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SR SAFETY REPORTING SPECIALIST

Full time Tiempo completo

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. essential functions receives, prepares and submits safety reports to applicable parties. ensures that all reports are compliant with regulatory timelines and country legislation and monitors this on a regular basis.  leads large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines.  provides input and feedback to aid the development of program and departmental procedural documents.  shares ideas and suggestions with team members. takes an active role in the development and implementation of ideas and suggestions.  liaises with relevant departments around safety reporting tasks and attends various meetings as required.  provides input, feedback and guidance to other team members and mentors new starters. ...


CLINICAL SUPPLIES OVERSIGHT MANAGER

Full time Tiempo completo

At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. we are seeking a in our global clinical supplies team. the role can be fully homebased. this role manages the full supply chain oversight for high complex global clinical trials. ensures project/study activities are in compliance with company and client requirements. mentors, trains and provides on-going support to junior team members. may act as main contact and escalation point for assigned clients. provides consultation services to clients and may develop and update client-specific manuals. builds and maintains client relationships. a day in the life develops study specific plans for each assigned project. meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets. integrates all clinical supplies activities into the su...


PV COORDINATOR

Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.discover impactful work:provides administrative safety support to the pharmacovigilance (pv) department. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to pv safety. may mentor or train new pv safety administration staff.a day in the life:• provides assistance and liaises with relevant teams and departments on a various range of administrative pv safety tasks, including audit readiness activities, meeting organisation, minute taking, filing, photocopying, work distribution, reconciling reports, end of day emails completing metrics and updating ppd systems with project allocation.• responsible for extract...


PROJ MGR CLIN SUPPLIES

Join to apply for the proj mgr clin supplies role at thermo fisher scientific continue with google continue with google join to apply for the proj mgr clin supplies role at thermo fisher scientific work schedule
standard (mon-fri) environmental conditions
office 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. the role
we are seeking an associate project/project manager to join our global clinical supplies team. this can be office based, hybrid, or fully homebased. a day in the life
this role provides complete oversight of supply chain for sophisticated global clinical trials. ensures project/study activities are in compliance with company and client requirements and acts as a representative for the department on all assigned projects. key responsibilities:
develops study specific plans for ...


LOGISTICS SPECIALIST I

Work schedule standard (mon-fri) environmental conditions office job description logistics specialist i join thermo fisher scientific inc. and excel in an exceptionally dynamic role as a logistics specialist i in bogota. this position offers a fantastic opportunity to collaborate with a world-class team and successfully implement logistics operations critical to advancing clinical projects. responsibilities coordinate product receipts from the arrival at our facilities until release in the gpm system. process medication and supply orders to medical facilities and request receipt acknowledgments. collaborate on new project initiations and coordinate with medical centers for shipment and return of materials. generate administrative starts for projects, crafting necessary folders and forms. monitor material transfer processes and request final product disposals. advise medical centers on shipment procedures, storage conditions, and documentation. detect and report deviations, complete investigations, and propose process improvements. collaborate in reception, dispatch, and return processes, ensuring deadlines are met. perform monthly service registrations, attend to comments, and ensure timely registration. develop metrics for suppliers, performance indicators, and reports for customers. complete all activities efficiently and safely. requirements bachelor's degree in engineering, logistics operations, health areas, administration, or related fields. at least one year of experience in similar tasks within the pharmaceutical industry or logistics companies. knowledge of gxp sta...


PV COORDINATOR

Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. discover impactful work: provides administrative safety support to the pharmacovigilance department. specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to safety reporting. may mentor or train new central safety reporting admin staff. a day in the life: • responsible for the submission of safety reports to applicable parties, including subsequent scanning, indexing and filing (both electronic and paper), safety tracker completion and quality check, and archiving in accordance with ...


VENDOR MANAGEMENT COORDINATOR

Work schedule standard (mon-fri) environmental conditions office job description are you an ambitious and proven professional looking for an exceptional opportunity to showcase your strong work ethic and skills? thermo fisher scientific inc. is seeking an individual with a track record of success in vendor management to join our world-class team of researchers. as a leader in the scientific industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. responsibilities: collaborate with cross-functional teams to determine vendor requirements and establish sourcing strategies manage vendor relationships and contracts, ensuring flawless execution and delivery conduct market research and competitive analysis to identify potential vendors develop and implement vendor performance metrics and conduct regular evaluations drive continuous improvement initiatives to optimize vendor management processes requirements: bachelor's degree in business administration or related field, or equivalent experience in the industry. previous experience in vendor management or procurement strong analytical and negotiation skills excellent communication and interpersonal skills proven ability to successfully implement vendor management strategies at thermo fisher scientific, we value diversity and inclusivity. we believe that collaboration and different perspectives drive innovation and lead to exceptional results. we are an equal opportunity employer and strictly prohibit discrimination based on race, color, religion, sex, sexual orientation, gender identity,...


LOGISTICS SPECIALIST I

Join to apply for the logistics specialist i role at thermo fisher scientific join to apply for the logistics specialist i role at thermo fisher scientific work schedule
standard (mon-fri) environmental conditions
office logistics specialist i join thermo fisher scientific inc. and excel in an exceptionally dynamic role as a logistics specialist i in bogota. this position offers a fantastic opportunity to collaborate with a world-class team and successfully implement logistics operations critical to advancing clinical projects. responsibilities
coordinate product receipts from the arrival at our facilities until release in the gpm system. process medication and supply orders to medical facilities and request receipt acknowledgments. collaborate on new project initiations and coordinate with medical centers for shipment and return of materials. generate administrative starts for projects, crafting necessary folders and forms. monitor material transfer processes and request final product disposals. advise medical centers on shipment procedures, storage conditions, and documentation. detect and report deviations, complete investigations, and propose process improvements. collaborate in reception, dispatch, and return processes, ensuring deadlines are met. perform monthly service registrations, attend to comments, and ensure timely registration. develop metrics for suppliers, performance indicators, and reports for customers. complete all activities efficiently and safely.
requirements
bachelor's degree in engineering, logistics operatio...


PROJ MGR CLIN SUPPLIES

Work schedule standard (mon-fri) environmental conditions office job description at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. the role we are seeking an associate project/project manager to join our global clinical supplies team. this can be office based, hybrid, or fully homebased. a day in the life this role provides complete oversight of supply chain for sophisticated global clinical trials. ensures project/study activities are in compliance with company and client requirements and acts as a representative for the department on all assigned projects. key responsibilities: develops study specific plans for each assigned project. meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets. integrates all clinical supplies activities into the supply chain to support p...


KEY ACCOUNTS MANAGER, GENETIC SCIENCES

Join to apply for the key accounts manager, genetic sciences role at thermo fisher scientific continue with google continue with google join to apply for the key accounts manager, genetic sciences role at thermo fisher scientific work schedule
standard (mon-fri) environmental conditions
office the role is to drive sales for gsd portfolio (real-time pcr, ce, dpcr, kits, and consumables into research, biotech, clinical markets. the role holder will use their technical, commercial knowledge and external context to contribute to and deliver profitable initiatives that build sales. the role holder will work closely with sales team for related product lines and applications to achieve sales figures. responsibilities include crafting, implementing, tracking, and reporting performances of the sales plan, targets, and forecasts. drive our clinical solutions by working with marketing and global business units. partner with our channels in the region and direct sales teams in colombia to identify and develop potential leads. the role is home based in bogotá-colombia. additional responsibilities are:
build pipeline of opp to support reaching aop for central latam subregion in academy, biotech’s and clinical segment drive business expansion in collaboration with support, sales, and market development drive adoption of our npis and continuous technical knowledge work together with local sales colleagues to ensure all possible actions are done to secure business in driven situations set up and undertake complex sales, anticipate pipeline changes, and has plans ...


SR PROJECT COORDINATOR

Join to apply for the sr project coordinator role at thermo fisher scientific join to apply for the sr project coordinator role at thermo fisher scientific work schedule
standard (mon-fri) environmental conditions
office 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. the role
we are seeking a senior project coordinator to join our global clinical supplies team. this role can be fully homebased. a day in the life
provides administrative and technical support to our global clinical supplies project team including planning, organizing and coordinating responsibilities of project administration. maintains procedures, guidelines and documentation. assists with maintaining project records and ensuring that all regulatory documents are correct, processed and approved. completes data entry and supports mai...


PV COORDINATOR

Full time Tiempo completo

At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. discover impactful work: provides administrative safety support to the pharmacovigilance department. specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to safety reporting. may mentor or train new central safety reporting admin staff. a day in the life: •responsible for the submission of safety reports to applicable parties, including subsequent scanning, indexing and filing (both electronic and paper), safety tracker completion and quality check, and archiving in accordance with sop’s and wpd’s. resolves simple problems with submission packs within minimal inp...


[I-643] - LOGISTICS SPECIALIST I

**actividades**: coordinar y dar cumplimiento a las actividades relacionadas con los proyectos a nível local. esto implica realizar, verificar, asesorar, documentar, generar reportes y mantener el flujo de comunicación dentro del equipo del proyecto para los procesos de recepción, almacenamiento, preparación y embalado de envíos, despacho, devolución, etiquetado/re-etiquetado, reconciliación y destrucción de medicamentos y de suministros clínicos. revisar e implementar los procesos de operaciones logísticas y de control de gestión operativa del establecimiento tercerista contratado por fisher clinical services. estas actividades se realizarán siguiendo las buenas prácticas de fabricación, almacenamiento y distribución, minimizando la cantidad de desvíos en calidad. todas estas operaciones logísticas deberán ser llevadas a cabo de acuerdo a las especificaciones, procedimientos, instrucciones y herramientas informáticas/administrativas requeridas por la compañía y/o cliente. **requisitos básicos mínimos**: - conocimientos de normas gmp, bioseguridad, regulaciones locales y sops. - paquete microsoft office. **evaluación de excel intermedio.**: - experiência en actividad logística y almacenamiento en productos farmacéuticos. **educación/experiência**: - graduados en áreas de la salud, ingeniería, operaciones logísticas, administración. - experiência de hasta **2/3 años en tareas similares en industria farmacéutica, cros, o compañías similares de logística.** idiomas**:inglés oral y escrito nível intermedio-se evaluará escritura.** **habilidades y/o competencia...


[VYL719] REGULATORY AFFAIRS SPECIALIST II

Work schedule standard (mon-fri) environmental conditions office responsabilidades: ejecutar actividades de solicitud, seguimiento y control de documentación requerida para la solicitud de los registros sanitarios de la compañía. solicitar información técnica y legal a los sitios de manufactura, y realizar la evaluación y preparación de expedientes regulatorios para la obtención y/o mantenimiento de registros sanitarios del portafolio de productos de thermo fisher en colombia, ecuador y países de la región centroamérica. realizar seguimiento a procesos de renovación de registros sanitarios consolidación y cargue de información requerida para dar cumplimiento con el estándar semántico para dispositivos médicos y reactivos de diagnóstico in vitro. mantenimiento de las bases de datos de registros sanitarios y tracking de procesos en curso en las plataformas corporativas dar seguimiento a los trámites regulatorios en curso. brindar soporte a los distribuidores en la obtención de documentos regulatorios. competencias técnicas: educación: químico farmaceútico, químico biólogo parasitólogo, bacteriólogo o áreas afines a la salud entre 3 y 5 años de experiência en la industria, específicamente en el área de asuntos regulatorios relacionados con reactivos de uso exclusivo en investigación (ruo), reactivos de diagnóstico in vitro (ivd) y dispositivos médicos ante el invima. conocimientos en la normativa local aplicable a productos para reactivos de uso exclusivo en investigación (ruo), reactivos de diagnóstico in vitro (ivd) y dispositivos médicos manejo y anális...


(CW-278) SCIENTIST II, FIELD APPLICATIONS

**objetivo de la función** brindar soporte científico a clientes, vendedores y distribuidores. las principales responsabilidades incluyen: 1) actuar en preventa, cuando sea necesario, siendo un consultor técnico ofreciendo a los clientes potenciales información técnica y demostraciones de productos que les ayuden en su decisión de compra; 2) brindar capacitación, asesoramiento técnico y solución de problemas a los usuarios de productos thermo fisher scientific, ya sea en campo o de forma remota; 3) capacitar a los clientes internos; 4) participar en congresos y eventos científicos del área (incluso como disertante). **responsabilidades** brindar capacitación y soporte técnico-científico a clientes internos y externos a través de visitas técnicas, teléfono o por correo electrónico, además de actividades secundarias como: visitas técnicas con el equipo comercial y participación en eventos de marketing. participar en eventos virtuales o presenciales realizados por la casa matriz para demostración de nuevas aplicaciones de productos y servicios. orientar al cliente en la elección del mejor producto y metodología, con el objetivo de satisfacer sus necesidades. ser capaz de asistir al cliente en la resolución de problemas de moderada complejidad relacionados con el uso de los productos de la empresa. demostrar equipos y reactivos en el centro de capacitación de la empresa o en los laboratorios de los clientes. asumir responsabilidades operativas y desarrollarse en las áreas de negocios corporativos a través de la ejecución de sus proyectos internos y demandas interdepartamenta...


RZS163 ANALISTA JR DE CONTABILIDAD

Funciones y responsabilidades: relevar y tener registro de contratos existentes entre el cliente y la compañía y solicitar los contratos faltantes. analizar las especificaciones contractuales en el momento de efectuar la facturación y pedir información adicional que avale los servicios prestados y no mencionados en el contrato. soportar el cierre financiero mensual para chile, colombia y perú. actualizar y dar seguimiento a la planilla de cobranzas. brindar soporte a la gerencia del área en tareas tales como: consultas bancarias, análisis de gastos, análisis de proveedores. analizar estados contables. participar en la creación de nuevas herramientas para optimizar los procedimientos del área. colaborar en el permanente fortalecimiento de los circuitos de control interno. desarrollar todas las actividades de manera eficiente y segura. otras tareas pueden ser requerida a fin de cumplir con los requerimientos del negocio. requisitos básicos mínimos: conocimientos de excel, outlook, paquete microsoft office, internet. sistema de gestión de finanzas conocimiento contable educación/experiência: estudiantes o graduados en áreas de contabilidad y/o finanzas sin experiência o experiência de hasta 1 año en tareas similares....


CB-376 LOGISTICS ASSOCIATE III

Descripcion:brindar soporte en los procesos de recepción, almacenamiento, preparación y embalado de envíos, despacho, devolución, etiquetado/re-etiquetado, reconciliación y destrucción de medicamentos y de suministros clínicos y demás actividades relacionadas con los proyectos a nível regional. generar reportes, marcar transacciones en sistema, generar reporte, actualizar información de trazabilidad de diferentes procesos. estas actividades se realizarán siguiendo las buenas prácticas de fabricación, almacenamiento y distribución, minimizando la cantidad de desvíos en calidad. todas estas operaciones logísticas deberán ser llevadas a cabo de acuerdo a las especificaciones, procedimientos, instrucciones y herramientas informáticas/administrativas requeridas por la compañía y/o cliente. funciones y responsabilldades: brindar asistencia al sector de coordinadores de proyectos, en el procesamiento de órdenes de envío, preparación de documentación requerida por los terceros para tal fin, coordinación de fechas de entrega con los centros, entre otros. a nível regional. soporte en el proceso de recepciones y documentación relacionada, a nível regional. ingreso de datos en tracking de recepciones, envíos y otros procesos críticos. actualización de estados de órdenes en el sistema. generación de reportes, métricas y otros. revisión de diferentes tipos de reportes como registros de temperaturas, compras, facturación. programación y seguimiento de devoluciones. seguimiento a retorno de cajas reutilizables e ingreso al sistema. brindar soporte y seguimiento a las actividades ...


REGULATORY AFFAIRS SPECIALIST II N-93

**work schedule** standard (mon-fri) **environmental conditions** office **responsabilidades**: - ejecutar actividades de solicitud, seguimiento y control de documentación requerida para la solicitud de los registros sanitarios de la compañía. - solicitar información técnica y legal a los sitios de manufactura, y realizar la evaluación y preparación de expedientes regulatorios para la obtención y/o mantenimiento de registros sanitarios del portafolio de productos de thermo fisher en colombia, ecuador y países de la región centroamérica. - realizar seguimiento a procesos de renovación de registros sanitarios - consolidación y cargue de información requerida para dar cumplimiento con el estándar semántico para dispositivos médicos y reactivos de diagnóstico in vitro. - mantenimiento de las bases de datos de registros sanitarios y tracking de procesos en curso en las plataformas corporativas - dar seguimiento a los trámites regulatorios en curso. - brindar soporte a los distribuidores en la obtención de documentos regulatorios. competencias técnicas: - educación: químico farmaceútico, químico biólogo parasitólogo, bacteriólogo o áreas afines a la salud - entre 3 y 5 años de experiência en la industria, específicamente en el área de asuntos regulatorios relacionados con reactivos de uso exclusivo en investigación (ruo), reactivos de diagnóstico in vitro (ivd) y dispositivos médicos ante el invima. - conocimientos en la normativa local aplicable a productos para reactivos de uso exclusivo en investigación (ruo), reactivos de diagnóstico in vitro (ivd) y dis...


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