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Cambridge (uk)

Found in Reed - an exciting opportunity for a Principal Statistician, located in our Cambridge, UK office. In this role you Job Description At AstraZeneca we are constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We?re pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we?re industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as together we explore synergies between small and large molecules. AstraZeneca has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent. Those who join AstraZeneca feel a sense of ownership about their future. They thrive with a recognised leader in the industry. AstraZeneca is an agile, fast-moving and emerging industry leader in oncology . We are a nimble organisation that values smart risk-takers. With AstraZeneca , you will be applying a creative approach to science while being at the forefront of a strong and rich pipeline of cutting-edge medicines. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterised by respect, integrity and growth opportunities. Our Oncology Pipeline Our robust pipeline includes investigational therapies in varied stages of clinical development, from recently approved products to earlier-stage molecules in clinical trials. We aspire to transform the lives of cancer patients, working to eliminate cancer as a cause of death in the future. We have an exciting opportunity for a Principal Statistician, located in our Cambridge, UK office. In this role you will provide statistical expertise for complex design and interpretation of clinical studies, regulatory submissions and commercialisation. You will also: Analyse internal and external information to inform design decisions and the development of decision criteria Develop a Statistical Analysis plan for complex studies and/or project deliveries Provide support to the complex study analysis, regulatory submissions including specification of overview documents and response to regulatory questions Contribute to the regulatory submissions including specification of overview documents and response to regulatory questions Identify opportunities for the application of modelling and simulation to improve study design Identify and apply statistical methodology to improve the process and delivery activities Perform ad hoc and exploratory data analyses Contribute to the development of best practice to improve quality, efficiency and effectiveness Summary and Qualifications Principal statisticians work with senior staff in providing statistical support to clinical trial design, data analysis and results interpretation for clinical studies at different phase of development. They engage in using modelling and simulations to exploit information to inform design and decision-making. They work with programming team (internal or external) to implementing statistical analysis plan. Work with the Global Product Statistician (GPS) as a statisticians? team to provide statistical input to compound development, and actively participate at the Clinical Trial team and the Clinical Development Sub-team Qualifications: MS or Ph.D. Statistics, Biostatistics, or Mathematics (containing a substantial statistical component) and preferably in pharma/healthcare or other relevant area Knowledge of the technical and regulatory requirements related to the role and able to guide others on these Experience in drug development, study design, and data analysis and interpretation Excellent communication skills and ability to build strong relationships Excellent collaboration skills required ? the energy to work across global & functional boundaries, both internally and externally Project management skills Ability to apply statistical expertise to complex problems, problem solving and quality focus Desirable Qualifications Experience in Oncology product development preferred Expert statistical programming skills (SAS and R) AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Statistician »
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(uk)

Found in EnvironmentJob - passionate about wetland conservation and river catchment restoration? The Working Wetlands project Devon Wildlife Trust, Exeter and Beaworthy, Devon, £29,130 pa plus 5 pension. Are you passionate about wetland conservation and river catchment restoration? The Working Wetlands project is one of the largest natural catchment management schemes in the South West to improve water quality and build the resilience and sustainability of 8 major catchments across Devon as part of South West Water?s Upstream Thinking programme. The programme has wide-reaching, positive impacts on the environment - increasing biodiversity, reducing energy us...

Jobs Working Wetlands Advisory Officer (Reservoirs) »
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(uk)

Found in EnvironmentJob - wetland conservation and river catchment restoration? The Working Wetlands project is one Devon Wildlife Trust, Beaworthy, Devon, £23,749 pa plus 5 pension. Are you passionate about wetland conservation and river catchment restoration? The Working Wetlands project is one of the largest natural catchment management schemes in the South West to improve water quality and build the resilience and sustainability of 8 major catchments across Devon as part of South West Water?s Upstream Thinking programme. The programme has wide-reaching, positive impacts on the environment - increasing biodiversity, reducing energy us...

Jobs Working Wetlands Advisory Officer (Tamar) »
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(uk)

Found in EnvironmentJob - water quality, wetland conservation and river catchment restoration? The Working Wetlands project Devon Wildlife Trust, Exeter, Devon, £23,749 pro rata plus 5 pension. Are you passionate about water quality, wetland conservation and river catchment restoration? The Working Wetlands project is one of the largest natural catchment management schemes in the South West to improve water quality and build the resilience and sustainability of 6 major catchments across Devon as part of South West Water?s Upstream Thinking programme. Working alongside South West Water and the Westcountry Rivers Trust, you will deliver an ambiti...

Jobs Working Wetlands Water Quality Officer »
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Cambridge (uk)

Found in Reed - and recognising their potential. Our ambition is to push the boundaries of science to change the practice Location: Cambridge Competitive Salary & Benefits At AstraZeneca when we see an opportunity for change we seize it and make it happen, because an opportunity no matter how small can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Our ambition is to push the boundaries of science to change the practice of medicine and transform the lives of patients living with cancer. To accomplish this, we focus on research & development and our commercial capabilities to deliver a new generation of medicines that have the potential to redefine cancer treatment. As a Principal Patient Safety Physician, you play a key role bringing deep clinical understanding and judgement to the patient safety risk perspective in benefit risk assessments. You will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and regulatory requirements. The role will be based in our Cambridge City House office, close to Cambridge Train Station. Main Duties and Responsibilities You will provide medico-scientific and clinical strategic leadership for assigned product(s). You will provide Disease Area strategic Patient Safety input to drug development and post-marketing programs across life-cycle of assigned substances and products ? e.g to dTPPs, patient populations, scientific understanding of toxicity-related mechanisms, ensure risk management commitments, risk mitigation and communication. You will define safety needs of Oncology TA disease areas with CoE and assure SSaMT interactions with PS Peer Review and SIRC. You will also lead regulatory communication and provide oversight of higher-level documents. We encourage you to closely follow medical developments within assigned areas to transform emerging data and trends into new plans You will lead medico-scientific and clinical contributions to RMPs for assigned products and to Periodic Reports including PBRERs, DSURs, etc. You will also coach and mentor junior Patient Safety staff and support SSaMTs in relevant Product teams. You may lead SSaMTs for key products in phase III/early launch phase. Additional responsibilities: Establish and lead SSaMT in accordance with PS Operating Model Agree SSaMT strategy and plan with GML, GCL and PSTAVP TA. Ensure SSaMT delivery of all elements of agreed plan to next project achievement, input to governance decisions and strategy to next achievement Ensure expert input to all elements (including SKGs) of design and interpretation, and efficient use of available tools and methodology (e.g. modelling and simulation) Establish and represent the ?safety view? of the assigned program(s) internally and externally Essential Requirements Degree in medicine and experience as a physician or academic clinician Extensive experience in designing, monitoring and implementing clinical trials and interpreting trial results Significant experience in advanced research and development Experience from strategic leadership of complex drug projects Therapeutic area expertise and commercial understanding Meaningful industry experience in Pharmacovigilance field Detailed understanding of pharmaceutical safety, reporting and surveillance processes and strong experience of Patient Safety as it relates to clinical trials and marketed products in any relevant field such as pharma, Regulatory Agency or Public Health agency Understanding of the medico-legal aspects of pharmacovigilance Proven leader of cross-functional delivery teams. Demonstrated ability to influence key business partners within and outside of company Proven proficiency with both written and verbal communications Desirable Requirements PhD in scientific discipline Extensive general medical knowledge Able to work across TAs and Functions Research background including peer reviewed publications Next steps? Apply now! AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Patient Safety Physician »
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Cambridge (uk)

Found in Reed - Senior Research Associate Location: Cambridge, Cambridgeshire Salary: Competitive, DOE Contract: 12 Senior Research Associate Location: Cambridge, Cambridgeshire Salary: Competitive, DOE Contract: 12-month Fixed term About the Role: To manufacture Abcam products according to their manufacturing batch records. Primary responsibilities: Manufacture Abcam products according to the manufacturing batch records (MBR?s). Actively participate in product improvement and process scale up Provide additional assistance in quality control when required Perform general laboratory duties as required Actively participate in laboratory and company meetings Maintain an accurate and complete record of all laboratory work performed Follow company health and safety guidelines for working in the laboratory Secondary responsibilities: Contribute to the company quality system Help with trouble shooting and technical issues with customer complaints when required Use and maintain company equipment according to company SOP?s and health and safety guidelines About You: At least 3 years? laboratory experience. A degree in a Life Science discipline is desirable. Experience working in scientific production is valuable. Experience of working with antibodies is advantageous. Production of colloidal gold or other nanoparticles would be useful. Ability to work accurately and follow both written and verbal instructions. Flexible approach to work. Team focussed with the ability to work effectively with others. About us: Ever since 1998, when our founder, Jonathan Milner, started selling antibodies from the back of his bike, Abcam has aimed to help scientific researchers make breakthroughs faster. We now have offices and labs in the UK, the US, China and Japan, and as we continue to grow, we remain ambitious, driven by our customers? success and their research needs. It?s our goal to provide a world-standard in protein research tools, technical support and delivery. When you join Abcam, you?ll join a global business with the passion and the vision to become the most influential company, and, best-loved brand in life sciences. Our culture is our key differentiator. We believe in empowering individuals, with responsibility given at an early stage. The working environment is fun and fast-paced, collaborative and outcome focused, with a strong customer focus. In addition to competitive salaries, we offer an attractive and flexible benefits package (which includes shares for eligible employees), a culture focused on wellbeing and opportunities for growth and development. If this sounds like you and you?d like to be a part of a fast paced, growing business with the vision to become the most influential company and best-loved brand in life sciences please apply now! No Agencies Please.

Jobs Senior Research Associate »
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Cambridge (uk)

Found in Reed - At AstraZeneca we are constantly pushing the boundaries of science to deliver life-changing At AstraZeneca we are constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We?re pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we?re industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as together we explore synergies between small and large molecules. AstraZeneca has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent. The Principal Statistical Programmer role has heavy emphasis on delivery while also focusing on leading a clinical program utilising project management and technical leadership abilities. This role is responsible for programming clinical trial analysis deliverables with quality and timeliness, with a hands-on and collaborative approach with other team members. This position requires high degree of independence, technical skills and ability to influence the team to get results without line management authority. Major Responsibilities: Review a clinical study protocol with regard to statistical programming responsibilities Review and provide input to a Statistical Analysis Plan (SAP) and Statistical Programming Plan (SPP) Review and provide input to Case Report Forms (CRFs) and external data transfer agreements Work cooperatively with and hold accountable clinical study team members including but not limited to the biostatistician, data manager, and medical writer Work cooperatively with and oversee a contract programming provider Assign tasks, set priorities, and provide technical help to clinical study programming teams Develop and maintain SDTM and ADaM specifications Program SDTMs, ADaMs, tables, figures, and listings (TFLs) according to approved specifications Provide accurate programming time estimates and risk mitigation plans to management or a study team Proactively inform management of the status of statistical programming deliverables and issues Oversee on-time delivery from clinical study programming teams and meet timelines for multiple concurrent studies Contribute to or initiate standards or process improvements Required Skills: Excellent SAS programming skills; contribute programming to a global library of macros Able to communicate clearly in oral or written form Advanced knowledge of CDISC standards and applying standards to complicated data Advanced knowledge of lab data processing and able to resolve issues Working knowledge of medical terms, the data coding process, and coding dictionaries Apply regulatory agency guidance in statistical programming responsibilities Preferred Skills: Able to program in other languages (e.g. R or S-PLUS, VBA, or Perl) Advanced knowledge of Unix commands; able to program shell scripts for complicated tasks Advanced knowledge of inferential statistics Requirements/Qualifications: Education : Minimum Bachelor?s Degree with concentration in Life Sciences, Computer Science, Mathematics, Statistics or a quantitative/analytical field. Experience : Extensive SAS programming experience in clinical studies including leading a clinical study programming team Supervision : Able to independently perform technical work and oversee a clinical study programming team AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Statistical Programming »
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(uk)

Found in GuardianJobs - c. £28,500 dependent upon experience: Medical Research Foundation : We need the very best people c. £28,500 dependent upon experience: Medical Research Foundation : We need the very best people to help deliver our vision of advancing medical research, improving human health and changing people?s lives. London (Greater)

Jobs Medical Research Foundation : Communications Officer »
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Cambridge (uk)

Found in Reed - the potential of science to address the unmet needs of patients around the world. We commit to those areas where At AstraZeneca, we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We?re passionate about the potential of science to address the unmet needs of patients around the world. We commit to those areas where we believe we can really change the course of medicine and bring big new ideas to life. Are you ready to work on one of the most exciting pipelines in the Oncology industry? AstraZeneca?s vision in Oncology is to push the boundaries of science to change the practice of medicine, transform the lives of patients living with cancer, and to ultimately eliminate cancer as a cause of death. A broad pipeline of next-generation medicines is focused principally on four disease areas - breast, ovarian, lung and haematological cancers. We are seeking highly motivated Senior Scientists in Immuno-Oncology with deep scientific and technical expertise spanning both in innate and/or adaptive immune cell biology (including roles with a focus on T cells, NK cells and/or myeloid cells) with a track record of scientific excellence to join our team in Cambridge, UK. As a Senior Scientist you will be a key member of a team focused on supporting immune-oncology projects through the drug discovery process. You will bring your theoretical and practical expertise in immunology to establish assay systems and deliver datasets that will have direct impact on immune-oncology research projects. Main Duties and Responsibilities Working in this laboratory-based position within the Immuno-Oncology Research group you will develop, design, conduct and analyse in vitro experiments to assess the function of our candidate drugs and help to dissect the mechanism of action of novel therapeutics targeting the immune system for cancer therapy. You will also review emerging literature and internal data to help in identifying new potential targets and contribute to target validation activities. A strong foundation in immunology / immuno-oncology, and depth of expertise in techniques for the analysis of immune function and phenotype is essential for this role. As a highly organised, self-motivated individual with a strong lab/practical background, you will stay up to date with relevant technical and intellectual scientific expertise in tumour immunology and have a genuine passion for this field of research! Essential Requirements A PhD, or equivalent experience, in immunology and/or immuno-oncology. Experience of a range of in vitro skills for the analysis of human immune cell function e.g. multiparameter flow cytometry, ELISA, primary immune cell co-cultures, molecular biology skills including transcriptomic, assessment of intracellular signaling and generation of engineered cell lines Strong interpersonal, influencing, negotiating and collaboration skills together with evidence of having used these to support problem solving and delivery in a collaborative environment. Depth of understanding and enthusiasm for immunology and immuno-oncology Proven track record of success in your research Data processing, statistical analysis and interpretation. Experience preparing written scientific reports (e.g. manuscripts) and oral presentations (e.g. slides, posters). Desirable Requirements We would encourage applications from candidates who have experience in the evaluation of immune function and in the application of complex immunological assays. Expertise in field of T cell exhaustion, tumour myeloid and/or NK biology Experience with visualizing/quantitating high content multi-parameter flow data and evaluation of transcriptomic datasets Experience working with patient-derived tumours/TILs an advantage Knowledge of the drug discovery process Publications in top tier scientific journals Next steps, Apply Today! AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Senior Scientist, In vitro, Oncology Research »
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Cambridge (uk)

Found in Reed - Senior Statistician /Principal Statistician Statistical Innovation Cambridge (UK) or Gothenburg Senior Statistician /Principal Statistician Statistical Innovation Cambridge (UK) or Gothenburg (Sweden) At AstraZeneca, we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity, even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people?s exceptional skills with those of people from all over the globe. Our Oncology Biometrics department is an integral part of the Oncology R&D organisation. We drive excellent design in order to generate the appropriate data needed for quality decision making. The goal of Oncology Biometrics is to deliver value to the pipeline by excellence in delivery, improved decision making and engaging and shaping the external environment whilst accessing and implementing innovative solutions. You will sit within our Statistical Innovation group in Oncology Biometrics (OBM) department, which is a methodological hub for statistical design and analysis of clinical trials. Working as part of Data Science and Analytics (DSA), you?ll be able to access technology at the forefront of science in an innovative environment, where you will have the scope to develop creative statistical ideas and approaches, and to apply them in your work. Main duties and responsibilities Joining a team of statistical methodology experts, you will provide key input as you work to find solutions to problems at critical stages in the drug development cycle. This is exciting and technically challenging work in a dynamic and constantly changing landscape. Your key focus will be on producing pragmatic solutions, often within a tight time scale where the emphasis will be to deliver first, then refine and develop your solutions thereafter. You will contribute to, or lead capability build in the development and implementation of innovative methodological approaches in oncology R&D. You will also provide expert consultancy on key issues for fellow statisticians working in our therapeutically aligned statistics groups, as well as medical scientists and other key roles across the business. This will involve participating in strategic activities such as capability build projects, which can directly impact improvements to the way clinical trials are designed and analysed in AstraZeneca. This will also involve developing and implementing new methodology, interacting with external scientists and regulators, through publications, presentations and cross-industry collaborations. There will also be a focus on proactively identifying new areas where Statistical Innovation can add value, developing collaborative relationships with the external scientific/academic community. Summary and Qualifications Senior statisticians and Principal Statisticians work with senior staff in providing statistical support to clinical trial design and analysis, data analysis and results interpretation for clinical studies at different phase of development. They engage in using modelling and simulations to exploit information to inform design and decision-making. They work with programming team (internal or external) to implementing statistical analysis plan. Partners both internally and externally including with equivalent role in Biopharma R&D Unit. Note: Level of the position will be determined through the interview process where skills, experience and capabilities can be demonstrated and evaluated. Qualifications: ? MS or PhD in Statistics or a related discipline, preferably followed by experience of independent academic research and/or clinical drug development ? Documented ability of delivering innovative statistical solutions in drug development and evaluation, study design, and data analysis and interpretation ? Track record of research and methodological development in Statistics ? Desire to apply your scientific competence on practical problems, for the benefit of patients Desirable Qualifications ? Knowledge / research experience in the development of statistical methodology related to the design of Late Phase clinical trials. ? High level of competence in global and cross-skilled collaborative working ? Strong knowledge of programming in R and/or SAS ? Broad awareness of statistical issues against the evolving scientific and regulatory landscape AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Senior/Principal Statistician, Statistical Innovation »
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Cambridge (uk)

Found in Reed - approach to science while being at the forefront of a strong and rich pipeline of cutting-edge medicines Those who join AstraZeneca feel a sense of ownership about their future. They thrive with a recognised leader in the industry. AstraZeneca is an agile, fast-moving and emerging industry leader. We are a nimble organisation that values smart risk-takers. With AstraZeneca, you will be applying a creative approach to science while being at the forefront of a strong and rich pipeline of cutting-edge medicines. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterised by respect, integrity and growth opportunities. Our Pipeline Our robust pipeline includes investigational therapies in varied stages of clinical development, from recently approved products to earlier-stage molecules in clinical trials. We aspire to transform the lives of patients around the world. We have an exciting opportunity available for a Senior Biostatistician in our Cambridge UK location. Position Summary Biometrics and Information Sciences (B&I) drives good design to generate data needed for quality decision making. Our goal is to deliver value to the pipeline by excellence in delivery, improving decision making and engaging and shaping the external environment while accessing and implementing innovative solutions. TA Statistics is the group that oversees and delivers all the statistical and programming contribution to design, decision-making, interpretations and communication internally and externally for the TA portfolio of projects and is engaged in shaping the TA external environment. Level of the Position is determined by candidate experience, skills and capabilities. Responsibilities Provides statistical support for standard design and interpretation of clinical programmes, regulatory submissions and commercialisation Under guidance of a more experienced statistician will undertake design and analysis of complex studies. Analysing internal and external information to inform design decisions and the development of decision criteria Applies modelling and simulation to inform study design, assess robustness of results etc Develop a Statistical Analysis plan for study and/or project delivery Produce analysis, supporting graphics and analysis tables for standard CSRs, GMA studies or publications Able to interpret, summarise and communicate results of standard studies. Contribute to the improvement of methodology and provide practical solutions for problems Apply statistical methodology to improve the process and delivery activities Contributes to the development of best practice to improve quality, efficiency and effectiveness Job Dimensions Accountable for the quality of their statistical work Requirements MSc/PhD in Statistics or Mathematics (containing a substantial statistical component) Knowledge of key technical and regulatory requirements Extensive experience of design, analysis and reporting of clinical studies in more than one setting Communication Skills Collaboration and Team Working Skills Competent Statistical Programmer (SAS and R) Desirable Collaboration required Ability to apply statistical expertise to problems, problem solving and quality focus. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Statistician »
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Cambridge (uk)

Found in Reed - Principal Programmer ? Early Oncology Location(s) ? Cambridge (UK); Permanent Salary - Competitive Principal Programmer ? Early Oncology Location(s) ? Cambridge (UK); Permanent Salary - Competitive salary and company benefits apply Would you like to be a part of a Programming group that has direct strategic impact on drug development, playing a key role in getting medicines to patients? At AstraZeneca every one of our employees makes a difference to patient lives every day. We are building on our strong pipeline and turning ideas into life-changing medicines that benefit patients around the globe. Our Oncology Biometrics department, of which Programming is a part of, is an integral part of the Oncology R&D organisation. We drive excellent design in order to generate the appropriate data needed for quality decision making. The goal of Oncology Biometrics is to deliver value to the pipeline by excellence in delivery, improved decision making and engaging and shaping the external environment whilst accessing and implementing innovative solutions. Ultimately, the Oncology Programming department oversees and delivers all of the programming contribution to internal decision making, regulatory submissions and reporting and commercial activities for the portfolio of drug projects within the Oncology R&D organisation. If you?re inspired by the possibilities of science to make a difference and ready to discover what you can do ? join us. Role You will provide statistical programming support and/or lead programming related activities for the analysis and reporting process including, but not limited to, Clinical Study Report development, regulatory submissions, commercialisation and the scientific utilisation of our data for AstraZeneca products. There are many career options you can pursue for progression including technical pathways, management of global projects or line management. You?ll be part of a global team that pulls together to put patients first. Responsibilities Reporting to an Associate Director/Director within the Oncology Programming group you will provide programming expertise in one or more of the following areas: Lead/contribute to the delivery of the Clinical Study Report , Study Data Tabulation Model/Analysis Data Model databases and Tables, Figures and Listings through both internal and external delivery models Lead/contribute to the statistical programming deliverables for regulatory submissions, including specification and delivery of overview databases, outputs and response to regulatory questions Produce and maintain technical database standards and programming specification documents Lead/contribute to the development of best practice to improve quality, efficiency and effectiveness Development Safety Update Reports, Periodic Benefit-Risk Evaluation Report, Investigators brochures Planning and executing the transfer and analysis of data for safety/efficacy monitoring boards/independent data monitoring committees Requirements To succeed in this role, you?ll be an enthusiastic individual with an understanding of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You?ll enjoy multitasking, collaborating as part of a global team, and have an appetite for solving problems. You will be an effective communicator, with a strong team focus who enjoys collaborating to achieve the best results. Desirable experience includes: BSc in a Mathematical (i.e. Applied Math, Engineering, etc.), Statistical, Computer Science or Life Science subject Excellent problem-solving skills Diligence ? attention to detail and ability to manage concurrent projects and activities Excellent verbal and written communication skills and ability to influence stakeholders Principal Programmer Extensive SAS programming expertise to an advanced level gained within a clinical drug development or healthcare environment Comprehensive knowledge of technical and regulatory requirements with submission experience Wide-ranging knowledge of CDSIC standards and industry best practices Travel ? willingness and ability to travel domestically and/or internationally Team centric approach: keen to take steps to understand and appreciate the roles, skills and strengths of others on the team Next Steps ? Apply today! To be considered for this exciting opportunity, please complete your application on our website at your earliest convenience. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Programmer »
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(uk)

Found in GuardianJobs - To £112,000: Health Research Authority: At the Health Research Authority (HRA), our core purpose To £112,000: Health Research Authority: At the Health Research Authority (HRA), our core purpose is to protect and promote the interests of patients and the public in health and social care London, Manchester, Bristol, Nottingham or Newcastle

Jobs Health Research Authority: Chief Digital Transformation Officer »
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Newcastle-Upon-Tyne (uk)

Found in Fish4Jobs - Competitive: Anonymous: SummaryDo you want to be part of a new and exciting people insights and analytics team?About HMRCHMRC is the UK�s tax, payments and customs authority, Newcastle Upon Tyne

Jobs Anonymous: Survey Design and Qualitative Research Officer »
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Nottinghamshire (uk)

Found in Fish4Jobs - Competitive: Anonymous: SummaryDo you want to be part of a new and exciting people insights and analytics team?About HMRCHMRC is the UK�s tax, payments and customs authority, Nottinghamshire

Jobs Anonymous: Survey Design and Qualitative Research Officer »
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Cambridge (uk)

Found in Reed - Position: Senior Data Scientist/Associate Principal Scientist in Bioinformatics (Emerging Position: Senior Data Scientist/Associate Principal Scientist in Bioinformatics (Emerging Innovations) Based in: Cambridge, UK or Waltham, US Salary: Competitive with excellent benefits At AstraZeneca we believe in the potential of our people and you?ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. Are you an experienced bioinformatician looking for an exciting new challenge? Join our data Sciences & Quantitative Biology team in Cambridge, UK or Waltham, US and you will play a key role in using data science to enable and support our external innovation activities. You will join a multi-disciplinary team of data scientists and researchers to improve how we position drugs to target disease and translate biological questions into data science problems and solutions. You will benefit professionally as a member of a globally operating data sciences department, whilst working in an embedded environment with our Emerging Innovations Unit. Emerging Innovations Background The Emerging Innovations Unit (EIU) is a small, virtual and externally-focused R&D group within AstraZeneca that takes an entrepreneurial approach delivering medicines to patients. We achieve this primarily by repurposing internal AZ assets for new diseases, both inside and outside of core therapeutic areas, through a combination of internal programs and through pioneering ?Open Innovation? partnerships with external investigators (refer to: http://). The EIU also identifies and oversees the ?incubation? of novel technologies that could become next generation approaches to discover and/or develop innovative pharmaceuticals or assist in identifying patient populations that could benefit from our medicines. There is a strong entrepreneurial culture both for developing your own projects and for mentoring internal and external collaborators. The EIU is a sub-function of the Discovery Sciences group within AstraZeneca BioPharmaceutical R&D, as is the Data Sciences & Quantitative Biology department. Our team is passionate about diversity and inclusion. We welcome candidates from a range of backgrounds. Your main responsibilities will involve Collaborate effectively with multi-disciplinary colleagues and other data scientists to manage and analyse data to generate insights relating to external innovation. Work may, for example, involve text mining and NLP, molecular analytical approaches to drug repositioning, and leveraging large-cohort genetic studies. Contribute to derivation and prioritisation of hypotheses for new drug positioning opportunities Communicate efficiently and effectively with biologists and other scientists to understand requirements and translate them into data science problems and solutions. Ensure scientific excellence in software, processes and results as well as being efficient and well documented. Qualifications, Skills and Experience Required Essential PhD, or equivalent experience, in bioinformatics, mathematics, statistics, or the life sciences A solid understanding of biological concepts, data and information types ? for example relating to diseases, preclinical assays, target identification and target validation, or drug repositioning. Experience with relevant computational tools such as R/R Shiny, Python, cloud-based systems, software versioning tools (e.g. Git/Github), databasing (SQL, NoSQL) and data integration. Good quantitative skills and statistical knowledge Experience in analysing NGS transcriptomics and genetics data Ability to work effectively in global multi-disciplinary teams Strong communication skills, with technical and non-technical collaborators Desirable Experience in analysis of other ?omics data, or multi-omics studies Experience in drug repositioning research Experience in drug discovery and disease research If you are interested in this role, please apply by submitting your CV as soon as possible. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Sr Data Scientist or Associate Principal Scientist »
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Cambridge (uk)

Found in Reed - achieve no matter where you start with us. Our scientific research and development is afforded the utmost At AstraZeneca we believe in the potential of our people and you?ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. Our scientific research and development is afforded the utmost respect so we give our people the same. We do everything we can to make sure each AstraZeneca person has everything they need to stretch themselves and see what they can achieve. Discovery Sciences is a multi-faceted department which drives early drug discovery across AstraZeneca?s global Innovative Medicines and Early Development (IMED) portfolio. Mechanistic Biology & Profiling (part of Discovery Sciences), is a global, multidisciplinary department responsible for mechanism-of-action studies and compound profiling for efficacy and pre-clinical safety in support of the Oncology, Cardiovascular, Renal & Metabolism (CVRM), Respiratory, Inflammation & Autoimmunity (RIA), and Neuroscience portfolios. As the Principal Scientist, Enzymology, within the Mechanistic Biology & Profiling Group in Cambridge, UK, you will pursue world-class medicines in new ways, combining our peoples? extraordinary skills with those of people from all over the globe. Main Duties and Responsibilities: Reporting directly to the Global Head of the Mechanistic Biology & Profiling Department you will set the vision and drive our strategy for the integration of mechanistic enzymology into projects to characterise our drug targets and their interactions with ligands, from generation of early understanding of the underlying biology through to aiding clinical dose prediction. You will lead our mission to provide early, impactful mechanistic enzymology insight to projects across the IMEDs, influencing globally through matrix teams to combine a variety of approaches including in vitro enzymology, pharmacology, and quantitative cell biology. You will be a recognized scientific leader, able to represent the discipline across a broad range of therapeutic projects and global initiatives within Discovery Sciences and IMEDs, and also externally. You will drive scientific and technical innovation, including through external collaboration and partnership. You will also be a key member of the Global Mechanistic Biology & Profiling Leadership Team, participating in setting and maintaining the strategic direction and scientific quality of the department. Essential Requirements: PhD in mechanistic enzymology significant postdoctoral experience (or equivalent in a drug discovery environment) Formal training and proven expertise in mechanistic enzymology and its role in drug discovery Consistent record of career progression, and significant external reputation in pre-steady-state and steady-state kinetics, gained through professional recognition, external presentation and publication in high-impact journals Extensive experience in pre-clinical drug discovery, with deep knowledge of the use of mechanistic enzymology to aid translation from model systems through to clinical dose prediction Proven track record of training and developing a world-class group of experts, and optimising team performance in a highly matrixed discovery project environment Extensive experience of establishing and leading external collaborations and technology change projects to advance organisational science capability Track record of delivering results across a diverse project portfolio by driving scientific, strategic, and people performance. Desirable Requirements: Strong leader - able to articulate a vision for disease- agnostic Discovery missions, set direction and inspire commitment for preclinical Discovery. Ability to influence internal expertise, capacity and resources to drive governance and decision-making regarding scientific portfolio support and technology development. Is future orientated and strategic in thinking style. Capability to express complex technological ideas in a clear and compelling way to engage and influence multiple stakeholder groups. Generates exceptional results by influencing, driving performance and collaborating across project boundaries. Strong financial acumen with ability to assess and drive significant technological investments. Robust decision making informed by business and financial acumen and an understanding of competitor strategy. Global mind-set, with expertise in developing cross-functional operating models. Preferable Location: Cambridge (UK), with global accountability. Salary: Competitive with excellent benefits. If you?re passionate about the possibilities of science to make a difference and ready to discover what you can do ? join us, we look forward to receiving your application! To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience ? it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Scientist, Enzymology, Mechanistic Biology & Profiling »
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Newport (uk)

Found in Reed - in a Newport Secondary area for September Secondary Science Teacher Every qualified teacher that works with us Hoop Education are an approved supplier to 16 local authorities in Wales and are committed to providing the highest level of customer service, with fair rates of pay, and clear and honest communication. Even during this worrying and unprecedented time, we at Hoop Education are still speaking to the Key Decision makers within the schools and we are currently recruiting for the following position for a school in a Newport Secondary area for September Secondary Science Teacher Every qualified teacher that works with us here at Hoop will: ? Be paid a minimum 127.72 per day (M1) ? Be allocated a designated education consultant from our teacher-led team, who will work with you to identify opportunities for your continued professional development ? Be given direct access to our online training platform, where you will be able to complete e-learning modules on Child Protection, Use of Reasonable Force, Moving and Handling, First Aid and Behaviour Management, as well as other available modules within the education sector. Duties will include: * Maintaining classroom discipline in line with the school discipline policy * Building rapport between yourself and pupils * Supporting pupils as they undertake work in line with the national curriculum priorities * Promoting the school ethos and adhering to all school policies and procedures * Working closely with all school colleagues and under direction of the school leadership team. The ideal candidate will: * Be a Qualified Science Teacher * Have experience of working in a Secondary School setting * Hold Qualified Teacher Status (QTS) * Be registered (or willing to register) with the Education Workforce Council (EWC) * Be a passionate practitioner with the desire to improve the education outcomes for all pupils * Have excellent organisational skills and be able to communicate effectively at all levels * Be able to support and promote the ethos of the school. Benefits include: * Free DBS check * Free training * Refer a friend and earn up to 150 * Weekly Pay * Flexible working hours. Due to the nature of this role, an enhanced DBS check will take place prior to employment. Hoop Education are proud to be a teacher led employment agency, with vast experience in placing candidates in their ideal job role. If you have the relevant skills and experience and are keen to find out more, then please click the apply button or email your CV to or call the office on

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Edinburgh (uk)

Found in Reed - JOB AD: Research Compiler Engineer - Programming languages - Edinburgh - Highly Competitive plus JOB AD: Research Compiler Engineer - Programming languages - Edinburgh - Highly Competitive plus fantastic benefits! MicroTECH Global are working with a globally well-known business who are currently going through huge amounts of growth and they are looking for a Research Compiler Engineer - Programming languages to join their business. The successful candidates will have good experiences in artificial intelligence, deep learning and heterogeneous computing techniques, be able to perform the research and engineering works from designing easy-to-use programming Models/APIs to optimizing low-level compiler back-ends for various AI accelerators. The candidate should have a very solid computer science background, good research and programming skills, compiler/system performance tuning capabilities. Research and prototyping in Compilers and Programming languages team, Edinburgh. Join the strategy and business plan. Exploring the newly AI programming frameworks/languages. Cooperation with the Informatics school of the University of Edinburgh in Compilers and programming languages area transfer the result from academic to industry. Experience required: PhD or top rankings bachelorship & Major in computer science Mainstream compilers like LLVM/GCC experience Familiar with modern processor architectures and quantitative analysis approach Good programming skills in C/C programming languages Familiar with parallel computation and heterogeneous computation like OpenCL/Cuda Ability to pick up and progress new technologies What you will receive in return: Competitive salary and incentive schemes plus employee discounts Competitive Group Personal Pension Scheme and life cover Private medical insurance and Cash Plan 24 days annual leave per annum, pro-rata, plus 9 public holidays Opportunity for training and development Flexible working To hear more about this fantastic role please get in touch with Christina McGuire @ MicroTECH Global. PLEASE NOTE: All applicants should hold the Right to Work in the UK without the requirement for work sponsorship. Research Compiler Engineer - Programming languages - Edinburgh - Highly Competitive plus fantastic benefits!

Jobs Research Compiler Engineer »
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Sheffield (uk)

Found in Reed - are looking to recruit a Research Assistant. This is a very exciting role to work alongside a large consumer Elevation Recruitment Group are currently working with a key client based in Sheffield who are looking to recruit a Research Assistant. This is a very exciting role to work alongside a large consumer sought after brand. Working to support the business owner, you will work 20 hours a week from home with some office based work required in the future. Working closely with the owner, you will support him in providing all aspects of both business and academic research. Key Accountabilities: - Produce required facts and figures for projects such as academic research papers, commercial company information - An ability to work both independently and compile accurate reports and presentations to deadline - An ability to communicate effectively with others, particularly regarding the presentation of data including economic stats, academic research and sports research - Able to work effectively under time pressure and the ability to understand and follow complex instructions Requirements: This role would suit someone who is looking for flexibility in their working hours and can work closely with a business owner If you have experience in an academic capacity i.e. phd student, teacher or PA this role could suit you. You must be proactive, hardworking and detail orientated Be willing to go above and beyond whenever required Have a high attention to detail Have a degree or equivalent (desirable) Elevation Business Support is a specialist division of Elevation Recruitment Group focusing on positions in Yorkshire and surrounding regions. If you match the specified criteria and are interested in discussing the position in more detail, we would love to hear from you. The position in more detail, we would love to hear from you.

Jobs Part-Time Research Assistant »
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Kent (uk)

Found in Fish4Jobs - 50000.00 - 65000.00 GBP Annual: Anonymous: Principal Design Engineer (Rail)KentPermanentImmediate 50000.00 - 65000.00 GBP Annual: Anonymous: Principal Design Engineer (Rail)KentPermanentImmediate StartGBP50,000 to GBP65,000An award-winning design consultancy with offices in Kent and Hampshi Kent

Jobs Anonymous: Principal Design (Rail) »
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Cambridge (uk)

Found in Reed - , and application. Research and development on GPU micro-architecture and provide new techniques for improving GPU Company: MicroTech Global are working with a globally well-known business which is rapidly growing, and they are looking for a Senior GPU Hardware Designer to join their team. The role is focus on platform development not application development. Role: Responsible for GPU performance and power modelling and analysis, including both hardware architecture and software framework like compiler, driver, operating system, and application. Research and development on GPU micro-architecture and provide new techniques for improving GPU hardware?s power, performance, and area. Research and development on new graphics and computing applications and provide the guideline of GPU hardware/software functionality requirements and relative implementations. Make significant contributions to silicon design/verification/debug and performance analysis. Deliver new technology or methodology to improve GPU rendering and computing performance and power efficiency in physical implementation level. Cowork with the SoC teammates, finish all GPU?s system level integration analysis and design include working flow, interface define, storage and interconnection, power strategy, low power policy and testing methodology Skills required: MS/PhD degree in EE/CE or relative field with 5 or more years of ASIC design experience, to be with direct experience working with mobile programmable graphics hardware design is preferred. Familiarity with graphics/compute/vision standard APIs (OpenGL, OpenGL ES, OpenCL, Vulkan, OpenVX, etc) Familiarity with Android graphics system architecture and workflow from application level to kernel level. Deep understanding on software and algorithm development using GPU, for example, 3D games, virtual reality, image processing, artificial intelligence, etc Strong skills in SOC low power analysis, methodology, workflow, and design. Strong skills in GPU performance modelling and analysis. What you will receive in return: Competitive salary Generous Group Personal Pension Scheme and life cover (subject to age and earnings) Private medical insurance and Cash Plan 25 days annual leave per annum, pro rata, plus 8 public days Excellent training and development programme Childcare vouchers Flexible working Free onsite parking Principal GPU Hardware Designer - Cambridge - Up to 100,000 plus fantastic benefits

Jobs Principal GPU Hardware Designer »
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Cambridge (uk)

Found in Reed - development of our innovative pipeline, transforming exciting science into valued new medicines and ensuring Location: Cambridge, England, United Kingdom Global Medicine Development drives late-stage development of our innovative pipeline, transforming exciting science into valued new medicines and ensuring patients around the world can access them. We are responsible for enabling the business to make critical pipeline and investment decisions, to ensure they select the right molecules to progress and to seize the right lifecycle management opportunities ? generating the data required to drive regulatory submissions for new medicines and expanded indications and generating the evidence that shows their true value. As the Principal Pharmacovigilance (PV) Scientist you will provide expertise to multiple and/or single but complex products in different stages of development as needed. You will provide oversight of safety documents and deliverables for these projects in collaboration with the Global Safety Physician (GSP) and other PV Scientists. You will lead PV strategy for safety documents and regulatory reports. The role would suit someone with scientific curiosity, and an enthusiasm for understanding the science and making a difference to patients. The remit of the role is flexible, with the unique opportunity to move around from early phase through to late phase and to post marketing. This allows for a wide breadth of experiences, opportunities to learn, grow and develop. Our team is enthusiastic, resilient and has a strong desire to follow the science. The pace is fast, with a new challenge each day. Main Responsibilities You will lead the strategy for proactive pharmacovigilance and risk management planning of complex or multiple products, including preparation of the safety aspects of Global Risk Management Plans and Risk Evaluation and Mitigation Strategies (REMS) in partnership with the GSP and others as appropriate. You will provide subject matter expertise in the therapeutic area and across multiple products. You will have the ability to lead cross-functional process improvement or other initiatives on behalf of the Patient Safety organization. You will perform duties as a Safety Strategy and Management Team (SSaMT) Leader for complex and/or multiple products. As a Safety expert you will lead presentation of complex issues to Safety Information Review Committee (SIRC). You will lead safety strategy for multiple or complex periodic regulatory documents (PBRERs, PSURs, DSURs) according to the agreed process and timelines. You lead safety strategy for regulatory submissions of new products, formulations or indications (NDA/BLA, MAA), in partnership with the GSP and other functional experts. You will lead negotiations and provides expertise to the PS component of contracts/agreements with third parties to ensure quality and integrity of agreements. You will take accountability and lead resolution of complex safety issues and mediates cross-functional agreement. You will have the ability to participate in due diligence activities. As a safety expert, you will also provide training and mentorship to new GSPs and PV Scientists in approved processes and systems. Essential Requirements A life sciences/pharmacy<br>ursing degree, and advanced Patient Safety and/or Clinical/Drug Development experience Fluent in written and verbal English Advanced knowledge of PV regulations MD/MSc/PhD in scientific discipline, preferred Advanced understanding of epidemiology, preferred Demonstrable experience working in/leading (safety &amp;/or scientific) activities across at least 4 of the following areas: Clinical Development (Early and/or Late Phase) Post-Marketing surveillance MAA/BLA Submissions Periodic Reports Risk Management Plans (from scratch) Governance Board Interactions If you are interested in this role please apply by submitting your CV. Thank you. AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, gender or gender orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Pharmacovigilance Scientist »
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Norwich (uk)

Found in Reed - An experienced and chartered Principal Structural Engineer is sought to join this reputable firm An experienced and chartered Principal Structural Engineer is sought to join this reputable firm. This role will be to effectively liaise effectively with external clients, agencies and other design consultants. The suitable candidate will be based in the company?s Norwich office. You will be responsible for leading an effective and professional structures team. The firm is a well established practice with several nationwide offices. The firm are Investors in People, IS09001 approved and hold various other accreditations. This will be a high profile role with longer term opportunity for progression and advancement for the right candidate. Key requirements for this candidate - Credible and professional Chartered Structural Engineer (MICE or MIStructE) with significant experience and knowledge of managing project teams Experience of managing projects and conceptual design Ability to confidently manage clients expectations Effective communicator both internally and externally Working on own initiative with energy and drive Extensive experience of most common building materials Sector knowledge in retail and data centres Build and maintain Client relations Ability to represent business at Senior level Technical capabilities to include British Standards &amp; Eurocodes Remuneration package includes: Excellent basic salary Significant Bonus Scheme Holiday - 25 days plus BH?s Healthcare Death in service benefit and life assurance Pension Scheme Annual Professional membership fees paid The successful candidate must have a proven track record of relevant experience coupled with a genuine desire to progress. Sam Davis Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

Jobs Principal Structural Engineer »
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Glasgow (uk)

Found in Reed - Principal Product Change Engineer A Product Change Engineer with PLM experience is required to work Principal Product Change Engineer A Product Change Engineer with PLM experience is required to work on a six month contract, with the possibility of extension for our Defence client based in Glasgow. This is a 6-month contract with a leading UK defence business. Overview of the Product Change Engineer contract role The role will play a critical role within the Hunter Class Frigate Program (HCF) Product Change Management team, bringing complex warship engineering product knowledge and experience to complement the process team. Reporting to the Engineering Manager Product Change, this will be the lead role in interfacing with the reference design engineering (Type 26 GCS) and product change teams to enable and co-ordinate impact assessment by HCF engineers of the design product changes on the HCF design. This role will represent the HCF engineering authority at the reference design Engineering Change Board. Key skills required for the Product Change Engineer Strong whole-of-ship product knowledge across different disciplines including an understanding of the key interfaces between ship systems and sub-systems Knowledge and ideally a user of existing product change and configuration management processes Integrated bill of materials (iBoM) and change management in Windchill knowledge Leadership (Requirements of the job for providing leadership and guidance to others Leadership of processes, the candidate shall be able to provide clear guidance on the use of engineering processes (e.g. change) to wide range of stakeholders The role is based in Glasgow - Commutable from Kilmarnock, Paisley, Greenock, Stirling and Falkirk with excellent access from Edinburgh If you are a Configuration/Change Engineer looking for a new contract either apply online or if would like to find out about other Engineering opportunities please contact Kris Foston on or phone Do you know anyone who might be looking for a new role? You could benefit from our candidate referral scheme. Contact me on the above contact details for more information. Outsource. Our People. Your Success. Outsource UK is one of the country?s largest and most successful independent recruitment consultancies, specialising in the IT, Digital, Financial Services and Engineering sectors. We recruit talented people for contract and permanent opportunities, offer a consultative approach and have a reputation for providing a superior service to both clients and candidates. The business focuses on building long lasting relationships based on reliability and trust. We do this by hiring and retaining a great team of recruitment consultants who listen and understand our client?s and candidate?s needs. Our Manchester office (which covers the whole of the UK) provides a &quot;one-stop shop&quot; to clients and candidates operating in the engineering and manufacturing sectors and, in addition to Engineers, we source and provide temporary/contract and permanent opportunities for IT, Programme Management and Support Professionals (including Procurement / Purchasing / Supply Chain, HR, Finance and Administrative Support). Please visit our website www.outsource-uk.co.uk

Jobs Principal Product Change Engineer »
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Bristol (uk)

Found in Reed - for an experienced Senior or Principal recruiter who?ll enjoy building on our existing client base and taking things Join a well-respected and successful B Corp Certified recruitment business with an extensive client base, established industry partnerships and a progressive and enjoyable environment Enjoy a truly engaging and collaborative team environment with the entire business supporting you every step of the way You bring the attitude and ambition and we?ll provide you with every possible tool you could wish for, a highly successful marketing programme and a personal development plan to ensure you achieve great things In 2019 ADLIB became one of a handful of B Corp recruitment businesses based in the UK. We?re committed to sustainability - economically, on a human level and for the environment. This is a newly created role, that calls for an experienced Senior or Principal recruiter who?ll enjoy building on our existing client base and taking things to a whole new level. Working with often complex organisations who will benefit from our services to attract the talent required to drive their sustainability programmes and business models forward. We?re seeking a Senior or Principal Recruiter with a deep understanding of sustainability issues who?d love to immerse themselves into the sector and build out a team of specialists. What you?ll be doing We?re looking for experienced Recruiter who is in recruitment for the long game. Ambitious, committed and authentic you?ll want to take advantage of our brand, knowledge, platform and industry contacts and support our growth. Naturally you?ll be blown away that we?re a B Corp business and will be playing a key part in continually supporting the advancement of our certification. You?ll make things happen, see everything as an opportunity, get a kick from breaking down doors, creating new relationships, whilst working within a structured and effective manner that builds a long term business. You?ll quickly understand the sustainability landscape and how this sits against the business plan, initially you?ll have a broad starting point across CSR &amp; Sustainability, energy and cleantech, responsible investment and corporate affairs and communications. As you grow, the team will ? operating across specialisms in line with market demand. Beyond recruitment you?ll enjoy building out industry partnerships and supporting the wider geographic development of our greentech meet up and more. You?ll be supported by a team approach to winning together, in the quest to collectively strengthen our proposition and success rates. In short, you?ll have a team of 30 plus consultants behind you, ready to share their industry and client knowledge. You?ll also enjoy working with a highly experienced marketing team who?ll work closely to ensure our proposition and client acquisition model is maximised at all times. What experience you?ll need A successful track record in recruitment goes without saying. We want to hear from either Senior or Principal level Recruiters who share our behaviours and bring a proven desire / understanding of sustainability issues and the associated talent market&nbsp; You?ll be well equipped to dig deep, source and build relationships with candidates and clients alike&nbsp; The ability to immerse yourself in their worlds, network and build trust will be essential to your success, alongside maintaining ADLIB?s reputation within a busy market place. You?ll have impeccable communication skills, attention to detail, enjoy winning business and creating opportunities for the short and long term. As for your career, it?s entirely down to you and where you want to take it to. What you?ll get in return for your talents Expect an adult environment, a base salary in line with your experience and previous success, bonus structure, 27.5 days holiday (plus bank holidays), health scheme, seriously nice offices, a B Corp stakeholder group for all to join, flexi-time scheme, ping pong, company lunches and drinks / pizza fridays (drinkers, non-drinkers, vegans, veggies, you?ll be in good company) and most importantly, you?ll be joining a collaborative team that?ll have your back from day one and support you every step of the way. What?s next? Get in touch with Nick for a confidential discussion.

Jobs Senior / Principal Recruiter »
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London (uk)

Found in Reed - of activities dealing with various sponsor types e.g. Charities, Research Councils, Industry, Government Offices Temporary Assignment 15- 16ph plus Holiday Pay Outline of Vacancy This diverse and challenging assignment will Support Research Grants Managers with the day to day running of the section, ensuring that an efficient service to both internal and external customers is maintained. Duties will involve a diverse range of activities dealing with various sponsor types e.g. Charities, Research Councils, Industry, Government Offices The preparation of claims and invoices in a frequency determined by the sponsor, ensuring accuracy of information and requiring an in-depth knowledge of the sponsors diverse rules and regulations. Reconciling the total value of the claim to the general ledger and making any necessary adjustments in agreement with other central service sections and academic departments. Failure to meet deadlines will result in the imposition of financial penalties by external sponsors Responsible for maintaining a schedule of claims and intuitively arranging an order of priority to meet the needs of the sponsor The efficient timing of invoice and claim submissions is essential to facilitate the Colleges cash flow The continuous process of updating the information held in Agresso when changes occur, in order to ensure the accuracy of the data produced, for both routine and management information reports which are regularly presented to academics, Heads of Department, Senior Officers, and the College Research Board To produce routine reports as required, from the general ledger and PCB modules in Agresso, for data analysis and the compilation of information to meet departmental and external sponsor requirements To initiate and enter journals onto Agresso relating to internal expenditure transfers and salary re-charges, paying careful attention to accuracy to avoid the misrepresentation of data To work closely with the Finance office to ensure accuracy of research grant expenditure and liaison with the Credit Control Section to assist with the collection of income on research grants and contracts Ensuring that regular budget/expenditure reports are sent to departments in a timely manner Monitoring budget control and alerting the relevant departmental administrators and grant holders to significant variances for appropriate action Monitoring transactions to the research salary suspense account and interacting with HR and departments to determine the correct budget code and correct source of funding To Apply Please email your up to date CV stating your current salary, notice period &amp; salary sought IMPORTANT NOTE Our aim is to respond to all successful applications within 5 days. If you haven?t been contacted within 5 days your application has been unsuccessful and your details will not be held further but we positively encourage you to apply for any other positions that you may see in the future. We apologise that we cannot contact everybody in person but thank you in advance for your interest. Adept Recruitment Ltd encourages applications from individuals of all ages &amp; backgrounds. Appointment will be made on merit alone but candidates must be able to demonstrate their ability to work in the UK. Adept Recruitment Ltd acts as an employment agency for permanent recruitment &amp; an employment business for temporary recruitment as defined by the Conduct of Employment Agencies &amp; Employment Business Regulations 2003.

Jobs Research Grants Officer 3 Month Temporary Assignment £15-£16ph »
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Cambridge (uk)

Found in Reed - Position: Senior Research Scientist, Sample Management Location: Cambridge Science Park Competitive Position: Senior Research Scientist, Sample Management Location: Cambridge Science Park Competitive Salary &amp; Excellent Company Benefits Are you a hardworking and experienced scientist, eager to join a company in the forefront of sample management technologies? Would you like to contribute to the continuous improvement of life changing projects? Apply for a Senior Research Scientist role to join our Sample Management team at AstraZeneca in Cambridge . In this position, you will be responsible for the storage and timely supply of chemical compounds to AstraZeneca?s drug discovery projects. Highly automated systems will be employed to supply small molecules to AstraZeneca scientists and partner organisations. You will be a part of the Discovery Sciences organisation, operating within an outstanding scientific environment to support drug discovery across each of AstraZeneca?s Therapeutic Areas. We work collaboratively within a Sample Management team, to provide support within agreed service levels with a strong customer focus. We strive hard to understand what fits customer needs and how to add value through our experience and capabilities. To maintain this position, we actively seek ways to improve our process and exploit new technologies. Main Duties and Responsibilities This position will give you the opportunity to work in a dynamic and enthusiastic environment, whilst delivering critical support to projects. You are passionate about supporting projects by providing compounds in the requested format - assay ready plates, serially diluted mother plates, formulations and solids. Continuous improvement is also a core activity, performed as individual and/or group projects within the local team and the global department. We will encourage you to act upon day-to-day issues that occur whilst processing samples and ensure business continuity. You will work with the following typical tasks: Working as part of a team to deliver research compounds in the requested format and to agreed timelines, for distribution both locally and globally to AZ customers and external collaborators Rapidly addressing customer queries with regards to Sample Management orders, software, processes and capabilities Working closely with internal project teams in the development of outstanding solutions to meet customer needs Remaining current in research/technological advancements and discovery programs Designing, performing and interpreting experiments independently to investigate process improvements and evaluate new technologies Achieving personal scientific visibility through project contributions, internal presentations and publications Ensuring your own work and that of your colleagues is performed in accordance with appropriate Safety, Health &amp; Environment (SHE), quality and compliance standards Minimum requirements Sample Management is a highly collaborative group, working to tight delivery schedules - so the ability to be comfortable working at a fast, goal-oriented pace, with a team focused attitude is essential to be successful in the role. We also believe you have: A BSc/MSc in a scientific/engineering subject area, and some shown experience A strong work ethic and customer focus Excellent problem-solving skills and ability to identify and implement improvement activities A passion for science, technology and innovation A track record in the performance of a range of practical skills, including non-routine sophisticated tasks, to a high level Excellent communication skills with a proactive and delivery focused approach Desirable Requirements Knowledge and experience of working in a sample management role Experience in operating liquid handling equipment Experience in operating integrated laboratory automation equipment Experience with Laboratory Information Management Systems (LIMS), or other tracking and scheduling software An understanding of the drug discovery process If this sounds like the next challenge for you ? apply today ! We look forward to your application no later than 5th June 2020 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Senior Research Scientist, Sample Management »
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Cardiff (uk)

Found in Fish4Jobs - Consultancy are looking for a Principal Design Engineer to work from their office in Cardiff.Ke Cardiff 50000.00 - 55000.00 GBP Annual: Anonymous: PRINCIPAL DESIGN ENGINEEREstablished Civil Engineering Consultancy are looking for a Principal Design Engineer to work from their office in Cardiff.Ke Cardiff

Jobs Anonymous: Principal Civil Engineer - Cardiff »
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Edinburgh (uk)

Found in Fish4Jobs - 45000.00 - 55000.00 GBP Annual: Anonymous: Job Title: Principal Transport Modeller Office 45000.00 - 55000.00 GBP Annual: Anonymous: Job Title: Principal Transport Modeller Office: Edinburgh, ScotlandSalary Range: GBP45,000 - GBP55,000 + benefitsA leading, multinational consultancy, Edinburgh

Jobs Anonymous: Principal Transport Modeller - Edinburgh »
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Cambridge (uk)

Found in Reed - Principal Statistician, Tool Development, Quantitative Solutions Location- Cambridge / Gothenburg Principal Statistician, Tool Development, Quantitative Solutions Location- Cambridge / Gothenburg / Gaithersburg Career Level ? E Description At AstraZeneca we?re driving leading-edge approaches to drug development across many business areas ? within Early Biometrics &amp; Statistical Innovation (EB&amp;SI) a data-centric focus is helping us work more efficiently and creatively to bring the right medicines to the right patients. Our biometrics teams use their expertise in statistics and programming to answer drug development objectives and reduce uncertainty in product development, driving better business decisions with quantitative reasoning. The Principal Statistician, Tool Development sits in our Quantitative Solutions (QS) group, within EB&amp;SI. QS is a centre of excellence for building high quality software tools to provide novel statistical analyses, advanced analytics and business solutions. Working as part of Data Science and AI (DS&amp;AI), you?ll be able to access technology at the forefront of science in an innovative environment, where you will have the scope to develop creative tool development ideas and approaches, and to apply them in your work. Main Duties and Responsibilities As a Principal Statistician, Tool Development you will be part of the Quantitative Solutions team providing high quality software solutions in support of the drug development portfolio, for example: Trial design simulations Network meta-analyses Data visualisations Decision making methodologies Machine learning Technical expertise on tool development to staff within EB&amp;SI, DS&amp;AI and across AstraZeneca Working alongside others, you will lead the development of new software tools, including providing statistical &amp; programming expertise, managing stakeholder interactions, delivering requirements analysis, proof of concept, user acceptance testing and project management. You will be responsible for improving the productivity, scalability and ease of use of existing tools and solutions, whilst ensuring that our statistical software tools are developed and validated to AstraZeneca and regulatory standards. You will also inspire and mentor more junior colleagues within the Quantitative Solutions group. In addition to the above, you will contribute to the development, sharing and support of new procedures and standards in software tool development, to enable QS to provide the business with a range of innovative solutions to a variety of technical questions in drug development. Requirements Essential MSc or PhD in biostatistics, mathematics, informatics or related subject Experience of statistical analysis, modelling &amp; simulation, and statistical computing, primarily using R Broad understanding of clinical drug development &amp; the pharmaceutical environment Desirable Experience, or understanding, of end-to-end software tool development and lifecycle management Knowledge of other programming languages (e.g. R-Shiny, Java, Python, Spotfire, C/C , VBA/VBS) would be advantageous AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

Jobs Principal Statistician, Tool Development, Quantitative Solutions »
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Newcastle (uk)

Found in Reed - Control Officer to be responsible for helping to maintain and improve the Quality Management System Exciting Medical Devices Development company seeks a highly self-motivated and enthusiastic Quality Control Officer to be responsible for helping to maintain and improve the Quality Management System by employing excellent attention to detail, managing time efficiently and effectively and bringing outstanding teamwork skills to the role. Duties may include: Check incoming material documentation/certification Physically inspect incoming materials Support the Engineering and Assay teams in testing of incoming materials and assisting with non-routine analyses. Perform investigations where required Perform finished product testing according to test methods and product specifications including qPCR on standard laboratory instrumentation including BioRad CFX96 and Qiagen Rotor-Gene Q Help to develop, validate and the perform finished product test methods to facilitate QC testing of instruments and consumables Liaise with the Purchasing and Sales teams to ensure all materials released in time for use Help to generate and maintain incoming material specifications Work with the Operations team to suitably oversee controlled temperature shipments of samples and products Input into supplier complaints where required Ensure all documentation for incoming materials is completed promptly and made available by PDF for batch review Assist with management of outsourcing raw material identity testing Raise QMS documentation for Deviations, Change Control, Supplier Complaint where relevant for incoming material QC Assist with management of laboratory supplies Perform all activities in a safe manner with strict adherence to company guidelines Work within the Quality team to maintain focused, effective progression in line with Company Quality objectives. Support other members of the Quality team by providing training and mentoring on areas of expertise. Effectively interact with Technical, Development, Manufacturing, Operations, Sales and Marketing and Planning teams. Ensure policies and procedures are properly understood, carried out and evaluated and that modifications are investigated if necessary. Help to train staff in Quality Control requirements. Investigate relevant standards and establish clearly defined Quality methods for staff to apply. Define Quality procedures in conjunction with R&amp;D and Operations staff. Maintain process controls and documentation procedures and identify areas for improvement and efficiency. Support product design review and change control systems. Participate in the Company audit schedules for both internal and external Quality audits. Monitor Quality indicators and helping to gather and track relevant data. Identify relevant Quality-related training needs and delivering training. QA/QC review of contractor documentation relating to validation and verification activities as well as device manufacture records. Skills and experience: Good attention to detail Proficiency in Microsoft software packages Proven experience in a controlled environment of document checking and review Ability to prioritise and time manage Life science or Chemistry qualifications A highly motivated, organized, proactive and enthusiastic individual with a proven ability to work with tact and diplomacy. A minimum of 2 years? experience in working within a Quality Management System, with some specific experience of working with medical devices. Experience of working with ISO 13485

Jobs QC Officer »
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Newcastle (uk)

Found in Reed - Control Officer to be responsible for helping to maintain and improve the Quality Management System Exciting Medical Devices Development company seeks a highly self-motivated and enthusiastic Quality Control Officer to be responsible for helping to maintain and improve the Quality Management System by employing excellent attention to detail, managing time efficiently and effectively and bringing outstanding teamwork skills to the role. Duties may include: Check incoming material documentation/certification Physically inspect incoming materials Support the Engineering and Assay teams in testing of incoming materials and assisting with non-routine analyses. Perform investigations where required Perform finished product testing according to test methods and product specifications including qPCR on standard laboratory instrumentation including BioRad CFX96 and Qiagen Rotor-Gene Q Help to develop, validate and the perform finished product test methods to facilitate QC testing of instruments and consumables Liaise with the Purchasing and Sales teams to ensure all materials released in time for use Help to generate and maintain incoming material specifications Work with the Operations team to suitably oversee controlled temperature shipments of samples and products Input into supplier complaints where required Ensure all documentation for incoming materials is completed promptly and made available by PDF for batch review Assist with management of outsourcing raw material identity testing Raise QMS documentation for Deviations, Change Control, Supplier Complaint where relevant for incoming material QC Assist with management of laboratory supplies Perform all activities in a safe manner with strict adherence to company guidelines Work within the Quality team to maintain focused, effective progression in line with Company Quality objectives. Support other members of the Quality team by providing training and mentoring on areas of expertise. Effectively interact with Technical, Development, Manufacturing, Operations, Sales and Marketing and Planning teams. Ensure policies and procedures are properly understood, carried out and evaluated and that modifications are investigated if necessary. Help to train staff in Quality Control requirements. Investigate relevant standards and establish clearly defined Quality methods for staff to apply. Define Quality procedures in conjunction with R&amp;D and Operations staff. Maintain process controls and documentation procedures and identify areas for improvement and efficiency. Support product design review and change control systems. Participate in the Company audit schedules for both internal and external Quality audits. Monitor Quality indicators and helping to gather and track relevant data. Identify relevant Quality-related training needs and delivering training. QA/QC review of contractor documentation relating to validation and verification activities as well as device manufacture records. Skills and experience: Good attention to detail Proficiency in Microsoft software packages Proven experience in a controlled environment of document checking and review Ability to prioritise and time manage Life science or Chemistry qualifications A highly motivated, organized, proactive and enthusiastic individual with a proven ability to work with tact and diplomacy. A minimum of 2 years? experience in working within a Quality Management System, with some specific experience of working with medical devices. Experience of working with ISO 13485

Jobs QC Officer »
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Newcastle (uk)

Found in Reed - Control Officer to be responsible for helping to maintain and improve the Quality Management System Exciting Medical Devices Development company seeks a highly self-motivated and enthusiastic Quality Control Officer to be responsible for helping to maintain and improve the Quality Management System by employing excellent attention to detail, managing time efficiently and effectively and bringing outstanding teamwork skills to the role. Duties may include: Check incoming material documentation/certification Physically inspect incoming materials Support the Engineering and Assay teams in testing of incoming materials and assisting with non-routine analyses. Perform investigations where required Perform finished product testing according to test methods and product specifications including qPCR on standard laboratory instrumentation including BioRad CFX96 and Qiagen Rotor-Gene Q Help to develop, validate and the perform finished product test methods to facilitate QC testing of instruments and consumables Liaise with the Purchasing and Sales teams to ensure all materials released in time for use Help to generate and maintain incoming material specifications Work with the Operations team to suitably oversee controlled temperature shipments of samples and products Input into supplier complaints where required Ensure all documentation for incoming materials is completed promptly and made available by PDF for batch review Assist with management of outsourcing raw material identity testing Raise QMS documentation for Deviations, Change Control, Supplier Complaint where relevant for incoming material QC Assist with management of laboratory supplies Perform all activities in a safe manner with strict adherence to company guidelines Work within the Quality team to maintain focused, effective progression in line with Company Quality objectives. Support other members of the Quality team by providing training and mentoring on areas of expertise. Effectively interact with Technical, Development, Manufacturing, Operations, Sales and Marketing and Planning teams. Ensure policies and procedures are properly understood, carried out and evaluated and that modifications are investigated if necessary. Help to train staff in Quality Control requirements. Investigate relevant standards and establish clearly defined Quality methods for staff to apply. Define Quality procedures in conjunction with R&amp;D and Operations staff. Maintain process controls and documentation procedures and identify areas for improvement and efficiency. Support product design review and change control systems. Participate in the Company audit schedules for both internal and external Quality audits. Monitor Quality indicators and helping to gather and track relevant data. Identify relevant Quality-related training needs and delivering training. QA/QC review of contractor documentation relating to validation and verification activities as well as device manufacture records. Skills and experience: Good attention to detail Proficiency in Microsoft software packages Proven experience in a controlled environment of document checking and review Ability to prioritise and time manage Life science or Chemistry qualifications A highly motivated, organized, proactive and enthusiastic individual with a proven ability to work with tact and diplomacy. A minimum of 2 years? experience in working within a Quality Management System, with some specific experience of working with medical devices. Experience of working with ISO 13485

Jobs QC Officer »
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Newcastle (uk)

Found in Reed - Control Officer to be responsible for helping to maintain and improve the Quality Management System Exciting Medical Devices Development company seeks a highly self-motivated and enthusiastic Quality Control Officer to be responsible for helping to maintain and improve the Quality Management System by employing excellent attention to detail, managing time efficiently and effectively and bringing outstanding teamwork skills to the role. Duties may include: Check incoming material documentation/certification Physically inspect incoming materials Support the Engineering and Assay teams in testing of incoming materials and assisting with non-routine analyses. Perform investigations where required Perform finished product testing according to test methods and product specifications including qPCR on standard laboratory instrumentation including BioRad CFX96 and Qiagen Rotor-Gene Q Help to develop, validate and the perform finished product test methods to facilitate QC testing of instruments and consumables Liaise with the Purchasing and Sales teams to ensure all materials released in time for use Help to generate and maintain incoming material specifications Work with the Operations team to suitably oversee controlled temperature shipments of samples and products Input into supplier complaints where required Ensure all documentation for incoming materials is completed promptly and made available by PDF for batch review Assist with management of outsourcing raw material identity testing Raise QMS documentation for Deviations, Change Control, Supplier Complaint where relevant for incoming material QC Assist with management of laboratory supplies Perform all activities in a safe manner with strict adherence to company guidelines Work within the Quality team to maintain focused, effective progression in line with Company Quality objectives. Support other members of the Quality team by providing training and mentoring on areas of expertise. Effectively interact with Technical, Development, Manufacturing, Operations, Sales and Marketing and Planning teams. Ensure policies and procedures are properly understood, carried out and evaluated and that modifications are investigated if necessary. Help to train staff in Quality Control requirements. Investigate relevant standards and establish clearly defined Quality methods for staff to apply. Define Quality procedures in conjunction with R&amp;D and Operations staff. Maintain process controls and documentation procedures and identify areas for improvement and efficiency. Support product design review and change control systems. Participate in the Company audit schedules for both internal and external Quality audits. Monitor Quality indicators and helping to gather and track relevant data. Identify relevant Quality-related training needs and delivering training. QA/QC review of contractor documentation relating to validation and verification activities as well as device manufacture records. Skills and experience: Good attention to detail Proficiency in Microsoft software packages Proven experience in a controlled environment of document checking and review Ability to prioritise and time manage Life science or Chemistry qualifications A highly motivated, organized, proactive and enthusiastic individual with a proven ability to work with tact and diplomacy. A minimum of 2 years? experience in working within a Quality Management System, with some specific experience of working with medical devices. Experience of working with ISO 13485

Jobs QC Officer »
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Newcastle (uk)

Found in Reed - Control Officer to be responsible for helping to maintain and improve the Quality Management System Exciting Medical Devices Development company seeks a highly self-motivated and enthusiastic Quality Control Officer to be responsible for helping to maintain and improve the Quality Management System by employing excellent attention to detail, managing time efficiently and effectively and bringing outstanding teamwork skills to the role. Duties may include: Check incoming material documentation/certification Physically inspect incoming materials Support the Engineering and Assay teams in testing of incoming materials and assisting with non-routine analyses. Perform investigations where required Perform finished product testing according to test methods and product specifications including qPCR on standard laboratory instrumentation including BioRad CFX96 and Qiagen Rotor-Gene Q Help to develop, validate and the perform finished product test methods to facilitate QC testing of instruments and consumables Liaise with the Purchasing and Sales teams to ensure all materials released in time for use Help to generate and maintain incoming material specifications Work with the Operations team to suitably oversee controlled temperature shipments of samples and products Input into supplier complaints where required Ensure all documentation for incoming materials is completed promptly and made available by PDF for batch review Assist with management of outsourcing raw material identity testing Raise QMS documentation for Deviations, Change Control, Supplier Complaint where relevant for incoming material QC Assist with management of laboratory supplies Perform all activities in a safe manner with strict adherence to company guidelines Work within the Quality team to maintain focused, effective progression in line with Company Quality objectives. Support other members of the Quality team by providing training and mentoring on areas of expertise. Effectively interact with Technical, Development, Manufacturing, Operations, Sales and Marketing and Planning teams. Ensure policies and procedures are properly understood, carried out and evaluated and that modifications are investigated if necessary. Help to train staff in Quality Control requirements. Investigate relevant standards and establish clearly defined Quality methods for staff to apply. Define Quality procedures in conjunction with R&amp;D and Operations staff. Maintain process controls and documentation procedures and identify areas for improvement and efficiency. Support product design review and change control systems. Participate in the Company audit schedules for both internal and external Quality audits. Monitor Quality indicators and helping to gather and track relevant data. Identify relevant Quality-related training needs and delivering training. QA/QC review of contractor documentation relating to validation and verification activities as well as device manufacture records. Skills and experience: Good attention to detail Proficiency in Microsoft software packages Proven experience in a controlled environment of document checking and review Ability to prioritise and time manage Life science or Chemistry qualifications A highly motivated, organized, proactive and enthusiastic individual with a proven ability to work with tact and diplomacy. A minimum of 2 years? experience in working within a Quality Management System, with some specific experience of working with medical devices. Experience of working with ISO 13485

Jobs QC Officer »
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SE11, ENG (uk)

Real Life Sciences

Found in ZipRecruiter - Reporting to the Chief Operating Officer of a fast growing Real World Evidence Research business&nbsp;...&nbsp;Epidemiological&#x2F;Statistical or Scientific qualifications are a bonus but not essential.Publication&nbsp;...

Jobs Principal Consultant - Real World Evidence »
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AL6, ENG (uk)

Roche

Found in ZipRecruiter - As Principal Data Scientist within Data Science Oncology, Personalized Healthcare (PHC) function&nbsp;...&nbsp;The evidence and insights will be used to inform the research and development of our molecules, and&nbsp;...

Jobs Principal Data Scientist, Data Science RWD Oncology »
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Surrey, ENG (uk)

Science Solutions Recruitment Ltd

Found in ZipRecruiter - This Regulatory Officer role is within an expanding firm who are globally known for their&nbsp;...&nbsp;research post I built up four years&#x27; experience in recruiting scientists into new jobs. Full&nbsp;...

Jobs Chemical Regulatory Submissions Officer - South East »
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Stevenage, ENG (uk)

GlaxoSmithKline

Found in ZipRecruiter - Our team (Research Statistics) collaborates with top laboratory and clinical scientists to advance&nbsp;...&nbsp;In this role, the Statistician &#x2F; Principal Statistician will be responsible for providing&nbsp;...

Jobs Principal Statistician or Statistician - Research (Non-Clinical) »
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SE11, ENG (uk)

IQVIA

Found in ZipRecruiter - IQVIA™ is the leading human data science company focused on helping healthcare clients find&nbsp;...&nbsp;The Senior Principal role in our EMEA Brand and Integrated Research Solutions team is critical for&nbsp;...

Jobs Senior Principal - Brand and Integrated Research Solutions (R1120854) »
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CB5, ENG (uk)

Newton Colmore Consulting

Found in ZipRecruiter - With this in mind, you will need to have a proved track record as a R&amp;D Engineer or Systems&nbsp;...&nbsp;Scientific recruitment specialists Newton Colmore Consulting, on +44 121 268 2240 or make an&nbsp;...

Jobs Principal Troubleshooting Research and Development Engineer »
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The previous job ads are the result from searching for:

Jobs Principal Research Officer Wetland Science

  Evaluation : 3.0 out of 5
based on 6 interactions.

Job Description At AstraZeneca we are constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We?re pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we?re industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as together we explore synergies between small and large molecules. AstraZeneca has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent. Those who join AstraZeneca feel a sense of ownership about their future. They thrive with a recognised leader in the industry. AstraZeneca is an agile, fast-moving and emerging industry leader in oncology . We are a nimble organisation that values smart risk-takers. With AstraZeneca , you will be applying a creative approach to science while being at the forefront of a strong and rich pipeline of cutting-edge medicines. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterised by...


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