{"row_id":0,"dateposted":"2023-08-18T00:00:00.000+0000","title":"Spécialiste Service Client, CDD 6 mois","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p><u>Découvrez un travail stimulant :<\/u><\/p><p><b>Offrez une excellente expérience à nos clients et fidélisez-les, maximisez les<\/b> <b>performances de l’e-business et alignez-vous sur les objectifs commerciaux globaux pour permettre la croissance. <\/b><\/p><p><u>Une journée chez Thermo Fisher :<\/u><\/p><ul><li>Respecter les procédures, les objectifs de performance et les règles du service à la clientèle<\/li><li>Fournir un service d’assistance de haute qualité à nos clients (téléphone, courriel ou tout autre moyen de communication)<\/li><li>Traiter toutes les demandes de renseignements par téléphone, par écrit ou sur le Web dans le respect des directives de la division. Transmettre les prix et les renseignements sur la disponibilité des produits aux clients.<\/li><li>Identifier et évaluer les besoins des clients pour assurer la satisfaction et diriger les activités vers les services appropriés<\/li><li>Établir des relations de confiance durables grâce à une communication ouverte et interactive<\/li><li>Travailler sur des missions ou des projets d’amélioration continue en équipe<\/li><li>Tenir à jour les rapports quotidiens du service clients, indiquer les informations en relation à nos indicateurs de performance journaliers.<\/li><li>Assurer la liaison avec les transporteurs<\/li><\/ul><p><u>Les clés du succès :<\/u><\/p><p><b>Éducation<\/b><\/p><ul><li>BAC+2 en équivalent relation client requis.<\/li><\/ul><p><b>Expérience<\/b><\/p><ul><li>Expérience avérée dans des fonctions administratives similaires<\/li><\/ul><p><b>Connaissances, compétences, aptitudes<\/b><\/p><p>Maîtrise de Microsoft Office.<\/p><ul><li>Capacité à travailler en équipe.<\/li><li>Excellentes compétences en gestion du temps.<\/li><li>Capacité à travailler sous pression et sur","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01201361"},"responsibilities":"Offrez une excellente expérience à nos clients et fidélisez-les, maximisez les performances de l’e-business et alignez-vous sur les objectifs commerciaux globaux pour permettre la croissance. Respecter les procédures, les objectifs de performance et les règles du service à la clientèle. Fournir un service d’assistance de haute qualité à nos clients (téléphone, courriel ou tout autre moyen de communication). Traiter toutes les demandes de renseignements par téléphone, par écrit ou sur le Web dans le respect des directives de la division. Transmettre les prix et les renseignements sur la disponibilité des produits aux clients. Identifier et évaluer les besoins des clients pour assurer la satisfaction et diriger les activités vers les services appropriés. Établir des relations de confiance durables grâce à une communication ouverte et interactive. Travailler sur des missions ou des projets d’amélioration continue en équipe. Tenir à jour les rapports quotidiens du service clients, indiquer les informations en relation à nos indicateurs de performance journaliers. Assurer la liaison avec les transporteurs. Résolution de conflits.","workhours":"40 hours per week","directapply":"false","skills":"résolution, demandes, service à la clientèle., service clients, renseignements, assistance, relation, grâce, évaluer, relation client, besoins des clients, directives, écrit, communication ouverte, gestion du temps, procédures, activités, service a la clientele, disponibilité, communication, transporteurs, travailler en équipe., capacité à travailler sous pression, relations de confiance, équipe, compétences interpersonnelles, qualité, indicateurs de performance, des produits, français, Team Manager - Emea Implementation Team & Saas, Upgrade & Implementation Consultant, Enterprise Client Services Team Manager, Technical Support Representative - Implementation & Production Data Support, Senior Manager - Workforce Management Solutions, Tools & IDE Support Analyst, Support Services - Business Analyst & Sales Manager & Project Manager & Enterprise Resource Planning & Customer Relationship Management Products, Manager - Platform Innovation Project Delivery, Manager - Product Implementation & Client Services, Information Technology Specialist & Customer Solution Adoption SAP Transportation Management","experiencerequirements":"BAC+2 en équivalent relation client requis.","occupationalcategory":"客户服务与技术支持","page_url":"https:\/\/jobs.thermofisher.com\/cn\/zh\/job\/TFSCGLOBALR01201361EXTERNALZHCN\/Sp%C3%A9cialiste-Service-Client-CDD-6-mois"}
{"row_id":1,"dateposted":"2023-09-06T00:00:00.000+0000","title":"Operator I, Manufacturing","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>Thermo Fisher Scientific Inc. (NYSE: TMO) es el líder mundial al servicio de la ciencia, con ingresos anuales de aproximadamente $40 mil millones. Nuestra misión es permitir que nuestros clientes hagan del mundo un lugar más saludable, limpio y seguro. Ya sea que nuestros clientes estén acelerando la investigación en ciencias de la vida, resolviendo desafíos analíticos complejos, aumentando la productividad en sus laboratorios, mejorando la salud de los pacientes mediante diagnósticos o desarrollando y fabricando terapias que cambian la vida, estamos aquí para ayudarlos. Nuestro equipo global de más de 100 000 colegas ofrece una combinación inigualable de tecnologías innovadoras, conveniencia de compra y servicios farmacéuticos a través de nuestras marcas líderes en la industria, que incluyen Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon y PPD. Para obtener más información, visite <a href=\\\"http:\/\/www.thermofisher.com\/\\\" target=\\\"_blank\\\">www.thermofisher.com<\/a><\/p><p><\/p><p>Bajo la supervisión directa del Líder de grupo, es responsable de las actividades de Ensamble, inspección y empaque de los componentes y productos terminados. Esto incluye llevar a cabo el proceso de despeje de línea, reportes de producción Hora por Hora, así como mantener el orden y limpieza del área, buscando en todas sus actividades asegurar la calidad de los productos","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01200494"},"responsibilities":"Thermo Fisher Scientific Inc. Bajo la supervisión directa del Líder de grupo, es responsable de las actividades de Ensamble, inspección y empaque de los componentes y productos terminados. Esto incluye llevar a cabo el proceso de despeje de línea, reportes de producción Hora por Hora, así como mantener el orden y limpieza del área, buscando en todas sus actividades asegurar la calidad de los productos que manufacturamos para nuestros clientes. Realizar inspecciones visuales de acuerdo con el estándar de defectos. Asegurar el llenado correcto de formatos requeridos en el proceso. Cumplir con todas las normas de seguridad. Llenar el reporte de Despeje de Línea en cada cambio de modelo. Seguir las instrucciones de las Hojas de Trabajo Estandar (SW). Identificar y llenar correctamente las etiquetas de scrap. Asegurar el llenado de los checklist de seguridad. Asegurar las 5’s del área. Asegurar el correcto llenado de los reportes de producción. Participar en las sesiones de entrenamiento en materia de medio ambiente (a las que sean convocados). Realizar sus tareas y responsabilidades respetando los controles para el cuidado del medio ambiente y la integridad de los empleados. Participar en las 4 Disciplinas de la Ejecución. Participar en actividades de PPI. Autoridades. riesgo","workhours":"40 hours per week","directapply":"false","skills":"manufactura, ppi, proceso, supervision, equipo global, componentes, inspección, limpieza, integridad, mejora continua, puntualidad, sistema de gestión ambiental, sesiones de entrenamiento, servicios, hora, escritura, Manufacturing & Quality Engineer, Manufacturing Process Engineer, Process Engineer, Manufacturing Engineer, Packaging Technician, Senior Manufacturing Engineer, Production Technician, Manufacturing Engineer - Manufacturing & Injection Moulding & Cad, Senior Process Engineer, Manufacturing Technician III","experiencerequirements":"Nuestro equipo global de más de 100 000 colegas ofrece una combinación inigualable de tecnologías innovadoras, conveniencia de compra y servicios farmacéuticos a través de nuestras marcas líderes en la industria, que incluyen Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon y PPD.","occupationalcategory":"Operacijos","page_url":"https:\/\/jobs.thermofisher.com\/lt\/lt\/job\/TFSCGLOBALR01200494EXTERNALLTLT\/Operator-I-Manufacturing"}
{"row_id":2,"dateposted":"2023-08-18T00:00:00.000+0000","title":"Manager, Planning","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p><span>Thermo Fisher Scientific is the world leader in serving science, with revenues of $40 billion. We help our customers accelerate life sciences research, address sophisticated analytical challenges, improve patient diagnostics and increase laboratory productivity. Through our best-in-class brands, we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive support. <\/span><\/p><p><\/p><p><b>Position Summary: <\/b>This role is part of the Southeast Asia & Taiwan Supply Chain and Commercial operations team, who's key objective is to e<span>nsure timely delivery of products and services to customers in an efficient and cost-effective manner. You will support the objective by helping improve the regional organizations planning capability cutting across different divisions, geographies, and product portfolios. <\/span><\/p><p><\/p><p><b>Key Responsibilities:<\/b><\/p><ul><li><p>Establish and lead regional planning team and function, defining org structure, Roles & Responsibilities, improvement plan and roadmap, aligning with cross functional partners on overall team strategy.<\/p><\/li><li><p>Identify and implement quick wins that drive improvements in fill rates, lead time reduction, or inventory and excess & obsolete (E&O) reduction.<\/p><\/li><li><p>Responsible for local SIOP process deployment and execution, with active engagement in forecasting processes, aligning demand and supply plan across functional teams<\/p><\/li><li><p>Regular review and update of demand history, trends, forecast, proactively communicating and collaborating with commercial teams to align commercial execution","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"value":"R-01199482","name":"Thermo Fisher Scientific"},"responsibilities":"Position Summary: This role is part of the Southeast Asia & Taiwan Supply Chain and Commercial operations team, who's key objective is to ensure timely delivery of products and services to customers in an efficient and cost-effective manner. You will support the objective by helping improve the regional organizations planning capability cutting across different divisions, geographies, and product portfolios. Establish and lead regional planning team and function, defining org structure, Roles & Responsibilities, improvement plan and roadmap, aligning with cross functional partners on overall team strategy. Identify and implement quick wins that drive improvements in fill rates, lead time reduction, or inventory and excess & obsolete (E&O) reduction. Responsible for local SIOP process deployment and execution, with active engagement in forecasting processes, aligning demand and supply plan across functional teams. Regular review and update of demand history, trends, forecast, proactively communicating and collaborating with commercial teams to align commercial execution with demand forecast, measured by continuously improved forecast accuracy. Development of mechanism to monitor overall supply plan and supplier performance, identify potential changes to stocking strategy, policy, parameters which improve fill rate, reduce lead time, optimize inventory & reduce E&O levels. Analyze and monitor overall inventory health, driving proactive actions","workhours":"40 hours per week","directapply":"false","skills":"supply chain, commercial operations, forecasting, regional planning, strategy, forecast, supply chain improvements, collaborating, logistics, proactive, analysis, training, supply chain optimization, data management, sql, industrial engineering, planning, potential, statistical data analysis, visualization, trends, lead time reduction, influence, communicator, life sciences, cross functional, development, Operations Manager - Plan Sponsor Support, Manager - Project Management, Manager - Development, Associate Director Strategy & Performance Management, Manager - Program Management, Assistant Training Manager Project, Senior Manager - Program Management, Operations Manager & Project Manager, Senior Manager - Development, Manager - Procurement","experiencerequirements":null,"occupationalcategory":"Operaciones","page_url":"https:\/\/jobs.thermofisher.com\/mx\/es\/job\/TFSCGLOBALR01199482EXTERNALESMX\/Manager-Planning"}
{"row_id":3,"dateposted":"2023-07-31T00:00:00.000+0000","title":"Praktikant\/in zur Mitarbeit im Labor (w\/m\/d)","description":"<p>Wissenschaft mit einem Jahresumsatz von rund 40 Milliarden US-Dollar. Unsere Mission ist es, unsere Kunden dabei zu unterstützen, die Welt gesünder, sauberer und sicherer zu machen. Wir unterstützen unsere Kunden, die biowissenschaftliche Forschung voranzutreiben, bei der Lösung komplexer analytischer Herausforderungen, der Steigerung der Produktivität in ihren Labors, der Verbesserung der Patientengesundheit durch Diagnostik oder der Entwicklung und Herstellung von lebensverbessernden Therapien. Unser globales Team von mehr als 100.000 KollegInnen bietet eine unübertroffene Kombination aus innovativen Technologien, komfortablen Einkaufsprozessen und pharmazeutischen Dienstleistungen durch unsere branchenführenden Marken, darunter Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon und PPD.<\/p><p><br>Seit dem Markteintritt im Jahre 2000 hat sich die Thermo Fisher Scientific GENEART GmbH zu einem der weltweit führenden Spezialisten bei der Herstellung synthetischer Gene und in der Synthetischen Biologie entwickelt. Das Unternehmen stellt Schlüsseltechnologienbereit für die Entwicklung und Herstellung neuer Medikamente, Dienstleistungen zur Verbesserung von Eiweißen (z.B. Industrieenzyme, Antikörper) oder zur Konstruktion von Zellen für komplexe biologische Prozesse (z.B. für den Einsatz in Zelltherapien). Heute ist GENEART eine 100%igeTochtergesellschaftvon Thermo Fisher Scientific Inc, dem weltweit führenden Partner für die Wissenschaft. Wir unterstützen unsere Kunden somit dabei die Welt gesünder, sauberer und sicherer zu machen- das ist unsere Mission!<\/p><p><br>Schau‘ dir auch das","hiringorganization":{"name":"Thermo Fisher"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher","value":"230271BR"},"responsibilities":"Das Unternehmen stellt Schlüsseltechnologienbereit für die Entwicklung und Herstellung neuer Medikamente, Dienstleistungen zur Verbesserung von Eiweißen (z.B. Industrieenzyme, Antikörper) oder zur Konstruktion von Zellen für komplexe biologische Prozesse (z.B. für den Einsatz in Zelltherapien). In dieser Position unterstützt Du das Team in der Abteilung Genes and Preps bei der Plasmid Präparation im Labor. Herstellung von Medien. Herstellung von Pufferlösungen. Plasmid Präparation aus E.coli in unterschiedlichen Quantitäten. Dokumentation der Produktionsprozesse (LIMS, Excel). Die Möglichkeit dein theoretisches Wissen in einem praktischen Arbeitsumfeld anzuwenden, wobei du mit den neuesten Technologien arbeitest und deine Arbeit einen wichtigen Beitrag zu unserem gemeinsamen Erfolg leistet. Praktikant (w\/m\/d) zur Mitarbeit im Labor.","workhours":"40 hours per week","directapply":"false","skills":"prozesse, zuverlässig, marken, herstellung, präparation, motiviert, solide, entwicklung und, e.coli, zellen, innovation, antikörper, wissenschaft, lims, ppd, arbeitsumfeld, globales team, einsatz, integrität, dienstleistungen, abteilung, verbesserung, unity, unternehmenskultur, konstruktion, erfahrungen, Coordonnateur de projets - Culture, Group Lead Ticketing & Operation, Sales Coordinator - Employment Process Outsourcing, Manager - Research & Development Ambulatory & Outpatient, Program Management Group Lead, Principal & Program Director, Recruitment Process Outsourcing, Project Administrator Module Export & Import Management, SAP IBP S&OP & DP & SP - Consultant - Supply Chain, Senior Manager - Designated Support Engineering, SAP PP & MM s & 4 Hana - Senior Consultant (Supply Chain)","experiencerequirements":"Unser globales Team von mehr als 100.000 KollegInnen bietet eine unübertroffene Kombination aus innovativen Technologien, komfortablen Einkaufsprozessen und pharmazeutischen Dienstleistungen durch unsere branchenführenden Marken, darunter Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon und PPD.","occupationalcategory":"Studentai ir praktikos","page_url":"https:\/\/jobs.thermofisher.com\/lt\/lt\/job\/TFSCGLOBAL230271BREXTERNALLTLT\/Praktikant-in-zur-Mitarbeit-im-Labor-w-m-d"}
{"row_id":4,"dateposted":"2023-08-14T00:00:00.000+0000","title":"Source Document Specialist","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p><b>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 – To enable 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.<\/b><\/p><p><\/p><p><b>Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on – now and in the future.<\/b><\/p><p><\/p><p><span>As a Source Document Specialist you will be responsible for the <\/span><span>creation, completion, and maintenance of clinical trial source documents. This <\/span><span>includes the preparation of documents and responding to queries from site staff members.<\/span><\/p><p><\/p><p><b><span>Key responsibilities are as follows: <\/span><\/b><\/p><p>- <span>Creates, completes <\/span><span>and maintains source documents for clinical studies (includes e-source).<\/span><\/p><p><span>- Reviews study protocols and utilizes sponsor provided materials and other <\/span><span>resources to include all essential elements of","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01196401"},"responsibilities":"As a Source Document Specialist you will be responsible for the creation, completion, and maintenance of clinical trial source documents. This includes the preparation of documents and responding to queries from site staff members. Creates, completes and maintains source documents for clinical studies (includes e-source). - Reviews study protocols and utilizes sponsor provided materials and other resources to include all essential elements of protocol into source documents. - Manages the version control of source documents. - Liaise with other functional\/departmental managers\/ Investigators to understand all necessary aspects and needs of source documents & criteria, and to ensure it meets requirements. - Distributes source documentation to site staff efficiently and in timelines. - Ensures sites are using the correct source document training. - May be required to provide initial and ongoing training to site staff in the completion of documents Quality and Compliance. - Ensures all source documents are prepared in accordance with GCP, ICH, FDA and other applicable regulatory guidelines. - Ensures quality and compliance by following established SOPs, ICH\/GCP, study-specific manuals and other applicable regulatory requirements. - Consistently demonstrates knowledge of the key principles of cross-functional project management . Ability to identify and remedy risks related to contractual deliverables","workhours":"40 hours per week","directapply":"false","skills":"Documentation, GCP, Project Management, Compliance, Translation, ICH, Regulatory, Training, Strong Attention to Detail, attention to detail, attention to , Clinical Trial, FDA, Clinical, Clinical Development, clinical research, Clinical Research Experience, clinical development guidelines, patient journey, Document Management Specialist, Applications Systems Training & Documentation Specialist, Infinitt Administrator, Document Administrator, Communications Specialist II, Proposal Coordinator, Information Management Specialist, Project Tracking Coordinator & Specialist, Publishing Specialist II, Technical Communications Specialist","experiencerequirements":null,"occupationalcategory":"Qualità e Affari Regolatori","page_url":"https:\/\/jobs.thermofisher.com\/it\/it\/job\/TFSCGLOBALR01196401EXTERNALITIT\/Source-Document-Specialist"}
{"row_id":5,"dateposted":"2023-08-02T00:00:00.000+0000","title":"Sr Customer Service Representative","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.<\/p><p><\/p><p><b>Responsibilities:<\/b><\/p><ul><li>Adhere to Thermo Fisher Scientific protocols, consistencies and procedures.<\/li><li>Ensure that Thermo Fisher’s customer satisfaction objectives are met or exceeded.<\/li><li>Provide high level of customer service to existing and new customer base.<\/li><li>Interface closely with sales, service, and management to ensure customer satisfaction is maximized.<\/li><li>Effectively communicate and exchange information among team members.<\/li><li>Support Practical Process Improvement (PPI) methodology and participate in initiatives as required.<\/li><li>Responsible for meeting all required department and company training goals and expectations.<\/li><li>Responsible for answering high volume of customer calls in the divisional call center and the ability to correctly direct callers to the proper company within Thermo Fisher, including other divisions.<\/li><li>Responsible for answering calls from customers, channel partners, distributors, and sales representatives for all Laboratory Products and accessing several different computer systems to obtain the necessary information to assist customers.<\/li><li>Process telephone orders placed with verbal P.O. or credit card.<\/li><li>Must have an understanding of all product lines and the product knowledge to accurately detail our","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01196389"},"responsibilities":"Adhere to Thermo Fisher Scientific protocols, consistencies and procedures. Ensure that Thermo Fisher’s customer satisfaction objectives are met or exceeded. Provide high level of customer service to existing and new customer base. Interface closely with sales, service, and management to ensure customer satisfaction is maximized. Effectively communicate and exchange information among team members. Support Practical Process Improvement (PPI) methodology and participate in initiatives as required. Responsible for meeting all required department and company training goals and expectations. Responsible for answering high volume of customer calls in the divisional call center and the ability to correctly direct callers to the proper company within Thermo Fisher, including other divisions. Responsible for answering calls from customers, channel partners, distributors, and sales representatives for all Laboratory Products and accessing several different computer systems to obtain the necessary information to assist customers. Process telephone orders placed with verbal P.O. or credit card. Responsible for communicating (written and verbal) daily with customers (both internal and external), distributors and sales representatives regarding sales channels, product lines, equipment, descriptions, features, terms and conditions, specifications, warranties, freight terms, deliveries, pricing, policies, freight estimates, inside delivery estimates, returns installation and any other requirements to fulfill the conditions of contracts and","workhours":"40 hours per week","directapply":"false","skills":"Sales, Customer Satisfaction, Customer Base, Product Knowledge, Orders, Management, Efficiency, communication, computer, Excellent Communication Skills, Company Training, Computer Systems, Process Improvement, Initiatives, Methodology, Cashier & Customer Service Representative, Senior Customer Service Representative, Customer Service Representative Professional, Teller & Customer Service Representative, Customer Services Representative, Centralized Customer Service Representative, Customer Service Representative Repairs, Sales Associate & Customer Service Representative, Customer Service Specialist, Contact Service Representative","experiencerequirements":{"monthsofexperience":"24"},"occupationalcategory":"Atencion al Cliente y Soporte tecnico","page_url":"https:\/\/jobs.thermofisher.com\/mx\/es\/job\/TFSCGLOBALR01196389EXTERNALESMX\/Sr-Customer-Service-Representative"}
{"row_id":6,"dateposted":"2023-09-07T00:00:00.000+0000","title":"Sr Manufacturing Engineering Technician","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>When you’re part of Thermo Fisher Scientific, you’ll do exciting work, and be part of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of $20 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.<br \/>Position Summary:<br \/>Responsibility for running and upkeep of machinery and equipment. To ensure all machinery and equipment is running efficiently, checked and maintained within laid down specifications. To achieve production targets in accordance with daily\/weekly manufacturing plan.<br \/>Adopt and live the Company’s 4-I values (Intensity, Integrity, Innovation & Involvement)<br \/>Responsibilities:<br \/>• Ensure that all equipment is maintained in a safe and reliable condition<br \/>• Carry out and record any periodic PPM checks which have been allocated and for which they are competent<br \/>• Carry out any mechanical and\/or electrical and\/or setting work within factory (within the scope of competence) including any work as may be required in any unit<br \/>• To assist in any training of other Production Technicians and to attend any training courses deemed necessary to enhance skill","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01194828"},"responsibilities":null,"workhours":"40 hours per week","directapply":"false","skills":"Manufacturing Engineer, Senior Manufacturing Engineer, Manufacturing Process Engineer, Manufacturing Technician III, Manufacturing Engineer - Manufacturing & Injection Moulding & Cad, Process Engineer, Manufacturing Engineering Intern, Senior Process Engineer, Manufacturing & Quality Engineer, Electrical Engineering Technician","experiencerequirements":null,"occupationalcategory":"Produktion & Fertigung","page_url":"https:\/\/jobs.thermofisher.com\/de\/de\/job\/TFSCGLOBALR01194828EXTERNALDEDE\/Sr-Manufacturing-Engineering-Technician"}
{"row_id":7,"dateposted":"2023-07-05T00:00:00.000+0000","title":"Psychometric Rater I","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>Essential Functions and Other Job Information: <br \/>Essential Functions<br \/>• Administers psychometric ratings for clinical trials conducted by a supervising <br \/>Principal Investigator in accordance to FDA, GCP, and protocol guidelines.<br \/>• Assumes a lead role on studies, facilitating study specific Psychometric Rater <br \/>training for new and on-going studies.<br \/>• Maintains ongoing study-specific communication with sponsors and site staff <br \/>regarding ratings-related protocol updates, clarifications and testing procedures.<br \/>• Identifies potential problems or inconsistencies and takes action as appropriate.<br \/>• Administers and interpret protocol specific scales to determine protocol eligibility <br \/>under the supervision of the Principal Investigator.<br \/>• Ensures subject safety by appropriately responding to any potential for harm to <br \/>self or others identified through the course of interviews and evaluations <br \/>performed.<br \/>• Actively works to maintain consistency in the performance of ratings for <br \/>individual subjects as well as for clinical trials.<br \/>• Maintains timely source documentation as well as sponsor required information.<br \/>• Completes all monitor and sponsor queries in a timely manner.<br \/>• Provides educational in-services for third party vendors providing protocol <br \/>specific care to subjects.<br \/>• Ensures adherence to COP’s, SOP’s and GCP (ICH GCP and local regulations).<br \/>Job Complexity","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01187321"},"responsibilities":"Administers psychometric ratings for clinical trials conducted by a supervising . Assumes a lead role on studies, facilitating study specific Psychometric Rater . Maintains ongoing study-specific communication with sponsors and site staff . regarding ratings-related protocol updates, clarifications and testing procedures. Identifies potential problems or inconsistencies and takes action as appropriate. Administers and interpret protocol specific scales to determine protocol eligibility . Ensures subject safety by appropriately responding to any potential for harm to . Actively works to maintain consistency in the performance of ratings for . Maintains timely source documentation as well as sponsor required information. Completes all monitor and sponsor queries in a timely manner. Provides educational in-services for third party vendors providing protocol . specific care to subjects. Ensures adherence to COP’s, SOP’s and GCP (ICH GCP and local regulations). Job Complexity Works on problems of diverse scope where analysis of data requires evaluation of . specialization; resolves a wide range of issues in creative ways. Normally receives little instruction on day-to-day work, general instructions on new . Demonstrates good judgment in selecting methods and techniques for . obtaining solutions. Business Represents the department as a prime contact on projects. Interacts with internal . Relationships and external","workhours":"40 hours per week","directapply":"false","skills":"Potential, Coordination, Facilitating, GCP, Evaluation, Testing, Specialization, Analysis, Complexity, ICH, Documentation, supervision, Presentation Skills, Outstanding Verbal, customer services, Quality Rater Search Evaluation, Research Assistant - Cognitive Social Development Laboratory, Animator & Maya Faculty, Research Scholar & Senior IT Mentor, Data Mining & Python Instructor, Research Assistant, Teaching & Research Assistant, Research Assistant & ERP Module Handler, Program Coordinator & Test Administrator, Policy & Research Assistant","experiencerequirements":null,"occupationalcategory":"Clinical Research","page_url":"https:\/\/jobs.thermofisher.com\/global\/en\/job\/TFSCGLOBALR01187321EXTERNALENGLOBAL\/Psychometric-Rater-I"}
{"row_id":8,"dateposted":"2023-09-15T00:00:00.000+0000","title":"Clinical Trial Coordinator","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p><b>Clinical Trial Coordinator - United Kingdom (Office based in Cambridge OR Home Based - specific locations)<\/b><\/p><p><\/p><p>PPD, part of Thermo Fisher Scientific, are currently hiring for Clinical Trial Coordinators to work in our Cambridge office OR Home based in the following UK locations: Belfast, Bristol, Plymouth\/Truro, Norwich\/Lincoln. These are strategic locations to support with business needs and CRA development plans.<\/p><p><\/p><p>This role is ideal for a Life Science graduate who wishes to kick start their career within clinical research and grow into a Clinical Research Associate position in the future.<\/p><p><\/p><p>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","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01201867"},"responsibilities":"Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants. Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking tools. Reviews regulatory documents for proper content. Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified. Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments. Assists with the identification of potential investigators and development\/distribution of initial protocol packets. May assist the project team with the preparation of regulatory compliance review packages. Builds meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes. Responsible for adhering to Good Clinical Practices, country specific regulations, PPD clinical research services \/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical\/clinical aspects of project implementation, execution, and closeout. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Discover Impactful Work.","workhours":"40 hours per week","directapply":"false","skills":"Clinical Trial, Good Clinical Practices, Clinical Research, Regulatory, Project Tracking, Regulatory Compliance, Project Implementation, Practice, PPD, Training, Willingness, Teamwork, Senior Clinical Research Assistant & Data Manager, Clinical Research Consultant, Clinical Research Technician, Protocol Manager, Associate Research Manager, Clinical Research Recruiter, Data Coordinator, Principal Research Assistant, Clinical Data Manager II, Principal Investigator","experiencerequirements":null,"occupationalcategory":"Clinical Research","page_url":"https:\/\/jobs.thermofisher.com\/global\/en\/job\/TFSCGLOBALR01201867EXTERNALENGLOBAL\/Clinical-Trial-Coordinator"}
{"row_id":9,"dateposted":"2023-05-19T00:00:00.000+0000","title":"QC Analysis Reviewer - Clinical Trial Manufacturing","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><div><p><span><span><span>Monza site is a world class contract manufacturing and development facility, specialized in aseptic injectable drugs. Joining 2000 colleagues on site, the selected candidate will experience a smart, international, and fast-growing environment. With revenues of $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.<\/span><\/span><\/span><\/p><p><span><span><span>The candidate will join the PDS Analysis Reviewer Team Leader in newly-built Pharmaceutical Development department and will perform required analysis to ensure that clients’ requests are met according to SOP, GMP and GLP.<\/span><\/span><\/span><\/p><p><span><span><span>Supporting the Analytical Development Supervisor in multiple task, the candidate will specifically be assigned the following activities:<\/span><\/span><\/span><\/p><p><\/p><p><span><span><span>PURPOSE OF THE POSITION \/ RESPONSIBILITY:<\/span><\/span><\/span><\/p><p><span><span><span>Based on the information received from the Manager and \/ or the Team Leader of the reference BU, it carries out the tasks and activities listed below for which it has been enabled by the appropriate training, in compliance with the company and departmental SOPs and the safety regulations in force. <\/span><\/span><\/span><\/p><p><\/p><p><span><span><span>SPECIFIC TASKS \/ PRIMARY ACTIVITIES:<\/span><\/span><\/span><\/p><ul><li><span><span><span>Implement the verification and evaluation activities of the analytical documentation issued by the laboratory in order to ensure the integrity of the data, through the correct programming of daily activities, the","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"value":"R-01169228","name":"Thermo Fisher Scientific"},"responsibilities":"The candidate will join the PDS Analysis Reviewer Team Leader in newly-built Pharmaceutical Development department and will perform required analysis to ensure that clients’ requests are met according to SOP, GMP and GLP. Supporting the Analytical Development Supervisor in multiple task, the candidate will specifically be assigned the following activities. Based on the information received from the Manager and \/ or the Team Leader of the reference BU, it carries out the tasks and activities listed below for which it has been enabled by the appropriate training, in compliance with the company and departmental SOPs and the safety regulations in force. Implement the verification and evaluation activities of the analytical documentation issued by the laboratory in order to ensure the integrity of the data, through the correct programming of daily activities, the control of the progress of the activities, in compliance with the priorities defined by their manager and company quality standards. Ensure the correct management of the relevant analytical documentation, from receipt, to control, archiving and traceability, according to current procedures and company quality standards. Contribute to the optimal technical training of laboratory staff, both in the insertion phase and on the occasion of the introduction of new tools,","workhours":"40 hours per week","directapply":"false","skills":"Evaluation, Compliance, Analytical, Analysis, Validation, Analytical Techniques, gmps, Quality Standards, Data Management, R&D, Instrumentation, GLP, GMP, Pharmaceutical Development, Development, Archiving, chromatographic data management, Contract Manufacturing, Chemistry, Cleaning Validation, Aseptic, Documentation, Safety Regulations, HPLC, Integrity, Management, Training, Technical Training, Responsibility, Programming, Senior Clinical Research Assistant & Data Manager, Senior Statistical Programmer, Statistical Programmer, Clinical Project Manager, Research Assistant Development, Quality, & Testing, Statistical SAS Programmer, Clinical Data Management Intern, Consultant - Quality Control, Development & Quality Assurance, Marketing Manager - Process Chromatography","experiencerequirements":null,"occupationalcategory":"Ricerca e Sviluppo","page_url":"https:\/\/jobs.thermofisher.com\/it\/it\/job\/TFSCGLOBALR01169228EXTERNALITIT\/QC-Analysis-Reviewer-Clinical-Trial-Manufacturing"}
{"row_id":10,"dateposted":"2023-05-16T00:00:00.000+0000","title":"Engineer II, Field Service","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>About Us<\/p><p><\/p><p>Thermo Fisher Scientific KK<\/p><p>Headquartered in Waltham, Massachusetts, USA, the company employs 90,000 people worldwide. With $35 billion in total revenue and $1 billion in R&D expenditures,<\/p><p><\/p><p>the Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services brands provide basic and applied training in a variety of fields worldwide<\/p><p><\/p><p>The company is widely penetrated by customers ranging from product development, quality control and assurance, and security to medical, pharmaceutical, and biopharmaceutical.<\/p><p><\/p><p><\/p><p><\/p><p>Crucial duties and Responsibilities<\/p><p><\/p><p>As a Field Engineer, you will perform repairs, routine inspections, installations, customer service item sales promotions, and customer training for analytical and analytical instruments and systems we manufacture and sell.<\/p><p>#On-site installation of sophisticated instruments<\/p><p>#Routine maintenance visits<\/p><p>#Provide additional value and corrective support<\/p><p>#Assisting other members of the team<\/p><p>#Prepare and submit work reports<\/p><p>#Provide user training on system maintenance<\/p><p>#Provide feedback to global product quality team<\/p><p>#Update and revise service process documentation<\/p><p>#Identification and reporting of unique issues related to business processes<\/p><p><\/p><p># Act as problem resolution authority and provide training<\/p><p><\/p><p><\/p><p><\/p><p>Professional Attraction<\/p><p><\/p><p>The most attractive thing about being a field service engineer is that we listen to our customers directly and respond to them.<\/p><p><\/p><p>We provide technical support to a wide range of customers, including companies, research institutes, and medical institutions, to help them seek their","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01184124"},"responsibilities":"As a Field Engineer, you will perform repairs, routine inspections, installations, customer service item sales promotions, and customer training for analytical and analytical instruments and systems we manufacture and sell. # Provide additional value and corrective support. # Prepare and submit work reports. # Provide user training on system maintenance. # Provide feedback to global product quality team. # Update and revise service process documentation. # Identification and reporting of unique issues related to business processes. # Act as problem resolution authority and provide training. The successful candidate will be involved in a large part of the service provided to customers after the installation of the equipment, and will play a role in improving customer happiness and equipment upgrades, as well as driving service sales growth. # Installation and operation of equipment. # Inspection and validation work. # Propose maintenance contracts\/paid repairs\/upgrades according to customer needs. Communicate efficiently with internal customers and partners 2. # E-learning allows you to acquire knowledge without time or location restrictions. #","workhours":"40 hours per week","directapply":"false","skills":"Installation, Training, Quality Control and Assurance, ISO 9001, Customer Training, Mechanical, Customer Service, System Maintenance, Maintenance Contracts, Job Rotation, Driving, Routine Maintenance, Site Installation, Reports, Technical Support, Product Development, R&D, Validation, Product Quality, Analytical, Product Knowledge, Analyzers, Internal Customers, Adaptability, Reporting, Problem Resolution, Customer Needs, E-Learning, Proposals, Electrical Engineer II, Field Service Technician, Engineering Support Technician, Reliability Systems Engineer, Engineering Tech & Field Service Representative, Electrical Controls Engineer, Engineering Technician, Electrical Engineering Technician, Controls Engineer, Facility Management Engineer","experiencerequirements":null,"occupationalcategory":"Servizio Clienti e Supporto Tecnico","page_url":"https:\/\/jobs.thermofisher.com\/it\/it\/job\/TFSCGLOBALR01184124EXTERNALITIT\/Engineer-II-Field-Service"}
{"row_id":11,"dateposted":"2023-05-03T00:00:00.000+0000","title":"Tissue Procurement specialist III","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.<\/p><p><\/p><p><b>Discover Impactful Work:<\/b><\/p><p>The Organ and Tissue Procurement Specialist III is responsible for supporting the supply chain of Thermo Fisher’s primary cell manufacturing operation. The primary responsibility of this position is coordinating and procuring human and animal organs and tissue for research.<\/p><p>The process of procuring human organs and tissues involves medically evaluating records and ensuring the overall quality is suitable for isolating cells. In addition, this individual will coordinate with external partners such as vendors and suppliers of services needed to complete the organ donation process (i.e., hospitals, tissue banks, OPOs, and transportation services).<\/p><p>Procuring animal organs and tissues involves collaboration with veterinarians and technicians from animal vendors and","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01171148"},"responsibilities":"Discover Impactful Work. The primary responsibility of this position is coordinating and procuring human and animal organs and tissue for research. The process of procuring human organs and tissues involves medically evaluating records and ensuring the overall quality is suitable for isolating cells. In addition, this individual will coordinate with external partners such as vendors and suppliers of services needed to complete the organ donation process (i.e., hospitals, tissue banks, OPOs, and transportation services). Procuring animal organs and tissues involves collaboration with veterinarians and technicians from animal vendors and may function as a surgical team member or consultant on the best methods for appropriately using an aseptic technique to recover the organ for research purposes. In addition, the Organ and Tissue Procurement Specialist III is responsible for documentation of all aspects of Tissue collection (i.e., IRBs, MTAs, contracts, consents) and maintains tissue reports and analyzes data for process improvement. Evaluates liver tissue turned down by transplant centers and allocated for research to determine suitability for hepatic isolation. Tissue Recovery Proficiency: Supports organ\/tissue management and inventory control, including acquisitions and logistics; reviews and interprets specimen-related data. Maintains competence with surgical recovery techniques. Manage surgical recovery protocols and specifications for acquiring human","workhours":"40 hours per week","directapply":"false","skills":"affirmative action, Clinical Experience, Clinical, Manufacturing, Physiology, Clinical Liaison, Aseptic, Research, Operations, Anatomy, Project Management, Evaluating, Innovation, Management, Collaborating, Logistics, Applications, Integrity, Science, Supply Chain, Teamwork, Process Improvement, SAFe, EEO, OPOS, Presentations, Reports, Clinical Skills, Good Clinical Practices, Analysis, Procuring, Clinical Contracts Associate I, Laboratory Analyst, Clinical Contracts Associate, Research Specialist III, Document Management Specialist, Technical Assistant, Transportation Management Coordinator Sergeant, Information Management Specialist, Quality Control & Management Coordinator, Data Acquisitions Specialist","experiencerequirements":{"monthsofexperience":"36"},"occupationalcategory":"Operacijos","page_url":"https:\/\/jobs.thermofisher.com\/lt\/lt\/job\/TFSCGLOBALR01171148EXTERNALLTLT\/$%7BresumeInfo.skills.suggestedSkills.length%20?%20'"}
{"row_id":12,"dateposted":"2023-08-23T00:00:00.000+0000","title":"Logistics Specialist","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>Job title : Logistics Specialist<\/p><p>Location : 인천 영종도<\/p><p><\/p><p><b>Job Description<\/b><\/p><p>Inventory Management & analysis<\/p><p>OPEX Management & analysis<\/p><p>KPI Management & analysis<\/p><p><span>Various DC Project management<\/span><\/p><p>Project MBO (Management By Objects) & Schedule management, Efficiency improvement & savings<\/p><p>Development and Maintenance of Automation System<\/p><p><\/p><p><b><span>Qualifications <\/span><\/b><\/p><p>재고관리 경험자<\/p><p><span>프로젝트 진도관리 및 성과분석 우수자<\/span><\/p><p>프로세스 기획력 우수 (PI, BPR, CI, Lean-Kaizen, Gemba 등)<\/p><p>물류 프로세스 지식<\/p><p>데이터분석력 (Excel, Powerpoint, Visio) 및 시스템활용능력(SAP, ORACLE) 우수자<\/p><p>문제 해결 및 의사 결정 능력<\/p><p>비즈니스 영어 능력 우대<\/p><p><\/p><p><b>Benefits:<\/b><\/p><p>We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company pension, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.<\/p><p><\/p><p><b>EEO\/Reasonable Accommodation:<\/b><\/p><p>Thermo Fisher Scientific is an EEO\/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.<\/p>","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"value":"R-01194995","name":"Thermo Fisher Scientific"},"responsibilities":"Inventory Management & analysis. Various DC Project management. Project MBO (Management By Objects) & Schedule management, Efficiency improvement & savings. Development and Maintenance of Automation System.","workhours":"40 hours per week","directapply":"false","skills":"Management, Inventory Management, opex management, dc project management, Project Management, Efficiency Improvement, SAP, kpi management, KPI, Analysis, automation system, Schedule Management, Automation, Development And Maintenance, Opex, Logistics Specialist, Operations & Logistics Manager, Export Operations Specialist, Sourcing & Logistics Analyst, Logistics Coordinator, Materials Planner, Team Member - Logistics Module of Project Manager, Procurement Analyst, Production & Operations Coordinator, Carrier Management Specialist","experiencerequirements":null,"occupationalcategory":"Výroba","page_url":"https:\/\/jobs.thermofisher.com\/cz\/cz\/job\/TFSCGLOBALR01194995EXTERNALCZCZ\/Logistics-Specialist"}
{"row_id":13,"dateposted":"2023-08-18T00:00:00.000+0000","title":"Medical Technologist","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>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.<\/p><p><span>Our Global Central Labs combines the expertise of a leading CRO, Clinical Research Services with global central labs that are among the world's largest dedicated exclusively to clinical trials.<\/span><br \/> <\/p><p><b>Major Job Responsibilities<\/b><\/p><p>The Medical Technologist performs, reviews, and interprets complex, esoteric, and routine chemical, hematological, coagulation, renal, lipid, and hormonal analyses by manual automated, and\/ or microscopic means. Performs a wide variety of clinical laboratory analyses including assays which define complicated disorders of the cardiovascular, endocrine, hematological, hemostatic, thrombolytic, and","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01196484"},"responsibilities":"The Medical Technologist performs, reviews, and interprets complex, esoteric, and routine chemical, hematological, coagulation, renal, lipid, and hormonal analyses by manual automated, and\/ or microscopic means. Performs a wide variety of clinical laboratory analyses including assays which define complicated disorders of the cardiovascular, endocrine, hematological, hemostatic, thrombolytic, and renal systems and evaluates individual and related laboratory data, recognizes patterns or trends that suggest significance of results. Integrates analytical results with specific and highly varied clinical trial protocols and evaluates the credibility, appropriateness, and accuracy of test results in order to facilitate entry or exclusion of subjects from research programs. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale.","workhours":"40 hours per week","directapply":"false","skills":"Clinical Laboratory, Cardiovascular, Microscopic, Clinical Trial, Hemostatic, Collaborative, Thrombolytic, critical thinking, Cooperative, Science, Facilitate, Organizational Skills, Analytical, Planning, Medical Technologist, Laboratory Assistant, Radiologic Technologist, Laboratory Technician, Certified Phlebotomy Technician, Technologist, Medical Assistant, Research Assistant - NLP-Medical Treatment Laboratory, Physician Assistant, Specimen Technician","experiencerequirements":{"monthsofexperience":"1"},"occupationalcategory":"Services de Laboratoire","page_url":"https:\/\/jobs.thermofisher.com\/fr\/fr\/job\/TFSCGLOBALR01196484EXTERNALFRFR\/Medical-Technologist"}
{"row_id":14,"dateposted":"2023-09-14T00:00:00.000+0000","title":"Systems Specialist - Document Control \/ Veeva Vault","description":"<p style=\\\"text-align:left\\\"><b><u>Job Description<\/u><\/b><\/p><p style=\\\"text-align:inherit\\\"><\/p><p>Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our clients to make the world healthier, safer, and cleaner.<\/p><p><\/p><p>Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical\/ biopharmaceutical company, all while maintaining full-time benefits.<\/p><p><\/p><p>This position is at a client clinical-stage biopharmaceutical company dedicated to the discovery, development and commercialization of next-generation bispecific and multifunctional biotherapeutics. The client's suite of complementary therapeutic platforms and its fully-integrated drug development engine provide the flexibility and compatibility to precisely engineer and develop highly-differentiated product candidates.<\/p><p><\/p><p>We are seeking a highly-motivated professional who is looking to grow their career. The Systems Specialist will generally support the Quality Systems team with a focus on the clean up of the electronic Document System (EDMS), Deviation\/Change Control programs and may assist with the GxP Training Learning Management System (LMS). This position will be based in Seattle.<\/p><p><\/p><h2><b>Essential Functions<\/b><\/h2><ul><li><p>Work with Document Control to generate","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01202853"},"responsibilities":"The Systems Specialist will generally support the Quality Systems team with a focus on the clean up of the electronic Document System (EDMS), Deviation\/Change Control programs and may assist with the GxP Training Learning Management System (LMS). Supports the Deviation and Change Control programs using the electronic Veeva Quality Management System (QMS). Assists Deviation\/Change Control Specialist on follow up, reporting and metrics development. Work with Document Control to generate reports and follow up on document progress as they approach approval. Participates with Document Control regarding clean up activities on going in the Veeva QualityDocs vault. Understands and supports the Veeva \\\"Quality Docs\\\" document control system and the quality systems associated with GxP operations. Supports GxP Training Program through verification that new users are set up correctly in the LMS (Learning Management System) in proper roles and user groups. Initiates and follows up on new GxP Training request using IT ticket system. Assists in following up and collecting all Job Descriptions and Curricula vitae as part of maintaining Training Files. Uses quality tools to assist in compilation, tracking, trending, and communicating QMS metrics in presentations, reports, and dashboards. Supports the maintenance and improvement of Quality Systems processes in general and the","workhours":"40 hours per week","directapply":"false","skills":"quality systems, document control, lms, qms, gxp, metrics, operations, document progress, quality tools, reporting, interpersonal, veeva, electronic document, electronic quality systems, reports, compilation, presentations, following up, customer service, microsoft office software, customer service oriented, interpersonal skills, Configuration Management Specialist- Staff, Senior Programmer - Sharepoint, Alfresco Engineer, Applications Systems Training & Documentation Specialist, Recruitment Systems Specialist, Project Coordinator & Senior Process Analyst, Document Management Specialist, Project Administrator Module Export & Import Management, Senior Specialist Systems Design & Manager, Order Operation Administrator","experiencerequirements":{"monthsofexperience":"24"},"occupationalcategory":"ラボラトリーサービス","page_url":"https:\/\/jobs.thermofisher.com\/jp\/ja\/job\/TFSCGLOBALR01202853EXTERNALJAJP\/Systems-Specialist-Document-Control-Veeva-Vault"}
{"row_id":15,"dateposted":"2023-06-01T00:00:00.000+0000","title":"Material Handler\/Shipping Clerk","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p><b><span>Warehouse Colleague - Daytime Shift<\/span><\/b> – Packing, Pulling Orders, Inventory<\/p><p>Some of the benefits you can expect:<\/p><ul><li>Medical, Dental, & Vision benefits are effective immediately upon employment<\/li><li>Earn up to 15 PTO (paid vacation) days in your 1st year<\/li><li>Paid holidays<\/li><li>401K program with 6% matching<\/li><li>Tuition Reimbursement & Employee Stock Purchase Programs<\/li><li>Room for growth<\/li><\/ul><p>This isn’t your ordinary warehouse job nor ordinary company. As a warehouse colleague, you will help deliver various types of products from life-saving personal protective equipment to microscopes for high school biology classrooms. You will be on the front lines of helping science make the world healthier, cleaner, and safer. We value hard work and dependability and in return, you’ll be rewarded with great pay, great benefits, and the satisfaction that you are making a difference in the world.<\/p><p><b><span>How will you make an impact?<\/span><\/b><\/p><p>We want enthusiastic, dependable, hard-working, standout colleagues that will make a difference for our customers and fellow colleagues every day. The impact you will have could be anything from delivering products that help a scientist discover a cure for cancer to helping a nurse care for a patient effectively because they have the right equipment.<\/p><p><b><span>What will you do?<\/span><\/b><\/p><ul><li>Process customer orders daily to meet their expectations<\/li><li>Work in one or","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01185825"},"responsibilities":"As a warehouse colleague, you will help deliver various types of products from life-saving personal protective equipment to microscopes for high school biology classrooms. You will be on the front lines of helping science make the world healthier, cleaner, and safer. Process customer orders daily to meet their expectations. Work in one or more process paths; receiving, picking, packing, or shipping. Package and label shipments according to standard operating procedures and complete documentation requirements for hazardous materials. Help ensure inventory is stored properly. Work with your team to make sure everyone has a great experience working at Thermo Fisher Scientific. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.","workhours":"40 hours per week","directapply":"false","skills":"PICKING, SHIPPING, Inventory, Orders, PACKING, handling hazardous materials, General warehouse, Warehouse, Customer Orders, Dependability, work independently, Documentation, Scanning, High Level Of Accuracy, Attention To Detail, EEO, Affirmative Action, chemicals, IMPACT, scanning equipment, PROCESS CUSTOMER ORDERS, Material Handler, Warehouse Clerk, Material Handler I, Forklift Operator, Warehouse Coordinator, Warehouse Supervisor, Warehouse Associate, Distribution Center Supervisor, Shipping Clerk, Warehouse Worker","experiencerequirements":null,"occupationalcategory":"Operacijos","page_url":"https:\/\/jobs.thermofisher.com\/lt\/lt\/job\/TFSCGLOBALR01185825EXTERNALLTLT\/Material-Handler-Shipping-Clerk"}
{"row_id":16,"dateposted":"2023-07-20T00:00:00.000+0000","title":"Site Payments Associate II","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>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.<\/p><p><\/p><p>Our goal-driven teams combine and deliver centralized support and solutions for the clinical trials, collaborating to improve processes, cycle and flexibility. We partner with our sites, businesses and colleagues around the world to decrease startup timelines and exceed expectations.<\/p><h2>Discover Impactful Work:<\/h2><p>Provides administrative, reporting, contractual and financial support to the department related to the processing of payments to investigative sites. Responsibilities include data compilation, issue\/risk resolution, and ensuring adherence to contractual guidelines and country regulations.<\/p><h2>A day in the Life:<\/h2><p>Compiles data from","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01195389"},"responsibilities":"Discover Impactful Work. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Provides administrative, reporting, contractual and financial support to the department related to the processing of payments to investigative sites. Responsibilities include data compilation, issue\/risk resolution, and ensuring adherence to contractual guidelines and country regulations. Compiles data from multiple sources to generate payments to sites in accordance with procedural documents and site contracts. Ensures adherence to country-specific regulations which affect and impact ability to pay. Manages payment responsibilities and workflow to meet contracted timelines and project deliverables. Builds and leads relationships with study sites and interface, on occasion, with clients for payment-specific issues. Responds to study-related escalations and resolves payment-related findings. Raises project risks appropriately. Trains study teams on site payment processes, including setting expectations around site payments' requirements and deliverables. May process investigator payments in middleware and financial system; manage refunds, credit notes, late payment fees, pre-payments or investigator meeting reimbursements. May build and enter budgets and SVTs; work on transparency reporting; perform study reconciliations; lead and maintain investigator funds tracker for studies transitioned to site payments. and perform applicable data entry of said documents. for all aspects of project","workhours":"40 hours per week","directapply":"false","skills":"Financial Systems, Financial, Reporting, Financial Support, CREDIT, organizational, Project Implementation, Regulatory, Country Regulatory, EDC, Good Clinical Practices, Documentation, Tax, Analyzing, Solid Computer Skills, computer, communication, Strong Attention to Detail, Organizational Skills, Training, english, Communication Skills, tax regulations, Senior Software Associate II, Service Analyst - Technical Support, Project Engineer Hardware & Software Consultant, Senior Project Manager Applications Services, Project Manager & Provisioning & Support Specialist, Manager Applications & Support Engineering, Implementation Manager - ERP Applications, Softwares Associate & Technical Delivery manager, Description Software Consultant, Applications & Production Support Engineer","experiencerequirements":null,"occupationalcategory":"Klinische Forschung","page_url":"https:\/\/jobs.thermofisher.com\/de\/de\/job\/TFSCGLOBALR01195389EXTERNALDEDE\/Site-Payments-Associate-II"}
{"row_id":17,"dateposted":"2023-07-25T00:00:00.000+0000","title":"Produktionsmitarbeiter (m\/w\/d)","description":"<div><p><span><span>Thermo Fisher Scientific Inc. ist der weltweit führende Partner für die Wissenschaft mit einem Umsatz von 40 Mrd. USD und 100.000 Mitarbeitern in 55 Ländern. <\/span><\/span><span><span>Unsere Mission ist es, unsere Kunden in die Lage zu versetzen, die Welt gesünder, sauberer und sicherer zu machen. Ob unsere Kunden die Biowissenschaftsforschung beschleunigen, komplexe analytische Herausforderungen lösen, die Diagnostik und Therapie von Patienten verbessern oder die Produktivität in ihren Labors steigern - wir sind hier, um sie zu unterstützen<\/span><\/span><span> <\/span><\/p><\/div><div><p><span> <\/span><\/p><\/div><div><p><span><span>Bei Patheon, Teil von Thermo Fisher Scientific in Linz, ist kein Tag wie der andere. Die pharmazeutische Wirkstofferzeugung bietet ein vielseitiges Aufgabengebiet, egal ob Sie in Forschung, Qualität, Produktion oder im Business tätig sind. Gemeinsam mit mehr als 750 KollegInnen tragen Sie aktiv dazu bei, diese Welt ein Stück gesünder zu machen.<\/span><\/span><span> <\/span><\/p><\/div><p><\/p><p>Als ProduktionsmitarbeiterIn sind sie für die Chargierung von Rohstoffen, das Bedienen von Anlagen und Apparaten sowie für die Überwachung des Produktionsprozesses und die Produktfinalisierung zuständig<br> <\/p><p><\/p><p><b>Ihre Aufgaben<\/b><\/p><ul><li>Überwachen des Herstellprozesses mittels Prozessleitsystem<\/li><li>Bedienen von Apparaten und PLS-Steuerungseinheiten<\/li><li>Steuern von Infrastrukturanlagen<\/li><li>Chargieren von Rohstoffen<\/li><li>Mitarbeit bei der Finalisierung bzw. Produktabfüllung<\/li><li>Unterstützung bei der Probeziehung<\/li><li>Dokumentation nach cGMP<\/li><\/ul><p><\/p><p><b>Ihre Qualifikationen<\/b><\/p><ul><li>Abgeschlossene Lehrausbildung, idealerweise in einem technischen Beruf<\/li><li>Technisches Verständnis und handwerkliches Geschick<\/li><li>Erfahrung in einem Produktionsbetrieb von Vorteil<\/li><li>Hohes Verantwortungsbewusstsein, Zuverlässigkeit<\/li><li>Bereitschaft zum Schichtdienst (5-Schicht)<\/li><li>Sehr gute","hiringorganization":{"name":"Thermo Fisher"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher","value":"230230BR"},"responsibilities":"Thermo Fisher Scientific Inc. Als ProduktionsmitarbeiterIn sind sie für die Chargierung von Rohstoffen, das Bedienen von Anlagen und Apparaten sowie für die Überwachung des Produktionsprozesses und die Produktfinalisierung zuständig. Ihre Aufgaben. Überwachen des Herstellprozesses mittels Prozessleitsystem. Bedienen von Apparaten und PLS-Steuerungseinheiten. Steuern von Infrastrukturanlagen. Chargieren von Rohstoffen. Mitarbeit bei der Finalisierung bzw. Produktabfüllung. Dann bewerben Sie sich mit den üblichen Unterlagen (bis max.","workhours":"40 hours per week","directapply":"false","skills":"zuverlässigkeit, integrität, verantwortungsbewusstsein, handwerkliches geschick, innovation, dokumentation, prozessleitsystem, produktionsbetrieb, unterlagen, technisches verständnis, cgmp, vorteil, überwachung des produktionsprozesses, unterstützung, bedienen von, unternehmenskultur, weiterbildung, Trainings Co-ordinator, Coordonnateur de projets - Culture, Sales Coordinator - Employment Process Outsourcing, Conseiller, Global Practice Lead - Recruitment Process Outsourcing, Group Lead Ticketing & Operation, Junior Manager Materials, Global Functional Lead - E-recruitment, Principal & Program Director, Recruitment Process Outsourcing, Junior Process Associate","experiencerequirements":null,"occupationalcategory":"Operacijos","page_url":"https:\/\/jobs.thermofisher.com\/lt\/lt\/job\/TFSCGLOBAL230230BREXTERNALLTLT\/Produktionsmitarbeiter-m-w-d"}
{"row_id":18,"dateposted":"2023-08-16T00:00:00.000+0000","title":"Accountant","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>At Thermo Fisher Scientific, our Finance teams are important to our business and functional teams to make educated, sound decisions that drive our Mission and make us a stable and trusted industry leader. From Financial Planning & Analysis, Tax, Treasury, Financial Reporting, Audit, Investor Relations, Strategy & Corporate Development to Accounting, our Finance functions have a diverse and global presence, providing significant opportunities to develop outstanding career experiences and perspectives. Ranked #95 on the 2021 Fortune 500 list and with revenues of more than $40 billion, you’ll discover endless opportunities to grow a rewarding career as part of the world leader serving science.<\/p><p><\/p><p>Reporting to the AR Supervisor, the Associate Accountant is responsible in supporting strategic credit control and collection framework, providing effective credit risk management and driving collections performance. Account Receivable includes Credit & Collections, Billing and Cash Applications. The position is responsible to achieve AR key metrics and deliverables to support our business objectives and includes, but not limited to, supporting project implementations and business partnering.<\/p><h2><\/h2><h2>Responsibilities include but are not limited to the following:<\/h2><ul><li>Perform Accounts Receivables duties in line with the company’s credit policies and procedures.<\/li><li>Perform periodic review of credit limits on customer accounts<\/li><li>Ensures orders are managed and","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01200355"},"responsibilities":"Reporting to the AR Supervisor, the Associate Accountant is responsible in supporting strategic credit control and collection framework, providing effective credit risk management and driving collections performance. The position is responsible to achieve AR key metrics and deliverables to support our business objectives and includes, but not limited to, supporting project implementations and business partnering. Perform Accounts Receivables duties in line with the company’s credit policies and procedures. Perform periodic review of credit limits on customer accounts. Ensures orders are managed and released timely in accordance to guidelines. Compile and maintain accurate and complete accounts receivable records in Cforia system to include contacts, status of past due, and any disputes identified. Work cross-functionally with FP&A, Commercial and Customer Services teams to resolve any outstanding discrepancies on AR. Assist in establishing and maintaining appropriate internal controls to ensure 100% SOX compliance. Participate in various finance SOP projects and initiatives to drive process improvements and automation. Participate and support on revenue recognition accounting. reviewing monthly and quarterly balance sheet reconciliations, and financial reporting packages. reviewing SAB104 for revenue recognition, and ensuring that transactions are accurately recorded in accordance with policies in the proper accounting periods. reviewing monthly ageing reports ad analysis. monitoring","workhours":"40 hours per week","directapply":"false","skills":"Accounting, b2b accounts receivable, Financial Reporting, Financial, Accounts Receivables, revenue recognition accounting, ACCOUNTS RECEIVABLE, Reporting, Revenue Recognition, FP&A, Credit Control, Internal Controls, Reports, Senior Management, Analysis, Business Partnering, Initiatives, Balance Sheet, Credit Risk Management, Key Metrics, Presenting, Independent, organized, communicator, Integrity, Senior Accountant, Accounting Manager, Accounting Analyst, Financial Accounting Manager, Junior Accountant, Lead Accountant, Staff Accountant, Accounting Supervisor, Assistant Controller, Financial Reporting Specialist - Corporate Finance & Accounting","experiencerequirements":{"monthsofexperience":"48"},"occupationalcategory":"财务","page_url":"https:\/\/jobs.thermofisher.com\/cn\/zh\/job\/TFSCGLOBALR01200355EXTERNALZHCN\/Accountant"}
{"row_id":19,"dateposted":"2023-09-14T00:00:00.000+0000","title":"Senior Automation Professional","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $50 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them.<\/p><p><\/p><p>Our global team of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.<\/p><p><\/p><p>Currently, we are looking for a <b>Senior Automation Professional <\/b>in Lengnau, Switzerland<\/p><p>In this function, you will part of the Manufacturing Engineering team in Lengnau, a state-of-the-art Drug Substance Manufacturing site for Biologic's.<\/p><p><\/p><p><b>Your Responsibilities:<\/b><\/p><ul><li>Contact person for the production team for the technical provision of the systems<\/li><li>GMP-compliant implementation and documentation of maintenance and repair work. (Planned and unplanned). Process and confirm notifications and orders in the maintenance management system<\/li><li>Compliance with regulations, especially regarding quality, ecology, and safety, especially the applicable standards and guidelines of the Electricity Act SR 734.0, Heavy Current Ordinance SR 734.2, NIV SR","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01201677"},"responsibilities":"In this function, you will part of the Manufacturing Engineering team in Lengnau, a state-of-the-art Drug Substance Manufacturing site for Biologic's. Contact person for the production team for the technical provision of the systems. GMP-compliant implementation and documentation of maintenance and repair work. ( Process and confirm notifications and orders in the maintenance management system. Compliance with regulations, especially regarding quality, ecology, and safety, especially the applicable standards and guidelines of the Electricity Act SR 734.0, Heavy Current Ordinance SR 734.2, NIV SR 734.27, NEV SR 734.26, NIN and relevant standards. Support for the maintenance planner (maintenance planner) in spare parts management. Ensuring compliance with contractually agreed processes in the assigned mandates. Solving of electrical\/automated systems and fault analyses, development and implementation of proposed solutions when recurring problems occur in collaboration with the system suppliers and the system owners. Provision of on-call service. Support in updating the system documentation (circuit diagrams, EMSR schemes). Handling and supervising external companies (service technicians). Ensures alignment and implementation to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.","workhours":"40 hours per week","directapply":"false","skills":"automation, validation, professional experience, calibration, management, manufacturing engineering, compliance, project execution, production, maintenance, gmp, manufacturing, development, siemens, responsibility, plant maintenance, maintenance management, safety, plc technology, spare parts, documentation, hvac systems, software design, hardware design, circuit diagrams, profibus, adaptability, virtualization, german is, dns, Practice Director - Automation Development & Quality Assurance, Robotic Process Automation (RPA) Senior Consultant, Applications Software Development Senior Consultant, Robotic Process Automation (RPA) Consultant, Software Development Senior Consultant, Associate Principal Software Quality Engineer, SAS Automation Programmer, Software Development Senior Analyst, Consulting & Senior Associate - Microsoft Dynamics, Senior Automation Tester","experiencerequirements":{"monthsofexperience":"36"},"occupationalcategory":"Operations","page_url":"https:\/\/jobs.thermofisher.com\/global\/en\/job\/TFSCGLOBALR01201677EXTERNALENGLOBAL\/Senior-Automation-Professional"}
{"row_id":20,"dateposted":"2023-07-11T00:00:00.000+0000","title":"Quality Engineer","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p><b>Profile<\/b><\/p><ul><li>HBO level \/ bachelor’s degree or HBO work- and think level.<\/li><li>Excellent knowledge of Dutch and English language.<\/li><li>A few years of work experience in Quality environment is required.<\/li><li>Flexible, able to cope with deadlines\/stress.<\/li><li>Detail- oriented and accurate.<\/li><li>Proactive approach.<\/li><li>Organized with good communication skills.<\/li><li>Knowledge of quality standards.<\/li><li>Must be able to communicate effectively with multiple levels of staff throughout the organization.<\/li><li>Possess strong organizational skills with the ability to manage and prioritize multiple tasks and meet deadlines.<\/li><li>Able to operate in an international multi-cultural environment.<\/li><li>Knowledge of Microsoft Office, Trackwise and Agile is a pre.<\/li><\/ul><p><\/p><p><\/p><p><b>Responsibilities<\/b><\/p><ul><li>Provide quality system leadership to assure internal policies are met.<\/li><li>Helps the Quality department with maintenance of Quality Management System.<\/li><li>Drives a culture of continuous improvement.<\/li><li>Is responsible for the site’s document control process.<\/li><li>Promote and monitor change control.<\/li><li>Keep quality documents actual.<\/li><li>Perform training to all site personnel on Quality procedures.<\/li><li>Works with Regulatory department on requirements of product and site registrations (applicable regulations).<\/li><li>Physical checks on products and shipments.<\/li><li>All employees at the EDC are required to perform their tasks in accordance with the EDC QMS and Thermo Fisher safety requirements.<\/li><li>All employees at the EDC are required to perform their tasks in accordance with the EDC QMS and Thermo Fisher safety requirements<\/li><li>Perform other duties as assigned by Quality Manager.<\/li><\/ul><p><\/p><p><\/p><p><b>Training and","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01189350"},"responsibilities":"Provide quality system leadership to assure internal policies are met. Helps the Quality department with maintenance of Quality Management System. Drives a culture of continuous improvement. Is responsible for the site’s document control process. Promote and monitor change control. Keep quality documents actual. Perform training to all site personnel on Quality procedures. Works with Regulatory department on requirements of product and site registrations (applicable regulations). Physical checks on products and shipments. Perform other duties as assigned by Quality Manager.","workhours":"40 hours per week","directapply":"false","skills":"Safety, organizational, Quality Procedures, Quality Standards, Continuous Improvement, Maintenance, QMS, document control process, ProActive, Document Control, TrackWise, Regulatory, Dutch, Agile, EDC, Leadership, Training, Quality Engineer, Senior Quality Engineer, Senior Quality Control Engineer, Principal Quality Engineer, Manufacturing & Quality Engineer, Reliability Engineer, Quality Engineering Lead, Software Quality Engineer, Senior Supplier Quality Assurance Engineer, Quality Engineer I","experiencerequirements":null,"occupationalcategory":"Operations","page_url":"https:\/\/jobs.thermofisher.com\/it\/it\/job\/TFSCGLOBALR01189350EXTERNALITIT\/Quality-Engineer"}
{"row_id":21,"dateposted":"2023-09-14T00:00:00.000+0000","title":"Developer II","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p><b>Responsibilities<\/b><\/p><p><\/p><p><b><span>Position Summary<\/span><\/b> <br \/> <br \/>The SAP ABAP Developer analyzes user requirements, procedures, and problems to automate processes or to improve existing systems. Provides technical knowledge, system design techniques, methodologies, tools, and standards applied in the IT and business environment. <\/p><p><\/p><p>As a key member of the SAP Core team, provide support to the business community for SAP in the ABAP Technical Development area. This includes all new projects as well as production support across all functions within SAP.<\/p><p><br \/> <br \/><b><span>Key Duties and Responsibilities<\/span><\/b> <\/p><ul><li>Applies company policies and procedures to resolve a variety of issues<\/li><li>Exercise judgment and independence in identifying next steps<\/li><li>Engage with other project personnel to ensure business application systems are developed in a way that aligns with architectural standards and established methodologies and practices<\/li><li>Provide programming knowledge, usually as a member of a project team, in the analysis, design, and development of SAP reports, interfaces, conversions, business forms, and user exits<\/li><li>Provide estimates for the programming and unit testing activities of a project when needed<\/li><li>Write new and modify existing data sources, infosets and queries<\/li><li>Develop and support interfaces to numerous legacy and third-party systems using a variety of techniques such as LSMW, BAPI, IDOC, RFC calls, BDC, and call transaction","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01201478"},"responsibilities":"Provides technical knowledge, system design techniques, methodologies, tools, and standards applied in the IT and business environment. Applies company policies and procedures to resolve a variety of issues. Exercise judgment and independence in identifying next steps. Provide programming knowledge, usually as a member of a project team, in the analysis, design, and development of SAP reports, interfaces, conversions, business forms, and user exits. Provide estimates for the programming and unit testing activities of a project when needed. Write new and modify existing data sources, infosets and queries. Perform program performance optimization and tuning where vital. Supervise and report to management on the status of project efforts, anticipating\/identifying issues that inhibit the attainment of project goals and implementing corrective actions. Practical experience in creating custom and enhance standard CDS view and AMDP class based on business requirement. The SAP ABAP Developer analyzes user requirements, procedures, and problems to automate processes or to improve existing systems. As a key member of the SAP Core team, provide support to the business community for SAP in the ABAP Technical Development area. Engage with other project personnel to ensure business application systems are developed in a way that aligns with architectural standards and established methodologies","workhours":"40 hours per week","directapply":"false","skills":"sap abap development, sdlc, abap, bapi, java, odata, eclipse, sap hana, sql, xml, technical development, sap, bi, idoc, computer science, architecture, netweaver 7.0, qm, business application, sap abap, netweaver, technical knowledge, data services, bdc, sm, programming languages, business objects, analytical, adobe forms, sap ecc, Developer II, Developer III, Developer I, Applications Developer II, Java Developer III, Software Developer - II, Software Developer III, UI Developer II, Developer IV, UI Developer III","experiencerequirements":{"monthsofexperience":"36"},"occupationalcategory":"Informatica, Dati e Tecnologie","page_url":"https:\/\/jobs.thermofisher.com\/it\/it\/job\/TFSCGLOBALR01201478EXTERNALITIT\/Developer-II"}
{"row_id":22,"dateposted":"2023-09-08T00:00:00.000+0000","title":"Medical Lab Technologist I","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><div><div><div><div><div><div><div><div><div><div><div>The Medical Technologist independently and without technical supervision performs low, moderate, and high complexity clinical laboratory testing as a generalist, with assignment in some or all of the following disciplines: urinalysis, coagulation, hematology, chemistry, special chemistry, and immunology. The Med Tech also troubleshoots laboratory equipment and methods and provides technical supervision of others as required.<\/div><div>ASCP Board Certification Required.<\/div><div><\/div><div>Responsibilities include:<\/div><ul><li>Perform clinical laboratory testing on samples according to established laboratory procedures, and verify\/report test results as requested by study protocol. Ensures quality laboratory results and prioritizes work to optimize timely result reporting. Accurately perform quality control\/assurance and proficiency testing as needed<\/li><li>Maintain complex laboratory equipment and correctly interpret assay validity as a CLIA qualified clinical laboratory testing professional<\/li><li>Perform and record instrument and test preventive maintenance, calibration, reagent, troubleshooting and other procedures required to establish, maintain, or monitor test performance<\/li><li>Perform, monitor and record disinfection and maintenance of general laboratory equipment and areas<\/li><li>Technically monitor and supervise medical laboratory technicians and students. This includes participation in the laboratory competency assessment program<\/li><\/ul><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><div><\/div><div><div><div><b>Qualifications - Internal\/External<\/b><\/div><div>Education and <span>Experience: Bachelor's<\/span> degree in Medical Technology or four-years of college plus ASCP certified Clinical Laboratory Scientist (NCA) or equivalent certification<\/div><div>Knowledge, Skills and Abilities: Ability to advise clinic staff in the proper","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"name":"Thermo Fisher Scientific","value":"R-01201395"},"responsibilities":"The Medical Technologist independently and without technical supervision performs low, moderate, and high complexity clinical laboratory testing as a generalist, with assignment in some or all of the following disciplines: urinalysis, coagulation, hematology, chemistry, special chemistry, and immunology. The Med Tech also troubleshoots laboratory equipment and methods and provides technical supervision of others as required. Responsibilities include:Perform clinical laboratory testing on samples according to established laboratory procedures, and verify\/report test results as requested by study protocol. Ensures quality laboratory results and prioritizes work to optimize timely result reporting. Accurately perform quality control\/assurance and proficiency testing as needed. Maintain complex laboratory equipment and correctly interpret assay validity as a CLIA qualified clinical laboratory testing professional. Perform and record instrument and test preventive maintenance, calibration, reagent, troubleshooting and other procedures required to establish, maintain, or monitor test performance. Perform, monitor and record disinfection and maintenance of general laboratory equipment and areas. Technically monitor and supervise medical laboratory technicians and students.","workhours":"40 hours per week","directapply":"false","skills":"clinical laboratory, medical laboratory, hematology, immunology, clinical, urinalysis, specimen collection, human anatomy, laboratory principles, laboratory equipment, calibration, testing, quality control, complexity, supervision, communication, applications, maintenance, disinfection, communication skills, preventive maintenance, customer service principles, chemistry, assay, research, reporting, troubleshooting, Medical Technologist, Laboratory Assistant, MRI Technologist, Specimen Technician, Laboratory Consultant, Ultrasound Technologist, Laboratory Technician, Laboratory Analyst, Certified Phlebotomy Technician, Computer Laboratory Assistant","experiencerequirements":{"monthsofexperience":"48"},"occupationalcategory":"ラボラトリーサービス","page_url":"https:\/\/jobs.thermofisher.com\/jp\/ja\/job\/TFSCGLOBALR01201395EXTERNALJAJP\/Medical-Lab-Technologist-I"}
{"row_id":23,"dateposted":"2023-08-11T00:00:00.000+0000","title":"Quality on the Floor Specialist (Clinical Trial Manufacturing)","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>Thermo Fisher Scientific è world leader in Serving Science.<\/p><p>La Business Unit PDS di Monza sta cercando un Quality on the Floor Specialist per l'unità di Pharmaceutical Development Service (DS)<\/p><p><\/p><p>Alle dipendenze del Quality on the floor Team Leader e del Quality Operations Senior Manager, si occupa della Batch Record Review dei lotti GMP nel rispetto delle procedure aziendali, degli standard di qualità e delle normative vigenti (leggi, norme GMP, FDA, etc.) e della sorveglianza delle attività produttive, diffondendo pro-attivamente la Quality Culture all’interno dei Reparti.<\/p><p><\/p><p><b>COMPITI SPECIFICI\/ATTIVITÀ PRIMARIE:<\/b><\/p><p><b>Batch Record Review<\/b><\/p><ul><li>Effettua la revisione dei lotti GMP rilevanti (siano essi ad uso umano\/veterinario oppure destinati a generare informazioni di carattere GMP, Es. MediaFill, lotti engineering per caratterizzazione, stabilità o registrazione) e ne verifica la conformità alle specifiche, alle procedure aziendali ed alle normative vigenti dichiarandola mediante l’utilizzo dell’apposita check-list.<\/li><\/ul><p><\/p><p><b>Supporto del Cliente<\/b><\/p><ul><li>Fornisce supporto ai Cliente in merito a questioni legate alla propria area di competenza, interfacciandosi direttamente con loro per risolvere quesiti legati alla revisione, al fine di consentire il corretto rilascio e la corretta gestione dei lotti GMP rilevanti.<\/li><\/ul><p><\/p><p><b>Sorveglianze periodiche nel Reparto Produzione<\/b><\/p><ul><li>Effettua sorveglianze periodiche delle attività produttive e promuove la Quality Culture diffondendola pro-attivamente all’interno dei Reparti.<\/li><li>Incoraggia la condivisione delle problematiche e","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"OTHER","identifier":{"name":"Thermo Fisher Scientific","value":"R-01199629"},"responsibilities":"Alle dipendenze del Quality on the floor Team Leader e del Quality Operations Senior Manager, si occupa della Batch Record Review dei lotti GMP nel rispetto delle procedure aziendali, degli standard di qualità e delle normative vigenti (leggi, norme GMP, FDA, etc.) e della sorveglianza delle attività produttive, diffondendo pro-attivamente la Quality Culture all’interno dei Reparti. Batch Record Review. Effettua la revisione dei lotti GMP rilevanti (siano essi ad uso umano\/veterinario oppure destinati a generare informazioni di carattere GMP, Es. MediaFill, lotti engineering per caratterizzazione, stabilità o registrazione) e ne verifica la conformità alle specifiche, alle procedure aziendali ed alle normative vigenti dichiarandola mediante l’utilizzo dell’apposita check-list. Fornisce supporto ai Cliente in merito a questioni legate alla propria area di competenza, interfacciandosi direttamente con loro per risolvere quesiti legati alla revisione, al fine di consentire il corretto rilascio e la corretta gestione dei lotti GMP rilevanti. Sorveglianze periodiche nel Reparto Produzione. Effettua sorveglianze periodiche delle attività produttive e promuove la Quality Culture diffondendola pro-attivamente all’interno dei Reparti. Incoraggia la condivisione delle problematiche e delle relative azioni correttive con il Reparto Produzione mediante huddle periodici. Supporta le funzioni del gruppo Quality System & Compliance nell’esecuzione di Fit & Finish e Oversight","workhours":"40 hours per week","directapply":"false","skills":"oversight, gestione, conformità, implementazione, competenza, interno, continuous improvement, comprensione, indagini, accordo, mbr, huddle, ottimizzazione, quality operations, procedure di qualità, procedure aziendali, distribuzione, qualità, stabilità, quality system, specifiche, ppi, politiche, revisione, training, supporto, esecuzione, attività, produzione, caratterizzazione, Process Developer - Operations, Production Manager - Materials Quality Assurance, Marketing Manager - Process Chromatography, Manufacturing Project Manager, Pharmaceutical Industry Team Lead, Global Process Engineer, Manufacturing & Quality Engineer, Senior Process Engineer, Packaging Engineer, Plant Quality Manager & Supplier Quality Manager","experiencerequirements":null,"occupationalcategory":"Výroba","page_url":"https:\/\/jobs.thermofisher.com\/cz\/cz\/job\/TFSCGLOBALR01199629EXTERNALCZCZ\/Quality-on-the-Floor-Specialist-Clinical-Trial-Manufacturing"}
{"row_id":24,"dateposted":"2023-07-06T00:00:00.000+0000","title":"Clinical Trial Coordinator - Netherlands","description":"<p><b><u>Job Description<\/u><\/b><\/p><p><\/p><p>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.<\/p><p>Our clinical department defines, develops and delivers clinical programs, ensuring the highest-quality review of data and effective interaction with study sites.<\/p><p>As a<span> <\/span><b>Clinical Trial Coordinator<\/b>, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract. Additional key responsibilities include:<\/p><ul><li>Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools<\/li><li>Reviews regulatory documents for proper content<\/li><li>Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified<\/li><li>Disseminates","hiringorganization":{"name":"Thermo Fisher Scientific"},"employmenttype":"FULL_TIME","identifier":{"value":"R-01186252","name":"Thermo Fisher Scientific"},"responsibilities":"At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Our clinical department defines, develops and delivers clinical programs, ensuring the highest-quality review of data and effective interaction with study sites. As a Clinical Trial Coordinator, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract. Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools. Reviews regulatory documents for proper content. Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified. Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments. Assists with the identification of potential investigators and development\/distribution of initial protocol packets. Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes. Responsible for adhering to Good Clinical Practices, country specific regulations, PPD\/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical\/clinical aspects of project implementation, execution, and closeout.","workhours":"40 hours per week","directapply":"false","skills":"Clinical Trial, Good Clinical Practices, CLINICAL RESEARCH, Development, Project Administration, Regulatory, Organisational, RESEARCH, Potential, Clinical, Project Tracking, Project Implementation, Distribution, Practice, PPD, Training, Efficiency, Technical Support, english, Senior Clinical Research Assistant & Data Manager, Clinical Research Consultant, Associate Research Manager, Principal Research Assistant, Senior Statistical Programmer, Leiomyosarcoma Implementation Consultant, Clinical Data Manager II, Clinical Research Technician, Research Associate It & Dissemination, Protocol Manager","experiencerequirements":null,"occupationalcategory":"Klinikiniai tyrimai","page_url":"https:\/\/jobs.thermofisher.com\/lt\/lt\/job\/TFSCGLOBALR01186252EXTERNALLTLT\/Clinical-Trial-Coordinator-Netherlands"}