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RRHH en más de 180 países, impulsamos tu crecimiento profesional, tus proyectos y tus éxitos.Iniciamos proceso interno para incorporar un/a.Business Development Specialist.Toledo (y Madrid Sur), con experiencia específica en apertura de mercado y.Se unirá a nuestro división de Staff Leasing Es

En Grupo Bimbo estamos en busca de colaboradores que quieran alimentar un mundo mejor.Quieres ser parte de una gran empresa que alimenta el mundo con grandes acciones?.Es tu oportunidad de colaborar con nosotros y pertenecer a una gran comunidad global que se encarga de llevar alimentos deliciosos y

En Grupo Bimbo estamos en busca de colaboradores que quieran alimentar un mundo mejor. ¿Quieres ser parte de una gran empresa que alimenta el mundo con grandes acciones? Es tu oportunidad de colaborar con nosotros y pertenecer a una gran comunidad global que se encarga de llevar alimentos deliciosos y nutritivos a las manos de todos. Grupo Bimbo es la mayor empresa de panificación del mundo. Estamos presentes en 39 países y cuatro continentes: América, Europa, África y Asia. Fabricamos más de 13.000 productos diferentes en categorías como pan, dulce, galletas y pan tostado. ¡Seguimos creciendo! Actualmente estamos buscando un Technical Services Technician. Misión: En dependencia del Manager de Servicios Técnicos , la misión principal es trabajar en la mejora de procesos en nuestras líneas de producción y en la implementación de nuevas tecnologías en todas las categorías en las que operamos . Funciones: • Escalar de la mano de los técnicos de I+D las recetas y procesos a nivel industrial en nuestras plantas de fabricación, para lo cual se necesita formación técnica y experiencia en el sector ., • Será necesario tener conocimiento sobre las materias primas y procesos necesarios en la industria de panificación para lo cual se requerirá poder interactuar con proveedores de ingredientes y maquinaria., • Es imprescindible tener disponibilidad para viajar a las diferentes fábricas que Bimbo Iberia tiene en España y Portugal así como viajar al extranjero si fuera necesario. Aproximadamente viajará un 50% de su tiempo., • Conocimiento avanzado de los procesos de panificación y pastelería., • Capacidad para innovar e investigar en nuevas tecnologías y procesos industriales., • Desempeñará el 100% de su trabajo en las fábricas y líneas de producción para lo cual ha de ser una persona que le apasione el control de procesos industriales y puesta a punto de nueva maquinaria y nuevos productos., • Se valorará experiencia en mejora continua ( Lean Manufacturing ) Requisitos: • Grado en Ingeniería Química, • Inglés medio / alto, • Excel Avanzado, • De 1 - 3 años de experiencia en posición similar Competencias: • Capacidad para trabajar en equipo, • Habilidades en comunicación, • Empatía, • Habilidades para trabajar en un entorno industrial bajo presión. “Le informamos que, de conformidad con la Ley Orgánica 3/2018, de Protección de Datos Personales y Garantía de los Derechos Digitales (LOPDGDD) y el Reglamento (UE) 216/679 General Europeo de Protección de Datos (RGPD), los datos personales que nos facilita quedarán almacenados en un fichero “Gestión de Personal” registrado por BIMBO (con denominación social BAKERY IBERIAN INVESTMENTS, S.L.), con la finalidad de analizar su perfil profesional a los efectos de hacerle partícipe en los procesos de selección que se desarrollen en BIMBO a la vista de los puestos/becas vacantes o de nueva creación que se originen periódicamente. “Asimismo, Vd. puede ejercer los derechos de acceso, rectificación, supresión, limitación, portabilidad y oposición, así como llevar a cabo cualquier aclaración dirigiéndose a BIMBO con domicilio en C/ Josep Pla, nº 2 Edificio B mar – 08019 BARCELONA adjuntando copia de su D.N.I. o documento identificativo, o a través del correo electrónico a la cuenta (adjuntando esta copia de su D.N.I. o documento identificativo o firmándolo con firma electrónica reconocida).

Planet Pharma are partnered with a leading global client who specializes in delivering high-quality home-based healthcare solutions. Established by clinical nurse specialists, the organisation offers tailored nursing services across diverse therapy areas, including drug administration, patient education, and clinical trial support. Our client is looking for experienced freelance nurses with a strong background in clinical trials or home visits to provide ad-hoc, home-based clinical services. Key Requirements: • Set up as a freelancer/Sole Trader, • Venipuncture, • Use of centrifuge, • ECG (performance only – interpretation not required), • Cannulation, • Port-a-Cath access & de-access, • Injection administration, • Owns a car and willing to travel, • Available for ad-hoc work About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Charlotte Fagan (Recruitment Manager) at Planet Pharma for more information: E: T:

Energizing a new world with Exide Technologies About us Exide Technologies () is an internationally leading provider of innovative and sustainable battery storage solutions for automotive and industrial applications. With more than 135 years of experience, Exide has developed and globally marketed innovative batteries and systems, contributing to the energy transition and driving a cleaner future. Exide Technologies' culture and strategy are centred on recycling, sustainability, and environmental responsibility. The company has 11 manufacturing and 3 recycling facilities across Europe, ensuring resilience and a low CO2 footprint with a local supply chain. With a team of 5,000 employees, we provide €1.6bn energy storage solutions and services to customers worldwide, every year. Exide Technologies’ Automotive Division manufactures 12V batteries for all powertrain concepts, covering internal combustion over to full electrician and off-road vehicles. We offer lead-acid and lithium-ion batteries for light and commercial vehicles, motorcycles, boats and more. We serve the OEMs and the Aftermarket with our and our customer’s top brands. About the job For our growing Automotive division in Manzanares (SPAIN) at the earliest possible date we are looking for a: HSE (Health, Safety & Environment) Plant Manager. What will your daily responsibilities include in this role? Will lead the HSE operations and activity is in the Manufacturing Plant, promoting a safeworking environment for the employees and contractors and the meeting of all legal requirements for HSE issues. Will drive the Technical HSE projects in terms of HSE technical requirements, best practices sharing, budget and scheduling follow up, lead the Risk Assessment process, implement the Company Management System and ensure the internal and external audit processes. Directs HSE programs and activities to ensure compliance with national and local laws and regulations and Company Policy. Main responsabilities • Development and implementation of the HSE program, Company Guidelines & HSE Management System., • Ensure the definition and project execution of investments and resources necessary for the implementation of HSE programs., • Prepare and analyze the EHS KPIs and reporting, ensuring data quality and timeliness., • Join the internal audit program in the division in collaboration with Corporate / BU HSE, participate in audits when necessary., • Ensure the definition and implementation of action plans to resolve the findings found., • Assure that periodic risk assessments are carried out in order to evaluate and provide actions and resources based on the findings., • Confirm proper communication & investigation of accidents and incidents, definition and implementation of action plans., • Plant inspections, assessment of HSE conditions., • Maintain HSE technical competency through continuing education and propose necessary programs., • Ensure identification, verification and compliance with legal and other Company and/or Customer requirements., • Meetings with external companies, suppliers and local authorities when required. What we ask for • University degree in Industrial Engineer or similar., • Master in Health and Safety., • Knowledge in ISO 45001 /14001., • At least 5 years of experience in a similar position preferably in an industrial environment., • Business fluent in English., • Proactive communication with colleagues and customers. What we offer We offer you a challenging, responsible and varied job in a modern, fast growing divison within an International Corporation. You can expect a highly collegial working environment with a reasonable scope for action and decision-making. You will benefit from exciting personal and professional development opportunities, additional corporate well-being initiatives, and several key benefits, including: • The opportunity to gain valuable experience within a large international corporation., • Pension Plan financed by the employer., • Offer of medical insurance on preferential terms., • Free Canteen Working with us means being engaged and agile. Our culture of continuous learning and commitment to sustainability and diversity create an environment where you can grow your skills and your career. Feel free to apply if you think you meet the criteria and are excited to join our project. Please submit your application along with an updated CV. A member of our Selection team will reach out to you. Best of luck! Our energy: It’s you! Together, we will be transforming the energy sector. Exide is an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability or gender identity. Exide is committed to sustainability and value creation, respecting the planet’s limits and fostering positive change for both the environment and people within the global energy storage system. Exide Technologies – Energizing a new world

In a few words Position: IT Compliance Location: Azuqueca de Henares, Spain (on-site) Experience: Over 1 year in similar roles in computer system validation and quality assurance Want to know more? CHEMO, part of the INSUD PHARMA group, is a global leader in pharmaceutical industrial operations wi

Grupo Cobra es una compañía global con más de 80 años de experiencia en ingeniería industrial y servicios especializados.

In short Position: Clinical Development Leader Location: Azuqueca de Henares. Experience: 3 to 5 years in similar roles. Want to know more?👇 INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs), and branded pharmaceutical products, adding value for human and animal health. INSUD PHARMA’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to become a #Challenger? What are we looking for?🔎 Planning, designing, organization, supervision of conduct and reporting of clinical trial contracted to Clinical Research Organizations (CRO) to enable studies execution within the planned timelines and in compliance with current GCP and other applicable requirements. The main focus is on pharmacokinetic (PK) and bioequivalence (BE) trials. Multicenter clinical trials and phase II and III trials may also be required with the necessary support. The challenge! • Assume overall responsibility for the plan, design, execution, reporting and evaluation of results of clinical trials as well as assure conduct of the trials in compliance with applicable requirements including but not limited to GCP. Specific responsibilities include:, • Design and manage the clinical trials according to plan and in compliance with applicable laws, regulations, and guidelines (ICH, EMA, FDA, and others)., • Participate in the selection of CROs and other external vendors and control the execution of all contracted activities and ensure that the activities are conducted in accordance with the requirements (cost, quality, and time)., • Review the necessary documentation before (e.g. Protocol, ICF, etc.), during (e.g. Monitoring etc.) and at the end (e.g. Study Report, etc.) of clinical trials., • Coordinate internal Chemo activities and procedures related with the conduct of the clinical trials (e.g. investigational medication shipment, etc.)., • Collaborate in the interaction with Health Authorities: Scientific Advices and Deficiency Letters., • Collaborate with other departments and experts (e.g. in Pharmaceutical Development, Regulatory, Pharmacovigilance, Project Management) to define strategies and plans for projects execution and execute clinical activities according to agreed plans., • Participate on the maintenance of GCP system through elaboration and/or review of SOPs, etc., • Contribute to the maintenance of GCP system through elaboration and/or review of SOPs, etc., • Specific Knowledge:, • Experience in global Clinical Development, primarily in PK and BE studies:, • Current knowledge of laws, regulations, and guidance (ICH, EMA, FDA, etc.) related to design and execution of clinical trials, primarily PK and BE studies as well as demonstrating bioequivalence in general., • Experience in studies design and studies program development., • Preparation and review of study documentation., • Implementation of trials in global environment: Site selection and management (clinical / bioanalytical sites, monitoring activities)., • Project management of multiple studies, • Experience in development of generic drugs and related methodologies: evaluation of in vitro dissolution studies results, evaluation of PK/BE studies results and reports, assessment of suitability of bioanalytical methods, in vitro/in vivo correlations etc. Experience (years/area): • Mandatory: Degree in Medicine, Pharmacy or Life Science, • Desired: Training/experience in Pharmacokinetics, bioequivalence studies and most of the relevant guidelines., • Fluent in English required, communicative level in Spanish preferred, knowledge of other languages will be an asset., • At least 3 years of experience in a similar position. Our Benefits! ⏰Flexible start hours from Monday to Friday (full 40-hour workweek). 📜Permanent contract. 💸Attractive salary package. 🥼Life and accident insurance. 🍽️Company cafeteria (free of charge). 🥼Co-payment for voluntary health insurance. 💸Benefits and Savings Club. 📈Development plans, internal mobility policy. ⭐And much more! How will the Selection Process be? 🕵️ ➡️Stay alert to your phone and email! Most likely, the first thing we will do is contact you through one of these two channels. ➡️Prepare well! We will continue with a face-to-face/virtual interview based on availability and as agreed; there may be one or two interviews, and depending on the type of process, there may also be some kind of test. ➡️Wait for the result! We care that you feel guided and know what to expect from us at every step of the selection process, so we will always try to inform you about the status of the process. 🔷Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we post. Your opportunity to become a new Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as established in current regulations - Organic Law 3/2007, and we do not discriminate against anyone based on ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

In a nutshell Position: Pharmaceutical Development Manager - External Operations Location: Azuqueca de Henares Experience: More than 5 years in the development of the position and duties described Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing expertise and experience in scientific research, development, manufacturing, sales and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs) and branded pharmaceutical products, with added value for human and animal health. INSUD PHARMA's activity is organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 commercial offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries around the world. INSUD PHARMA believes in innovation and sustainable development. What are we looking for? We are recruiting a Pharmaceutical Development Manager – External Operations to join the R&D team at one of our plants located in Azuqueca de Henares. The challenge! As Pharmaceutical Development Manager - External Operations, you will lead, coordinate and supervise pharmaceutical development projects carried out at Insud Pharma Group's sites outside Spain and with external partners. Your mission: to ensure the highest quality development and smooth technology transfer of solid oral and semi-solid dosage forms from external centres to our flagship plant in Spain, driving the success of the portfolio in multiple markets. Specific responsibilities • Provide strategic oversight of R&D projects developed at Insud Pharma Group plants outside Spain and through external partners such as CDMOs worldwide, primarily in solid oral and semi-solid dosage forms., • Manage all formulation, analytical and process development activities, from pre-formulation to industrialisation, ensuring overall compliance with corporate objectives, regulatory requirements and project deadlines., • Supervise, guide and inspire a high-performance team; define annual objectives aligned with the company's strategy and foster a culture of innovation, engagement and continuous improvement., • Review, approve and validate project documentation (development, analytical, regulatory, clinical) prepared by international and third-party teams, ensuring the most rigorous standards for regulatory submission and audit readiness., • Drive seamless technology transfer and product scaling, ensuring robust implementation in Spanish production (Liconsa), including plant preparation, process reproducibility, equipment qualification and comprehensive technical documentation., • Align projects and coordinate effectively with global cross-functional teams: Clinical Development, Production, Regulatory Affairs, Business Development, Supply Chain, Quality, among others., • Propose optimal resource allocation and lead change initiatives to enhance capacity, efficiency and adoption of best practices in internal and external networks., • Monitor KPIs for deadline compliance, document quality, process reproducibility and submission/approval rates; proactively address project risks and leverage new opportunities., • Present project status and strategic recommendations to senior management and global leadership, acting as a visible benchmark for external innovation, excellence, and patient-centred value., • Higher degree in Pharmacy, Pharmaceutical Sciences, Chemistry or related field., • ≥5 years of experience in pharmaceutical development, with proven experience in managing international projects and with third parties (/CDMOs); experience in generic drug development highly valued., • Solid knowledge of formulation, analytical and process development—especially for solid and semi-solid oral forms; practical experience in scale-up, technology transfer and regulatory submissions (FDA/EMA and others) required., • Fluency in English (spoken/written); Spanish and/or other languages will be a significant advantage., • Proven leadership of multidisciplinary and multicultural teams; able to align diverse stakeholders in a highly dynamic and matrix environment., • Excellent project management, negotiation, and interpersonal skills; proven track record in problem solving, innovation, and meeting objectives on time and within budget., • Willingness to travel internationally to external sites and collaborating organisations as needed. Monday to Friday working hours, with flexible start times between 8:00 a.m. and 9:30 a.m. and finish times depending on start time, from 4:30 p.m. onwards. Permanent contract. Attractive salary package. Life and accident insurance. Co-payment for voluntary health insurance. Benefits and Savings Club. Development plans, internal mobility policy. And much more! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must be in line with the needs and demands of society, and therefore is committed to equal opportunities and treatment between men and women, as set out in current legislation on the matter -Organic Law 3/2007, and we do not discriminate against anyone on the basis of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Xiromed is a vertically integrated generic company focused on delivering high quality & value products to the US and some European markets. Xiromed’s vision is to be a high quality provider of generic pharmaceuticals that bring enhanced value to our patients, customers and the healthcare system. We strive to bring broad based access to drug products across dosage forms, therapeutic areas and market channels. We continue to invest strongly in state of the art infrastructure across technology, manufacturing and quality systems to build a strong and diversified portfolio of offerings. The biggest asset that makes us who we are will always be our people across the organization, who epitomize the passion, leadership, integrity and the culture of success at our company. Global Responsibility Bringing Xiromed EU portfolio pipeline, internal and external, to the market in accordance with the goals and business plan of the business unit, including but not limited to ensure the launch is properly planned, technically prepared, and timely implemented and finally launched into the markets. Specific Responsibilities • Improve BCs generally format and forecasting accuracy Business Case and involvement in launch/replenishment order., • System for launch planning (lead implementation and maintenance of such system – probably will be SAP based)., • Active part in COGs negotiation for launches and existing portfolio – renegotiate where margin low., • Manage the forecasting and order placement of the launches., • Inhouse portfolio coordination & configurations for regulatory and business cases., • Launch Management, being part of the launch team and leading a number of launches. Competencies/Career level Innovation, communication, teamwork, adaptability/flexibility, productivity, sense of urgency, initiative/problems solving Requirements and personal skills • Education: University Degree in Pharmacy or similar., • Languages: Fluent Spanish and English, knowledge of other languages will be an asset., • Experience (years/area): 4 years in Launch and Project Management. Business Development Gx- Experience network for COGs negotiation., • Specific Knowledge: Systems implementation/maintenance., • Travels: Open to travel., • Personal skills: Flexibility, open and cooperative attitude, teamwork good communication/organizational skills and problems solving. COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

En pocas palabras Chemo Azuqueca de Henares, Castilla-La Mancha, España (Presencial) En pocas palabras Posición: Analista de Estabilidades de Control de Calidad -Temporal Localización: Azuqueca de Henares. Experiencia: Al menos 2 años en funciones similares. ¿Quieres saber más? Chemo, parte del Grupo InsudPharma, es una empresa líder en la cadena de valor farmacéutica, con compromiso firme hacia la innovación, la calidad y el desarrollo sostenible. En Chemo creemos que la excelencia en cada proceso es la base para contribuir a la salud humana y animal a nivel global. ¿Preparado para formar parte de un equipo comprometido con la calidad? ¿Qué buscamos? • Realizar análisis siguiendo los métodos analíticos aprobados de lotes de producto terminado, intermedios y materias primas., • Cuidar equipos y materiales conforme a los procedimientos aprobados para garantizar la calidad de los datos analíticos., • Mantener el lugar de trabajo limpio y ordenado., • Realizar muestreos de materias primas, intermedios y producto final., • Seguir todos los procedimientos operativos y generales aprobados., • Bajo supervisión de técnico o supervisor, realizar ensayos que apoyen la validación de nuevos métodos analíticos., • Obtener y revisar la documentación relacionada con los análisis realizados., • Realización de análisis siguiendo los métodos analíticos aprobados de lotes de producto terminado, intermedios y materias primas., • Cuidado de equipos y materiales, siguiendo los procedimientos aprobados con el fin de garantizar la calidad de los datos analíticos obtenidos., • Mantener el lugar de trabajo limpio y ordenado., • Muestreo de materias primas, intermedios y producto final., • Seguimiento de todos lo procedimientos operativos o generales aprobados., • Bajo supervisión de un técnico o supervisor realización de ensayos que conduzcan a la validación de nuevos métodos de análisis. ¿Qué necesitas? • FP en Análisis y Control o Licenciatura en Ciencias (Química, Biología, Farmacia, o afines)., • Mínimo 2 años de experiencia en control de calidad o áreas relacionadas., • Conocimiento de procedimientos analíticos y normativas vigentes. Contrato temporal (sustitución) Turnos rotativos M/T/N. Seguro médico privado. Atractivo paquete salarial. Seguro de vida y accidentes. Copago en el seguro voluntario de salud. Club de Beneficios y Ahorro. Planes de desarrollo, política de movilidad interna. ¡Muchos más Planes de desarrollo profesional y formación continua ¿Cómo será el proceso de Selección? • Contacto inicial vía telefónica o email., • 1 o 2 entrevistas presenciales. ¡Estate atento/a al teléfono y al correo! Seguramente lo primero que haremos será contactarte por alguna de las dos vías. ¡Prepárate bien! Continuaremos con una entrevista presencial/virtual según la disponibilidad y acordemos, en el proceso puede haber entre una y dos entrevistas y según el tipo de proceso puede haber también algún tipo de prueba. ¡Espera el resultado! Nos preocupamos de que cada proceso de selección os sintáis guiados y sabiendo qué esperar de nosotros, por lo que procuraremos indicaros siempre el estado del proceso. COMPROMISO CON LA IGUALDAD DE OPORTUNIDADES En Chemo y Grupo InsudPharma promovemos y garantizamos la igualdad de género, la no discriminación por razón de etnia, religión, orientación sexual, discapacidad o cualquier otra condición personal o social. Nuestro compromiso es generar un ambiente laboral inclusivo, diverso y respetuoso para todas las personas.

Qualentum lanza el programa de .Una oportunidad para iniciar un plan de carrera en una compañía española de impacto global, presente en 50 países y con más de 24.Formación técnica especializada en Análisis de Datos y Nuevas Tecnologías, .Título Propio de UNIR, que potenciará tu futuro p

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Work within a global organisation that values agility, innovation, and personal growth over rigid hierarchy.

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AC-FIX (GLOBAL PIPING SYSTEMS, S.

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If interested, please apply here or share me your Cv at Snavlani@redglobal.

Decskill nació en 2014 como una consultora de Talento IT, con la misión principal de aportar valor a través del conocimiento.Capacitamos a las empresas para enfrentar los desafíos del mundo digital disponiendo a nuestros clientes modelos de negocios que aseguren Capacitación Tecnológica, Flexi

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En Safeguard Global, líder en soluciones de RRHH en más de 180 países, impulsamos tu crecimiento profesional, tus proyectos y tus éxitos.

The purpose of this role is to shape and execute the networks IFRS strategy as determined by the Global Leadership Team (GLT) and the Global IFRS Steering Committee (IFRS SC). Evidence of a global mindset including an understanding of the external forces impacting our future sustainable growth. Prev

Consultor Senior SAP SD – Proyecto de Implementación Global | Barcelona (Híbrido). En Vortech PCI Group, estamos buscando un Consultor Senior SAP SD para unirse a un proyecto internacional con una empresa líder global que opera en múltiples regiones. Capacidad para liderar equipos multifuncion

Te apasiona el medioambiente y la gestión eficiente del agua?.Aguas residuales, centrándose en la elaboración de ofertas competitivas para licitaciones, además de apoyo a la gestión de las explotaciones.Como Personal Técnico de Estudios y Ofertas, tus responsabilidades incluirán:.Análisis de

Operamos a nivel local-global desde 18 países, donde contamos con 78 centros de entrega globales, y más de 20. En Quest Global creemos que la ingeniería tiene el poder único de resolver los problemas del presente que marcarán el camino hacia el futuro. Quest Global es un lugar donde nuestra gen

RED Global is supporting one of our key international partners in their search for a.

Desde COS GLOBAL SERVICES, estamos buscando un.

Somos una empresa dedicada al desarrollo de productos para la limpieza del hogar y el cuidado personal propios y como proveedores.Contamos con más de 40 años de experiencia en el sector químico.Lo que empezó como un pequeño negocio familiar, se ha convertido en un.Queremos incorporar a una pers

Consultor/a Senior especializado/a en Global Transaction Banking (GTB). Tu misión será liderar proyectos de consultoría de negocio, poniendo al cliente corporativo en el centro y ayudando a las entidades a diseñar su futuro en el ámbito del Global Transaction Banking. Analizarás competencia, v

Norconsulting selecciona un perfil de.Ingeniero/a de Alta Tensión (Subestaciones / Protección y Control).Quieres conocer más detalles del puesto?.Diseño y cálculo de sistemas eléctricos.Coordinación con equipos multidisciplinares.Supervisión técnica de los entregables, asegurando el.Interac

We are currently looking for an experienced.S/4HANA rollout for a leading pharmaceutical company.Remote + Onsite in Kiel every 3 weeks.Candidate can be based anywhere in Europe.Strong knowledge of SAP S/4HANA.Proven background in the pharmaceutical sector.Expertise in integration between SAP QM and

Use of Amadeus Global Distribution System - Refreshment training may be provided.

El candidato seleccionado liderará las actividades funcionales de FICO en las distintas fases del proyecto, desde la evaluación inicial hasta el soporte post go-live.Implementación y configuración del módulo SAP FICO S/4HANA según los requerimientos del negocio.Liderar actividades de conversi�