At ABB, we are dedicated to addressing global challenges. Our core values: care, courage, curiosity, and collaboration - combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to empower everyone to create sustainable solutions.Write the next chapter of your ABB story.This position reports toRegional Product Group ManagerYour role and responsibilitiesIn this role, you will have the opportunity to act as a design authority for an engineering discipline with low to medium complexity for SCADA and Control & Protections assignments. Each day, you will complete assignments on small projects or portions of larger projects in a cost-effective manner. You will also showcase your expertise by applying basic design thinking/design for excellence concepts in projects.The work model for the role is: Hybrid {}This role contributes to the Electrification business area, and their Distribution Solutions division in Chile. Your main stakeholders will be both internal and external customers from the Operations and Engineering areas.You will be mainly accountable for: Development of engineering for Control & Protections and SCADA systems Evaluating, selecting and applying standard techniques and procedures to carry out engineering tasks. Integration and control of suppliers of the assigned resources Communicating with customers Support in activities associated to the integration, testing, installation and adequate performance of Control & Protections and SCADA. Preparation of project documents within the deliverable scope.Qualifications For The RoleYou desirably have over five (5) years of experience in the execution of tasks related to Control & Protection and SCADA engineering, being able to develop SCADA architectures as required, and have experience in the configuration and development of SCADA applications.You have an intermediate English level and can hold technical conversations independently, as well as are able to communicate effectively with customers overseas.You are an autonomous, knowledge driven and solution oriented professional. You can exercise technical leadership and can communicate technical information with ease to stakeholders at all levels of an organization.You have a professional degree in Electrical, Electronics, Telecommunications or Automation EngineeringYou have availability to travel when assignments require it.More about usWe value people from different backgrounds. Apply today for your next career step within ABB and visit www.abb.com to learn about the impact of our solutions across the globe. #MyABBStory94210490 Nivel de antigüedad: No correspondeTipo de empleo: Jornada completaFunción laboral: Ingeniería y Tecnología de la informaciónSectores: Fabricación de electrodomésticos y productos eléctricos y electrónicos

DescriptionClinical Trial ManagerSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.Discover what our 29,000 employees, across 110 countries already know:WORK HERE MATTERS EVERYWHEREWhy Syneos HealthWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.Job Responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT). Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/Central Monitors) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Employs strategic thinking and problem-solving skills to propose and implement risk mitigations. Participates and presents in key meetings such as Kick Off Meeting. Serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members. This may include accompanying CRA team members to sites for observation or conflict resolution. Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. Ensures CTMS, dashboards and other systems are set up and available for use by the clinical team, including overseeing user acceptance testing (UAT) as needed. Ensures access and audit trail reviews are conducted as required. Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans and timelines for the study. Oversees resourcing allocations for CRAs and Central Monitors, site assignments and study team members' conduct, and identifies risks to delivery or quality. Ensures quality of the clinical monitoring, central monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and / or tracking tools. Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs),Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency) according to plan. Understands the monitoring strategy required for the study and, where required, participates in the development of the study risk assessment plan. Is accountable for their assigned clinical team members' understanding, ongoing compliance and delivery according to the stated monitoring strategy, CMP/SMP, and risk plans. Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity. Document requested revisions and approvals in CTMS. Ensures these deliverables are provided according to company and/or sponsor specifications, including delivery deadlines. Interacts with the client and other functional departments related to clinical monitoring, central monitoring and site management activities and deliverables. Provides status updates on the clinical deliverables and risks to clients, project management and leadership as per departmental or study agreements. Provides solutions for obstacles in protocol execution and site management. Demonstrates understanding of other functions' roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations. This may include data management, study start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central Monitors assigned to the study and routinely assesses study-specific process and training compliance, CMP compliance, and identifies emerging risks. May develop and support execution of corrective action plans at site and study level. Supports and completes activities to achieve data cut and lock deadlines. Provides feedback to line managers on staff performance including strengths as well as areas for development.QualificationsWhat we’re looking for Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience Ability to lead and align teams in the achievement of project milestones Capable of working in an international environment Previous clinical trial experience in site management Preferred experience with risk-based monitoring and clinical or central monitoring Familiar with financial principles and budget management practices Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills Good communication, presentation and interpersonal skills among project team and with sites Basic conflict resolution skills Ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project. Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues Moderate travel may be required, approximately 20%Get to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos HealthAdditional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Nivel de antigüedad: IntermedioTipo de empleo: Jornada completaFunción laboral: Investigación, Analista y Tecnología de la informaciónSectores: Investigación biotecnológica, Fabricación de productos farmacéuticos y Servicios de investigación

¿Quiénes somos?Somos la empresa de tecnología y negocios más prestigiosa de Iberoamérica. Nuestra red regional permite responder rápidamente a la demanda, con especialistas en cada problemática y aplicando innovación tecnológica a cada negocio.📢 ¿Qué buscamos?Nos encontramos en la búsqueda de un Project Manager Senior con Certificación SAP Business One y experiencia funcional – Excluyente. ¿Qué tareas deberá hacer el perfil que se sume?Establecer los objetivos, plazos y cronograma del proyecto.Asignar las tareas a los equipos y supervisar su progreso.Controlar la eficiencia, el progreso y la calidad del proyecto.Detectar problemas a tiempo y tomar medidas para minimizarlos, dentro de otras funciones. 💪 ¿Qué necesitamos? (requisitos )Contar con experiencia comprobable como PM con experiencia funcional.Contar con certificación SAP Business One. (Excluyente)Disponibilidad para trabajar por proyecto con posibilidad de extensión. Completa disponibilidad para trabajar en modalidad presencial en Santiago centro. !!Considera los requisitos antes de postular!! Mucho Éxito. Nivel de antigüedad: IntermedioTipo de empleo: Jornada completaFunción laboral: Tecnología de la informaciónSectores: Servicios y consultoría de TI

¿Buscas estabilidad laboral, un excelente ambiente de trabajo y oportunidades para desarrollarte profesionalmente? ¡Esta es tu oportunidad! En Sertus, valoramos el compromiso, la responsabilidad y las ganas de crecer.¿Qué ofrecemos?Sueldo: $700.000 Liquido Horario: Lunes - Jueves: 08:30 a 18:30 hrsViernes 08:30 a 17:30 hrsColación Funciones principales: •⁠ ⁠Cumplir con requisitos del sistema de gestión y de la norma NCh-ISO 17025 vigente. •⁠ ⁠Ayudar en la recepción y entrega de equipos a clientes. •⁠ ⁠Ingreso en sistema informático y etiquetado de equipos. •⁠ ⁠Realizar toma de datos supervisado (calibración/ensayo) durante los procesos en laboratorio. •⁠ ⁠Realizar lectura y análisis de fichas técnicas y/o manuales de equipos a calibrar/ensayar •⁠ ⁠Identificar si existen anomalías de datos obtenidos en o durante la calibración/ensayo •⁠ ⁠Digitalización de resultados en formularios de certificados/informes. •⁠ ⁠Realizar verificaciones intermedias y mantenciones a equipos patrones. •⁠ ⁠Mantener limpio y ordenado áreas de trabajo y laboratorio en general. ¿Qué buscamos?-Conocimiento en norma NCh/ISO 17025 vigente.-Conocimiento de equipos patrones y equipos a calibrar/ensayar. -Experiencia en ensayos a medidores eléctricos.¡Te esperamos para construir juntos un futuro lleno de logros y crecimiento! Nivel de antigüedad: No correspondeTipo de empleo: Jornada completaSectores: Servicios de recursos humanos

Empresa líder en la gestión medioambiental con presencia nivel nacional, requiere incorporar a importante proyecto a Conductores Profesionales para operar camiones de recolección en la RM, con base ubicada en Quilicura.El servicio es un importante proyecto de sustentabilidad, donde se busca obtener de manera selectiva los residuos clasificables como reciclables, los cuales pueden tener una segunda utilidad y así contribuir de una manera más eficiente a la gestión de residuos.La principal función es conducir camiones de recolección para el retiro de residuos reciclables, esto según plan de trabajo y rutas establecidas por la supervisión, siguiendo normas de seguridad.Requisitos Experiencia en conducción de alto tonelaje (Comprobable) Poseer Licencia de conducir profesional A2 Ley 18.290 o A4 – A5 Ley 19.495. Disponibilidad para trabajar de lunes a viernes de 08:00 a 16:00 horas, sábado de 08:00 a 15:00 horas. Conocimientos básicos de utilización de app smartphone Disponibilidad inmediata, para comenzar la última semana de septiembreCondiciones LaboralesRenta liquida de $ 700.000 + variables Nivel de antigüedad: IntermedioTipo de empleo: Contrato por obraFunción laboral: Gestión y ManufacturaSectores: Servicios medioambientales

Importante empresa del rubro textil requiere incorporar a su equipo de trabajo Vendedor Full Time para tiendas de Región Metropolitana.Este Talento Será Responsable DeGestionar Venta de productos de nuestra tiendaAtención al cliente Recepción y Reposición de mercadería Toma de inventariosRequisitosEnseñanza media completa Experiencia en Venta Manejo de Estrategias de Ventas Disponibilidad para trabajar Full Time 44 horas semanales (Horario Mall)Ofrecemos Renta Líquida 560.000 + Comisiones Contrato inicial a plazo fijo, para luego y según evaluación de desempeño acceder a indefinido con beneficios asociados, tales como: Descuento en Productos de la tienda. Seguro Complementario de Salud. Aguinaldo en fechas patrias y navidad, entre otrosComo organización, valoramos la inclusión, por lo que nuestras vacantes están alineadas con la Ley 21.690 de Inclusión Laboral. ¡Te invitamos a postular con nosotros y ser parte de nuestro gran equipo! Nivel de antigüedad: IntermedioTipo de empleo: Contrato por obraFunción laboral: Ventas y Desarrollo empresarialSectores: Comercio al por menor de prendas de vestir y moda

¿Tienes ganas de hacer la diferencia y alcanzar tu mejor versión? En Walmart Chile nos transformamos día a día con orgullo y pasión para brindar la mejor experiencia omnicanal y generar un impacto real en nuestros colaboradores, clientes y comunidades. Somos el Retail minorista más grande del mundo y el tercer empleador más grande de Chile. En Chile nos puedes encontrar a través de nuestras plataformas digitales Lider App y lider.cl, y nuestros formatos Lider, Express de Lider, Super Bodega aCuenta y Central Mayorista. ¡Pero eso no es todo! Para lograr la experiencia de compra de excelencia que buscamos, contamos también con nuestras plantas productivas y centros de distribución. La diversidad, el desarrollo y el bienestar de nuestros colaboradores nos moviliza y son parte de nuestro ADN. Somos personas trabajando para personas y buscamos que puedas potenciar tu talento con nosotros. Únete a nuestro propósito de Ahorrarle dinero a nuestros clientes para que puedan vivir mejor y acompáñanos a impactar a más de miles de familias.Descripción del Rol El team de Health & Safety está buscando a su próximo/a Prevencionista de Riesgos para hacer la diferencia en nuestro equipo de Gerencia Ética y Cumplimiento, reportando a Supervisor Health & Safety Lider. Valoramos tu historia y eso que nos hace únicos. Es por eso que impulsamos un ambiente de trabajo inclusivo, en donde puedes ser tu mejor versión y hacer la diferencia junto a nosotr@s. *Esta oferta laboral se rige bajo la Ley Nº 21.015 que incentiva la inclusión de personas con discapacidad al mundo laboral. Tus principales desafíos serán:Asesorar y dirigir acciones preventivas que se enfoquen a disminuir la tasa de accidentabilidad y siniestralidad de la unidad de negocio a cargo, focalizando el trabajo colaborativo con la operación para lograr objetivos.Aplicar y gestionar el cumplimiento de los protocolos MINSAL, Protocolos Internacionales y Programa de Higiene Ocupacional.Comunicar de manera efectiva a las líneas de mando, respecto a los lineamientos de H&S. Hacer uso de medios comunicación efectivos, que permitan un alcance mayor a la operación.Revisión, seguimiento y control a las actividades relacionadas a controlar emergencias que afecten la continuidad operacional de Walmart Chile.Realizar seguimiento al programa de trabajo de terceras partes (EE.CC). Revisión y auditorias establecidas para el control documental y legal en plataforma SICOP.Integrar y dar seguimiento a las plataformas digitales que almacenan data de gestión, tanto interna como externa (mutual de seguridad).Gestionar procesos KPI y organizar funcionalmente proyectos propios y de sus reportes.Realizar gestión preventiva de multas. Identificar causas principales que afecten al negocio. Dando seguimiento mensual de cada uno de los centros de trabajo identificando los incumplimientos regulatorios.¿Qué esperamos de ti?Eres Ingeniero/a en Prevención de Riesgos.Tienes experiencia aplicando el rol de Prevencionista de Riesgo. Te manejas con Microsoft Office en un nivel Básico-Intermedio.Tienes Disponibilidad para Trabajar a Plazo Fijo .Nuestros BeneficiosPotenciamos tu bienestar para que puedas vivir mejor, por eso contamos con muchísimos beneficios para ti. Te dejamos algunos:Cuida a los tuyos: Sabemos lo importante que es tu familia por eso te entregamos hasta un mes con goce de sueldo para cuidarlos en caso de enfermedades catastróficas o accidentes graves.Asesoría Financiera: Te entregamos orientación y asesorías relacionadas con la protección y planificación de tus finanzas personales y familiares. Seguro complementario de salud: ¡La salud es lo primero! por eso te ofrecemos un seguro de salud complementario a tu sistema previsional, que cubre distintas prestaciones.Convenios con gimnasios: Ejercita tu cuerpo a un solo click con precios preferenciales con gimnasios en convenio.*Los beneficios dependerán de las condiciones de contrato y antigüedad, formato y/o unidad de negocio de Walmart Chile* Si quieres conocer más de nuestra Compañía, ingresa a: https://www.somoswalmartchile.cl/ Nivel de antigüedad: Algo de responsabilidadTipo de empleo: Jornada completaFunción laboral: Control de calidadSectores: Comercio al por menor de comestibles y Comercio al por menor

AVEVA is a global leader in industrial software. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals and minerals – safely, efficiently and more sustainably.We’re the first software business in the world to have our sustainability targets validated by the SBTi, and we’ve been recognized for the transparency and ambition of our commitment to diversity, equity, and inclusion. We’ve also recently been named as one of the world’s most innovative companies.If you’re a curious and collaborative person who wants to make a big impact through technology, then we want to hear from you! Find out more at AVEVA Careers.For more information about our privacy policy and how to manage cookies, visit our Privacy Policy.Location: Santiago, Chile (Remote with once-a-week meetings with local team)Time zone: Working with clients/vendors/teams from Argentina, Chile and USKey Responsibilities - You will do:Manage the collection of outstanding accounts receivable.Communicate with clients to follow up on overdue payments.Reconcile accounts and resolve discrepancies.Prepare and send invoices.Provide regular reports on receivables status to management.Collaborate with other departments to ensure smooth workflow.Requirements - You will have:3+ years of experience in accounts receivable or a related role.Strong attention to detail and organizational skills.Excellent communication and interpersonal skills.Proficiency in accounting software and MS Office (especially Excel).Ability to work independently and as part of a team.English language proficiency - Advanced/bilingualOracle knowledge or experience (A PLUS)AVEVA requires all successful applicants to undergo and pass a comprehensive background check before they start employment. Background checks will be conducted in accordance with local laws and may, subject to those laws, include proof of educational attainment, employment history verification, proof of work authorization, criminal records, identity verification, credit check. Certain positions dealing with sensitive and/or third party personal data may involve additional background check criteria.AVEVA is an Equal Opportunity Employer. We are committed to being an exemplary employer with an inclusive culture, developing a workplace environment where all our employees are treated with dignity and respect. We value diversity and the expertise that people from different backgrounds bring to our business.Come and join AVEVA to create the transformative technology that enables our customers to engineer a better world. Nivel de antigüedad: Sin experienciaTipo de empleo: Jornada completaFunción laboral: Contabilidad/Auditorías y FinanzasSectores: Desarrollo de software