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The alliance of bioversity international and the international center for tropical agriculture (ciat) delivers research-based solutions that harness agricultural biodiversity and sustainably transform food systems to improve people’s lives in a clima...
Overview major oil and gas company is seeking a data scientist to join the global optimizer department. the global optimizer development department (god) charter is to optimize crude allocation and the operations of global manufacturing facilities in order to maximize revenue, increase profitability, and capture international market opportunities. your primary role is to analyze and structure large amounts of raw live and historical data, build algorithms and solutions around the data to drive decision making within the company. your role will be at the core of the forecasting and predictive digital strategy of the company, to support the development of state-of-the-art solution for the downstream digital center. duties and responsibilities - formulate and lead multi-faceted analytic studies against large volumes of data. - interpret and analyze data using exploratory mathematic and statistical techniques based on the scientific method. - coordinate research and analytic activities utilizing various data points (unstructured and structured) and employ programming to clean, massage, and organize the data. - experiment against data points, provide information based on experiment results and provide previously undiscovered solutions to command data challenges. - lead all data experiments tasked by the data science team. - coordinate with data engineers to build data environments providing data identified by data analysts, data integrators, knowledge managers, and intel analysts. - develop methodology and processes for prioritization and scheduling of projects. - analyze p...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. we have a vacancy for a vendor management coordinator in our global clinical supplies team. a day in the life: supports the day to day operations of the study drug, comparators and ancillaries management. coordinates with vendors and assists with vendor management when clinical supplies services are required to be outsourced ensures all activities are completed in compliance with company good practices and client requirements. completes ongoing training on new regulations concerning all clinical supplies and gxp activities. participates in and supports department project teams. may coordinate or serve as a liason cross-functionally. asks for quotations to vendors and verify them against what was requ...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. our detailed, goal-oriented pharmacovigilance colleagues manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring. as part of your work with beginning-to-end trial experience, you will expand your knowledge and experience working on clinical trials through every stage of drug development. this includes management and oversight of all contracted services. discover impactful work: as a safety reporting specialist, you will be responsible for receipt, submission, and subsequent tracking of expedited and periodic safety reports pertaining to the department’s projects. you will as...
Our client is seeking senior sensor scientist or physicist with expertise in sensor geometry, image fusion, and remote sensing to support advanced research and development efforts. this role is ideal for a technically driven professional with a strong foundation in mathematics and sensor/target phenomenology. ***please note: they are hiring for both dayton, oh and columbia, md*** responsibilities - design and implement advanced algorithms for sensor homography, image stitching, and scene reconstruction. - conduct applied research in remote sensing and multi-sensor data exploitation to support real-world mission objectives. - develop image processing and computer vision solutions to improve the usability and interpretation of complex data. - collaborate with cross-functional teams to integrate algorithms into scalable tools and operational systems. - prepare technical documentation, white papers, and briefings for internal stakeholders and external partners. - offer subject matter expertise to support proposal development and client engagement activities. qualifications - master’s degree or ph.d. in physics, mathematics, electrical or aerospace engineering, or a closely related field. - at least 5 years of experience in image analysis, sensor modeling, or remote sensing applications. - in-depth understanding of sensor/target phenomenology and imaging principles. - proficiency in python with hands-on experience using scientific libraries such as numpy, scipy, and opencv. - demonstrated ability to create and deploy algorithms in research or mission-focus...
Medical scientific liaison - immunology - location: bogotá, colombia - 80% of travel expected - job type: permanent, full time about the job our team: msls are the extension of the medical function in the field. they build and develop enduring ‘win-win' relationships with healthcare professionals and institutions, creating constructive partnerships with internal and external stakeholders to disseminate scientific information and generate insights. msls provide field or hybrid medical support that is aligned and integrated to the overall medical strategy within the bu. key deliverables: - hcp/kol engagement plans - customer engagement reports (entries in crm) - insights - kab survey evaluation interdependencies: - office-based medical (medical manager), rwe, heva, pharmacovigilance, csu, medinfo (gmi) - commercial operations, market access, public affairs - external customers (scientific external experts, patient organizations, medical societies, health authorities, etc.) main responsibilities: - engages proactively and reactively with healthcare professionals and institutions - engages external stakeholders on medical and scientific information exchange for the therapeutic area during one-to-one interactions and group settings - organises and engages kols & hcps during local group scientific meetings (hospital staff meetings, webinars, etc) according to the stakeholder engagement plan, aligned with country medical plan - develops and maintains trusted partnerships, through scientific engagement and exchange, with healthcare professionals and institutions in a rapi...
By clicking the “apply” button, i understand that my employment application process with takeda will commence and that the information i provide in my application will be processed in line with takeda’s privacy notice and terms of use. i further attest that all information i submit in my employment application is true to the best of my knowledge. job description role objective the medical science liaison albania, montenegro, north macedonia could be based in any of the 3 countries and will be responsible for: - providing local country (albania, montenegro and north macedonia) field-based support from the medical function in order to achieve the company’s goals. - identifying and develop strong sustainable peer to peer relationships with external stakeholders to support the medical/scientific credibility of the company - being an expert on the disease areas under designated therapeutic area responsibility accountabilities - continuously screen, review and analyze scientific literature; generate summaries & critical assessments if appropriate - use specific disease and product knowledge to develop takeda in a given therapy area; i.e. answer medical/technical unsolicited enquiries from hcps, provide accurate and non-promotional scientific information relating to licensed and unlicensed indications following unsolicited requests from hcps, etc. - proactively identify and develop long term peer-to-peer relationships with opinion leaders and other relevant stakeholders in order to understand their needs, segment them accordingly and implement targeted approach and tact...
Descripción de la empresa sgs es el líder mundial en inspección, verificación, análisis, capacitación y certificación. es considerada como el principal referente mundial en calidad e integridad, contamos con más de 95.000 colaboradores y una red de más de 2.400 oficinas y laboratorios por el mundo. descripción del empleo responsible for assigning, reviewing, exporting, analyzing, and delivering clinical study images and image analysis data to study sponsors or to internal statistics department. also performs image analysis using device software or external computer programs. may provide programming support for this software. also assists in the research and setup of new imaging instrumentation, software, and development of supporting documentation to be used on clinical trials. job functions: - review and export study images collected on clinical trials. - perform image analysis using built-in software and external computer programs for clinical studies. - engage with scientific, clinic, quality, information technology, and other teams to ensure image analysis is performed accurately and delivered by the deadline. - assist in data management - create high quality presentations to assist internal and external clients in understanding image acquisition and analysis methods and results - research and contribute to new image analysis methodologies - set up new imaging equipment/instrumentation and related software for use in clinical trials. - assist in the design and implementation of efficient workflows for various types of image analysis - draft work instructions for,...
Are you a stem expert fluent in spanish (latin america), eager to shape the future of ai? large‑scale language models are evolving from clever chatbots into powerful engines of scientific discovery and technical problem-solving. with high‑quality training data, tomorrow's ai can democratize world‑class education, keep pace with cutting‑edge research, and streamline work for engineers, scientists, and analysts everywhere. that training data begins with you—we need your expertise to help power the next generation of ai. we're looking for stem specialists who live and breathe mathematics, physics, chemistry, engineering, data science, computer science, and scientific computing. you'll challenge advanced language models on topics like thermodynamics, mechanics, calculus, statistics, materials science, electronics, algorithm design, and quantitative modeling—documenting every failure mode so we can harden model reasoning. on a typical day, you will converse with the model on real-world stem problem-solving scenarios and theoretical technical questions, verify factual accuracy and logical soundness, capture reproducible error traces, and suggest improvements to our prompt engineering and evaluation metrics. a bachelor's or master's degree in a stem discipline is ideal; published research, engineering design experience, data analysis projects, or coding portfolios signal fit. clear, metacognitive communication—"showing your work"—is essential. ready to turn your stem expertise into the knowledge base for tomorrow's ai? apply today and start teaching the model that will tea...
Tasks: responsible for developing, reviewing, finalizing, and maintaining clinical trial documents such as informed consent forms. applies knowledge of gcp guidelines, regulatory requirements, regulatory framework of privacy standards and biological samples standards, therapeutic area(s), and investigational medicinal products (imps) to review and develop informed consent forms (icf). ensures that the content of the master informed consent form is consistent with the corresponding protocol and fully informs the subject of all information about the research study that a potential research subject will need to know to decide if they want to enroll in the study. ensures that research participants can easily understand the content and the scientific and medical language of the consent form. ensures that documents are written/edited in compliance with the global industry standards ensures client-specific guidance and requirements are included within the master informed consent form during development and review supports the development, review, and approval of master templates to ensure effective and timely execution of protocol/site activation create, review, and revise training material and plans to support the training requirements of the team. responsible for timely and appropriate communication to all stakeholders, as applicable liaise with pm/designee to communicate any trends, outstanding issues, safety concerns, or any other activity or lack thereof which may jeopardize the clinical trial delivery or patient safety from the task assigned. skills: strong knowl...
Company description work with us. change the world. at aecom, we're delivering a better world. whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. we are the world's trusted infrastructure consulting firm, partnering with clients to solve the world’s most complex challenges and build legacies for future generations. there has never been a better time to be at aecom. with accelerating infrastructure investment worldwide, our services are in great demand. we invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. we're one global team driven by our common purpose to deliver a better world. join us. job description aecom's enterprise capabilities team has an immediate opportunity available for acoustician iv for employment in bogota, colombia. the responsibilities include but are not limited to: - generally requires multi-disciplinary knowledge. - makes recommendations on work methods and procedures and technical innovations by devising practical and economical solutions to problems in own discipline. - makes recommendations on research requests, objectives, priorities, and timing. - assess need for change and recommends development of standards. - assess work against standards, objectives and specifications. - utilizes a...
Company description work with us. change the world. at aecom, we're delivering a better world. whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. we are the world's trusted infrastructure consulting firm, partnering with clients to solve the world’s most complex challenges and build legacies for future generations. there has never been a better time to be at aecom. with accelerating infrastructure investment worldwide, our services are in great demand. we invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. we're one global team driven by our common purpose to deliver a better world. join us. job description aecom's enterprise capabilities team has an immediate opportunity available for acoustician iv for employment in bogota, colombia. the responsibilities include but are not limited to: - generally requires multi-disciplinary knowledge. - makes recommendations on work methods and procedures and technical innovations by devising practical and economical solutions to problems in own discipline. - makes recommendations on research requests, objectives, priorities, and timing. - assess need for change and recommends development of standards. - assess work against standards, objectives and specifications. - utilizes a...
Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific inc., our mission is to make the world healthier, cleaner, and safer. as a sr cm analyst i, you will play a pivotal role in advancing global health initiatives through world-class clinical research. our collaborative environment, dedication to excellence, and brand-new resources will empower you to excel and make a global impact. centralized monitoring (cm) is an integral part of ppd’s risk-based quality management (rbqm) strategy. we deliver risk surveillance and centralized statistical monitoring, combining the power of statistical and analytical tools with expertise from operationally experienced staff to monitor and manage clinical study data. ongoing data assessments from our centralized monitoring group facilitates dynamic adaptation of monitoring plans with a focus on critical-to-quality risks that drive data quality and have the greatest impact on data integrity and subject safety. job responsibilities - serve as the centralized monitoring functional lead, with knowledge in rbqm methodologies, tools, and processes. - lead activities such as developing centralized monitoring plans and generating findings reports. - manage review timelines and support budget management. - serve as functional representative, communicating and working with the study team. - ensure reviews are complete, generate reports, and lead centralized monitoring review meetings to discuss issues and risks with the study team. - contribute to risk assessment through department ris...
Company description abbvie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. we strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our allergan aesthetics portfolio. for more information about abbvie, please visit us at www.abbvie.com. follow @abbvie on x, facebook, instagram, youtube, linkedin and tik tok. job description medical science liaisons (msls) are key members of the affiliate medical department. these field-based roles focus on medical and scientific engagement with abbvie stakeholders (including research and healthcare professionals, payers, and providers). the focus of this role is on interacting with and supporting the needs of thought leaders. msls work to communicate information and facilitate dialogue about abbvie’s marketed products, compounds in development and the related disease states, in a strictly scientific, non-promotional manner, and in full compliance with applicable national laws and regulations, guidelines, codes of conduct, abbvie’s policies and procedures and accepted standards of best practice. the msl serves to enhance the scientific credibility of abbvie with established and emerging thought leaders, by supporting scientific dialogue and collaborations in the areas of research, medical and scientific exchange, including facilitation of requests for scientific and medical information. msls also participate in t...
Are you a coding expert fluent in spanish (latin america) eager to shape the future of ai? large‑scale language models are evolving from clever chatbots into powerful engines of scientific discovery. with high‑quality training data, tomorrow's ai can democratize world‑class education, keep pace with cutting‑edge research, and streamline software development for engineers everywhere. that training data begins with you—we need your expertise to help power the next generation of ai. we're looking for coding specialists who live and breathe algorithms, data structures, software architecture, frontend and backend development, cloud infrastructure, and systems programming—and who can do so fluently in spanish (latin america). you'll challenge advanced language models on topics like asynchronous programming, restful api integration, memory management, object-oriented design, secure coding practices, and debugging distributed systems—documenting every failure mode so we can harden model reasoning. on a typical day, you will converse with the model on software engineering tasks and technical scenarios in spanish (latin america), verify logical accuracy and coding fluency, assess naturalness and correctness of spanish language usage, capture reproducible error traces, and suggest improvements to our prompt engineering and evaluation metrics. a bachelor's, master's, or phd in computer science, software engineering, or a closely related technical field is ideal; real-world coding experience, technical writing in spanish, or open-source contributions signal fit. clear, metacogniti...
Coding specialist (fluent in spanish - latin america) - ai trainer join to apply for the coding specialist (fluent in spanish - latin america) - ai trainer role at invisible expert marketplace coding specialist (fluent in spanish - latin america) - ai trainer join to apply for the coding specialist (fluent in spanish - latin america) - ai trainer role at invisible expert marketplace get ai-powered advice on this job and more exclusive features. are you a coding expert fluent in spanish (latin america) eager to shape the future of ai? large‑scale language models are evolving from clever chatbots into powerful engines of scientific discovery. with high‑quality training data, tomorrow’s ai can democratize world‑class education, keep pace with cutting‑edge research, and streamline software development for engineers everywhere. that training data begins with you—we need your expertise to help power the next generation of ai. we’re looking for coding specialists who live and breathe algorithms, data structures, software architecture, frontend and backend development, cloud infrastructure, and systems programming—and who can do so fluently in spanish (latin america). you’ll challenge advanced language models on topics like asynchronous programming, restful api integration, memory management, object-oriented design, secure coding practices, and debugging distributed systems—documenting every failure mode so we can harden model reasoning. on a typical day, you will converse with the model on software engineering tasks and technical scenarios in spanish (latin ame...
Company description abbvie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. we strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our allergan aesthetics portfolio. for more information about abbvie, please visit us at www.abbvie.com. follow @abbvie on x, facebook, instagram, youtube, linkedin and tik tok. job description primary job function the role ensures compliance with cluster north laws and abbvie's guidelines in executing multi country observational studies (mcos) and oversees their conduction, tracking, remuneration, and database management. it leads the development of evidence generation projects, supports medical affairs teams, manages audits, and participates in gap assessment processes. the role aligns projects with global and local product strategies, leads regulatory processes and scientific partnerships, and supports the medical director in budget planning. core job responsibilities - ensure mcos compliance with cluster north laws and abbvie's sops/guidelines. - oversee mcos conduction, tracking, remuneration, and database reporting. - lead diverse evidence generation projects and support medical affairs in real world evidence (rwe). - manage strategies and planning for audits and ensure service provider qualifications. - participate in the "gap assessment" process and manage the selection of investigation centers and investi...
Igc pharma sas is a subsidiary of a usa-based clinical stage biotech company committed to driving innovation and improving patient outcomes for alzheimer’s. as we expand our r&d; efforts, we are seeking a grants and non-dilutive funding manager to oversee and lead all grant application activities in collaboration with our third-party partners. this role is a leadership position, requiring critical thinking, science, and project coordination skills. job description: the grants and funding manager will be responsible for the planning, preparation, submission, and monitoring of all grant and non-dilutive funding applications on behalf of igc pharma. the ideal candidate will collaborate closely with internal teams—including research, clinical, and regulatory affairs—as well as a designated third-party company that provides specialized support in generating grant leads, grant writing, and funding strategies. this position will report to the managing director and will serve as the primary liaison for grants and agencies including alz, addf, and others. key responsibilities: - identify grant opportunities relevant to igc pharma's therapeutic areas and pipeline. - lead the preparation and submission of grant applications, ensuring alignment with agency guidelines and strategic company objectives. - manage timelines, deliverables, and internal resource coordination for multiple simultaneous submissions. - act as the point of contact for all grant-related communications with third-party consultants, funding agencies, and collaborators. - collaborate with internal subject matter e...
Msl oncology solid tumors bogota cundinamarca, co - function: research & development - job type: full-time job id: r00131116 company description abbvie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. we strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our allergan aesthetics portfolio. job description medical science liaisons (msls) are key members of the affiliate medical department. these field-based roles focus on medical and scientific engagement with abbvie stakeholders (including research and healthcare professionals, payers, and providers). the focus of this role is on interacting with and supporting the needs of thought leaders. msls work to communicate information and facilitate dialogue about abbvie’s marketed products, compounds in development and the related disease states, in a strictly scientific, non-promotional manner, and in full compliance with applicable national laws and regulations, guidelines, codes of conduct, abbvie’s policies and procedures and accepted standards of best practice. the msl serves to enhance the scientific credibility of abbvie with established and emerging thought leaders, by supporting scientific dialogue and collaborations in the areas of research, medical and scientific exchange, including facilitation of requests for scientific and medical information. msls also participate in the initiation...
Company description abbvie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. we strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our allergan aesthetics portfolio. for more information about abbvie, please visit us at www.abbvie.com. follow @abbvie on x, facebook, instagram, youtube, linkedin and tik tok (https://www.tiktok.com/@abbvie) . job description medical science liaisons (msls) are key members of the affiliate medical department. these field-based roles focus on medical and scientific engagement with abbvie stakeholders (including research and healthcare professionals, payers, and providers). the focus of this role is on interacting with and supporting the needs of thought leaders. msls work to communicate information and facilitate dialogue about abbvie’s marketed products, compounds in development and the related disease states, in a strictly scientific, non-promotional manner, and in full compliance with applicable national laws and regulations, guidelines, codes of conduct, abbvie’s policies and procedures and accepted standards of best practice. the msl serves to enhance the scientific credibility of abbvie with established and emerging thought leaders, by supporting scientific dialogue and collaborations in the areas of research, medical and scientific exchange, including facilitation of requests for scientific a...
**work schedule** standard (mon-fri) **environmental conditions** office **job description** at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. we have a vacancy for a vendor management coordinator in our global clinical supplies team. a day in the life: supports the day to day operations of the study drug, comparators and ancillaries management. coordinates with vendors and assists with vendor management when clinical supplies services are required to be outsourced ensures all activities are completed in compliance with company good practices and client requirements. completes ongoing training on new regulations concerning all clinical supplies and gxp activities. participates in and supports department project teams. may coordinate or serve as a liason cross-functionally. asks for quotations to vend...
Company description abbvie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. we strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our allergan aesthetics portfolio. for more information about abbvie, please visit us at www.abbvie.com. follow @abbvie on x, facebook, instagram, youtube, linkedin and tik tok (https://www.tiktok.com/@abbvie) . job description primary job function the role ensures compliance with cluster north laws and abbvie's guidelines in executing multi country observational studies (mcos) and oversees their conduction, tracking, remuneration, and database management. it leads the development of evidence generation projects, supports medical affairs teams, manages audits, and participates in gap assessment processes. the role aligns projects with global and local product strategies, leads regulatory processes and scientific partnerships, and supports the medical director in budget planning. core job responsibilities + ensure mcos compliance with cluster north laws and abbvie's sops/guidelines. + oversee mcos conduction, tracking, remuneration, and database reporting. + lead diverse evidence generation projects and support medical affairs in real world evidence (rwe). + manage strategies and planning for audits and ensure service provider qualifications. + participate in the gap assessment process and m...
Company description eurofins scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. from the food you eat, to the water you drink, to the medicines you rely on, eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. the eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agro-science contract research organization services. it is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in contract development and manufacturing organizations. it also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. in over 30 years, eurofins has grown from one laboratory in nantes, france to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. in 2021, eurofins generated total revenues of eur 6.72 billion, and has been amon...
Company description eurofins scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. from the food you eat, to the water you drink, to the medicines you rely on, eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. the eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agro-science contract research organization services. it is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in contract development and manufacturing organizations. it also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. in over 30 years, eurofins has grown from one laboratory in nantes, france to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. in 2021, eurofins generated total revenues of eur 6.72 billion, and has been amon...
**work schedule** standard (mon-fri) **environmental conditions** office **job description** at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. discover impactful work: provides administrative safety support to the pharmacovigilance (pv) department. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to pv safety. may mentor or train new pv safety administration staff. a day in the life: • provides assistance and liaises with relevant teams and departments on a various range of administrative pv safety tasks, including audit readiness activities, meeting organisation, minute taking, filing, photocopying, work distribution, reconciling reports, end of day emails completing metrics and updating ppd systems wit...
Data scientist / applied scientist (mid and senior levels) data scientist / applied scientist (mid and senior levels) we are hiring multiple data scientists and applied scientists across latam to join the microsoft 365 team. these are remote positions, allowing you to work from the comfort of your home! as part of our team, you will help shape one of microsoft’s fastest-growing cloud services. your work will directly impact copilot, enabling personalized, context-aware experiences that empower millions of users across microsoft 365. do you want to collaborate closely with software engineers, product managers, and researchers to design, implement, and evaluate models and algorithms that continuously adapt and improve based on user interactions and feedback? do you want to leverage advanced machine learning and information retrieval to predict and optimize memory content selection, representation, and lifecycle management. you will work at the forefront of applied ai and machine learning, shaping the future of intelligent productivity tools. you will contribute to a culture of innovation, continuous learning, and experimentation. about the team the substrate core substrate team powers the infrastructure that underpins microsoft 365’s most critical services and copilot. we are a high-impact, forward-looking team focused on building intelligent, scalable, and cost-efficient platforms that enable microsoft to deliver world-class productivity experiences to billions of users. our mission is to drive operational excellence and innovation across the m365 fleet ...
Company description abbvie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. we strive to have a remarkable impact on people's lives across s...
Work schedule standard (mon-fri) environmental conditions office job description job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission ...
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