We have an exciting opportunity for an experienced scientist to join a growing therapeutics organisation. You will contribute to cutting-edge research in the development of therapeutics for veterinary diseases. The role requires expertise in in vitro assay development, molecular pharmacology, and cell biology. As a Principal Scientist, you must also have a strong leadership background. Key Responsibilities: Implement cutting-edge pharmacological and immunological assays to characterize antibody candidates and assess their therapeutic potential. Collaborate closely with cross-functional teams, including molecular biologists, protein engineers translational scientists and our dedicated CMC Group, to advance drug discovery programs from target validation to clinical development. Provide scientific leadership and guidance to project and laboratory teams as an expert in the field, fostering a culture of innovation, scientific rigor, and excellence. Present research findings and project updates to internal stakeholders, external collaborators, and scientific conferences. Be at the cutting-edge of emerging trends, technologies, and advancements in the fields of in vitro assay development and execution. Guide a multidisciplinary laboratory team to design, produce and test biological candidate antibodies for veterinary use Drive innovation and implement novel approaches, methodologies, and technologies to enhance drug discovery and development efforts through continuous improvement. Contribute to the scientific community through publications, presentations, and participation in scientific forums. Drive antibody discovery efforts through target identification, antibody generation, and lead optimization strategies. Qualifications/Experience: Ph.D. in Pharmacology, Immunology, Molecular Biology, or equivalent with a minimum of 10 years of industry experience in in vitro pharmacology in drug discovery, preferably with significant antibody experience. Proven track record of scientific leadership and expertise in pharmacology, antibody development, and preclinical drug discovery. Strong background in immunology, cell biology, and molecular biology techniques relevant to antibody discovery and characterization. Demonstrated ability to lead and mentor scientific teams, drive collaborative research efforts, and communicate effectively across interdisciplinary teams. Excellent problem-solving skills, analytical thinking, and ability to thrive in a dynamic and fast-paced research environment. Proficiency in data analysis software, statistical methods, and bioinformatics tools for data interpretation and visualization. Ability to work as an expert cross-functionally, working with colleagues in discovery, early development, clinical and manufacturing. Ability to communicate at all levels within the organisation and act as an advocate for the company with external collaborators and partners. Highly competent across cell-biology, in vitro pharmacology and in vitro assay disciplines with specific expertise in analytical software tools, data analysis and interpretation. This is an exciting and demanding role for an ambitious individual looking to learn, grow and contribute in a lab-based role.
Apr 20, 2024
Full time
We have an exciting opportunity for an experienced scientist to join a growing therapeutics organisation. You will contribute to cutting-edge research in the development of therapeutics for veterinary diseases. The role requires expertise in in vitro assay development, molecular pharmacology, and cell biology. As a Principal Scientist, you must also have a strong leadership background. Key Responsibilities: Implement cutting-edge pharmacological and immunological assays to characterize antibody candidates and assess their therapeutic potential. Collaborate closely with cross-functional teams, including molecular biologists, protein engineers translational scientists and our dedicated CMC Group, to advance drug discovery programs from target validation to clinical development. Provide scientific leadership and guidance to project and laboratory teams as an expert in the field, fostering a culture of innovation, scientific rigor, and excellence. Present research findings and project updates to internal stakeholders, external collaborators, and scientific conferences. Be at the cutting-edge of emerging trends, technologies, and advancements in the fields of in vitro assay development and execution. Guide a multidisciplinary laboratory team to design, produce and test biological candidate antibodies for veterinary use Drive innovation and implement novel approaches, methodologies, and technologies to enhance drug discovery and development efforts through continuous improvement. Contribute to the scientific community through publications, presentations, and participation in scientific forums. Drive antibody discovery efforts through target identification, antibody generation, and lead optimization strategies. Qualifications/Experience: Ph.D. in Pharmacology, Immunology, Molecular Biology, or equivalent with a minimum of 10 years of industry experience in in vitro pharmacology in drug discovery, preferably with significant antibody experience. Proven track record of scientific leadership and expertise in pharmacology, antibody development, and preclinical drug discovery. Strong background in immunology, cell biology, and molecular biology techniques relevant to antibody discovery and characterization. Demonstrated ability to lead and mentor scientific teams, drive collaborative research efforts, and communicate effectively across interdisciplinary teams. Excellent problem-solving skills, analytical thinking, and ability to thrive in a dynamic and fast-paced research environment. Proficiency in data analysis software, statistical methods, and bioinformatics tools for data interpretation and visualization. Ability to work as an expert cross-functionally, working with colleagues in discovery, early development, clinical and manufacturing. Ability to communicate at all levels within the organisation and act as an advocate for the company with external collaborators and partners. Highly competent across cell-biology, in vitro pharmacology and in vitro assay disciplines with specific expertise in analytical software tools, data analysis and interpretation. This is an exciting and demanding role for an ambitious individual looking to learn, grow and contribute in a lab-based role.
AWE have an exciting opportunity for a Theoretical Scientist , to work as a Prompt Diagnostician within our Design Physics Group , to develop modelling techniques and undertake reanalysis our underground test (UGT) data. Location: Aldermaston, West Berkshire . We are located between Reading and Basingstoke, with onsite parking. Due to the classified nature of this role, it is anticipated that the successful candidate will need to spend the entirety of their time working on site at AWE Aldermaston during their working hours. Package: £31,000 - £35,000 (depending on your suitability, qualifications, and level of experience) Closing Date: 1st May 2024 The Role The prompt diagnostics team are a small team within the Design Physics Group. Our mission is to assess, process and interpret the data recorded from the diagnostics fielded on previous underground ground tests (UGTs) prior to the Comprehensive Test Ban Treaty. This data forms the basis for understanding and validation of the complex physics models of nuclear warheads, which are used by our Design Physics colleagues to underwrite the performance and safety of existing and future designs. Key Responsibilities Planning, development and validation of theoretical models and software codes designed to replicate the physical mechanisms which occur in the diagnostics fielded on underground tests. Undertaking reanalysis of underground test data, using modern methods, to provide comparable data for our developing modelling capabilities. Working collaboratively with our international colleagues, sharing methods, ideas and knowledge to enhance your work. Present your own scientific achievements to the team, function and project through published work and presentations. The Company may require you to fulfil any other reasonable duties aligned to your position from time to time in line with business needs. Who Are We Looking For? To be considered for this role, you will need the following: A degree in physics, maths, computer science or an equivalent STEM-based discipline. Knowledge of scientific programming, using languages such as Python, Fortran, C++, or a similar high-level language. Willing to travel overseas as required. Whilst not on the check list, we are interested in hearing from candidates who can demonstrate some of the following: A methodical approach to complex problem solving using technical knowledge. A clear and concise communication approach, both oral and written. Excellent team working ability, with a proactive approach and the ability to prioritise a varied workload, ensuring timely delivery with minimum supervision. The ability to capture and communicate technical requirements effectively. Understanding and knowledge of radiation detection and measurement techniques. Broad understanding of basic physics concepts, in particular, nuclear, particle and electromagnetic physics. Experience of GEANT4 or MCNP modelling would be advantageous. Knowledge of electronics is desirable but not essential. What will you get from us? As part of our People Promise, AWE ( one of the best 25 big companies to work for in the UK ) has a range of benefits to suit you. These include: Time to recharge your batteries with 270 hours of annual leave (including Bank Holidays). 9-day working fortnight - every other Friday off work. Flexible working hours. Consideration for flexible working arrangements so that your work may fit in with your lifestyle. Just let us know on your application if you wish to work part time. Family friendly policies: Maternity Leave - 39 Weeks Full Pay and Paternity Leave - 4 Weeks Full Pay. Opportunities for Professional Career Development that include funding for the annual membership of a relevant professional body, access to mentors and training. Employee Assistance Programme and Occupational Health Services. A market leading contributory pension scheme (we will pay between 9% and 13% of your pensionable pay depending on your own contribution). Life Assurance. Discounts - access to savings on a wide range of everyday spending savings. Special Leave Policy including paid time off for volunteering, public service (including reserve forces) and caring for your family. A host of voluntary & core benefits to suit your health and wellbeing - more information available on our careers site. Important things you need to know: You must be a UK national who has been resident in the UK for the past 10 years. Interviews will be 90 minutes in length and will be held over Microsoft Teams. You will be required to prepare a 10-minute presentation in advance. Candidates must be willing and able to obtain and maintain the necessary security clearance for the role. This will be funded by AWE. Agencies: Please note that we do not out-source our recruitment
Apr 20, 2024
Full time
AWE have an exciting opportunity for a Theoretical Scientist , to work as a Prompt Diagnostician within our Design Physics Group , to develop modelling techniques and undertake reanalysis our underground test (UGT) data. Location: Aldermaston, West Berkshire . We are located between Reading and Basingstoke, with onsite parking. Due to the classified nature of this role, it is anticipated that the successful candidate will need to spend the entirety of their time working on site at AWE Aldermaston during their working hours. Package: £31,000 - £35,000 (depending on your suitability, qualifications, and level of experience) Closing Date: 1st May 2024 The Role The prompt diagnostics team are a small team within the Design Physics Group. Our mission is to assess, process and interpret the data recorded from the diagnostics fielded on previous underground ground tests (UGTs) prior to the Comprehensive Test Ban Treaty. This data forms the basis for understanding and validation of the complex physics models of nuclear warheads, which are used by our Design Physics colleagues to underwrite the performance and safety of existing and future designs. Key Responsibilities Planning, development and validation of theoretical models and software codes designed to replicate the physical mechanisms which occur in the diagnostics fielded on underground tests. Undertaking reanalysis of underground test data, using modern methods, to provide comparable data for our developing modelling capabilities. Working collaboratively with our international colleagues, sharing methods, ideas and knowledge to enhance your work. Present your own scientific achievements to the team, function and project through published work and presentations. The Company may require you to fulfil any other reasonable duties aligned to your position from time to time in line with business needs. Who Are We Looking For? To be considered for this role, you will need the following: A degree in physics, maths, computer science or an equivalent STEM-based discipline. Knowledge of scientific programming, using languages such as Python, Fortran, C++, or a similar high-level language. Willing to travel overseas as required. Whilst not on the check list, we are interested in hearing from candidates who can demonstrate some of the following: A methodical approach to complex problem solving using technical knowledge. A clear and concise communication approach, both oral and written. Excellent team working ability, with a proactive approach and the ability to prioritise a varied workload, ensuring timely delivery with minimum supervision. The ability to capture and communicate technical requirements effectively. Understanding and knowledge of radiation detection and measurement techniques. Broad understanding of basic physics concepts, in particular, nuclear, particle and electromagnetic physics. Experience of GEANT4 or MCNP modelling would be advantageous. Knowledge of electronics is desirable but not essential. What will you get from us? As part of our People Promise, AWE ( one of the best 25 big companies to work for in the UK ) has a range of benefits to suit you. These include: Time to recharge your batteries with 270 hours of annual leave (including Bank Holidays). 9-day working fortnight - every other Friday off work. Flexible working hours. Consideration for flexible working arrangements so that your work may fit in with your lifestyle. Just let us know on your application if you wish to work part time. Family friendly policies: Maternity Leave - 39 Weeks Full Pay and Paternity Leave - 4 Weeks Full Pay. Opportunities for Professional Career Development that include funding for the annual membership of a relevant professional body, access to mentors and training. Employee Assistance Programme and Occupational Health Services. A market leading contributory pension scheme (we will pay between 9% and 13% of your pensionable pay depending on your own contribution). Life Assurance. Discounts - access to savings on a wide range of everyday spending savings. Special Leave Policy including paid time off for volunteering, public service (including reserve forces) and caring for your family. A host of voluntary & core benefits to suit your health and wellbeing - more information available on our careers site. Important things you need to know: You must be a UK national who has been resident in the UK for the past 10 years. Interviews will be 90 minutes in length and will be held over Microsoft Teams. You will be required to prepare a 10-minute presentation in advance. Candidates must be willing and able to obtain and maintain the necessary security clearance for the role. This will be funded by AWE. Agencies: Please note that we do not out-source our recruitment
Description A personalised women's healthcare company, tailoring and monitoring medications based on unique biological profiles; medical history, mental health, genetics, and hormone levels. We enable women to understand their hormones, monitor their reproductive health and take control of their bodies. ABOUT THE ROLE + TEAM At Tuune, we are a diverse team of healthcare, design, and technology experts who've long believed that it's time for the medical world to acknowledge the fact that each woman is unique. A "one-size-fits-all" approach to women's health is damaging and simply not good enough anymore. As the Head of Research and Innovation at Tuune it will be your job to guide the direction of our scientific advancements, working as part of a cross-functional team alongside doctors, engineers, and designers, we're data-driven and favor lean methodologies. This role reports to the Chief Medical Officer and CEO of Tuune. A key part of the role will be driving product innovation within the company and nurturing a culture of scientific excellence. This is an exciting opportunity to make your mark on a new product that has the potential to impact millions of women's lives. YOUR MISSION As Tuune's Head of Research and Innovation you will be instrumental to the impact and success of our clinical product. WHAT YOU NEED TO SUCCEED A versatile biologist deeply passionate about women's health and precision medicine with strong analytical skills and the ability to diagnose problems and productionise research. In order to be successful in this role, you will need: 5+ years of industry experience (pharma, diagnostics, or medical devices) Advanced scientific degree (PhD and/or PostDoc) in a relevant field like Reproductive Medicine or Clinical Pharmacology Ability to work in the fast-paced but rigorous environment of a healthtech start-up Excellent communication skills with an ability to communicate complex science clearly and simply An interest in and understanding of female physiology, hormones, genetics and genetic testing Nice to have: Clinical pharmacology background with experience in reproductive health Experience working with patient data Experience managing a team of scientists Previously worked on contraceptives or female hormones Successfully executed studies that brought medical innovation through the FDA approval process Able to demonstrate an understanding of reproductive biology applied to drug discovery Requirements Your role is to: Participate in defining overall concept and strategy for developing science collaborations at Tuune, create roadmaps for initiating new and maintaining current research collaborations, develop and set research roadmaps for internal feasibility studies and validation priorities Define research aims and methods, design protocols, and drive the execution of internal and external research projects in collaboration with Tuune's medical and data science teams Generate internal literature reviews on relevant scientific topics Monitor scientific literature for advances in relevant fields Refine and improve the long-term scientific vision, create a scientific strategy that is aligned with Tuune's product vision and business goals, develop and set a research roadmap for feasibility studies and validation priorities Structuring data for subsequent analysis and interpretation Guide and mentor the research team at Tuune to ensure the research activities are carried out to the highest standards Work with bioinformaticians and software engineers developing algorithmic methods and tools, provide pharmacology input for new developments Benefits We have a full range of benefits, including share options, competitive salaries, private medical insurance, and a contributory pension scheme. We understand that everyone has their own work rhythm and believe in a flexible working schedule. When you need a break, you have unlimited holidays that you can use throughout the year. WE ARE AN EQUAL OPPORTUNITY EMPLOYER We commit to creating an environment that enables everyone to perform at their best. We're an equal opportunity employer dedicated to building a diverse and inclusive team. Tuune focuses on Mobile, Mobile Commerce, Digital Health, and Mobile Application. Their company has offices in United Kingdom and Greater London. They have a small team that's between 11-50 employees. You can view their website at
Apr 20, 2024
Full time
Description A personalised women's healthcare company, tailoring and monitoring medications based on unique biological profiles; medical history, mental health, genetics, and hormone levels. We enable women to understand their hormones, monitor their reproductive health and take control of their bodies. ABOUT THE ROLE + TEAM At Tuune, we are a diverse team of healthcare, design, and technology experts who've long believed that it's time for the medical world to acknowledge the fact that each woman is unique. A "one-size-fits-all" approach to women's health is damaging and simply not good enough anymore. As the Head of Research and Innovation at Tuune it will be your job to guide the direction of our scientific advancements, working as part of a cross-functional team alongside doctors, engineers, and designers, we're data-driven and favor lean methodologies. This role reports to the Chief Medical Officer and CEO of Tuune. A key part of the role will be driving product innovation within the company and nurturing a culture of scientific excellence. This is an exciting opportunity to make your mark on a new product that has the potential to impact millions of women's lives. YOUR MISSION As Tuune's Head of Research and Innovation you will be instrumental to the impact and success of our clinical product. WHAT YOU NEED TO SUCCEED A versatile biologist deeply passionate about women's health and precision medicine with strong analytical skills and the ability to diagnose problems and productionise research. In order to be successful in this role, you will need: 5+ years of industry experience (pharma, diagnostics, or medical devices) Advanced scientific degree (PhD and/or PostDoc) in a relevant field like Reproductive Medicine or Clinical Pharmacology Ability to work in the fast-paced but rigorous environment of a healthtech start-up Excellent communication skills with an ability to communicate complex science clearly and simply An interest in and understanding of female physiology, hormones, genetics and genetic testing Nice to have: Clinical pharmacology background with experience in reproductive health Experience working with patient data Experience managing a team of scientists Previously worked on contraceptives or female hormones Successfully executed studies that brought medical innovation through the FDA approval process Able to demonstrate an understanding of reproductive biology applied to drug discovery Requirements Your role is to: Participate in defining overall concept and strategy for developing science collaborations at Tuune, create roadmaps for initiating new and maintaining current research collaborations, develop and set research roadmaps for internal feasibility studies and validation priorities Define research aims and methods, design protocols, and drive the execution of internal and external research projects in collaboration with Tuune's medical and data science teams Generate internal literature reviews on relevant scientific topics Monitor scientific literature for advances in relevant fields Refine and improve the long-term scientific vision, create a scientific strategy that is aligned with Tuune's product vision and business goals, develop and set a research roadmap for feasibility studies and validation priorities Structuring data for subsequent analysis and interpretation Guide and mentor the research team at Tuune to ensure the research activities are carried out to the highest standards Work with bioinformaticians and software engineers developing algorithmic methods and tools, provide pharmacology input for new developments Benefits We have a full range of benefits, including share options, competitive salaries, private medical insurance, and a contributory pension scheme. We understand that everyone has their own work rhythm and believe in a flexible working schedule. When you need a break, you have unlimited holidays that you can use throughout the year. WE ARE AN EQUAL OPPORTUNITY EMPLOYER We commit to creating an environment that enables everyone to perform at their best. We're an equal opportunity employer dedicated to building a diverse and inclusive team. Tuune focuses on Mobile, Mobile Commerce, Digital Health, and Mobile Application. Their company has offices in United Kingdom and Greater London. They have a small team that's between 11-50 employees. You can view their website at
As part of PwC's global strategy, The New Equation, we're investing significantly in skills, capabilities and technologies to address the breadth and complexity of the challenges that our clients face with their businesses and in society. One of our responses to this was establishing Tech Central, a technology focused function working alongside other PwC teams. Tech Central is rapidly growing and the environment that our people work in is fuelled by ingenuity, collaboration and innovation. Our people are skilled and passionate about the work they do. As part of the team you'll experience an environment consisting of a wide range of technologies with ample room for you to learn, grow and innovate. About the team Building technology assets is one of our top priorities in Tech Central, and you will be part of our AI and Emerging Technology team. The team is customer focused and you'll solve data science problems in collaboration with other technical specialists in the team and our lines of service. The Role Contribute to data science engagements with key clients and lines of business Contribute to the delivery of core data science assets (such as our SaaS platforms) for ourselves and our clients Collaborate with non-technical stakeholders to define project objectives, scope, and deliverables, in order to translate our data science capabilities into tangible value Craft and manage project documentation, data analyses, presentations, and timelines, ensuring clear communication and understanding of findings and their commercial implications Skills and Experience Delivering significant and valuable advanced analytics projects and/or assets in industry and professional services Engagement of technical and senior stakeholders, including visualisation of results and presenting to senior stakeholders Experience with experiment design and measurement Delivery of projects on time and in budget for high profile clients Understanding of requirements for software engineering and data governance in data science We make extensive use of the following technologies in our team. Python for data science SQL for data processing Git for version control Azure / GCP Cloud Skills we'd like to hear about Data Manipulation and Analysis Data Visualisation Machine Learning/Software Engineering Model Deployment LLM Validation
Apr 18, 2024
Full time
As part of PwC's global strategy, The New Equation, we're investing significantly in skills, capabilities and technologies to address the breadth and complexity of the challenges that our clients face with their businesses and in society. One of our responses to this was establishing Tech Central, a technology focused function working alongside other PwC teams. Tech Central is rapidly growing and the environment that our people work in is fuelled by ingenuity, collaboration and innovation. Our people are skilled and passionate about the work they do. As part of the team you'll experience an environment consisting of a wide range of technologies with ample room for you to learn, grow and innovate. About the team Building technology assets is one of our top priorities in Tech Central, and you will be part of our AI and Emerging Technology team. The team is customer focused and you'll solve data science problems in collaboration with other technical specialists in the team and our lines of service. The Role Contribute to data science engagements with key clients and lines of business Contribute to the delivery of core data science assets (such as our SaaS platforms) for ourselves and our clients Collaborate with non-technical stakeholders to define project objectives, scope, and deliverables, in order to translate our data science capabilities into tangible value Craft and manage project documentation, data analyses, presentations, and timelines, ensuring clear communication and understanding of findings and their commercial implications Skills and Experience Delivering significant and valuable advanced analytics projects and/or assets in industry and professional services Engagement of technical and senior stakeholders, including visualisation of results and presenting to senior stakeholders Experience with experiment design and measurement Delivery of projects on time and in budget for high profile clients Understanding of requirements for software engineering and data governance in data science We make extensive use of the following technologies in our team. Python for data science SQL for data processing Git for version control Azure / GCP Cloud Skills we'd like to hear about Data Manipulation and Analysis Data Visualisation Machine Learning/Software Engineering Model Deployment LLM Validation
Machine Learning Engineer Analytics Centre of Excellence (ACOE) London/Hybrid The Analytics Centre of Excellence (ACOE) is positively impacting patient lives through the anticipation and delivery of Decision Intelligence solutions that increase clinical trial success, shorten drug development timelines, and reduce costs in bringing new drugs to market, getting much-needed drugs to patients faster through successful clinical trial delivery. Our vision at the ACOE is that every decision our users and clients make in R&D is made through Decision Intelligence, allowing speedy access to safe, novel, and effective treatments for all patients. ACOE Product Portfolio: In trial strategy, we are using Machine Learning (ML) to recommend countries and clinical trial sites and accurately predict clinical study timelines. We are deploying ML at clinical trial sites to read Electronic Medical Records data and find undiagnosed patients that are otherwise challenging to identify. We are optimizing our patient outreach targeting and are predicting participant dropout. In addition, problems in patient recruitment are being solved with ML. Further upstream in R&D we are predicting clinical trial outcomes, drug-protein interactions, repurposing drugs and even leveraging ML to optimize molecules. Job Overview Develop fit for purpose AIML models/algorithms/processes to address pharma/healthcare applications and innovative products upon completion of prototypes followed by the building of production grade algorithms/automation engines for client deliverables. Test for viability to deliver final products to clients. Able to bring newly researched ideas to reality quickly and on a large scale. Design, build, test, and deliver products from post-prototype to client delivery. Essential Functions Facilitates the transformation of machine learning research domain expertise in the areas of human data into viable prototypes Facilitates the development of features of models on individual projects and/or products with guidance and support from others Develops understanding of the creation of new algorithms through working alongside other Machine Learning Engineers and Machine Learning Research Scientists Facilitates the building and training of new production grade algorithms that can learn from complex, high dimensionality data to uncover patterns from which machine learning models and applications can be developed Uses a variety of techniques to improve the performance of individual natural language processing and/or machine learning algorithms Facilitates the testing and validation of models to determine viability for deployment with guidance and support from others Consult for internal and external clients, implement solution development and innovation to meet clients' needs, facilitate client AI project technical delivery What we're looking for Master's Degree Master's Degree in Machine Learning, Statistics, Computer Science, Physics, Math, or related field Several years' experience working on creating machine learning algorithms Programming experience using one or more of the following: Python, Java, C++, R, Go, Kubernetes, Deep learning or equivalent. Python (Scikit-learn, Tensor Flow, Pandas, NumPy, SciPy) SQL, Linux/mac command-line tools Experience with building, testing, measuring, and deploying machine learning models in production Familiarity with ML algorithms (classification, regression) and processes (how to build models, assess their goodness of fit, etc.) Familiarity with agile software development lifecycle (SCRUM, Kanban, etc.) Previous experience of owning, maintaining, and enhancing software data products Attention to clarity of code, ease of development, and correctness of implementations Good knowledge of software development best practices including testing, continuous integration, and DevOps tools Preferred Requirements: Knowledge and experience of Hierarchical Modelling Experience with clinical domain and with regulated data Used Deep Neural Network libraries such as Tensor Flow, especially with Bayesian Neural Networks Knowledge of cloud systems such as AWS, Azure, GCP and containerization such as Docker Experience working with large, real-world datasets Demonstrated in-depth understanding of product development lifecycle Demonstrated aptitude for and interest in peer mentorship Experience deploying code into production through CI/CD tools Knowledge of biostatistics/life sciences/healthcare technology Knowledge of UX principles Experience working in the Hadoop ecosystem Why Join? Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. You will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry. You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. It's an exciting time to join and reimagine what's possible in healthcare. IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential. We thank all applicants for their interest; however only those selected for interview will be contacted. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
Apr 18, 2024
Full time
Machine Learning Engineer Analytics Centre of Excellence (ACOE) London/Hybrid The Analytics Centre of Excellence (ACOE) is positively impacting patient lives through the anticipation and delivery of Decision Intelligence solutions that increase clinical trial success, shorten drug development timelines, and reduce costs in bringing new drugs to market, getting much-needed drugs to patients faster through successful clinical trial delivery. Our vision at the ACOE is that every decision our users and clients make in R&D is made through Decision Intelligence, allowing speedy access to safe, novel, and effective treatments for all patients. ACOE Product Portfolio: In trial strategy, we are using Machine Learning (ML) to recommend countries and clinical trial sites and accurately predict clinical study timelines. We are deploying ML at clinical trial sites to read Electronic Medical Records data and find undiagnosed patients that are otherwise challenging to identify. We are optimizing our patient outreach targeting and are predicting participant dropout. In addition, problems in patient recruitment are being solved with ML. Further upstream in R&D we are predicting clinical trial outcomes, drug-protein interactions, repurposing drugs and even leveraging ML to optimize molecules. Job Overview Develop fit for purpose AIML models/algorithms/processes to address pharma/healthcare applications and innovative products upon completion of prototypes followed by the building of production grade algorithms/automation engines for client deliverables. Test for viability to deliver final products to clients. Able to bring newly researched ideas to reality quickly and on a large scale. Design, build, test, and deliver products from post-prototype to client delivery. Essential Functions Facilitates the transformation of machine learning research domain expertise in the areas of human data into viable prototypes Facilitates the development of features of models on individual projects and/or products with guidance and support from others Develops understanding of the creation of new algorithms through working alongside other Machine Learning Engineers and Machine Learning Research Scientists Facilitates the building and training of new production grade algorithms that can learn from complex, high dimensionality data to uncover patterns from which machine learning models and applications can be developed Uses a variety of techniques to improve the performance of individual natural language processing and/or machine learning algorithms Facilitates the testing and validation of models to determine viability for deployment with guidance and support from others Consult for internal and external clients, implement solution development and innovation to meet clients' needs, facilitate client AI project technical delivery What we're looking for Master's Degree Master's Degree in Machine Learning, Statistics, Computer Science, Physics, Math, or related field Several years' experience working on creating machine learning algorithms Programming experience using one or more of the following: Python, Java, C++, R, Go, Kubernetes, Deep learning or equivalent. Python (Scikit-learn, Tensor Flow, Pandas, NumPy, SciPy) SQL, Linux/mac command-line tools Experience with building, testing, measuring, and deploying machine learning models in production Familiarity with ML algorithms (classification, regression) and processes (how to build models, assess their goodness of fit, etc.) Familiarity with agile software development lifecycle (SCRUM, Kanban, etc.) Previous experience of owning, maintaining, and enhancing software data products Attention to clarity of code, ease of development, and correctness of implementations Good knowledge of software development best practices including testing, continuous integration, and DevOps tools Preferred Requirements: Knowledge and experience of Hierarchical Modelling Experience with clinical domain and with regulated data Used Deep Neural Network libraries such as Tensor Flow, especially with Bayesian Neural Networks Knowledge of cloud systems such as AWS, Azure, GCP and containerization such as Docker Experience working with large, real-world datasets Demonstrated in-depth understanding of product development lifecycle Demonstrated aptitude for and interest in peer mentorship Experience deploying code into production through CI/CD tools Knowledge of biostatistics/life sciences/healthcare technology Knowledge of UX principles Experience working in the Hadoop ecosystem Why Join? Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. You will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry. You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. It's an exciting time to join and reimagine what's possible in healthcare. IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential. We thank all applicants for their interest; however only those selected for interview will be contacted. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
Who are we? Our team is the first in the world to use autonomous vehicles on public roads using end-to-end deep learning. With our multi-national world-class technical team, we're building things differently. We don't think it's scalable to tell an algorithm how to drive through hand-coded rules and expensive HD maps. Instead, we believe that machine learning algorithms learning from experience and data will allow our driver to be more intelligent and capable of easily adapting to new environments. Our aim is to be the future of self-driving cars: the first to deploy in 100 cities across the world bringing autonomy to everyone, everywhere. The impact you will have: We're looking for an experienced Applied Scientist with expertise in synthetic data to join our Vision & Graphics team. You'll be at the forefront of advancing our innovative neural simulator, Ghost Gym , developing and applying groundbreaking research to generate thousands of simulated scenarios. These scenarios are critical for training, testing, and debugging our end-to-end AI driving models, contributing significantly to the creation of safe and reliable AI driving technology. You will play a crucial role in designing, developing, and deploying innovative AI models. You will focus on generating and utilizing synthetic data to train and validate our AI systems, ensuring they meet the highest standards of accuracy and reliability. Challenges you will own: Lead the development and implementation of synthetic data generation techniques to support the training and testing of AI models. Collaborate with cross-functional teams to understand requirements and create realistic, scalable synthetic datasets tailored to specific AI applications. Apply state-of-the-art machine learning and deep learning methodologies to improve the fidelity and efficiency of synthetic data. Conduct rigorous validation and testing of AI models using synthetic data, identifying and addressing gaps in performance. Stay abreast of the latest research and technological advancements in synthetic data and neural rendering, integrating new findings into our workflows. This could involve opportunities to publish research findings in top-tier journals and conferences, contributing to the scientific community and establishing Wayve as a leader in the field. What you will bring: Must haves: Proven expertise in synthetic data generation and application in AI model training and testing. Strong foundation in machine learning, deep learning, and neural rendering techniques. Strong programming skills in Python, with experience in deep learning frameworks such as PyTorch. Demonstrable experience with tools relevant to synthetic data generation. Excellent problem-solving skills and the ability to work independently as well as in a team environment. Demonstrated ability to work collaboratively in a fast-paced, innovative, interdisciplinary team environment. Desirable: Experience with dynamic scene reconstruction and rendering, particularly in outdoor environments. Familiarity with parallel computing, GPU programming, and optimization techniques. PhD or MSc in Computer Science, Computer Engineering, or a related field, with a focus on computer graphics, computer vision, or machine learning. Our offer: A position to shape the future of autonomous driving, and thus to tackle one of the biggest challenges of our time Immersion in a team of world-class researchers, engineers and entrepreneurs Competitive compensation and stock options On-site chef and bar, lots of fun socials, a workplace nursery scheme and more! Help relocating/travelling to London, with visa sponsorship Flexible working hours - we trust you to do your job well, at times that suit you and your team. Wayve is built by people from all walks of life. We believe that it is our differences that make us stronger, and our unique perspectives and backgrounds that allow us to build something different. We are proud to be an equal opportunities workplace, where we don't just embrace diversity but nurture it - so that we all thrive and grow.
Apr 17, 2024
Full time
Who are we? Our team is the first in the world to use autonomous vehicles on public roads using end-to-end deep learning. With our multi-national world-class technical team, we're building things differently. We don't think it's scalable to tell an algorithm how to drive through hand-coded rules and expensive HD maps. Instead, we believe that machine learning algorithms learning from experience and data will allow our driver to be more intelligent and capable of easily adapting to new environments. Our aim is to be the future of self-driving cars: the first to deploy in 100 cities across the world bringing autonomy to everyone, everywhere. The impact you will have: We're looking for an experienced Applied Scientist with expertise in synthetic data to join our Vision & Graphics team. You'll be at the forefront of advancing our innovative neural simulator, Ghost Gym , developing and applying groundbreaking research to generate thousands of simulated scenarios. These scenarios are critical for training, testing, and debugging our end-to-end AI driving models, contributing significantly to the creation of safe and reliable AI driving technology. You will play a crucial role in designing, developing, and deploying innovative AI models. You will focus on generating and utilizing synthetic data to train and validate our AI systems, ensuring they meet the highest standards of accuracy and reliability. Challenges you will own: Lead the development and implementation of synthetic data generation techniques to support the training and testing of AI models. Collaborate with cross-functional teams to understand requirements and create realistic, scalable synthetic datasets tailored to specific AI applications. Apply state-of-the-art machine learning and deep learning methodologies to improve the fidelity and efficiency of synthetic data. Conduct rigorous validation and testing of AI models using synthetic data, identifying and addressing gaps in performance. Stay abreast of the latest research and technological advancements in synthetic data and neural rendering, integrating new findings into our workflows. This could involve opportunities to publish research findings in top-tier journals and conferences, contributing to the scientific community and establishing Wayve as a leader in the field. What you will bring: Must haves: Proven expertise in synthetic data generation and application in AI model training and testing. Strong foundation in machine learning, deep learning, and neural rendering techniques. Strong programming skills in Python, with experience in deep learning frameworks such as PyTorch. Demonstrable experience with tools relevant to synthetic data generation. Excellent problem-solving skills and the ability to work independently as well as in a team environment. Demonstrated ability to work collaboratively in a fast-paced, innovative, interdisciplinary team environment. Desirable: Experience with dynamic scene reconstruction and rendering, particularly in outdoor environments. Familiarity with parallel computing, GPU programming, and optimization techniques. PhD or MSc in Computer Science, Computer Engineering, or a related field, with a focus on computer graphics, computer vision, or machine learning. Our offer: A position to shape the future of autonomous driving, and thus to tackle one of the biggest challenges of our time Immersion in a team of world-class researchers, engineers and entrepreneurs Competitive compensation and stock options On-site chef and bar, lots of fun socials, a workplace nursery scheme and more! Help relocating/travelling to London, with visa sponsorship Flexible working hours - we trust you to do your job well, at times that suit you and your team. Wayve is built by people from all walks of life. We believe that it is our differences that make us stronger, and our unique perspectives and backgrounds that allow us to build something different. We are proud to be an equal opportunities workplace, where we don't just embrace diversity but nurture it - so that we all thrive and grow.
We are currently recruiting for a Senior Scientist - Assay Development for a Biotechnology company based in Oxfordshire. As a Senior Scientist you will use your expertise in developing assay to support the company's therapeutic development programme. Responsibilities include: Design and develop novel assays (immunoassay and ligand binding assays) Design and run various experiments developing new research methods. Troubleshoot assays and equipment. Work with colleagues to deliver research objectives. Ideal candidates with have a PhD in Molecular Biology, Cell Biology, or Biochemistry with further experience (industry or Post Doc) in developing immunoassay and ligand binding assays. Experience in AD biomarker discovery, validation, and clinical translation is desirable long with experience in/ or knowledge of aptamers. To apply please send your CV to Peter at Rowland Talent Solutions. Please note: candidates need the right to work in the UK to be considered for Scientist role. Key words: ELISA, Assay, Molecular, immunoassay, biomarker, researcher, diagnostic
Apr 17, 2024
Full time
We are currently recruiting for a Senior Scientist - Assay Development for a Biotechnology company based in Oxfordshire. As a Senior Scientist you will use your expertise in developing assay to support the company's therapeutic development programme. Responsibilities include: Design and develop novel assays (immunoassay and ligand binding assays) Design and run various experiments developing new research methods. Troubleshoot assays and equipment. Work with colleagues to deliver research objectives. Ideal candidates with have a PhD in Molecular Biology, Cell Biology, or Biochemistry with further experience (industry or Post Doc) in developing immunoassay and ligand binding assays. Experience in AD biomarker discovery, validation, and clinical translation is desirable long with experience in/ or knowledge of aptamers. To apply please send your CV to Peter at Rowland Talent Solutions. Please note: candidates need the right to work in the UK to be considered for Scientist role. Key words: ELISA, Assay, Molecular, immunoassay, biomarker, researcher, diagnostic
Invertebrate Genetics Research Scientist About this opportunity: The Invertebrate Genetics team within the department of Bioscience conducts critical research to support development and improve understanding of novel insecticides. This is a unique chance for a molecular geneticist who specialises in invertebrates to apply their expertise to propose, design and execute experiments to this end. If successful, you will be part of a team using molecular genetic approaches to address questions on mode of action / resistance of active ingredients, and to define and execute strategies to support target led discovery programs. You will work with the Insect Control Lead Generation team and be part of a larger cross-functional project team working towards these goals. Accountabilities: • Assist with the maintenance and enhancement of the invertebrate molecular laboratory, adapting to current business priorities and adopting adjacent/novel technologies or equipment where appropriate. • Develop protocols / define experimental strategies to support insecticide projects and programs • Develop a broad awareness of insect physiology and seek to identify genotypes which could be used as tools for insecticide mode-of-action validation, determination and for exploring mechanisms of resistance. • Introduce new technologies, techniques or ways of working to improve productivity of existing projects/platforms. • Contribute to the automation of invertebrate platforms to support insecticide/nematicide projects and active ingredient discovery. • Maintain awareness of project key strategic goals. Propose, design, and carry out appropriate experiments using invertebrates to achieve these goals. • Communicate outcomes of experimental activities with stakeholders. • Maintain high standards of HSE compliance, which includes following all risk assessments, reporting of safety incidents and supporting the lab stewards community when requested. Experience & skills: • Must have a degree in a relevant science discipline. Appropriate technical science background is critical. • Must have worked with model or pest invertebrates with experience in molecular genetic approaches. • First-hand experience of micro-injection techniques in invertebrate species is desirable. • Experience in invertebrate husbandry and handling of DEFRA licenced insects is desirable • Excellent note keeping and organisational skills • Knowledge of bioinformatic approaches and ability to work with and interrogate large datasets is desirable. • Ability to interact effectively with colleagues. Good influencing skills. With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.
Apr 16, 2024
Contractor
Invertebrate Genetics Research Scientist About this opportunity: The Invertebrate Genetics team within the department of Bioscience conducts critical research to support development and improve understanding of novel insecticides. This is a unique chance for a molecular geneticist who specialises in invertebrates to apply their expertise to propose, design and execute experiments to this end. If successful, you will be part of a team using molecular genetic approaches to address questions on mode of action / resistance of active ingredients, and to define and execute strategies to support target led discovery programs. You will work with the Insect Control Lead Generation team and be part of a larger cross-functional project team working towards these goals. Accountabilities: • Assist with the maintenance and enhancement of the invertebrate molecular laboratory, adapting to current business priorities and adopting adjacent/novel technologies or equipment where appropriate. • Develop protocols / define experimental strategies to support insecticide projects and programs • Develop a broad awareness of insect physiology and seek to identify genotypes which could be used as tools for insecticide mode-of-action validation, determination and for exploring mechanisms of resistance. • Introduce new technologies, techniques or ways of working to improve productivity of existing projects/platforms. • Contribute to the automation of invertebrate platforms to support insecticide/nematicide projects and active ingredient discovery. • Maintain awareness of project key strategic goals. Propose, design, and carry out appropriate experiments using invertebrates to achieve these goals. • Communicate outcomes of experimental activities with stakeholders. • Maintain high standards of HSE compliance, which includes following all risk assessments, reporting of safety incidents and supporting the lab stewards community when requested. Experience & skills: • Must have a degree in a relevant science discipline. Appropriate technical science background is critical. • Must have worked with model or pest invertebrates with experience in molecular genetic approaches. • First-hand experience of micro-injection techniques in invertebrate species is desirable. • Experience in invertebrate husbandry and handling of DEFRA licenced insects is desirable • Excellent note keeping and organisational skills • Knowledge of bioinformatic approaches and ability to work with and interrogate large datasets is desirable. • Ability to interact effectively with colleagues. Good influencing skills. With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.
AWE have an exciting opportunity for a Theoretical Scientist , to work as a Prompt Diagnostician within our Design Physics Group , to develop modelling techniques and undertake reanalysis our underground test (UGT) data. Location: Aldermaston, West Berkshire . We are located between Reading and Basingstoke, with onsite parking. Due to the classified nature of this role, it is anticipated that the successful candidate will need to spend the entirety of their time working on site at AWE Aldermaston during their working hours. Package: 31,000 - 35,000 (depending on your suitability, qualifications, and level of experience) Closing Date: 1st May 2024 The Role The prompt diagnostics team are a small team within the Design Physics Group. Our mission is to assess, process and interpret the data recorded from the diagnostics fielded on previous underground ground tests (UGTs) prior to the Comprehensive Test Ban Treaty. This data forms the basis for understanding and validation of the complex physics models of nuclear warheads, which are used by our Design Physics colleagues to underwrite the performance and safety of existing and future designs. Key Responsibilities Planning, development and validation of theoretical models and software codes designed to replicate the physical mechanisms which occur in the diagnostics fielded on underground tests. Undertaking reanalysis of underground test data, using modern methods, to provide comparable data for our developing modelling capabilities. Working collaboratively with our international colleagues, sharing methods, ideas and knowledge to enhance your work. Present your own scientific achievements to the team, function and project through published work and presentations. The Company may require you to fulfil any other reasonable duties aligned to your position from time to time in line with business needs. Who Are We Looking For? To be considered for this role, you will need the following: A degree in physics, maths, computer science or an equivalent STEM-based discipline. Knowledge of scientific programming, using languages such as Python, Fortran, C++, or a similar high-level language. Willing to travel overseas as required. Whilst not on the check list, we are interested in hearing from candidates who can demonstrate some of the following: A methodical approach to complex problem solving using technical knowledge. A clear and concise communication approach, both oral and written. Excellent team working ability, with a proactive approach and the ability to prioritise a varied workload, ensuring timely delivery with minimum supervision. The ability to capture and communicate technical requirements effectively. Understanding and knowledge of radiation detection and measurement techniques. Broad understanding of basic physics concepts, in particular, nuclear, particle and electromagnetic physics. Experience of GEANT4 or MCNP modelling would be advantageous. Knowledge of electronics is desirable but not essential. What will you get from us? As part of our People Promise, AWE ( one of the best 25 big companies to work for in the UK ) has a range of benefits to suit you. These include: Time to recharge your batteries with 270 hours of annual leave (including Bank Holidays). 9-day working fortnight - every other Friday off work. Flexible working hours. Consideration for flexible working arrangements so that your work may fit in with your lifestyle. Just let us know on your application if you wish to work part time. Family friendly policies: Maternity Leave - 39 Weeks Full Pay and Paternity Leave - 4 Weeks Full Pay. Opportunities for Professional Career Development that include funding for the annual membership of a relevant professional body, access to mentors and training. Employee Assistance Programme and Occupational Health Services. A market leading contributory pension scheme (we will pay between 9% and 13% of your pensionable pay depending on your own contribution). Life Assurance. Discounts - access to savings on a wide range of everyday spending savings. Special Leave Policy including paid time off for volunteering, public service (including reserve forces) and caring for your family. A host of voluntary & core benefits to suit your health and wellbeing - more information available on our careers site. Important things you need to know: You must be a UK national who has been resident in the UK for the past 10 years. Interviews will be 90 minutes in length and will be held over Microsoft Teams. You will be required to prepare a 10-minute presentation in advance. Candidates must be willing and able to obtain and maintain the necessary security clearance for the role. This will be funded by AWE. Agencies: Please note that we do not out-source our recruitment
Apr 15, 2024
Full time
AWE have an exciting opportunity for a Theoretical Scientist , to work as a Prompt Diagnostician within our Design Physics Group , to develop modelling techniques and undertake reanalysis our underground test (UGT) data. Location: Aldermaston, West Berkshire . We are located between Reading and Basingstoke, with onsite parking. Due to the classified nature of this role, it is anticipated that the successful candidate will need to spend the entirety of their time working on site at AWE Aldermaston during their working hours. Package: 31,000 - 35,000 (depending on your suitability, qualifications, and level of experience) Closing Date: 1st May 2024 The Role The prompt diagnostics team are a small team within the Design Physics Group. Our mission is to assess, process and interpret the data recorded from the diagnostics fielded on previous underground ground tests (UGTs) prior to the Comprehensive Test Ban Treaty. This data forms the basis for understanding and validation of the complex physics models of nuclear warheads, which are used by our Design Physics colleagues to underwrite the performance and safety of existing and future designs. Key Responsibilities Planning, development and validation of theoretical models and software codes designed to replicate the physical mechanisms which occur in the diagnostics fielded on underground tests. Undertaking reanalysis of underground test data, using modern methods, to provide comparable data for our developing modelling capabilities. Working collaboratively with our international colleagues, sharing methods, ideas and knowledge to enhance your work. Present your own scientific achievements to the team, function and project through published work and presentations. The Company may require you to fulfil any other reasonable duties aligned to your position from time to time in line with business needs. Who Are We Looking For? To be considered for this role, you will need the following: A degree in physics, maths, computer science or an equivalent STEM-based discipline. Knowledge of scientific programming, using languages such as Python, Fortran, C++, or a similar high-level language. Willing to travel overseas as required. Whilst not on the check list, we are interested in hearing from candidates who can demonstrate some of the following: A methodical approach to complex problem solving using technical knowledge. A clear and concise communication approach, both oral and written. Excellent team working ability, with a proactive approach and the ability to prioritise a varied workload, ensuring timely delivery with minimum supervision. The ability to capture and communicate technical requirements effectively. Understanding and knowledge of radiation detection and measurement techniques. Broad understanding of basic physics concepts, in particular, nuclear, particle and electromagnetic physics. Experience of GEANT4 or MCNP modelling would be advantageous. Knowledge of electronics is desirable but not essential. What will you get from us? As part of our People Promise, AWE ( one of the best 25 big companies to work for in the UK ) has a range of benefits to suit you. These include: Time to recharge your batteries with 270 hours of annual leave (including Bank Holidays). 9-day working fortnight - every other Friday off work. Flexible working hours. Consideration for flexible working arrangements so that your work may fit in with your lifestyle. Just let us know on your application if you wish to work part time. Family friendly policies: Maternity Leave - 39 Weeks Full Pay and Paternity Leave - 4 Weeks Full Pay. Opportunities for Professional Career Development that include funding for the annual membership of a relevant professional body, access to mentors and training. Employee Assistance Programme and Occupational Health Services. A market leading contributory pension scheme (we will pay between 9% and 13% of your pensionable pay depending on your own contribution). Life Assurance. Discounts - access to savings on a wide range of everyday spending savings. Special Leave Policy including paid time off for volunteering, public service (including reserve forces) and caring for your family. A host of voluntary & core benefits to suit your health and wellbeing - more information available on our careers site. Important things you need to know: You must be a UK national who has been resident in the UK for the past 10 years. Interviews will be 90 minutes in length and will be held over Microsoft Teams. You will be required to prepare a 10-minute presentation in advance. Candidates must be willing and able to obtain and maintain the necessary security clearance for the role. This will be funded by AWE. Agencies: Please note that we do not out-source our recruitment
Overview: Morgan Advanced Materials is a world leader in advanced materials science and engineering of ceramics, carbon and composites. We operate in a series of well-defined markets where our applications expertise offers our customers a valuable differentiator, engineering high-specification materials, components and sub-assembly parts that solve their challenging technical problems. The Thermal Ceramics division designs, manufactures and installs a broad range of thermal insulation products that significantly reduce energy consumption and emissions in a variety of high temperature processing applications. Our product offering is extensive and covers application needs from Industrial to Commercial markets. Group Key Figures: Revenue £950m (2021), 7,500 employees, manufacturing in 30+ countries, and customers in 100+ countries. A UK PLC with head office located in Windsor, Berkshire UK. Listed on London Stock Exchange; Member of the FTSE 250 Index. The primary purpose of the Scientist role is to support current business through QC and forensics, project management and H&S regulatory compliance, as well as develop new business through areas such as innovation in chemistry, process and application of high temperature insulating refractories. The Scientist role would also be expected to contribute to relevance in the support activities and innovation in the development activities through formal technical knowledge. Where required the role would also undertake some supervisory responsibilities. Responsibilities: Performs basic experimental and technical investigations towards the acquisition of new knowledge. Design chemical, physical, engineering for laboratory-scale tests and protocols, with a view to proving fitness-for-use / product specifications or process validation. Overseas testing may be required. Interpret and report test results with implications for further design. Chooses, specifies, and acquires all equipment and consumable relating to said technical activity. Schedules and undertakes equipment maintenance and calibration. Performs risk assessments on new tests and equipment prior to use. Form links with external suppliers to conduct proving trials with their products. Establish the need for technology change. Apply stage gate methodology to projects. Weekly, monthly, and yearly reporting on project as required. Execute the role ethically and in accordance with the Morgan Leadership Behaviours. Actively participate Environmental, Health & Safety improvement initiatives, in particular Morgan Thank Safe, Take 5 and other safety-related initiatives and reporting requirements, leading by example at all times. Actively participate in the 'ThinkSAFE' processes (e.g. safety tours, etc.). Have adequate knowledge of health and safety regulations in order to ensure compliance within the areas of responsibility and ensure all statutory registers and records are maintained. Ensure all employees within the team are competent, adequately trained, supervised, and have the relevant information to enable them to carry out their duties safely. The role will require periodic domestic and international travel. Some travel periods may require extended stays when relating to production trials. Qualifications: Essential Engineering Degree, Masters or MBA educated (or equivalent role-based experience) Strong written and verbal communication skills. Has operated in a similar decentralised business before with demonstrable personal credibility Desirable Extensive knowledge and experience in relevant field Previous experience of working within a large organisation Familiar with the Thermal production sites on a global basis and the associated operations personal (internal candidates) Working knowledge of Stage Gate methodology and other PMO tools Understanding of the Capex process Multi-language proficiency for regions served by Morgan Morgan Advanced Materials is an EEO/AA/M/W/D/V Employer
Sep 24, 2022
Full time
Overview: Morgan Advanced Materials is a world leader in advanced materials science and engineering of ceramics, carbon and composites. We operate in a series of well-defined markets where our applications expertise offers our customers a valuable differentiator, engineering high-specification materials, components and sub-assembly parts that solve their challenging technical problems. The Thermal Ceramics division designs, manufactures and installs a broad range of thermal insulation products that significantly reduce energy consumption and emissions in a variety of high temperature processing applications. Our product offering is extensive and covers application needs from Industrial to Commercial markets. Group Key Figures: Revenue £950m (2021), 7,500 employees, manufacturing in 30+ countries, and customers in 100+ countries. A UK PLC with head office located in Windsor, Berkshire UK. Listed on London Stock Exchange; Member of the FTSE 250 Index. The primary purpose of the Scientist role is to support current business through QC and forensics, project management and H&S regulatory compliance, as well as develop new business through areas such as innovation in chemistry, process and application of high temperature insulating refractories. The Scientist role would also be expected to contribute to relevance in the support activities and innovation in the development activities through formal technical knowledge. Where required the role would also undertake some supervisory responsibilities. Responsibilities: Performs basic experimental and technical investigations towards the acquisition of new knowledge. Design chemical, physical, engineering for laboratory-scale tests and protocols, with a view to proving fitness-for-use / product specifications or process validation. Overseas testing may be required. Interpret and report test results with implications for further design. Chooses, specifies, and acquires all equipment and consumable relating to said technical activity. Schedules and undertakes equipment maintenance and calibration. Performs risk assessments on new tests and equipment prior to use. Form links with external suppliers to conduct proving trials with their products. Establish the need for technology change. Apply stage gate methodology to projects. Weekly, monthly, and yearly reporting on project as required. Execute the role ethically and in accordance with the Morgan Leadership Behaviours. Actively participate Environmental, Health & Safety improvement initiatives, in particular Morgan Thank Safe, Take 5 and other safety-related initiatives and reporting requirements, leading by example at all times. Actively participate in the 'ThinkSAFE' processes (e.g. safety tours, etc.). Have adequate knowledge of health and safety regulations in order to ensure compliance within the areas of responsibility and ensure all statutory registers and records are maintained. Ensure all employees within the team are competent, adequately trained, supervised, and have the relevant information to enable them to carry out their duties safely. The role will require periodic domestic and international travel. Some travel periods may require extended stays when relating to production trials. Qualifications: Essential Engineering Degree, Masters or MBA educated (or equivalent role-based experience) Strong written and verbal communication skills. Has operated in a similar decentralised business before with demonstrable personal credibility Desirable Extensive knowledge and experience in relevant field Previous experience of working within a large organisation Familiar with the Thermal production sites on a global basis and the associated operations personal (internal candidates) Working knowledge of Stage Gate methodology and other PMO tools Understanding of the Capex process Multi-language proficiency for regions served by Morgan Morgan Advanced Materials is an EEO/AA/M/W/D/V Employer
Job Description Reading Scientific Services Ltd (RSSL) is a cutting-edge Contract Research Organisation (CRO), providing research, analysis and consultancy to the life science, healthcare and food sectors. As a Senior Scientist, t he role of Biopharmaceutical Chromatograph er is to provide strong technical direction and analytical expertise throughout the discovery, development and delivery phases of the drug life cycle. The scope includes development, optimization and validation of analytical methods that aid full characterization of materials used in biopharmaceutical innovation and delivery (concept materials through to the established proteins and peptides). The Senior Scientist II role will p lay a key role in ensuring that bio pharmaceutical projects within the Ph armaceutical Development laboratory are performed and supervised effectively and accurately within agreed timescales and to appropriate quality standards. The role will coach a team of scientist s, providing technical direction, and will be responsible for reviewing and authorising of certificates of analysis, interpretive scientific reports, method development and validations and authorizing competencies within the area of expertise . Detailed responsibilities: Technical Essentials 1. Provide high quality customer service at all times by ensuring effective organisation of assigned workload, integrity of analytical data generated and timely/accurate provision of results. 2. Responsible for a portfolio of analytical projects including investigation and characterisation of biopharmaceuticals using chromatographic method development and validation . 3. Implementation of solutions to technical challenges and support creation of new business opportunities 4. Perform data checking and provide interpretatio n of results for routine and complex testing 5. Generate certificate analysis and external interpretive reports. 6. Expert user in the use of software packages relevant to the role : Laboratory's LIMS system, Q-Pulse, Chemwatch , Openlab . 7. Provide training and supervise staff in routine activities , methods and interpretation. 8. Provide t echnical direction in area of expertise within and across departments , including maintenance and troubleshooting of laboratory equipment . Communication & Influence 1. Work as part of an efficient analytical team 2. To liase with clients, business development and line management to ensure effective communication of project proposals and results. 3. Provide expert advice and lead client and stake holders meetings and audits 4. Deliver presentations to clients and stakeholders 5. Contribute to both technical and business strategy including influencing senior management Key Leadership and supervision 1. Use Technical expertise to coach/ mentor a team of S cientists and Technicians 2. Plan own workload and projects for junior staff 3. T rain and coach junior members of the team as required. More about this role Knowledge: including education, qualifications and training Educated to Degree or PhD in a relevant scientific discipline or equivalent relevant experience in a laboratory. U nderstanding of chromatographic lab equipment, HPLC (SEC, IEX), CE , FPLC, techniques In-depth knowledge of both technical area of expertise & business environment including regulatory requirements Good knowledge of laboratory quality and accreditation systems (GMP) Work schedule: The standard hours for this role are Monday to Friday 9-5. There is scope for flexible start and finish times for example to allow for taking children to school No Relocation support available Business Unit Summary Reading Scientific Services, Ltd. (RSSL) is a cutting-edge contract research organization (CRO), providing research, analysis and consultancy to the food and pharmaceutical sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 60 countries. We were recognized in 2019 as an Enlightened Employer, Women in Business and Thames Valley Tech finalists and in 2018, one of our family members earned the Food & Drink Federation's Scientist of the Year. Enriched by our parent company, Mondelēz International, our diverse team of 300 includes 23 nationalities, creating a family feel as we strive toward our mission of "Science Enhancing Lives." Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Regular Analytical Science Science & Engineering
Sep 24, 2022
Full time
Job Description Reading Scientific Services Ltd (RSSL) is a cutting-edge Contract Research Organisation (CRO), providing research, analysis and consultancy to the life science, healthcare and food sectors. As a Senior Scientist, t he role of Biopharmaceutical Chromatograph er is to provide strong technical direction and analytical expertise throughout the discovery, development and delivery phases of the drug life cycle. The scope includes development, optimization and validation of analytical methods that aid full characterization of materials used in biopharmaceutical innovation and delivery (concept materials through to the established proteins and peptides). The Senior Scientist II role will p lay a key role in ensuring that bio pharmaceutical projects within the Ph armaceutical Development laboratory are performed and supervised effectively and accurately within agreed timescales and to appropriate quality standards. The role will coach a team of scientist s, providing technical direction, and will be responsible for reviewing and authorising of certificates of analysis, interpretive scientific reports, method development and validations and authorizing competencies within the area of expertise . Detailed responsibilities: Technical Essentials 1. Provide high quality customer service at all times by ensuring effective organisation of assigned workload, integrity of analytical data generated and timely/accurate provision of results. 2. Responsible for a portfolio of analytical projects including investigation and characterisation of biopharmaceuticals using chromatographic method development and validation . 3. Implementation of solutions to technical challenges and support creation of new business opportunities 4. Perform data checking and provide interpretatio n of results for routine and complex testing 5. Generate certificate analysis and external interpretive reports. 6. Expert user in the use of software packages relevant to the role : Laboratory's LIMS system, Q-Pulse, Chemwatch , Openlab . 7. Provide training and supervise staff in routine activities , methods and interpretation. 8. Provide t echnical direction in area of expertise within and across departments , including maintenance and troubleshooting of laboratory equipment . Communication & Influence 1. Work as part of an efficient analytical team 2. To liase with clients, business development and line management to ensure effective communication of project proposals and results. 3. Provide expert advice and lead client and stake holders meetings and audits 4. Deliver presentations to clients and stakeholders 5. Contribute to both technical and business strategy including influencing senior management Key Leadership and supervision 1. Use Technical expertise to coach/ mentor a team of S cientists and Technicians 2. Plan own workload and projects for junior staff 3. T rain and coach junior members of the team as required. More about this role Knowledge: including education, qualifications and training Educated to Degree or PhD in a relevant scientific discipline or equivalent relevant experience in a laboratory. U nderstanding of chromatographic lab equipment, HPLC (SEC, IEX), CE , FPLC, techniques In-depth knowledge of both technical area of expertise & business environment including regulatory requirements Good knowledge of laboratory quality and accreditation systems (GMP) Work schedule: The standard hours for this role are Monday to Friday 9-5. There is scope for flexible start and finish times for example to allow for taking children to school No Relocation support available Business Unit Summary Reading Scientific Services, Ltd. (RSSL) is a cutting-edge contract research organization (CRO), providing research, analysis and consultancy to the food and pharmaceutical sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 60 countries. We were recognized in 2019 as an Enlightened Employer, Women in Business and Thames Valley Tech finalists and in 2018, one of our family members earned the Food & Drink Federation's Scientist of the Year. Enriched by our parent company, Mondelēz International, our diverse team of 300 includes 23 nationalities, creating a family feel as we strive toward our mission of "Science Enhancing Lives." Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Regular Analytical Science Science & Engineering
Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - Stevenage Posted Date: Aug 9 2022 Are you energized by an opportunity to strategize on projects and improve platform capabilities across the Clinical Biomarker Group? If so, this Clinical Biomarker Specialist role could be an exciting opportunity to explore. The Clinical Biomarker Specialist will report to the Clinical Biomarker Lead to enhance clinical biomarker strategies for projects and improve platform capabilities across the Clinical Biomarker group. Working as part of the Clinical Biomarkers Team, the Clinical Biomarker Specialist will employ cutting edge technologies and procedures to discover and support technical validation of biomarkers to strengthen clinical biomarker strategies at all stages of clinical development to ensure optimally informed decision making in drug development. The Clinical Biomarker Specialist role provides an opportunity to gain clinical experience and for future development into the Clinical Biomarker Lead role. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Technical validation of biomarkers for use in clinical trials and in observational studies. Working with internal technology groups, Contract Research Organisations and collaborators to deliver clinical biomarker assays. Providing input on biomarker-related elements of study trial design and conduct and incorporating biomarkers into clinical protocols, Study Reference Manuals and Central Lab Worksheets. Ensuring alignment of biomarker outputs with data management, statistics, and modelling/simulation requirements. Liaise with other parts of the organization to resolve study biomarker issues. Evaluating the value and suitability of new technologies for potential use in clinical trials. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: PhD-educated scientist (or equivalent) in life sciences (background/degree in immunology an advantage) with at least 2 years of experience in pharmaceutical industry supporting pipeline progression. Experience with the discovery, validation and implementation of biomarkers. Excellent communication skills and positive can-do attitude. Good interpersonal and matrix working skills. Preferred Qualifications: If you have the following characteristics, it would be a plus: In depth knowledge of GCP principles. Experience of clinical implementation of biomarker technologies. at least 2 years of experience in pharmaceutical industry supporting pipeline progression. Why GSK? Our values and expectationsare at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Operating at pace and agile decision-making - using evidence and applying judgement to balance pace, rigour and risk. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Continuously looking for opportunities to learn, build skills and share learning. Sustaining energy and well-being. Building strong relationships and collaboration, honest and open conversations. Budgeting and cost-consciousness. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1- (US Toll Free) or +1 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.
Sep 24, 2022
Full time
Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - Stevenage Posted Date: Aug 9 2022 Are you energized by an opportunity to strategize on projects and improve platform capabilities across the Clinical Biomarker Group? If so, this Clinical Biomarker Specialist role could be an exciting opportunity to explore. The Clinical Biomarker Specialist will report to the Clinical Biomarker Lead to enhance clinical biomarker strategies for projects and improve platform capabilities across the Clinical Biomarker group. Working as part of the Clinical Biomarkers Team, the Clinical Biomarker Specialist will employ cutting edge technologies and procedures to discover and support technical validation of biomarkers to strengthen clinical biomarker strategies at all stages of clinical development to ensure optimally informed decision making in drug development. The Clinical Biomarker Specialist role provides an opportunity to gain clinical experience and for future development into the Clinical Biomarker Lead role. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Technical validation of biomarkers for use in clinical trials and in observational studies. Working with internal technology groups, Contract Research Organisations and collaborators to deliver clinical biomarker assays. Providing input on biomarker-related elements of study trial design and conduct and incorporating biomarkers into clinical protocols, Study Reference Manuals and Central Lab Worksheets. Ensuring alignment of biomarker outputs with data management, statistics, and modelling/simulation requirements. Liaise with other parts of the organization to resolve study biomarker issues. Evaluating the value and suitability of new technologies for potential use in clinical trials. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: PhD-educated scientist (or equivalent) in life sciences (background/degree in immunology an advantage) with at least 2 years of experience in pharmaceutical industry supporting pipeline progression. Experience with the discovery, validation and implementation of biomarkers. Excellent communication skills and positive can-do attitude. Good interpersonal and matrix working skills. Preferred Qualifications: If you have the following characteristics, it would be a plus: In depth knowledge of GCP principles. Experience of clinical implementation of biomarker technologies. at least 2 years of experience in pharmaceutical industry supporting pipeline progression. Why GSK? Our values and expectationsare at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Operating at pace and agile decision-making - using evidence and applying judgement to balance pace, rigour and risk. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Continuously looking for opportunities to learn, build skills and share learning. Sustaining energy and well-being. Building strong relationships and collaboration, honest and open conversations. Budgeting and cost-consciousness. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1- (US Toll Free) or +1 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.
Job Description Reading Scientific Services Ltd (RSSL) is a cutting-edge Contract Research Organisation (CRO), providing research, analysis and consultancy to the food and pharmaceutical sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 60 countries. In 2021, we've been recognised as Employer of the Year and Business of the Year at the Thames Valley Business Awards, and in past years have achieved OBN's Best CRO and Women in Business Enlightened Employer. Enriched by our parent company Mondelēz International, our diverse team includes 23 nationalities from 300 members, creating a family feel as we strive towards our mission of "Science Enhancing Lives". In this role, you work independently to organize project teams and establish project technical scope and approach, and manage project design and delivery while still retaining a hands-on approach to analytical work. Your work includes large, complex projects that may be multi-department, cross-functional, and multi-country in nature. You offer people leadership, execute strategies or goals to meet business needs and interact independently with senior management and stakeholders. How you will contribute You will provide technical direction and leadership-which includes training and mentoring junior team members-in the laboratory to ensure that complex projects are completed on time and with the appropriate analytical and regulatory standards. In this role, you will review and approve scientific reports, method development and validations, authorize competencies in your area of expertise and independently perform complex method development and design validations protocols. In addition, you will maintain and troubleshoot lab equipment, ensure a clean, tidy and safe working environment, and perform and approve risk assessments. Excellent communication skills will be required of you because you will write technical reports, check data, offer interpretations of results and interact with internal and external holders using influencing and presentation skills to present project proposals and results. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Laboratory requirements and practices Analytical technology in your area of expertise and the desire to develop in-depth and broader technical expertise Scientific understanding and the ability to independently conduct chemical analysis in relevant area Verbal and written communication skills with the ability to build your network and technical credibility with external clients and internal teams Problem solving and planning resources to maintain a consistent workflow to deliver projects Organizational skills, including time management and priority setting No Relocation support available Business Unit Summary Reading Scientific Services, Ltd. (RSSL) is a cutting-edge contract research organization (CRO), providing research, analysis and consultancy to the food and pharmaceutical sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 60 countries. We were recognized in 2019 as an Enlightened Employer, Women in Business and Thames Valley Tech finalists and in 2018, one of our family members earned the Food & Drink Federation's Scientist of the Year. Enriched by our parent company, Mondelēz International, our diverse team of 300 includes 23 nationalities, creating a family feel as we strive toward our mission of "Science Enhancing Lives." Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Regular Analytical Science Science & Engineering
Sep 24, 2022
Full time
Job Description Reading Scientific Services Ltd (RSSL) is a cutting-edge Contract Research Organisation (CRO), providing research, analysis and consultancy to the food and pharmaceutical sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 60 countries. In 2021, we've been recognised as Employer of the Year and Business of the Year at the Thames Valley Business Awards, and in past years have achieved OBN's Best CRO and Women in Business Enlightened Employer. Enriched by our parent company Mondelēz International, our diverse team includes 23 nationalities from 300 members, creating a family feel as we strive towards our mission of "Science Enhancing Lives". In this role, you work independently to organize project teams and establish project technical scope and approach, and manage project design and delivery while still retaining a hands-on approach to analytical work. Your work includes large, complex projects that may be multi-department, cross-functional, and multi-country in nature. You offer people leadership, execute strategies or goals to meet business needs and interact independently with senior management and stakeholders. How you will contribute You will provide technical direction and leadership-which includes training and mentoring junior team members-in the laboratory to ensure that complex projects are completed on time and with the appropriate analytical and regulatory standards. In this role, you will review and approve scientific reports, method development and validations, authorize competencies in your area of expertise and independently perform complex method development and design validations protocols. In addition, you will maintain and troubleshoot lab equipment, ensure a clean, tidy and safe working environment, and perform and approve risk assessments. Excellent communication skills will be required of you because you will write technical reports, check data, offer interpretations of results and interact with internal and external holders using influencing and presentation skills to present project proposals and results. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Laboratory requirements and practices Analytical technology in your area of expertise and the desire to develop in-depth and broader technical expertise Scientific understanding and the ability to independently conduct chemical analysis in relevant area Verbal and written communication skills with the ability to build your network and technical credibility with external clients and internal teams Problem solving and planning resources to maintain a consistent workflow to deliver projects Organizational skills, including time management and priority setting No Relocation support available Business Unit Summary Reading Scientific Services, Ltd. (RSSL) is a cutting-edge contract research organization (CRO), providing research, analysis and consultancy to the food and pharmaceutical sectors. Whether we are creating new products, validating medicines or solving investigations, we take pride in being a leader in our field, serving clients from across 60 countries. We were recognized in 2019 as an Enlightened Employer, Women in Business and Thames Valley Tech finalists and in 2018, one of our family members earned the Food & Drink Federation's Scientist of the Year. Enriched by our parent company, Mondelēz International, our diverse team of 300 includes 23 nationalities, creating a family feel as we strive toward our mission of "Science Enhancing Lives." Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Regular Analytical Science Science & Engineering
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross functional team, you deliver the RDQ activities required to complete new product development, portfolio maintenance and/or productivity projects with an emphasis on meeting the desired consumer experience. How you will contribute With the support and guidance of a manager, you will organize and execute projects in line with RDQ, marketing and manufacturing requirements, effectively communicating status and risks. You will plan and conduct pilot plant and factory trials in accordance with good manufacturing practice and HACCP requirements and development activities (e.g. product shelf-life testing, designing for quality, consumer test preparation etc.). You will also write technical reports that will require the analysis and interpretation of results and that lead to conclusions and recommendations and create and maintain accurate consumer-led specifications. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Food science, science, or engineering ideally in a fast-moving consumer goods market Working on teams and independently with the guidance of a manager Prioritizing and managing activities Identifying problems proactively and creating and implementing solutions independently Applying fundamental technical understanding to interpret and analyze data to reach clear conclusions Communicating effectively verbally and in writing, including technical writing Putting the consumer at the heart of development activities More about this role What you need to know about this position: Ernest Jackson & Co Ltd exists to deliver the best tasting healthcare products to consumers. Unique to Mondelez international, Ernest Jackson has a locally managed Research and Development function whose goal is to: Develop the right healthcare products to meet the needs of the consumer and enable a competitive edge for the business. As a member of the R&D department this role develops new; food, nutraceutical and pharmaceutical products for predominantly UK markets but also international export. You will develop recipes, specifications, standards and manufacturing procedures for new products. Creating protocols for safe and effective trialing and testing, and producing reports that justify the efficacy of our products for release to market. This will all be completed in accordance with GMP, HACCP, ICH, MHRA, FDA, FSSC and health & safety guidelines and regulations. The Research and Development Department performs a wide range of projects in support of Ernest Jackson Business Objectives. Therefore, as well as product development, the development scientist is also expected to support process upgrades and production efficiencies. In this role you will support other business functions in ensuring any changes to process consider and mitigate the impact to product. This will include supporting and running trials, validation work, process design and supporting the creation of process parameters. You will be expected to work in an organised manner within tight deadlines to ensure that projects are delivered within expected time scales. The role holder will have or develop a working knowledge of both licenced medicine regulations and the nutritional landscape in order to design and develop new products that meet market and regulatory needs. The successful individual will be required to conduct project work on a wide range of projects, from development of new functional food (nutraceutical) products (most likely supporting another scientist), reviewing and controlling raw material changes, collating and reviewing product data used to justify characteristics including but not limited to analytical data of vitamins and minerals and organoleptic data of finished products. The successful individual would need to be able to work flexibly from site, we'd aim to retain at least a Mdlz 50:50 time split between home and office. The individual will need to supervise trials on site, support changes, conduct testing and taste panels on site. Looking for a candidate that can start as soon as possible The successful candidate would most likely be involved in our sustainability goals, investigating the impact of recyclable materials on our products and their shelf life What extra ingredients you will bring: Strong communication skills to sell ideas and solutions to senior stakeholders Inquisitive; the successful candidate will support with root cause investigations, looking for someone who will keep digging, keep investigating and ruling things out, good at crunching data. Process orientated; R&D support the business in maintaining robust GMP processes Data driven; goes without saying we crunch data and solve a lot of issues that require evidence Other stuff The successful individual will have exposure to pharmaceutical products and pharmaceutical development but unlikely to lead on any pharmaceutical projects, might be a selling point Potentially open to individuals with Engineering background instead of food development/Chemistry/science background if they're the right fit Education / Certifications: Must BSc in Chemistry, life science, or other scientific discipline Proficient in MS Office applications especially Word, Excel, and PowerPoint Fluent in English (written and spoken communication) Preferred Experience in product development Some experience in the FMCG sector Experience in a lab environment (we don't develop in one, but some skills are transferable) Experience in project-based work/development Knowledge in Food product law/technical aspects of food development Job specific requirements: Must Be able to work in an agile manor, capable of working on multiple tracks of work/objectives at once Be inquisitive, want to learn and develop their understanding, willing to ask questions and reasons Strong interpersonal skills, good influencing ability Passion Understand timelines/deadlines Good ability to plan and organise own work, prioritising where necessary Integrity/honesty/trust Attention to detail Process orientated: won't struggle with prescriptive processes or being bound by pharmaceutical regulations Preferred Confident presenting ideas Strong stakeholder management and persuasion skills Good commercial awareness Analytical thought process: able to define ways to test and prove concepts, a rigorous scientific approach Financial understanding of costs/impacts/benefits Work schedule: This is a maternity cover fixed term contract. This role offers hybrid working. The responsibilities of this position are performed within the framework of a regional business model that is defined and managed by Mondelēz Europe GmbH, Switzerland . No Relocation support available Business Unit Summary At Mondelez Europe, we are proud, not only of the iconic brands we make, but also of the people who make them. Our delicious products are created in 52 plants across Europe by more than 28,000 passionate people. We are the top maker of chocolate and biscuits and a leading maker of gum and candy. We make sure our powerful global brands and local jewels like Cadbury , Milka and Alpen Gold chocolates, Oreo , belVita , LU and Tuc biscuits, and Stimorol and Dirol gums get safely into our customers hands-and mouths. Great people and great brands. That's who we are. Join us on our journey to continue leading the future of snacking around the world by offering the right snack, for the right moment, made the right way. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Temporary (Fixed Term) Product development Science & Engineering
Sep 23, 2022
Full time
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. Working as part of a cross functional team, you deliver the RDQ activities required to complete new product development, portfolio maintenance and/or productivity projects with an emphasis on meeting the desired consumer experience. How you will contribute With the support and guidance of a manager, you will organize and execute projects in line with RDQ, marketing and manufacturing requirements, effectively communicating status and risks. You will plan and conduct pilot plant and factory trials in accordance with good manufacturing practice and HACCP requirements and development activities (e.g. product shelf-life testing, designing for quality, consumer test preparation etc.). You will also write technical reports that will require the analysis and interpretation of results and that lead to conclusions and recommendations and create and maintain accurate consumer-led specifications. What you will bring A desire to drive your future and accelerate your career and the following experience and knowledge: Food science, science, or engineering ideally in a fast-moving consumer goods market Working on teams and independently with the guidance of a manager Prioritizing and managing activities Identifying problems proactively and creating and implementing solutions independently Applying fundamental technical understanding to interpret and analyze data to reach clear conclusions Communicating effectively verbally and in writing, including technical writing Putting the consumer at the heart of development activities More about this role What you need to know about this position: Ernest Jackson & Co Ltd exists to deliver the best tasting healthcare products to consumers. Unique to Mondelez international, Ernest Jackson has a locally managed Research and Development function whose goal is to: Develop the right healthcare products to meet the needs of the consumer and enable a competitive edge for the business. As a member of the R&D department this role develops new; food, nutraceutical and pharmaceutical products for predominantly UK markets but also international export. You will develop recipes, specifications, standards and manufacturing procedures for new products. Creating protocols for safe and effective trialing and testing, and producing reports that justify the efficacy of our products for release to market. This will all be completed in accordance with GMP, HACCP, ICH, MHRA, FDA, FSSC and health & safety guidelines and regulations. The Research and Development Department performs a wide range of projects in support of Ernest Jackson Business Objectives. Therefore, as well as product development, the development scientist is also expected to support process upgrades and production efficiencies. In this role you will support other business functions in ensuring any changes to process consider and mitigate the impact to product. This will include supporting and running trials, validation work, process design and supporting the creation of process parameters. You will be expected to work in an organised manner within tight deadlines to ensure that projects are delivered within expected time scales. The role holder will have or develop a working knowledge of both licenced medicine regulations and the nutritional landscape in order to design and develop new products that meet market and regulatory needs. The successful individual will be required to conduct project work on a wide range of projects, from development of new functional food (nutraceutical) products (most likely supporting another scientist), reviewing and controlling raw material changes, collating and reviewing product data used to justify characteristics including but not limited to analytical data of vitamins and minerals and organoleptic data of finished products. The successful individual would need to be able to work flexibly from site, we'd aim to retain at least a Mdlz 50:50 time split between home and office. The individual will need to supervise trials on site, support changes, conduct testing and taste panels on site. Looking for a candidate that can start as soon as possible The successful candidate would most likely be involved in our sustainability goals, investigating the impact of recyclable materials on our products and their shelf life What extra ingredients you will bring: Strong communication skills to sell ideas and solutions to senior stakeholders Inquisitive; the successful candidate will support with root cause investigations, looking for someone who will keep digging, keep investigating and ruling things out, good at crunching data. Process orientated; R&D support the business in maintaining robust GMP processes Data driven; goes without saying we crunch data and solve a lot of issues that require evidence Other stuff The successful individual will have exposure to pharmaceutical products and pharmaceutical development but unlikely to lead on any pharmaceutical projects, might be a selling point Potentially open to individuals with Engineering background instead of food development/Chemistry/science background if they're the right fit Education / Certifications: Must BSc in Chemistry, life science, or other scientific discipline Proficient in MS Office applications especially Word, Excel, and PowerPoint Fluent in English (written and spoken communication) Preferred Experience in product development Some experience in the FMCG sector Experience in a lab environment (we don't develop in one, but some skills are transferable) Experience in project-based work/development Knowledge in Food product law/technical aspects of food development Job specific requirements: Must Be able to work in an agile manor, capable of working on multiple tracks of work/objectives at once Be inquisitive, want to learn and develop their understanding, willing to ask questions and reasons Strong interpersonal skills, good influencing ability Passion Understand timelines/deadlines Good ability to plan and organise own work, prioritising where necessary Integrity/honesty/trust Attention to detail Process orientated: won't struggle with prescriptive processes or being bound by pharmaceutical regulations Preferred Confident presenting ideas Strong stakeholder management and persuasion skills Good commercial awareness Analytical thought process: able to define ways to test and prove concepts, a rigorous scientific approach Financial understanding of costs/impacts/benefits Work schedule: This is a maternity cover fixed term contract. This role offers hybrid working. The responsibilities of this position are performed within the framework of a regional business model that is defined and managed by Mondelēz Europe GmbH, Switzerland . No Relocation support available Business Unit Summary At Mondelez Europe, we are proud, not only of the iconic brands we make, but also of the people who make them. Our delicious products are created in 52 plants across Europe by more than 28,000 passionate people. We are the top maker of chocolate and biscuits and a leading maker of gum and candy. We make sure our powerful global brands and local jewels like Cadbury , Milka and Alpen Gold chocolates, Oreo , belVita , LU and Tuc biscuits, and Stimorol and Dirol gums get safely into our customers hands-and mouths. Great people and great brands. That's who we are. Join us on our journey to continue leading the future of snacking around the world by offering the right snack, for the right moment, made the right way. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Temporary (Fixed Term) Product development Science & Engineering
Owlstone Medical ( ()) is on a mission to save 100,000 lives and $1.5 billion in healthcare costs through the development and application of Breath Biopsy , which enables the non-invasive collection and analysis of biomarkers in exhaled breath for early disease detection and precision medicine. We are currently seeking a Senior Biostatistician with clinical research and biomarker discovery experience to be a member of our Clinical and Translational Science Department. The candidate will contribute to the mission of the company by providing input into clinical study designs and trial protocols and will ensure that data analysis and interpretation of results are statistically sound and meet the desired study objectives. The Senior Biostatistician will work in a cross-functional team to support Owlstone s clinical test development and customer services business. Key responsibilities: Perform appropriate statistical analyses at all phases of the project, from clinical protocol development and study design through final analysis and reporting of results Evaluate clinical research studies and prepare statistical analysis plans that provide sound approaches to support a continuum of study goals, from biomarker discovery through clinical test development Apply appropriate statistical methodologies to analyze the data, including, but not limited to, hypothesis testing, regression models, multivariate analyses, machine learning, and network-based analyses Program and analyze data using Python or R; demonstrate good programming practices through proper documentation and commenting; perform appropriate QA to ensure accuracy and consistency of results Effectively communicate statistical methods and results to cross-functional team members, clinical collaborators, and others with a variety of technical expertise (including lay audience) Maintaining technical knowledge and skills appropriate for the role, including staying current with innovative statistical methodologies that are relevant to clinical research Requirements Technical Competencies: A thorough understanding of sample size, study power, precision, and their application in clinical trials and/or observational studies Proficient in translating clinical research questions into testable hypotheses Adept in communicating the assumptions, limitations, and advantages or disadvantages of statistical methods and describing preferred alternatives when key assumptions are not met Working proficiency in Python (to the level of package writing) or R (capable of implementing statistical or computational methods) Demonstrated ability to take initiative and be proactive in your approach to work, with an independent, creative, and open mindset Desirable Experience: Statistical experience working with CROs or the biopharmaceutical industry Application of statistical design and analysis for biomarker discovery and validation Experience with metabolomics (or other omics) data from clinical or epidemiologic studies Experience working closely with clinical biologists and translational scientists to analyze and interpret clinical datasets Strong publication record or other demonstrable track record of performance and collaboration Familiarity with IRB/ethics and regulatory documentation Qualifications: PhD or equivalent combination of education, training and experience in (bio) statistics or a related discipline, preferably with demonstrable experience working in a clinical, biomedical, or commercial environment
Sep 22, 2022
Full time
Owlstone Medical ( ()) is on a mission to save 100,000 lives and $1.5 billion in healthcare costs through the development and application of Breath Biopsy , which enables the non-invasive collection and analysis of biomarkers in exhaled breath for early disease detection and precision medicine. We are currently seeking a Senior Biostatistician with clinical research and biomarker discovery experience to be a member of our Clinical and Translational Science Department. The candidate will contribute to the mission of the company by providing input into clinical study designs and trial protocols and will ensure that data analysis and interpretation of results are statistically sound and meet the desired study objectives. The Senior Biostatistician will work in a cross-functional team to support Owlstone s clinical test development and customer services business. Key responsibilities: Perform appropriate statistical analyses at all phases of the project, from clinical protocol development and study design through final analysis and reporting of results Evaluate clinical research studies and prepare statistical analysis plans that provide sound approaches to support a continuum of study goals, from biomarker discovery through clinical test development Apply appropriate statistical methodologies to analyze the data, including, but not limited to, hypothesis testing, regression models, multivariate analyses, machine learning, and network-based analyses Program and analyze data using Python or R; demonstrate good programming practices through proper documentation and commenting; perform appropriate QA to ensure accuracy and consistency of results Effectively communicate statistical methods and results to cross-functional team members, clinical collaborators, and others with a variety of technical expertise (including lay audience) Maintaining technical knowledge and skills appropriate for the role, including staying current with innovative statistical methodologies that are relevant to clinical research Requirements Technical Competencies: A thorough understanding of sample size, study power, precision, and their application in clinical trials and/or observational studies Proficient in translating clinical research questions into testable hypotheses Adept in communicating the assumptions, limitations, and advantages or disadvantages of statistical methods and describing preferred alternatives when key assumptions are not met Working proficiency in Python (to the level of package writing) or R (capable of implementing statistical or computational methods) Demonstrated ability to take initiative and be proactive in your approach to work, with an independent, creative, and open mindset Desirable Experience: Statistical experience working with CROs or the biopharmaceutical industry Application of statistical design and analysis for biomarker discovery and validation Experience with metabolomics (or other omics) data from clinical or epidemiologic studies Experience working closely with clinical biologists and translational scientists to analyze and interpret clinical datasets Strong publication record or other demonstrable track record of performance and collaboration Familiarity with IRB/ethics and regulatory documentation Qualifications: PhD or equivalent combination of education, training and experience in (bio) statistics or a related discipline, preferably with demonstrable experience working in a clinical, biomedical, or commercial environment
Most companies try to meet expectations, dunnhumby exists to defy them. Using big data, deep expertise and AI-driven platforms to decode the 21st century human experience - then redefine it in meaningful and surprising ways that put customers first. Across digital, mobile and retail. For brands like Tesco, Coca-Cola, Procter & Gamble and PepsiCo. We're looking for a talented Research Data Scientist who expects more from their career. It's a chance to extend and improve dunnhumby's Price & Promotions scientific portfolio. It's an opportunity to work with a market-leading business to explore new opportunities for us and influence global retailers. Joining our Data Science team, you'll work with world class and passionate people to apply machine learning, statistical, and econometrics methods to business problems. You'll support our high-performing Price & Promotions experts by developing mathematical models, creative methods to address new and complex problems and perform data analysis and model validation. You'll also have the opportunity to document and present analysis to internal teams and clients. What we expect from you Passion about designing generative models from first principles whenever possible. Pragmatic approach to modelling with a care to preserve theoretical validity and practical use. Good working knowledge any of: Maximum Likelihood Theory, Mixed Effects Models, Hierarchical Models, Bayesian Inference (MAP/Sampling). If the above points resonate with you, it is also likely that you will have: Degree or equivalent in a statistical or mathematical subject. Postgraduate degree or recent relevant experience of conducting research or mathematical analysis, especially in the domains of statistics, physics, econometrics or machine learning. Ability to prototype solutions using e.g. Python, R, Matlab to facilitate testing of algorithms on large data sets. Good understanding of machine learning techniques, with applications to classification, regression, and clustering. Working knowledge of databases and SQL What you can expect from us We won't just meet your expectations. We'll defy them. You will work within a team of collaborative and curious colleagues, who are passionate about injecting scientific rigour into their solutions. You'll enjoy the comprehensive rewards package you'd expect from a leading technology company. But also, a degree of personal flexibility you might not expect. Plus, thoughtful perks, like flexible working hours and your birthday off. You'll also benefit from an investment in cutting-edge technology that reflects our global ambition. But with a nimble, small-business feel that gives you the freedom to play, experiment and learn. And we don't just talk about diversity and inclusion. We live it every day - with thriving networks including dh Women's Network, dh Proud, dh Parent's & Carer's, dh One and dh Thrive as the living proof. Everyone's invited. Our approach to Flexible Working At dunnhumby, we value and respect difference and are committed to building an inclusive culture by creating an environment where you can balance a successful career with your commitments and interests outside of work. We believe that you will do your best at work if you have a work / life balance. Some roles lend themselves to flexible options more than others, so if this is important to you please raise this with your recruiter, as we are open to discussing agile working opportunities during the hiring process.
Sep 21, 2022
Full time
Most companies try to meet expectations, dunnhumby exists to defy them. Using big data, deep expertise and AI-driven platforms to decode the 21st century human experience - then redefine it in meaningful and surprising ways that put customers first. Across digital, mobile and retail. For brands like Tesco, Coca-Cola, Procter & Gamble and PepsiCo. We're looking for a talented Research Data Scientist who expects more from their career. It's a chance to extend and improve dunnhumby's Price & Promotions scientific portfolio. It's an opportunity to work with a market-leading business to explore new opportunities for us and influence global retailers. Joining our Data Science team, you'll work with world class and passionate people to apply machine learning, statistical, and econometrics methods to business problems. You'll support our high-performing Price & Promotions experts by developing mathematical models, creative methods to address new and complex problems and perform data analysis and model validation. You'll also have the opportunity to document and present analysis to internal teams and clients. What we expect from you Passion about designing generative models from first principles whenever possible. Pragmatic approach to modelling with a care to preserve theoretical validity and practical use. Good working knowledge any of: Maximum Likelihood Theory, Mixed Effects Models, Hierarchical Models, Bayesian Inference (MAP/Sampling). If the above points resonate with you, it is also likely that you will have: Degree or equivalent in a statistical or mathematical subject. Postgraduate degree or recent relevant experience of conducting research or mathematical analysis, especially in the domains of statistics, physics, econometrics or machine learning. Ability to prototype solutions using e.g. Python, R, Matlab to facilitate testing of algorithms on large data sets. Good understanding of machine learning techniques, with applications to classification, regression, and clustering. Working knowledge of databases and SQL What you can expect from us We won't just meet your expectations. We'll defy them. You will work within a team of collaborative and curious colleagues, who are passionate about injecting scientific rigour into their solutions. You'll enjoy the comprehensive rewards package you'd expect from a leading technology company. But also, a degree of personal flexibility you might not expect. Plus, thoughtful perks, like flexible working hours and your birthday off. You'll also benefit from an investment in cutting-edge technology that reflects our global ambition. But with a nimble, small-business feel that gives you the freedom to play, experiment and learn. And we don't just talk about diversity and inclusion. We live it every day - with thriving networks including dh Women's Network, dh Proud, dh Parent's & Carer's, dh One and dh Thrive as the living proof. Everyone's invited. Our approach to Flexible Working At dunnhumby, we value and respect difference and are committed to building an inclusive culture by creating an environment where you can balance a successful career with your commitments and interests outside of work. We believe that you will do your best at work if you have a work / life balance. Some roles lend themselves to flexible options more than others, so if this is important to you please raise this with your recruiter, as we are open to discussing agile working opportunities during the hiring process.
Principle Scientist / Technical Lead, London Based, £50-55k + 20% bonus + expenses Are you up for a challenge ? Do you want to lead the way and take your career to the next level ? Great read on We are looking for a self starter, a dynamic, entrepreneurial scientist who wants to take their next step and drive a company forward . This is a new role for someone who wants the ultimate challenge Reporting into Managing Director/Chief Scientific Officer, the Principal Scientist/Technical Lead is responsible for delivery of technical projects and implementation of technical services for the pathology business unit. You will be leading project that could involved with the implementation of technical services which span a wide array of disciplines, technologies and assays including biochemistry, haematology, immunoassay, molecular diagnostics. Validation and verification of new assays and analysers including drafting verification/validation protocols, procuring required materials, executing protocols and ensuring completion of verifications and conformance with acceptance criteria. Authoring technical documentation including Standard Operating Procedures, verification/validation protocols, technical reports, compiling and submitted data etc Technical review of prospective vendors to ensure adherence to required ISO standards as well as internal operational and technical requirements. Onboarding of new analysers, assays and equipment ensuring verification and validation is completed. What will you need to have ? Professional registration with the Health and Care Professions Council (HCPC). Experience across an array of pathology disciplines including biochemistry, haematology, immunology and molecular diagnostics. 10 years experience in a pathology/clinical laboratory. Demonstrable experience of leading on technical projects. Strong experience with technical processes such as validation and verification. Super organised: used to juggling multiple projects with different priorities and working to short deadlines Strong attention to detail: our team rely on us to ensure projects run perfectly Tech savvy: confident using MS Office Have a growth mindsight: we're growing fast, and you'll be expected to offer ideas where processes can be improved and drive your own personal development Excellent verbal and written skills: you should be able to draft clear, concise communications, adapting tone & style as appropriate If you want to a confidential chat, apply now
Feb 26, 2022
Full time
Principle Scientist / Technical Lead, London Based, £50-55k + 20% bonus + expenses Are you up for a challenge ? Do you want to lead the way and take your career to the next level ? Great read on We are looking for a self starter, a dynamic, entrepreneurial scientist who wants to take their next step and drive a company forward . This is a new role for someone who wants the ultimate challenge Reporting into Managing Director/Chief Scientific Officer, the Principal Scientist/Technical Lead is responsible for delivery of technical projects and implementation of technical services for the pathology business unit. You will be leading project that could involved with the implementation of technical services which span a wide array of disciplines, technologies and assays including biochemistry, haematology, immunoassay, molecular diagnostics. Validation and verification of new assays and analysers including drafting verification/validation protocols, procuring required materials, executing protocols and ensuring completion of verifications and conformance with acceptance criteria. Authoring technical documentation including Standard Operating Procedures, verification/validation protocols, technical reports, compiling and submitted data etc Technical review of prospective vendors to ensure adherence to required ISO standards as well as internal operational and technical requirements. Onboarding of new analysers, assays and equipment ensuring verification and validation is completed. What will you need to have ? Professional registration with the Health and Care Professions Council (HCPC). Experience across an array of pathology disciplines including biochemistry, haematology, immunology and molecular diagnostics. 10 years experience in a pathology/clinical laboratory. Demonstrable experience of leading on technical projects. Strong experience with technical processes such as validation and verification. Super organised: used to juggling multiple projects with different priorities and working to short deadlines Strong attention to detail: our team rely on us to ensure projects run perfectly Tech savvy: confident using MS Office Have a growth mindsight: we're growing fast, and you'll be expected to offer ideas where processes can be improved and drive your own personal development Excellent verbal and written skills: you should be able to draft clear, concise communications, adapting tone & style as appropriate If you want to a confidential chat, apply now
Laboratory technical coordinator Excellent opportunity for a laboratory coordinator within a pharmaceutical testing laboratory. Kenton Black is a recruitment partner to a global pharmaceutical laboratory who are looking for a laboratory technical coordinator to join their team based in Kent. This person will be responsible in resolving customer queries, and reporting results to external clients. This is an ideal position for a pharmaceutical chemist/ scientist who is looking for more of an office based role where they would be utilizing their knowledge to resolve client queries and provide technical solutions. This role can be home based. Key responsibilities First point of contact for all external client technical enquires Support project teams in setting up analytical testing at contract research organizations Keep up to date with analytical testing happening within the laboratory with clients Reviewing data returned from CROs against the work order. Preparation and/or checking of technical documentation Data retrieval, document preparation and verification for regulatory filings Review of analytical experiments for Drug Substance and Drug Product that may include transfer of methods, analysis of samples, validation experiments or stability data. Requirements Essential Degree in Pharmaceutical Science or equivalent Previous experience in working within pharmaceutical R&D testing laboratory is essential Excellent experience in using techniques such as HPLC, GC, NMR, MS, Karl Fisher, Dissolution and UV Experience in interpretation of technical data Desired Experience in method validation and stability testing is highly desired Previous experience in managing projects, liaising with external clients is highly desired Experience with reviewing GMP analytical experiments for drug substance and drug product desirable. Experience with writing the analytical sections for regulatory filings desirable
Feb 26, 2022
Full time
Laboratory technical coordinator Excellent opportunity for a laboratory coordinator within a pharmaceutical testing laboratory. Kenton Black is a recruitment partner to a global pharmaceutical laboratory who are looking for a laboratory technical coordinator to join their team based in Kent. This person will be responsible in resolving customer queries, and reporting results to external clients. This is an ideal position for a pharmaceutical chemist/ scientist who is looking for more of an office based role where they would be utilizing their knowledge to resolve client queries and provide technical solutions. This role can be home based. Key responsibilities First point of contact for all external client technical enquires Support project teams in setting up analytical testing at contract research organizations Keep up to date with analytical testing happening within the laboratory with clients Reviewing data returned from CROs against the work order. Preparation and/or checking of technical documentation Data retrieval, document preparation and verification for regulatory filings Review of analytical experiments for Drug Substance and Drug Product that may include transfer of methods, analysis of samples, validation experiments or stability data. Requirements Essential Degree in Pharmaceutical Science or equivalent Previous experience in working within pharmaceutical R&D testing laboratory is essential Excellent experience in using techniques such as HPLC, GC, NMR, MS, Karl Fisher, Dissolution and UV Experience in interpretation of technical data Desired Experience in method validation and stability testing is highly desired Previous experience in managing projects, liaising with external clients is highly desired Experience with reviewing GMP analytical experiments for drug substance and drug product desirable. Experience with writing the analytical sections for regulatory filings desirable
Our client is a consultancy who help redefine lab/ R&D informatics strategy and support the 'lab of the future' with digital transformation projects. Their expertise covers the entire lifecycle from business case creation, requirements definition, vendor/ technology selection and implementation and validation. Project: The customer is going through a lab transformation activity and as part of that they have new lab systems to implement and existing systems to interface/integrate. These systems range from LIMS/ELN to compound management systems, plate handling systems and sample storage systems etc KEY DUTIES AND RESPONSIBILITIES: To deliver informatics solutions - ELNs/ LIMS. Project manage to ensure delivery against budget, scope and timelines. Manage project risks. Conduct requirements gathering. Design and develop solutions based on the defined user requirements. Contribute to systems architectural design. Coordinate and manage validation and user acceptance processes. Collaborate with business teams and technology vendors. Conduct business process analysis and system design. Conduct requirements gathering. Document user stories KEY SKILLS & EXPERIENCE Proven experience in delivering and managing laboratory informatics projects. You will be comfortable leading detailed technical conversations with both scientists and lab informatics software specialists. You will have laboratory experience to support the understanding and complexity of science workflows in scope. You will have in-depth experience with ELNs (Electronic Laboratory Notebooks) or LIMS (laboratory Information Management Systems) The client has deemed these roles outside of IR35.
Feb 26, 2022
Contractor
Our client is a consultancy who help redefine lab/ R&D informatics strategy and support the 'lab of the future' with digital transformation projects. Their expertise covers the entire lifecycle from business case creation, requirements definition, vendor/ technology selection and implementation and validation. Project: The customer is going through a lab transformation activity and as part of that they have new lab systems to implement and existing systems to interface/integrate. These systems range from LIMS/ELN to compound management systems, plate handling systems and sample storage systems etc KEY DUTIES AND RESPONSIBILITIES: To deliver informatics solutions - ELNs/ LIMS. Project manage to ensure delivery against budget, scope and timelines. Manage project risks. Conduct requirements gathering. Design and develop solutions based on the defined user requirements. Contribute to systems architectural design. Coordinate and manage validation and user acceptance processes. Collaborate with business teams and technology vendors. Conduct business process analysis and system design. Conduct requirements gathering. Document user stories KEY SKILLS & EXPERIENCE Proven experience in delivering and managing laboratory informatics projects. You will be comfortable leading detailed technical conversations with both scientists and lab informatics software specialists. You will have laboratory experience to support the understanding and complexity of science workflows in scope. You will have in-depth experience with ELNs (Electronic Laboratory Notebooks) or LIMS (laboratory Information Management Systems) The client has deemed these roles outside of IR35.
LIMS Administrator The LIMS Administrator role is responsible for the uptime, performance and security access of users to the software system. The role forms a vital trouble shooting link between laboratory users who supply data in, and Data Scientists who analyse and process data out. Critical to the role is an understanding of the key stages in the molecular biology process of PCR and sample traceability requirements for ISO standards 15189. Are you looking for a change to work for an organisation that makes a difference in the society? Then this is the right role for you! The Rosalind Franklin Laboratory is part of the NHS Test and Trace Lighthouse Laboratory network and is at the heart of UK Health Security Agency's plans for managing coronavirus. What's in it for you? £40,000 pa, £20.51 per hour 10% Retention Payment 4 days on and 4 days off 18 months temporary contract Responsibilities Uptime, Performance and Security access of users to the LIMS software system Work closely with IT team to ensure the right tools and equipment had been supplied to access LIMS inside and outside the lab Data Entry Work with quality team to ensure good change control, release management and documentation to maintain the validation Essential Criteria BSc in BIological Science/ IT qualifiation within proven laboratory experience Super-User or software management experience Knowledge in medical diagnostic testing Expert use of database and data analysis Experience in software training
Feb 24, 2022
Contractor
LIMS Administrator The LIMS Administrator role is responsible for the uptime, performance and security access of users to the software system. The role forms a vital trouble shooting link between laboratory users who supply data in, and Data Scientists who analyse and process data out. Critical to the role is an understanding of the key stages in the molecular biology process of PCR and sample traceability requirements for ISO standards 15189. Are you looking for a change to work for an organisation that makes a difference in the society? Then this is the right role for you! The Rosalind Franklin Laboratory is part of the NHS Test and Trace Lighthouse Laboratory network and is at the heart of UK Health Security Agency's plans for managing coronavirus. What's in it for you? £40,000 pa, £20.51 per hour 10% Retention Payment 4 days on and 4 days off 18 months temporary contract Responsibilities Uptime, Performance and Security access of users to the LIMS software system Work closely with IT team to ensure the right tools and equipment had been supplied to access LIMS inside and outside the lab Data Entry Work with quality team to ensure good change control, release management and documentation to maintain the validation Essential Criteria BSc in BIological Science/ IT qualifiation within proven laboratory experience Super-User or software management experience Knowledge in medical diagnostic testing Expert use of database and data analysis Experience in software training