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About Group-IB Founded in 2003 and headquartered in Singapore, Group-IB is a leading creator of cybersecurity technologies to investigate, prevent, and fight digital crime. Combating cybercrime is in the company’s DNA, shaping its technological capabilities to defend businesses and citizens and support law enforcement operations. Group-IB’s Digital Crime Resistance Centers (DCRCs) are located in the Middle East, Europe, Central Asia, and Asia-Pacific to help critically analyze and promptly mitigate regional and country-specific threats. These mission-critical units help Group-IB strengthen its contribution to global cybercrime prevention and continually expand its threat-hunting capabilities. Each of us can help make the world a safer place. Join us! The role: As a Business Development Manager , you will be an essential part of the European Sales Team and, in particular, of the Iberia Team, helping to generate new great business opportunities and promoting our solutions across Spain. You will be reporting directly to the Sales Manager. By deep-diving into the industry, you will have a chance to advance your career in cybersecurity sales and deliver our solutions. Tasks to solve: Develop and manage existing customer accounts in Spain and hunt for new business. Support existing and grow the right IT channel ecosystem. Execute campaigns to target new sales opportunities through follow-up and outbound cold calls/emails. Work closely with the Sales Teams, Partner Channel, and Marketing teams on lead management. Develop our commercial business in your territory under the guidance of the relevant sales executives and ensure an accurate overview and forecasts. Target, educate and persuade new customers to use Group-IB products. Update and maintain clients database details within CRM diligently. Qualifications 5+ years of experience selling Cybersecurity and/or Fraud Protection solutions. Experience in cybersecurity vendors or system integrators is a plus. Hunter and results-driven individual seeking an opportunity to further develop their cybersecurity sales career. Client-centric mindset and approach. Good understanding of the indirect sales channels. Excellent analytical, communication, and presentation skills. Strong passion for cybersecurity and high-tech technologies Fluency in English and Spanish. Why GROUP-IB? Your happiness is important to us: We want every single team member to be happy. Continuing professional development: At Group-IB, you can choose from various paths to growth: progress as an expert, advance to a management position, try your hand in another department, relocate abroad, or launch a new business area. Group-IB.A team with extensive international expertise: Do you have experience but are looking for exciting challenges? By choosing us, you will be choosing complex tasks and continuously improving your skills in a fast-growing international company . Globally recognized technologies: Group-IBs members are located in 25 countries, and our products and services are sold in 60 countries. What’s more, Gartner, IDC, and Forrester have ranked our technologies among the best in their class. We work with over 450 international partners and about 500 clients . A culture created by each of us: Group-IB’s employees speak many different languages and understand one another. We respect each others beliefs, share common values, and strive toward the happiness of every employee . Economic stability: Group-IBs sustainable growth helps rapidly develop careers that would take years to progress as far as most other companies. What else should you know: Flexible schedule: Group-IB does not have fixed working hours. You choose your schedule. We adhere to the principle advocated by Steve Jobs: “We have to work not 12 hours and head. Certificates and training courses : Group-IB specialists hold over 1,000 professional certificates, including CEH, CISSP, OSCP, GIAC, MCFE, BSI, as well as some rare ones that would be a source of pride for experts in forensics, penetration testing, and reverse engineering worldwide. We have an incentive program that helps employees achieve certifications at the companys expense. Challenges: A wide selection of GIB programs helps you improve soft skills, gain new competencies, and receive monetary rewards. The initiative is rewarded: At Group-IB, you can bring your most daring ideas to life. The company encourages technical blogging, writing articles, building sports teams, and other creative activities.

Buscamos un/a apasionado/a del mundo de la Automoción con experiencia en gestión de proyectos en Madrid ¿Quiénes somos? Somos MIGSO-PCUBED , la consultora líder en Project Management , parte del grupo ALTEN . Contamos con más de 3.300 consultores en Europa, Norteamérica, Asia y Australia. Damos soporte a nuestros clientes en gestión de proyectos y PMO , participando en proyectos de I+D, industrialización, mejora de procesos y transformación . Trabajamos en sectores como Automoción, Aeronáutica, Ferrocarril, Defensa, Energía, Servicios Financieros, Telecomunicaciones, Tecnología & Media y Sector Público . ¿Cómo será tu día a día? Control y seguimiento de presupuestos y costes de proyectos industriales. Identificación, análisis y gestión de riesgos . Seguimiento del avance del proyecto (plazos, hitos y entregables). Elaboración de informes de estado a nivel proyecto y portfolio, con manejo de distintos KPI . Soporte en la gestión de proyectos a los diferentes departamentos implicados (ingeniería, calidad, producción, compras, etc.). Coordinación de los distintos equipos involucrados en el proyecto. Tu perfil Grado o Licenciatura en Ingeniería . Experiencia mínima de 1 año en gestión de proyectos en el sector automoción . Nivel de inglés B2/C1 , con capacidad para comunicarte en entornos internacionales. Manejo de herramientas como SAP, Excel, MS Project, Power BI (u otras similares). Persona dinámica, comprometida , con buenas habilidades de comunicación, acostumbrada a trabajar con múltiples interlocutores y en equipo. ¡Trabajar con nosotros es una experiencia única por varias razones! ✨ Aquí tienes algunos puntos clave: Desarrollo profesional : Ofrecemos un plan formativo robusto para impulsar tu crecimiento y habilidades, además de oportunidades de formación en idiomas para expandir tus horizontes ¡Diviértete mientras trabajas! Nuestros eventos corporativos y actividades de team building te permiten conectar con colegas, construir relaciones sólidas y disfrutar de momentos memorables Flexibilidad que importa : Tu bienestar es fundamental, por eso ofrecemos retribución flexible que incluye Ticket Restaurante, transporte y guardería, para adaptarnos a tus necesidades Tu salud es nuestra prioridad: Ofrecemos un completo seguro médico para cuidar de ti Cultura de bienestar : Nos preocupamos por ti. Nuestras políticas promueven la igualdad, la desconexión digital y disponemos de espacios de trabajo acogedores que fomentan un entorno positivo y equilibrado para todos. ¿Crees que encajas en la descripción? presenta tu solicitud hoy y comienza tu viaje en MIGSO-PCUBED ✈ #MORETHANJUSTAJOB

SW Spain es una firma de servicios profesionales con amplia trayectoria en España, especializada en auditoría, consultoría, fiscal, legal y servicios digitales . Forma parte de SW International , una red global en rápida expansión con presencia en más de 95 oficinas , más de 12.000 profesionales y una fuerte base en la región de Asia-Pacífico, lo que la convierte en un socio estratégico para empresas con ambiciones internacionales. La firma opera a través de SW Auditores España S.L.P. y SW Advisory España S.L.P. , ofreciendo servicios tanto al sector público como al privado, abarcando compañías de todos los tamaños y sectores. Buscamos un Consultor Senior con experiencia en Corporate Finance y/o Transaction Services para participar en proyectos de M&A, Valoraciones y Financial Due Diligence . Responsabilidades Ejecutar Financial Due Diligence (QoE, EBITDA, working capital, cash flow, deuda). Apoyar y coordinar procesos de M&A (buy-side y sell-side). Elaborar V aloraciones y modelos financieros. Preparar materiales clave (teasers, IMs, informes TS, presentaciones). Gestionar relación con clientes. Requisitos Mínimo 3 años en Corporate Finance, TS, M&A. Se valorara positivamente experiencia previa en Auditoría Financiera Dominio de Excel, contabilidad y herramientas de modelización y análisis financiero. Experiencia en FDD y valoración. Inglés alto y excelentes habilidades de comunicación. Qué ofrecemos Participación en operaciones relevantes. Desarrollo profesional y formación continua. Entorno flexible

About Group-IB Founded in 2003 and headquartered in Singapore, Group-IB is a leading creator of cybersecurity technologies to investigate, prevent, and fight digital crime. Combating cybercrime is in the company’s DNA, shaping its technological capabilities to defend businesses and citizens and support law enforcement operations. Group-IB’s Digital Crime Resistance Centers (DCRCs) are located in the Middle East, Europe, Central Asia, and Asia-Pacific to help critically analyze and promptly mitigate regional and country-specific threats. These mission-critical units help Group-IB strengthen its contribution to global cybercrime prevention and continually expand its threat-hunting capabilities. Each of us can help make the world a safer place. Join us! The role: This new hire will be working with cybercrime fighters and helping big financial institutions across the European region to stop fraud! Tasks to solve: Investigate Fraud Activity: Analyze suspicious user sessions and behavioral patterns to detect and understand fraudulent behaviour across web and mobile platforms protected by Group-IB Fraud Protection. Improve Detection Logic: Develop and fine-tune fraud detection rules, leveraging behavioural, technical, and contextual data to stay ahead of emerging fraud techniques. Research & Monitor Threats: Stay informed on evolving fraud tactics and contribute to internal knowledge bases with insights and documentation. Collaborate on Product Development: Share feedback with product and engineering teams based on hands-on usage of the Group-IB Fraud Protection to help enhance usability, detection capabilities, and analyst workflows. Support Client Investigations: Work directly with Group-IB customers, helping them interpret alerts, understand fraud scenarios, and enhance their fraud protection strategies. Prepare Actionable Reports: Deliver clear, structured fraud analysis reports to internal and external customers, highlighting findings, root causes, and risk recommendations. Qualifications: 3+ years of experience in a similar job. Proficiency in Python for data manipulation and analysis (e.g., using pandas, NumPy, etc.) Knowledge in Jupyter. Ability to work with raw, semi-structured, or structured data and adapt it to present to clients. Excellent analytical thinking, with a structured approach to problem-solving and investigation. Experience working with SQL and large datasets. Experience working within the Financial Institutions in Risk roles. Fluency in English and French OR Italian. Submit your resume in ENGLISH, please. Nice to have: Working experience in i-Gaming. Knowledge of web and mobile application architectures. Cybersecurity acumen (interested in or at least engaged with it) Why GROUP-IB? Your happiness is important to us: We want every single team member to be happy. Continuing professional development: At Group-IB, you can choose from various paths to growth: progress as an expert, advance to a management position, try your hand in another department, relocate abroad, or launch a new business area. Group-IB.A team with extensive international expertise: Do you have experience but are looking for exciting challenges? By choosing us, you will be choosing complex tasks and continuously improving your skills in a fast-growing international company . Globally recognized technologies: Group-IBs members are located in 25 countries, and our products and services are sold in 60 countries. What’s more, Gartner, IDC, and Forrester have ranked our technologies among the best in their class. We work with over 450 international partners and about 500 clients . A culture created by each of us: Group-IB’s employees speak many different languages and understand one another. We respect each others beliefs, share common values, and strive toward the happiness of every employee . Economic stability: Group-IBs sustainable growth helps rapidly develop careers that would take years to progress as far as most other companies. What else should you know: Flexible schedule: Group-IB does not have fixed working hours. You choose your schedule. We adhere to the principle advocated by Steve Jobs: “We have to work not 12 hours and head. ”Health: If anything goes wrong, don’t worry — we offer health insurance. Certificates and training courses : Group-IB specialists hold over 1,000 professional certificates, including CEH, CISSP, OSCP, GIAC, MCFE, BSI, as well as some rare ones that would be a source of pride for experts in forensics, penetration testing, and reverse engineering worldwide. We have an incentive program that helps employees achieve certifications at the companys expense. Challenges: A wide selection of GIB programs helps you improve soft skills, gain new competencies, and receive monetary rewards. The initiative is rewarded: At Group-IB, you can bring your most daring ideas to life. The company encourages technical blogging, writing articles, building sports teams, and other creative activities

¿Quiénes somos?: Neotalent Conclusion es una de las mayores especialistas del mercado ibérico en captación y gestión de talento informático y de ingeniería. Como parte del grupo neerlandés Conclusion, que se compone por un ecosistema de 25 empresas y 3.600 empleados, nos centramos en aumentar la capacidad tecnológica de nuestros clientes y acelerar la transformación digital de los mismos. En Neotalent Conclusion, somos especialistas del talento. Atraemos a los mejores profesionales y los combinamos con los proyectos más ambiciosos, en el momento justo. Nuestro éxito radica en la inversión en innovación, orientación a resultados y, por encima de todo, en la garantía de que las personas tengan carreras felices y realizadoras. Con más de 25 años de experiencia, Neotalent Conclusion cuenta con oficinas en Madrid, Lisboa y Oporto. Nuestra compañía está formada por un equipo de más de 850 profesionales entre sus diferentes áreas de operación. Neotalent, the responsive people. Más información en y . Buscamos un Product Owner para uno de nuestros clientes del sector seguros 2 días presenciales en Barcelona Contrato Indefinido con Neotalent Conclusion Proyecto: DevOps Competitive Center, centrado en el DevOps lifecycle y en la implementación de prácticas DevOps. Rol: Product Owner (PO) con perfil técnico. Metodología de trabajo Agile Confluence para gestion de backlog Herramientas de CI/CD: Kubernetes, ArgoCD y SonarQube. Colaboración con el equipo de SRE, stakeholders, product managers y tech leads. Nice to have: Experiencia en el sector seguros, para comprender mejor la estrategia y la regulación del sector. Tecnologías principales: Azure (principal plataforma cloud), AWS y Kubernetes. Idioma de trabajo: Inglés. Contribuir a la definición e implementación de la visión y estrategia del producto. Colaborar con equipos multifuncionales para asegurar la entrega exitosa del producto. Descripción del servicio: Actuar como la voz del cliente y defensor de las necesidades de los usuarios. Priorizar y gestionar el product backlog alineándolo con los objetivos de negocio. Facilitar ceremonias ágiles y procesos de toma de decisiones. Entregables del servicio: Traducir las solicitudes de stakeholders y clientes en requisitos técnicos. Proporcionar soluciones a los problemas planteados. Ejecutar la hoja de ruta ( roadmap ) definida junto con el Product Manager. Priorizar y gestionar el product backlog con el equipo de desarrollo. Mejora y evolución del producto. Experiencia / Conocimientos: Obligatorio Experiencia previa trabajando con equipos de desarrollo de aplicaciones. Experiencia en tecnologías cloud. Conocimiento de los principales impulsores y estrategia de IT en torno al uso del cloud público. Experiencia demostrada gestionando múltiples stakeholders y proveedores clave. Deseable Experiencia con la plataforma Azure, GitHub y el ciclo de vida de desarrollo de software ( SDLC ) en general. Conocimientos de arquitectura de aplicaciones IT. Cualificaciones del servicio: Al menos 4 años de experiencia en gestión de productos IT o gestión de proyectos Experiencia con AWS, Azure,Kubernetes, SRE. Experiencia organizando y planificando eventos con stakeholders clave. Entorno de trabajo en inglés. Contexto internacional, con equipos remotos y organización matricial. Capacidad para trabajar en un entorno colaborativo y también de forma independiente. Interacción regular con stakeholders . Viajes internacionales ocasionales (Europa, EE. UU. y Asia) para apoyar nuevos proyectos. Por qué unirte a nosotros: Trabajar en proyectos desafiantes para grandes clientes Aprender más sobre tecnologías emergentes Posibilidad de trabajar de forma remota Acceso a formación continua y certificaciones Disfrutar de un plan de compensación flexible ... ¡y mucho más!

¿Te interesaría seguir desarrollándote profesionalmente en una compañía líder a nivel mundial en el sector editorial, con presencia internacional en mercados clave de Europa, América, África, Asia y Oceanía, y con un firme compromiso con la cultura, la diversidad lingüística y la difusión del conocimiento? Desde Oxigent Technologies seleccionamos un/a Consultor de Integraciones SAP para participar en un proyecto de integraciones tecnológicas entre SAP, EDI, transportistas y plataformas B2B dentro del área de Comercial y Logística, ubicado en Barcelona. ¿Cuáles serán tus funciones principales? Responsable de los procesos de integración relacionados con: Entrada de pedidos Confirmaciones de albaranes y facturas Procesos de disponibilidad (entradas/salidas) Integración con plataforma propia B2B WebClientes Integración de ventas de clientes (Sell-Outs) Integración y comunicación con transportistas / carriers Monitorización proactiva de interfaces e integraciones Resolución de incidencias técnicas Mantenimiento evolutivo y correctivo Implementación de nuevas integraciones y mejoras Análisis funcional-técnico de nuevos requerimientos Validación y control de integridad de datos (especialmente sell-outs y tracking logístico) Documentación técnica de interfaces y procesos Coordinación con equipos internos y externos Interlocución técnica con proveedores EDI y transportistas Para ello, ¿qué vas a necesitar? Experiencia en entornos SAP integrados Experiencia en integraciones mediante: ficheros, RFC, Webservices, APIs Experiencia trabajando con datos comerciales y logísticos Experiencia en integraciones con terceros (clientes, proveedores o carriers) Capacidad de análisis técnico y funcional Experiencia en resolución de incidencias en entornos productivos ¿Qué te ofrecemos? Contratación indefinida a través de Oxigent. Salario acorde a la experiencia aportada (entre 30.000 - 34.000 euros brutos anuales). Modelo híbrido - 50% remoto 50% oficina, 2/3 días rotativo Cheque Formación para desarrollarte en las áreas profesionales que más te interesen. Seguro médico privado. Retribución flexible aplicable a seguro médico, restaurante, transporte, guardería y formación. Aplicación de acceso a gimnasios y actividades deportivas en toda España con descuentos. ¡Y muchos otros beneficios! ¡Únete al equipo de Oxigent! Empresa comprometida con la sostenibilidad y la igualdad de oportunidades, donde el talento y la tecnología no entienden de género.

INTERNATIONAL RECRUITMENT & HR EXPERTS ACROSS THE PLASTICS, PACKAGING, SPECIALITY CHEMICALS, LIFE SCIENCES, BIOPOLYMER, FOOD ADDITIVES & INGREDIENTS, ENERGY AND RECYCLING SECTORS SINCE 1975. Sales Manager Applicants must have polymer resin trading or distribution experience Based in Spain Job ref: CST/64783 Salary: Attractive based on experience The Company: Our client is the Chemical trading division of an International conglomerate that has been active in the import/export trade and the development of new business for nearly five decades. The main task of the Chemicals division is the import and export of chemicals of all kinds, their derivatives and various chemical end products for customers in Europe and Asia. This role is a new position created to develop sales and business of polyolefins primarily in Portugal and Northern Spain regions. Key Responsibilities: Regular customer visits and sales of our product range as well as the acquisition and performance of sales-oriented tasks through regular telephone customer contacts Responsibility for sales, turnover and contribution margin for the assigned area Active sales acquisition and identification of sales opportunities Submission of offers and price negotiations with the customer on site Obtaining market information as well as determining and monitoring the competitive situation Ensuring proper and timely order and shipping processing Customer acquisition, visits and support Complaint processing and sales correspondence Order and shipping processing of complete order, also for third countries Create calculations, statistics and offers Provide a weekly report on business activities (including sales performance versus budget) and the market environment Provide visit reports & all relevant feedback in CRM Analysis of customer, competitor and market trends and demand structure in defined area Person profile: Professional sales experience of more than 10 years Working experience in trading or distribution company as a polymer resin trader, especially PE & PP items in Northern Spain and Portugal region Fluent in Spanish and English languages. An ability to speak Portuguese is highly desirable MS Office skills Willingness to travel and an independent, goal-oriented and systematic way of working Outstanding interpersonal skills across cultures For reasons of better legibility, the simultaneous use of the language forms male, female and diverse (f/m/d) is avoided. All personal designations apply equally to all genders. For EU roles, candidates must be eligible to work and live in the European Union. Proof of eligibility will be required with your application. To apply please contact Conrad Taylor 0044 (0) 1789 207070 CONNECT WITH ME ON LINKEDIN. Why select Listgrove? Five Decades of Market Intelligence Unrivalled Industry Networks Recognised International brand HR Qualified Professionals Throughout 2026 & 2027 you can meet with Listgrove at the following exhibitions: Interpack, France Innovation Plasturgie, Interplas UK, Plast Milan, Fakuma, ArabPlast, NPE 2027. Performance through People. Please visit for more information on our services, global success and testimonials. Listgrove Limited Registered in England No: 01197713

Group-IB: Founded in 2003 and headquartered in Singapore, Group-IB is a leading creator of cybersecurity technologies to investigate, prevent, and fight digital crime. Combating cybercrime is in the company’s DNA, shaping its technological capabilities to defend businesses, citizens, and support law enforcement operations. Group-IB’s Digital Crime Resistance Centers (DCRCs) are located in the Middle East, Europe, Central Asia, and Asia-Pacific to help critically analyze and promptly mitigate regional and country-specific threats. These mission-critical units help Group-IB strengthen its contribution to global cybercrime prevention and continually expand its threat-hunting capabilities. Each of us can help make the world a safer place. Join us! The role: Group-IB is a partner of INTERPOL, Europol, and a cybersecurity solutions provider recommended by SWIFT and OSCE. Such partnerships give us advantages in our everyday duties. We do deep research on malware and public presentation of complex research. We participate in IR and perform as experts at conferences and in the mass media. Our reports are used by thousands of people all over the world. And we invite you to our global team. Tasks to solve: Research activities of various cyber threat groups, collecting IoCs and TTPs focusing on the Dark Web. Work on client requests from the European region, including analysing malicious and phishing campaigns, investigating attackers infrastructure, and creating detection and hunting rules. Research malicious campaigns, attacker infrastructure, and related activities. Perform analytical work during research to attribute campaigns and tools to specific threat groups, identify common patterns in malicious infrastructure, and create hunting and detection rules. Prepare detailed reports summarising the results of research. Contribute to the continuous improvement of company products. Create public articles and presentations for events, including cybersecurity community conferences. Apply for this role if you have: Authorisation to work in Europe. 4+ years of experience as a Threat Intelligence Analyst focusing on the Dark Web. Graduated in cybersecurity, computer science, information technology, or a related field (or have equivalent experience). Have an understanding of cybersecurity fundamentals, including cyber threat landscapes, attack vectors, TTPs, and malware types. Knowledge of Python and Bash (this last one is preferable) Extensive knowledge of concepts such as the MITRE ATT&CK framework, Cyber Kill Chain, and TTPs. Have excellent OSINT and analytical skills, with the ability to recognize patterns and trends, connect the dots, and draw reasonable conclusions. Understand OPSEC principles. Have basic knowledge of scripting languages. Understand common network protocols. Have a basic understanding of the cyber threat industry. Are proficient in technical language and capable of writing technical reports. Why choose Group-IB: Your happiness is important to us: We want every single team member to be happy. Continuing professional development: At Group-IB, you can choose from various paths to growth: progress as an expert, advance to a management position, try your hand in another department, relocate abroad, or launch a new business area at Group-IB. A team with extensive international expertise: Do you have experience but are looking for exciting challenges? By choosing us, you will be choosing complex tasks and continuously improving your skills in a fast-growing international company. Globally recognised technologies: Group-IBs members are located in 25 countries, and our products and services are sold in 60 countries. What’s more, Gartner, IDC, and Forrester have ranked our technologies among the best in their class. We work with over 450 international partners and about 500 clients. A culture created by each of us: Group-IB’s employees speak many different languages and understand one another. We respect each others beliefs, share common values, and strive toward the happiness of every employee. Economic stability: Group-IBs sustainable growth helps rapidly develop careers that would take years to progress as far as most other companies. What else should you know: Flexible schedule: Group-IB does not have fixed working hours. You choose your own schedule. We adhere to the principle advocated by Steve Jobs: “We have to work not 12 hours, and head.” Certificates and training courses: Group-IB specialists hold over 1,000 professional certificates, including CEH, CISSP, OSCP, GIAC, MCFE, BSI, as well as some rare ones that would be a source of pride for experts in forensics, penetration testing, and reverse engineering worldwide. We have an incentive program that helps employees achieve certifications at the companys expense. Challenges: A wide selection of GIB programs helps you improve soft skills, gain new competencies, and receive monetary rewards. The initiative is rewarded: At Group-IB, you can bring your most daring ideas to life. The company encourages technical blogging, writing articles, building sports teams, and other creative activities.

Buscamos una persona con experiencia en logística y comercio internacional. Se encargará de gestionar la parte administrativa de los contratos y coordinar las operaciones logísticas de exportación, en contacto con transportistas, clientes y proveedores. Lugar de Trabajo: Mas Pujó, Santa Margarida i els Monjos Incorporación: Immediata DESCRIPCIÓN FUNCIONES: 1.BACK OFFICE Redacción de contratos y gestión de firmas Obtención de CDC firmados Introducción de facturas de contratos y cierre de los mismos para poder facturar Países: Principalmente con Europa pero también Asia y América del Norte 2.LOGíSTICA: Gestión de retiradas de contratos realizados: coordinación de transportista, comprador y vendedor, verificación de documentos, seguimiento de pagos, resolución rápida y eficaz de incidencias 3. OTROS: Asistir a Export Manager Gestión de viajes: compra de billetes avión, búsqueda hoteles, etc. Asistencia telefónica CARACTERÍSTICAS GENERALES: -Transporte: Necesario disponer de permiso de conducción y también de un medio de transporte propio puesto que no hay una conexión con red pública de transporte. -Disponibilidad para viajar puntualmente FORMACIÓN/CONOCIMIENTOS: Auxiliar Administrativo Asistente de dirección Comercio Internacional IDIOMAS: Francés: Nivel alto Alemán: Indispensable Nivel alto Inglés: Indispensable Nivel alto Español: Nivel alto Catalán: Nivel alto EXPERIENCIA LABORAL: Mínimo de 3 años de experiencia laboral en alguno/s de los siguientes equipos: • Departamento comercial • Departamento logístico • Empresa familiar Horarios / Jornada Entrada flexible de 8 a 9 y salida flexible entre 17 y 18 horas Se valorará persona: • Empática • Dinámica, ágil y proactiva, • Muy ordenada y organizada • Espíritu de superación y mejora • Profesionalidad

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are seeking a Cleaning Validation Specialist to support cleaning validation activities within a GMP-regulated pharmaceutical manufacturing environment. Responsibilities include, but are not limited to: • Support the planning and execution of cleaning validation activities for manufacturing equipment and facilities., • Assist in the preparation and review of validation protocols and reports ., • Participate in sampling activities and support analysis of validation data., • Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure compliance with GMP requirements ., • Support risk assessments and validation strategies related to equipment cleaning processes., • Contribute to investigations, deviations, and CAPA actions associated with cleaning validation., • Maintain and organize validation documentation according to regulatory and internal quality standards ., • Assist in preparing documentation for internal audits and regulatory inspections . Required Qualifications: • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Biotechnology, Chemistry, Chemical Engineering, or Life Sciences ., • Minimum 1 year of experience in the pharmaceutical, biotechnology, or related regulated industry (internships or academic projects are also considered)., • Basic understanding of GMP principles and pharmaceutical manufacturing environments., • Strong attention to detail and good analytical skills., • Ability to work collaboratively in cross-functional teams ., • Fluent in English and Spanish Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

About Linglong Linglong Tire is a leading Chinese tire manufacturer with production facilities and research centers in Asia, North America and Europe. With around 19,500 employees worldwide Linglong has the elite of the global tire industry in its teams. Through sales networks in over 170 countries and relations to world-class automakers Linglongs reliable quality is more and more appreciated. As a sponsor of Real Madrid and Chelsea and due to the opening of our new production site in Serbia, we are constantly expanding our brand presence in the European market. We are looking for a Tire Subjective Evaluation Engineer (m/f/d) to expand our R&D team in Spain. Responsibility • Perform subjective evaluation of tire & vehicle performance for OEM and aftermarket, • Produce detailed and clear subjective evaluation reports, • Establish and maintain alignment with OEM customer engineers, • Participate in joint tests with OEM customers in preferred/OEM proving grounds, • Develop and update subjective evaluation methods based on customer requirements, • Create positive relationships with European Tire and Vehicle Magazine partners, • Assist in the coordination and management of all European testing activities Qualification • Academic Degree in engineering or in a field associated with the role, • Multiple years of experience in the field of subjective tire evaluation for European OEMs, • Fluent in English (written and spoken), • German language proficiency is an advantage, • AKF/OE PG and Industrie-Pool licenses, • Open-minded team player, who takes initiative, with strong communication skills What we offer • Unlimited Contract, • Performance Bonus, • An amazing open minded and international team, • Being part of the success of an international growing brand, • Opportunity for professional and personal growth

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking a GMP Analytical Lab Consultant - Maintenance & Qualification to support Quality Control laboratory activities within a GMP environment. The role involves managing qualification, calibration, maintenance, and troubleshooting of chemical laboratory instrumentation, ensuring compliance and proper performance of QC equipment. Responsibilities include, but are not limited to: • Perform Periodic Qualification (IQ, OQ, PQ) of Chemical Quality Control laboratory instrumentation , including: HPLC, UPLC, GC, balances, pH meters, Karl Fischer titrators, AAS, UV-Vis, IR spectrophotometers, climatic chambers, DSC, TGA, TOC analyzers ., • Author and execute IQ, OQ, and PQ protocols and generate final qualification reports ., • Monitor equipment performance, calibration status, and daily functionality checks to ensure GMP compliance ., • Coordinate and manage relationships with vendors and external suppliers ., • Plan and schedule qualification, calibration, and maintenance activities ., • Oversee activity planning and procurement of kits and consumables ., • Execute preventive maintenance and troubleshooting activities on laboratory instruments. Preventive Maintenance & Troubleshooting – HPLC • Detector diagnostics and troubleshooting, • Flow cell cleaning and lamp replacement, • Pump diagnostics and replacement of seals, pistons, and fittings, • Diagnosis of mechanical faults (arms, needle, injector systems), • Replacement of tubing, fittings, frits, filters, gaskets, and capillaries, • Cleaning of solvent inlet filters (dip sticks), • System flushing to remove precipitates and contamination, • Leak detection and seal integrity checks, • Diagnosis and replacement of syringes, septa, O-rings, injectors, and liners Required Qualifications: • Degree in scientific disciplines, • Experience of working in GMP environment, • Strong knowledge of analytical laboratory instrumentation and qualification processes (IQ/OQ/PQ)., • Spanish native, english at least B2 Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are seeking a Senior Regulatory Affairs & Pharmacovigilance Specialist to support both local and international regulatory and PV activities. The role combines hands-on regulatory work with pharmacovigilance oversight, ensuring compliance across Spain and LATAM markets. Key Responsibilities Regulatory Affairs (RA): • Analyze EU regulatory strategies and provide recommendations to clients, • Author full technical dossiers (Modules 1–5) from scratch, • Manage variations, renewals, labeling updates, and Health Authority interactions, • Support regulatory activities in LATAM markets, • Support PV activities and reporting obligations in Spain and EU, • Ensure compliance with local and international safety regulations, • Assist in signal detection, risk management, and safety documentation, • Coordinate with global PV teams to align processes and reporting Requirements • 4–5 years of experience in Regulatory Affairs and/or Pharmacovigilance in pharma or consultancy, • Strong knowledge of EU and Spanish regulations, • Experience in global or corporate regulatory/PV environments, • Fluency in Spanish and English (C1–C2); Nice-to-Have knowledge of Italian and/or Portuguese, • Experience with LATAM regulatory/PV activities, • Exposure to Medical Devices, Veterinary, Cosmetics, or Food Supplements, • Strong interest in or experience with pharmacovigilance systems and processes Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

MONTAJES DELSAZ ❗Estamos buscando talento para unirse a nuestro equipo en Montajes Delsaz ❗ Somos una empresa líder en salas limpias para sectores clave como el Farmacéutico, Biotech y Ciencias de la salud, entre otros. ❤️ ¿Por qué Montajes Delsaz? Nos apasiona lo que hacemos y trabajamos para ofrecer un entorno laboral donde puedas sentirte valorado y desarrollarte profesionalmente. Promovemos una cultura empresarial basada en el trabajo en equipo, la comunicación y el respeto, porque sabemos que el esfuerzo y el compromiso de nuestro equipo son la clave para alcanzar el éxito. En Montajes Delsaz, apostamos por el talento de las personas y en su capacidad para marcar la diferencia, porque eso es lo que nos hace únicos. ▶️ ¿Quieres conocernos mejor? Descubre más sobre nuestra empresa y los proyectos que llevamos a cabo en este video: 🔎 ¿Qué buscamos? COMERCIAL NACIONAL E INTERNACIONAL La misión de la posición es que desarrolle y gestione las relaciones comerciales con los clientes internacionales y nacionales, asegurando el cumplimiento de los objetivos de ventas globales, la apertura de nuevos mercados y la fidelización de la cartera actual. Que actúe como nexo entre la empresa y los distintos mercados internacionales y nacionales, adaptando la estrategia comercial a cada contexto cultural, legal y económico. 🎯 ¿Cuáles serán tus funciones? Funciones: • Identificar, contactar y negociar con clientes potenciales en mercados internacionales y nacionales., • Participar en ferias, misiones comerciales y eventos de networking en el extranjero., • Gestionar procesos de exportación y coordinación logística junto al departamento correspondiente., • Elaborar ofertas comerciales, contratos y seguimiento de pedidos internacionales y nacionales., • Analizar tendencias del mercado, competencia y oportunidades de expansión., • Cumplir con objetivos de ventas y márgenes establecidos para cada zona geográfica., • Adaptar estrategias comerciales al marco legal y fiscal de cada país., • Coordinarse con equipos de marketing, producción y finanzas para asegurar la satisfacción del cliente. 🎯 Lo que buscamos en ti Formación requerida: Titulación universitaria en Ingeniería, Arquitectura, Farmacia o similar Deseable poseer Máster en Comercio Exterior, Negociación Internacional, Dirección Comercial o MBA. Formación continua en tendencias del mercado global y técnicas de venta. Competencias: Experiencia comprobada en ventas internacionales y desarrollo de negocios globales (>5 años). Dominio del inglés (C1-C2); otros idiomas valorables (francés, alemán, portugués, etc.). Experiencia previa en negociación con distribuidores, grandes cuentas, canales internacionales, sectores como construcción, ingeniería, instalaciones, etc. Se valorará muy positivamente poseer experiencia técnica y/o comercial previa en mercados específicos (Europa, LATAM, Asia, …) en el sector Pharma. Conocimiento de comercio exterior, Incoterms, aduanas, normativa internacional. Manejo avanzado de CRM, ERPs comerciales (Salesforce, SAP, etc.). Capacidad de análisis de mercados internacionales y nacionales. Habilidades de negociación multiculturales. Disponibilidad para viajar a nivel nacional e internacional (>30%). Permiso de conducir. Habilidades: Alta orientación a resultados y cierre de ventas. Comunicación clara y persuasiva en entornos multiculturales. Adaptabilidad y resiliencia en entornos cambiantes. Capacidad de organización y autonomía. Empatía y construcción de relaciones a largo plazo. Pensamiento estratégico con visión global. Toma de decisiones. Trabajo en equipo y cooperación. Tolerancia a la presión. Si te apasionan los retos, es tu oportunidad, no dudes en inscribirte, nosotros estaremos encantados de conocerte. 🤝 ¿Qué ofrecemos? • Contrato indefinido., • Jornada completa., • Salario competitivo según experiencia y valía., • Centro de trabajo situado en Barcelona. 💡 ¿Te interesa? ¡Estamos deseando conocerte! Inscríbete ahora y únete a Montajes Delsaz para formar parte de un equipo que valora tu talento.

A leading teleradiology provider across Europe and the UK, supporting a global network of 350+ subspecialized radiologists. The company focuses on delivering accurate, timely radiology reporting through advanced technology to improve patient care and help healthcare providers manage increasing imaging demand. With an international presence across multiple locations, it offers 24/7 remote reporting services for hospitals and clinics, enabling efficient handling of both routine and urgent diagnostic imaging. An important partner of The Teleconsult Group is Meditecs, developing the technology that drives the integration and interoperability projects since 2018. Meditecs is a Spanish company specialized in healthcare interoperability, with more than 16 years of experience in hospital and regional projects in Spain, Europe, UK, Asia, with ongoing projects in Canada, US, and Latin America. Through its own technology, MT Smart Connect, Meditecs' solutions integrate: medical devices (diagnostic imaging, laboratory, patient monitoring, etc.), electromedicine equipment, EHR and consultation management systems, HIS, LIS, RIS and PACS, medical cloud platforms, and any other healthcare system or data source, making use of technologies or standards: To serve as the strategic "Human Firewall" and primary translator between Teleconsult’s diverse business departments and the Meditecs development team. By mastering the art of requirements interception and solution design, you will eliminate development bottlenecks, provide business stakeholders with predictable timelines, and ensure every line of code adds maximum value to the company. The Technical Product Owner is the ultimate gatekeeper of the development lifecycle. You are responsible for the entire journey of a feature from the initial spark of a business need, through rigorous technical design with architects, to the final validation of a high-quality software release. Serve as the sole point of entry for all software requests. You will "intercept" ad-hoc communications from different departments to protect the development team's focus and efficiency. Architectural Partnership: Work hand-in-hand with Meditecs’ Software Architects and Senior Developers to bridge the gap between business "vision" and technical "reality." Technical Design Review: Participate in designing system workflows, API integrations, and data models to ensure they are scalable and align with Teleconsult’s existing ecosystem (existing custom ERP with several dashboards, integrated with Agfa Enterprise Imaging). Feasibility Analysis: Act as a sounding board for the technical team to identify potential constraints, technical debt, or risks early in the design phase. Project Governance & Delivery Management Develop and maintain a transparent project roadmap. Cost & Resource Estimation: Collaborate with technical leads to provide accurate effort estimations (time and cost) for new initiatives, enabling data-driven decision-making for leadership. Quality, Compliance & UAT Gatekeeper of Quality: Define and oversee User Acceptance Testing (UAT). You are the final authority who confirms that the delivered software meets the original business requirements and quality standards. Governance: Ensure all solutions comply with company policies regarding Data Privacy (GDPR) and Information Security. General Know the Environmental, Quality and Information Security objectives and goals established for the company. Follow the policy and procedures in the Environmental, Quality and Information Security Management related to your role. Experience: 6+ years as a Product Owner, Technical Project Manager, or Senior Systems Analyst. Web Ecosystems: Proven experience managing complex, data-heavy web applications and dashboards. Mastery of Bitbucket and modeling tools (UML, BPMN, …). Technical Literacy: Strong understanding of API-led architecture, SQL, and SaaS environments (ideally Google Cloud Platform). Methodology: Deep knowledge of Agile/Scrum and the ability to adapt it to a multi-project remote environment. Preferably knowledge of JIRA and Confluence. Diplomatic Authority: The ability to say "no" or "not yet" to senior stakeholders firmly but professionally. Fluent in English and Spanish (mandatory), with the ability to simplify complex technical concepts for non-technical users. If you are a structured and technically fluent Product Owner who thrives at the intersection of business and development, we would love to hear from you. net and Mobile: +44 (0) 7367 425270.

Addetto Customer Service JSP, il principale produttore europeo di Dispositivi di Protezione Individuale (DPI), è alla ricerca di un/una Customer Service Executive entusiasta e professionale da inserire nel nostro dinamico team con sede a Barcelona Spain Il nostro impegno in JSP è progettare e produrre prodotti innovativi che non solo salvino vite umane, ma che ci distinguano anche dalla concorrenza. JSP è cresciuta considerevolmente negli ultimi 5 anni. Abbiamo investito a livello globale, passando da tre siti produttivi nel Regno Unito a stabilimenti dislocati in tutta Europa, negli Stati Uniti e in Asia. Nel 2018 abbiamo inoltre inaugurato uno stabilimento produttivo di livello internazionale in Germania. In qualità di Customer Service Executive, fornirai un servizio clienti d’eccellenza a tutti i clienti JSP, dimostrando una solida comprensione delle loro esigenze, gestendo le richieste con rapidità e precisione e mostrando empatia verso le loro problematiche, offrendo al contempo soluzioni proattive. Tutte queste attività dovranno essere svolte con cordialità e professionalità, al fine di posizionare il servizio clienti di JSP come punto di riferimento del mercato. Obiettivi / Responsabilità • Inserire, monitorare e aggiornare il portafoglio ordini (inserimento, controllo e gestione dei back order), • Informare e aggiornare i clienti sullo stato dei loro ordini, incluse eventuali modifiche delle date di consegna, • Gestire, se necessario, le consegne in collaborazione con il centro logistico e i trasportatori, • Gestire il servizio post-vendita interfacciandosi con la forza vendita e con i clienti, • Assicurare la corretta applicazione dei listini, delle tariffe e delle regole commerciali aziendali, • Gestire le controversie con i clienti, monitorando note di credito e resi, • Supportare l’apertura di nuovi account cliente, • Inserire nuovi contatti e aggiornare i dati anagrafici dei clienti (indirizzi, referenti e contatti), • Collaborare con i team di vendita per la gestione dei clienti ed eventuali attività di follow-up Competenze • Madrelingua italiana, • Buona conoscenza della lingua spagnola scritta e parlata, • Ottima conoscenza della lingua inglese (livello minimo C1), utilizzata quotidianamente; la sede centrale dell’azienda è a Oxford, Regno Unito, • Esperienza nell’amministrazione delle vendite e/o nel servizio clienti considerata un plus, • Buona conoscenza del pack Office, • Gradita familiarità con SAGE X3 o sistemi CRM analoghi, • Affidabilità, buone capacità organizzative e atteggiamento positivo e collaborativo, • Un’esperienza pregressa nel settore dei Dispositivi di Protezione Individuale (DPI) sarà considerata un valore aggiunto Requisiti • Almeno 1 anno di esperienza in ambito Customer Service

Teleconsult Group A leading teleradiology provider across Europe and the UK, supporting a global network of 350+ subspecialized radiologists. The company focuses on delivering accurate, timely radiology reporting through advanced technology to improve patient care and help healthcare providers manage increasing imaging demand. With an international presence across multiple locations, it offers 24/7 remote reporting services for hospitals and clinics, enabling efficient handling of both routine and urgent diagnostic imaging. An important partner of The Teleconsult Group is Meditecs, developing the technology that drives the integration and interoperability projects since 2018. Meditecs is a Spanish company specialized in healthcare interoperability, with more than 16 years of experience in hospital and regional projects in Spain, Europe, UK, Asia, with ongoing projects in Canada, US, and Latin America. Through its own technology, MT Smart Connect, Meditecs' solutions integrate: medical devices (diagnostic imaging, laboratory, patient monitoring, etc.), electromedicine equipment, EHR and consultation management systems, HIS, LIS, RIS and PACS, medical cloud platforms, and any other healthcare system or data source, making use of technologies or standards: HL7 V2.X, HL7, FHIR, ASTM E1381, DICOM, IHE Profiles. Job overview To serve as the strategic Human Firewall and primary translator between Teleconsult’s diverse business departments and the Meditecs development team. Your mission is to transform a high volume of fragmented, ad-hoc requirements into a structured, technically sound, and prioritized product roadmap. By mastering the art of requirements interception and solution design, you will eliminate development bottlenecks, provide business stakeholders with predictable timelines, and ensure every line of code adds maximum value to the company. Primary Accountability The Technical Product Owner is the ultimate gatekeeper of the development lifecycle. You will sit at the intersection of business strategy and technical execution, ensuring that the Meditecs team is never distracted by conflicting priorities. You are responsible for the entire journey of a feature from the initial spark of a business need, through rigorous technical design with architects, to the final validation of a high-quality software release. Key Responsibilities 1. Requirements Engineering (Gathering, Interception & Validation) • Rigorous Validation: Critically evaluate every request against business goals. You must ensure that requirements are feasible, necessary, and fully understood before they ever reach the backlog., • Specification Mastery: Translate business needs into high-fidelity functional specifications, user stories, and clear acceptance criteria that leave no room for developer ambiguity. 2. Collaborative Solution Design • Technical Design Review: Participate in designing system workflows, API integrations, and data models to ensure they are scalable and align with Teleconsult’s existing ecosystem (existing custom ERP with several dashboards, integrated with Agfa Enterprise Imaging)., • Detailed documentation: Functional specifications using UML standardized visual diagrams (Use Case, Statechart, Activity/Process flow… ), • Feasibility Analysis: Act as a sounding board for the technical team to identify potential constraints, technical debt, or risks early in the design phase. 3. Project Governance & Delivery Management • Roadmap & Timeline Ownership: Develop and maintain a transparent project roadmap. You are responsible for providing stakeholders with realistic delivery timelines and progress updates., • Cost & Resource Estimation: Collaborate with technical leads to provide accurate effort estimations (time and cost) for new initiatives, enabling data-driven decision-making for leadership. 4. Quality, Compliance & UAT • Gatekeeper of Quality: Define and oversee User Acceptance Testing (UAT). You are the final authority who confirms that the delivered software meets the original business requirements and quality standards., • Governance: Ensure all solutions comply with company policies regarding Data Privacy (GDPR) and Information Security. 5. General • Know the company policies., • Know the Environmental, Quality and Information Security objectives and goals established for the company., • Follow the policy and procedures in the Environmental, Quality and Information Security Management related to your role., • Properly manage the assets assigned to you., • Properly manage risks if you own any risk identified by the organization., • Actively participate in the adoption and implementation of corrective and improvement actions. Requirements Education & Experience • Experience: 6+ years as a Product Owner, Technical Project Manager, or Senior Systems Analyst., • Web Ecosystems: Proven experience managing complex, data-heavy web applications and dashboards. Skills & Competencies Technical Skills • Expert Documentation: Mastery of Bitbucket and modeling tools (UML, BPMN, …)., • Technical Literacy: Strong understanding of API-led architecture, SQL, and SaaS environments (ideally Google Cloud Platform)., • Methodology: Deep knowledge of Agile/Scrum and the ability to adapt it to a multi-project remote environment., • Preferably knowledge of JIRA and Confluence. Soft Skills • Communication: Fluent in English and Spanish (mandatory), with the ability to simplify complex technical concepts for non-technical users. If you are a structured and technically fluent Product Owner who thrives at the intersection of business and development, we would love to hear from you. This is a unique opportunity to take ownership of complex, high-impact products while shaping how requirements are transformed into scalable solutions. Apply directly or reach out to discuss how your experience aligns with this role. Contact our Head of Recruitment, Leticia Calva at and Mobile: +44 (0) 7367 425270.

Buscamos un ingeniero/a con experiencia en Project Management que quiera incorporarse a nuestro equipo de consultores/as. Quien somos 🙌 Somos MIGSO-PCUBED la consultora Líder en Project Management, parte del grupo ALTEN. 🌍Actualmente contamos con más de 3.300 consultores, operando en Europa, Norte América, Asia y Australia. 🤝🏻 Damos soporte a nuestros clientes en gestión de proyectos y PMO. MIGSO-PCUBED brinda su apoyo a proyectos de I+D, TIC y transformación para nuestros clientes. Tenemos una amplia cartera de Proyectos en sectores como Aeronáutica, Automoción, Ferrocarril, Defensa, Energía, Servicios Financieros, Telecomunicaciones, Tecnología & Media, y Sector Público. 💻 ¿Cómo será tu día a día? • Planificar el proyecto involucrando a todos los departamentos afectados (compras, ingeniería, etc...)., • Controlar presupuestos y costes., • Estudiar y gestionar posibles riesgos., • Hacer seguimientos del avance del proyecto., • Elaboración de informes detallados de avance tanto a nivel proyecto como a nivel portfolio, con manejo de varios KPI, • Analizar procesos y realizar una mejora continua de ellos, • Proporcionar soporte de gestión de proyectos a los distintos departamentos implicados a todos los niveles de gobierno. 👀¿Quién eres? • Estas graduado/licenciado en ingeniería o tienes un master en gestión de proyectos, • Tienes una experiencia profesional de mínimo 3 años en gestión de proyectos, • Tienes una comunicación fluida en inglés (B2/C1), • Manejo de alguna herramientas: SAP, Excel, MS Project, • Eres una persona dinámica, comprometida, a la que le gusta estar en contacto con diferentes interlocutores y que sabe trabajar en equipo. ¿Porqué trabajar con nosotros? ¡Trabajar con nosotros es una experiencia única por varias razones! Aquí tienes algunos puntos clave: • Desarrollo profesional: Ofrecemos un plan formativo robusto para impulsar tu crecimiento y habilidades, además de oportunidades de formación en idiomas para expandir tus horizontes., • ¡Diviértete mientras trabajas! Nuestros eventos corporativos y actividades de team building te permiten conectar con colegas, construir relaciones sólidas y disfrutar de momentos memorables., • Flexibilidad que importa: Tu bienestar es fundamental, por eso ofrecemos retribución flexible que incluye Ticket Restaurante, transporte y guardería, para adaptarnos a tus necesidades., • Tu salud es nuestra prioridad: Ofrecemos un completo seguro médico para cuidar de ti., • Cultura de bienestar: Nos preocupamos por ti. Nuestras políticas promueven la igualdad, la desconexión digital y disponemos de espacios de trabajo acogedores que fomentan un entorno positivo y equilibrado para todos. ¡Únete a MIGSO-PCUBED y conviértete en un/a Experto/a en Project Management! 👨 💻👩 💻 #ProjectManager #GestiónDeProyectos #MejoraContinua #SAP #MSProject #InglésB2 #MoreThanJustAJob

Sobre Hebron, S.A.: Somos una empresa situada en La Llagosta dedicada a la fabricación y distribución de productos químicos. Pertenecemos al grupo Otsuka, empresa japonesa referente en Asia. Con el 85% de nuestras ventas internacionales en la zona EMEA, somos líderes en el sector y nos comprometemos con la innovación y la calidad. Ofrecemos un entorno dinámico y colaborativo, donde valoramos y cuidamos el bienestar y el equilibrio entre la vida laboral y personal de nuestra plantilla. Tu misión Buscamos a un profesional con alta motivación y experiencia para desempeñarse como HSE Technician en nuestro equipo. Bajo la dirección del Manufacturing General Manager, será responsable de proporciona soporte en todas las actividades relacionadas con Seguridad, Prevención y Medioambiente de la empresa. En el área de Seguridad y Prevención, coordinará el Servicio de Prevención Ajeno, asegurando su correcto funcionamiento; asegurará el cumplimiento legal en materia de prevención de riesgos laborales y realizará las acciones que mantienen a la empresa con un estándar de seguridad adecuado. En el área de Medioambiente, supervisará y gestionará todos los vectores ambientales de la empresa (residuos, emisiones atmosféricas, aguas residuales, suelos…) y se encarga de mantener la ISO14001 así como la Autorización Ambiental. Tus Responsabilidades Principales • Coordinar las reuniones periódicas y las actividades del Servicio de Prevención Ajeno (SPA) tanto de Especialidades Técnicas como de Vigilancia de la Salud., • Participar en la Evaluación de Riesgo de todos los puestos de trabajo de la empresa y resolver las acciones de mejora propuestas por el SPA., • Participar en el Comité de Seguridad y Salud (CSS) y el Comité de Autoprotección (AC) como secretario/a., • Investigar accidentes e incidentes cuando ocurran y definir medidas correctivas y preventivas., • Cumplir y asegurar el cumplimiento de las normas de seguridad de la empresa., • Ser Recurso Preventivo de la compañía y realizar/ firmar los permisos de trabajo necesarios., • Supervisar y realizar, cuando se requiera, los Permisos de Trabajo Especial y/o los Planes Específicos de Seguridad de aquellos trabajos con especial peligrosidad., • Trabajar, junto con las empresas externas que vayan a trabajar en las instalaciones, la Coordinación de Actividades Empresariales (CAE) y los Permisos de Trabajo necesarios., • Participar en la realización y dar soporte al cumplimiento del Plan de Autoprotección (PAU)., • Identificar, divulgar y aplicar la normativa relacionada con el Medioambiente (Vertido de aguas, emisiones atmosféricas, suelos contaminados, gestión de residuos, control de la legionela…) y los cambios legislativos que puedan afectar a la compañía en el campo de Seguridad y Prevención., • Realizar las acciones necesarias para el cumplimiento legal en materia de Prevención de Riesgos Laborales, Medioambiente y Seguridad Industrial (APQ, DOPEX, RD1215, …)., • Definir, gestionar, homologar junto al SPA y suministrar los EPIs necesarios para protección del personal., • Gestión de SP bajo la norma ISO 45.001 y MA bajo la norma ISO 14.001. Documentar, gestionar y pasar las auditorias. Gestionar la política y objetivos de SP y MA., • Reportar periódicamente indicadores y a OCC los datos necesarios de SP y MA., • Asegurar la gestión de los residuos. Buscar proveedores para los residuos y coordinar con fábrica y administración la correcta realización de las tareas., • Control de las energías (Gas, electricidad) y agua. Incluida la contratación y control presupuestario de empresas relacionadas con las actividades medioambientales (residuos, agua, energía…). Proponer medidas de reducción., • Cumplimentar toda la documentación oficial requerida asociada MA (Declaración Residuos, DUCA…) y a SP (Gravamen Protección Civil, ANPAQ,…), • Consecución y mantenimiento de la Licencia Ambiental para Hebron., • Controlar el Budget de SP, Residuos y Energía., • Formar o coordinar la formación externa en el campo de Seguridad y Prevención y Medioambiente a toda la plantilla., • Ejecutar o asegurar la realización de las acciones y proyectos relacionados con MA y SP solicitadas. ¿Qué necesitas para aplicar? Ingeniería Química o Industria o similar. Máster PRL / Máster Gestión Ambiental o afines. Inglés nivel B1-B2 Autocad Conocimientos básicos de reglamentación aplicable a industria y legalización de equipos. 2-3 años de experiencia en puesto similar Lo que ofrecemos • Incorporación inmediata a tiempo completo y con contrato indefinido., • Entorno de trabajo profesional, estable y colaborativo., • Horario Flexible, • Menú diario por 1,20€, • Salario competitivo, • Oportunidades de formación y desarrollo Hebron es una empresa que ofrece igualdad de oportunidades. Estamos comprometidos con la diversidad y la construcción de un equipo que represente una variedad de antecedentes, perspectivas y habilidades. Los procesos de selección se fundamentan en la transparencia y la no discriminación, tomando como base las calificaciones, el mérito y la necesidad del negocio. Nuestro objetivo es ser un equipo diverso, en un entorno inclusivo donde podamos seguir creciendo juntos.

PLG is a global life‑science services provider offering product development, lifecycle management, consulting, and digital solutions. With offices across Europe, North America, and Asia, it continues to grow through organic expansion and strategic acquisitions that strengthen its capabilities and footprint. The M&A Sr. Associate / Specialist will play a key role in executing PLG’s buy-and-build strategy. The role involves identifying potential acquisition targets, managing the end-to-end transaction process, coordinating due diligence, and supporting integration planning. Working closely with senior management and private equity stakeholders, the Mergers and Acquisitions Manager will contribute to the evaluation and execution of strategic investments across the life sciences services sector MISSIONS: • Financial Analysis:, • Conduct research and financial analysis to evaluate potential M&A opportunities, including financial statements, valuation metrics, and key performance indicators., • Analyze industry trends, competitive landscapes, and market conditions to assess the financial and strategic viability of potential transactions., • Prepare financial projections and scenario analyses to evaluate the potential impact of M&A activities on the company's financials., • Due Diligence:, • Lead due diligence process by gathering and analyzing relevant information, including financial, tax, legal, commercial and operational DD., • Assist in coordinating due diligence efforts with various internal teams and external advisors, ensuring comprehensive evaluation of target companies., • Identify risks, opportunities, and synergies associated with potential transactions, and provide recommendations based on due diligence findings., • Documentation and Reporting:, • Prepare detailed reports, including Commercial DD and M&A presentations for the executive board summarizing the analysis and key findings., • Assist in drafting and reviewing transaction-related documentation, such as letters of intent, sellers purchase agreements, and disclosure schedules., • Maintain organized and updated master target list with last information available. transaction records, including financial models, due diligence materials, and other relevant documentation., • Interactions:, • Work closely with teams from various departments including finance, sales, HR, quality, and IT to foster collaboration and achieve shared objectives., • Engage with M&A advisors, auditors, and the management of target companies to facilitate smooth transactions and integration processes., • Maintain regular and effective communication with the Post-Merger Integration (PMI) team, providing updates on ongoing transactions and coordinating efforts to ensure successful integration., • Keep abreast of market trends, regulatory changes, and best practices pertaining to M&A activities. Provide valuable insights and recommendations to enhance the company's M&A strategy. THE SUCCESSFUL APPLICANT • Minimum of 4-6 years of relevant business experience in areas such as M&A, transaction services, private equity, corporate development, strategy consulting, or venture capital., • Excellent in conducting comprehensive financial analysis and modeling, with strong analytical skills to interpret complex financial data and perform valuation analysis., • Demonstrated expertise in deal structuring, valuation, and financial/M&A modeling., • Knowledge of business strategy and its application in a corporate context., • Exceptional financial acumen and understanding of financial concepts., • Demonstrated experience managing multiple transactions simultaneously, • Advanced proficiency in Office tools, particularly Excel and PowerPoint., • Proven project management capabilities, including the ability to independently plan, manage, and deliver projects., • Strategic thinker with a collaborative approach and proactive mindset., • Excellent communication, influencing, negotiation, and organizational skills., • Ability to cultivate and keep strong relationships., • Possesses integrity, analytical skills, and critical thinking abilities., • International experience in a professional capacity., • Fluent in both written and spoken English. French is a plus., • Willingness to travel occasionally, approximately 2-3 days every 2 months., • Previous experience in the Life Sciences and/or consulting services industry is highly advantageous. WHAT WE CAN OFFER • The possibility of working in hybrid mode;, • A dynamic, multicultural working environment;, • A long-term career plan, • An interesting and extensive salary package A flat organizational structure with close collaboration and communication with management and cross departments

PLG is a global life‑science services provider offering product development, lifecycle management, consulting, and digital solutions. With offices across Europe, North America, and Asia, it continues to grow through organic expansion and strategic acquisitions that strengthen its capabilities and footprint. The M&A Sr. Associate / Specialist will play a key role in executing PLG’s buy-and-build strategy. The role involves identifying potential acquisition targets, managing the end-to-end transaction process, coordinating due diligence, and supporting integration planning. Working closely with senior management and private equity stakeholders, the Mergers and Acquisitions Manager will contribute to the evaluation and execution of strategic investments across the life sciences services sector MISSIONS: • Financial Analysis:, • Conduct research and financial analysis to evaluate potential M&A opportunities, including financial statements, valuation metrics, and key performance indicators., • Analyze industry trends, competitive landscapes, and market conditions to assess the financial and strategic viability of potential transactions., • Prepare financial projections and scenario analyses to evaluate the potential impact of M&A activities on the company's financials., • Due Diligence:, • Lead due diligence process by gathering and analyzing relevant information, including financial, tax, legal, commercial and operational DD., • Assist in coordinating due diligence efforts with various internal teams and external advisors, ensuring comprehensive evaluation of target companies., • Identify risks, opportunities, and synergies associated with potential transactions, and provide recommendations based on due diligence findings., • Documentation and Reporting:, • Prepare detailed reports, including Commercial DD and M&A presentations for the executive board summarizing the analysis and key findings., • Assist in drafting and reviewing transaction-related documentation, such as letters of intent, sellers purchase agreements, and disclosure schedules., • Maintain organized and updated master target list with last information available. transaction records, including financial models, due diligence materials, and other relevant documentation., • Interactions:, • Work closely with teams from various departments including finance, sales, HR, quality, and IT to foster collaboration and achieve shared objectives., • Engage with M&A advisors, auditors, and the management of target companies to facilitate smooth transactions and integration processes., • Maintain regular and effective communication with the Post-Merger Integration (PMI) team, providing updates on ongoing transactions and coordinating efforts to ensure successful integration., • Keep abreast of market trends, regulatory changes, and best practices pertaining to M&A activities. Provide valuable insights and recommendations to enhance the company's M&A strategy. THE SUCCESSFUL APPLICANT • Minimum of 4-6 years of relevant business experience in areas such as M&A, transaction services, private equity, corporate development, strategy consulting, or venture capital., • Excellent in conducting comprehensive financial analysis and modeling, with strong analytical skills to interpret complex financial data and perform valuation analysis., • Demonstrated expertise in deal structuring, valuation, and financial/M&A modeling., • Knowledge of business strategy and its application in a corporate context., • Exceptional financial acumen and understanding of financial concepts., • Demonstrated experience managing multiple transactions simultaneously, • Advanced proficiency in Office tools, particularly Excel and PowerPoint., • Proven project management capabilities, including the ability to independently plan, manage, and deliver projects., • Strategic thinker with a collaborative approach and proactive mindset., • Excellent communication, influencing, negotiation, and organizational skills., • Ability to cultivate and keep strong relationships., • Possesses integrity, analytical skills, and critical thinking abilities., • International experience in a professional capacity., • Fluent in both written and spoken English. French is a plus., • Willingness to travel occasionally, approximately 2-3 days every 2 months., • Previous experience in the Life Sciences and/or consulting services industry is highly advantageous. WHAT WE CAN OFFER • The possibility of working in hybrid mode;, • A dynamic, multicultural working environment;, • A long-term career plan, • An interesting and extensive salary package A flat organizational structure with close collaboration and communication with management and cross departments

Ready to join the future of work? Come join a remote and hybrid first*, global company spanning across the Americas, Europe, Asia, and Africa for A Job That Works for You. You will become among 900+ Guardians worldwide spread across 50+ countries, embracing YOUR unique approach to work. 🌎 Our vision of the future of work is “work in any way” which offers flexibility for where you work, empowering you to define your ideal work environment, unbound by the traditional notions of what work should look like. Most importantly, it puts people first! 🤩 (*As standard we are a remote-first company, however some roles are required to have more of an office presence - we are happy to confirm this during our initial call 😊) We’re seeking a Dutch speaking Business Development Representative (BDR) to join our high-performing EMEA sales team in Barcelona. This is an opportunity to be part of a fast-growing global company, helping HR and business leaders expand their workforce across borders. How you will make a difference: As our Business Development Representative, you’ll be at the forefront of driving Safeguard Global’s growth across Netherlands and the wider EMEA region. This is your opportunity to make a real impact. Identifying high-potential opportunities, sparking meaningful conversations, and opening doors with HR, Finance, and C-suite leaders. You won’t just be booking meetings, you’ll be shaping our pipeline, uncovering real business challenges, and positioning our global employment solutions as the answer. Working closely with our Account Executives, Marketing, and Partnerships teams, you’ll play a key role in building momentum, creating demand, and generating new business opportunities that power our continued growth. 🚀 • Drive new business growth by proactively prospecting and qualifying leads through outbound channels (calls, emails, social) and following up on inbound interest., • Engage and influence Dutch-speaking HR, Finance, and Operations leaders, uncovering their challenges and positioning Safeguard Global’s solutions as the answer., • Partner closely with Account Executives to build targeted account strategies and ensure seamless handover of high-quality opportunities., • Fuel the top of the funnel by leveraging marketing campaigns, events, and partner channels to generate demand and pipeline., • Own your pipeline data, keeping Salesforce up to date and providing clear visibility into performance and pipeline health., • Hit (and exceed) your targets, delivering against monthly KPIs for meetings, opportunities, and revenue contribution., • Continuously level up your skills by embracing feedback, coaching, and collaboration to refine your outreach and maximise impact. What will make you stand out: • Proven experience in business development or sales, ideally within B2B SaaS, HR Tech, or global workforce solutions—bringing a strong understanding of how to generate and qualify opportunities., • Fluent Dutch speaker with strong English skills, confident communicating with a wide range of stakeholders across regions., • A natural communicator, able to build rapport quickly, deliver compelling messages, and engage decision-makers with confidence., • Driven, curious, and resilient, with a genuine hunger to hit—and exceed—targets., • Highly organised and adaptable, comfortable managing multiple conversations and opportunities at once in a fast-paced environment., • Tech-savvy, with experience using CRM systems like Salesforce and sales engagement tools to stay efficient and data-driven., • Based in Barcelona, with the flexibility to thrive in a hybrid or remote setup. Who we are and what we do: Safeguard Global is…global! We enable global expansion without the risk by helping 1,500+ customers recruit, hire, manage, and pay employees in nearly 190 countries. Join us to meet diverse talent, explore new cultures, and connect with amazing folks from around the globe. ✈️ Our Global Benefits • 👨 💻 Autonomy and Flexibility (work in any way): Remote first, with the flexibility to include life needs like school runs and gym breaks in your schedule, all while maintaining a high standard of work., • 🌴 Generous leave: Enjoy a competitive leave package including paid bonding leaves for new additions to your family, • 🎁 Make a difference: Get 2 paid charitable days off to contribute to causes you believe in, • 💰 Corporate bonus/SIP: All Guardians are eligible for our annual bonus scheme or sales incentive plan., • ✈️ International environment: Grow your network internationally and collaborate across the world. Interact, discover cultures, and tap into local expertise., • ⭐ Human centered culture: We emphasize the people factor in everything we do. Our nurturing culture ensures your ideas reach our leaders and your contributions get the recognition they deserve., • 📚 Learning: We support your continuous growth by providing access to 2 learning platforms, where you can learn at your own pace.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are seeking a Senior Regulatory Affairs & Pharmacovigilance Specialist to support both local and international regulatory and PV activities. The role combines hands-on regulatory work with pharmacovigilance oversight, ensuring compliance across Spain and LATAM markets. Key Responsibilities Regulatory Affairs (RA): • Analyze EU regulatory strategies and provide recommendations to clients, • Author full technical dossiers (Modules 1–5) from scratch, • Manage variations, renewals, labeling updates, and Health Authority interactions, • Support regulatory activities in LATAM markets, • Support PV activities and reporting obligations in Spain and EU, • Ensure compliance with local and international safety regulations, • Assist in signal detection, risk management, and safety documentation, • Coordinate with global PV teams to align processes and reporting Requirements • 4–5 years of experience in Regulatory Affairs and/or Pharmacovigilance in pharma or consultancy, • Strong knowledge of EU and Spanish regulations, • Experience in global or corporate regulatory/PV environments, • Fluency in Spanish and English (C1–C2); Nice-to-Have knowledge of Italian and/or Portuguese, • Experience with LATAM regulatory/PV activities, • Exposure to Medical Devices, Veterinary, Cosmetics, or Food Supplements, • Strong interest in or experience with pharmacovigilance systems and processes Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are seeking a Senior Regulatory Affairs & Pharmacovigilance Specialist to support both local and international regulatory and PV activities. The role combines hands-on regulatory work with pharmacovigilance oversight, ensuring compliance across Spain and LATAM markets. Key Responsibilities Regulatory Affairs (RA): • Analyze EU regulatory strategies and provide recommendations to clients, • Author full technical dossiers (Modules 1–5) from scratch, • Manage variations, renewals, labeling updates, and Health Authority interactions, • Support regulatory activities in LATAM markets, • Support PV activities and reporting obligations in Spain and EU, • Ensure compliance with local and international safety regulations, • Assist in signal detection, risk management, and safety documentation, • Coordinate with global PV teams to align processes and reporting Requirements • 4–5 years of experience in Regulatory Affairs and/or Pharmacovigilance in pharma or consultancy, • Strong knowledge of EU and Spanish regulations, • Experience in global or corporate regulatory/PV environments, • Fluency in Spanish and English (C1–C2); Nice-to-Have knowledge of Italian and/or Portuguese, • Experience with LATAM regulatory/PV activities, • Exposure to Medical Devices, Veterinary, Cosmetics, or Food Supplements, • Strong interest in or experience with pharmacovigilance systems and processes Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Ready to join the future of work? Come join a remote and hybrid first*, global company spanning across the Americas, Europe, Asia, and Africa for A Job That Works for You. You will become among 900+ Guardians worldwide spread across 50+ countries, embracing YOUR unique approach to work. 🌎 Our vision of the future of work is “work in any way” which offers flexibility for where you work, empowering you to define your ideal work environment, unbound by the traditional notions of what work should look like. Most importantly, it puts people first! 🤩 (*As standard we are a remote-first company, however some roles are required to have more of an office presence - we are happy to confirm this during our initial call 😊) How you will make a difference: As our Global Solutions Advisor (Account Executive), you will work with clients across the Spanish region and wider EMEA Markets using your Spanish language skills to build strong relationships and understand their growth ambitions. You’ll guide organisations through the challenges of global expansion and workforce management, owning the full sales cycle from first conversation to close. Based in Spain with occasional travel to our Barcelona office, your work will help clients expand confidently anywhere in the world. • Develop sales opportunities by proactively nurturing opportunities from self-generated leads, marketing lists, and warm leads across the organisation., • Develop and manage your own portfolio of prospects, ensuring consistent growth and engagement., • Plan and execute targeted sales activities to consistently achieve and exceed your targets., • Own the full sales journey, from identifying prospects to progressing and closing deals., • Engage HR, Finance, and C-Suite stakeholders to uncover needs, align solutions, and build compelling business cases., • Develop and present customised proposals, leading contract negotiations to secure deals that deliver value for both clients and the business., • Build and maintain a reliable pipeline while forecasting weekly and monthly sales with accuracy., • Collaborate with channel partners, sharing insights on lead performance and guiding them to provide high-quality opportunities., • Respond to and follow up on all sales enquiries via email, phone, and occasional client visits, delivering exceptional client experiences., • Stay up to date on HR and global employment trends to bring insight and value to every client conversation., • Actively represent Safeguard Global at industry events, forging connections, expanding your network, and uncovering new business opportunities. What will make you stand out: • Proven track record in B2B consultative sales, ideally within HR Tech, Payroll, SaaS, or Employer-of-Record (EOR) solutions., • Strong fluency in Spanish and English is essential, • Experience managing complex sales cycles and engaging multiple decision-makers across HR, Finance, and C-Suite., • Exceptional communication, negotiation, and presentation skills., • Highly organised, self-motivated, and comfortable taking ownership of opportunities independently., • Ability to understand client needs and deliver tailored solutions that create real value., • Collaborative mindset, able to work effectively with colleagues, customers, and business partners., • Results-driven with a focus on building long-term client relationships and achieving business outcomes. What you will get joining our Sales Team: • Selling top-notch services with a high need at a market leader company, • First-class sales enablement training program based on value selling, individual coaching program, • Continuous learning on how companies operate globally, • Opportunities to travel and visit exciting places, • Ownership of your quota achievement, work with autonomy and flexibility for your best performance, • High performing standards that will make you grow your career, • Energetic, international, and fun environment Who we are and what we do: Safeguard Global is…global! We enable global expansion without the risk by helping 1,500+ customers recruit, hire, manage, and pay employees in nearly 190 countries. Join us to meet diverse talent, explore new cultures, and connect with amazing folks from around the globe. ✈️ Our Global Benefits • 👨 💻 Autonomy and Flexibility (work in any way): Remote first, with the flexibility to include life needs like school runs and gym breaks in your schedule, all while maintaining a high standard of work., • 🌴 Generous leave: Enjoy a competitive leave package including paid bonding leaves for new additions to your family, • 🎁 Make a difference: Get 2 paid charitable days off to contribute to causes you believe in, • 💰 Corporate bonus/SIP: All Guardians are eligible for our annual bonus scheme or sales incentive plan., • ✈️ International environment: Grow your network internationally and collaborate across the world. Interact, discover cultures, and tap into local expertise., • ⭐ Human centered culture: We emphasize the people factor in everything we do. Our nurturing culture ensures your ideas reach our leaders and your contributions get the recognition they deserve., • 📚 Learning: We support your continuous growth by providing access to 2 learning platforms, where you can learn at your own pace. Next Steps: To apply, please click on the following link. We wish you the best with your application. Welcome to the future of work!

Title: SailPoint Developer / IAM Engineer Location: Spain / Europe (Hybrid) We are searching for a SailPoint Developer / Identity & Access Management (IAM) Engineer to support one of our global pharmaceutical organisations in Spain. This is a hands-on, high-impact role within a global life sciences leader, helping to shape the next generation of IAM services and automation. Why this role? You’ll join a team driving a major modernisation of IAM—designing and optimising automated workflows, integrating test automation into CI/CD, and ensuring robust compliance across the identity lifecycle. You’ll work closely with a Spain-based team, with regular in-person workshops that accelerate onboarding, collaboration, and delivery. The Opportunity: What You’ll Do • Develop & enhance SailPoint solutions (IdentityIQ preferred) and IAM workflows (joiner–mover–leaver, access requests, certifications), • Automate identity lifecycle processes and compliance activities (e.g., access recertification) using scripting and APIs (PowerShell, Python, REST), • Embed test automation in CI/CD pipelines; maintain robust, audit-ready test suites; support regression and platform reliability, • Monitor & operate the SailPoint/ IAM environment; troubleshoot issues, optimise performance, and contribute to platform stability, • Collaborate across engineering, security, and product teams to set best practices and help define a new target architecture What You Bring • SailPoint expertise (IdentityIQ strongly preferred) and solid understanding of IAM fundamentals (policies, entitlements, joiner–mover–leaver), • Java proficiency for SailPoint development/customisations, plus scripting (PowerShell and/or Python) and REST API experience, • Familiarity with CI/CD and modern toolchains (e.g., Bitbucket/Git, Jira, Confluence); experience integrating automation into pipelines, • Experience with test automation (frameworks/tools agnostic) and SQL for data validation and troubleshooting, • Clear, structured problem-solving mindset; strong communication in English (Spanish is a plus) Nice to Have • Hands-on with Azure AD / Entra and broader IAM ecosystem, • ITIL understanding (change, incident, problem) and experience in regulated environments, • Background in life sciences or other highly regulated sectors Work Model & Location • Spain-based candidates preferred; proximity to Barcelona or willing to travel advantageous for workshops and onboarding, • Hybrid: day-to-day remote with in-person workshops ~ monthly sometimes less (2–3 days); willingness to come on-site for onboarding and key sessions If you have the skills and experience for this opportunity, then please apply or email Loren your CV today to . Loren is a Client Partner at Haybury Search covering Europe, UK, North America and Asia.

Title: SailPoint Developer / IAM Engineer Location: Spain / Europe (Hybrid) We are searching for a SailPoint Developer / Identity & Access Management (IAM) Engineer to support one of our global pharmaceutical organisations in Spain. This is a hands-on, high-impact role within a global life sciences leader, helping to shape the next generation of IAM services and automation. Why this role? You’ll join a team driving a major modernisation of IAM—designing and optimising automated workflows, integrating test automation into CI/CD, and ensuring robust compliance across the identity lifecycle. You’ll work closely with a Spain-based team, with regular in-person workshops that accelerate onboarding, collaboration, and delivery. The Opportunity: What You’ll Do • Develop & enhance SailPoint solutions (IdentityIQ preferred) and IAM workflows (joiner–mover–leaver, access requests, certifications), • Automate identity lifecycle processes and compliance activities (e.g., access recertification) using scripting and APIs (PowerShell, Python, REST), • Embed test automation in CI/CD pipelines; maintain robust, audit-ready test suites; support regression and platform reliability, • Monitor & operate the SailPoint/ IAM environment; troubleshoot issues, optimise performance, and contribute to platform stability, • Collaborate across engineering, security, and product teams to set best practices and help define a new target architecture What You Bring • SailPoint expertise (IdentityIQ strongly preferred) and solid understanding of IAM fundamentals (policies, entitlements, joiner–mover–leaver), • Java proficiency for SailPoint development/customisations, plus scripting (PowerShell and/or Python) and REST API experience, • Familiarity with CI/CD and modern toolchains (e.g., Bitbucket/Git, Jira, Confluence); experience integrating automation into pipelines, • Experience with test automation (frameworks/tools agnostic) and SQL for data validation and troubleshooting, • Clear, structured problem-solving mindset; strong communication in English (Spanish is a plus) Nice to Have • Hands-on with Azure AD / Entra and broader IAM ecosystem, • ITIL understanding (change, incident, problem) and experience in regulated environments, • Background in life sciences or other highly regulated sectors Work Model & Location • Spain-based candidates preferred; proximity to Barcelona or willing to travel advantageous for workshops and onboarding, • Hybrid: day-to-day remote with in-person workshops ~ monthly sometimes less (2–3 days); willingness to come on-site for onboarding and key sessions If you have the skills and experience for this opportunity, then please apply or email Loren your CV today to . Loren is a Client Partner at Haybury Search covering Europe, UK, North America and Asia.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in Barcelona. This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities. Responsibilities include, but are not limited to: • Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems., • Prepare, review, and execute C&Q and validation documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports)., • Collaborate with cross-functional teams (Engineering, QA, Validation, Manufacturing) to ensure compliance with GMP, regulatory guidelines, and project timelines., • Review technical documentation, P&IDs, FAT/SAT protocols, and vendor manuals., • Identify, troubleshoot, and document deviations, ensuring timely resolution., • Ensure all activities meet GMP, FDA, EMA, and ICH requirements., • Provide project updates and progress reports to stakeholders. Required Qualifications: • Bachelor’s degree in Engineering, Life Sciences, or related field., • At least 1 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants, • Strong knowledge of GMP, FDA, and EU regulations., • Excellent analytical, problem-solving, and communication skills., • Ability to work independently and collaboratively in a project environment., • Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant in Barcelona. This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities. Responsibilities include, but are not limited to: • Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems., • Prepare, review, and execute C&Q and validation documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports)., • Collaborate with cross-functional teams (Engineering, QA, Validation, Manufacturing) to ensure compliance with GMP, regulatory guidelines, and project timelines., • Review technical documentation, P&IDs, FAT/SAT protocols, and vendor manuals., • Identify, troubleshoot, and document deviations, ensuring timely resolution., • Ensure all activities meet GMP, FDA, EMA, and ICH requirements., • Provide project updates and progress reports to stakeholders. Required Qualifications: • Bachelor’s degree in Engineering, Life Sciences, or related field., • At least 1 year of experience in IQ/OQ/PQ protocol development and execution and C&Q for pharmaceutical/biotech facilities, including construction of production plants, • Strong knowledge of GMP, FDA, and EU regulations., • Excellent analytical, problem-solving, and communication skills., • Ability to work independently and collaboratively in a project environment., • Spanish native, English fluent (at least B2) Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are currently seeking a GMP Analytical Lab Consultant - Maintenance & Qualification to support Quality Control laboratory activities within a GMP environment. The role involves managing qualification, calibration, maintenance, and troubleshooting of chemical laboratory instrumentation, ensuring compliance and proper performance of QC equipment. Responsibilities include, but are not limited to: • Perform Periodic Qualification (IQ, OQ, PQ) of Chemical Quality Control laboratory instrumentation, including: HPLC, UPLC, GC, balances, pH meters, Karl Fischer titrators, AAS, UV-Vis, IR spectrophotometers, climatic chambers, DSC, TGA, TOC analyzers., • Author and execute IQ, OQ, and PQ protocols and generate final qualification reports., • Monitor equipment performance, calibration status, and daily functionality checks to ensure GMP compliance., • Coordinate and manage relationships with vendors and external suppliers., • Plan and schedule qualification, calibration, and maintenance activities., • Oversee activity planning and procurement of kits and consumables., • Execute preventive maintenance and troubleshooting activities on laboratory instruments. Preventive Maintenance & Troubleshooting – HPLC • Detector diagnostics and troubleshooting, • Flow cell cleaning and lamp replacement, • Pump diagnostics and replacement of seals, pistons, and fittings, • Diagnosis of mechanical faults (arms, needle, injector systems), • Replacement of tubing, fittings, frits, filters, gaskets, and capillaries, • Cleaning of solvent inlet filters (dip sticks), • System flushing to remove precipitates and contamination, • Leak detection and seal integrity checks, • Diagnosis and replacement of syringes, septa, O-rings, injectors, and liners Required Qualifications: • Degree in scientific disciplines, • Experience of working in GMP environment, • Strong knowledge of analytical laboratory instrumentation and qualification processes (IQ/OQ/PQ)., • Spanish native, english at least B2 Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are looking for a Process Validation Specialist to support validation activities related to aseptic filling operations within a GMP-regulated pharmaceutical manufacturing environment. Responsibilities include, but are not limited to: Support the planning and execution of process validation activities related to filling operations. Assist in the preparation and review of validation documentation , including protocols and reports. Participate in Process Performance Qualification (PPQ) activities and other validation lifecycle activities. Support data collection and analysis during validation runs and routine manufacturing. Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure GMP compliance . Contribute to investigations, deviations, and CAPA actions related to filling processes. Assist with risk assessments and continuous improvement initiatives for manufacturing processes. Support preparation of documentation for internal audits and regulatory inspections . Required Qualifications: Bachelor’s or Master’s degree in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or a related field . Minimum 1 year of experience in the pharmaceutical, biotechnology, or related regulated industry (internships or thesis projects are also considered). Basic knowledge of GMP and pharmaceutical manufacturing processes . Strong organizational and analytical skills. Ability to work effectively in cross-functional teams . Fluent in English and Spanish Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are looking for a Process Validation Specialist to support validation activities related to aseptic filling operations within a GMP-regulated pharmaceutical manufacturing environment. Responsibilities include, but are not limited to: • Support the planning and execution of process validation activities related to filling operations., • Assist in the preparation and review of validation documentation , including protocols and reports., • Participate in Process Performance Qualification (PPQ) activities and other validation lifecycle activities., • Support data collection and analysis during validation runs and routine manufacturing., • Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure GMP compliance ., • Contribute to investigations, deviations, and CAPA actions related to filling processes., • Assist with risk assessments and continuous improvement initiatives for manufacturing processes., • Support preparation of documentation for internal audits and regulatory inspections . Required Qualifications: • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or a related field ., • Minimum 1 year of experience in the pharmaceutical, biotechnology, or related regulated industry (internships or thesis projects are also considered)., • Basic knowledge of GMP and pharmaceutical manufacturing processes ., • Strong organizational and analytical skills., • Ability to work effectively in cross-functional teams ., • Fluent in English and Spanish Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation . PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Kreab es una consultora de Asuntos Públicos y Comunicación fundada en Suecia en 1970. Con fuerte presencia en mercados de Europa, Asia, EEUU, África y América Latina, desde donde ayudamos a nuestros clientes a alcanzar sus objetivos de posicionamiento, notoriedad y reputación corporativa, aumentando su capacidad de influencia y asesorándoles en la representación de sus intereses y a identificar riesgos políticos y regulatorios. En España contamos con más de 160 profesionales repartidos entre las oficinas de Madrid, Barcelona y Valencia. Trabajamos juntamente con nuestros compañeros de Bruselas, con los que sumamos un equipo de más cien consultores especializados en Asuntos Públicos, Regulación y procesos legislativos europeos. Kreab Bruselas se ha consolidado como una de las tres consultoras de Asuntos Públicos más fuertes del mercado europeo. Además, desde España, KREAB lidera su crecimiento en América Latina y África, donde ya contamos con oficinas en con oficinas en Colombia, Ecuador, Bolivia, Chile, Brasil, Panamá, Perú y Argentina. En Kreab precisamos incorporar un consultor senior para el área de Comunicación Corporativa en nuestra oficina de Barcelona . Valoramos perfiles que tengan un recorrido en el mundo de la comunicación corporativa, con experiencia de 5-7 años en agencia de comunicación. Realizarás las siguientes funciones: Contacto habitual con periodistas y medios de comunicación consumer-lifestyle. Apoyo en análisis de información y comunicación con periodistas Colaborar en la elaboración de informes trimestrales/anuales y press clippings Coordinarse con los portavoces internos de la compañía y buscar y gestionar información interna para desarrollar acciones específicas de comunicación Apoyo en la asistencia a eventos y coordinación de contenidos Apoyo en la elaboración de propuestas y planes estratégicos de comunicación. ♀️ Requisitos del puesto: Grado en Comunicación, Periodismo, Publicidad y Relaciones Públicas.. Valorable Máster en Comunicación Corporativa Nivel C1 de inglés Competencias y habilidades clave para el puesto: Proactividad Capacidad de gestión Trabajo en equipo Ganas de trabajar Ilusión Actitud positiva Ideas innovadoras ¿Qué Podemos ofrecerte? Modalidad híbrida de trabajo Días de vacaciones por Convenio + 5 Días Kreab. Retribución flexible (seguro de salud, transporte, guardería...) Formación por parte de la empresa para que puedas seguir desarrollándote y promocionar dentro del plan de carrera que existe para ti. Acceso a ventajas y descuentos por formar parte de Kreab. Excelente ambiente de trabajo integrándote en un equipo dinámico. En Kreab, nos comprometemos a fomentar un entorno laboral diverso e inclusivo, donde cada miembro de nuestro equipo, sin distinción de género, edad, origen étnico, condición social o económica, orientación sexual, expresión o identidad de género, estado físico o de salud, religión, afiliación política u cualquier otra diferencia o condición, tenga la oportunidad de desarrollarse y alcanzar su máximo potencial. Trabajamos incansablemente cada día para lograr este objetivo, asegurando procesos de selección imparciales y brindando igualdad de oportunidades.

¿Quieres impulsar la transformación industrial del sector Farmacéutico? En MIGSO-PCUBED, líder global en consultoría de gestión de proyectos , buscamos Project Management Officers (PMO) para unirse a nuestro equipo y colaborar con clientes del sector farmacéutico en proyectos estratégicos. Si buscas un entorno donde tu trabajo importa, donde puedes crecer y donde se apuesta de verdad por el desarrollo profesional, esta puede ser tu oportunidad. ¿Quiénes somos? Somos MIGSO-PCUBED la consultora Líder en Project Management. Actualmente contamos con más de 3.300 consultores, operando en Europa, Norte América, Asia y Australia. Damos soporte a nuestros clientes en gestión de proyectos y PMO. MIGSO-PCUBED brinda su apoyo a proyectos de I+D, TIC y transformación para nuestros clientes. Tenemos una amplia cartera de Proyectos en sectores como Aeronáutica, Automoción, Ferrocarril, Defensa, Energía, Servicios Financieros, Telecomunicaciones, Tecnología & Media, y Sector Público. ¿Cómo será tu día a día? ️ • Planificar el proyecto involucrando a todos los departamentos afectados (compras, ingeniería, etc...)., • Controlar presupuestos y costes., • Estudiar y gestionar posibles riesgos., • Hacer seguimientos del avance del proyecto., • Elaboración de informes detallados de avance tanto a nivel proyecto como a nivel portfolio, con manejo de varios KPI, • Analizar procesos y realizar una mejora continua de ellos, • Proporcionar soporte de gestión de proyectos a los distintos departamentos ¿Te interesa? Entonces encajarás si… • Estas graduado/licenciado en ingeniería, • Tienes mínimo 2 años de experiencia en gestión de proyectos en sectores industriales., • Tienes una comunicación fluida en inglés (B2/C1), • Manejo de alguna herramientas : SAP, Excel, MS Project, Power bi, • Eres una persona dinámica, comprometida, a la que le gusta estar en contacto con diferentes interlocutores y que sabe trabajar en equipo. ¿Por qué MIGSO-PCUBED? ⭐ ¡Trabajar con nosotros es una experiencia única por varias razones! Desarrollo profesional. Ofrecemos un plan formativo robusto para impulsar tu crecimiento y habilidades, además de oportunidades de formación en idiomas para expandir tus horizontes. ¡Diviértete mientras trabajas! Nuestros eventos corporativos y actividades de team building te permiten conectar con colegas, construir relaciones sólidas y disfrutar de momentos memorables. ♂️ Flexibilidad que importa. Tu bienestar es fundamental. Ofrecemos retribución flexible que incluye Ticket Restaurante, transporte y guardería, para adaptarnos a tus necesidades. Tu salud es nuestra prioridad. Contamos con un completo seguro médico para cuidar de ti y de tu tranquilidad. Cultura de bienestar. Promovemos la igualdad, la desconexión digital y contamos con espacios de trabajo acogedores para fomentar un entorno positivo y equilibrado. ¿Quieres dar un paso adelante en tu carrera PMO? Si te interesa formar parte de un proyecto de referencia y crecer dentro de una empresa líder en Project Management, estaremos encantados de conocerte. Presenta tu solicitud hoy y comienza tu viaje en MIGSO-PCUBED ✈ #MORETHANJUSTAJOB

We’re not hiring a Designer. We’re looking for the Architect that will lead our next high-value projects and brand evolution. 🚀 Most designers see a floor plan. You see a theatre of conversion. At Pro Expo, we don’t just build structures; we architect business catalysts. We are seeking a visionary who bridges the gap between structural engineering precision and marketing psychology. You are not a designer—you are a spatial storyteller who understands that a €250k+ investment must deliver more than beauty; it must deliver a measurable competitive advantage. Are you the one? • You have 10+ years of battle-tested experience in the world’s top exhibition agencies., • You use AI tools not just for speed, but to explore the boundaries of what’s possible in spatial design., • You thrive in the high-pressure environment of Global RFPs, leading multidisciplinary teams to victory in Europe, Asia, and the Americas. What Pro Expo Offers: • Strategic Autonomy: Lead the creative vision for our most ambitious international projects., • Remote/Freelance Flexibility: We prioritize talent over location. Remote work arrangements can be considered upon successful completion of the probation period., • Exciting projects with leading global brands in Europe, Asia, and the Americas: Work with leading global brands on high-impact activations. If your portfolio doesn't just show stands, but shows strategies that won the room, we need to talk. Please send us your CV and portfolio to , along with a short note on why you’d like to join Pro Expo. A portfolio is required as part of the application and should include at least two or three examples of stand or event space designs, mentioning “Senior Concept Designer” in the subject line.

Teleconsult Group A leading teleradiology provider across Europe and the UK, supporting a global network of 350+ subspecialized radiologists. The company focuses on delivering accurate, timely radiology reporting through advanced technology to improve patient care and help healthcare providers manage increasing imaging demand. With an international presence across multiple locations, it offers 24/7 remote reporting services for hospitals and clinics, enabling efficient handling of both routine and urgent diagnostic imaging. An important partner of The Teleconsult Group is Meditecs, developing the technology that drives the integration and interoperability projects since 2018. Meditecs is a Spanish company specialized in healthcare interoperability, with more than 16 years of experience in hospital and regional projects in Spain, Europe, UK, Asia, with ongoing projects in Canada, US, and Latin America. Through its own technology, MT Smart Connect, Meditecs' solutions integrate: medical devices (diagnostic imaging, laboratory, patient monitoring, etc.), electromedicine equipment, EHR and consultation management systems, HIS, LIS, RIS and PACS, medical cloud platforms, and any other healthcare system or data source, making use of technologies or standards: HL7 V2.X, HL7, FHIR, ASTM E1381, DICOM, IHE Profiles. Job overview To serve as the strategic Human Firewall and primary translator between Teleconsult’s diverse business departments and the Meditecs development team. Your mission is to transform a high volume of fragmented, ad-hoc requirements into a structured, technically sound, and prioritized product roadmap. By mastering the art of requirements interception and solution design, you will eliminate development bottlenecks, provide business stakeholders with predictable timelines, and ensure every line of code adds maximum value to the company. Primary Accountability The Technical Product Owner is the ultimate gatekeeper of the development lifecycle. You will sit at the intersection of business strategy and technical execution, ensuring that the Meditecs team is never distracted by conflicting priorities. You are responsible for the entire journey of a feature from the initial spark of a business need, through rigorous technical design with architects, to the final validation of a high-quality software release. Key Responsibilities 1. Requirements Engineering (Gathering, Interception & Validation) • Rigorous Validation: Critically evaluate every request against business goals. You must ensure that requirements are feasible, necessary, and fully understood before they ever reach the backlog., • Specification Mastery: Translate business needs into high-fidelity functional specifications, user stories, and clear acceptance criteria that leave no room for developer ambiguity. 2. Collaborative Solution Design • Technical Design Review: Participate in designing system workflows, API integrations, and data models to ensure they are scalable and align with Teleconsult’s existing ecosystem (existing custom ERP with several dashboards, integrated with Agfa Enterprise Imaging)., • Detailed documentation: Functional specifications using UML standardized visual diagrams (Use Case, Statechart, Activity/Process flow… ), • Feasibility Analysis: Act as a sounding board for the technical team to identify potential constraints, technical debt, or risks early in the design phase. 3. Project Governance & Delivery Management • Roadmap & Timeline Ownership: Develop and maintain a transparent project roadmap. You are responsible for providing stakeholders with realistic delivery timelines and progress updates., • Cost & Resource Estimation: Collaborate with technical leads to provide accurate effort estimations (time and cost) for new initiatives, enabling data-driven decision-making for leadership. 4. Quality, Compliance & UAT • Gatekeeper of Quality: Define and oversee User Acceptance Testing (UAT). You are the final authority who confirms that the delivered software meets the original business requirements and quality standards., • Governance: Ensure all solutions comply with company policies regarding Data Privacy (GDPR) and Information Security. 5. General • Know the company policies., • Know the Environmental, Quality and Information Security objectives and goals established for the company., • Follow the policy and procedures in the Environmental, Quality and Information Security Management related to your role., • Properly manage the assets assigned to you., • Properly manage risks if you own any risk identified by the organization., • Actively participate in the adoption and implementation of corrective and improvement actions. Requirements Education & Experience • Experience: 6+ years as a Product Owner, Technical Project Manager, or Senior Systems Analyst., • Web Ecosystems: Proven experience managing complex, data-heavy web applications and dashboards. Skills & Competencies Technical Skills • Expert Documentation: Mastery of Bitbucket and modeling tools (UML, BPMN, …)., • Technical Literacy: Strong understanding of API-led architecture, SQL, and SaaS environments (ideally Google Cloud Platform)., • Methodology: Deep knowledge of Agile/Scrum and the ability to adapt it to a multi-project remote environment., • Preferably knowledge of JIRA and Confluence. Soft Skills • Communication: Fluent in English and Spanish (mandatory), with the ability to simplify complex technical concepts for non-technical users. If you are a structured and technically fluent Product Owner who thrives at the intersection of business and development, we would love to hear from you. This is a unique opportunity to take ownership of complex, high-impact products while shaping how requirements are transformed into scalable solutions. Apply directly or reach out to discuss how your experience aligns with this role. Contact our Head of Recruitment, Leticia Calva at and Mobile: +44 (0) 7367 425270.

Ravago es un grupo internacional fundado en 1961 y con sede en Luxemburgo, líder global en la fabricación y distribución de plásticos, caucho y productos químicos. Opera en Europa, Norteamérica, Asia y África, y da servicio a una amplia variedad de industrias mediante una cartera completa de materiales plásticos, compuestos, elastómeros, químicos y soluciones recicladas. Puedes encontrar más información en . MISIÓN Y RESPONSABILIDADES Tu misión Ser la persona referente en nóminas y gestión del dato del área de People & Culture, formando parte de Ravago Business Shared Services Iberia, que asegure procesos ágiles, exactos y totalmente alineados con las necesidades del negocio. Responsabilidades • Gestionar el ciclo completo de nómina de distintas legal entities en Iberia, coordinando el trabajo con la consultoría externa y asegurando la correcta aplicación de diversos convenios colectivos., • Revisar, validar y garantizar la exactitud mensual de todas las nóminas, gestionando un alto volumen de empleados., • Administrar y mantener datos de HR en los sistemas globales y locales, asegurando integridad, estructura y consistencia del dato., • Elaborar y actualizar informes, KPI’s y dashboards para dar visibilidad fiable al negocio., • Resolver consultas laborales y administrativas de empleados y managers con un enfoque de excelente servicio al cliente interno., • Participar en auditorías y asegurar el cumplimiento normativo en todos los procesos de People. QUÉ NECESITAMOS • Experiencia previa en consultoría (nómina/laboral/compensación/procesos) o en empresas con fuerte interacción con consultoras., • Capacidad demostrada para mejorar procesos y resolver incidencias complejas., • Sólidos conocimientos de nómina y legislación laboral española., • Experiencia gestionando volúmenes altos de empleados y distintos convenios., • Perfil muy ordenado, estructurado y riguroso con el dato., • Excelentes habilidades de atención al cliente interno., • Inglés alto (B2/C1)., • Valorable experiencia generalista en RRHH. QUÉ OFRECEMOS • Incorporarte al área de People & Culture de una compañía líder en la distribución de químicos e ingredientes, con un rol clave en la mejora de procesos, la calidad del dato y la experiencia empleado., • Proyecto estable a jornada completa, con un paquete retributivo competitivo y acorde a tu experiencia., • Comedor corporativo subvencionado, con menú diario a un coste reducido para empleados/as., • Política de teletrabajo, con un modelo híbrido que favorece la conciliación., • Acceso a beneficios corporativos adicionales, que se detallarán durante el proceso de selección., • Un entorno internacional, colaborativo y en plena transformación, donde podrás participar en proyectos transversales de digitalización y mejora continua dentro del área People.

About Linglong Linglong Tire is a leading Chinese tire manufacturer with production facilities and research centers in Asia, North America and Europe. With around 19,500 employees worldwide Linglong has the elite of the global tire industry in its teams. Through sales networks in over 170 countries and relations to world-class automakers Linglongs reliable quality is more and more appreciated. As a sponsor of Real Madrid and Chelsea and due to the opening of our new production site in Serbia, we are constantly expanding our brand presence in the European market. We are looking for a Tire Subjective Evaluation Engineer (m/f/d) to expand our R&D team in Spain. Responsibility • Perform subjective evaluation of tire & vehicle performance for OEM and aftermarket, • Produce detailed and clear subjective evaluation reports, • Establish and maintain alignment with OEM customer engineers, • Participate in joint tests with OEM customers in preferred/OEM proving grounds, • Develop and update subjective evaluation methods based on customer requirements, • Create positive relationships with European Tire and Vehicle Magazine partners, • Assist in the coordination and management of all European testing activities Qualification • Academic Degree in engineering or in a field associated with the role, • Multiple years of experience in the field of subjective tire evaluation for European OEMs, • Fluent in English (written and spoken), • German language proficiency is an advantage, • AKF/OE PG and Industrie-Pool licenses, • Open-minded team player, who takes initiative, with strong communication skills What we offer • Unlimited Contract, • Performance Bonus, • An amazing open minded and international team, • Being part of the success of an international growing brand, • Opportunity for professional and personal growth

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora. We are currently seeking a QA Support Technician will be part of the Quality Assurance Department and will ensure GMP compliance of qualification activities related to equipment, facilities, and plant utilities within a pharmaceutical environment. Responsibilities include, but are not limited to: • Act as Quality Assurance approver for initial qualification protocols and reports (IQ/OQ/PQ)., • Review and approve requalification protocols and reports for: HVAC systems, Nitrogen systems, • Compressed air systems and Warehouse temperature mapping, • Ensure qualification documentation complies with GMP requirements and internal procedures., • Review and approve investigations and CAPA plans related to deviations involving equipment and facilities., • Monitor CAPA implementation and ensure timely closure., • Assess CAPA effectiveness prior to final closure., • Provide QA oversight of modification activities performed by Engineering., • Review and approve qualification plans for associated equipment., • Evaluate and approve change controls related to equipment and facilities, ensuring proper GMP and regulatory impact assessment., • Collaborate cross-functionally with Engineering, Production, and other relevant departments. Required Qualifications: • Degree in Chemical Engineering or similar technical/scientific field., • Experience in a GMP-regulated pharmaceutical environment., • Proven background in equipment, facilities, and utilities qualification (IQ/OQ/PQ)., • Experience in deviation management, CAPA, and change control., • Solid knowledge of GMP regulations, HVAC systems, and plant utilities., • Strong analytical skills, attention to detail, and ability to work cross-functionally. Next Steps Upon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. In the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process. Working at PQE Group As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. xcskxlj PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. Apply now and take the first step towards an amazing future with us.

Kreab es una consultora de Asuntos Públicos y Comunicación fundada en Suecia en 1970. Con fuerte presencia en mercados de Europa, Asia, EEUU, África y América Latina, desde donde ayudamos a nuestros clientes a alcanzar sus objetivos de posicionamiento, notoriedad y reputación corporativa, aumentando su capacidad de influencia y asesorándoles en la representación de sus intereses y a identificar riesgos políticos y regulatorios. ¿Es usted el candidato adecuado para esta oportunidad? Asegúrese de leer la descripción completa a continuación. En España contamos con más de 160 profesionales repartidos entre las oficinas de Madrid, Barcelona y Valencia. Trabajamos juntamente con nuestros compañeros de Bruselas, con los que sumamos un equipo de más cien consultores especializados en Asuntos Públicos, Regulación y procesos legislativos europeos. Kreab Bruselas se ha consolidado como una de las tres consultoras de Asuntos Públicos más fuertes del mercado europeo. Además, desde España, KREAB lidera su crecimiento en América Latina y África, donde ya contamos con oficinas en con oficinas en Colombia, Ecuador, Bolivia, Chile, Brasil, Panamá, Perú y Argentina. En Kreab precisamos incorporar un consultor senior para el área de Comunicación Corporativa en nuestra oficina de Barcelona. Valoramos perfiles que tengan un recorrido en el mundo de la comunicación corporativa, con experiencia de 5-7 años en agencia de comunicación. Realizarás las siguientes funciones: • Contacto habitual con periodistas y medios de comunicación consumer-lifestyle., • Apoyo en análisis de información y comunicación con periodistas, • Colaborar en la elaboración de informes trimestrales/anuales y press clippings, • Coordinarse con los portavoces internos de la compañía y buscar y gestionar información interna para desarrollar acciones específicas de comunicación, • Apoyo en la asistencia a eventos y coordinación de contenidos, • Apoyo en la elaboración de propuestas y planes estratégicos de comunicación. Requisitos del puesto: • Grado en Comunicación, Periodismo, Publicidad y Relaciones Públicas.., • Valorable Máster en Comunicación Corporativa, • Nivel C1 de inglés Competencias y habilidades clave para el puesto: • Proactividad, • Capacidad de gestión, • Trabajo en equipo, • Ganas de trabajar, • Ilusión, • Actitud positiva, • Ideas innovadoras ¿Qué Podemos ofrecerte? • Modalidad híbrida de trabajo, • Días de vacaciones por Convenio + 5 Días Kreab., • Retribución flexible (seguro de salud, transporte, guardería...), • Formación por parte de la empresa para que puedas seguir desarrollándote y promocionar dentro del plan de carrera que existe para ti., • Acceso a ventajas y descuentos por formar parte de Kreab., • Excelente ambiente de trabajo integrándote en un equipo dinámico. En Kreab, nos comprometemos a fomentar un entorno laboral diverso e inclusivo, donde cada miembro de nuestro equipo, sin distinción de género, edad, origen étnico, condición social o económica, orientación sexual, expresión o identidad de género, estado físico o de salud, religión, afiliación política u cualquier otra diferencia o condición, tenga la oportunidad de desarrollarse y alcanzar su máximo potencial. xcskxlj Trabajamos incansablemente cada día para lograr este objetivo, asegurando procesos de selección imparciales y brindando igualdad de oportunidades.

Buscamos un ingeniero/a con experiencia en Project Management que quiera incorporarse a nuestro equipo de consultores/as. Somos MIGSO-PCUBED la consultora Líder en Project Management, parte del grupo ALTEN. Actualmente contamos con más de 3.300 consultores, operando en Europa, Norte América, Asia y Australia. Damos soporte a nuestros clientes en gestión de proyectos y PMO. MIGSO-PCUBED brinda su apoyo a proyectos de I+D, TIC y transformación para nuestros clientes. Tenemos una amplia cartera de Proyectos en sectores como Aeronáutica, Automoción, Ferrocarril, Defensa, Energía, Servicios Financieros, Telecomunicaciones, Tecnología & Media, y Sector Público. ¿Elaboración de informes detallados de avance tanto a nivel proyecto como a nivel portfolio, con manejo de varios KPI Proporcionar soporte de gestión de proyectos a los distintos departamentos implicados a todos los niveles de gobierno. ¿Estas graduado/licenciado en ingeniería o tienes un master en gestión de proyectos Tienes una experiencia profesional de mínimo 3 años en gestión de proyectos Tienes una comunicación fluida en inglés (B2/C1) Manejo de alguna herramientas: SAP, Excel, MS Project Eres una persona dinámica, comprometida, a la que le gusta estar en contacto con diferentes interlocutores y que sabe trabajar en equipo. ¿Trabajar con nosotros es una experiencia única por varias razones! Desarrollo profesional: Ofrecemos un plan formativo robusto para impulsar tu crecimiento y habilidades, además de oportunidades de formación en idiomas para expandir tus horizontes. ~¡Flexibilidad que importa: Tu bienestar es fundamental, por eso ofrecemos retribución flexible que incluye Ticket Restaurante, transporte y guardería, para adaptarnos a tus necesidades. ~ Tu salud es nuestra prioridad: Ofrecemos un completo seguro médico para cuidar de ti. ~ Nuestras políticas promueven la igualdad, la desconexión digital y disponemos de espacios de trabajo acogedores que fomentan un entorno positivo y equilibrado para todos. ¡Únete a MIGSO-PCUBED y conviértete en un/a Experto/a en Project Management! #ProjectManager #GestiónDeProyectos #MejoraContinua #SAP #MSProject #InglésB2 #MoreThanJustAJob"

En ESTAL , compañía de referencia en el sector del packaging premium de vidrio, seguimos impulsando el crecimiento internacional de nuestras Business Units y reforzando nuestra red global de fabricación. Buscamos incorporar un/a Sourcing Technician para una Business Unit en fase de expansión, con un papel clave el desarrollo de proveedores industriales, principalmente en Asia, sin limitar la actividad a otros mercados internacionales. Esta posición es esencial para reforzar la competitividad, reducir riesgos de suministro y fortalecer nuestra capacidad negociadora tanto con proveedores como con cliente , actuando como una fuente clave de información estratégica para la BU. ¿Cuál será tu impacto? Identificarás, evaluarás y desarrollarás proveedores de packaging de vidrio y componentes asociados (decoración, cierres, accesorios), con foco principal en Asia. Reducirás el riesgo industrial de la BU , mapeando y desarrollando alternativas para todos los artículos estratégicos en Europa y Asia, disminuyendo dependencias críticas y garantizando continuidad de suministro. Impulsarás el crecimiento con cliente , abriendo acceso a nuevos proveedores y nuevas categorías de producto que nos permitan ser más competitivos y ampliar nuestra propuesta de valor. Contribuirás activamente a la gestión de costes durante todo el año , monitorizando energía, materias primas y tendencias de mercado para reforzar negociaciones con proveedores y con cliente. Fortalecerás nuestra posición negociadora y la protección de márgenes , aportando alternativas reales y conocimiento de mercado que incrementen el poder negociador de la BU. Participarás en procesos de homologación de proveedores y en el seguimiento de primeras producciones, asegurando un arranque industrial sólido. Harás seguimiento del desempeño de proveedores (calidad, servicio, costes y lead times) y apoyarás planes de mejora continua. Coordinarás visitas a proveedores, auditorías y validaciones industriales . Trabajarás de forma transversal con NPD, Calidad, Sostenibilidad, Supply Chain , asegurando cumplimiento normativo y de cliente. ¿Qué buscamos? Formación técnica (Ingeniería, Ciencias o similar). Experiencia de 2 a 5 años en sourcing, compras técnicas o gestión de proveedores industriales. Experiencia previa en packaging de vidrio muy valorable. Experiencia trabajando con fabricación en Asia o proveedores internacionales . Perfil estructurado, proactivo y resolutivo, con buenas habilidades de comunicación intercultural. Inglés fluido (imprescindible); otros idiomas serán valorables. Disponibilidad para viajar internacionalmente , principalmente a Asia. ¿Qué ofrecemos? Un rol clave en una Business Unit en crecimiento, con impacto directo en la estrategia industrial. Exposición internacional y trabajo directo con proveedores y cliente. Entorno innovador, colaborativo y orientado al crecimiento. Posibilidad de trabajar en Sant Feliu de Guíxols o Barcelona. Desarrollo profesional en una compañía referente en packaging premium de vidrio. Si te apasiona el mundo de las compras internacionales y quieres formar parte de un entorno dinámico, global y exigente, ¡esta oportunidad es para ti! ¡Te estamos esperando en ESTAL! ESTAL es una empresa comprometida con la igualdad de oportunidades. No discriminamos por origen, cultura, religión, identidad o expresión de género, nacionalidad, edad, discapacidad, estado civil, orientación sexual o cualquier otra condición protegida por la ley. Nos esforzamos por crear un ambiente diverso e inclusivo y animamos a todas las personas cualificadas a presentar su candidatura.

A leading teleradiology provider across Europe and the UK, supporting a global network of 350+ subspecialized radiologists. The company focuses on delivering accurate, timely radiology reporting through advanced technology to improve patient care and help healthcare providers manage increasing imaging demand. With an international presence across multiple locations, it offers 24/7 remote reporting services for hospitals and clinics, enabling efficient handling of both routine and urgent diagnostic imaging. An important partner of The Teleconsult Group is Meditecs, developing the technology that drives the integration and interoperability projects since 2018. Meditecs is a Spanish company specialized in healthcare interoperability, with more than 16 years of experience in hospital and regional projects in Spain, Europe, UK, Asia, with ongoing projects in Canada, US, and Latin America. Through its own technology, MT Smart Connect, Meditecs' solutions integrate: medical devices (diagnostic imaging, laboratory, patient monitoring, etc.), electromedicine equipment, EHR and consultation management systems, HIS, LIS, RIS and PACS, medical cloud platforms, and any other healthcare system or data source, making use of technologies or standards: To serve as the strategic "Human Firewall" and primary translator between Teleconsult’s diverse business departments and the Meditecs development team. By mastering the art of requirements interception and solution design, you will eliminate development bottlenecks, provide business stakeholders with predictable timelines, and ensure every line of code adds maximum value to the company. The Technical Product Owner is the ultimate gatekeeper of the development lifecycle. You are responsible for the entire journey of a feature from the initial spark of a business need, through rigorous technical design with architects, to the final validation of a high-quality software release. Serve as the sole point of entry for all software requests. You will "intercept" ad-hoc communications from different departments to protect the development team's focus and efficiency. Architectural Partnership: Work hand-in-hand with Meditecs’ Software Architects and Senior Developers to bridge the gap between business "vision" and technical "reality." Technical Design Review: Participate in designing system workflows, API integrations, and data models to ensure they are scalable and align with Teleconsult’s existing ecosystem (existing custom ERP with several dashboards, integrated with Agfa Enterprise Imaging). Feasibility Analysis: Act as a sounding board for the technical team to identify potential constraints, technical debt, or risks early in the design phase. Project Governance & Delivery Management Develop and maintain a transparent project roadmap. Cost & Resource Estimation: Collaborate with technical leads to provide accurate effort estimations (time and cost) for new initiatives, enabling data-driven decision-making for leadership. Quality, Compliance & UAT Gatekeeper of Quality: Define and oversee User Acceptance Testing (UAT). You are the final authority who confirms that the delivered software meets the original business requirements and quality standards. Governance: Ensure all solutions comply with company policies regarding Data Privacy (GDPR) and Information Security. General Know the Environmental, Quality and Information Security objectives and goals established for the company. Follow the policy and procedures in the Environmental, Quality and Information Security Management related to your role. Experience: 6+ years as a Product Owner, Technical Project Manager, or Senior Systems Analyst. Web Ecosystems: Proven experience managing complex, data-heavy web applications and dashboards. Mastery of Bitbucket and modeling tools (UML, BPMN, …). Technical Literacy: Strong understanding of API-led architecture, SQL, and SaaS environments (ideally Google Cloud Platform). Methodology: Deep knowledge of Agile/Scrum and the ability to adapt it to a multi-project remote environment. Preferably knowledge of JIRA and Confluence. Diplomatic Authority: The ability to say "no" or "not yet" to senior stakeholders firmly but professionally. Fluent in English and Spanish (mandatory), with the ability to simplify complex technical concepts for non-technical users. If you are a structured and technically fluent Product Owner who thrives at the intersection of business and development, we would love to hear from you. net and Mobile: +44 (0) 7367 425270.

Buscas nuevos retos? Somos MIGSO-PCUBED la consultora Líder en Project Management, parte del grupo ALTEN.Actualmente contamos con más de 3.Europa, Norte América, Asia y Australia.Damos soporte a nuestros clientes en gestión de proyectos y PMO.MIGSO-PCUBED brinda su apoyo a proyectos de I+D,

A leading teleradiology provider across Europe and the UK, supporting a global network of 350+ subspecialized radiologists. The company focuses on delivering accurate, timely radiology reporting through advanced technology to improve patient care and help healthcare providers manage increasing imaging demand. With an international presence across multiple locations, it offers 24/7 remote reporting services for hospitals and clinics, enabling efficient handling of both routine and urgent diagnostic imaging. An important partner of The Teleconsult Group is Meditecs, developing the technology that drives the integration and interoperability projects since 2018. Meditecs is a Spanish company specialized in healthcare interoperability, with more than 16 years of experience in hospital and regional projects in Spain, Europe, UK, Asia, with ongoing projects in Canada, US, and Latin America. Through its own technology, MT Smart Connect, Meditecs' solutions integrate: medical devices (diagnostic imaging, laboratory, patient monitoring, etc.), electromedicine equipment, EHR and consultation management systems, HIS, LIS, RIS and PACS, medical cloud platforms, and any other healthcare system or data source, making use of technologies or standards: To serve as the strategic "Human Firewall" and primary translator between Teleconsult’s diverse business departments and the Meditecs development team. By mastering the art of requirements interception and solution design, you will eliminate development bottlenecks, provide business stakeholders with predictable timelines, and ensure every line of code adds maximum value to the company. The Technical Product Owner is the ultimate gatekeeper of the development lifecycle. You are responsible for the entire journey of a feature from the initial spark of a business need, through rigorous technical design with architects, to the final validation of a high-quality software release. Serve as the sole point of entry for all software requests. You will "intercept" ad-hoc communications from different departments to protect the development team's focus and efficiency. Architectural Partnership: Work hand-in-hand with Meditecs’ Software Architects and Senior Developers to bridge the gap between business "vision" and technical "reality." Technical Design Review: Participate in designing system workflows, API integrations, and data models to ensure they are scalable and align with Teleconsult’s existing ecosystem (existing custom ERP with several dashboards, integrated with Agfa Enterprise Imaging). Feasibility Analysis: Act as a sounding board for the technical team to identify potential constraints, technical debt, or risks early in the design phase. Project Governance & Delivery Management Develop and maintain a transparent project roadmap. Cost & Resource Estimation: Collaborate with technical leads to provide accurate effort estimations (time and cost) for new initiatives, enabling data-driven decision-making for leadership. Quality, Compliance & UAT Gatekeeper of Quality: Define and oversee User Acceptance Testing (UAT). You are the final authority who confirms that the delivered software meets the original business requirements and quality standards. Governance: Ensure all solutions comply with company policies regarding Data Privacy (GDPR) and Information Security. General Know the Environmental, Quality and Information Security objectives and goals established for the company. Follow the policy and procedures in the Environmental, Quality and Information Security Management related to your role. Experience: 6+ years as a Product Owner, Technical Project Manager, or Senior Systems Analyst. Web Ecosystems: Proven experience managing complex, data-heavy web applications and dashboards. Mastery of Bitbucket and modeling tools (UML, BPMN, …). Technical Literacy: Strong understanding of API-led architecture, SQL, and SaaS environments (ideally Google Cloud Platform). Methodology: Deep knowledge of Agile/Scrum and the ability to adapt it to a multi-project remote environment. Preferably knowledge of JIRA and Confluence. Diplomatic Authority: The ability to say "no" or "not yet" to senior stakeholders firmly but professionally. Fluent in English and Spanish (mandatory), with the ability to simplify complex technical concepts for non-technical users. If you are a structured and technically fluent Product Owner who thrives at the intersection of business and development, we would love to hear from you. net and Mobile: +44 (0) 7367 425270.

A leading teleradiology provider across Europe and the UK, supporting a global network of 350+ subspecialized radiologists. The company focuses on delivering accurate, timely radiology reporting through advanced technology to improve patient care and help healthcare providers manage increasing imaging demand. With an international presence across multiple locations, it offers 24/7 remote reporting services for hospitals and clinics, enabling efficient handling of both routine and urgent diagnostic imaging. An important partner of The Teleconsult Group is Meditecs, developing the technology that drives the integration and interoperability projects since 2018. Meditecs is a Spanish company specialized in healthcare interoperability, with more than 16 years of experience in hospital and regional projects in Spain, Europe, UK, Asia, with ongoing projects in Canada, US, and Latin America. Through its own technology, MT Smart Connect, Meditecs' solutions integrate: medical devices (diagnostic imaging, laboratory, patient monitoring, etc.), electromedicine equipment, EHR and consultation management systems, HIS, LIS, RIS and PACS, medical cloud platforms, and any other healthcare system or data source, making use of technologies or standards: To serve as the strategic "Human Firewall" and primary translator between Teleconsult’s diverse business departments and the Meditecs development team. By mastering the art of requirements interception and solution design, you will eliminate development bottlenecks, provide business stakeholders with predictable timelines, and ensure every line of code adds maximum value to the company. The Technical Product Owner is the ultimate gatekeeper of the development lifecycle. You are responsible for the entire journey of a feature from the initial spark of a business need, through rigorous technical design with architects, to the final validation of a high-quality software release. Serve as the sole point of entry for all software requests. You will "intercept" ad-hoc communications from different departments to protect the development team's focus and efficiency. Architectural Partnership: Work hand-in-hand with Meditecs’ Software Architects and Senior Developers to bridge the gap between business "vision" and technical "reality." Technical Design Review: Participate in designing system workflows, API integrations, and data models to ensure they are scalable and align with Teleconsult’s existing ecosystem (existing custom ERP with several dashboards, integrated with Agfa Enterprise Imaging). Feasibility Analysis: Act as a sounding board for the technical team to identify potential constraints, technical debt, or risks early in the design phase. Project Governance & Delivery Management Develop and maintain a transparent project roadmap. Cost & Resource Estimation: Collaborate with technical leads to provide accurate effort estimations (time and cost) for new initiatives, enabling data-driven decision-making for leadership. Quality, Compliance & UAT Gatekeeper of Quality: Define and oversee User Acceptance Testing (UAT). You are the final authority who confirms that the delivered software meets the original business requirements and quality standards. Governance: Ensure all solutions comply with company policies regarding Data Privacy (GDPR) and Information Security. General Know the Environmental, Quality and Information Security objectives and goals established for the company. Follow the policy and procedures in the Environmental, Quality and Information Security Management related to your role. Experience: 6+ years as a Product Owner, Technical Project Manager, or Senior Systems Analyst. Web Ecosystems: Proven experience managing complex, data-heavy web applications and dashboards. Mastery of Bitbucket and modeling tools (UML, BPMN, …). Technical Literacy: Strong understanding of API-led architecture, SQL, and SaaS environments (ideally Google Cloud Platform). Methodology: Deep knowledge of Agile/Scrum and the ability to adapt it to a multi-project remote environment. Preferably knowledge of JIRA and Confluence. Diplomatic Authority: The ability to say "no" or "not yet" to senior stakeholders firmly but professionally. Fluent in English and Spanish (mandatory), with the ability to simplify complex technical concepts for non-technical users. If you are a structured and technically fluent Product Owner who thrives at the intersection of business and development, we would love to hear from you. net and Mobile: +44 (0) 7367 425270.

Ravago es un grupo internacional fundado en 1961 y con sede en Luxemburgo, líder global en la fabricación y distribución de plásticos, caucho y productos químicos. Opera en Europa, Norteamérica, Asia y África, y da servicio a una amplia variedad de industrias mediante una cartera completa de materiales plásticos, compuestos, elastómeros, químicos y soluciones recicladas. Puedes encontrar más información en . MISIÓN Y RESPONSABILIDADES Tu misión Ser la persona referente en nóminas y gestión del dato del área de People & Culture, formando parte de Ravago Business Shared Services Iberia, que asegure procesos ágiles, exactos y totalmente alineados con las necesidades del negocio. Responsabilidades • Gestionar el ciclo completo de nómina de distintas legal entities en Iberia, coordinando el trabajo con la consultoría externa y asegurando la correcta aplicación de diversos convenios colectivos., • Revisar, validar y garantizar la exactitud mensual de todas las nóminas, gestionando un alto volumen de empleados., • Administrar y mantener datos de HR en los sistemas globales y locales, asegurando integridad, estructura y consistencia del dato., • Elaborar y actualizar informes, KPI’s y dashboards para dar visibilidad fiable al negocio., • Resolver consultas laborales y administrativas de empleados y managers con un enfoque de excelente servicio al cliente interno., • Participar en auditorías y asegurar el cumplimiento normativo en todos los procesos de People. QUÉ NECESITAMOS • Experiencia previa en consultoría (nómina/laboral/compensación/procesos) o en empresas con fuerte interacción con consultoras., • Capacidad demostrada para mejorar procesos y resolver incidencias complejas., • Sólidos conocimientos de nómina y legislación laboral española., • Experiencia gestionando volúmenes altos de empleados y distintos convenios., • Perfil muy ordenado, estructurado y riguroso con el dato., • Excelentes habilidades de atención al cliente interno., • Inglés alto (B2/C1)., • Valorable experiencia generalista en RRHH. QUÉ OFRECEMOS • Incorporarte al área de People & Culture de una compañía líder en la distribución de químicos e ingredientes, con un rol clave en la mejora de procesos, la calidad del dato y la experiencia empleado., • Proyecto estable a jornada completa, con un paquete retributivo competitivo y acorde a tu experiencia., • Comedor corporativo subvencionado, con menú diario a un coste reducido para empleados/as., • Política de teletrabajo, con un modelo híbrido que favorece la conciliación., • Acceso a beneficios corporativos adicionales, que se detallarán durante el proceso de selección., • Un entorno internacional, colaborativo y en plena transformación, donde podrás participar en proyectos transversales de digitalización y mejora continua dentro del área People.

Everience is an international consulting group delivering AI-augmented digital services and placing people at the heart of the AI revolution.With a presence in Europe, Africa, Asia and America, Everience offers its 4,000-strong workforce the most demanding and stimulating environment in which to tra