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Join IQVIA Biotech – Where Innovation Meets Impact \n \n At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won’t just be part of the process—you’ll be at the forefront of it. You'll gain early insights into groundbreaking therapies and novel diseases, often before they reach the broader scientific community. \n If you're passionate about innovation and eager to make a real difference in the world of biotech, this is your opportunity to thrive. \n \n Responsibilities \n \n • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. \n • Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. \n • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. \n • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. \n • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. \n • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. \n • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. \n • Collaborate and liaise with study team members for project execution support as appropriate. \n • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. \n • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. \n \n Qualifications \n • Minimum of 1 year of experience of on-site monitoring experience \n • Experience monitoring Oncology studies is a must \n • Bachelor's Degree in scientific discipline or health care preferred \n • Equivalent combination of education, training and experience may be accepted in lieu of degree. \n • Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). \n • Good therapeutic and protocol knowledge as provided in company training. \n • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer, iPhone and iPad (where applicable). \n • Written and verbal communication skills including good command of English language. \n • Organizational and problem-solving skills. \n • Effective time and financial management skills. \n • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. \n \n This role is not eligible for UK visa sponsorship \n \n IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com \n \n IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. \n

Join IQVIA Biotech – Where Innovation Meets Impact \n \n At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won’t just be part of the process—you’ll be at the forefront of it. You'll gain early insights into groundbreaking therapies and novel diseases, often before they reach the broader scientific community. \n If you're passionate about innovation and eager to make a real difference in the world of biotech, this is your opportunity to thrive. \n \n Responsibilities \n \n • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. \n • Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. \n • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. \n • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. \n • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. \n • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. \n • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. \n • Collaborate and liaise with study team members for project execution support as appropriate. \n • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. \n • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. \n \n Qualifications \n • Minimum of 1 year of experience of on-site monitoring experience \n • Experience monitoring Oncology studies is a must \n • Bachelor's Degree in scientific discipline or health care preferred \n • Equivalent combination of education, training and experience may be accepted in lieu of degree. \n • Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). \n • Good therapeutic and protocol knowledge as provided in company training. \n • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer, iPhone and iPad (where applicable). \n • Written and verbal communication skills including good command of English language. \n • Organizational and problem-solving skills. \n • Effective time and financial management skills. \n • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. \n \n This role is not eligible for UK visa sponsorship \n \n IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com \n \n IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. \n

Join Us on Our Mission to Drive Healthcare Forward \n \n IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. \n \n Job Overview \n Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. \n \n Essential Functions \n • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. \n • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. \n • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. \n • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. \n • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. \n • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. \n • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. \n • Collaborate and liaise with study team members for project execution support as appropriate. \n • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. \n • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. \n \n Qualifications \n • Bachelor's Degree Degree in scientific discipline or health care preferred. Req \n • Requires at least 1 of year of on-site monitoring experience. Req \n • Equivalent combination of education, training and experience may be accepted in lieu of degree. Req \n • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. \n • i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. \n • Good therapeutic and protocol knowledge as provided in company training. \n • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). \n • Written and verbal communication skills including good command of English language. \n • Organizational and problem-solving skills. \n • Effective time and financial management skills. \n • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. \n \n Please note - this role is not eligible for UK visa sponsorship \n \n IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com \n \n IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. \n

Join Us on Our Mission to Drive Healthcare Forward \n \n IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. \n \n Job Overview \n Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. \n \n Essential Functions \n • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. \n • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. \n • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. \n • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. \n • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. \n • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. \n • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. \n • Collaborate and liaise with study team members for project execution support as appropriate. \n • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. \n • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. \n \n Qualifications \n • Bachelor's Degree Degree in scientific discipline or health care preferred. Req \n • Requires at least 1 of year of on-site monitoring experience. Req \n • Equivalent combination of education, training and experience may be accepted in lieu of degree. Req \n • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. \n • i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. \n • Good therapeutic and protocol knowledge as provided in company training. \n • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). \n • Written and verbal communication skills including good command of English language. \n • Organizational and problem-solving skills. \n • Effective time and financial management skills. \n • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. \n \n Please note - this role is not eligible for UK visa sponsorship \n \n IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com \n \n IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. \n

Company DescriptionSyngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. Maximise your chances of a successful application to this job by ensuring your CV and skills are a good match. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group.Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture.Job DescriptionAt Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success. To support this mission, we are seeking a Senior Formulation Development Chemist to join our Formulation Development Department within the Product Technology and Engineering Group. Key responsibilities will include:Acting as a lead formulation scientist within technical project(s) to bring formulated products to market.Independently defining formulation workplans, delivering and validating own technical data.Engaging independently with technical and non-technical functions across the organization.Actively identifying and exploring opportunities to generate broad IP in own projects.Providing technical support of formulated products in the market.Training colleagues with the ability to effectively supervise less experienced members of staff when required.Developing broad technical knowledge of experimental techniques and staying up to date on developments in the field.QualificationsWhat we are looking forFirst degree in Chemistry or closely related scientific discipline with PhD in Chemistry or related scientific discipline, or relevant industrial experience within the chemical industry, preferably in a formulation-based role.Basic knowledge of project management.Hands-on experience of working in laboratory with proven track record of working safely, independently and efficiently.Basic knowledge of data science with skills to support experiment design and data analysis.Experience in developing formulations for commercial application with an understanding of the compromises needed during product development is desired.Additional InformationDue to high interest in this position, we will only consider applications that include: (1) a CV, and (2) a cover letterexplaining your motivation and suitability for the role.Our siteJealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range.What we offerExtensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance.Up to 31.5 days annual holiday plus 8 UK bank holidays.A position which contributes to valuable and impactful work in a stimulating and international environment. The opportunity to develop and apply your science within the chemical industry.A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members.Learning culture and wide range of training options.Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Magazine for the 8th consecutive year.Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott’s Hill has Disability Confident certification. xrnqpay We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott’s Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.SummaryType: Full-timeFunction: Research

Company DescriptionSyngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. Make your application after reading the following skill and qualification requirements for this position. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group.Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture.Job DescriptionWe have an exciting opportunity for a passionate and experienced Technical Expert • Ecotoxicologist to join our dynamic Global Science Delivery team and work within a highly collaborative team of study managers and technical experts. Within the role you will apply your scientific background to provide ecotoxicology data and insights to project teams, and support the registration of sustainable crop protection products. You will drive the design, delivery and interpretation of critical ecotoxicology studies, demonstrating expertise in a range of terrestrial and/or aquatic disciplines, partnering with our strategic global Contract Research Organisation (CRO) network to deliver best-in-class technical inputs and timely delivery of critical endpoints. Key responsibilities will include:Ensuring the timely delivery of business-critical data generated at CROs to support the development and registration of new active ingredients and existing products globally.Being responsible for protocol design, evaluation of data and reviewing/authorising company reports.Elucidating insights from ecotoxicology data and reporting expert conclusions to technical teams.Independently providing technical assistance and innovative solutions to facilitate transfer of technical knowledge.Utilising your expert knowledge and understanding of ecotoxicology as well as relevant global regulatory guidance documents and their implication to our study designs.QualificationsWhat we are looking forMinimum BSc in Biology, Ecotoxicology, Environmental Toxicology, or a closely related field.Experience conducting ecotoxicology studies under GLP environment.Good knowledge of global ecotoxicology data requirements for Plant Protection Products, preferably with an understanding of the current regulatory landscape and new guidance/guideline development.Experience of generating key insights from data sets.Ability to work collaboratively as part of a diverse team to achieve project goals with strong organisation and time management proficiency.Capability of applying analytical thinking to solve problems with excellent attention to detail.Ability to learn and apply new skills promptly.Experience with Biological plant protection products (microbials, biostimulants, and biocontrols), including qPCR and microbiology methods is highly desirable.Additional InformationOur siteJealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range.Additionally, we could consider candidates based at Sao Paulo, Brazil beside Jealott's Hill, UK.What we offerExtensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance (depends on the contracting country).Flexible working.A position which contributes to valuable and impactful work in a stimulating and international environment. Learning culture and a wide range of training options.Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal.Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott’s Hill has Disability Confident certification. xrnqpay We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott’s Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.SummaryType: Full-timeFunction: Research

Company DescriptionSyngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. Do not pass up this chance, apply quickly if your experience and skills match what is in the following description. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group.Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture.Job DescriptionAre you a proactive problem solver with a passion for driving technical innovation? If so, we have good news as we are looking for an experienced DMPK/ADME Technical Expert to join our Analytical Metabolism and Methods (AMM) group within Product Safety. Within this role, you will make a key impact in projects by delivering innovative study designs to aid our understanding of the Absorption, Distribution, Metabolism and Excretion (ADME) and Pharmacokinetics (PK) and/or Toxicokinetics (TK) of chemicals in mammalian toxicology species. You will work within a highly collaborative team of study managers and technical experts, while applying your scientific expertise to interpret complex DMPK/ADME data for project teams, directly supporting the development and registration of sustainable crop protection products. A recent example is the registration of TYMIRIUM technology which protects crops against soil-borne pests. Additionally you will build effective partnerships with Contract Research Organisations (CROs), directing external study execution and collaborating to resolve technical challenges to secure the timely delivery of externally placed studies. Key responsibilities will include:Overseeing CRO delivery: Ensuring the timely delivery of business critical data generated at CROs, while being responsible for study strategy documents, protocol design, evaluation of data and reviewing/authorising company reports.Delivering technical insights: Elucidating insights from ADME and PK/TK data and reporting expert conclusions to metabolism teams.Applying regulatory expertise: Utilising your expert knowledge and understanding of ADME, PK/TK as well as relevant global regulatory guidance documents and their implication to optimise and de-risk our study designs. Keeping abreast of changes to regulatory guidelines and requirements.Partnering with CROs: Independently providing technical guidance and problem-solving support to external suppliers, where appropriate, to facilitate transfer of technical knowledge.Driving continuous improvement: Leading or contributing to the creation and optimisation of new processes, technical guidance documents and report templates to improve efficiency and consistency across the team.Serving as a scientific contributor within the ADME, PK/TK expert area, providing expertise to metabolism teams and other functional areas as required.QualificationsWhat we are looking forMinimum of a degree or equivalent in a biology- or chemistry-related discipline.Significant knowledge in the areas of DMPK/ADME, with expertise in pharmacokinetics and/or toxicokinetics.Familiarity of global Regulatory Test Guidelines (e.g. OECD 417) relevant to ADME and toxicokinetics studies conducted to GLP standards for the registration of crop protection chemicals.Experience in translating complex datasets into key safety or regulatory insights to inform decision making.Practical knowledge of quantitative PK/TK principles, including non-compartmental analysis (NCA), calculation of key PK/TK parameters.Proven ability to work collaboratively within diverse scientific teams (e.g., toxicologists, modellers, metabolism specialists) and with external stakeholders (industry, contract research or regulatory agencies) to achieve project goals.Capability to organise, prioritise, and track complex scientific deliverables across multiple projects, applying strong attention to detail and analytical thinking to solve problems in scientific experiments to maintain quality and delivery to agreed timelines.Excellent oral and written communication skills, with the ability to prepare technical reports and presentations to articulate complex technical matters clearly.Willingness to learn and ability to apply new skills promptly.In-depth understanding of in vitro and in vivo xenobiotic mammalian metabolism, including metabolite identification, metabolic pathway elucidation, and cross-species comparison would be desirable.Experience managing services delivered through third-party organisations, ensuring quality, milestone adherence, and budget discipline would be advantageous.Additional InformationOur siteJealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range.What we offerExtensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance.Up to 31.5 days annual holiday.Large campus environment.A position which contributes to valuable and impactful work in a stimulating and international environment. The chance to work as part of a global team to address the current and future needs of the agricultural sector.Learning culture and wide range of training options.Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal.Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott’s Hill has Disability Confident certification. xrnqpay We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott’s Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.SummaryType: Full-timeFunction: Research

Company DescriptionSyngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. Applying for this role is straight forward Scroll down and click on Apply to be considered for this position. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group.Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture.Job DescriptionAre you a proactive problem solver with a passion for driving technical innovation? Do you enjoy solving complex analytical problems and delivering innovative technical solutions? If so, we have good news, as we have an exciting opportunity for an experienced Environmental Fate Metabolism Study Manager to join our Analytical Methods & Metabolism (AMM) team and take on the challenge of elucidating the metabolic fate of our active ingredients in the environment. Working within a highly collaborative team of study managers and technical experts, you will have the challenge to apply your scientific background to fate metabolism data and share insights to project teams to support the registration of sustainable crop protection products. A recent example is the registration of TYMIRIUM technology which protects crops against soil-borne pests. Within the role you will solve analytical problems and build relationships with Contract Research Organisations (CROs) to deliver innovative technical solutions and critical endpoints. Key responsibilities will include:Ensuring the timely delivery of business critical data generated at CROs, being responsible for protocol design, evaluation of data and reviewing/authorising company reports.Elucidating insights from fate metabolism data and reporting expert conclusions to metabolism teams.Independently providing technical assistance and innovative solutions to external suppliers to facilitate transfer of technical knowledge.Developing expert knowledge and understanding of fate metabolism as well as relevant global regulatory guidance documents and their implication to our study designs.Serving as a scientific contributor, providing expertise to metabolism teams and other functional areas as required.QualificationsWhat we are looking forDegree or equivalent in a biology/chemistry or related discipline.Experience of conducting or managing environmental fate metabolism studies to meet GLP standards and familiarity of the relevant Regulatory Test Guidelines .Experience of generating key insights from data sets.Active scientific participation and collaboration with colleagues in industry, contract research or regulatory agencies.Ability to collaborate effectively in diverse teams, demonstrating strong organizational and analytical problem solving skills.Keen attention to detail and adaptability to learn and apply new skills.Knowledge of compound metabolism in the environment would be beneficial.Experience of accessing services through third-party organisations would be advantageous.Additional InformationOur siteJealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range.What we offerExtensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance.Up to 31.5 days annual holiday.Large campus environment.A position which contributes to valuable and impactful work in a stimulating and international environment. The chance to work as part of a global team to address the current and future needs of the agricultural sector.Learning culture and wide range of training options.Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal.Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott’s Hill has Disability Confident certification. xrnqpay We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott’s Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.SummaryType: Full-timeFunction: Research

Company DescriptionSyngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group.Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture.Job DescriptionAre you a proactive problem solver with a passion for driving technical innovation? Do you enjoy solving complex analytical problems and delivering innovative technical solutions? If so, we have good news, as we have an exciting opportunity for a Crop Metabolism Study Manager to join our Analytical Methods & Metabolism (AMM) team and take on the challenge of elucidating the metabolic fate of our active ingredients in crops and processed commodities. Working within a highly collaborative team of study managers and technical experts, you will have the change to apply your scientific background to provide crop metabolism data and insights to project teams to support the registration of sustainable crop protection products. A recent example is the registration of TYMIRIUM technology which protects crops against soil-borne pests. Key responsibilities will include:Ensuring the timely delivery of business critical data generated at CROs, being responsible for protocol design, evaluation of data and reviewing/authorising company reports.Elucidating insights from crop metabolism data and reporting expert conclusions to metabolism teams.Independently provide technical assistance and innovative solutions to external suppliers to facilitate transfer of technical knowledge.Developing expert knowledge and understanding of crop metabolism as well as relevant global regulatory guidance documents and their implication to our study designs.Serving as a scientific contributor, providing expertise to metabolism teams and other functional areas as required.QualificationsWhat we are looking forDegree or equivalent in a biology/chemistry or related discipline.Experience of generating key insights from data sets.Active scientific participation and collaboration with colleagues in industry, contract research or regulatory agencies.Ability to collaborate effectively in diverse teams, demonstrating strong organizational and analytical problem solving skills.Keen attention to detail and adaptability to learn and apply new skills.An understanding of the metabolism of xenobiotics in crops would be beneficial.Knowledge of plant physiology would be advantageous.Additional InformationOur siteJealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range.What we offerExtensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance.Up to 31.5 days annual holiday.Large campus environment.A position which contributes to valuable and impactful work in a stimulating and international environment. The chance to work as part of a global team to address the current and future needs of the agricultural sector.Learning culture and wide range of training options.Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal.Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: Jealott’s Hill has Disability Confident certification. xrnqpay We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott’s Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you.SummaryType: Full-timeFunction: Research

Company DescriptionSyngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. Increase your chances of an interview by reading the following overview of this role before making an application. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture.Job DescriptionWe are looking for a hands-on, senior-level Software Engineer with deep Python expertise to build reliable internal platforms and developer-enablement capabilities. This is an engineering-first role: strong software design, coding fluency and practical problem-solving are essential.You will apply AI in pragmatic ways-such as designing document search and conversational experiences using Retrieval-Augmented Generation (RAG)-while maintaining a high bar for engineering quality, security, scalability and operational excellence.What You’ll DoDesign, build and maintain production-grade Python services, libraries and developer tools.Apply modern Python practices, including packaging, type hints, asynchronous programming and maintainable API design.Create shared libraries, service templates and engineering standards that enable multiple internal teams to build consistently and efficiently.Build and evolve AI-enabled capabilities, including RAG-based search and conversational solutions over internal documentation and knowledge sources.Define robust evaluation approaches for AI-assisted features, balancing usefulness, reliability, security and cost.Develop and maintain CI/CD pipelines and cloud-native delivery practices using Docker, Kubernetes and Terraform.Establish strong testing, code quality, documentation-as-code and secure software development practices.Improve application performance, scalability and reliability through profiling, benchmarking, observability and architectural improvements.Implement monitoring, alerting and operational standards for platform services.Conduct thorough code reviews, mentor engineers and raise engineering standards across the team.Partner with engineering, product and scientific stakeholders to translate complex needs into practical, scalable technical solutions.QualificationsRequired QualificationsSignificant hands-on experience as a Software Engineer, with strong, production-level proficiency in Python. Equivalent depth in Java may also be considered.Demonstrated ability to write clean, maintainable and well-tested code, and to solve complex engineering problems independently.Strong experience with modern Python practices: packaging, dependency management, typing, async programming and service/API development.Experience designing and maintaining reusable libraries, service templates or internal developer platforms used by multiple teams.Strong knowledge of software quality practices, including automated testing, code reviews, CI/CD and release engineering.Practical experience with Docker, Kubernetes and Infrastructure as Code, ideally Terraform.Experience with observability, monitoring, alerting, performance profiling and benchmarking.Solid understanding of secure coding practices, vulnerability management and security considerations in software delivery.Applied understanding of Generative AI and LLM patterns, particularly RAG. You should be able to explain and design an approach for document search or conversational interfaces over enterprise content.Strong written and spoken English, with the ability to communicate effectively across technical and non-technical stakeholders.Preferred QualificationsExperience building internal platforms, developer tools or products adopted by several engineering teams.Experience in agriculture, life sciences, scientific computing or another regulated enterprise environment.Experience working in distributed, international engineering organisations.Track record of technical leadership, mentoring or leading cross-team engineering initiatives.Familiarity with AI/ML frameworks and tools used in software development environments.What Success Looks LikeYou are an engineer first: someone who can go deep in code, make sound technical decisions and deliver durable software in production. You use AI thoughtfully and practically-not as a substitute for engineering fundamentals, but as a capability embedded in reliable, secure and scalable platforms.Additional InformationWhy Syngenta?• Meaningful impact: help build technology that supports scientific innovation and sustainable agriculture.• Complex, modern challenges: work on high-scale platforms and systems with room for technical judgement. xrnqpay • Collaborative environment: partner with global engineering, R&D and product communities.• Growth: broaden your influence through challenging work, visible outcomes and a global networkSummaryType: Full-timeFunction: Information Technology

Syngenta Group UK is seeking a Crop Metabolism Study Manager to lead metabolic fate studies within the Analytical Methods & Metabolism (AMM) team, applying scientific expertise to generate data that supports registration of sustainable crop protection products. You will design and review CRO studies, interpret crop metabolism results, and provide expert insights to project teams while collaborating across disciplines in an international environment. #J-18808-Ljbffr

Johnson & Johnson MedTech Electrophysiology is seeking a dynamic and commercially minded Marketing Lead to drive strategic growth across the UK & Ireland business. This senior leadership position will be responsible for developing and executing integrated marketing strategies that accelerate market growth, strengthen customer partnerships, and support the successful adoption of innovative electrophysiology technologies. The successful candidate will combine strategic thinking, commercial execution and customer focus to deliver sustainable business growth while collaborating closely with local, regional and global stakeholders., Strategic Marketing Leadership • Develop and execute the UK & Ireland marketing strategy aligned with business objectives., • Translate global and regional priorities into impactful local market initiatives., • Identify market opportunities, customer needs and emerging trends to inform business strategy., • Lead annual marketing planning processes and associated investment decisions., • Ensure effective lifecycle management across the electrophysiology portfolio., • Drive market adoption and customer engagement through innovative marketing programmes., • Support the successful introduction and commercialisation of new technologies and solutions., • Develop customer-focused value propositions that address clinical and operational challenges., • Monitor competitive dynamics and market trends to inform strategic decision-making., • Partner with commercial teams to maximise growth opportunities and customer value., • Build and maintain strong relationships with key healthcare stakeholders and opinion leaders., • Support educational initiatives, scientific programmes and professional development activities., • Represent Johnson & Johnson MedTech at industry congresses, customer meetings and professional events., • Serve as a trusted partner to customers in advancing patient care and healthcare outcomes., • Lead, develop and inspire a high-performing marketing organisation., • Foster a culture of innovation, collaboration and accountability., • Coach and develop talent while creating an environment where individuals can thrive., • Champion inclusion, diversity and employee engagement., • Work closely with Sales, Medical Affairs, Professional Education, Health Economics, Market Access, Finance and other cross-functional partners., • Collaborate with EMEA and Global teams to ensure alignment of strategy and execution., • Drive organisational excellence through strong stakeholder management and effective communication., • Bachelor's degree or equivalent qualification in Marketing, Business, Life Sciences or a related field., • Significant experience within healthcare, medical devices, pharmaceuticals or a related industry., • Proven track record of developing and executing successful commercial and marketing strategies., • Demonstrated leadership experience in high-performance environments., • Strong analytical, strategic thinking and problem-solving capabilities., • Excellent communication, influencing and stakeholder management skills., • Ability to operate effectively within a complex matrix organisation., • Experience within cardiovascular, electrophysiology or medical technology sectors., • MBA or postgraduate qualification., • Experience working within multinational organisations and regional/global structures., • Experience leading product launches and market development initiatives., • Strong commercial acumen, • Strategic leadership capability, • Customer-centric thinking, • Change leadership, • Talent development and coaching, • Collaborative leadership style, • Data-driven decision making, • High levels of integrity and accountability, • Candidates must be willing and able to travel extensively throughout the UK & Ireland., • A minimum of three days per week customer-facing travel is required., • Occasional international travel may be required., • Brand Marketing, Brand Positioning Strategy, Business Alignment, Business Storytelling, Business Valuations, Cross-Functional Collaboration, Customer Intelligence, Data Analysis, Data-Driven Decision Making, Digital Strategy, Execution Focus, Financial Analysis, Go-to-Market Strategies, Industry Analysis, Market Research, Negotiation, Organizing, Problem Solving, Product Development Lifecycle, Product Portfolio Management, Product Strategies, Program Management, Strategic Thinking, Tactical Planning, Technical Credibility At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com (.) . At Johnson & Johnson, we provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and where solutions are personalised. At Johnson & Johnson, you'll join a purpose-driven organisation committed to transforming healthcare and improving patient outcomes globally. You'll have the opportunity to work alongside talented colleagues, develop your career, and make a meaningful impact on patients, healthcare systems and society. This is a unique opportunity to shape the future of one of the most innovative and rapidly growing areas within cardiovascular care. This version is much closer to a standard external J&D posting and avoids disclosing the UK&I EP operating model, team composition, reporting lines, headcount structure or capability deployment. It should be suitable for LinkedIn, Workday or external recruiter use with minimal HR review. #J-18808-Ljbffr

About Syngenta At Syngenta Crop Protection, we're pioneering solutions that safeguard global food security while championing sustainable agriculture. As a world market leader headquartered in Switzerland, we empower farmers with innovative crop protection technologies that defend against nature's toughest challenges. We unite advanced science with digital solutions to develop intelligent crop protection that maximizes yields while minimizing environmental impact. Join our mission of revolutionizing plant protection from seed to harvest. At Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success. To support this mission, we are seeking a motivated Technical Expert – Toxicology to join our dynamic team based in Jealott’s Hill as Technical Expert in the EU regulatory toxicology team. In this role, you will contribute to ensuring the safety and regulatory compliance of our crop protection products in the European market. You will support human toxicology technical project inputs into multidisciplinary EU teams, interpret complex scientific data, and engage with regulatory requirements for active substances, metabolites, and product registration processes. • Support toxicology project data management and contribute to strategy development for EU project teams, • Prepare and review toxicology sections of regulatory submissions for EU plant protection product registrations and renewals, • Collaborate with risk assessment teams to communicate safety evaluations, • Work cross-functionally to support integrated strategies for new product development and extending existing product registrations, • Engage with regulatory authorities (EFSA, ECHA, etc.) and contribute to regulatory forums as appropriate, • Stay current with EU regulations, scientific developments, and emerging issues in toxicology, • Contribute to technical training and best practices within the EU toxicology team, • Participate in industry task forces and working groups as required, • Degree in life sciences, biology, biomedicine, chemistry, or a related field — PhD preferred, • Good knowledge of EU regulatory frameworks, ideally in the r plant protection products sector, • Experience in managing toxicology projects and contributing to regulatory submissions, • Strong scientific writing and data interpretation skills, • Experience or background in risk assessment and safety evaluation of chemical substances is a distinct advantage, • Excellent communication and interpersonal skills, with the ability to interact effectively with diverse stakeholders, • Ability to work effectively within cross-functional teams, • Familiarity with current trends and emerging issues in toxicology and risk assessment, • Ability to utilise digital skills would be an advantage This role offers the opportunity to broaden your expertise beyond hazard assessment into non-dietary risk assessment (NDRA), with structured development pathways available for candidates who demonstrate aptitude and interest in this area. Candidates with an existing foundation in risk assessment methodology are particularly encouraged to apply. Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. • A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members., • Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance., • Up to 31.5 days annual holiday plus 8 UK bank holidays., • 36-hour working week. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture. We are looking for a Staff Engineer, Cloud Foundations to lead the technical direction of a multi-cloud foundation that enables every engineering team to build securely, reliably and with clear cost visibility. This is an opportunity to work at the intersection of advanced technology and agricultural R&D, partnering with engineers, product leaders and scientific stakeholders on capabilities with real-world impact. Help accelerate the digital capabilities that support more sustainable agriculture and scientific innovation. • Lead and apply deep expertise in multi-cloud architecture (AWS and GCP) to deliver durable, scalable outcomes that support organizational growth., • Lead and apply deep expertise in organization-scale Terraform and infrastructure as code to deliver durable, scalable outcomes., • Lead and apply deep expertise in cloud networking and governance to deliver durable, scalable outcomes., • Lead and apply deep expertise in FinOps instrumentation and cloud economics to deliver durable, scalable outcomes., • Lead and apply deep expertise in AI-assisted engineering with rigorous review to deliver durable, scalable outcomes., • Lead and apply deep expertise in technical leadership without line authority to deliver durable, scalable outcomes., • Collaborate across engineering, product and scientific teams to translate complex needs into practical solutions., • Set a high bar for quality, documentation and thoughtful use of AI-assisted engineering., • Mentor and develop engineering talent by sharing cloud architecture knowledge and best practices across teams., • Establish and enforce cloud security standards, compliance frameworks and governance policies to protect organizational assets., • Drive incident response protocols and reliability improvements to ensure high availability of cloud infrastructure., • Conduct architecture reviews and provide technical guidance on cloud design decisions to ensure alignment with organizational standards., • Demonstrable experience in multi-cloud architecture: AWS and GCP, • Demonstrable experience in organization-scale Terraform and infrastructure as code, • Demonstrable experience in cloud networking and governance, • Demonstrable experience in FinOps instrumentation and cloud economics, • Demonstrable experience in AI-assisted engineering with rigorous review, • Demonstrable experience in technical leadership without line authority, • Demonstrable experience in platform-as-product mindset, • Demonstrable experience in stakeholder management with hyperscalers, • Demonstrable experience in cloud security standards, compliance frameworks and governance policy development, • Demonstrable experience in incident response protocols and reliability engineering, • Strong communication skills and the ability to influence across technical and non-technical stakeholders, • Proven ability to conduct architecture reviews and provide technical guidance on cloud design decisions, • Fluent English, written and spoken, • AWS or GCP Certification, • Experience in agriculture, life sciences, scientific computing or a regulated enterprise environment, • Experience building platforms, products or services used by multiple internal teams, • Experience working in distributed, international engineering organisations, • Experience in cost optimisation and cloud economics management, • Experience mentoring and developing engineering talent in cloud architecture practices, • Meaningful impact: help build technology that supports scientific innovation and sustainable agriculture., • Complex, modern challenges: work on high-scale platforms and systems with room for technical judgement., • Collaborative environment: partner with global engineering, R&D and product communities., • Growth: broaden your influence through challenging work, visible outcomes and a global network. #J-18808-Ljbffr

Syngenta Group, a leader in agricultural technology, seeks a Staff Engineer to shape the cloud foundations across multi-cloud environments. You will collaborate with engineering, product and scientific teams to deliver secure, scalable platforms with clear cost visibility and strong governance. This role emphasizes AI-assisted engineering and high standards for reliability and security. You will mentor teams, drive architecture reviews, and set best practices that align with organizational #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture. About the role The HPC Lead is responsible for owning and evolving the High Performance Computing infrastructure for R&D scientists, including clusters, GPU provisioning, storage, and notebook infrastructure. This role serves as the technical and strategic anchor for HPC workloads for scientific computing and adjacent AI/ML needs. You will combine platform strategy, architecture, operational leadership, and partnership with scientific stakeholders while acting as a senior, hands-on contributor. What you will do Own the HPC infrastructure and work directly with engineers on cluster configuration, GPU provisioning, storage tier management, scheduler tuning, and notebook infrastructure. Define and own the HPC architecture roadmap, including cluster topology, GPU fleet composition, storage architecture, job-scheduling strategy, and the trajectory toward modern orchestration. Drive GPU procurement and investment strategy, evaluating vendor proposals critically, and making investment decisions with architectural confidence. Manage HPC capacity plans, hardware maintenance, support vendors, and contractor relationships, defining SLA design and the build-versus-buy decision for physical maintenance. Partner closely with scientists, computational specialists, and bioinformaticians to understand their workloads and ensure the HPC estate meets their evolving requirements. Use AI coding and productivity tools for automation scripts, infrastructure-as-code, operational runbooks, and performance analysis. Lead, mentor, and develop engineering teams to drive technical excellence, foster a culture of continuous improvement, and build deep HPC expertise across the organization. Establish and monitor HPC performance metrics, KPIs, and optimization targets; conduct regular performance profiling and capacity forecasting to ensure efficient resource utilization. Develop and maintain comprehensive documentation, operational runbooks, and knowledge management systems to ensure operational continuity and enable team self-sufficiency. Oversee budget planning, financial forecasting, and strategic procurement decisions for HPC infrastructure investments, ensuring cost-effectiveness and alignment with organizational priorities. Establish and enforce security protocols, compliance standards, and disaster recovery procedures for the HPC environment, ensuring business continuity and data protection. Communicate HPC strategy, status, and recommendations to executive stakeholders and cross-functional teams, translating technical concepts for non-technical audiences. Required Qualifications • Expert-level depth in HPC infrastructure, including cluster management, GPU provisioning (NVIDIA, A100/H100 generation), MPI, storage (Lustre, NFS, object storage), and job scheduling., • Expert understanding of GPU architecture, including generations, interconnects (NVLink, InfiniBand), memory profiles, and their implications for scientific workloads., • Strong experience with modern orchestration and the architectural trajectory toward Kubernetes-native HPC environments (e.g., GPU operators, Kubernetes scheduler extensions)., • Strong strategic capability in defining maintenance and support strategies, evaluating vendor contract structures, and managing hardware investments., • Strong ability to understand scientific workloads, conversing credibly with computational scientists and bioinformaticians to translate their needs into infrastructure solutions., • Strong proficiency in using AI-assisted engineering tools as a primary workflow for infrastructure automation., • Demonstrated leadership experience managing and mentoring technical teams, with a track record of building high-performing engineering organizations and fostering a culture of continuous improvement., • Proven expertise in budget planning, financial forecasting, and strategic procurement decisions for technology infrastructure investments., • Experience establishing and monitoring performance metrics, KPIs, and optimization targets; demonstrated capability in capacity forecasting and resource utilization analysis., • Strong background in developing and maintaining comprehensive documentation, operational runbooks, and knowledge management systems for complex technical environments. Bonus Points • Experience in agriculture, life sciences, scientific computing, or a regulated enterprise environment., • Experience building platforms, products, or services used by multiple internal teams., • Experience working in distributed, international engineering organisations., • Familiarity with popular scientific computing frameworks and libraries (e.g., TensorFlow, PyTorch, HPC libraries)., • Background in security protocols, compliance standards, and disaster recovery procedures for enterprise infrastructure environments., • Experience communicating complex technical concepts to executive stakeholders and cross-functional teams. Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff.Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. We offer a position which contributes to valuable and impactful work in a stimulating and international environment. The opportunity to develop and apply your science within the chemical industry. The chance to work as part of a global team to address the current and future needs of the agricultural sector. Learning culture and wide range of training options. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: careers/working-syngenta/diversity-and-inclusion #J-18808-Ljbffr

Syngenta is seeking a Staff Engineer, Cloud Foundations to lead the technical direction of a multi-cloud foundation. You will enable every engineering team to build securely, reliably and with clear cost visibility, partnering with engineering, product and scientific stakeholders on capabilities with real-world impact. Based in Bracknell, UK, you will accelerate digital capabilities to support sustainable agriculture and scientific innovation, while mentoring teams and setting governance #J-18808-Ljbffr

Lilly seeks a dynamic quantitative scientist to own population PK/PD modeling across programs, using NONMEM/Monolix and R. You will author analysis plans and regulatory submission reports, and lead end-to-end modeling efforts with scientific rigor. Collaborate with statistics, regulatory, medical, and clinical development, driving automation and AI integration, and communicating results clearly to teams and senior partners. #J-18808-Ljbffr

Syngenta Crop Protection is seeking a senior AI infrastructure lead to drive scalable AI platforms. You will oversee MLOps, model serving, vector databases, and HPC/GPU scheduling while ensuring responsible AI practices across distributed teams. Collaborate with engineering, product, and scientific groups to translate needs into practical AI-enabled solutions, shaping roadmaps and governance across a global R&D ecosystem. This role is on-site at Jealott's Hill near Bracknell, UK. #J-18808-Ljbffr

We’re looking for a seasoned Oncology ACE (Allucent Center of Expertise) Therapeutic Strategy Head to join our A-team. In this role, you’ll be responsible for shaping and driving our organization’s Oncology strategy, integrating scientific, operational, and commercial perspectives to ensure the successful capture and delivery of Oncology trials. With your expertise, you will bridge therapeutic insight with the ability to work with internal SMEs to create differentiated strategic operational solutions for Allucent’s clients. This position will not have any direct reports but will have matrixed oversight and accountability of therapeutically aligned project leadership and SME resources to enable portfolio performance management. At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. • Partner to develop, define, and execute Allucent’s overarching ACE Oncology strategy that aligns with our corporate and market opportunity goals across all phases of drug development., • Serve as an internal Oncology expert providing leadership across high value opportunities and ensure., • Lead the discussion around possible innovative and efficient operational models for Oncology trials, leveraging internal expertise across multidisciplinary scientific and operational functions., • Direct development of a therapeutic ecosystem of internal and external SMEs & Partners to differentiate Allucent’s go to market offering., • Have accountability for delivery performance across the Oncology portfolio, ensuring studies meet or exceed quality, timeline, and budget expectations., • Establish and monitor leading and lagging operational and financial KPIs specific to Oncology to enable proactive portfolio performance management., • Lead operational governance for key clients in the Oncology portfolio, providing strategic oversight and escalation support as required., • Champion operational innovation, such as decentralized or hybrid trial models, real-world data integration, and digital solutions that enhance Oncology study efficiency., • Partner with Medical, Biostatistics, Regulatory, and Data Operations to ensure Oncology trials are strategically and operationally optimized., • Contribute to process improvement initiatives that enhance efficiency and effectiveness of delivery solutions across the Oncology portfolio., • Partner with Marketing and Business Development and internal/external SMEs to position Allucent as a thought leader in the Oncology drug development space., • Lead operational strategy development key opportunities to support improved opportunity capture., • Cultivate relationships with key Oncology sponsors, thought leaders, and academic collaborators., • Identify new growth opportunities in Oncology, including emerging indications, novel modalities, and biomarker-driven strategies., • Participate as a key contributor to the executive operational leadership team for Allucent, • Provide mentorship and leadership to therapeutic leads, project directors, and operational teams within Oncology. Advanced degree in life sciences (MS, PhD, or equivalent). Background in Oncology, or related field preferred. Minimum 15 years of clinical research and development experience with a focus on Oncology within a CRO, pharma, or biotech environment. Demonstrated success leading Oncology programs or portfolios across multiple indications and study phases. Proven ability to align therapeutic insight with operational strategy. Strong experience collaborating with and influencing across multiple scientific and operational disciplines. Track record of client engagement, operational strategy, and managing large portfolios of work to achieve commercial and delivery goals Strategic thinker with strong business acumen and operational insight. Excellent communicator, capable of translating scientific and operational concepts for diverse audiences. Highly collaborative, able to influence across functions and levels without direct authority. Entrepreneurial, adaptable, and motivated by building excellence in a growth-oriented CRO environment. Competitive salaries and a comprehensive benefits package. The salary band will be different per country and will be shared with you in the first phone screen with Talent Acquisition. Departmental Study/Training for furthering professional development Mentoring opportunities Internal growth opportunities and career progression Financially rewarding internal employee referral program Eligibility for our internal employee recognition programs for going above and beyond on projects Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees Our mission is to help bring new therapies to light. When you work at Allucent, that means applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments. If you’re passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow. Together we SHINE. find more information about our values. #J-18808-Ljbffr

Hewlett Packard Enterprise is seeking an HPC & AI Application Performance Engineer to optimise complex HPC and AI workloads. You will work with customers on-site in the UK and with regional teams to maximise performance, scalability, and value from HPC/AI investments. The role focuses on analysing applications, solving challenging problems, and contributing to cutting‑edge projects in scientific discovery and engineering across a distributed team. #J-18808-Ljbffr

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. The Global Pharmacokinetics/Pharmacodynamics and Pharmacometrics (PK/PD & PMx) Department serves as the functional leader in research and development across the value chain, from preclinical lead molecule identification through clinical post-approval. Our mission is to accelerate the development of innovative medicines by applying mechanistic reasoning and quantitative modeling to complex systems. We partner across disciplines to simplify and enable critical decisions. We are leaders in model-informed drug discovery and development. Using deep quantitative thinking, we work best with hard questions, and our insight shapes the medicines that reach patients. The PMx team operates across all phases of drug development and serves as a strategic scientific partner to project teams, regulatory functions, and senior leadership. We are currently investing in automation, AI/ML integration, and standardized modeling workflows to accelerate timelines and expand our impact. We seek dynamic, curious, and collaborative quantitative scientists ready to engage and work on life-changing therapies for patients. This role is for a scientist who wants to own the modeling and simulation on real programs and be trusted with the answer. You will develop and apply population PK and PK/PD models independently, author the analysis plans and reports behind them, and work as a scientific partner and not as an analysis service. Your work will span multiple programs within PK/PD & PMx. You will take it to project teams and department forums, and build the judgment that turns a modeling result into a development decision. • Independently develop, evaluate, and apply population PK and PK/PD models to answer defined development questions, using NONMEM and/or Monolix with R for data handling, diagnostics, and simulation., • Serve as PMx lead on assigned programs: primary author of the analysis plan, author of the modeling report to regulatory submission standard, and accountable owner of the analysis end to end., • Provide scientific input to project teams on dose, regimen, patient population, and development strategy, including dose justification, exposure-response analyses, and responses to health authority questions., • Perform quality control and quality review of modeling deliverables, and support scientific oversight of vendor-delivered analyses., • Identify where modeling can answer a question the team has not thought to ask, and say so., • Partner with the PK/PD project leader on the quantitative strategy for your programs, starting from the scientific question and determining the best approach to answer it., • Build a cross-functional network across statistics, regulatory, medical, ADME, toxicology, and clinical development. Show up wherever modeling input or output is being discussed, and be engaged in those conversations., • Bring your work to the department forums, including scientific project reviews, and be open about what is still uncertain., • Elevate the people around you: share what you learn rather than holding it., • Use and extend the department's automation stack in day-to-day delivery., • Contribute to shared tooling, templates, and standards so the next analysis starts further along than the last one., • Communicate quantitative results clearly and at the level appropriate to the audience, from project teams to senior partners., • Share work externally over time, through scientific meetings, publications, and regulatory interactions., • Communicate clearly, concisely, and on time, in writing and in person. Seek feedback actively and give it constructively., • PhD in pharmacometrics, population pharmacokinetics/pharmacodynamics, computational sciences, engineering, chemistry, statistics or a related modelling area., • Experience in population PK and/or PK/PD modeling. Thorough understanding of pharmacokinetic and/or pharmacodynamic principles, along with an ability to clearly communicate theories and concepts to specialist and non-specialist audiences., • Experience using relevant software such as NONMEM (or Monolix), R, and mrgsolve., • Hands-on experience across the full modeling workflow: dataset specification and creation, exploratory data analysis, covariate evaluation and modeling, model evaluation (VPC, NPDE, goodness-of-fit), simulation, and reporting., • Experience contributing to a regulatory submission or a health authority response., • Reproducible analysis practice, including version control (Git) and literate reporting such as Quarto., • Active engagement with AI and automation in a pharmacometrics context, including hands-on experience with tools, curiosity about what is possible, and the judgment to tell where automation helps and where scientific judgment has to stay human. We are in the middle of a transformation and this person will be part of it., • Comfort working when the question is not yet fully defined, and a willingness to propose the approach rather than wait to be handed one., • Adept at working with cross-functional colleagues., • Excellent self-management and organizational skills, with the ability to prioritize across several programs. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL). Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $153,000 - $246,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture. About the role We are seeking a Lead, AI Enablement Technologies to run a cross-cutting strategic function within Engineering and Technology. This role makes AI a first-class, measured, and safely operated capability across R&D IT. You will own the engineering "how" of AI: infrastructure, technology choices, engineering practice, and the platform that business-facing AI products run on. What you will do Own the operational performance of the AI Enablement function across five key workloads: HPC and scientific compute, AI inference and serving infrastructure, agentic foundations, AI-assisted engineering, and AI upskilling for R&D. Direct line management for area leads, guiding specialists in HPC, scientific AI inference, and engineering AI. Drive the technology roadmap for AI infrastructure across R&D IT, including model serving stacks, inference optimisation patterns, guardrails frameworks, vector database choices, and evaluation harnesses. Manage HPC investments, including GPU procurement and cluster lifecycle, grounded in utilisation data and scientific demand forecasts. Partner with peer data, analytics, and bioinformatics IT functions to define API contracts, cost attribution models, and shared scientific-computing patterns. Own the evaluation and safety framework for AI at scale, including red-teaming, prompt-injection testing, and model performance tracking. Build consensus on cross-boundary technical patterns and author Architecture Decision Records (ADRs). Establish and monitor key performance indicators (KPIs) for infrastructure utilisation, cost efficiency, and system reliability, ensuring accountability across the AI Enablement function. Develop and deliver comprehensive capability-building programmes for R&D teams, including training on AI best practices, platform usage, and responsible AI principles. Manage vendor relationships and technology partnerships to ensure optimal selection, integration, and support of AI infrastructure components and tools. What you will bring Expert-level technical depth in AI infrastructure and MLOps, including model serving at scale, inference optimization, vector databases, and LLM-adjacent tooling. Strong scientific HPC literacy (e.g., Slurm, GPU scheduling, scientific-computing workflows) to credibly direct HPC specialists and engage with scientists. Proven engineering leadership experience running specialist teams and hiring senior/staff engineers. Strong strategic navigation skills to partner effectively across boundaries without being captured by vendors or peer functions. Hands-on habits; you still read code, review architecture, and evaluate tools directly. Exceptional communication skills, able to explain complex AI infrastructure to executives and engineers alike. Demonstrated experience designing and implementing safety frameworks, including red-teaming methodologies, adversarial testing, and model performance evaluation at scale. Proven track record in managing technology budgets, capital expenditure planning, and cost optimization across infrastructure investments. Experience authoring and socializing technical architecture decisions and design documentation across cross-functional teams. Strong vendor management and technology partnership experience, with ability to evaluate, negotiate, and integrate third‑party solutions effectively. Hands-on experience with popular ML frameworks, tools, and platforms (e.g., PyTorch, TensorFlow, Kubernetes, Ray, or equivalent) to maintain technical credibility and inform infrastructure decisions. Demonstrated success leading large-scale technology initiatives or organizational transformations, with ability to drive adoption and change management across diverse stakeholder groups. Strong metrics-driven mindset with proven ability to establish, track, and optimize key performance indicators for infrastructure utilization, cost efficiency, and system reliability. Experience building and scaling high-performing engineering teams in fast-growing or matrix organizational environments. Familiarity with responsible AI governance frameworks, compliance requirements, and industry best practices for AI safety and ethics. Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott's Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. We offer a position which contributes to valuable and impactful work in a stimulating and international environment. The opportunity to develop and apply your science within the chemical industry. The chance to work as part of a global team to address the current and future needs of the agricultural sector. Learning culture and wide range of training options. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: careers/working-syngenta/diversity-and-inclusion #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture. Are you a proactive problem solver with a passion for driving technical innovation? Do you enjoy solving complex analytical problems and delivering innovative technical solutions? If so, we have good news, as we have an exciting opportunity for a Crop Metabolism Study Manager to join our Analytical Methods & Metabolism (AMM) team and take on the challenge of elucidating the metabolic fate of our active ingredients in crops and processed commodities. Working within a highly collaborative team of study managers and technical experts, you will have the change to apply your scientific background to provide crop metabolism data and insights to project teams to support the registration of sustainable crop protection products. A recent example is the registration of TYMIRIUM® technology which protects crops against soil-borne pests. Key responsibilities will include: • Ensuring the timely delivery of business critical data generated at CROs, being responsible for protocol design, evaluation of data and reviewing/authorising company reports., • Elucidating insights from crop metabolism data and reporting expert conclusions to metabolism teams., • Independently provide technical assistance and innovative solutions to external suppliers to facilitate transfer of technical knowledge., • Developing expert knowledge and understanding of crop metabolism as well as relevant global regulatory guidance documents and their implication to our study designs., • Serving as a scientific contributor, providing expertise to metabolism teams and other functional areas as required. What we are looking for • Degree or equivalent in a biology/chemistry or related discipline., • Experience of generating key insights from data sets., • Active scientific participation and collaboration with colleagues in industry, contract research or regulatory agencies., • Ability to collaborate effectively in diverse teams, demonstrating strong organizational and analytical problem solving skills., • Keen attention to detail and adaptability to learn and apply new skills., • An understanding of the metabolism of xenobiotics in crops would be beneficial., • Knowledge of plant physiology would be advantageous. Our site Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer • Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance., • Up to 31.5 days annual holiday., • A position which contributes to valuable and impactful work in a stimulating and international environment., • The chance to work as part of a global team to address the current and future needs of the agricultural sector., • Learning culture and wide range of training options. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: careers/working-syngenta/diversity-and-inclusion Jealott’s Hill has Disability Confident certification. We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott’s Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you. By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply #J-18808-Ljbffr

This role has been designed as ‘’Onsite’ with an expectation that you will primarily work from an HPE partner/customer office. Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work. We help companies connect, protect, analyze, and act on their data and applications wherever they live, from edge to cloud, so they can turn insights into outcomes at the speed required to thrive in today’s complex world. Our culture thrives on finding new and better ways to accelerate what’s next. We know varied backgrounds are valued and succeed here. We have the flexibility to manage our work and personal needs. We make bold moves, together, and are a force for good. If you are looking to stretch and grow your career our culture will embrace you. Open up opportunities with HPE. Location: UK Type: permanent- full time At Hewlett Packard Enterprise, we are at the forefront of delivering High Performance Computing (HPC) and Artificial Intelligence (AI) solutions that power some of the world's most advanced research, innovation, and business outcomes. Our team of highly skilled professionals supports customers across EMEA and LATAM, providing expertise in HPC and AI infrastructure, application performance, benchmarking, optimisation, and advanced technical support. We are looking for an experienced HPC & AI Application Performance Engineer to join our distributed team and help customers maximise the performance, scalability, and impact of their HPC and AI environments. This is an exciting opportunity to work alongside leading researchers, software engineers, technology partners, and some of the most innovative organisations in the world. You will play a key role in analysing and optimising complex HPC and AI applications, solving challenging technical problems, and helping customers unlock greater value from their technology investments. Working across a diverse range of industries and research environments, you will contribute to cutting-edge projects that are shaping the future of scientific discovery, engineering, and artificial intelligence. • Provide advanced technical expertise and support to major HPE HPC and AI customer environments across EMEA and LATAM., • Work both on-site with UK customers and remotely with organisations across the wider region., • Analyse customer applications and workloads to identify opportunities for performance improvement, optimisation, and scalability., • Investigate complex software and infrastructure issues, acting as a trusted technical link between customer support teams and HPE R&D., • Support strategic business opportunities by providing technical expertise for large-scale HPC and AI bids and tenders., • Deliver technical workshops, training sessions, and presentations for customers and colleagues., • Share knowledge, best practices, and innovative ideas across the team and wider HPC and AI community., • Contribute to the development of tools, methodologies, and research initiatives that improve customer productivity and service delivery. We're seeking an individual with a strong technical background, excellent problem-solving abilities, and a passion for helping customers succeed. • Bachelor's degree (or equivalent experience) in Science, Technology, Engineering, Mathematics, or a related field., • UK citizenship with the ability to obtain required security clearances for specific UK customer environments., • Strong understanding of HPC and AI architectures, software environments, and performance analysis techniques., • Experience troubleshooting complex technical issues and working collaboratively with engineering and R&D teams., • Programming experience in C, C++, or Fortran, alongside strong Python skills., • Experience with GPU programming technologies such as CUDA, OpenACC, or OpenMP Offload., • Knowledge of parallel programming frameworks including MPI and OpenMP., • Familiarity with build systems, scripting, and batch processing environments., • Experience using performance profiling and optimisation tools., • Strong communication skills with the ability to explain complex technical concepts to a variety of audiences., • Fluent written and spoken English., • Master's degree or PhD in a relevant scientific, engineering, or technical discipline., • Experience in application domains such as:, • Weather and climate modelling, • Computational Fluid Dynamics (CFD), • Artificial Intelligence and Machine Learning, • Data Science, • Knowledge of container technologies, system software, and monitoring solutions., • Become a trusted technical advisor to customers and colleagues., • Help customers achieve measurable improvements in application performance and scalability., • Build strong partnerships with customers, engineering teams, and research communities., • Contribute to strategic HPC and AI projects across multiple industries., • Drive innovation by developing new tools, methodologies, and approaches to complex challenges., • Continuously learn and adapt to emerging technologies and computing paradigms., • Work with some of the world's leading HPC and AI experts., • Collaborate with research institutions, technology partners, and innovative customers., • Contribute to cutting-edge projects that advance scientific research and technological innovation., • Influence future products and solutions through direct engagement with HPE engineering and development teams., • Access ongoing learning, career development, and growth opportunities., • Be part of a collaborative and supportive team that values innovation, curiosity, and customer success. If you're passionate about solving complex technical challenges and want to make a direct impact on some of the world's most advanced computing environments, we'd love to hear from you. HPE is committed to creating an inclusive and accessible workplace and encourages applications from all qualified individuals, including those with disabilities. If you believe you require accommodation during any stage of the application or interview process, please submit your request by completing our secure form linked here. Note: This option is reserved for applicants needing assistance/reasonable accommodation related to a disability. We strive to provide our team members and their loved ones with a comprehensive suite of benefits that supports their physical, financial and emotional wellbeing. We also invest in your career because the better you are, the better we all are. We have specific programs catered to helping you reach any career goals you have — whether you want to become a knowledge expert in your field or apply your skills to another division. We are unconditionally inclusive in the way we work and celebrate individual uniqueness. We know varied backgrounds are valued and succeed here. We have the flexibility to manage our work and personal needs. We make bold moves, together, and are a force for good. Follow @HPECareers on Instagram to see the latest on people, culture and tech at HPE. #unitedkingdom TCP_05 HPE is an Equal Employment Opportunity/ Veterans/Disabled/LGBT employer. We do not discriminate on the basis of race, gender, or any other protected category, and all decisions we make are made on the basis of qualifications, merit, and business need. Our goal is to be one global team that is representative of our customers, in an inclusive environment where we can continue to innovate and grow together. Please click here: Equal Employment Opportunity. HPE will comply with all applicable laws related to employer use of arrest and conviction records, including laws requiring employers to consider for employment qualified applicants with criminal histories. #J-18808-Ljbffr

Syngenta Group is seeking an HPC Lead to own and evolve the High Performance Computing infrastructure for R&D scientists in the UK. You will manage clusters, GPU provisioning, storage, and orchestration, while partnering with researchers and bioinformaticians to optimize workloads and deliver scalable, secure compute. You will drive strategy, architecture, and procurement decisions, mentor engineering teams, and ensure cost-effective operation with robust documentation and runbooks. #J-18808-Ljbffr

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Marketing Strategic Marketing Professional Wokingham, Berkshire, United Kingdom Travel: This field-based leadership role requires a minimum of three days per week travel across the UK & Ireland. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and where solutions are personalised. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow. Learn more at www.jnj.com . Johnson & Johnson MedTech Electrophysiology is seeking a dynamic and commercially minded Marketing Lead to drive strategic growth across the UK & Ireland business. This senior leadership position will be responsible for developing and executing integrated marketing strategies that accelerate market growth, strengthen customer partnerships, and support the successful adoption of innovative electrophysiology technologies. The successful candidate will combine strategic thinking, commercial execution and customer focus to deliver sustainable business growth while collaborating closely with local, regional and global stakeholders. Strategic Marketing Leadership • Develop and execute the UK & Ireland marketing strategy aligned with business objectives., • Translate global and regional priorities into impactful local market initiatives., • Identify market opportunities, customer needs and emerging trends to inform business strategy., • Lead annual marketing planning processes and associated investment decisions., • Ensure effective lifecycle management across the electrophysiology portfolio.Business Growth & Market Development, • Drive market adoption and customer engagement through innovative marketing programmes., • Support the successful introduction and commercialisation of new technologies and solutions., • Develop customer-focused value propositions that address clinical and operational challenges., • Monitor competitive dynamics and market trends to inform strategic decision-making., • Partner with commercial teams to maximise growth opportunities and customer value.Customer Engagement, • Build and maintain strong relationships with key healthcare stakeholders and opinion leaders., • Support educational initiatives, scientific programmes and professional development activities., • Represent Johnson & Johnson MedTech at industry congresses, customer meetings and professional events., • Serve as a trusted partner to customers in advancing patient care and healthcare outcomes.People Leadership, • Lead, develop and inspire a high-performing marketing organisation., • Foster a culture of innovation, collaboration and accountability., • Coach and develop talent while creating an environment where individuals can thrive., • Champion inclusion, diversity and employee engagement.Cross-Functional Collaboration, • Work closely with Sales, Medical Affairs, Professional Education, Health Economics, Market Access, Finance and other cross-functional partners., • Collaborate with EMEA and Global teams to ensure alignment of strategy and execution., • Drive organisational excellence through strong stakeholder management and effective communication., • Bachelor's degree or equivalent qualification in Marketing, Business, Life Sciences or a related field., • Significant experience within healthcare, medical devices, pharmaceuticals or a related industry., • Proven track record of developing and executing successful commercial and marketing strategies., • Demonstrated leadership experience in high-performance environments., • Strong analytical, strategic thinking and problem-solving capabilities., • Excellent communication, influencing and stakeholder management skills., • Ability to operate effectively within a complex matrix organisation., • Experience within cardiovascular, electrophysiology or medical technology sectors., • MBA #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever-increasing population while taking care of our planet. Join us and help shape the future of agriculture. Are you a proactive problem solver with a passion for driving technical innovation? If so, we have good news as we are looking for an experienced DMPK/ADME Technical Expert to join our Analytical Metabolism and Methods (AMM) group within Product Safety. Within this role, you will make a key impact in projects by delivering innovative study designs to aid our understanding of the Absorption, Distribution, Metabolism and Excretion (ADME) and Pharmacokinetics (PK) and/or Toxicokinetics (TK) of chemicals in mammalian toxicology species. You will work within a highly collaborative team of study managers and technical experts, while applying your scientific expertise to interpret complex DMPK/ADME data for project teams, directly supporting the development and registration of sustainable crop protection products. A recent example is the registration of TYMIRIUM® technology which protects crops against soil-borne pests. Additionally you will build effective partnerships with Contract Research Organisations (CROs), directing external study execution and collaborating to resolve technical challenges to secure the timely delivery of externally placed studies. Key responsibilities will include: • Overseeing CRO delivery: Ensuring the timely delivery of business critical data generated at CROs, while being responsible for study strategy documents, protocol design, evaluation of data and reviewing/authorising company reports., • Delivering technical insights: Elucidating insights from ADME and PK/TK data and reporting expert conclusions to metabolism teams., • Applying regulatory expertise: Utilising your expert knowledge and understanding of ADME, PK/TK as well as relevant global regulatory guidance documents and their implication to optimise and de-risk our study designs. Keeping abreast of changes to regulatory guidelines and requirements., • Partnering with CROs: Independently providing technical guidance and problem-solving support to external suppliers, where appropriate, to facilitate transfer of technical knowledge., • Driving continuous improvement: Leading or contributing to the creation and optimisation of new processes, technical guidance documents and report templates to improve efficiency and consistency across the team., • Serving as a scientific contributor within the ADME, PK/TK expert area, providing expertise to metabolism teams and other functional areas as required. What we are looking for • Minimum of a degree or equivalent in a biology- or chemistry-related discipline., • Significant knowledge in the areas of DMPK/ADME, with expertise in pharmacokinetics and/or toxicokinetics., • Familiarity of global Regulatory Test Guidelines (e.g. OECD 417) relevant to ADME and toxicokinetics studies conducted to GLP standards for the registration of crop protection chemicals., • Experience in translating complex datasets into key safety or regulatory insights to inform decision making., • Practical knowledge of quantitative PK/TK principles, including non-compartmental analysis (NCA), calculation of key PK/TK parameters., • Proven ability to work collaboratively within diverse scientific teams (e.g., toxicologists, modellers, metabolism specialists) and with external stakeholders (industry, contract research or regulatory agencies) to achieve project goals., • Capability to organise, prioritise, and track complex scientific deliverables across multiple projects, applying strong attention to detail and analytical thinking to solve problems in scientific experiments to maintain quality and delivery to agreed timelines., • Excellent oral and written communication skills, with the ability to prepare technical reports and presentations to articulate complex technical matters clearly., • Willingness to learn and ability to apply new skills promptly., • In-depth understanding of in vitro and in vivo xenobiotic mammalian metabolism, including metabolite identification, metabolic pathway elucidation, and cross-species comparison would be desirable., • Experience managing services delivered through third-party organisations, ensuring quality, milestone adherence, and budget discipline would be advantageous. Our site Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott's Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer • Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance., • Up to 31.5 days annual holiday., • A position which contributes to valuable and impactful work in a stimulating and international environment., • The chance to work as part of a global team to address the current and future needs of the agricultural sector., • Learning culture and wide range of training options. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: careers/working-syngenta/diversity-and-inclusion Jealott's Hill has Disability Confident certification. We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott's Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you. #J-18808-Ljbffr

Job ID: 01876102Posted: Posted 18 Days AgoStart Date: 2026-09-28Location: GB-DUR-SEDGEFIELD-001 ~ Orbit Net Park ~ SEDGEFIELD (External Site); Glenrothes, Fife; Gloucester, South Gloucestershire; Manchester, Lancashire; Winnersh, Wokingham; High Wycombe, BuckinghamshireCountry: United KingdomTime Type: Full timeDate Posted:2026-09-28 Applying for this role is straight forward Scroll down and click on Apply to be considered for this position. Country:United Kingdom Location:Sedgefield, Durham Position Role Type:HybridAt RTX, the world's largest aerospace and defense company, 185,000 great minds are united by purpose and inspired to make a difference solving the world’s most complex problems. With our three market leading businesses, world-class operations and investments in research and development, we offer capabilities and opportunity no one else can. Together, we push the boundaries of known science and find new ways to connect and protect our world. Raytheon brings the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today’s mission and stay ahead of tomorrow’s threat. We deliver solutions that help our nation and allies defend freedoms and deter aggression, creating a safer, more secure world. Join us and help shape the future of aerospace and defense.Raytheon NORSS is seeking an exceptional Space Systems Chief Engineer to help shape the future of our space business.As the most senior engineering leader within the NORSS team, you will serve as the organisation’s technical authority, providing strategic direction across our space portfolio and leading multidisciplinary teams to deliver innovative, mission-critical capabilities. This is a unique opportunity to influence the technical vision, growth, and long-term success of a rapidly expanding space business.The ideal candidate will have a background with defence, academia, commercial, and scientific space exposure. You will combine deep expertise in space systems engineering with proven leadership in technology strategy, innovation, investment planning, business growth, and risk management. You will be expected to provide technical leadership at the highest level, shaping both current programmes and future capability development.We are particularly interested in candidates who have played a leading role in the development and delivery of technologies in Earth Observation, Space Domain Awareness (SDA) and Space-based ISR mission architectures.Above all, you will be a technical leader with the credibility, vision and drive to inspire engineering teams, engage customers and stakeholders, and ensure the successful delivery of complex space missions that advance both customer objectives and Raytheon NORSS's strategic ambitions. This Role reports into the Space and ISR Mission Area business lead and the Head of Engineering for Software and Services.Skills and Experience - A 2:1 bachelor’s degree in a relevant field (physics, mathematics, engineering or science).Excellent communication skills (written and oral), to articulate and communicate technical detail clearly and concisely with colleagues, customers and partner organisations at all levels. Able to prepare detailed reports and present where necessary.Knowledge of Space and Ground Segment architectures.Experience of Systems Engineering and full lifecycle development process.Working understanding and experience of software development process.A strong understanding of Space Domain Awareness (SDA) or Space-based ISR systems.Knowledge of secure remote data handling architectures.Experience in bid submission, including solution definition, technical bid writing and review.Experience writing and reviewing technical white papers and studies.Engineering team leadership and line management.A working understanding of modern digital technologies and practices, including cloud platforms, data security, and machine learning. xrnqpay Desirable - Understanding of orbital mechanics and orbit determinationKnowledge of space domain awareness software packages and toolsetsExperience with a variety of ground and space-based SDA sensors and their use Broad understanding of the space environment and spacecraft design and operationFamiliarity with RF and Optical systems for ground and space-based SDA missions and operationsProgramme and portfolio management experienceAgile and waterfall development methodologiesEngineering team development and supervision through relevant training and mentoringECSS Standards compliance including Software and Systems EngineeringFamiliarity with CCSDS standards for space data and information systemsDevelopment of Technology Roadmaps for technology maturation from TRL1 to TRL9Unit, Subsystem, System and Platform QualificationEnvironmental testing experienceWorking understanding of digital data cloud platforms#LI-LM1RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law. Privacy Policy and Terms:Click on this link to read the Policy and Terms

Company DescriptionSyngenta Group, a global leader in agricultural technology and innovation, employs 60,000 people across more than 100 countries to transform agriculture through tailor-made solutions for farmers, society, and our planet. All potential applicants are encouraged to scroll through and read the complete job description before applying. Our diverse portfolio encompasses seeds, crop protection, nutrition products, agronomic solutions, and digital services, all designed to help farmers produce healthy food, feed, fiber, and fuel while conserving natural resources and protecting the environment. Our mission is to address critical challenges such as climate change and food security through sustainable practices and cutting-edge solutions, while safeguarding the planet's resources. Jealott's Hill International Research Centre is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety, technical support of our product range and seeds research.Job DescriptionPurposeAt Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success.Syngenta's Dietary Risk Assessment team is seeking a Dietary Safety Assessor based in Jealott's Hill. In this role, you will ensure the safety and regulatory compliance of our crop protection products across the European market, directly contributing to the success of farmers and the sustainability of agriculture.Key Responsibilities:Undertake dietary risk assessment projects for the Europe team, delivering timely safety inputs that drive European and global business objectives.Prepare and critically review dietary safety sections of regulatory dossiers for EU plant protection product registrations, renewals, and lifecycle management.Contribute to innovative solutions and strategies to address complex cross-functional challenges and champion science-based regulatory positions.Communicate scientific outcomes and regulatory positions to internal stakeholders and regulatory meetings.Strategic Contribution & Communication:Partner with toxicology, residue chemistry, and cross-functional teams to develop integrated safety evaluations and strategies for new products and existing registrations.Represent Syngenta at regulatory forums and build productive relationships with EU authorities (competent authorities, EFSA, European Commission).Stay at the forefront of EU regulations (Reg 1107/2009, EFSA guidance), scientific developments, and emerging issues in dietary risk assessment and human safety.Actively participate in industry task forces, working groups, and scientific initiatives.QualificationsEducation & Experience:BSc, MSc, or Ph.D. in toxicology, food science, chemistry, biology, or related life science discipline.Minimum 3 years of experience in consumer/human safety assessment, preferably within the agrochemical, pharmaceutical, or food safety sectors.Technical Excellence:Working knowledge of EU regulatory frameworks and dietary risk assessment methodologies for plant protection products.Strong scientific writing skills with expertise in critical data interpretation and risk assessment of chemical substances.Understanding of EU regulations (Reg 1107/2009, EFSA guidance) and ability to stay current with evolving scientific developments.Experience representing organizations in regulatory forums and engaging with EU authorities (competent authorities, EFSA, European Commission).Core Competencies:Communication Excellence: Outstanding written and verbal communication skills with the ability to translate complex scientific concepts for diverse audiences.Strategic Innovation: Ability to think strategically, develop creative solutions, and navigate complex problems in dynamic regulatory environments.Additional InformationWhat we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. We offer a position which contributes to valuable and impactful work in a stimulating and international environment. A vibrant growth and learning culture with a wide range of formal and informal training opportunities, a self-paced learning platform, onsite lectures and seminars, as well as mentoring in technical skills and professional competencies. Onsite restaurant, gym and fitness classes. The chance to be part of a diverse scientific community that is working to address the future needs of the agricultural sector and help feed an ever-increasing population. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. xrnqpay Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: SummaryType: Full-timeFunction: Research

Company Description Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. Please ensure you read the below overview and requirements for this employment opportunity completely. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture. Job DescriptionDrive data-driven discovery in crop protection by applying advanced computational approaches to solve complex biological challenges. In this role, you will collaborate with scientists across Crop Protection Research, developing and deploying bioinformatics tools, machine learning models, and data workflows that generate insights from diverse biological datasets—directly supporting the development of safer, more sustainable agricultural solutions. Key Responsibilities Develop and apply state-of-the-art computational methods to address key challenges in Crop Protection Bioscience. Design, test, and deploy data analysis tools, workflows, and modelling approaches using iterative, evidence-based methods. Communicate analytical results, insights, and recommendations clearly to both technical and non-technical audiences. Guide scientists on data quality, integrity, and suitability for analysis. Collaborate across the Bioscience Digital team and wider R&D data community to share learning and drive innovation. Monitor external scientific and computational developments and identify opportunities for application within Bioscience. QualificationsMSc/PhD in computational biology, data science, natural sciences, or a related discipline, with a focus on data analysis, machine learning, or multi-omics data integration. Strong hands-on experience with Python and R for bioinformatics, data analysis, and visualisation. Confidence building, validating, and testing machine learning models. Experience with high-performance computing, version control systems, and reproducible digital workflows. Ability to work autonomously and communicate effectively with researchers across diverse scientific disciplines. Enthusiasm for innovation and solving complex biological problems through computational approaches. Additional InformationSite Details Jealott's Hill International Research Centre UK is situated in pleasant semi-rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance. Up to 31.5 days annual holiday. Flexible working We offer a position which contributes to valuable and impactful work in a stimulating and international environment. The opportunity to develop and apply your science within the chemical industry. The chance to work as part of a global team to address the current and future needs of the agricultural sector. Learning culture and wide range of training options. Syngenta has been ranked as a top 5 employer and number 1 in agriculture by Science Journal. xrnqpay Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: SummaryType: Full-timeFunction: Research

Syngenta is seeking a Staff Engineer, Decision Support & Planning Optimization to lead AI-powered decision making for R&D. You will mentor engineers, design scalable backend services, and collaborate across engineering, product and scientific teams to deliver auditable, secure systems with strong do

Syngenta Crop Protection seeks a Senior Data Scientist – Predictive Science to develop ML/GenAI models guiding discovery and development in Crop Protection.You will connect diverse scientific data with business decisions and work with international researchers to deliver robust insights.You will l

Syngenta Crop Protection is seeking a senior leader to drive durable, scalable IT solutions across R&D applications and day-two operations. You will mentor high-performing teams and shape engineering management practices for reliable service delivery. Based at Jealott's Hill UK, you will collaborate with engineering, product, and scientific teams to translate complex needs into practical solutions, establish KPIs, and manage budgets and vendor relationships. #J-18808-Ljbffr

CBRE Global Workplace Solutions is a leading global provider of integrated facilities and corporate real estate management. We are currently recruiting an extra works manager for our contract based in Bracknell. CBRE Global Workplace Solutions is recruiting an Extra Works Manager to join the team at Syngenta, Bracknell. This role takes end‑to‑end ownership of all additional works across the contract, from initial request and site survey through quotation, customer approval, mobilisation, safe delivery, quality assurance, and formal close‑out. Working across a diverse campus of offices, laboratories and glasshouses, the successful candidate will coordinate engineering teams and specialist contractors, ensuring all works are delivered safely, on time, within scope, and to a high standard, while providing day‑to‑day leadership to a small team. • Take full ownership of all additional works from initial request through to completion and close‑out., • Review requests to establish scope, priorities, access requirements, operational constraints and resource needs., • Organise engineers and specialist contractors to attend site and survey proposed works., • Review quotations for technical suitability, accuracy, completeness, value for money and alignment with the required scope., • Ensure quotations clearly capture labour, materials, access requirements, permits, specialist support, programmes and exclusions., • Upload and manage quotations through WebQuote, maintaining visibility of outstanding submissions and customer approvals., • Control variations and prevent unauthorised work from commencing before approval is obtained., • Maintain accurate records of approvals, work in progress, costs and completion status., • Ensure asset changes resulting from additional works are communicated to the Asset Manager, including details of removed, replaced, redundant or newly installed assets., • Support the maintenance of accurate asset records and associated documentation., • Validate completion information to enable timely commercial close‑out and invoicing., • Develop and maintain delivery plans for approved works packages., • Coordinate engineering resources, contractors, materials, access requirements, isolations and site logistics., • Agree programmes and delivery dates with stakeholders while minimising disruption to operations., • Manage works involving multiple trades and contractors, resolving delays, dependencies and delivery issues proactively., • Attend and supervise critical, higher‑risk or out‑of‑hours activities when required., • Ensure works are completed within agreed scope, programme and quality standards., • Review and accept suitable Risk Assessments and Method Statements (RAMS) before work begins., • Ensure Authority to Work processes, permits, isolations and site controls are in place where required., • Confirm contractors have completed site inductions and understand local site rules and restrictions., • Host contractors on site, coordinate access and monitor compliance with approved RAMS and site requirements., • Challenge unsafe behaviours or inadequate controls and stop work where there is an immediate safety, quality or compliance concern., • Ensure work areas are left safe, secure, clean and ready for operational use., • Provide day‑to‑day leadership and management of the carpentry team., • Allocate and prioritise workloads across additional works, planned activities and reactive requirements., • Monitor productivity, workmanship, safe working practices and timely completion of tasks., • Identify training, competency, resource, tooling and material requirements., • Provide clear expectations, regular communication, coaching and support to maintain high standards of safety, quality and customer service., • Inspect completed works and verify compliance with approved scope and quality requirements., • Ensure defects, incomplete items and snagging issues are rectified before work is accepted., • Obtain and retain relevant certificates, commissioning records, warranties, photographs, test results and completion documentation., • Confirm work areas have been reinstated and communicate completion to relevant stakeholders., • Maintain clear, auditable records throughout the lifecycle of each additional works project., • Strong planning, organisational and prioritisation skills., • Effective written and verbal communication skills., • Ability to review work scopes and contractor quotations., • Commercial awareness and an understanding of cost control., • Competence in Microsoft Office and electronic work‑management systems., • Experience managing additional works, minor works, projects or facilities activities., • Experience coordinating engineers and contractors., • Supervisory or team leadership experience., • Experience monitoring quality standards and closing out completed works., • Relevant technical, trade or facilities management experience., • Sound knowledge of contractor control, RAMS, permit systems and Authority to Work processes., • Understanding of mechanical, electrical, building fabric and general facilities management activities., • Appropriate health and safety training., • A proactive, organised and accountable approach., • A strong commitment to safety and customer service., • Confidence to challenge unsafe practices or poor‑quality work., • Ability to remain calm and decisive when resolving operational issues., • Commitment to seeing work through to full completion., • Experience using WebQuote or a similar quotation workflow system., • IOSH Managing Safely or equivalent qualification., • Relevant technical or project management qualification., • Knowledge of facilities management within a scientific, laboratory, pharmaceutical or regulated environment., • Experience managing carpentry, fabric or multi‑skilled trade teams., • Experience working across a large operational campus. When you join CBRE, you become part of the global leader in commercial real estate services and investment that helps businesses and people thrive. We are dynamic problem solvers and forward‑thinking professionals who create significant impact. Our collaborative culture is built on our shared values — respect, integrity, service and excellence — and we value the diverse perspectives, backgrounds and skillsets of our people. At CBRE, you have the opportunity to chart your own course and realize your potential. We welcome all applicants. We value human interaction to understand each candidate's unique experience, skills and aspirations. We do not use artificial intelligence (AI) tools to make hiring decisions, and we ask that candidates disclose any use of AI in the application and interview process. #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture. We are looking for a hands-on, senior-level Software Engineer with deep Python expertise to build reliable internal platforms and developer-enablement capabilities. This is an engineering-first role: strong software design, coding fluency and practical problem-solving are essential. You will apply AI in pragmatic ways-such as designing document search and conversational experiences using Retrieval-Augmented Generation (RAG)-while maintaining a high bar for engineering quality, security, scalability and operational excellence. • Design, build and maintain production-grade Python services, libraries and developer tools., • Apply modern Python practices, including packaging, type hints, asynchronous programming and maintainable API design., • Create shared libraries, service templates and engineering standards that enable multiple internal teams to build consistently and efficiently., • Build and evolve AI-enabled capabilities, including RAG-based search and conversational solutions over internal documentation and knowledge sources., • Define robust evaluation approaches for AI-assisted features, balancing usefulness, reliability, security and cost., • Develop and maintain CI/CD pipelines and cloud-native delivery practices using Docker, Kubernetes and Terraform., • Establish strong testing, code quality, documentation-as-code and secure software development practices., • Improve application performance, scalability and reliability through profiling, benchmarking, observability and architectural improvements., • Implement monitoring, alerting and operational standards for platform services., • Conduct thorough code reviews, mentor engineers and raise engineering standards across the team., • Partner with engineering, product and scientific stakeholders to translate complex needs into practical, scalable technical solutions. Required Qualifications • Significant hands-on experience as a Software Engineer, with strong, production-level proficiency in Python. Equivalent depth in Java may also be considered., • Demonstrated ability to write clean, maintainable and well-tested code, and to solve complex engineering problems independently., • Strong experience with modern Python practices: packaging, dependency management, typing, async programming and service/API development., • Experience designing and maintaining reusable libraries, service templates or internal developer platforms used by multiple teams., • Strong knowledge of software quality practices, including automated testing, code reviews, CI/CD and release engineering., • Practical experience with Docker, Kubernetes and Infrastructure as Code, ideally Terraform., • Experience with observability, monitoring, alerting, performance profiling and benchmarking., • Solid understanding of secure coding practices, vulnerability management and security considerations in software delivery., • Applied understanding of Generative AI and LLM patterns, particularly RAG. You should be able to explain and design an approach for document search or conversational interfaces over enterprise content., • Strong written and spoken English, with the ability to communicate effectively across technical and non-technical stakeholders., • Experience building internal platforms, developer tools or products adopted by several engineering teams., • Experience in agriculture, life sciences, scientific computing or another regulated enterprise environment., • Experience working in distributed, international engineering organisations., • Track record of technical leadership, mentoring or leading cross-team engineering initiatives., • Familiarity with AI/ML frameworks and tools used in software development environments. You are an engineer first: someone who can go deep in code, make sound technical decisions and deliver durable software in production. You use AI thoughtfully and practically-not as a substitute for engineering fundamentals, but as a capability embedded in reliable, secure and scalable platforms. Why Syngenta? • Meaningful impact: help build technology that supports scientific innovation and sustainable agriculture., • Complex, modern challenges: work on high-scale platforms and systems with room for technical judgement., • Collaborative environment: partner with global engineering, R&D and product communities., • Growth: broaden your influence through challenging work, visible outcomes and a global network #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow productively and sustainably. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision-making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. No matter what your position, you will have a vital role in safely feeding the world and taking care of our planet. Join us and help shape the future of agriculture. We are looking for a Staff Engineer, Cloud Foundations to lead the technical direction of a multi-cloud foundation that enables every engineering team to build securely, reliably and with clear cost visibility. This is an opportunity to work at the intersection of advanced technology and agricultural R&D, partnering with engineers, product leaders and scientific stakeholders on capabilities with real‑world impact. Help accelerate the digital capabilities that support more sustainable agriculture and scientific innovation. What You'll Do • Lead and apply deep expertise in multi-cloud architecture (AWS and GCP) to deliver durable, scalable outcomes that support organizational growth., • Lead and apply deep expertise in organization-scale Terraform and infrastructure as code to deliver durable, scalable outcomes., • Lead and apply deep expertise in cloud networking and governance to deliver durable, scalable outcomes., • Lead and apply deep expertise in FinOps instrumentation and cloud economics to deliver durable, scalable outcomes., • Lead and apply deep expertise in AI-assisted engineering with rigorous review to deliver durable, scalable outcomes., • Lead and apply deep expertise in technical leadership without line authority to deliver durable, scalable outcomes., • Collaborate across engineering, product and scientific teams to translate complex needs into practical solutions., • Set a high bar for quality, documentation and thoughtful use of AI-assisted engineering., • Mentor and develop engineering talent by sharing cloud architecture knowledge and best practices across teams., • Establish and enforce cloud security standards, compliance frameworks and governance policies to protect organizational assets., • Drive incident response protocols and reliability improvements to ensure high availability of cloud infrastructure., • Conduct architecture reviews and provide technical guidance on cloud design decisions to ensure alignment with organizational standards. What You Bring • Demonstrable experience in multi-cloud architecture: AWS and GCP, • Demonstrable experience in organisation-scale Terraform and infrastructure as code, • Demonstrable experience in cloud networking and governance, • Demonstrable experience in FinOps instrumentation and cloud economics, • Demonstrable experience in AI-assisted engineering with rigorous review, • Demonstrable experience in technical leadership without line authority, • Demonstrable experience in platform-as-product mindset, • Demonstrable experience in stakeholder management with hyperscalers, • Demonstrable experience in cloud security standards, compliance frameworks and governance policy development, • Demonstrable experience in incident response protocols and reliability engineering, • Strong communication skills and the ability to influence across technical and non-technical stakeholders, • Proven ability to conduct architecture reviews and provide technical guidance on cloud design decisions, • Fluent English, written and spoken, • AWS or GCP Certification Bonus Points • Experience in agriculture, life sciences, scientific computing or a regulated enterprise environment, • Experience building platforms, products or services used by multiple internal teams, • Experience working in distributed, international engineering organisations, • Experience in cost optimisation and cloud economics management, • Experience mentoring and developing engineering talent in cloud architecture practices Why Syngenta? Meaningful impact: help build technology that supports scientific innovation and sustainable agriculture. Complex, modern challenges: work on high-scale platforms and systems with room for technical judgement. Collaborative environment: partner with global engineering, R&D and product communities. Growth: broaden your influence through challenging work, visible outcomes and a global network. By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply #J-18808-Ljbffr

Syngenta Crop Protection is a leader in agricultural innovation, bringing breakthrough technologies and solutions that enable farmers to grow healthy and nutritious food while taking care of the planet. We offer a leading portfolio of crop protection solutions for plant and soil health, as well as digital solutions that transform the decision‑making capabilities of farmers. Our 17,900 employees serve to advance agriculture in more than 90 countries around the world. Syngenta Crop Protection is headquartered in Basel, Switzerland, and is part of the Syngenta Group. Our employees reflect the diversity of our customers, the markets where we operate and the communities which we serve. Regardless of your position, you will have a vital role in safely feeding an ever‑increasing population while taking care of our planet. Join us and help shape the future of agriculture. Are you a proactive problem solver with a passion for driving technical innovation? Do you enjoy solving complex analytical problems and delivering innovative technical solutions? If so, we have good news, as we have an exciting opportunity for an experienced Environmental Fate Metabolism Study Manager to join our Analytical Methods & Metabolism (AMM) team and take on the challenge of elucidating the metabolic fate of our active ingredients in the environment. Working within a highly collaborative team of study managers and technical experts, you will have the challenge to apply your scientific background to fate metabolism data and share insights to project teams to support the registration of sustainable crop protection products. A recent example is the registration of TYMIRIUM® technology which protects crops against soil‑borne pests. Within the role you will solve analytical problems and build relationships with Contract Research Organisations (CROs) to deliver innovative technical solutions and critical endpoints. Key responsibilities will include: • Ensuring the timely delivery of business critical data generated at CROs, being responsible for protocol design, evaluation of data and reviewing/authorising company reports., • Elucidating insights from fate metabolism data and reporting expert conclusions to metabolism teams., • Independently providing technical assistance and innovative solutions to external suppliers to facilitate transfer of technical knowledge., • Developing expert knowledge and understanding of fate metabolism as well as relevant global regulatory guidance documents and their implication to our study designs., • Serving as a scientific contributor, providing expertise to metabolism teams and other functional areas as required. What we are looking for • Degree or equivalent in a biology/chemistry or related discipline., • Experience of conducting or managing environmental fate metabolism studies to meet GLP standards and familiarity of the relevant Regulatory Test Guidelines ., • Experience of generating key insights from data sets., • Active scientific participation and collaboration with colleagues in industry, contract research or regulatory agencies., • Ability to collaborate effectively in diverse teams, demonstrating strong organizational and analytical problem solving skills., • Keen attention to detail and adaptability to learn and apply new skills., • Knowledge of compound metabolism in the environment would be beneficial., • Experience of accessing services through third‑party organisations would be advantageous. Our site Jealott's Hill International Research Centre UK is situated in pleasant semi‑rural surroundings between Bracknell and Maidenhead and is the place of work for approximately 800 Syngenta scientists and support staff. Jealott’s Hill is one of the main global research and development sites and key activities include research into discovery of new active ingredients, new formulation technologies, product safety and technical support of our product range. What we offer • Extensive benefits package including a generous pension scheme, bonus scheme, private medical & life insurance., • Up to 31.5 days annual holiday., • Large campus environment., • A position which contributes to valuable and impactful work in a stimulating and international environment., • The chance to work as part of a global team to address the current and future needs of the agricultural sector., • Learning culture and wide range of training options. Syngenta has been ranked as atop 5 employer and number 1 in agriculture by Science Journal. Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Learn more about our D&I initiatives here: careers/working-syngenta/diversity-and-inclusion Jealott’s Hill has Disability Confident certification. We are committed to making all stages of our recruitment process accessible to all candidates and our Jealott’s Hill site are a Disability Confident Level 2 Employer. Please let us know if you need any assistance or reasonable adjustments throughout your application and we will do everything we can to support you. #J-18808-Ljbffr

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. At Boston Scientific, you will find a collaborative culture driven by a passion for inno

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