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We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. Main Responsibilities : As a USP Manufacturing Technician , your responsibilities will include: Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader. Ensure the correct training of the personnel in charge. Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms. Participate in internal / external audits as required by the Quality Assurance Department. Comply and ensure compliance with GMP standards within the work team. Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB). Investigate and propose new methods or process innovations to optimize and improve the work in the area. Ensure proper compliance with regulations and correct completion of current documentation. Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager. Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB). Supervise the correct completion of the new equipment entry documentation. Supervise the correct training of the personnel in charge, if any. Carry out the distribution and supervision of daily activities. Write and keep updated the documentation associated with the production processes carried out in the USP area. Control / monitoring of orders placed in the USP production area using ERP software. Assesment criteria: Education: Bachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. Languages: Fluent in Spanish . Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: GMP/GLP regulations With industrial-scale bioreactors Cell Cultures Microbiological analysis techniques Upstream production positions Biotechnology / Biopharmaceutical Sector Other requirements: Open to work in shifts. Software package: Office. User level. Why 3PBiovian? A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. ...And so much more! Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. It's within us .

En Etalentum seleccionamos para una empresa del sector de fabricación electrónica (EMS), especializada en el montaje de tarjetas electrónicas y conjuntos electromecánicos, un/a Responsable de Producción, Procesos y Métodos, para la zona de Ribera Navarra. Se trata de una posición estratégica dentro de planta, con responsabilidad directa sobre producción y mejora de procesos, en un entorno técnico, dinámico y orientado a la excelencia operativa. La persona seleccionada liderará el área productiva, asegurando el cumplimiento de los objetivos en términos de calidad, eficiencia, costes y servicio al cliente. Funciones principales • Gestionar y asegurar el cumplimiento de los objetivos de producción (volumen, calidad, costes, plazos y estándares medioambientales). - Dirigir el área de Procesos y Métodos, desarrollando y optimizando útiles y métodos de fabricación. - Planificar y controlar la producción en función de las necesidades de cliente y compromisos de entrega. - Definir objetivos departamentales, establecer planes de acción y realizar su seguimiento. - Coordinar y liderar el equipo de producción, fomentando su desarrollo y desempeño. - Elaborar y controlar el presupuesto del área (costes fijos, variables, recursos y servicios externos). - Realizar seguimiento de KPIs productivos e impulsar planes de mejora continua. - Analizar desviaciones y poner en marcha acciones correctivas y preventivas. - Garantizar el cumplimiento de procedimientos internos, normas de planta y estándares de orden y limpieza. - Impulsar la optimización de procesos, tiempos y recursos productivos. Requisitos • Formación técnica o Ingeniería Industrial, Electrónica o similar. - Experiencia previa en gestión de producción en entorno industrial, preferiblemente en fabricación electrónica. - Conocimientos en planificación productiva, control de costes y mejora continua. - Experiencia en gestión y coordinación de equipos. - Capacidad de liderazgo, organización y orientación a resultados. Se valorará • Experiencia en empresas EMS o montaje de PCBA. - Conocimientos en Lean Manufacturing, 5S u otras metodologías de mejora continua. - Perfil proactivo, resolutivo y con visión global de planta. - Capacidad de trabajo transversal con los departamentos de calidad, compras e ingeniería. Se ofrece • Incorporación estable en empresa consolidada del sector. - Posición con responsabilidad y autonomía en la toma de decisiones. - Participación activa en proyectos de mejora y crecimiento industrial. - Entorno técnico, colaborativo y orientado a la excelencia operativa. - Condiciones económicas acordes a la experiencia y valía aportada.

We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. Main Responsibilities: As a DSP Manufacturing Technician , your responsibilities will include: Achieve the objectives set by the Team Leader and the DSP manufacturing manager. Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms. Comply with good manufacturing practice (GMP), as well as occupational health and safety standards. Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer. Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations. Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan. Carry out the control and supervision, the stock of materials needed to perform the daily activities. Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators. Program chromatography methods in UNICORN to ensure the correct execution of DSP processes. Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities. Participate in internal / external audits as required by the Quality Assurance Department. Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB). Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks. Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB). Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department. Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). Assesment criteria: Education: Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.). University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.). Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: GMP/GLP regulations Chromatographic equipment Packed chromatographic columns Experience with ÄKTA Experience with Unicorn Other requirements: Open to work in shifts. Office Software Package: User Level. Unicorn Software Package: User Level. Why 3PBiovian? A permanent and stable position in a competitive growing company. A competitive time off package with 41 paid days of vacation. Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) All new hires who reside outside Navarra are provided with a relocation service and/or assistance. Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. We encourage the participation of our employees in solidarity events such as charity races, social donations... We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. We have a high-impact work environment with flat hierarchies and short decision-making processes. ...And so much more! Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. It's within us.

En Etalentum seleccionamos para una empresa del sector de fabricación electrónica (EMS), especializada en el montaje de tarjetas electrónicas y conjuntos electromecánicos, un/a Responsable de Producción, Procesos y Métodos, para la zona de Ribera Navarra. Se trata de una posición estratégica dentro de planta, con responsabilidad directa sobre producción y mejora de procesos, en un entorno técnico, dinámico y orientado a la excelencia operativa. La persona seleccionada liderará el área productiva, asegurando el cumplimiento de los objetivos en términos de calidad, eficiencia, costes y servicio al cliente. Funciones principales • Gestionar y asegurar el cumplimiento de los objetivos de producción (volumen, calidad, costes, plazos y estándares medioambientales). - Dirigir el área de Procesos y Métodos, desarrollando y optimizando útiles y métodos de fabricación. - Planificar y controlar la producción en función de las necesidades de cliente y compromisos de entrega. - Definir objetivos departamentales, establecer planes de acción y realizar su seguimiento. - Coordinar y liderar el equipo de producción, fomentando su desarrollo y desempeño. - Elaborar y controlar el presupuesto del área (costes fijos, variables, recursos y servicios externos). - Realizar seguimiento de KPIs productivos e impulsar planes de mejora continua. - Analizar desviaciones y poner en marcha acciones correctivas y preventivas. - Garantizar el cumplimiento de procedimientos internos, normas de planta y estándares de orden y limpieza. - Impulsar la optimización de procesos, tiempos y recursos productivos. Requisitos • Formación técnica o Ingeniería Industrial, Electrónica o similar. - Experiencia previa en gestión de producción en entorno industrial, preferiblemente en fabricación electrónica. - Conocimientos en planificación productiva, control de costes y mejora continua. - Experiencia en gestión y coordinación de equipos. - Capacidad de liderazgo, organización y orientación a resultados. Se valorará • Experiencia en empresas EMS o montaje de PCBA. - Conocimientos en Lean Manufacturing, 5S u otras metodologías de mejora continua. - Perfil proactivo, resolutivo y con visión global de planta. - Capacidad de trabajo transversal con los departamentos de calidad, compras e ingeniería. Se ofrece • Incorporación estable en empresa consolidada del sector. - Posición con responsabilidad y autonomía en la toma de decisiones. - Participación activa en proyectos de mejora y crecimiento industrial. - Entorno técnico, colaborativo y orientado a la excelencia operativa. - Condiciones económicas acordes a la experiencia y valía aportada.

📢We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a USP Manufacturing Technician, your responsibilities will include: • Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader., • Ensure the correct training of the personnel in charge., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal / external audits as required by the Quality Assurance Department., • Comply and ensure compliance with GMP standards within the work team., • Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB)., • Investigate and propose new methods or process innovations to optimize and improve the work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB)., • Supervise the correct completion of the new equipment entry documentation., • Supervise the correct training of the personnel in charge, if any., • Carry out the distribution and supervision of daily activities., • Write and keep updated the documentation associated with the production processes carried out in the USP area., • Control / monitoring of orders placed in the USP production area using ERP software. 📚 Assesment criteria: Education: Bachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • With industrial-scale bioreactors, • Cell Cultures, • Microbiological analysis techniques, • Upstream production positions, • Biotechnology / Biopharmaceutical Sector Other requirements: • Open to work in shifts., • Software package: Office. User level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a USP Manufacturing Technician, your responsibilities will include: • Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader., • Ensure the correct training of the personnel in charge., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal / external audits as required by the Quality Assurance Department., • Comply and ensure compliance with GMP standards within the work team., • Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB)., • Investigate and propose new methods or process innovations to optimize and improve the work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB)., • Supervise the correct completion of the new equipment entry documentation., • Supervise the correct training of the personnel in charge, if any., • Carry out the distribution and supervision of daily activities., • Write and keep updated the documentation associated with the production processes carried out in the USP area., • Control / monitoring of orders placed in the USP production area using ERP software. 📚 Assesment criteria: Education: Bachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • With industrial-scale bioreactors, • Cell Cultures, • Microbiological analysis techniques, • Upstream production positions, • Biotechnology / Biopharmaceutical Sector Other requirements: • Open to work in shifts., • Software package: Office. User level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

Comienza tu andadura profesional con nosotros! Oferta de empleo como Supervisor o Supervisora de Producción en Stellantis Zaragoza. Supervisora o Supervisor de Producción.

We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. Main Responsibilities: As a DSP Manufacturing Technician , your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. It's within us.

Technical Product Manager Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción. We’re looking for a Technical Product Manager to drive the development and success of innovative connectivity products in a fast-paced, product-driven environment. What you’ll do: • Own the full product lifecycle from requirements to launch, • Collaborate cross-functionally with engineering, sales, and support teams, • Translate technical insights into clear, customer-facing documentation, • Support go-to-market initiatives and product adoption, • Work with broadband and network technologies in real-world applications, • Engage with customers and represent products in external settings What we’re looking for: • ~3 years’ experience in product management or engineering, • Background in telecommunications, xcskxlj networking, or related technologies, • Strong analytical, communication, and stakeholder management skills, • Proactive mindset with a passion for technology Interested or know someone who could be a great fit? Feel free to reach out or apply

Empresa multinacional del sector industrial.Zaragoza, en el polígono Plaza.Puede obtener más detalles sobre la naturaleza de esta vacante y lo que se espera de los solicitantes leyendo la información a continuación.Coordinar y supervisar el área productiva, liderando a un equipo de personas y a

Shape the Future of Digital Commerce with Your Visionary Expertise Lea el resumen de esta oportunidad para comprender qué habilidades, incluidas las habilidades interpersonales relevantes y el dominio de paquetes de software, se requieren. About Miravia: Miravia is an innovative e-commerce platform, part of Alibaba Group, that connects buyers and sellers effortlessly. We are committed to providing a dynamic shopping experience by partnering with forward-thinking brands across diverse categories. Based in Madrid, we collaborate with global teams to develop the e-commerce platforms of tomorrow. About the Role: We are looking for a data-driven Customer-Facing Product Operations Manager to drive the performance and user experience of key customer-facing products, including search functionality, product detail pages (PDP), and customer service tools. You will play a central role in optimizing our digital platform by translating user insights into actionable improvements, ensuring seamless product launches, and supporting strategic decision-making through analytics. This role is ideal for someone who thrives in a fast-paced environment, combines strong analytical skills with business acumen, and enjoys collaborating across product, tech, and operations teams. Key Responsibilities: • Manage and optimize customer-facing product features based on the product team’s strategy, with a focus on search, PDP, and customer journey tools., • Partner with cross-functional teams to identify user needs, analyze behavioral data, and implement UX improvements that boost engagement and conversion., • Lead end-to-end product launch plans — from planning to execution — ensuring timely delivery and alignment with business goals., • Serve as a bridge between users and the product team: collect feedback, uncover pain points, and translate insights into prioritized enhancements., • Monitor product performance using KPIs, conduct A/B tests, and deliver data-backed recommendations to improve key metrics., • Prepare regular reports for stakeholders, highlighting trends, risks, and opportunities for optimization. Requirements: • Bachelor’s degree in Business, Marketing, or a related field; focus on digital products or e-commerce is preferred., • Minimum of 3 years of experience in product operations, ideally within a tech-driven or e-commerce environment., • Strong analytical mindset — proficiency in SQL is required. Ability to extract, interpret, and visualize data to guide strategy., • Fluent in English (written and spoken); Mandarin/Chinese language skills are a valuable plus., • Proven ability to manage multiple priorities in a dynamic setting, with strong time management and organizational skills., • Excellent communication and collaboration skills — able to work effectively with diverse teams and stakeholders. Application Process: Ready to embark on this journey with us? Please send your CV in English! Please note this role requires to work 100% from the office. Our offices are very centric tough: Metro Station Avenida de América (Madrid). Whether you tick every box or bring a unique blend of skills, we want to hear from you. Diversity is our strength, and we encourage applications from those who bring distinct perspectives to our team. xcskxlj Join Miravia, and let's shape the e-commerce landscape together!

¿Tienes experiencia en producción y estás buscando un proyecto creativo y diferente? ¡Esta puede ser tu oportunidad! . Desde Productores de Sonrisas, empresa productora de espectáculos, especializada en la creación y realización de shows y circos, estamos en búsqueda de un/a profesional de producción para incorporarse a nuestro equipo para un proyecto de gira por distintas ciudades de España, con capacidad para coordinar aspectos técnicos, logísticos y operativos durante el recorrido. ¿Posee las habilidades y la experiencia adecuadas para este puesto? Siga leyendo para descubrirlo y envíe su solicitud. Responsabilidades • Ejecución de las necesidades de los departamentos técnicos, • Coordinación de permisos con ayuntamientos, • Coordinación con el equipo artístico para necesidades, • Coordinación en campo de las necesidades durante el montaje, • Producción en espectáculo durante las actuaciones, • Relación con proveedores, • Control de facturas y caja Requisitos • Mínimo 2 años en departamento de producción, • Disponibilidad completa para viaje y movilización, • Habilidades de comunicación, • Organizado y Planificado, • Persona responsable, con autonomía y proáctiva, • Carnet de conducir y coche propio, • Control y tolerancia al estrés. xcskxlj ¿Qué ofrecemos? • Posibilidades de desarrollo profesional, • Salario acorde a experiencia de candidato, • Contrato de larga duración

Shape the Future of Digital Commerce with Your Visionary Expertise ¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo en la descripción a continuación. About Miravia: Miravia is an innovative e-commerce platform, part of Alibaba Group, that connects buyers and sellers effortlessly. We are committed to providing a dynamic shopping experience by partnering with forward-thinking brands across diverse categories. Based in Madrid, we collaborate with global teams to develop the e-commerce platforms of tomorrow. Your role: We seek a strategic Senior Manager, Product & Content Compliance to safeguard our platform against illegal products and harmful UGC while balancing business growth with evolving legal mandates. Key Responsibilities: Product Compliance Strategy & Execution Lead the development and implementation of strategies to detect, review, and action prohibited/illegal product listings using smart automation and manual oversight. Create, update, and enforce Seller Policies and SOPs to align with local and EU regulations (e.g., consumer safety, restricted items) and platform standards. Design and optimize smart detection rules to flag high-risk products, ensuring scalability and accuracy. Manage an operations team responsible for manual reviews of product listings, appeals, and seller reports. Define permissible product categories, set requirements (e.g., certifications, documentation), and enforce restrictions. Collaborate with Legal, Product, and Engineering teams to integrate new compliance requirements. User-Generated Content (UGC) Compliance Develop and execute strategies to monitor and moderate prohibited UGC (reviews, images, videos) in compliance with laws and platform guidelines. Establish content policies and moderation workflows, balancing user expression with safety. Build smart detection systems to identify harmful content (e.g., hate speech, fraud) and reduce false positives. Oversee a team handling UGC reviews, user reports, and appeals, ensuring timely resolution. Partner with Product and Data teams to implement UGC compliance tools. Cross-Functional Leadership Advise senior leadership on compliance risks, trends, and mitigation strategies. Drive process improvements through data analysis, automation, and stakeholder feedback. Manage compliance-related projects end-to-end, ensuring alignment with business goals. Requirements: • 4+ years in compliance, trust & safety, or risk management (e-commerce or tech preferred)., • Deep understanding of EU e-commerce regulations (e.g., GPSR, DSA, etc)., • Operational Excellence: Proven ability to build policies, manage teams, and optimize workflows., • Fluent in English (written/spoken); Spanish proficiency is a strong plus., • Problem-Solving: Ability to navigate complex compliance challenges with a business-centric approach., • Bachelor’s degree in Law, Business, Technology, or related field. Application Process: Ready to embark on this journey with us? Please send your CV in English! Please note this role requires to work 100% from the office. Our offices are very centric tough: Metro Station Avenida de América (Madrid). Whether you tick every box or bring a unique blend of skills, we want to hear from you. Diversity is our strength, and we encourage applications from those who bring distinct perspectives to our team. xcskxlj Join Miravia, and let's shape the e-commerce landscape together!

OPEN TO CANDIDATES IN NORTH AMERICA, LATIN AMERICA, AND EUROPE ¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura hoy mismo. UATP is a global payments network simplifying payments in one of the most complex industries. We make it easy for businesses to make or accept any type of payment; open new markets, drive growth and reduce costs for Issuers, Merchants, vendors, agents, aggregators and more. Our team has decades of experience with the ever-changing payments landscape, and our reliable and proven technology ensures our global customers get more from every payment experience. The Manager, Product Management, Merchant Solutions, will play a pivotal role in building and scaling our next-generation payment platform capabilities for the travel and airline industry. This role will support the definition and execution of product requirements, collaborate with cross-functional teams, and help ensure the successful delivery of complex payment solutions that support global merchants. The position requires a combination of technical depth, product expertise, and a strong understanding of the business of payments. This full-time remote position may be located in North America, Latin America, or Europe and reports directly to the Managing Director, Product Management, Merchant Solutions. Key Responsibilities • Collaborate with leadership in shaping the product roadmap, and support requirement gathering, backlog definition, and feature delivery., • Translate business needs into detailed product requirements, including sequence diagrams, flow diagrams, and swim lane diagrams., • Work closely with system architects, developers, QA testers, DevOps, and business analysts to deliver scalable and resilient payment solutions., • Contribute to defining and monitoring non-functional requirements (performance, availability, resilience, security) critical for cloud-based systems., • Engage with external partners (PSPs, acquirers, fraud and tokenization providers, FX services, etc.) to ensure successful API integrations and efficient payment flows., • Support the design and delivery of core payment platform capabilities that improve efficiency, scalability, and reliability., • Stay on top of payment industry trends, including emerging technologies and evolving payment methods, to align product evolution with customer and market needs., • Collaborate with commercial, compliance, and operations teams to ensure product development supports business objectives., • Contribute to business cases, requirement documents, and executive-level presentations to support stakeholder alignment., • Provide input and support for the go-to-market strategy for new features and maintain feedback loops with customers. Qualifications • Bachelor’s degree in technical field (e.g., Computer Science, Engineering, Information Systems) or equivalent professional experience., • 5+ years of experience in product management, ideally with direct involvement in building payment systems., • Deep knowledge of payment flows (e.g., credit cards, account-to-account payments, real-time payments, BNPL, refunds, voids, reversals, settlement)., • Strong technical expertise, with proven experience working with APIs, cloud-native architectures, and non-functional requirements for high-scale systems., • Proficiency in creating detailed requirement documentation, including process flows, sequence diagrams, and technical specifications., • Proven track record of working effectively with cross-functional technical teams (architects, developers, QA, DevOps)., • Strong business acumen in payments; experience with payment orchestration platforms or multi-PSP environments is highly desirable., • Experience in airline or travel industry payments is a strong plus., • Excellent communication skills with the ability to bridge technical and business discussions., • Fluency in English (written and verbal) required; additional languages are a plus., • Must reside in North America, Latin America, or Europe and be authorized to work in the country of residence without visa sponsorship., • Ability and willingness to travel up to 15% internationally and to work flexible hours to support global teams. This job posting is intended to describe the general nature and level of work to be performed by the individual assigned to this position; it is not to be construed as an exhaustive list of all responsibilities, duties, and skills required. Staff may be required to perform duties outside of their normal responsibilities as needed. xcskxlj UATP is an equal opportunity employer.

About MAKE MAKE is building the financial layer for the global creator economy — payouts, multi-currency accounts, virtual cards, earnings splits, and payroll, all in one place. We're at an inflection point: millions of creators need a bank that actually understands them, and most have never had one. You'll help build it — and shape what it becomes. Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. About the role As a Senior Product Manager at MAKE, you'll own a meaningful part of our roadmap. The surface is wide — payouts, multi-currency accounts, virtual cards, splits, crypto — and where you focus will depend on your background and what excites you most. This is an early-stage environment: the roadmap is live, the team is lean, and the decisions you make ship to real users fast. You'll work directly with end-users and partners, not just internal stakeholders — bringing their signal back into what we build. You'll also be expected to improve how we work, not just what we ship. This role is deeply technical and deeply human at the same time. You'll thrive here if you have • 5+ years of product management in fintech, neobanking, or payments, • Startup experience that goes beyond job titles: you've operated in a small, fast team where you owned outcomes end-to-end, made calls with incomplete information, and moved without waiting for permission., • Tech-Savvy & Integration depth: you've owned or closely collaborated on API integrations at scale. You write requirements and technical specs that engineers comprehend and actually trust., • Strong UX instincts: you believe great financial products remove anxiety, not just friction. You've run user research, turned messy insights into elegant flows, and kept iterating based on real feedback loops rather than assumptions., • Client-facing fluency: you're comfortable leading scoping calls with partners. You know how to surface the right requirements, pressure-test their constraints, and translate what you hear into something the team can actually build and ship., • Hands-on global banking and payment knowledge: SWIFT, SEPA, ACH, or real-time payments., • Comfort with ambiguity and early-stage speed: you know when to ship and learn vs. when to slow down for compliance, security, and scalability. You don't confuse busyness with momentum. Bonus points • Experience with card issuing (BIN sponsorship, scheme rules, tokenisation via Apple/Google Pay)., • Exposure to crypto rails or stablecoin on/off ramp as a complementary fiat layer., • You've shipped developer-facing API products — you understand what good DX looks like and can write specs that make external integrators successful What’s in it for You • Competitive compensation package with potential for stock options., • Relocation opportunity to the Canary Islands (Tenerife) with a comprehensive relocation package, • Ownership and autonomy to shape MAKE’s compliance vision from the ground up., • Collaborative, fast-paced startup culture - work directly with founders and senior leadership. xcskxlj, • The chance to define compliance in one of fintech’s most exciting frontiers - the Creator Economy.

About the Role We are looking for a Senior Technical Product Manager to join our life sciences R&D product team, supporting large-scale digital transformation initiatives for a leading pharmaceutical client. This role requires a strong combination of technical depth, product strategy, and stakeholder management, focused on complex platform products used by researchers, scientists, and data engineers across computational chemistry and small molecule drug discovery domains. You will take ownership of strategic products or portfolios of applications, driving continuous discovery, innovation, and measurable business value within a hybrid delivery model that combines agile execution with structured governance frameworks (PDLC). This is a highly collaborative, partnership-driven role where you will work closely with engineering teams, business stakeholders, and multi-vendor environments to deliver impactful R&D solutions. Aumente sus posibilidades de llegar a la fase de entrevista leyendo la descripción completa del puesto y enviando su solicitud sin demora. What You’ll Do • Own the end-to-end product lifecycle for R&D platform products, from strategy and roadmap definition to delivery and continuous value validation, • Lead products through structured governance frameworks (e.g., PDLC), ensuring alignment across strategy, requirements, architecture, and launch checkpoints, • Drive product discovery through user research, stakeholder engagement, and continuous feedback loops with scientists and business users, • Translate complex scientific and technical requirements into clear product plans, user stories, and prioritized backlogs, • Collaborate closely with engineering, data, and business teams to define solutions, manage dependencies, and ensure successful delivery, • Drive release planning, UAT, and launch readiness across technical and non-technical stakeholders, • Operate effectively within a hybrid delivery model, balancing agile execution with structured governance requirements, • Leverage AI tools (e.g., Gemini Pro, Atlassian AI) to enhance prioritization, velocity forecasting, and product insights, • Apply data-driven techniques such as sentiment analysis and predictive analytics to inform backlog prioritization and decision-making, • Co-develop AI/GenAI use cases with stakeholders to improve research workflows and product capabilities, • Promote automation in documentation and requirements generation through AI-powered solutions, • Maintain high-quality documentation and communicate progress, risks, and outcomes to stakeholders and governance forums What You Bring • 8+ years of experience in product management, ideally in technical or platform-based environments, • Experience in computational chemistry or small molecule drug discovery workflows, particularly in areas such as molecular modeling, assay data, or compound-related platforms, • Experience working in regulated or complex domains (e.g., life sciences), with the ability to bridge technical and non-technical audiences, • Experience delivering AI-native or data-intensive products, including the application of AI/GenAI capabilities within product environments, is highly valued, • Proven ability to define product xcskxlj strategy, manage roadmaps, and deliver business value in complex environments, • Strong experience translating ambiguous requirements into structured documentation and actionable plans, • Solid understanding of agile methodologies and experience working within hybrid delivery models, • Advanced proficiency with tools such as Jira and Confluence for backlog management and documentation, • Strong technical background, with experience working with cloud platforms (GCP preferred), APIs, and data-driven systems, • Ability to collaborate effectively with engineers, data teams, and business stakeholders Nice to Have • Experience with high-performance computing (HPC) environments or large-scale data processing, • Familiarity with authentication systems (e.g., SSO, LDAP) and enterprise security models, • Experience working in multi-vendor environments, • Knowledge of data movement challenges related to large-scale scientific datasets, • Cloud certifications (e.g., GCP Professional Cloud Architect)

About us For more than 25 years, our global network of passionate technologists and pioneering craftspeople has delivered cutting-edge technology and game-changing consulting to companies on the brink of AI driven digital transformation. Since 2001, we have grown into a full service digital consulting company with 6000+ professionals working on a worldwide ambition. Driven by the desire to make a difference, we keep innovating. Fuelling the growth of our company with our knowledge worker culture. When teaming up with Xebia, expect in-depth expertise based on an authentic, value-led, and high quality way of working that inspires all we do. ¿Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación. At Xebia, we put ‘People First’—committed to attracting diverse talent and fostering an inclusive, respectful workplace where everyone is valued for their contributions. We welcome all individuals and evaluate solely on the quality of their work and teamwork. About the Role We are looking for a Senior Technical Product Manager to join our life sciences R&D product team, supporting large-scale digital transformation initiatives for a leading pharmaceutical client. This role requires a strong combination of technical depth, product strategy, and stakeholder management, focused on complex platform products used by researchers, scientists, and data engineers across biology, chemistry, and computational science domains. You will take ownership of strategic products or portfolios of applications, driving continuous discovery, innovation, and measurable business value within a hybrid delivery model that combines agile execution with structured governance frameworks (PDLC). This is a highly collaborative, partnership-driven role where you will work closely with engineering teams, business stakeholders, and multi-vendor environments to deliver impactful R&D solutions. What You’ll Do • Own the end-to-end product lifecycle for R&D platform products, from strategy and roadmap definition to delivery and continuous value validation, • Lead products through structured governance frameworks (e.g., PDLC), ensuring alignment across strategy, requirements, architecture, and launch checkpoints, • Drive product discovery through user research, stakeholder engagement, and continuous feedback loops with scientists and business users, • Translate complex scientific and technical requirements into clear product plans, user stories, and prioritized backlogs, • Collaborate closely with engineering, data, and business teams to define solutions, manage dependencies, and ensure successful delivery, • Drive release planning, UAT, and launch readiness across technical and non-technical stakeholders, • Operate effectively within a hybrid delivery model, balancing agile execution with structured governance requirements, • Leverage AI tools (e.g., Gemini Pro, Atlassian AI) to enhance prioritization, velocity forecasting, and product insights, • Apply data-driven techniques such as sentiment analysis and predictive analytics to inform backlog prioritization and decision-making, • Co-develop AI/GenAI use cases with stakeholders to improve research workflows and product capabilities, • Promote automation in documentation and requirements generation through AI-powered solutions, • Maintain high-quality documentation and communicate progress, risks, and outcomes to stakeholders and governance forums What You Bring • 8+ years of experience in product management, ideally in technical or platform-based environments, • Experience in structural biology, protein science, or nucleic acid-based drug discovery workflows is highly valued, particularly in areas such as protein structure analysis, structural data platforms, or oligonucleotide design systems, • Experience working in regulated or complex domains (e.g., life sciences), with the ability xcskxlj to bridge technical and non-technical audiences, • Experience delivering AI-native or data-intensive products, including the application of AI/GenAI capabilities within product environments, is highly valued, • Proven ability to define product strategy, manage roadmaps, and deliver business value in complex environments, • Strong experience translating ambiguous requirements into structured documentation and actionable plans, • Solid understanding of agile methodologies and experience working within hybrid delivery models, • Advanced proficiency with tools such as Jira and Confluence for backlog management and documentation, • Strong technical background, with experience working with cloud platforms (GCP preferred), APIs, and data-driven systems, • Ability to collaborate effectively with engineers, data teams, and business stakeholders Nice to Have • Experience with high-performance computing (HPC) environments or large-scale data processing, • Familiarity with authentication systems (e.g., SSO, LDAP) and enterprise security models, • Experience working in multi-vendor environments, • Knowledge of data movement challenges related to large-scale scientific datasets, • Cloud certifications (e.g., GCP Professional Cloud Architect)

📢We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a DSP Manufacturing Technician, your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). 📚 Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a DSP Manufacturing Technician, your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). 📚 Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

Join Tether and Shape the Future of Digital Finance At Tether, we’re not just building products, we’re pioneering a global financial revolution. Our cutting-edge solutions empower businesses—from exchanges and wallets to payment processors and ATMs—to seamlessly integrate reserve-backed tokens across blockchains. By harnessing the power of blockchain technology, Tether enables you to store, send, and receive digital tokens instantly, securely, and globally, all at a fraction of the cost. Transparency is the bedrock of everything we do, ensuring trust in every transaction. Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. Innovate with Tether Tether Finance: Our innovative product suite features the world’s most trusted stablecoin, USDT, relied upon by hundreds of millions worldwide, alongside pioneering digital asset tokenization services. But that’s just the beginning: Tether Power: Driving sustainable growth, our energy solutions optimize excess power for Bitcoin mining using eco-friendly practices in state-of-the-art, geo-diverse facilities. Tether Data: Fueling breakthroughs in AI and peer-to-peer technology, we reduce infrastructure costs and enhance global communications with cutting-edge solutions like KEET, our flagship app that redefines secure and private data sharing. Tether Education: Democratizing access to top-tier digital learning, we empower individuals to thrive in the digital and gig economies, driving global growth and opportunity. Tether Evolution: At the intersection of technology and human potential, we are pushing the boundaries of what is possible, crafting a future where innovation and human capabilities merge in powerful, unprecedented ways. Why Join Us? Our team is a global talent powerhouse, working remotely from every corner of the world. If you’re passionate about making a mark in the fintech space, this is your opportunity to collaborate with some of the brightest minds, pushing boundaries and setting new standards. We’ve grown fast, stayed lean, and secured our place as a leader in the industry. If you have excellent English communication skills and are ready to contribute to the most innovative platform on the planet, Tether is the place for you. Are you ready to be part of the future? About the job The Senior Technical Product Manager will be responsible for the overall product leadership of Hadron, including product vision, roadmap definition, and delivery execution. The role serves as the single point of accountability for the platform to serve institutional client needs, engineering delivery, and regulatory/compliance requirements. Unlike a traditional Product Manager role, this position requires clear decision-making authority to: • Set and enforce roadmap priorities, including pushing back on non-essential requests., • Coordinate with external engineering partners and maintain scope discipline., • Resolve conflicts between client requests, technical feasibility, and compliance constraints., • Make go/no-go decisions on integrations, product features, and releases., • Ensure product development aligns with the long-term architecture and scalability of the Hadron platform. Critical Context Hadron serves institutional clients globally with diverse and often conflicting tokenization requirements, including different asset classes, blockchain networks, compliance frameworks, and distribution models. The Product Manager must manage this complexity by maintaining a clear product strategy, prioritizing ruthlessly, and preventing scope creep. The role requires strong ownership and the ability to make difficult prioritization decisions in a fast-moving institutional environment. Tokenization, end-to-end • You have personally built, shipped, or owned a tokenization product — from asset onboarding and smart contract specification through to custody integration, investor cap table management, and secondary transfer mechanics., • You can walk through the full token lifecycle (issuance, transfer, redemption, corporate actions, burn) without needing to look anything up, and you understand the tradeoffs between different implementation approaches., • You understand custody models: the difference between self-custody, qualified custodian models, omnibus vs. segregated wallet structures, and what each means for compliance and operational risk., • You have practical knowledge of on-chain settlement mechanics and how they interact with traditional T+1/T+2 settlement rails (DTCC, Euroclear, SWIFT)., • You are fluent in token standards across multiple chains and understand when to reach for ERC-20, ERC-1400, or proprietary structures, and why. TradFi depth • You have a strong grasp of how institutional financial infrastructure works: how funds are structured and administered, how broker-dealers clear and settle, how banks manage trust and custody relationships, and how prime brokerage operates., • You understand the instruments being tokenized: money market funds, bonds, structured credit, equities, real estate, commodities including how each is priced, transferred, and serviced in the traditional world., • You are comfortable with regulatory frameworks relevant to tokenized assets such as MiCA, Reg D/S, MAS MAS notice, VARA and can identify the compliance constraints that must be encoded into product design., • You can read and rapidly interpret institutional documents: RFPs, term sheets, custody agreements, and due diligence questionnaires, and translate them into product requirements without extensive hand-holding. Institutional demand, rapid translation • You have worked directly with institutional clients such as asset managers, banks, sovereign funds, family offices as the primary product owner, and you know how to manage their expectations and extract signals from noise., • You can hear a new institutional use case or a complex integration requirement and rapidly assess feasibility, scope, and priority, without needing days to research the basics., • You have experience distinguishing between requests that reveal genuine product gaps and those that are bespoke client customisations and you know how to handle both without derailing the roadmap. Key Responsibilities Product Strategy & Roadmap • Define and maintain the Hadron product roadmap., • Prioritize product initiatives based on market demand, technical feasibility, and business impact., • Maintain a clear product vision for Hadron across multiple asset classes and blockchain networks., • Translate business and market needs into clear product requirements., • Maintain the product backlog and development priorities., • Coordinate development cycles and feature releases., • Act as the primary interface between product and engineering., • Coordinate development work with internal engineers and external technology partners., • Maintain clear documentation of product features, APIs, and platform capabilities., • Collect and structure feedback from institutional clients and internal teams., • Identify recurring integration challenges and translate them into product improvements.

If you like technology and enjoy working on innovative and diverse projects, your place is here. If you don’t know us yet, we are a global technology provider offering a complete portfolio of solutions in Payment, Mobile, Data and Identity. With over 65 years of experience, we have built a solid legacy that continues to grow. Today, we are more than 4,000 employees across 14 countries, working to create a more trustworthy and secure world. Compruebe a continuación si tiene lo necesario para esta oportunidad y, si es así, envíe su solicitud lo antes posible. We are currently looking for a Jr. Product Operations Analyst to join our Marketing, Product & Strategy team in Madrid (hybrid model). This opportunity is ideal for early-career professionals who are eager to learn how product organizations operate and want to gain hands-on experience in product execution, operations, and cross-functional collaboration. What will you do? • Support the day-to-day operations of the Product team, • Maintain and update documentation, trackers, and knowledge repositories, • Ensure product information is accurate and consistent across tools, • Execute and improve recurring Product Operations processes, • Identify inefficiencies and contribute to process improvements, • Prepare reports and dashboards, turning data into actionable insights, • Ensure data accuracy and reliability across systems, • Collaborate with Product, Engineering, Marketing, and other teams, • Follow up on action items and ensure smooth communication between stakeholders What are we looking for? • Bachelor’s degree in Engineering, Data, Technology, business, or a related field, • No prior professional experience required (internships are a plus), • Professional level of English and Spanish both spoken and written, • Strong organizational and time-management skills, • Analytical mindset and ability to work with data and digital tools, • Proactive attitude with a willingness to learn and improve processes, • Strong communication and collaboration skills, • Interest in Product, technology, and continuous improvement What do we offer? • A collaborative and international environment where people support each other, • Competitive salary aligned with experience, • Private health and life insurance, • A strong focus on your well-being and professional growth If you believe this opportunity is a good fit for you, we encourage you to apply via LinkedIn or send your CV to: Our Culture At Valid, we foster an inclusive, diverse, and innovative environment where everyone can thrive. We are committed to equal opportunities and a workplace free from discrimination. xcskxlj We put people at the core of everything we do, building our culture on trust, transparency, and teamwork, empowering talent and driving sustainable growth.

Company Description Based in the sunny Valencia region of Spain, we are a co-packing and private label beverage manufacturer. We specialize in crafting high-quality beverages, from RTD's, functional beverages, energy drinks to premium wine on can. We serve beverage brands all over Europe, Africa and the USA. CAN IT Spain is growing in a rapid but sustainable way, and our team is an integral part of this growth. Aunque la experiencia profesional y las cualificaciones son clave para este puesto, asegúrese de comprobar si posee las habilidades interpersonales preferibles antes de solicitar, si se requieren. Role Description We are seeking a full-time Process Operator for the beverage production at our co-packing facility in Castellón de la Plana, Spain. The Process Operator is responsible for the production of all our beverages. This varies from quality inspection and preparation of bulk shipments to our factory to in house beverage production, where we blend and carbonate drinks ourselves. xcskxlj You will be working alongside the canning and packaging team, who will can the drinks that you have prepared for them. We want you to have • Experience as an operator in food, beverage, or process industry, • Knowledge of HACCP, • Technical insight and attention to detail, • Spanish or English language skills What do we offer • Competitive salary + shift allowance, • Support on relocating / moving, • Work with modern production equipment, • Career growth opportunities

Grupo Loxam, multinacional líder en alquiler y venta de maquinaria selecciona un “Operario/a Modular para su delegación de Las Palmas de Gran Canaria.

¡Capitole sigue creciendo y queremos hacerlo contigo! Asegúrese de enviar su solicitud rápidamente para maximizar sus posibilidades de ser considerado para una entrevista. Lea la descripción completa del puesto a continuación. Estamos buscando un/a Senior Product Manager (Discovery), para incorporarse a una de las multinacionales de retail más reconocidas a nivel global, que está en un momento crítico de transformación de su modelo de gestión de contenidos digitales a gran escala. Buscamos a alguien que sepa lo que significa gestionar contenido en entornos complejos, multi-país y multi-canal, y que tenga el criterio para decidir si construir o comprar la solución correcta. El impacto será directo en cómo la compañía gestiona su contenido digital a nivel global. Lo que vas a encontrar: • Un rol enfocado en Product Discovery — tu misión es diagnosticar el AS-IS, hacer el benchmark de soluciones y definir la hoja de ruta hacia un modelo escalable y automatizado., • Interlocución directa con liderazgo senior — reportarás a perfiles de alto nivel y tendrás autonomía real para tomar decisiones estratégicas., • Un problema concreto y complejo: Build vs. Buy — ¿herramienta de mercado o desarrollo ad hoc? Tú liderarás la respuesta., • Trabajo con ecosistemas CMS headless (Contentstack, Contentful, AEM) y arquitecturas multi-country/multisite., • Posición puente entre negocio y tecnología — coordinarás stakeholders de branding, comunicación, edición e ingeniería., • Un entorno donde la resolución de ambigüedad y el criterio estratégico son más valorados que la ejecución táctica. Buscamos a alguien que: • Tenga +5 años de experiencia en Content Operations, Digital Content Management o como CMS Product Owner., • Haya liderado procesos de estrategia y transformación en entornos de contenido digital complejo., • Conozca en profundidad el ecosistema CMS headless — Contentstack, Contentful o AEM — y arquitecturas multi-country/multisite., • Tenga mentalidad de Product Manager — no de Project Manager ni de gestor operativo., • Sea capaz de moverse con soltura en entornos ambiguos y traducir complejidad en decisiones claras., • Haya trabajado con stakeholders de negocio y equipos técnicos de forma simultánea., • Resida en Barcelona o alrededores — imprescindible. Ubicación: Hibrido (2 días oficina) Vallès Oriental. Horario: L-J 8,5h · V 6h · Flexibilidad de entrada entre 8:00 y 9:30h. Idiomas: Ingles B2 (Preferentemente) ¿Por qué CAPITOLE? • Presupuesto individual de formación de 1.200€, • Paquete de retribución flexible, • Grandes descuentos en centros deportivos, • Seguro médico privado gratuito, • Revisiones mensuales con tu equipo para recibir feedback continuo, • Team buildings cada dos meses — ¡No te puedes perder la fiesta de verano ni la cena de Navidad !, • Comunidades tecnológicas internas para compartir conocimiento, • Descuentos en marcas internacionales para empleados (Club Capitole) ¿Aún no nos conoces? ¡Descúbrenos! xcskxlj ¡No dudes en enviarnos tu perfil junto a tu portfolio — estamos deseando conocerte! Capitole | Empowering people, unlocking technology innovation

iVascular somos una empresa de Medical Devices ubicada en Sant Vicenç dels Horts. La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes. Nos especializamos en el desarrollo, fabricación y comercialización de dispositivos médicos avanzados para el tratamiento de enfermedades cardio, neuro y endovasculares. Nuestro foco está en ofrecer soluciones mínimamente invasivas que realmente mejoran la calidad de vida de los pacientes y convertirnos en un referente en el ámbito vascular potenciando el valor de la tecnología y la innovación. Para ello, controlamos internamente todo el proceso: desde la investigación y desarrollo hasta la producción, esterilización y distribución. Esto lo llamamos Integración Vertical, y nos permite garantizar máxima calidad, innovación continua y una gran agilidad para adaptarnos a las necesidades del mercado. Somos una empresa nacional en fase de crecimiento y expansión internacional, con filiales ya constituidas en Europa, América y Asia. Nuestro propósito es muy claro: desarrollar tecnologías que salvan y mejoran vidas. Nos encontramos en búsqueda de un GLOBAL PRODUCT MANAGER (Cardiovascular) para reportar a nuestras oficinas centrales localizadas en Barcelona. Tu principal objetivo será el desarrollo e implementación, en el área asignada, de las estrategias de Marketing para cumplir con los objetivos globales de la empresa reportando al Global Marketing Director. FUNCIONES y RESPONSABILIDADES • Diseñar el material del Packaging (embalaje) del producto: Packaging, etiqueta, IFUs., • Desarrollar y actualizar estudios de mercado y benchmarking (evaluación comparativa) para cada producto coordinándose con el equipo de I+D., • Liderar el desarrollo e implementación del Plan de MKT Global de los productos del área asignada. Definir el posicionamiento global del producto y los mensajes de cada producto., • Desarrollar materiales promocionales acorde con el posicionamiento: catálogos, página web, RRSS, presentaciones de producto., • Responsable de la definición de las estrategias de lanzamiento y del plan de acción de los productos., • Proponer e implementar el plan de acción de los productos: registro post marketing, workshops internacionales, casos clínicos, reimpresiones de publicaciones de referencia o publicaciones de artículos en revistas especializadas y revistas que soporten la estrategia de comunicación., • Desarrollar planes de formación y herramientas necesarias para dar soporte al propio equipo de ventas y a los distribuidores., • Responsable de los presupuestos y programas de inversión en el área de Marketing aprobados en el Plan de MKT necesarios para conseguir los objetivos fijados., • Analizar, investigar y proyectar la evolución de los competidores en los diferentes mercados, anticipando las necesidades para la adecuada adaptación del producto en las características del mercado., • Proporcionar soporte de campo., • Crear una red de KoL que den soporte al área de responsabilidad., • Responsable del LCM (ciclo de vida del producto). PERFIL DESEADO • Estudios: grado/licenciatura/ingeniería en la rama de ciencias (biomédicas, biotecnología, bioingeniería, medicina, biología, farmacia, ingeniería, químicas o similares)., • Idiomas: español e inglés (nivel C1). Se realizará prueba de nivel. Otros idiomas, aportarán un valor añadido: francés, alemán, italiano, árabe., • Experiencia +5 años de experiencia en puesto similar., • Conocimientos específicos: formación complementaria en marketing, ventas y análisis de mercados, MBA o Máster en Marketing., • Viajes: ocasionalmente (ferias y congresos)., • Habilidades personales:, • Persona organizada con capacidad de planificación estratégica, orientado a resultados, con pensamiento sintético y analítico., • Trabajo en equipo con flexibilidad y adaptabilidad., • Capacidad de negociación y acostumbrado a trabajar con objetivos claros., • Capaz de realizar demostraciones y presentaciones de los dispositivos que involucran/inspiren a los médicos y comerciales. QUE OFRECEMOS • Contrato Indefinido y estable en un proyecto con un alto impacto a nivel global y en pleno proceso de expansión internacional., • Desarrollo profesional y personal en un ambiente joven y dinámico., • Salario competitivo en base a la experiencia y un atractivo paquete de beneficios., • Horario flexible para la conciliación personal/familiar. De L-J puedes entrar entre las 7 y las 9h y salir a partir de las 16:30h. Los viernes hacemos jornada intensiva de 8 a 14h., • Retribución flexible (tickets restaurante, transporte y guardería)., • Acceso al programa iWellness: gimnasio y fisioterapeuta en nuestras instalaciones., • Eventos y obsequios corporativos. xcskxlj, • Comedor propio de la empresa subvencionado.

At Astek we are looking for an IT Project & Product Manager to join a dynamic and innovative environment within the energy sector, supporting real-time operations, renewable energy activities, and data-driven transformation. Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud. You will act as a key link between business teams and IT development, ensuring that digital solutions are delivered efficiently, reliably, and with a strong end-to-end product vision. Main responsibilities: • Collect, analyze, and document business requirements, • Translate business needs into functional and technical specifications, • Coordinate Agile development cycles (sprint planning, backlog refinement, reviews), • Manage product backlog in collaboration with business stakeholders, • Lead medium and long-term IT projects end-to-end, • Coordinate testing, UAT, and deployments across environments, • Monitor incidents, prioritize issues, and ensure timely resolution, • Collaborate with infrastructure, cloud, cybersecurity, and support teams, • Promote continuous improvement and Agile best practices Who are you? • 4+ years of experience as an IT Project Manager, Product Owner, or similar role, • Strong experience working in Agile environments, • Solid understanding of software architectures, APIs, data flows, and CI/CD, • Experience with tools such as JIRA, • Interest in energy markets and digital innovation within the sector, • Fluent in English (Spanish is a plus) Who are we? Since 2015, Astek Iberia has been accompanying its customers in their development throughout Spain (Madrid, Barcelona, Valencia, Basque Country, Andalusia, Galicia, etc.). Founded in France in 1988, Astek is a global player in engineering and technology consulting, present in five continents and 25 countries. With expertise in a wide range of industrial and service sectors, Astek is an essential partner, supporting its customers in an intelligent deployment of their products and services, and in the implementation of their digital transformation. Today we are more than 8,000 employees, committed every day to promote the complementarity between digital technologies and complex systems engineering. Our style is to have flexible schedules and highly value the well-being of our employees. Why join us? You will grow professionally in a company in constant development and evolution. You will benefit from a personalized follow-up of your professional projects as close as possible to your ambitions. You will make a real contribution to the company's development in real time. You will enjoy 23 days of vacation (in addition to holidays) that you will be able to choose whenever you want. You will join our team: diverse, multicultural and constantly growing. You will have days full of good energy and good atmosphere. ..although you still have a lot to discover! Shall we meet? xcskxlj If you want to participate in the process, apply from here attaching your CV (in English) as detailed as possible and we will tell you more.

Spares in Motion supports wind turbine owners and operators by helping them source wind turbine spare parts. We offer procurement services to companies that perform maintenance on wind turbines in Europe, Asia, and North America. For our Madrid office we are seeking an experienced Product and Supply Chain Specialist to support our plans to expand our footprint in the Wind Aftermarket. This role requires a professional who is not only a strategic planner but also a hands-on doer, responsible for both ensuring we are ready to support newer turbine platforms and assisting our Sales Managers with complex and large requests. La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes. Job Responsibilities: As the Product Manager for Main Components and Decommissioning Projects, you will be instrumental in scaling our biggest revenue driver. Key responsibilities include: • Supplier Relationship Development: Develop the relationship with suppliers of main components and wind turbines decommissioning companies., • Supplier Evaluation & Qualification: Define and implement robust processes to evaluate and qualify these new suppliers., • Supply Chain Development: Partner with sales to develop the supply chain of main components., • Data Custodianship & Automation: Act as the custodian of Main component and dismantling projects data. Responsible for defining the data models and keeping them up to date with inputs from sales, using process automation., • Sales Support: Partner with the Global Sales team to provide technical expertise in complex and large sales opportunities and ensure insights are captured in our internal systems., • Scalable Growth: Define and implement a scalable process to increase the sales of main components by 4x within the next 2 years., • Digital Lead Generation: Partner with the website product manager to use the website as an effective sales lead generator for main components customers and suppliers., • Market Intelligence: Monitor the wind aftermarket landscape to identify emerging needs for newer fleets and translate these into development, procurement, and sales actions., • Technical Expertise: Act as the subject matter expert for both internal teams and external clients regarding components, systems, and turbine technology. Job Requirements: The ideal candidate will have a deep technical understanding of the wind energy sector combined with a proactive, entrepreneurial mindset. • Experience: A minimum of 3–5 years of professional experience specifically within the wind energy sector is mandatory, preferably in spare parts procurement or aftermarket support. Experience with GE, Gamesa, Vestas, or Siemens turbines is a plus., • Knowledge: Deep understanding of wind turbine components and the differences between major OEM platforms., • Analytical Mindset: Comfortable working with large datasets to generate new knowledge and insights that can be leveraged by the organization., • Technical Skills: Advanced Proficiency in Microsoft Excel is required, for example, using complex formulas, Pivot Tables, and Data Modeling., • Global Mindset & Cultural Competence: Ability to communicate effectively with a diverse, international sales and procurement team. You must be highly skilled at bridging cultural differences to successfully negotiate and build lasting partnerships with suppliers based in different countries., • Travel Required: Visiting suppliers is of paramount importance to this role. The candidate must be willing and able to travel frequently to conduct on-site evaluations and foster in-person relationships across various international locations., • Work Ethic: An entrepreneurial spirit who thrives in a fast-paced environment and takes full ownership of the complete portfolio of spare parts and components., • Location: Living in the Madrid area. If you are a driven professional ready to seize this exciting opportunity and contribute significantly to the growth of the renewable energy sector, we encourage you to apply. xcskxlj Join Spares in Motion as we revolutionize the wind turbine spare parts market and drive sustainable change.

OPERARIOS/AS DE EXPEDICIONES PRODUCCIÓN Y LOGISTICA.

About Xebia With over 20 years of experience, our global network of passionate technologists and pioneering craftsmen deliver cutting-edge technology and game-changing consulting to companies on the brink of transformation. Since 2001, we have grown from a Java company into a full-service digital consulting company with 4500+ professionals working on a worldwide ambition. We are organized in complementary chapters – teams with a tremendous amount of knowledge and experience within a particular field, such as Agile, DevOps, Data and AI, Cloud, Software Technology, Functional Programming, Low Code, and Microsoft. We help the world’s top 250 companies and category leaders overcome digital challenges, embrace innovation, adopt new technology, and implement new business models. In addition to high-quality consulting, we also provide offshoring and nearshoring services. For more details please visit are seeking a Senior Product Manager specializing in Chemistry Products | Cheminformatics to lead our product transformation efforts in the life sciences domain. This senior role requires deep expertise in cheminformatics and the ability to drive strategic product initiatives while managing complex stakeholder relationships. In this position, you'll manage software products that serve computational chemists, medicinal chemists, and drug discovery scientists. Your products may include molecular design and visualization platforms, chemical structure databases and search tools, compound property prediction systems, reaction planning and synthesis design applications, and molecular simulation and docking platforms. You'll be responsible for understanding how chemists work—from hit identification and lead optimization to ADME/Tox prediction—and translating these complex scientific workflows into product requirements that balance user needs with technical feasibility. The ideal candidate understands the cheminformatics landscape, including molecular descriptors, fingerprints, similarity searching, and structure-activity relationships. You'll work closely with computational chemists and wet-lab scientists to ensure products deliver meaningful scientific value, while also driving the modernization of legacy chemistry applications into scalable, cloud-based platforms that integrate with broader drug discovery pipelines. ¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo en la descripción a continuación. What You’ll Do: Product Knowledge Transfer • Document existing product knowledge, including use cases, usage metrics, business processes, technical specifications, and documentation, • Analyze current product landscape, use cases, business processes and customer needs, • Follow existing processes to develop comprehensive product requirements, • Serve as the primary point of contact for business requests for assigned products, • Map relevant stakeholders (influence, needs, communication frequency) and develop tailored engagement strategies, • Execute stakeholder engagement strategies with agreed objectives, • Fulfill Product Manager responsibilities during product development phases Essential Core Skills • Strong business use case analysis capabilities, • Experience conducting user interviews, • Proven stakeholder mapping and management abilities, • Excellent requirements documentation writing skills, • Working knowledge of software product development, • Working knowledge of Cloud technologies, • Exceptional verbal and written communication skills, • Proven agile development experience, • Cheminformatics expertise required, • Deep understanding of chemistry software workflows and computational chemistry applications, • Ability to communicate effectively with both technical teams and scientific users in the chemistry domain Recommended Scientific Background & Technical Chemistry Expertise – Technical Product Management • Background in Chemistry, computational chemistry, or related scientific discipline, • Expertise in chemical compounding, simulations, and computational prediction, • Ability to understand and synthesize chemical characteristics, • Experience collaborating with in-lab chemists and scientists for scientific readouts, • Familiarity with Schrödinger products (lab design, data flow enablement, ordering process improvement), • Experience in pharmaceutical or regulated industry environments, • Understanding of authentication systems (SSO, LDAP), • Knowledge of zero-downtime deployment strategies, • Experience with high-performance computing (HPC) environments, • Background in managing external vendor relationships and integration points, • Familiarity with Google Cloud Platform services and architecture, • Understanding of security and compliance requirements in enterprise environments, • Certification in relevant cloud technologies (GCP, etc.), • Experience migrating HPC workloads to cloud environments (specifically GCP), • Knowledge of GCP's HPC-specific offerings and configurations, • Familiarity with scientific or research computing applications common in pharmaceutical environments At Xebia, you will get the chance to work with passionate professionals within their field of expertise. We offer more than just a job, we offer a career. We are looking forward to working with you! Xebia is committed to creating an inclusive and diverse environment and is proud to be an equal-opportunity employer. xcskxlj All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, or age. Please feel free to share your preferred pronouns with us during the application process.

Jefe/a de Producción para proyectos en Jamaica, Montego Bay. Planificar la producción de obra en coordinación con el Jefe de Obra.

Únete a COPASA como Jefe/a de Producción en obra ferroviaria! ¿Tienes experiencia en producción de obra y te apasionan los grandes proyectos de infraestructura? En COPASA buscamos incorporar un/a Jefe/a de Producción para la ejecución del tramo Tafalla–Campanas de la Línea de Alta V

Si combinas visión de negocio con base técnica sólida y quieres liderar de verdad una división tecnológica, esta posición es para ti. Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición. Para nuestro cliente VENCO ELECTRONICA ( ), distribuidor de valor añadido con más de 40 años de trayectoria en electrónica industrial, especializado en soluciones para sectores como Defensa, Médico, Industrial y Transporte, estamos seleccionando un/a Product Manager – Sistemas Embebidos (Embedded Systems). Venco acompaña al cliente desde la concepción del proyecto hasta su integración. Aquí cada ingeniero conoce en profundidad el sector y el producto: la especialización es la norma, no la excepción. Tu misión Serás el responsable de la línea de Sistemas Embebidos de VENCO: definirás el roadmap tecnológico, identificarás oportunidades de negocio y asegurarás la rentabilidad y el crecimiento sostenido de la división. Tus responsabilidades principales • Liderar la división Embedded con responsabilidad directa sobre resultados., • Definir y ejecutar el roadmap de producto, incorporando hardware, software y servicios de vanguardia., • Gestionar el ciclo de vida completo del producto: selección, negociación con partners internacionales, posicionamiento competitivo y gestión end-of-life., • Actuar como referente técnico y comercial para el equipo de ventas. Tu perfil • Formación en Ingeniería (Electrónica, Telecomunicaciones o similar)., • Mínimo 5 años de experiencia como Product Manager, Director Técnico-Comercial o rol similar en electrónica industrial B2B., • Conocimiento profundo de sistemas embebidos y gestión del ciclo de vida de productos., • Experiencia en negociación y gestión de acuerdos con partners internacionales., • Inglés técnico avanzado., • Disponibilidad para viajar por España y Portugal., • El proyecto incluye un periodo de inmersión formativa presencial en las oficinas de L'Hospitalet de Llobregat. ¿Qué te ofrecemos? • Liderazgo estratégico real sobre una división clave de la empresa., • Paquete retributivo competitivo: fijo más variable ilimitado ligado al crecimiento y rentabilidad de la línea., • Modelo híbrido con enfoque en resultados., • Plan de retribución flexible a medida., • Entorno colaborativo con interacción directa con Ingeniería, Compras y Ventas. Si quieres convertir tu visión tecnológica en crecimiento real, nos interesa conocerte. Si combines visió de negoci amb una base tècnica sòlida i vols liderar de debò una divisió tecnològica, aquesta posició és per a tu. Per al nostre client VENCO ELECTRÒNICA ( ), distribuïdor de valor afegit amb més de 40 anys de trajectòria en electrònica industrial, especialitzat en solucions per a sectors com Defensa, Mèdic, Industrial i Transport, estem seleccionant un/a Product Manager – Sistemes Encastats. Venco acompanya el client des de la concepció del projecte fins a la seva integració. Aquí cada enginyer coneix en profunditat el sector i el producte: l'especialització és la norma, no l'excepció. La teva missió Seràs el responsable de la línia de Sistemes Encastats de VENCO: definiràs el roadmap tecnològic, identificaràs oportunitats de negoci i asseguraràs la rendibilitat i el creixement sostingut de la divisió. Les teves responsabilitats principals • Liderar la divisió Embedded amb responsabilitat directa sobre els resultats., • Definir i executar el roadmap de producte, incorporant maquinari, programari i serveis d'avantguarda., • Gestionar el cicle de vida complet del producte: selecció, negociació amb partners internacionals, posicionament competitiu i gestió end-of-life., • Formació en Enginyeria (Electrònica, Telecomunicacions o similar)., • Mínim 5 anys d'experiència com a Product Manager, Director Tècnic-Comercial o rol similar en electrònica industrial B2B., • Coneixement profund de sistemes encastats i gestió del cicle de vida de productes., • Experiència en negociació i gestió d'acords amb partners internacionals., • Anglès tècnic avançat., • Disponibilitat per viatjar per Espanya i Portugal., • Lideratge estratègic real sobre una divisió clau de l'empresa., • Paquet retributiu competitiu: fix més variable il·limitat lligat al creixement i rendibilitat de la línia., • Model híbrid amb enfocament en resultats., • Pla de retribució flexible a mida., • Entorn col·laboratiu amb interacció directa amb Enginyeria, Compres i Vendes. xcskxlj Si vols convertir la teva visió tecnològica en creixement real, ens interessa conèixer-te.

We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. Main Responsibilities : As a USP Manufacturing Technician , your responsibilities will include: • Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader., • Ensure the correct training of the personnel in charge., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal / external audits as required by the Quality Assurance Department., • Comply and ensure compliance with GMP standards within the work team., • Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB)., • Investigate and propose new methods or process innovations to optimize and improve the work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB)., • Supervise the correct completion of the new equipment entry documentation., • Supervise the correct training of the personnel in charge, if any., • Carry out the distribution and supervision of daily activities., • Write and keep updated the documentation associated with the production processes carried out in the USP area. Education: Bachelor's degree in Pharmacy; La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto. Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc. Desirable but not required Master's degree or equivalent in related fields. Languages: Fluent in Spanish . Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • With bioreactors, • Cell Cultures, • Microbiological analysis techniques, • Upstream production positions, • Open to work in shifts., • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes. We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. xcskxlj It's within us .

Bigle es una empresa líder en el sector Legal Tech, con presencia en Barcelona, Madrid y Bogotá. Nuestra misión es transformar la gestión legal y documental de las empresas mediante soluciones tecnológicas avanzadas, ayudando a optimizar la eficiencia, reducir riesgos y garantizar el cumplimiento normativo en sus operaciones legales. Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo. Ofrecemos una suite integral de productos diseñada para potenciar las Legal Operations y liderar la transformación digital en el sector legal: • Bigle CLM: Nuestra plataforma de Contract Lifecycle Management (CLM) gestiona todo el ciclo de vida de los contratos, desde la creación automatizada y los flujos de trabajo hasta la negociación, firma electrónica y seguimiento de obligaciones y renovaciones., • Bigle Libra: Nuestro asistente de inteligencia artificial generativa, especializado en el ámbito legal, que ayuda a analizar, resumir, traducir y generar contenido legal, optimizando procesos y proporcionando recomendaciones inteligentes para los equipos legales., • Bigle Sign: Una solución de firma electrónica avanzada que garantiza transacciones rápidas, seguras y conformes a normativas internacionales., • Bigle Academy: Una plataforma educativa que capacita a equipos legales y de negocio en la adopción de Legal Tech, promoviendo la profesionalización y el éxito en las Legal Operations. Con Bigle, las organizaciones no solo optimizan sus procesos legales, sino que se posicionan como líderes en innovación dentro del ámbito de Legal Operations, estableciendo nuevos estándares de excelencia y transformación digital en el sector. Nos apasiona la tecnología, la innovación y la usabilidad. Queremos transformar, de manera radical y a nivel global, la forma de llevar a cabo las operaciones legales. Pensamos que las personas merecen dedicar su tiempo a realizar tareas que aporten valor añadido, y que fomenten el crecimiento personal, liberándose de tareas repetitivas que pueden ser automatizadas por la tecnología. Además, queremos contribuir a proteger el medio ambiente, creando procesos completamente digitales que ayuden a reducir drásticamente el consumo de papel. Descripción de la oferta Bigle no ha parado de crecer desde su creación y buscamos profesionales intrépidos que quieran seguir creciendo con nosotros y hacer un impacto global con nuestra tecnología ¿Te gustaría formar parte de esta aventura? Estamos en la búsqueda de un/a Product Owner / Product Manager, con perfil híbrido que combine visión estratégica de producto con ejecución ágil en el día a día. Esta persona actuará como puente entre negocio y tecnología, transformando la visión de la compañía en un roadmap accionable y trabajando estrechamente con el CTO y el equipo de desarrollo para maximizar el valor entregado. Funciones y Responsabilidades Estrategia de Producto • Traducir la visión del negocio en un roadmap de producto claro y priorizado, • Identificar oportunidades y gaps de producto mediante research de usuarios, análisis de mercado y competencia, • Definir métricas de éxito y KPIs de producto, • Alinear stakeholders (CEO, CTO, Marketing, Ventas, Customer Success), • Analizar datos de uso y comportamiento para priorizar iniciativas, • Validar hipótesis mediante experimentos y feedback de clientes, • Priorizar iniciativas utilizando marcos como RICE, MoSCoW o Value vs Effort, • Asegurar que el roadmap equilibre impacto de negocio, valor usuario y viabilidad técnica Ejecución ágil • Ser responsable del backlog de producto (Asana), • Traducir el roadmap en historias de usuario claras y accionables, • Definir criterios de aceptación y alcance funcional, • Planificar sprints junto con CTO, asegurando entrega de valor real al usuario, • Resolver dudas funcionales y de negocio del equipo técnico, • Validar entregables antes de release, • Colaborar con el CTO para asegurar viabilidad técnica, • Equilibrar deuda técnica vs entrega de valor, • Gestionar nuevas peticiones asegurando su evaluación y priorización antes de su incorporación al backlog Requisitos Experiencia • 2–5 años en roles de Product Manager, Product Owner o híbrido PM/PO, • Experiencia trabajando con equipos de desarrollo ágiles, • Valorable experiencia previa en startups o entornos de rápido crecimiento, • Valorable background técnico (ex-desarrollador, analista técnico, etc.) Formación • Grado en Ingeniería, ADE o similar, • Valorable MBA o formación específica en producto, • Valorable certificaciones Agile (PSPO, CSPO, Scrum Product Owner) Competencias clave: • Definición y priorización de roadmap de producto, • Gestión de backlog y delivery en entornos Agile, • Análisis de datos y toma de decisiones basada en impacto, • Research de usuarios y validación de hipótesis, • Comunicación negocio–tecnología y gestión de stakeholders, • Pensamiento crítico y analítico, • Liderazgo por influencia y autonomía, • Capacidad de priorización y foco en valor, • Mentalidad hands-on y orientación a ejecución Qué ofrecemos • Ser parte de la revolución Legal Tech que transformará los procesos legales para siempre. Apreciarás tu impacto todos los días., • Compañeros de equipo increíbles: Ganamos juntos. Aprendemos juntos. Nos gusta trabajar en equipo y aprender unos de otros., • Cultura: la pasión por la innovación, el espíritu aventurero y la búsqueda de la excelencia son nuestros valores fundamentales., • Comunidad tecnológica: somos parte de la vibrante escena de empresas tecnológicas de Barcelona. Estarás rodeado de personas inteligentes e inspiradoras., • Flexibilidad para trabajar en remoto., • Oficina agradable con un entorno abierto en el centro de Barcelona y Madrid, con gran terraza con vistas a la ciudad, 2 cantinas, gimnasio, vestuarios y duchas. Otra información y proceso • Incorporación: Inmediata., • Ubicación preferente del candidato: Barcelona o Madrid., • Flexibilidad para trabajar en remoto. xcskxlj, • Entorno de trabajo agradable y flexible. Datos de contacto • E-mail: (MAD) Calle de María de Molina, 39, 3ª planta, 28006 Madrid (BOG) Bogotá, Chico 94, Cra. 11 No. 93a - 83, Bogotá, 110221 Colombia

Desde EBA, filial de GRUPO SANJOSE, precisamos incorporar un/una jefe/a de producción para obra de edificación en Vitoria. Por favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación. Si te incorporas a nuestra plantilla, formarás parte de los equipos de obra encargados de llevar las siguientes funciones: • Control técnico y económico del proyecto., • Optimización del proyecto., • Control de certificación., • Control de materiales., • Control de tajos., • Trato directo con subcontratas. ¿Qué esperamos de ti? Buscamos un perfil que cumpla con los siguientes requisitos: -Formaciones requeridas para el puesto: Grado en Edificación, Grado en Ing. Civil, Máster Camino, Canales y Puertos. -Valorable experiencia previa y salario en función de valía. -Al menos 1 año de experiencia desempeñando funciones similares -Se valorará acreditar el curso básico de prevención de riesgos laborales (60 h). -Ubicación: Vitoria. Grupo Empresarial San José cree en la diversidad como parte importante del éxito de sus equipos de trabajo. xcskxlj Garantizando un entorno inclusivo en el que se fomenta el respeto, pertenencia y compromiso para que todas las personas puedan participar en igualdad de oportunidades en los procesos de selección sin importar su sexo, edad, origen étnico o cultural, religión o creencias, orientación sexual, identidad y expresión de género, discapacidad u otras características personales o sociales.

Somos un grupo empresarial internacional con más de 3.500 empleados y presencia consolidada en diferentes países de Europa y América. Dentro de nuestras estrategias de desarrollo corporativo apostamos decididamente por el crecimiento de nuestra línea de negocio de construcción de edificación, habiendo incrementado notablemente en los últimos ejercicios nuestro volumen de negocio y equipo de profesionales. Descubra exactamente qué habilidades, experiencia y cualificaciones necesitará para tener éxito en este puesto antes de enviar su solicitud a continuación. Nuestras líneas de negocio más importantes son la construcción de infraestructuras, promoción de infraestructuras y servicios en régimen concesional, ejecución de obras de electrificación ferroviaria, proyectos de edificación, transporte ferroviario de mercancías y servicios de mantenimiento, revisión y reparación de maquinaria ferroviaria. Actualmente, tenemos varios proyectos en la zona de Madrid y necesitamos incorporar Jefes/as de Producción para, bajo la supervisión del Jefe/a de Obra, supervisar y controlar la ejecución de obras de la dirección de edificación. ¿Qué buscamos? • Experiencia 2-5 años en las funciones propias del puesto., • Formación en Arquitectura Técnica, Ingeniería de Edificación, Ingeniería de Caminos, Canales y Puertos, etc., • Disponibilidad incorporación: inmediata. xcskxlj Ofrecemos posibilidad de incorporación a un grupo multinacional, condiciones económicas competitivas y estabilidad profesional.

Role Summary We are seeking an AI Product Manager to lead the development and commercialization of next-generation AI-powered IVF solutions. This role is critical in transforming laboratory data into actionable clinical intelligence, enabling fertility clinics to improve outcomes, reduce variability, and scale operations through AI. You will own the full lifecycle of AI-driven products (e.g., embryo ranking, lab workflow intelligence, predictive analytics), working across clinical, engineering, and commercial teams globally. ¿Es usted el candidato adecuado para esta oportunidad? Asegúrese de leer la descripción completa a continuación. Key Responsibilities 1. AI Product Strategy & Portfolio Ownership • Define and drive the global product strategy for AI-enabled IVF solutions, • Build a scalable AI roadmap integrating:, • Embryo assessment algorithms, • Time-lapse imaging data, • Laboratory workflow analytics, • Identify new AI opportunities aligned with clinical impact and revenue growth 2. AI Product Development • Lead full product lifecycle:, • Concept → Data strategy → Model development → Clinical validation → Launch → Iteration, • Translate clinical and commercial needs into AI model requirements and product features, • Work closely with data science teams to:, • Define training datasets and annotation standards, • Set model performance benchmarks (AUC, sensitivity, specificity), • Ensure continuous model improvement through real-world data 3. Clinical Integration & Validation • Partner with embryologists and IVF clinics to ensure real-world usability, • Design and support clinical validation studies, • Translate AI outputs into clinically interpretable insights, • Ensure products support decision-making without increasing clinical risk 4. Data & Platform Strategy • Define and manage the data ecosystem, including:, • Time-lapse imaging data, • Patient and cycle data, • Lab operational data, • Develop feedback loops to improve AI models using global clinical datasets, • Ensure data integrity, traceability, and scalability 5. Regulatory & Compliance Alignment • Work with QARA teams to support documentation for AI validation and regulatory submissions, • Ensure AI transparency and explainability 6. Cross-Functional Project Management • Act as the bridge between:, • AI / Data Science teams, • Clinical & Application teams, • Regulatory & Quality, • Commercial & Marketing, • Drive alignment across global teams (EMEA, APAC, US), • Lead agile development cycles and product prioritization 7. Commercialization & Market Adoption • Define product positioning, pricing strategy, and value proposition, • Support go-to-market strategy and distributor enablement, • Work with marketing on scientific messaging and KOL engagement, • Monitor adoption metrics and continuously optimize product-market fit Requirements xcskxlj • Bachelor’s or Master’s degree in Biomedical Engineering, Computer Science, Data Science or Life Sciences. Advanced degree (MSc / PhD) preferred, • 6+ years of product management experience in Medical devices, Digital health, AI-driven healthcare products, • Proven experience launching AI or data-driven products, • IVF / reproductive medicine experience is highly preferred, • Strong understanding of Machine learning fundamentals, Data pipelines and model validation, AI performance metrics and limitations, • Ability to collaborate effectively with engineering and data science teams, • Familiar with IVF laboratory workflows, Embryology or reproductive medicine, Time-lapse imaging systems, • Strategic thinking with strong execution capability, • Ability to operate in a complex, global environment, • Strong stakeholder management across technical and non-technical teams, • Customer-centric mindset (clinicians, lab managers, distributors), • Mandarin Chinese speaking preferred

About Life5 Life5 is a Pan-European insurtech operating across Spain, Italy, and France. We are fundamentally changing how life insurance is distributed and underwritten. Having successfully navigated a strategic restructuring to reach breakeven, we operate with a highly leveraged, lean strike team. No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. We don't operate like a traditional insurance distributor; we operate as a tech-first orchestrator. We translate complex, legacy underwriting logic into dynamic, frictionless digital funnels, ensuring the end-customer gets the protection they need without the traditional hassle. While we are a B2C-first company at our core, we are actively expanding our backend infrastructure to become the API layer that powers B2B2C channels, traditional brokers, and broader cross-sell ecosystems. The Role As the Founder Associate / Growth PM, you will act as the Second Brain to the CEO. You will step into a highly cross-functional role designed to unblock our most critical strategic and growth initiatives. We don't need you to write code, but we need you to understand product logic and human behavior. You will bridge the gap between high-level business strategy (unit economics, carrier negotiations), technical infrastructure, and deep customer empathy (designing B2C conversion funnels, financial calculators, and modern broker tools). What You Will Actually Do • Growth & Conversion Operations: Analyze our B2C acquisition funnels—from top-of-funnel paid media to our bottom-of-funnel human advisory team. Dive into the data to identify friction points and deploy programmatic solutions that drive down Customer Acquisition Cost (CAC) and increase Lifetime Value (LTV)., • Platform & B2B2C Expansion: While keeping the end-user in mind, you will help design the operational rollout of our infrastructure plays. This involves understanding the friction of traditional brick-and-mortar brokers and translating that into scalable digital tools., • Partner Negotiations: Assist the CEO in high-stakes discussions with legacy insurance carriers and reinsurers, preparing the analytical frameworks and business cases required to secure the products our customers actually want. Who We Are Looking For • The High-Velocity Thinker: You have 1 to 3 years of experience in top-tier strategy consulting (McKinsey, BCG, Bain, etc.), investment banking, or a high-growth startup environment., • High IQ + High EQ: You are just as comfortable dissecting unit economics, CAC, and conversion data in a spreadsheet as you are sitting in a boardroom presenting a digital roadmap to a legacy insurance executive., • Fearless Learner: You don't need a background in insurtech, but you must possess the intellectual horsepower to learn regulatory frameworks and product nuances in days, not months., • Bias for Action: You prefer launching, measuring, and iterating over building 40-slide theoretical decks. What We Offer • Compensation: Competitive base salary + Equity. We want you incentivized by the Enterprise Value you are helping to build., • True Ownership: You will have a front-row seat and a steering wheel in a Pan-European scale-up. xcskxlj, • Mentorship & Leverage: You will work directly with the CEO and learn cutting-edge methodologies for leveraging automation and technology to build and scale products at unprecedented speeds.

Join MOBIS Spain Electrified Powertrain – Driving the Future of EV Batteries Innovation! Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. we're at the forefront of EV battery assembly innovation. As a cutting-edge subsidiary of Hyundai Mobis, our Pamplona-based team ensures the safe, efficient, and high-performance operations. If you're eager to join a dynamic, international team driving major advancements in electrified powertrain technology, this is your invitation. Collaborate with top-tier professionals, engage in smart manufacturing, and play a crucial role in accelerating the electric revolution. Quality Assurance Specialist (QA) Quality Assurance and Customer RequirementsAct as the QA representative towards the customer for quality-related topics, deviations, claims, and notifications.Support customer audits, assessments, and quality review meetings. Field Claims Management and Market QualityReceive and evaluate quality incidents detected at vehicle assembly plants or in the market.Coordinate with customers, service organizations, and local entities for the technical review of claims. Field Return Parts AnalysisPerform analysis of returned field parts.Conduct visual, functional, and data analysis.Carry out traceability-based analysis (lot, serial number, production history). Provide technical support in responsibility analysis related to field claims.Coordinate with internal departments (QA, Production, Purchasing) and Quality HQ. Implement actions to prevent recurrence based on field claims data.Horizontally deploy lessons learned to similar projects and products. Minimum of 3 years of experience in quality management or related areas.Experience in customer quality support for components in sectors such as automotive, electronics, machinery, or semiconductors (preferred).Solid knowledge of Quality Management Systems (ISO 9001, IATF 16949) and experience with VDA 6.3 audits .English level B2 minimum ; knowledge of German is a plus.Knowledge of adhesives, welding, and battery systems is desirable. xcskxlj Every qualified applicant will receive equal consideration for employment.

Seeking a proactive Upstream Technician for a Manufacturing Operations Department. Responsibilities include ensuring compliance with GMP standards, preparing and developing production processes for biological molecules, and participating in audits and investigations.

Join MOBIS Spain Electrified Powertrain – Driving the Future of EV Batteries Innovation! Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. we're at the forefront of EV battery assembly innovation. As a cutting-edge subsidiary of Hyundai Mobis, our Pamplona-based team ensures the safe, efficient, and high-performance operations. If you're eager to join a dynamic, international team driving major advancements in electrified powertrain technology, this is your invitation. Collaborate with top-tier professionals, engage in smart manufacturing, and play a crucial role in accelerating the electric revolution. Quality Assurance Specialist (QA) Quality Assurance and Customer RequirementsAct as the QA representative towards the customer for quality-related topics, deviations, claims, and notifications.Support customer audits, assessments, and quality review meetings. Field Claims Management and Market QualityReceive and evaluate quality incidents detected at vehicle assembly plants or in the market.Coordinate with customers, service organizations, and local entities for the technical review of claims. Field Return Parts AnalysisPerform analysis of returned field parts.Conduct visual, functional, and data analysis.Carry out traceability-based analysis (lot, serial number, production history). Provide technical support in responsibility analysis related to field claims.Coordinate with internal departments (QA, Production, Purchasing) and Quality HQ. Implement actions to prevent recurrence based on field claims data.Horizontally deploy lessons learned to similar projects and products. Minimum of 3 years of experience in quality management or related areas.Experience in customer quality support for components in sectors such as automotive, electronics, machinery, or semiconductors (preferred).Solid knowledge of Quality Management Systems (ISO 9001, IATF 16949) and experience with VDA 6.3 audits .English level B2 minimum ; knowledge of German is a plus.Knowledge of adhesives, welding, and battery systems is desirable. xcskxlj Every qualified applicant will receive equal consideration for employment.

Buscamos un Jefe de Producción para obra ferroviaria en Navarra. Supervisará la planificación, ejecución, costes y coordinación de proveedores en un proyecto de gran envergadura.

Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo.Nuestro cliente, Exkal, líder en el sector de la refrigeración comercial, busca incorporar un/a Manager de Producción con experiencia en entornos productivos.Perf

Si tienes experiencia en el sector automovilístico es genial, pero si no, ¡no te preocupes! Te formaremos y ayudaremos desde el primer momento. En Adecco creemos en la igualdad de oportunidades y apostamos por el Talento Sin Etiquetas. Se valorará experiencia en líneas de

En Adecco creemos en la igualdad de oportunidades y apostamos por el Talento Sin Etiquetas.

En Adecco creemos en la igualdad de oportunidades y apostamos por el Talento Sin Etiquetas.

Buscamos un Jefe de Producción para obra ferroviaria en Navarra.

España, con una trayectoria de más de un siglo y un firme compromiso con la seguridad, la sostenibilidad y la excelencia operativa.Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo.Ciclo formativo de Grado Superior