hire within an expanding team, focused on building and scaling platforms that underpin mission critical solutions. Operating at the forefront of data, cloud, and AI driven innovation, they offer an environment where engineers can work on complex, high impact challenges with real world significance. The Candidate: This would suit a candidate with a strong background in data or analytics platform engineering, who is comfortable working across both software development and infrastructure. You'll enjoy solving complex technical challenges, working in dynamic environments, and collaborating closely with Data Scientists and MLOps teams. A pragmatic, adaptable mindset is key, along with a passion for building scalable, secure systems that enable data driven outcomes. You should also be comfortable working in secure, highly regulated environments. The Role: We are seeking Senior and Principal Analytics Platform Engineers to join a growing team delivering high impact solutions within a secure environment. You will play a key role in designing, building, and evolving a modern analytics platform, supporting the full lifecycle from development through to deployment and ongoing optimisation. This is a hands on role offering exposure to a broad and evolving technology landscape. Due to the nature of the work, you will be operating within a highly secure environment with specific access requirements. Key Duties: Design, build and evolve scalable analytics and data platforms. Contribute across the full software development lifecycle. Support cloud migration and data management initiatives. Develop, test and deploy new platform capabilities. Troubleshoot and enhance existing analytics services. Provide hands on support to Data Scientists and MLOps teams. Tackle complex engineering challenges across a varied tech stack. Requirements: Strong experience with Python. Experience with Kubernetes and Docker. Understanding of CI/CD pipelines (e.g. GitLab). Exposure to data platforms, MLOps or machine learning environments. Spark or Scala. AWS services (e.g. S3). Elasticsearch or graph databases. OIDC/OAuth. Node.js or React. To apply for this Analytics Platform Engineer permenent job, please click the button below and submit your latest CV. Curo Services endeavour to respond to all applications. However, this may not always be possible during periods of high volume. Thank you for your patience. Curo Resourcing Ltd acts as an Employment Business for contract and temporary recruitment as well as an Employment Agency in relation to permanent vacancies.
Clinical Research Radiotherapy Physicist NHS AfC: Band 7 Main area Radiotherapy Grade NHS AfC: Band 7 Contract 7 months (Fixed term: 7 months) Hours Part time - 33.75 hours per week Job ref 282-SB1281 Employer The Royal Marsden NHS Foundation Trust Employer type NHS Site The Royal Marsden Hospital Town Sutton Salary £53,751 - £60,651 pro rata Salary period Yearly Closing 01/03/:59 Job overview We are looking for an enthusiastic physicist to join the Radiotherapy Physics group at the Sutton branch of the Royal Marsden Hospital for a fixed term for 7 months until 30 September 2026 (at 0.9 FTE). This post will be actively engaged in research functions and also fulfil clinical roles to allow others time for research. It is therefore suitable for someone with a research background who would like to be more involved in clinical work or a clinical physicist interested in research. The Radiotherapy Department in Sutton has 5 Elekta linacs, an Elekta Unity MR-Linac, a Cyberknife S7 and two Accuray Radixact units. Treatment planning is performed using the RayStation treatment planning system. We have established workflows for adaptive radiotherapy (both online and plan of the day), 4DCT, and breathhold techniques. The radiotherapy physics group consists of 40 physicists, dosimetrists and engineers and forms a substantial part of the Royal Marsden/Institute of Cancer Research Joint Department of Physics, through which we have many active research collaborations, most notably on the MR-linac which was the first in the UK to treat patients. Main duties of the job The post holder will provide specialist support to all aspects of the clinical, scientific and technical Radiotherapy Physics Service to Radiotherapy. The post holder will undertake research projects during dedicated time and to disseminate results and assist with the translation of research work into the clinic where appropriate. The post holder has clinical and scientific responsibilities for day-to-day essential complex treatment planning and checking and performing Quality Assurance and dosimetry and analysing results. Work closely with the Principal Physicist in all areas. Working for our organisation The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals - one in Chelsea, London, and one in Sutton, Surrey - as well as a Medical Daycare Unit in Kingston Hospital. At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do. At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements. Detailed job description and main responsibilities For further information please refer to the Job Description & Person Specification Undertake research activities associated with the adaptive and advanced Radiotherapy pathways, aligned with departmental development plans. Produce complex treatment plans. Carry out associated dosimetry calculations and verification measurements, in accordance with clinical prescription and agreed procedures. Analyse requirements and make complex judgements regarding treatment parameters and patient dose effects to produce the required dose distribution over the treatment volume, using computerised planning systems as appropriate. Participate in the commissioning of new radiotherapy treatment equipment, including the preparation and checking of complex beam data for treatment planning systems. Undertake both routine and complex dosimetry measurements, following procedures and/or guidelines as appropriate. Perform quality control, dosimetry and other measurements and procedures on highly complex, patient-critical treatment machines. Participate in the day to day, complex commissioning activities on new equipment installations, carefully analysing and checking measured data. Supervise the professional work of junior radiotherapy physics, trainees and dosimetrist staff working in areas or on projects being managed by the post holder. Provide practical training to physicists, medical and radiographer staff on aspects of Radiotherapy Physics, including clinical governance, ethics, audit and ISO systems. Person specification Qualifications Good (1st or 2nd class) Honours degree in a relevant subject MSc in radiation Physics (or equivalent) PhD in relevant subject or equivalent specialised scientific knowledge IPEM Diploma or equivalent in Medical Physics or Medical Engineering. Registration Working towards achieving or HCPC Registered as a Clinical Scientist Scientific/Technical/Specialist Basic knowledge across the range of working procedures and practices in radiotherapy physics, building on theoretical knowledge and practical experience. Practical experience in clinical radiotherapy treatment planning and in the use of dosimetry equipment in radiotherapy. Specialist training on and practical experience with a range of radiotherapy treatment & simulation/scanning equipment, including clinical applications. Demonstrable experience in radiotherapy physics research, ideally covering all aspects from conception to clinical implementation IT Able to use Excel, Word, etc. to set up documents and spreadsheets, extract information Experience in programming (e.g. in one or more of Python, C++, JAVA, R, MATLAB) Able to set up and manage the acquisition, structure and networking of information, including image transfer formats Communication Able to communicate highly complex information at postgraduate level to other professional groups Proven track record of presenting scientific papers at national and international conferences and write up scientific material for publication Communication Able to train groups of other professional staff Able to deliver teaching and training on highly complex subjects Able to deal with complex and unpredictable situations Understanding of hazards posed by, and precautions needed with: Ionising radiation, lasers, electrical hazards The Royal Marsden values diversity and is committed to the recruitment and retention of underrepresented minority groups. We particularly welcome applications from Black, Asian and minority ethnic candidates, LGBTQ+ candidates and candidates with disabilities. As a Disability Confident Employer, we are working to create a workplace that enables all staff to reach their full potential. We are committed to this because we know that greater diversity and inclusion will lead to an even greater positive impact for the people we serve. Due to the high volumes of applications we receive, we reserve the right to close any adverts before the published closing date once we have received a sufficient number of applications. We advise you to submit your application as early as possible to prevent disappointment. Please ensure your information is accurate to avoid errors with processing your application. All applicants will be contacted by email to the address supplied on your application. Applicants are advised to check their email accounts regularly and to ensure that email filters are set to allow our emails. Flu Vaccination - What We Expect of our Staff At The Royal Marsden we have an immune compromised patient population who we must protect as much as we can against the flu virus. Each year, seasonal flu affects thousands of people in the UK. Occurring mainly in winter, it is an infectious respiratory disease capable of producing symptoms ranging from those similar to a common cold, through to very severe or even fatal disease. The wellbeing of our staff and patients is of the upmost importance to us, and it is the expectation of The Royal Marsden that all patient-facing staff have an annual flu vaccination, provided free of charge by the Trust. Employer certification / accreditation badges The postholder will have access to vulnerable people in the course of their normal duties and as such this post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service to check for any previous criminal convictions. Name Alex Dunlop Job title Advanced Clinical Research Physicist Email address Additional information For further details contact: Michael Thomas, Head of Radiotherapy Physics (Sutton), () or Alex Dunlop, Advanced Clinical Research Physicist, . click apply for full job details
Feb 27, 2026
Full time
Clinical Research Radiotherapy Physicist NHS AfC: Band 7 Main area Radiotherapy Grade NHS AfC: Band 7 Contract 7 months (Fixed term: 7 months) Hours Part time - 33.75 hours per week Job ref 282-SB1281 Employer The Royal Marsden NHS Foundation Trust Employer type NHS Site The Royal Marsden Hospital Town Sutton Salary £53,751 - £60,651 pro rata Salary period Yearly Closing 01/03/:59 Job overview We are looking for an enthusiastic physicist to join the Radiotherapy Physics group at the Sutton branch of the Royal Marsden Hospital for a fixed term for 7 months until 30 September 2026 (at 0.9 FTE). This post will be actively engaged in research functions and also fulfil clinical roles to allow others time for research. It is therefore suitable for someone with a research background who would like to be more involved in clinical work or a clinical physicist interested in research. The Radiotherapy Department in Sutton has 5 Elekta linacs, an Elekta Unity MR-Linac, a Cyberknife S7 and two Accuray Radixact units. Treatment planning is performed using the RayStation treatment planning system. We have established workflows for adaptive radiotherapy (both online and plan of the day), 4DCT, and breathhold techniques. The radiotherapy physics group consists of 40 physicists, dosimetrists and engineers and forms a substantial part of the Royal Marsden/Institute of Cancer Research Joint Department of Physics, through which we have many active research collaborations, most notably on the MR-linac which was the first in the UK to treat patients. Main duties of the job The post holder will provide specialist support to all aspects of the clinical, scientific and technical Radiotherapy Physics Service to Radiotherapy. The post holder will undertake research projects during dedicated time and to disseminate results and assist with the translation of research work into the clinic where appropriate. The post holder has clinical and scientific responsibilities for day-to-day essential complex treatment planning and checking and performing Quality Assurance and dosimetry and analysing results. Work closely with the Principal Physicist in all areas. Working for our organisation The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals - one in Chelsea, London, and one in Sutton, Surrey - as well as a Medical Daycare Unit in Kingston Hospital. At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do. At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements. Detailed job description and main responsibilities For further information please refer to the Job Description & Person Specification Undertake research activities associated with the adaptive and advanced Radiotherapy pathways, aligned with departmental development plans. Produce complex treatment plans. Carry out associated dosimetry calculations and verification measurements, in accordance with clinical prescription and agreed procedures. Analyse requirements and make complex judgements regarding treatment parameters and patient dose effects to produce the required dose distribution over the treatment volume, using computerised planning systems as appropriate. Participate in the commissioning of new radiotherapy treatment equipment, including the preparation and checking of complex beam data for treatment planning systems. Undertake both routine and complex dosimetry measurements, following procedures and/or guidelines as appropriate. Perform quality control, dosimetry and other measurements and procedures on highly complex, patient-critical treatment machines. Participate in the day to day, complex commissioning activities on new equipment installations, carefully analysing and checking measured data. Supervise the professional work of junior radiotherapy physics, trainees and dosimetrist staff working in areas or on projects being managed by the post holder. Provide practical training to physicists, medical and radiographer staff on aspects of Radiotherapy Physics, including clinical governance, ethics, audit and ISO systems. Person specification Qualifications Good (1st or 2nd class) Honours degree in a relevant subject MSc in radiation Physics (or equivalent) PhD in relevant subject or equivalent specialised scientific knowledge IPEM Diploma or equivalent in Medical Physics or Medical Engineering. Registration Working towards achieving or HCPC Registered as a Clinical Scientist Scientific/Technical/Specialist Basic knowledge across the range of working procedures and practices in radiotherapy physics, building on theoretical knowledge and practical experience. Practical experience in clinical radiotherapy treatment planning and in the use of dosimetry equipment in radiotherapy. Specialist training on and practical experience with a range of radiotherapy treatment & simulation/scanning equipment, including clinical applications. Demonstrable experience in radiotherapy physics research, ideally covering all aspects from conception to clinical implementation IT Able to use Excel, Word, etc. to set up documents and spreadsheets, extract information Experience in programming (e.g. in one or more of Python, C++, JAVA, R, MATLAB) Able to set up and manage the acquisition, structure and networking of information, including image transfer formats Communication Able to communicate highly complex information at postgraduate level to other professional groups Proven track record of presenting scientific papers at national and international conferences and write up scientific material for publication Communication Able to train groups of other professional staff Able to deliver teaching and training on highly complex subjects Able to deal with complex and unpredictable situations Understanding of hazards posed by, and precautions needed with: Ionising radiation, lasers, electrical hazards The Royal Marsden values diversity and is committed to the recruitment and retention of underrepresented minority groups. We particularly welcome applications from Black, Asian and minority ethnic candidates, LGBTQ+ candidates and candidates with disabilities. As a Disability Confident Employer, we are working to create a workplace that enables all staff to reach their full potential. We are committed to this because we know that greater diversity and inclusion will lead to an even greater positive impact for the people we serve. Due to the high volumes of applications we receive, we reserve the right to close any adverts before the published closing date once we have received a sufficient number of applications. We advise you to submit your application as early as possible to prevent disappointment. Please ensure your information is accurate to avoid errors with processing your application. All applicants will be contacted by email to the address supplied on your application. Applicants are advised to check their email accounts regularly and to ensure that email filters are set to allow our emails. Flu Vaccination - What We Expect of our Staff At The Royal Marsden we have an immune compromised patient population who we must protect as much as we can against the flu virus. Each year, seasonal flu affects thousands of people in the UK. Occurring mainly in winter, it is an infectious respiratory disease capable of producing symptoms ranging from those similar to a common cold, through to very severe or even fatal disease. The wellbeing of our staff and patients is of the upmost importance to us, and it is the expectation of The Royal Marsden that all patient-facing staff have an annual flu vaccination, provided free of charge by the Trust. Employer certification / accreditation badges The postholder will have access to vulnerable people in the course of their normal duties and as such this post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service to check for any previous criminal convictions. Name Alex Dunlop Job title Advanced Clinical Research Physicist Email address Additional information For further details contact: Michael Thomas, Head of Radiotherapy Physics (Sutton), () or Alex Dunlop, Advanced Clinical Research Physicist, . click apply for full job details
Principal Ecologist A Principal Ecologist is required to join a leading consultancy. This is an exciting opportunity to join an environment to lead on projects where your efforts will be rewarded and recognised. You will work on a diverse workload delivering projects for the public and private sectors across the UK including exciting infrastructure and renewables projects. You will be responsible for growing, managing and mentoring an ecological team, plus have strong technical ability and able to lead and mentor and develop business. You will have previous experience working with Bats and be confident in planning and undertaking habitat surveys. To Be considered for this role you must have: Right To Live & Work in the UK Protected species license (ideally bats) Good report writing skills Full UK driving license. In return, you will join a forward-thinking consultancy and receive a competitive package, paid overtime arrangement. You'll join a business that supports and looks after it's staff with excellent progression opportunities available. Coastal Engineer / Scientist We are seeking an experienced Coastal Engineer / Scientist to play a key technical and leadership role within the Coastal & Marine Environment team. You will lead on a range of coastal projects, providing expertise in hydrodynamics, geomorphology, flooding, and environmental asse Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical, Ecology and Environmental Contract Type: Permanent Town/City: Bristol Structural Engineer We are seeking a Structural Engineer with approximately five years of experience to join their growing team. In this role, you will be involved in the design and delivery of a wide range of structural projects, preparing calculations, technical drawings, and reports while collabo Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical Contract Type: Permanent Town/City: London/Leeds/Glasgow Geotechnical Engineer (First) We are seeking a Geotechnical Engineer with around five years of experience to join their growing team. In this role, you will contribute to the delivery of high quality geotechnical design and analysis across a range of civil engineering projects. You'll be responsible for prepa Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: London/Leads Geotechnical Engineer (Second) In this role, you will support the geotechnical and design teams by contributing to geoenvironmental assessments, ground investigation projects, and interpretative reporting. You will be responsible for the preparation of technical reports, data analysis, and contributing to the Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: Newcastle Contracts Department Lead This position will focus on overseeing the reporting and quality output from the Contracts Department. As this is a UK wide role, the successful candidate can be based in any of the client's four regional offices-Durham, Glasgow, Manchester, or Hungerford. The role will involve m Salary: Competitive Sector: Geotechnical Contract Type: Full time Town/City: England/Scotland
Feb 27, 2026
Full time
Principal Ecologist A Principal Ecologist is required to join a leading consultancy. This is an exciting opportunity to join an environment to lead on projects where your efforts will be rewarded and recognised. You will work on a diverse workload delivering projects for the public and private sectors across the UK including exciting infrastructure and renewables projects. You will be responsible for growing, managing and mentoring an ecological team, plus have strong technical ability and able to lead and mentor and develop business. You will have previous experience working with Bats and be confident in planning and undertaking habitat surveys. To Be considered for this role you must have: Right To Live & Work in the UK Protected species license (ideally bats) Good report writing skills Full UK driving license. In return, you will join a forward-thinking consultancy and receive a competitive package, paid overtime arrangement. You'll join a business that supports and looks after it's staff with excellent progression opportunities available. Coastal Engineer / Scientist We are seeking an experienced Coastal Engineer / Scientist to play a key technical and leadership role within the Coastal & Marine Environment team. You will lead on a range of coastal projects, providing expertise in hydrodynamics, geomorphology, flooding, and environmental asse Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical, Ecology and Environmental Contract Type: Permanent Town/City: Bristol Structural Engineer We are seeking a Structural Engineer with approximately five years of experience to join their growing team. In this role, you will be involved in the design and delivery of a wide range of structural projects, preparing calculations, technical drawings, and reports while collabo Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical Contract Type: Permanent Town/City: London/Leeds/Glasgow Geotechnical Engineer (First) We are seeking a Geotechnical Engineer with around five years of experience to join their growing team. In this role, you will contribute to the delivery of high quality geotechnical design and analysis across a range of civil engineering projects. You'll be responsible for prepa Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: London/Leads Geotechnical Engineer (Second) In this role, you will support the geotechnical and design teams by contributing to geoenvironmental assessments, ground investigation projects, and interpretative reporting. You will be responsible for the preparation of technical reports, data analysis, and contributing to the Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: Newcastle Contracts Department Lead This position will focus on overseeing the reporting and quality output from the Contracts Department. As this is a UK wide role, the successful candidate can be based in any of the client's four regional offices-Durham, Glasgow, Manchester, or Hungerford. The role will involve m Salary: Competitive Sector: Geotechnical Contract Type: Full time Town/City: England/Scotland
A Principal Ecologist is required to join a leading multinational, multi disciplinary consultancy. This is an exciting opportunity to join an environment to lead on projects where your efforts will be rewarded and recognised. You will work on a diverse workload delivering projects for the public and private sectors across the UK including exciting infrastructure and renewables projects. You will be responsible for growing, managing and mentoring an ecological team, plus have strong technical ability and able to lead and mentor and develop business. You will have previous experience working with Bats and be confident in planning and undertaking habitat surveys. You will have: Full membership of CIEEM ( or working towards) Previous experience leading a team UK driver License In return you will receive a competitive salary, car allowance and an excellent benefits package including a share incentive scheme, option to buy holiday, life assurance and more. We are seeking an experienced Coastal Engineer / Scientist to play a key technical and leadership role within the Coastal & Marine Environment team. You will lead on a range of coastal projects, providing expertise in hydrodynamics, geomorphology, flooding, and environmental asse Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical, Ecology and Environmental Contract Type: Permanent Town/City: Bristol We are seeking a Structural Engineer with approximately five years of experience to join their growing team. In this role, you will be involved in the design and delivery of a wide range of structural projects, preparing calculations, technical drawings, and reports while collabo Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical Contract Type: Permanent Town/City: London/Leeds/Glasgow We are seeking a Geotechnical Engineer with around five years of experience to join their growing team. In this role, you will contribute to the delivery of high-quality geotechnical design and analysis across a range of civil engineering projects. You'll be responsible for prepa Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: London/Leeds In this role, you will support the geotechnical and design teams by contributing to geoenvironmental assessments, ground investigation projects, and interpretative reporting. You will be responsible for the preparation of technical reports, data analysis, and contributing to the Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: Newcastle This position will focus on overseeing the reporting and quality output from the Contracts Department. As this is a UK-wide role, the successful candidate can be based in any of the client's four regional offices-Durham, Glasgow, Manchester, or Hungerford. The role will involve m Salary: Competitive Sector: Geotechnical Contract Type: Full time Town/City: England/Scotland
Feb 27, 2026
Full time
A Principal Ecologist is required to join a leading multinational, multi disciplinary consultancy. This is an exciting opportunity to join an environment to lead on projects where your efforts will be rewarded and recognised. You will work on a diverse workload delivering projects for the public and private sectors across the UK including exciting infrastructure and renewables projects. You will be responsible for growing, managing and mentoring an ecological team, plus have strong technical ability and able to lead and mentor and develop business. You will have previous experience working with Bats and be confident in planning and undertaking habitat surveys. You will have: Full membership of CIEEM ( or working towards) Previous experience leading a team UK driver License In return you will receive a competitive salary, car allowance and an excellent benefits package including a share incentive scheme, option to buy holiday, life assurance and more. We are seeking an experienced Coastal Engineer / Scientist to play a key technical and leadership role within the Coastal & Marine Environment team. You will lead on a range of coastal projects, providing expertise in hydrodynamics, geomorphology, flooding, and environmental asse Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical, Ecology and Environmental Contract Type: Permanent Town/City: Bristol We are seeking a Structural Engineer with approximately five years of experience to join their growing team. In this role, you will be involved in the design and delivery of a wide range of structural projects, preparing calculations, technical drawings, and reports while collabo Salary: Competitive Sector: Civil & Structural Engineering, Geotechnical Contract Type: Permanent Town/City: London/Leeds/Glasgow We are seeking a Geotechnical Engineer with around five years of experience to join their growing team. In this role, you will contribute to the delivery of high-quality geotechnical design and analysis across a range of civil engineering projects. You'll be responsible for prepa Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: London/Leeds In this role, you will support the geotechnical and design teams by contributing to geoenvironmental assessments, ground investigation projects, and interpretative reporting. You will be responsible for the preparation of technical reports, data analysis, and contributing to the Salary: Competitive Sector: Geotechnical Contract Type: Permanent Town/City: Newcastle This position will focus on overseeing the reporting and quality output from the Contracts Department. As this is a UK-wide role, the successful candidate can be based in any of the client's four regional offices-Durham, Glasgow, Manchester, or Hungerford. The role will involve m Salary: Competitive Sector: Geotechnical Contract Type: Full time Town/City: England/Scotland
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Principal Research Scientist in United Kingdom. As a Principal Research Scientist, you will lead high-impact research initiatives that shape the integrity, quality, and governance of open knowledge systems. You will collaborate with senior leadership and global stakeholders to design and execute studies that inform strategy and operational decisions. This role involves mentoring researchers, translating complex findings into actionable recommendations, and advocating for scientific rigor within multidisciplinary environments. You will work across diverse time zones, contribute to public-facing research, and help define best practices in your domain. Your work will directly influence long-term strategies and the evolution of large-scale collaborative platforms. This position is fully remote, with occasional travel, and offers the opportunity to engage with cutting-edge research while impacting communities worldwide. Accountabilities Lead a strategic research portfolio focused on knowledge integrity and online community governance. Mentor and guide individual contributors to execute high-quality, impactful research projects. Translate complex research findings into actionable insights for leadership, legal, and communications teams. Conduct rapid, authoritative evaluation of external research to identify risks, opportunities, and methodological insights. Engage with global scientific communities, representing organizational research perspectives and promoting best practices. Collaborate with cross-functional teams to integrate research outcomes into policy, systems, and tools. Requirements PhD and at least five years of experience in research, science, or related fields. Proven track record of scholarly publications and service within relevant scientific communities. 3+ years of strategic technical leadership in large or matrixed organizations or equivalent academic experience. Advanced expertise in AI, NLP, ML frameworks, or mixed-method research applied to online communities or human-system interaction. Ability to manage complex portfolios while mentoring contributors and balancing high-level strategy with technical details. Strong analytical, organizational, and communication skills, capable of translating nuanced scientific findings for non-technical stakeholders. Experience collaborating with legal, communications, or cross-disciplinary teams is a plus. Comfortable working remotely across time zones and traveling periodically for stakeholder engagement. Benefits Fully remote work with flexible schedules. Opportunity to lead high-profile research initiatives with global impact. Collaboration with multidisciplinary teams and communities. Competitive compensation commensurate with experience and location. Travel opportunities up to four times per year to participate in strategic events. Engagement with thought leaders, scientific communities, and standards organizations. Supportive environment for professional growth, mentoring, and knowledge sharing. Why Apply Through Jobgether? We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
Feb 27, 2026
Full time
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Principal Research Scientist in United Kingdom. As a Principal Research Scientist, you will lead high-impact research initiatives that shape the integrity, quality, and governance of open knowledge systems. You will collaborate with senior leadership and global stakeholders to design and execute studies that inform strategy and operational decisions. This role involves mentoring researchers, translating complex findings into actionable recommendations, and advocating for scientific rigor within multidisciplinary environments. You will work across diverse time zones, contribute to public-facing research, and help define best practices in your domain. Your work will directly influence long-term strategies and the evolution of large-scale collaborative platforms. This position is fully remote, with occasional travel, and offers the opportunity to engage with cutting-edge research while impacting communities worldwide. Accountabilities Lead a strategic research portfolio focused on knowledge integrity and online community governance. Mentor and guide individual contributors to execute high-quality, impactful research projects. Translate complex research findings into actionable insights for leadership, legal, and communications teams. Conduct rapid, authoritative evaluation of external research to identify risks, opportunities, and methodological insights. Engage with global scientific communities, representing organizational research perspectives and promoting best practices. Collaborate with cross-functional teams to integrate research outcomes into policy, systems, and tools. Requirements PhD and at least five years of experience in research, science, or related fields. Proven track record of scholarly publications and service within relevant scientific communities. 3+ years of strategic technical leadership in large or matrixed organizations or equivalent academic experience. Advanced expertise in AI, NLP, ML frameworks, or mixed-method research applied to online communities or human-system interaction. Ability to manage complex portfolios while mentoring contributors and balancing high-level strategy with technical details. Strong analytical, organizational, and communication skills, capable of translating nuanced scientific findings for non-technical stakeholders. Experience collaborating with legal, communications, or cross-disciplinary teams is a plus. Comfortable working remotely across time zones and traveling periodically for stakeholder engagement. Benefits Fully remote work with flexible schedules. Opportunity to lead high-profile research initiatives with global impact. Collaboration with multidisciplinary teams and communities. Competitive compensation commensurate with experience and location. Travel opportunities up to four times per year to participate in strategic events. Engagement with thought leaders, scientific communities, and standards organizations. Supportive environment for professional growth, mentoring, and knowledge sharing. Why Apply Through Jobgether? We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
