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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.

Destacada empresa industrial fabricante de productos de consumo duradero, desea incorporar a su organización: PROJECT MANAGER Reportando directamente al Responsable del Departamento de Márqueting, se encargará de coordinar el desarrollo de nuevos productos desde la aprobación del concepto hasta la entrega de producción, actuando como enlace operativo entre Márqueting y los equipos técnicos (Diseño, Ingeniería, Abastecimiento, Empaquetado, Cumplimiento, Operaciones). Deberá traducir los briefings de márqueting en planes de proyecto estructurados, cronogramas y listas de tareas, definiendo y supervisando los hitos del proyecto y realizando un seguimiento del progreso del mismo, garantizando la alineación con el plazo y el alcance acordados. Identificará posibles riesgos, retrasos o cuellos de botella y se encargará de facilitar soluciones con los equipos pertinentes. Organizará y documentará las reuniones interdisciplinarias y los seguimientos, manteniendo la documentación del proyecto estructurada, incluyendo especificaciones, estado del empaque, aprobaciones de material gráfico y actualizaciones de producción. Deberá apoyar la coordinación del muestreo, las pruebas, la validación de compliance y las aprobaciones de preproducción. Finalmente, garantizará una comunicación fluida entre departamentos durante todo el proceso de desarrollo, contribuyendo a la optimización de procesos y a una mejor colaboración entre equipos. Se requiere: • Graduado ADE y/o Diplomatura en Marketing, o similar., • Imprescindible alto nivel de inglés. Se valorará conocimiento de otros idiomas., • Experiencia mínima de 5 años en puestos de similares características en sectores de consumo duradero comercializados a través de canales parecidos a los del grupo (grandes almacenes, hipermercados, detallistas especializados, detallistas e-commerce, mayoristas, distribuidores internacionales), • Disponibilidad para trabajar 100% presencial. Empresa comprometida con la igualdad de oportunidades entre mujeres, hombres y personas LGTBI y con la igualdad de trato y no discriminación.

Do you want to be part of a team with a real impact on global health? At Noucor, a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide 🌍. We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Main Tasks: • Ensure that all processes related to clinical trials are performed in compliance with GCP (Good Clinical Practice) and applicable quality standards., • Provide QA support to clinical trial activities, including documentation review and quality oversight of internal teams and external partners (CROs, service providers)., • Evaluate and manage quality issues, deviations, CAPAs, change controls and complaints related to Clinical Trials., • Support quality activities related to Investigational Medicinal Products (IMPs) in collaboration with Pharmaceutical Development and Analytical Development., • Maintain awareness of applicable quality regulations and compliance requirements impacting clinical development and R&D activities. Requirements: • Degree in Pharmacy, Chemistry, Biology, or similar., • Fluent in English and Spanish., • Experience in Good Clinical Practices (GCP); knowledge of GMP requirements for IMPs in clinical trials (formerly Annex 13)., • Good command of MS Office., • High willingness to learn and take on new challenges and responsibilities., • Motivation, teamwork, and good communication skills. We Offer: 🤩 Work within a great team of professionals with a very good work environment. ⚙️ Innovative work environment focused on continuous improvement. 🚀 Continuous learning and development. 💼 Competitive benefits package and flexible schedule. 📍 Offices in Palau-solità i Plegamans. 💰 Competitive salary. Interested in joining us? At Noucor, we believe in the value of diverse teams. We therefore welcome and consider all applications regardless of gender, age, background, sexual orientation, gender identity, or any other personal characteristic. If you meet most of the requirements and are motivated by the project, we would be pleased to hear from you.

COMSER is looking for a Qualification and Validation Technician for the GMP Compliance Services area.We are a company that provides services to the pharmaceutical industry. Our purpose is to help and streamline the industrialization of new medicines that improve people's quality of life. Our focus is on injectable medicines that need to be manufactured in an aseptic environment. What do we offer? • Career plan with personalized professional development in the pharmaceutical sector. In a growing company with many opportunities., • Being part of a multidisciplinary team, where scientific and engineering profiles stand out; where your creative proposals will be valued., • Being the direct interlocutor with our clients during the execution of projects., • Good and young work environment. What will your main functions be? • Design and develop equipment or process validation protocols according to GMP and in accordance with the client's user requirements., • Execution and review of the protocols, with subsequent analysis of the results., • Continuous improvement of the validation documentation and updating of standards adaptable to each project What do we expect from you? That you have a scientific-technical university education (chemical sciences, pharmacy, biology, chemical engineering or similar) and/or training acquired in the development of your usual profession. • That you are an analytical, planned, resolute, results-oriented and dynamic person., • Knowledge of GMP regulations, aseptic manufacturing and the lyophilization technique is a plus., • Availability to travel (national and international)., • Full professional level of English (written and spoken)., • Own vehicle for travel to client sites. At COMSER, we value and respect diversity. We firmly believe that having a diverse team is key to success and innovation. That's why we offer equal opportunities to all candidates, regardless of their gender, age, race, religion, sexual orientation, disability, or any other characteristic. If you believe you fit the profile and are interested in starting a new professional project, do not hesitate to apply for the offer and contact us. We want to meet you!

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.

Syntegon Telstar S.R.U. is a company of the Syntegon group, which operates worldwide. As a brand specialized in the development of GMP projects of consulting, engineering, construction and integrated process equipment, we serve companies linked to the life sciences market (pharmaceutical and biotechnology, healthcare, cosmetics, veterinary and food industries), as well as hospitals, laboratories and research centers. We also offer solutions with the application of vacuum and high vacuum technologies for traditional and high-tech industries in the energy and aerospace sectors, as well as scientific experimentation. Apply now and become part of our team! Job Description We are looking for a process‑driven and highly dedicated Automation Engineer with a passion for challenging commissioning projects. In this role, you will work at the intersection of automation, process engineering, and regulatory requirements—contributing directly to the performance, reliability, and compliance of our cutting‑edge isolator systems. • Develop and adapt PLC software (Siemens TIA Portal) for advanced isolator systems, • Conduct comprehensive functional tests and support process validation activities, • Collaborate closely with process engineers to ensure alignment with regulatory standards, • Support extensive on‑site commissioning activities at customer facilities (often in shift models), • Analyse technical issues, perform troubleshooting, and drive continuous process improvements, • Create and maintain technical documentation and software standards, • Provide technical support to project management, service teams, and qualification functions Qualifications • Solid experience in PLC programming; Siemens TIA Portal is a must‑have, • Bachelor’s or Master’s degree in Electrical Engineering, Automation Engineering, Mechatronics, or a related field, • 2–5 years of relevant professional experience in automation, machine control, pharmaceutical equipment, or process environments, • Willingness to work with control engineering topics and expand expertise, • Strong understanding of process environments; experience in aseptic production is a clear advantage, • Willingness to travel internationally (approx. 15–20%), • Beneficial: Siemens Step7 Classic, • Good command of English and the ability to work both independently and collaboratively, • A structured, reliable working style with a strong sense of responsibility Additional Information Please note that we can only submit your CV in English. For Syntegon and its subsidiaries, diversity is a key concern. We explicitly welcome an environment where all employees, regardless of gender, age, origin, religion, sexual orientation, gender identity, or special needs, are treated equally. If this job posting uses only the male form, it is for readability purposes and refers to individuals of all genders.

Estamos colaborando con una compañía especializada en servicios GMP para la industria farmacéutica, que busca incorporar un/a Técnico/a de Cualificación y Validación junior para reforzar su equipo de Compliance. Su misión es clara: acompañar la industrialización de nuevos medicamentos que impactan directamente en la calidad de vida de las personas, especialmente en el ámbito de los inyectables fabricados en entorno aséptico. 🚀 ¿Qué se ofrece? • Plan de carrera y desarrollo profesional personalizado dentro del sector Pharma, • Incorporación a un entorno en crecimiento, con proyectos variados y recorrido a largo plazo., • Trabajo en un equipo multidisciplinar con perfiles científicos y de ingeniería, donde se valora la iniciativa y las nuevas ideas., • Rol con contacto directo con cliente durante la ejecución de proyectos., • Buen ambiente laboral, joven y colaborativo. 🧩 ¿Cuáles serán tus responsabilidades? • Diseño y elaboración de protocolos de cualificación y validación de equipos y procesos bajo normativa GMP., • Ejecución, revisión y análisis de resultados de dichos protocolos., • Mejora continua de la documentación de validación y actualización de estándares según cada proyecto. 🎯 ¿Qué perfil buscamos? • Formación universitaria en áreas científico-técnicas: Química, Farmacia, Biología, Ingeniería Química o similar (o experiencia equivalente)., • Persona analítica, organizada, resolutiva, orientada a resultados y con actitud proactiva., • Se valorará conocimiento en GMP, fabricación aséptica y liofilización., • Disponibilidad para viajar (nacional e internacional)., • Nivel alto de inglés (oral y escrito)., • Carnet de conducir y vehículo propio para desplazamientos a planta. Compromiso con la Igualdad de Oportunidades: En Solutia GHS garantizamos que todos nuestros procesos de selección se desarrollan en base a criterios objetivos, valorando únicamente las competencias, la experiencia y el talento de las personas candidatas. Promovemos la igualdad de oportunidades y no toleramos ningún tipo de discriminación por razón de sexo, género, edad, origen, raza, religión, orientación sexual, identidad de género, discapacidad o cualquier otra circunstancia personal o social. Asimismo, nuestra política retributiva se rige por el principio de equidad salarial ante el desempeño de las mismas funciones, reforzando nuestro compromiso con un entorno laboral diverso, inclusivo y respetuoso.

Syntegon Telstar S.R.U. is a company of the Syntegon group, which operates worldwide. As a brand specialized in the development of GMP projects of consulting, engineering, construction and integrated process equipment, we serve companies linked to the life sciences market (pharmaceutical and biotechnology, healthcare, cosmetics, veterinary and food industries), as well as hospitals, laboratories and research centers. We also offer solutions with the application of vacuum and high vacuum technologies for traditional and high-tech industries in the energy and aerospace sectors, as well as scientific experimentation. Apply now and become part of our team! Job Description We are looking for a Mechanical Engineer for our offices in Terrassa (Barcelona) with at least 2 years of experience in designing special-purpose machinery for the pharmaceutical sector (ideally filling machinery) or the packaging industry. The role involves designing and developing this special machinery in 3D, as well as preparing all associated technical documentation. Main responsabilities: • Development of mechanical solutions, creation of models and drawings, preparation of mock-ups, optimization of existing assemblies, and preparation and updating of functional specifications, flow diagrams, and pneumatic schematics., • Technical calculations and sizing, including strength calculations, service life and tolerance analyses, as well as the use of simulation tools and, when appropriate, FEM analysis for design validation., • Documentation of modifications and data maintenance in ERP/PLM systems: creation and updating of Bills of Materials (BOM) in SAP, as well as initiating catalog part requests (workflow)., • Conducting risk assessments, preparing functional specifications, leading Design Qualification workshops, and participating in systematic design reviews., • Planning, coordinating, and supervising prototypes, tests, and trials; evaluating the results and deriving the necessary design modifications., • Technical support for assembly, pre‑assembly, service, and purchasing; rapid implementation of design modifications in case of complaints, with a high level of responsiveness and proactivity., • Compliance with and application of relevant standards and guidelines (machine safety, pharmaceutical requirements), as well as participation in the standardization and continuous improvement of design standards., • Coordination with customers and suppliers: technical communication with the customer, support during acceptances/tests, and coordination with external suppliers for data management and manufacturing. Qualifications • University degree in Mechanical Engineering, Mechatronics, Precision Engineering, or an equivalent technical qualification; academic certificate., • Experience in the design and construction of special-purpose machinery, ideally in pharmaceutical filling lines or comparable pharmaceutical equipment., • Extensive hands-on experience with 3D CAD (ideally SolidWorks/DBWorks) including a demonstrable portfolio of CAD models/drawings., • Experience with SAP (master data, Bills of Materials, classification, etc.) and with database systems., • Familiarity with design workflows, Design Reviews, functional specifications, risk assessments, process flow diagrams, and pneumatic schematics., • Hands-on experience with prototypes/testing, assembly support, and customer acceptance activities., • Interdisciplinary mindset (mechanical, electrical engineering, automation, and process technology) with a focus on overall customer‑oriented functionality. Additional Information Please note that we can only process your CV in English. For Syntegon and its subsidiaries, diversity is a key concern. We explicitly welcome an environment where all employees, regardless of gender, age, origin, religion, sexual orientation, gender identity, or special needs, are treated equally. If this job posting uses only the male form, it is for readability purposes and refers to individuals of all genders.

Si, como nosotros, trabajas mejor cuando se confía en ti, súmate a nuestro equipo >> En Elis apostamos por las personas, les damos responsabilidades y las acompañamos en su crecimiento. Formarás parte de un grupo internacional con más de 75 años de historia, líder en su sector y comprometido con la economía circular. Don’t choose Elis si buscas rutina. Pero si te motiva la gestión de flotas y la optimización operativa, en nuestra organización buscamos incorporar un/a Gestor/a de Flota que lidere la gestión integral de nuestra flota de vehículos comerciales, de empresa e industriales (camiones y furgonetas).sigue leyendo 👇 🎯 Tu misión Serás responsable de garantizar la disponibilidad, eficiencia operativa, control de costes y cumplimiento normativo de toda la flota, trabajando de forma transversal con distintos departamentos y proveedores externos cumpliendo los procedimientos y estándares del grupo. 🔧 ¿Qué harás? ➢ Gestión integral de flota (turismos e industrial). ➢ Coordinación de altas, bajas, renovaciones y sustituciones. ➢ Supervisión de mantenimiento, ITV, seguros y documentación. ➢ Gestión de contratos de renting/leasing y relación con proveedores. ➢ Soporte y atención a empleados/as usuarios de flota. ➢ Participar en negociaciones con proveedores de complejidad media. ➢ Gestionar pedidos, contratos y seguimiento de entregas para distintos centros. ➢ Actuar como interlocutor entre proveedores y la empresa. ➢ Elaborar reporting periódico y seguimiento de KPIs. ➢ Garantizar el cumplimiento de procedimientos, compliance y estándares de grupo. 👤 ¿A quién buscamos? ➢ Formación universitaria en ADE, Ingeniería o similar ➢ 3-5 años de experiencia en gestión de flotas ➢ Conocimiento de normativa y contratos de renting/leasing. ➢ Excel nivel avanzado (Power Bi es un plus) ➢ Nivel de inglés para entorno profesional ➢ Perfil analítico, organizado y con capacidad de gestión. 🎁 ¿Qué ofrecemos? ➢ Contrato indefinido en un grupo sólido y en crecimiento ➢ Un rol con impacto directo en la optimización de compras y costes ➢ Desarrollo profesional dentro de un entorno internacional ➢ Salario competitivo y beneficios sociales 👉 ¿Te interesa el reto? Únete a Elis y forma parte de un equipo que impulsa la eficiencia y la mejora continua en nuestras operaciones. ELIS MANOMATIC, S.A.U. te informa que es la entidad responsable del tratamiento de tus datos personales con el fin de valorar tu candidatura para vacantes presentes o futuras a cubrir en nuestra organización. Para más información sobre el tratamiento de tus datos o sobre cómo ejercer sus derechos de derechos de acceso, rectificación, supresión, limitación, portabilidad y oposición, puedes acceder a nuestro portal web en el apartado política de privacidad. ELIS MANOMATIC, S.A.U. no discriminará directa o indirectamente a los candidatos y candidatas en los procesos de selección, por razones de sexo, estado civil, edad, origen racial o étnico, condición social, religión o convicciones, ideas políticas, orientación sexual, afiliación o no a un sindicato, así como por razón de lengua Que ELIS MANOMATIC, S.A.U. se compromete a actuar bajo el principio de igualdad de trato y de oportunidades entre todo el personal que realicen el mismo trabajo. ELIS MANOMATIC, S.A.U. se dispone a adoptar medidas que eviten cualquier forma de discriminación entre hombres y mujeres. En los procesos de selección, realizarán iniciativas para contratar mujeres en áreas donde la presencia femenina esté subrepresentada o dar preferencia a la contratación de mujeres en igualdad de condiciones.

We are Applus+ Laboratories, the division of the Applus+ Group that provides testing, certification, and product development engineering services. In the IT & CYBERSECURITY laboratory, we are accredited to perform a wide range of security evaluations for payment schemes, identification, and IT security. We are seeking for passionate hardware and embedded system security professional passionates to join our team and learn this field. Perform vulnerability analysis and penetration testing on real hardware and software products, analysing source code and using reverse engineering techniques. We are looking for a Junior Cybersecurity Engineer to join our team and perform vulnerability analysis and penetration testing on real hardware and software products, analysing source code and using reverse engineering techniques. Essential job responsibilities • Acquire knowledge of key customer's technological solutions, • Gain understanding of cybersecurity requirements for products and customer facilities, • Carry out hardware and software security evaluations in different frameworks., • Perform ad-hoc evaluations, subject to customer constraints and needs., • Work with technology vendors to help meet security certification requirements, • Identify and resolve challenges to ensure certification project success, • Write technical reports and communicate effectively with customers, testing laboratories, and other stakeholders, • Conduct security evaluations in compliance with certification standards, primarily for Smart Cards and embedded systems., • Perform advanced technical security analyses, including:, • -Secure source code reviews for embedded and payment systems., • -High Assurance Vulnerability Analysis (VA)., • -Advanced penetration testing using Side Channel Analysis (SCA) and Fault Injection (FI) techniques. To be considered, candidates must possess • Education: Technical background such as Computer Science, Telecommunication, Electronics, Mathematics or equivalent degree., • Coding experience with Python / C / C++, • Experience with laboratory equipment such as oscilloscopes is desirable, • Documentary experience with Git, • Languages: Spanish and English (at least B2), • Experience in the same position: 0-2 years, • Strong analytical and communication skills, • Self-starter with a passion for professional growth, • Passion for technology and cybersecurity Our current stack and tools: • Programming Language, Python, C/ C++, • Git, • Operative Systems, UNIX Based OS Benefits • Permanent contract., • Full-time position., • 23 vacation days and 3 personal days., • Flexible compensation plan (health insurance, transportation, childcare, meal vouchers)., • Employee parking., • Green spaces and wellness activities, including yoga classes, to promote well-being., • Subsidized menu with reduced prices. Are you passionate about cybersecurity? Do you want to be part of a team of top experts? This is the company for you! Applus+ Laboratories is an equal opportunity employer. We are committed to evaluating all applications equally based on skills, achievements, and experience, regardless of race, nationality, gender, age, disability, sexual orientation, gender identity, or any other classification protected by law

Applus+ es una de las compañías líderes mundiales en ensayo, inspección y certificación, con presencia en más de 65 países en los 5 continentes y un equipo de más de 25.000 personas. Puedes consultar nuestros proyectos en la web: Hemos experimentado un gran desarrollo durante los últimos años, gracias a nuestro equipo humano que consideramos que son pieza clave y estratégica en el desarrollo de esta compañía. ¿Te gustaría ser parte de nuestro equipo? Actualmente estamos seleccionando un/a Compliance Assurance Specialist para incorporarse a nuestro departamento de Compliance Corporativo. Buscamos un/a profesional con sólida experiencia en auditoría de Compliance e Internal control, con perfil analítico y financiero. Esta persona reportará a la Chief Compliance Officer del Grupo y contribuirá activamente al desarrollo y ejecución del programa de Compliance Assurance, enfocado en verificar la implementación efectiva del modelo de Compliance de Applus+ en todas las entidades del Grupo. Responsabilidades principales: • Colaborar en el diseño y ejecución del plan de revisiones de Compliance a nivel global, evaluando la eficacia de los controles implementados y el cumplimiento de los procedimientos corporativos., • Realizar revisiones tanto presenciales como en remoto en las distintas entidades del Grupo, identificando oportunidades de mejora y apoyando en la definición de planes de acción., • Participar en investigaciones internas relacionadas con posibles desviaciones o incumplimientos, aportando un enfoque riguroso y objetivo en el análisis., • Diseñar e implantar herramientas y sistemas para la realización de auditorías remotas y el seguimiento continuo de indicadores de cumplimiento, incluyendo el uso de plataformas como Power BI., • Mantenerse al día sobre prácticas internacionales, marcos normativos relevantes y tendencias en compliance, contribuyendo a la mejora continua del sistema de control interno., • Elaborar informes de conclusiones para el equipo de Compliance y otras áreas implicadas, presentando los hallazgos, riesgos y recomendaciones de forma clara y estructurada. Requisitos: • Formación universitaria en Finanzas, Auditoría, Administración y Dirección de Empresas, Economía, Ingeniería o similares., • Mínimo 10 años de experiencia profesional, preferentemente en auditoría interna, control de riesgos o Compliance en compañías multinacionales o firmas de auditoría., • Experiencia demostrada en el diseño y ejecución de planes de revisión o auditoría de Compliance, y en el seguimiento de controles., • Alto dominio de herramientas de análisis y visualización de datos (especialmente Power BI)., • Buenas habilidades interpersonales, con capacidad para comunicar de forma clara, persuasiva y empática, especialmente en contextos multiculturales o cuando se actúe como figura de revisión en remoto o presencial., • Capacidad para trabajar de forma autónoma y gestionar tareas complejas con criterio y responsabilidad., • Disponibilidad para viajar internacionalmente de forma frecuente., • Nivel alto de inglés (C1 o superior). Se valorará el conocimiento de otros idiomas. Se valorará especialmente: • Certificaciones profesionales relevantes como Certified Internal Auditor (CIA), Certified Fraud Examiner (CFE), Certified in Risk and Control Management (CRMA) u otras relacionadas con aseguramiento, control interno o prevención del fraude., • Experiencia en la implantación de sistemas de control remoto o tecnologías emergentes aplicadas a compliance., • Conocimiento práctico de estándares internacionales de control interno, marcos regulatorios y normativas sectoriales aplicables a grupos multinacionales.

Kanguro es una startup de logística de última milla con alto potencial de crecimiento nacida en Barcelona con un propósito claro: liderar la transformación tecnológica de la logística. Operamos una red universal de puntos de recogida en España y estamos en plena expansión a Alemania, Francia y Portugal, combinando IA y tecnología propia para hacer la entrega y recogida de paquetes más eficiente para el carrier, más cómoda para el cliente y más sostenible para todos. ¿En qué consiste la posición? Buscamos un/a becario/a de RRHH que nos ayude a mantener al equipo alineado, con seguimiento real de objetivos, rendimiento y cumplimiento de políticas internas. Tu día a día estará centrado en hacer validaciones recurrentes con empleados de todos los niveles — especialmente perfiles de nivel medio y senior — para asegurar que los objetivos se cumplen, las evaluaciones de rendimiento ocurren y las políticas de trabajo presencial/remoto se respetan. No es un rol administrativo clásico. Vas a tener conversaciones reales con gente senior y acceso directo a dirección. Responsabilidades Seguimiento de rendimiento y OKRs • Apoyar en la ejecución de ciclos recurrentes de validación de rendimiento para todos los empleados, con foco en perfiles mid-to-senior, • Hacer seguimiento del progreso de OKRs por equipo: asegurar que los objetivos se definen, revisan y actualizan en la cadencia acordada, • Preparar informes resumen de rendimiento para dirección, destacando gaps de alineamiento y contribuciones destacadas, • Monitorizar y validar el cumplimiento de las políticas de trabajo híbrido: días presenciales, días remotos y excepciones, • Mantener registros de asistencia y presencia; señalar patrones que se desvíen de lo acordado, • Ayudar a diseñar y desplegar encuestas periódicas de satisfacción y engagement, • Analizar resultados y preparar insights accionables para dirección, • Mantener y actualizar registros de empleados, contratos y documentación de RRHH, • Apoyar en coordinación de procesos de selección cuando sea necesario, • Tareas administrativas relacionadas con nómina, beneficios y compliance legal ¿Qué perfil buscamos? • Estudiante o recién graduado/a en Recursos Humanos, Psicología, Relaciones Laborales, ADE o similar, • Elegible para convenio de prácticas con universidad o escuela de negocios española, • Muy organizado/a: capaz de gestionar múltiples seguimientos con muchas personas sin que se caiga nada, • Cómodo/a trabajando con hojas de cálculo (Excel/Google Sheets) y creando trackers desde cero, • Buena comunicación escrita y verbal en castellano; inglés necesario, • Discreción y profesionalidad — manejarás datos sensibles de rendimiento y personal, • Mentalidad proactiva: no esperas a que te digan qué hacer, señalas problemas y propones mejoras, • Valorable: familiaridad con herramientas de RRHH (BambooHR, Factorial, Personio), herramientas de encuestas, o conocimiento básico de legislación laboral española, • Catalán valorable ¿Qué ofrecemos? • Convenio de prácticas (6 meses, con posibilidad de extensión o incorporación), • Remuneración de 900€/mes, • Oficina en Sant Cugat del Vallès, delante de la estación de Mirasol (FGC), • Presencialidad: 4–5 días en oficina (la presencia es clave para este rol), • Horario flexible compatible con compromisos universitarios, • Responsabilidad real desde el primer día, • Acceso directo a dirección y exposición a cómo se gestiona una empresa en crecimiento, • Equipo con muy buen ambiente, joven y multidisciplinar, • Trabajar en una empresa donde la inteligencia artificial es parte del día a día, no solo un claim ¿Cómo aplicar? El responsable de este proceso de selección es Josep Francesc Cortés. Si te interesa la posición y cumples los requisitos, envía un email a dirigido a Josep Francesc, adjuntando tu CV y una carta de motivación donde nos cuentes quién eres y por qué te interesa este rol en Kanguro; qué puedes aportar al equipo de People; y tu disponibilidad.

Specifically, we are looking for a Product Engineer with German to work on an innovative automotive project located in Vallès Occidental area (Barcelona). Functions: Defining and ensuring the development stages and the technical feasibility of the project, complying with customer's milestones. Searching and applying the technical solutions taking into account the quality standard. Reviewing and re-thinking the technical design in collaboration with the design team. Leading the FMEA's implementation of the product and quality tools during the product development phases, ensuring compliance with the quality requirements, regulations and standards of the countries where the product will be used. Leading the product approval activities. Analyzing the results of the product technical test reports and to find the necessary technical countermeasures solutions together with the Quality Design Engineer. Working together with manufacturing team in the industrialization of the products. Managing product modifications during development phase. Supporting the competitiveness of the business unit by optimizing costs, quality and product performance, adopting new technical solutions, optimizing components in terms of cost, quality and manufacturing capacity. Ensuring the optimization of components in terms of cost, quality and manufacturing capacity together with the Purchasing department and suppliers. Be in continuous contact with the customer engineering. Managing the development of CAD designs taking into account customer's requirements and ensuring quality in the production process, as follow: Carrying out the parameterization and drawing of the product components. Carrying out preliminary studies and numerical definitions of the different components of the product with CAD Tools. Designing the components and assembly of the CAD Tools product. Requirements: Engineering degree, equivalent degree or consolidated experience in the role. Good professional level of English, German and Spanish (spoken and written). Minimum experience of 2-3 years in similar position. Previous experience in mechanical positions. Knowledge of CAD design SW Experience in the design of plastic materials and knowledge of the automotive sector will be a plus. What we offer? Innovative project on a TIER1 company. Be part of one of the best automotive companies. Be part of a multinational company in a multicultural environment with a continuous and free trainings at your service. Permanent contract and salary according to your professional background. Healthcare insurance. Hybrid work. ¿Quieres saber más de nosotros? En Formel D estamos comprometidos con la igualdad de oportunidades y el respeto a la diversidad. Analizamos cada candidatura con transparencia y objetividad, evitando cualquier tipo de sesgo por género, procedencia, orientación sexual, discapacidad o cualquier otra condición personal.

Destacada empresa industrial fabricante de productos de consumo duradero, desea incorporar a su organización: PROJECT MANAGER Reportando directamente al Responsable del Departamento de Márqueting, se encargará de coordinar el desarrollo de nuevos productos desde la aprobación del concepto hasta la entrega de producción, actuando como enlace operativo entre Márqueting y los equipos técnicos (Diseño, Ingeniería, Abastecimiento, Empaquetado, Cumplimiento, Operaciones). Deberá traducir los briefings de márqueting en planes de proyecto estructurados, cronogramas y listas de tareas, definiendo y supervisando los hitos del proyecto y realizando un seguimiento del progreso del mismo, garantizando la alineación con el plazo y el alcance acordados. Identificará posibles riesgos, retrasos o cuellos de botella y se encargará de facilitar soluciones con los equipos pertinentes. Organizará y documentará las reuniones interdisciplinarias y los seguimientos, manteniendo la documentación del proyecto estructurada, incluyendo especificaciones, estado del empaque, aprobaciones de material gráfico y actualizaciones de producción. Deberá apoyar la coordinación del muestreo, las pruebas, la validación de compliance y las aprobaciones de preproducción. Finalmente, garantizará una comunicación fluida entre departamentos durante todo el proceso de desarrollo, contribuyendo a la optimización de procesos y a una mejor colaboración entre equipos. Se requiere: Graduado ADE y/o Diplomatura en Marketing, o similar. Imprescindible alto nivel de inglés. Se valorará conocimiento de otros idiomas. Experiencia mínima de 5 años en puestos de similares características en sectores de consumo duradero comercializados a través de canales parecidos a los del grupo (grandes almacenes, hipermercados, detallistas especializados, detallistas e-commerce, mayoristas, distribuidores internacionales) Disponibilidad para trabajar 100% presencial. Empresa comprometida con la igualdad de oportunidades entre mujeres, hombres y personas LGTBI y con la igualdad de trato y no discriminación.

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.

Syntegon Telstar S.R.U. is a company of the Syntegon group, which operates worldwide. As a brand specialized in the development of GMP projects of consulting, engineering, construction and integrated process equipment, we serve companies linked to the life sciences market (pharmaceutical and biotechnology, healthcare, cosmetics, veterinary and food industries), as well as hospitals, laboratories and research centers. We also offer solutions with the application of vacuum and high vacuum technologies for traditional and high-tech industries in the energy and aerospace sectors, as well as scientific experimentation. Apply now and become part of our team! Job Description We are looking for a process‑driven and highly dedicated Automation Engineer with a passion for challenging commissioning projects. In this role, you will work at the intersection of automation, process engineering, and regulatory requirements—contributing directly to the performance, reliability, and compliance of our cutting‑edge isolator systems. Develop and adapt PLC software (Siemens TIA Portal) for advanced isolator systems Conduct comprehensive functional tests and support process validation activities Collaborate closely with process engineers to ensure alignment with regulatory standards Support extensive on‑site commissioning activities at customer facilities (often in shift models) Analyse technical issues, perform troubleshooting, and drive continuous process improvements Create and maintain technical documentation and software standards Provide technical support to project management, service teams, and qualification functions Qualifications Solid experience in PLC programming; Siemens TIA Portal is a must‑have Bachelor’s or Master’s degree in Electrical Engineering, Automation Engineering, Mechatronics, or a related field 2–5 years of relevant professional experience in automation, machine control, pharmaceutical equipment, or process environments Willingness to work with control engineering topics and expand expertise Strong understanding of process environments; experience in aseptic production is a clear advantage Willingness to travel internationally (approx. 15–20%) Beneficial: Siemens Step7 Classic Good command of English and the ability to work both independently and collaboratively A structured, reliable working style with a strong sense of responsibility Additional Information Please note that we can only submit your CV in English. For Syntegon and its subsidiaries, diversity is a key concern. We explicitly welcome an environment where all employees, regardless of gender, age, origin, religion, sexual orientation, gender identity, or special needs, are treated equally. If this job posting uses only the male form, it is for readability purposes and refers to individuals of all genders.

About us redarbor is the #1 HR Tech company in Latam. We help 75 million people a month to find a job and more than 150,000 companies to recruit and engage the best talent. Our projects We are leaders in job sites and apps with our employment platforms Computrabajo (the leader in Latin America), OCC in Mexico, and Infojobs and Catho in Brazil, as well as our HR software solutions Pandapé Genoma. Redarbor in figures 2013 founded +1100 collaborators 17 offices HR Tech 1# in Latam and 2# global online employment group We help more than 75 million people a month to find a job We are the best company to work for in Spain, according to GPTW. Who are we looking for? We are looking for a detail-oriented and analytical Corporate Audit Specialist with 3 years of professional experience in financial consolidation and reporting. In this role, you will report directly to the Head of Consolidation & Audit , acting as the key support in managing the Group’s financial reporting, international audits, and the integrity of our consolidated data. The ideal candidate is proactive, organized, and comfortable working in a fast-paced, international environment. You have a strong understanding of accounting principles and enjoy transforming complex financial data into accurate and meaningful reports. Your role? As a Consolidation Specialist, you will be responsible for preparing and reviewing consolidated financial statements , ensuring compliance with applicable accounting standards (such as IFRS or local GAAP). You will support the monthly, quarterly, and annual closing processes , coordinate with subsidiaries to collect financial data, analyze variances, and contribute to improving consolidation processes and internal controls to meet audit standards. You will work closely with finance teams across different regions to ensure accuracy, consistency, and timely reporting. You are the person we are looking for, if: You have approximately 3 years of experience in financial consolidation, audit, or corporate accounting. You hold a degree in Finance, Accounting, Business Administration, or a related field. You have a solid understanding of accounting standards (e.g., IFRS or local GAAP) with specific knowledge of IFRS 16, IFRS 9, IFRS 3 and NIC 21. You have proven experience in the preparation of individual and consolidated annual accounts. You are proficient in Excel and familiar with consolidation or ERP systems (e.g., SAP,Navision, Oracle, or similar tools). You demonstrate strong analytical skills and attention to detail. You have good communication skills and feel comfortable interacting with international stakeholders. You are fluent in English You bring experience in: Preparing consolidated financial statements under IFRS and management reports. Supporting month-end and year-end closing processes ensuring the robustness of our internal controls. Managing financial data from multiple subsidiaries, handling multi-currency environments and foreign exchange and analyzing financial variances. Supervise the collection and rigorous review of reporting packages from all subsidiaries, ensuring they are received on time and in the required format for the monthly and annual closing. Performing intercompany reconciliations, eliminating intercompany transactions and managing complex foreign exchange impacts. As a Consolidation Specialist, you will play a pivotal role in the coordination of both consolidated and individual audits, acting as the key interlocutor for external auditors to ensure the audit process for the Group. You will work hand-in-hand with local finance teams to ensure that all audit requirements are met accurately and on time.. Review and monitor the implementation of the Group’s accounting policies, ensuring total homogeneity in criteria between all subsidiaries. Improving financial processes and ensuring compliance with internal controls. If you aspire to join a leading company in its industry, working alongside a highly skilled team within a dynamic and international environment, we would love to connect with you even if you don't meet all the requirements. Your interest is valued, and we look forward to getting to know you better! Our benefits: Permanent Contract • flexible working hours + day off on your BIRTHDAY • December 24th, 31th. 23 working days of VACATION . We reward seniority with additional vacation days for every 2 years worked, up to a maximum of 5 extra days. Shortened workdays during Christmas, Easter, July, and August. Shortened workday on your child's birthday to spend more time with them on their special day. Hybrid Teleworking Model : 2 days in the office and 3 days from home. 100% Remote Work : 5 weeks a year + Christmas and Easter + specific long weekends + 2 weeks in August. Training Program : in-person courses + unlimited online training for specific skills from home. Individual budget for certifications and events. Languages : free online English and Portuguese classes. Parking : 50% subsidized cost for monthly parking at the office building. Gym : 70% subsidized membership fee. Physiotherapy : 50% subsidized monthly cost for a physiotherapist. Healthy meals : subsidized cost of your chosen menu. Ophthalmology : fixed annual subsidy for prescription lenses and contact lenses. Fresh fruit, coffee, and tea available daily. Family Day, Afterwork events, Team Building activities, etc. And much more.. At REDARBOR we work to promote an inclusive culture that seeks equity and values different perspectives. This translates to gender, religion, people with disabilities, LGBTQ+, ethnicity, and diversity of experience. We work all our searches based on this premise. Join our team!

Applus+ es una de las compañías líderes mundiales en ensayo, inspección y certificación, con presencia en más de 65 países en los 5 continentes y un equipo de más de 25.000 personas. Puedes consultar nuestros proyectos en la web: Hemos experimentado un gran desarrollo durante los últimos años, gracias a nuestro equipo humano que consideramos que son pieza clave y estratégica en el desarrollo de esta compañía. ¿Te gustaría ser parte de nuestro equipo? Actualmente estamos seleccionando un/a Compliance Assurance Specialist para incorporarse a nuestro departamento de Compliance Corporativo. Buscamos un/a profesional con sólida experiencia en auditoría de Compliance e Internal control, con perfil analítico y financiero. Esta persona reportará a la Chief Compliance Officer del Grupo y contribuirá activamente al desarrollo y ejecución del programa de Compliance Assurance, enfocado en verificar la implementación efectiva del modelo de Compliance de Applus+ en todas las entidades del Grupo. Responsabilidades principales: • Colaborar en el diseño y ejecución del plan de revisiones de Compliance a nivel global, evaluando la eficacia de los controles implementados y el cumplimiento de los procedimientos corporativos., • Realizar revisiones tanto presenciales como en remoto en las distintas entidades del Grupo, identificando oportunidades de mejora y apoyando en la definición de planes de acción., • Participar en investigaciones internas relacionadas con posibles desviaciones o incumplimientos, aportando un enfoque riguroso y objetivo en el análisis., • Diseñar e implantar herramientas y sistemas para la realización de auditorías remotas y el seguimiento continuo de indicadores de cumplimiento, incluyendo el uso de plataformas como Power BI., • Mantenerse al día sobre prácticas internacionales, marcos normativos relevantes y tendencias en compliance, contribuyendo a la mejora continua del sistema de control interno., • Elaborar informes de conclusiones para el equipo de Compliance y otras áreas implicadas, presentando los hallazgos, riesgos y recomendaciones de forma clara y estructurada. Requisitos: • Formación universitaria en Finanzas, Auditoría, Administración y Dirección de Empresas, Economía, Ingeniería o similares., • Mínimo 10 años de experiencia profesional, preferentemente en auditoría interna, control de riesgos o Compliance en compañías multinacionales o firmas de auditoría., • Experiencia demostrada en el diseño y ejecución de planes de revisión o auditoría de Compliance, y en el seguimiento de controles., • Alto dominio de herramientas de análisis y visualización de datos (especialmente Power BI)., • Buenas habilidades interpersonales, con capacidad para comunicar de forma clara, persuasiva y empática, especialmente en contextos multiculturales o cuando se actúe como figura de revisión en remoto o presencial., • Capacidad para trabajar de forma autónoma y gestionar tareas complejas con criterio y responsabilidad., • Disponibilidad para viajar internacionalmente de forma frecuente., • Nivel alto de inglés (C1 o superior). Se valorará el conocimiento de otros idiomas. Se valorará especialmente: • Certificaciones profesionales relevantes como Certified Internal Auditor (CIA), Certified Fraud Examiner (CFE), Certified in Risk and Control Management (CRMA) u otras relacionadas con aseguramiento, control interno o prevención del fraude., • Experiencia en la implantación de sistemas de control remoto o tecnologías emergentes aplicadas a compliance., • Conocimiento práctico de estándares internacionales de control interno, marcos regulatorios y normativas sectoriales aplicables a grupos multinacionales.

Syntegon Telstar S.R.U. is a company of the Syntegon group, which operates worldwide. As a brand specialized in the development of GMP projects of consulting, engineering, construction and integrated process equipment, we serve companies linked to the life sciences market (pharmaceutical and biotechnology, healthcare, cosmetics, veterinary and food industries), as well as hospitals, laboratories and research centers. We also offer solutions with the application of vacuum and high vacuum technologies for traditional and high-tech industries in the energy and aerospace sectors, as well as scientific experimentation. Apply now and become part of our team! Job Description We are looking for a process‑driven and highly dedicated Automation Engineer with a passion for challenging commissioning projects. In this role, you will work at the intersection of automation, process engineering, and regulatory requirements—contributing directly to the performance, reliability, and compliance of our cutting‑edge isolator systems. • Develop and adapt PLC software (Siemens TIA Portal) for advanced isolator systems, • Conduct comprehensive functional tests and support process validation activities, • Collaborate closely with process engineers to ensure alignment with regulatory standards, • Support extensive on‑site commissioning activities at customer facilities (often in shift models), • Analyse technical issues, perform troubleshooting, and drive continuous process improvements, • Create and maintain technical documentation and software standards, • Solid experience in PLC programming; Siemens TIA Portal is a must‑have, • Bachelor’s or Master’s degree in Electrical Engineering, Automation Engineering, Mechatronics, or a related field, • 2–5 years of relevant professional experience in automation, machine control, pharmaceutical equipment, or process environments, • Willingness to work with control engineering topics and expand expertise, • Strong understanding of process environments; experience in aseptic production is a clear advantage, • Willingness to travel internationally (approx. 15–20%), • Beneficial: Siemens Step7 Classic, • Good command of English and the ability to work both independently and collaboratively

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.

We are Applus+ Laboratories, the division of the Applus+ Group that provides testing, certification, and product development engineering services. In the IT & CYBERSECURITY laboratory, we are accredited to perform a wide range of security evaluations for payment schemes, identification, and IT security. We are seeking for passionate hardware and embedded system security professional passionates to join our team and learn this field. Perform vulnerability analysis and penetration testing on real hardware and software products, analysing source code and using reverse engineering techniques. We are looking for a Junior Cybersecurity Engineer to join our team and perform vulnerability analysis and penetration testing on real hardware and software products, analysing source code and using reverse engineering techniques. Essential job responsibilities • Acquire knowledge of key customer's technological solutions, • Gain understanding of cybersecurity requirements for products and customer facilities, • Carry out hardware and software security evaluations in different frameworks., • Perform ad-hoc evaluations, subject to customer constraints and needs., • Work with technology vendors to help meet security certification requirements, • Identify and resolve challenges to ensure certification project success, • Write technical reports and communicate effectively with customers, testing laboratories, and other stakeholders, • Conduct security evaluations in compliance with certification standards, primarily for Smart Cards and embedded systems., • Perform advanced technical security analyses, including:, • -Secure source code reviews for embedded and payment systems., • -High Assurance Vulnerability Analysis (VA)., • -Advanced penetration testing using Side Channel Analysis (SCA) and Fault Injection (FI) techniques. To be considered, candidates must possess • Education: Technical background such as Computer Science, Telecommunication, Electronics, Mathematics or equivalent degree., • Coding experience with Python / C / C++, • Experience with laboratory equipment such as oscilloscopes is desirable, • Documentary experience with Git, • Languages: Spanish and English (at least B2), • Experience in the same position: 0-2 years, • Strong analytical and communication skills, • Self-starter with a passion for professional growth, • Passion for technology and cybersecurity Our current stack and tools: • Programming Language, Python, C/ C++, • Git, • Operative Systems, UNIX Based OS Benefits • Permanent contract., • Full-time position., • 23 vacation days and 3 personal days., • Flexible compensation plan (health insurance, transportation, childcare, meal vouchers)., • Employee parking., • Green spaces and wellness activities, including yoga classes, to promote well-being., • Subsidized menu with reduced prices. Are you passionate about cybersecurity? Do you want to be part of a team of top experts? This is the company for you! Applus+ Laboratories is an equal opportunity employer. We are committed to evaluating all applications equally based on skills, achievements, and experience, regardless of race, nationality, gender, age, disability, sexual orientation, gender identity, or any other classification protected by law

We are Applus+ Laboratories, the division of the Applus+ Group that provides testing, certification, and product development engineering services. In the IT & CYBERSECURITY laboratory, we are accredited to perform a wide range of security evaluations for payment schemes, identification, and IT security. We are seeking for passionate hardware and embedded system security professional passionates to join our team and learn this field. Perform vulnerability analysis and penetration testing on real hardware and software products, analysing source code and using reverse engineering techniques. We are looking for a Junior Cybersecurity Engineer to join our team and perform vulnerability analysis and penetration testing on real hardware and software products, analysing source code and using reverse engineering techniques. Essential job responsibilities • Acquire knowledge of key customer's technological solutions, • Gain understanding of cybersecurity requirements for products and customer facilities, • Carry out hardware and software security evaluations in different frameworks., • Perform ad-hoc evaluations, subject to customer constraints and needs., • Work with technology vendors to help meet security certification requirements, • Identify and resolve challenges to ensure certification project success, • Write technical reports and communicate effectively with customers, testing laboratories, and other stakeholders, • Conduct security evaluations in compliance with certification standards, primarily for Smart Cards and embedded systems., • Perform advanced technical security analyses, including:, • -Secure source code reviews for embedded and payment systems., • -High Assurance Vulnerability Analysis (VA)., • -Advanced penetration testing using Side Channel Analysis (SCA) and Fault Injection (FI) techniques. To be considered, candidates must possess • Education: Technical background such as Computer Science, Telecommunication, Electronics, Mathematics or equivalent degree., • Coding experience with Python / C / C++, • Experience with laboratory equipment such as oscilloscopes is desirable, • Documentary experience with Git, • Languages: Spanish and English (at least B2), • Experience in the same position: 0-2 years, • Strong analytical and communication skills, • Self-starter with a passion for professional growth, • Passion for technology and cybersecurity Our current stack and tools: • Programming Language, Python, C/ C++, • Git, • Operative Systems, UNIX Based OS Benefits • Permanent contract., • Full-time position., • 23 vacation days and 3 personal days., • Flexible compensation plan (health insurance, transportation, childcare, meal vouchers)., • Employee parking., • Green spaces and wellness activities, including yoga classes, to promote well-being., • Subsidized menu with reduced prices. Are you passionate about cybersecurity? Do you want to be part of a team of top experts? This is the company for you! Applus+ Laboratories is an equal opportunity employer. We are committed to evaluating all applications equally based on skills, achievements, and experience, regardless of race, nationality, gender, age, disability, sexual orientation, gender identity, or any other classification protected by law

Estamos colaborando con una compañía especializada en servicios GMP para la industria farmacéutica, que busca incorporar un/a Técnico/a de Cualificación y Validación junior para reforzar su equipo de Compliance. Su misión es clara: acompañar la industrialización de nuevos medicamentos que impactan directamente en la calidad de vida de las personas, especialmente en el ámbito de los inyectables fabricados en entorno aséptico. 🚀 ¿Qué se ofrece? • Plan de carrera y desarrollo profesional personalizado dentro del sector Pharma, • Incorporación a un entorno en crecimiento, con proyectos variados y recorrido a largo plazo., • Trabajo en un equipo multidisciplinar con perfiles científicos y de ingeniería, donde se valora la iniciativa y las nuevas ideas., • Rol con contacto directo con cliente durante la ejecución de proyectos., • Buen ambiente laboral, joven y colaborativo. 🧩 ¿Cuáles serán tus responsabilidades? • Diseño y elaboración de protocolos de cualificación y validación de equipos y procesos bajo normativa GMP., • Ejecución, revisión y análisis de resultados de dichos protocolos., • Mejora continua de la documentación de validación y actualización de estándares según cada proyecto. 🎯 ¿Qué perfil buscamos? • Formación universitaria en áreas científico-técnicas: Química, Farmacia, Biología, Ingeniería Química o similar (o experiencia equivalente)., • Persona analítica, organizada, resolutiva, orientada a resultados y con actitud proactiva., • Se valorará conocimiento en GMP, fabricación aséptica y liofilización., • Disponibilidad para viajar (nacional e internacional)., • Nivel alto de inglés (oral y escrito)., • Carnet de conducir y vehículo propio para desplazamientos a planta. Compromiso con la Igualdad de Oportunidades: En Solutia GHS garantizamos que todos nuestros procesos de selección se desarrollan en base a criterios objetivos, valorando únicamente las competencias, la experiencia y el talento de las personas candidatas. Promovemos la igualdad de oportunidades y no toleramos ningún tipo de discriminación por razón de sexo, género, edad, origen, raza, religión, orientación sexual, identidad de género, discapacidad o cualquier otra circunstancia personal o social. Asimismo, nuestra política retributiva se rige por el principio de equidad salarial ante el desempeño de las mismas funciones, reforzando nuestro compromiso con un entorno laboral diverso, inclusivo y respetuoso.

Esta persona reportará a la Chief Compliance Officer del Grupo y contribuirá activamente al desarrollo y ejecución del programa de Compliance Assurance, enfocado en verificar la implementación efectiva del modelo de Compliance de Applus+ en todas las entidades del Grupo. Mantenerse al día sobre

COMSER is looking for a Qualification and Validation Technician for the GMP Compliance Services area.We are a company that provides services to the pharmaceutical industry. Our purpose is to help and streamline the industrialization of new medicines that improve people's quality of life. Our focus is on injectable medicines that need to be manufactured in an aseptic environment. What do we offer? • Career plan with personalized professional development in the pharmaceutical sector. In a growing company with many opportunities., • Being part of a multidisciplinary team, where scientific and engineering profiles stand out; where your creative proposals will be valued., • Being the direct interlocutor with our clients during the execution of projects., • Good and young work environment. What will your main functions be? • Design and develop equipment or process validation protocols according to GMP and in accordance with the client's user requirements., • Execution and review of the protocols, with subsequent analysis of the results., • Continuous improvement of the validation documentation and updating of standards adaptable to each project What do we expect from you? That you have a scientific-technical university education (chemical sciences, pharmacy, biology, chemical engineering or similar) and/or training acquired in the development of your usual profession. • That you are an analytical, planned, resolute, results-oriented and dynamic person., • Knowledge of GMP regulations, aseptic manufacturing and the lyophilization technique is a plus., • Availability to travel (national and international)., • Full professional level of English (written and spoken)., • Own vehicle for travel to client sites. At COMSER, we value and respect diversity. We firmly believe that having a diverse team is key to success and innovation. That's why we offer equal opportunities to all candidates, regardless of their gender, age, race, religion, sexual orientation, disability, or any other characteristic. If you believe you fit the profile and are interested in starting a new professional project, do not hesitate to apply for the offer and contact us. We want to meet you!

Syntegon Telstar S.R.U. is a company of the Syntegon group, which operates worldwide. As a brand specialized in the development of GMP projects of consulting, engineering, construction and integrated process equipment, we serve companies linked to the life sciences market (pharmaceutical and biotechnology, healthcare, cosmetics, veterinary and food industries), as well as hospitals, laboratories and research centers. We also offer solutions with the application of vacuum and high vacuum technologies for traditional and high-tech industries in the energy and aerospace sectors, as well as scientific experimentation. Apply now and become part of our team! Job Description We are looking for a Mechanical Engineer for our offices in Terrassa (Barcelona) with at least 2 years of experience in designing special-purpose machinery for the pharmaceutical sector (ideally filling machinery) or the packaging industry. The role involves designing and developing this special machinery in 3D, as well as preparing all associated technical documentation. Main responsabilities: • Development of mechanical solutions, creation of models and drawings, preparation of mock-ups, optimization of existing assemblies, and preparation and updating of functional specifications, flow diagrams, and pneumatic schematics., • Technical calculations and sizing, including strength calculations, service life and tolerance analyses, as well as the use of simulation tools and, when appropriate, FEM analysis for design validation., • Documentation of modifications and data maintenance in ERP/PLM systems: creation and updating of Bills of Materials (BOM) in SAP, as well as initiating catalog part requests (workflow)., • Conducting risk assessments, preparing functional specifications, leading Design Qualification workshops, and participating in systematic design reviews., • Planning, coordinating, and supervising prototypes, tests, and trials; evaluating the results and deriving the necessary design modifications., • Technical support for assembly, pre‑assembly, service, and purchasing; rapid implementation of design modifications in case of complaints, with a high level of responsiveness and proactivity., • Compliance with and application of relevant standards and guidelines (machine safety, pharmaceutical requirements), as well as participation in the standardization and continuous improvement of design standards., • University degree in Mechanical Engineering, Mechatronics, Precision Engineering, or an equivalent technical qualification; academic certificate., • Experience in the design and construction of special-purpose machinery, ideally in pharmaceutical filling lines or comparable pharmaceutical equipment., • Extensive hands-on experience with 3D CAD (ideally SolidWorks/DBWorks) including a demonstrable portfolio of CAD models/drawings., • Experience with SAP (master data, Bills of Materials, classification, etc.) and with database systems., • Familiarity with design workflows, Design Reviews, functional specifications, risk assessments, process flow diagrams, and pneumatic schematics., • Hands-on experience with prototypes/testing, assembly support, and customer acceptance activities.

Do you want to be part of a team with a real impact on global health? At Noucor, a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide 🌍. We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team. Main Tasks: • Ensure that all processes related to clinical trials are performed in compliance with GCP (Good Clinical Practice) and applicable quality standards., • Provide QA support to clinical trial activities, including documentation review and quality oversight of internal teams and external partners (CROs, service providers)., • Evaluate and manage quality issues, deviations, CAPAs, change controls and complaints related to Clinical Trials., • Support quality activities related to Investigational Medicinal Products (IMPs) in collaboration with Pharmaceutical Development and Analytical Development., • Maintain awareness of applicable quality regulations and compliance requirements impacting clinical development and R&D activities. Requirements: • Degree in Pharmacy, Chemistry, Biology, or similar., • Fluent in English and Spanish., • Experience in Good Clinical Practices (GCP); knowledge of GMP requirements for IMPs in clinical trials (formerly Annex 13)., • Good command of MS Office., • High willingness to learn and take on new challenges and responsibilities., • Motivation, teamwork, and good communication skills. We Offer: 🤩 Work within a great team of professionals with a very good work environment. ⚙️ Innovative work environment focused on continuous improvement. 🚀 Continuous learning and development. 💼 Competitive benefits package and flexible schedule. 📍 Offices in Palau-solità i Plegamans. 💰 Competitive salary. Interested in joining us? At Noucor, we believe in the value of diverse teams. We therefore welcome and consider all applications regardless of gender, age, background, sexual orientation, gender identity, or any other personal characteristic. If you meet most of the requirements and are motivated by the project, we would be pleased to hear from you.

Kanguro es una startup de logística de última milla con alto potencial de crecimiento nacida en Barcelona con un propósito claro: liderar la transformación tecnológica de la logística. Operamos una red universal de puntos de recogida en España y estamos en plena expansión a Alemania, Francia y Portugal, combinando IA y tecnología propia para hacer la entrega y recogida de paquetes más eficiente para el carrier, más cómoda para el cliente y más sostenible para todos. ¿En qué consiste la posición? Buscamos un/a becario/a de RRHH que nos ayude a mantener al equipo alineado, con seguimiento real de objetivos, rendimiento y cumplimiento de políticas internas. Tu día a día estará centrado en hacer validaciones recurrentes con empleados de todos los niveles — especialmente perfiles de nivel medio y senior — para asegurar que los objetivos se cumplen, las evaluaciones de rendimiento ocurren y las políticas de trabajo presencial/remoto se respetan. No es un rol administrativo clásico. Vas a tener conversaciones reales con gente senior y acceso directo a dirección. Responsabilidades Seguimiento de rendimiento y OKRs • Apoyar en la ejecución de ciclos recurrentes de validación de rendimiento para todos los empleados, con foco en perfiles mid-to-senior, • Hacer seguimiento del progreso de OKRs por equipo: asegurar que los objetivos se definen, revisan y actualizan en la cadencia acordada, • Preparar informes resumen de rendimiento para dirección, destacando gaps de alineamiento y contribuciones destacadas, • Monitorizar y validar el cumplimiento de las políticas de trabajo híbrido: días presenciales, días remotos y excepciones, • Mantener registros de asistencia y presencia; señalar patrones que se desvíen de lo acordado, • Ayudar a diseñar y desplegar encuestas periódicas de satisfacción y engagement, • Analizar resultados y preparar insights accionables para dirección, • Mantener y actualizar registros de empleados, contratos y documentación de RRHH, • Apoyar en coordinación de procesos de selección cuando sea necesario, • Tareas administrativas relacionadas con nómina, beneficios y compliance legal ¿Qué perfil buscamos? • Estudiante o recién graduado/a en Recursos Humanos, Psicología, Relaciones Laborales, ADE o similar, • Elegible para convenio de prácticas con universidad o escuela de negocios española, • Muy organizado/a: capaz de gestionar múltiples seguimientos con muchas personas sin que se caiga nada, • Cómodo/a trabajando con hojas de cálculo (Excel/Google Sheets) y creando trackers desde cero, • Buena comunicación escrita y verbal en castellano; inglés necesario, • Discreción y profesionalidad — manejarás datos sensibles de rendimiento y personal, • Mentalidad proactiva: no esperas a que te digan qué hacer, señalas problemas y propones mejoras, • Valorable: familiaridad con herramientas de RRHH (BambooHR, Factorial, Personio), herramientas de encuestas, o conocimiento básico de legislación laboral española, • Catalán valorable ¿Qué ofrecemos? • Convenio de prácticas (6 meses, con posibilidad de extensión o incorporación), • Remuneración de 900€/mes, • Oficina en Sant Cugat del Vallès, delante de la estación de Mirasol (FGC), • Presencialidad: 4–5 días en oficina (la presencia es clave para este rol), • Horario flexible compatible con compromisos universitarios, • Responsabilidad real desde el primer día, • Acceso directo a dirección y exposición a cómo se gestiona una empresa en crecimiento, • Equipo con muy buen ambiente, joven y multidisciplinar, • Trabajar en una empresa donde la inteligencia artificial es parte del día a día, no solo un claim ¿Cómo aplicar? El responsable de este proceso de selección es Josep Francesc Cortés. Si te interesa la posición y cumples los requisitos, envía un email a dirigido a Josep Francesc, adjuntando tu CV y una carta de motivación donde nos cuentes quién eres y por qué te interesa este rol en Kanguro; qué puedes aportar al equipo de People; y tu disponibilidad.

Destacada empresa industrial fabricante de productos de consumo duradero, desea incorporar a su organización: PROJECT MANAGER Reportando directamente al Responsable del Departamento de Márqueting, se encargará de coordinar el desarrollo de nuevos productos desde la aprobación del concepto hasta la entrega de producción, actuando como enlace operativo entre Márqueting y los equipos técnicos (Diseño, Ingeniería, Abastecimiento, Empaquetado, Cumplimiento, Operaciones). Deberá traducir los briefings de márqueting en planes de proyecto estructurados, cronogramas y listas de tareas, definiendo y supervisando los hitos del proyecto y realizando un seguimiento del progreso del mismo, garantizando la alineación con el plazo y el alcance acordados. Identificará posibles riesgos, retrasos o cuellos de botella y se encargará de facilitar soluciones con los equipos pertinentes. Organizará y documentará las reuniones interdisciplinarias y los seguimientos, manteniendo la documentación del proyecto estructurada, incluyendo especificaciones, estado del empaque, aprobaciones de material gráfico y actualizaciones de producción. Deberá apoyar la coordinación del muestreo, las pruebas, la validación de compliance y las aprobaciones de preproducción. Finalmente, garantizará una comunicación fluida entre departamentos durante todo el proceso de desarrollo, contribuyendo a la optimización de procesos y a una mejor colaboración entre equipos. Se requiere: • Graduado ADE y/o Diplomatura en Marketing, o similar., • Imprescindible alto nivel de inglés. Se valorará conocimiento de otros idiomas., • Experiencia mínima de 5 años en puestos de similares características en sectores de consumo duradero comercializados a través de canales parecidos a los del grupo (grandes almacenes, hipermercados, detallistas especializados, detallistas e-commerce, mayoristas, distribuidores internacionales), • Disponibilidad para trabajar 100% presencial. Empresa comprometida con la igualdad de oportunidades entre mujeres, hombres y personas LGTBI y con la igualdad de trato y no discriminación.

Syntegon Telstar S.R.U. is a company of the Syntegon group, which operates worldwide. As a brand specialized in the development of GMP projects of consulting, engineering, construction and integrated process equipment, we serve companies linked to the life sciences market (pharmaceutical and biotechnology, healthcare, cosmetics, veterinary and food industries), as well as hospitals, laboratories and research centers. We also offer solutions with the application of vacuum and high vacuum technologies for traditional and high-tech industries in the energy and aerospace sectors, as well as scientific experimentation. Apply now and become part of our team! Job Description We are looking for a Mechanical Engineer for our offices in Terrassa (Barcelona) with at least 2 years of experience in designing special-purpose machinery for the pharmaceutical sector (ideally filling machinery) or the packaging industry. The role involves designing and developing this special machinery in 3D, as well as preparing all associated technical documentation. Main responsabilities: • Development of mechanical solutions, creation of models and drawings, preparation of mock-ups, optimization of existing assemblies, and preparation and updating of functional specifications, flow diagrams, and pneumatic schematics., • Technical calculations and sizing, including strength calculations, service life and tolerance analyses, as well as the use of simulation tools and, when appropriate, FEM analysis for design validation., • Documentation of modifications and data maintenance in ERP/PLM systems: creation and updating of Bills of Materials (BOM) in SAP, as well as initiating catalog part requests (workflow)., • Conducting risk assessments, preparing functional specifications, leading Design Qualification workshops, and participating in systematic design reviews., • Planning, coordinating, and supervising prototypes, tests, and trials; evaluating the results and deriving the necessary design modifications., • Technical support for assembly, pre‑assembly, service, and purchasing; rapid implementation of design modifications in case of complaints, with a high level of responsiveness and proactivity., • Compliance with and application of relevant standards and guidelines (machine safety, pharmaceutical requirements), as well as participation in the standardization and continuous improvement of design standards., • University degree in Mechanical Engineering, Mechatronics, Precision Engineering, or an equivalent technical qualification; academic certificate., • Experience in the design and construction of special-purpose machinery, ideally in pharmaceutical filling lines or comparable pharmaceutical equipment., • Extensive hands-on experience with 3D CAD (ideally SolidWorks/DBWorks) including a demonstrable portfolio of CAD models/drawings., • Experience with SAP (master data, Bills of Materials, classification, etc.) and with database systems., • Familiarity with design workflows, Design Reviews, functional specifications, risk assessments, process flow diagrams, and pneumatic schematics., • Hands-on experience with prototypes/testing, assembly support, and customer acceptance activities.

Ensure compliance with reporting requirements from BaFin Bundesbank Bank of Spain and European authorities (EBA ECB). Knowledge of European banking regulations and reporting standards particularly in Germany and Spain is a plus. Honda Bank GmbH is part of Hondas financial operations in Europe combin

Si, como nosotros, trabajas mejor cuando se confía en ti, Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto. súmate a nuestro equipo >> En Elis apostamos por las personas, les damos responsabilidades y las acompañamos en su crecimiento. Formarás parte de un grupo internacional con más de 75 años de historia , líder en su sector y comprometido con la economía circular. Don’t choose Elis si buscas rutina. Pero si te motiva la gestión de flotas y la optimización operativa, en nuestra organización buscamos incorporar un/a Gestor/a de Flota que lidere la gestión integral de nuestra flota de vehículos comerciales, de empresa e industriales (camiones y furgonetas).sigue leyendo Tu misión Serás responsable de garantizar la disponibilidad, eficiencia operativa, control de costes y cumplimiento normativo de toda la flota, trabajando de forma transversal con distintos departamentos y proveedores externos cumpliendo los procedimientos y estándares del grupo. ¿Qué harás? Gestión integral de flota (turismos e industrial). Coordinación de altas, bajas, renovaciones y sustituciones. Supervisión de mantenimiento, ITV, seguros y documentación. Gestión de contratos de renting/leasing y relación con proveedores. Soporte y atención a empleados/as usuarios de flota. Participar en negociaciones con proveedores de complejidad media. Gestionar pedidos, contratos y seguimiento de entregas para distintos centros. Actuar como interlocutor entre proveedores y la empresa. Elaborar reporting periódico y seguimiento de KPIs. Garantizar el cumplimiento de procedimientos, compliance y estándares de grupo. ¿A quién buscamos? Formación universitaria en ADE, Ingeniería o similar 3-5 años de experiencia en gestión de flotas Conocimiento de normativa y contratos de renting/leasing. Excel nivel avanzado (Power Bi es un plus) Nivel de inglés para entorno profesional Perfil analítico, organizado y con capacidad de gestión. ¿Qué ofrecemos? Contrato indefinido en un grupo sólido y en crecimiento Un rol con impacto directo en la optimización de compras y costes Desarrollo profesional dentro de un entorno internacional Salario competitivo y beneficios sociales ¿Te interesa el reto? Únete a Elis y forma parte de un equipo que impulsa la eficiencia y la mejora continua en nuestras operaciones. ELIS MANOMATIC, S.A.U. te informa que es la entidad responsable del tratamiento de tus datos personales con el fin de valorar tu candidatura para vacantes presentes o futuras a cubrir en nuestra organización. Para más información sobre el tratamiento de tus datos o sobre cómo ejercer sus derechos de derechos de acceso, rectificación, supresión, limitación, portabilidad y oposición, puedes acceder a nuestro portal web en el apartado política de privacidad. ELIS MANOMATIC, S.A.U. no discriminará directa o indirectamente a los candidatos y candidatas en los procesos de selección, por razones de sexo, estado civil, edad, origen racial o étnico, condición social, religión o convicciones, ideas políticas, orientación sexual, afiliación o no a un sindicato, así como por razón de lengua Que ELIS MANOMATIC, S.A.U. se compromete a actuar bajo el principio de igualdad de trato y de oportunidades entre todo el personal que realicen el mismo trabajo. ELIS MANOMATIC, S.A.U. se dispone a adoptar medidas que eviten cualquier forma de discriminación entre hombres y mujeres. xcskxlj En los procesos de selección, realizarán iniciativas para contratar mujeres en áreas donde la presencia femenina esté subrepresentada o dar preferencia a la contratación de mujeres en igualdad de condiciones.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. Position Do you have a passion for software engineering and technology? Do you want to have a meaningful contribution in a SW of top‑notch systems that save lives? If so, this is your position! Our Instrumentation Development Chapter is responsible for the design and development of instrumentation (pre‑analytics, analyzers, post‑analyzers and lab automation solutions) for the future Core Laboratory. We are looking for self‑motivated software engineers to join our exceptional engineering teams that are building solutions for our Coagulation instrumentation. You will be part of an ongoing transformation in the healthcare industry, working in one of the future product teams in Roche, responsible for creating an intuitive core platform that has a great impact on users. Responsibilities * • Participate in all phases of software development from feasibility studies through design, development, testing and bug fixing including software maintenance., • Participate in defining user stories, their estimation, planning, and implementation within the software development team., • Produce code based on software requirements, the project’s software architecture and other project guidelines; Unit and subsystem specifications that document their implementation., • Do accurate code design and implementation including the tests to verify the code against unit and/or subsystem specification., • Review and analyze your source code as well as on request the source code of your peers in the software development team., • Review application design, functionality, usability and performance to enhance it., • Provide work status and issue notification within the software development team and if required to software project management., • Share expertise and experience with less experienced software engineers and actively support their knowledge improvement., • Permanently improve the software development workflow to increase quality and efficiency by exchanging know‑how with other software engineers and stakeholders. Requirements * • Bachelor’s degree in Computer Science or similar from the software sector., • At least 8 years of work experience in hands‑on software development., • Experience with cybersecurity and what it means from the software engineering point of view., • Strong knowledge in the following technologies: Microsoft .NET Framework, .NET 8.0, C#, .NET Core, XAML., • PostgreSQL database (version 17), Oracle database and Entity Framework., • Automated Testing framework (MS Test, Selenium, Winapp driver)., • Continuous integration/deployment (like Azure DevOps and GIT)., • Good knowledge of design patterns., • Working experience in Object Oriented Analysis and Design using UML, writing formal specifications and requirements., • Excellent knowledge of software and application design and architecture best practices., • Strong team player, open minded and enthusiastic to learn, strong communication and collaboration., • Experience working in agile software development environments (Scrum, SAFe), ideally a SAFe certification and practical experience acting as a Scrum Master are highly desirable., • High level of written and spoken English., • Interpersonal communication skills, influence and inspiration, capable of dealing with complex situations., • Strong technical background and good problem‑solving skills., • Positive, open minded, communicative and proactive mindset., • Takes responsibility for a team or technical concept. Additional Qualifications * • Experience with product delivery in regulated industries with good understanding of compliance topics such as information security and design control is a strong plus., • Prior experience in developing and delivering software for Medical Devices is a strong plus. Personal Traits * • Self‑organized and responsible., • A team player, who listens to their colleagues but is not afraid to assert themselves., • Looking for a purpose where your work will have a real impact in patient lives. Your work is meaningful to you., • Passionate and naturally curious., • Looking for solving real‑world problems and proposing actual plans., • Not afraid to fail and learn. We will provide you with an excellent work environment, international projects and a company which strongly believes that the employees are the biggest strength, so you’ll be able to make your own decisions and dedicate time to propose new and innovative changes, optimize processes and find ways to increase efficiency. We also offer competitive compensation and excellent social benefits like flexible work schedule and home office policies, medical insurance, pension plan, allowances for marriage and birth, training related to your career development, gym, meal allowance, flexible remuneration scheme with its fiscal advantages and other benefits. We offer a flexible working model which allows home office and remote work. xcskxlj Roche is an Equal Opportunity Employer. #J-18808-Ljbffr

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