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Colaborar en el cumplimentar los objetivos marcados de servicio, satisfacción de clientes y eficacia de los procesos wellness.Colaborar y apoyar en la supervisión y control del cumplimiento de protocolos.Proponer y coordinar las ofertas para la captación de clientes, diseño de promociones, etc.G

Gestionar y controlar los procesos definidos para el desarrollo del servicio.Lograr el Plan de Ventas y generación de ingresos del departamento: planificará acciones de dinamización y promoción, y formará al equipo para la venta.Organizar y coordinar los diferentes servicios de Restauración/Ba

Ejecutar, de manera cualificada, autónoma y responsable, el servicio y venta de alimentos y bebidas.Recibir a los clientes y acomodarles en caso de que sea necesario.Ofrecer atención directa al cliente en el consumo de alimentos y bebidas.Encargarse de la preparación, montaje y desmontaje de los

Experiencia mínima de 2 años en puesto similar en sistemas preventivos y correctivos en Hoteles. Verificar el buen funcionamiento de todas las instalaciones y maquinaria del Hotel, asegurando el correcto uso de las mismas y que su mantenimiento esté en el mejor estado posible.

Empresas: Barceló Hotel Group Participar con alguna autonomía y responsabilidad en el servicio y venta de alimentos y bebidas.Conservar adecuadamente su zona y utensilios de trabajo.Preparar áreas de trabajo para el servicio.Colaborar en el servicio al cliente.Preparar el montaje del servicio, me

Empresas: Barceló Hotel Group Verificar el buen funcionamiento de todas las instalaciones y maquinaria del Hotel, asegurando el correcto uso de las mismas y que su mantenimiento esté en el mejor estado posible. Experiencia mínima de 2 años en puesto similar en sistemas preventivos y correctivo

Empresas: Barceló Hotel Group Participar con alguna autonomía y responsabilidad en el servicio y venta de alimentos y bebidas.Conservar adecuadamente su zona y utensilios de trabajo.Preparar áreas de trabajo para el servicio.Colaborar en el servicio al cliente.Preparar el montaje del servicio, me

Empresas: Barceló Hotel Group Participar con alguna autonomía y responsabilidad en el servicio y venta de alimentos y bebidas.Conservar adecuadamente su zona y utensilios de trabajo.Preparar áreas de trabajo para el servicio.Colaborar en el servicio al cliente.Preparar el montaje del servicio, me

Empresas: Barceló Hotel Group Participar con alguna autonomía y responsabilidad en el servicio y venta de alimentos y bebidas.Conservar adecuadamente su zona y utensilios de trabajo.Preparar áreas de trabajo para el servicio.Colaborar en el servicio al cliente.Preparar el montaje del servicio,

Supervisar la limpieza y mantenimiento de las instalaciones, avisando a la Gobernanta y al Jefe de mantenimiento de cualquier posible incidencia.

Empresas: Barceló Hotel Group Supervisar e intervenir en la prestación de los servicios de comidas y/o bebidas (restaurantes, bares, etc.Planificar tiempo y recursos: elaboración de turnos, control de stocks.Organizar y asignar las mesas a los camareros que dependen de él.Corregir las actuacio

Empresas: Barceló Hotel Group Recepción del cliente en las instalaciones.

Empresas: Barceló Hotel Group Gestionar y controlar los procesos definidos para el desarrollo del servicio.Lograr el Plan de Ventas y generación de ingresos del departamento: planificará acciones de dinamización y promoción, y formará al equipo para la venta.Organizar y coordinar los diferen

Grupo Gransolar busca un Project Developer para sus oficinas de Almería. El candidato gestionará el desarrollo de proyectos solares y almacenamiento, permisos, licencias y el diseño técnico para plantas híbridas FV+BESS, colaborando con equipos multidisciplinares. Se requieren ingenierías superiores y 8–10 años de experiencia en renovables, con inglés C1. Ofrecemos contrato indefinido, seguro médico y seguro de vida, y un entorno dinámico. #J-18808-Ljbffr

Straumann Group is seeking an experienced CSV and Test Management Lead in a hybrid Madrid/Wroclaw setting. You will drive validation and test strategies for SAP and other enterprise applications, ensuring compliance with GxP and regulatory standards. The role requires 10+ years in CSV/QM/Test/PM with leadership experience, fluency in English, and a strategic mindset to guide cross-functional teams through validation activities across the global IT landscape. #J-18808-Ljbffr

Empresas: Barceló Hotel Group Ejecutar, de manera cualificada, autónoma y responsable, el servicio y venta de alimentos y bebidas.Recibir a los clientes y acomodarles en caso de que sea necesario.Ofrecer atención directa al cliente en el consumo de alimentos y bebidas.Encargarse de la preparaci

Empresas: Barceló Hotel Group El auxiliar de noche en la recepción de un hotel es responsable de garantizar el correcto funcionamiento del establecimiento durante el turno nocturno, realizando tareas de vigilancia y seguridad mediante rondas periódicas por las instalaciones, prestando apoyo y a

Buscamos Jefe de Obra (h/m) para obras de canalizaciones Ubicación: Almería Funciones: Gestión económica y técnica: Controlar los costes de materiales, mano de obra, subcontratas y servicios asociados al contrato.

Job Title: Pepper Breeding Director (M/F) Contract type: Permanent • Lead and manage Pepper breeding activities for Europe, Americas, Middle East and Africa in accordance with the Limagrain Vegetable Seeds (LVS) R&D Strategy., • Direct Pepper breeding programs with Breeding Coordinators and Breeders to achieve goals and objectives set during Strategic Crop reviews, Breeding Program reviews, Development Management review., • Actively develop breeding teams and individuals (technical & managerial competencies)., • Promote constructive global interactions and exchanges with breeding programs in other crops, with Asia colleagues and across Limagrain Vegetable Seeds., • Define and manage the Pepper breeding organization with regard to staff, budget, and technology resources associated with the development and execution of each breeding program to deliver objectives., • Act as interface with marketing teams to secure alignment of breeding programs with market needs. Lead the development strategies and directions for Pepper., • As part of the Breeding Leadership Team, collaborate with breeding management throughout the world, and contribute to global R&D strategy, breeding program reviews., • Work together with LVS counterpart and marketing leaders in order to contribute to strategic Crop Reviews and Project Portfolio definition and build Pepper R&D Strategy., • Represent R&D in cross functional committee: maximize crop market share & profitability and develop products, align on strategy priorities and main projects., • Define the Pepper breeding organization in regard to Global Strategy, staff, budget, and technology resources associated with the development and implementation of each breeding program., • Work together with R&D Operation and Trait & Technology Application leaders by providing direction/priorities for the implementation of the breeding programs at each site., • Collaborate with other breeding leaders and technology teams to advance on the breeding strategic roadmap initiatives and optimize the breeding process., • Act as R&D leader for Spain. As delegated, represent the Business Unit HM.Clause in collaborations or partnerships with the group (LVS), as well as with external organizations such as universities and institutes., • Manage Pepper breeding teams (breeding coordinators & breeders) and ensure a framework of management, training and skill development for teams and individuals., • Ensure the implementation, among the breeding teams, of the company rules., • Responsible for breeding budget, OPEX execution throughout the year., • Minimum of master’s degree in an Agronomic and/or Biological Science, with specialization in plant genetics and breeding., • At least 10 years of management and product development experience, including five years of experience managing a breeding program., • Must be proficient both in Spanish and in English; French is a plus., • Strong leadership and management skills. Open-minded, positive attitude, and capacity to lead change., • Result-oriented. Long‑ & short‑term vision. Financial analysis for strategic decision making. Ability to create innovative environment., • Willingness to travel frequently, domestic & international (30%)., • We offer you an attractive compensation package as well as numerous development opportunities within HM.CLAUSE and Limagrain Group., • This position is located in Almeria, Spain. HM. CLAUSE, Business Unit of Group Limagrain, is an innovative global leader in the development, production, and commercialization of vegetable seeds. HM. CLAUSE belongs to the top 5 vegetable seed entities in the world. With over 2,000 varieties in more than 20 vegetable crops, HM. CLAUSE provides innovative solutions to growers worldwide. HM. CLAUSE is a company committed to diversity and inclusion. #J-18808-Ljbffr

Permanent contract / Full-time Are you passionate about making a real impact in agricultural research? Do you enjoy collaborating on research projects? Are you seeking to combine your experience of genetics and plant breeding with project coordination in regulatory framework? Do you thrive in planning and organising in a deadline and compliance driven environment? Continue reading to find out more about our new opportunity for an EMEA R&D Projects Coordinator. Reporting to the Head of Laboratories for EMEA, you will work in close collaboration with Research, Legal, and Finance teams across the region to: • Identify and Manage collaborative projects:, • Identify opportunities for collaboration with private and public institutions in the sector., • Contribute to the draft and design of collaborative projects with partners., • Submit and manage project funding applications with various institutions., • Coordinate and monitor approved projects., • Manage project documentation and requirements for regulatory compliance., • Administer national funding and tax incentive schemes:, • Submit, and manage, applications to tax incentive programs., • Prepare technical reports, coordinating with research teams to obtain information., • Coordinate the process of certification management to obtain the Binding Motivated Report and meet legal and fiscal requirements., • Manage documentation within the established deadlines and for compliance purposes., • Intellectual Property (IP) Evaluate IP opportunities:, • Oversee and coordinate IP preparation and filing., • Organize and communicate arbitration and negotiations in collaboration with the Legal Department. You could be based in either Spain, France or South Africa. • you are fluent in English and Spanish (verbal and writing, formal and scientific) and have:, • An M.Sc with 5 years’ experience/ PhD specializing in genetics or plant breeding., • Strong project management skills, • Excellent communication and collaboration abilities, • Solid analytical and organizational skills, • Ability to interpret and apply regulations, • High attention to detail and strong problem-solving mindset You will be part of the Sakata Vegetables EMEA team, part of the international Sakata Group. What makes Sakata different is that while being a key international player in the seed business, the company keeps a family spirit. This means 3 things: it’s a people-oriented company where it is easy to communicate at all levels you will work closely with your colleagues and customers and will never be far from the fields as a result of its Japanese origins, you'll be working for a stable company with an emphasis on long-term. Working at Sakata offers you the opportunity to join a well-established company in the seed industry. As part of the team, you will experience a people-oriented culture while working alongside colleagues from different nationalities across Europe, Africa, and the Middle East. #J-18808-Ljbffr

La persona seleccionada será responsable de la gestión integral y funcionamiento operativo de una estación de Investigación y Desarrollo (I+D), asegurando la correcta coordinación de los equipos, instalaciones, recursos y actividades necesarias para dar soporte a los departamentos de Mejora Gen

Permanent contract / Full-time Are you passionate about making a real impact in agricultural research? Do you enjoy collaborating on research projects? Are you seeking to combine your experience of genetics and plant breeding with project coordination in regulatory framework? Do you thrive in planning and organising in a deadline and compliance driven environment? Continue reading to find out more about our new opportunity for an EMEA R&D Projects Coordinator. A valuable member of the Research team, you will play a key role in facilitating the progress towards strategic research goals within EMEA by coordinating research projects with external partners, managing applications for funding and tax incentives, and taking responsibility for coordinating Intellectual Property matters. • Identify and Manage collaborative projects, • Identify opportunities for collaboration with private and public institutions in the sector., • Contribute to the draft and design of collaborative projects with partners., • Submit and manage project funding applications with various institutions., • Coordinate and monitor approved projects., • Manage project documentation and requirements for regulatory compliance., • Administer national funding and tax incentive schemes, • Submit, and manage, applications to tax incentive programs., • Prepare technical reports, coordinating with research teams to obtain information., • Coordinate the process of certification management to obtain the Binding Motivated Report and meet legal and fiscal requirements., • Manage documentation within the established deadlines and for compliance purposes., • Intellectual Property (IP), • Evaluate IP opportunities, • Oversee and coordinate IP preparation and filing, • Organize and communicate arbitration and negotiations in collaboration with the Legal Department You could be based in either Spain, France or South Africa. You are fluent in English and Spanish (verbal and writing, formal and scientific) and have: • An M.Sc with 5 years’ experience/ PhD specializing in genetics or plant breeding., • Strong project management skills, • Excellent communication and collaboration abilities, • Solid analytical and organizational skills, • Ability to interpret and apply regulations, • High attention to detail and strong problem-solving mindset You will be part of the Sakata Vegetables EMEA team, part of the international Sakata Group. What makes Sakata different is that while being a key international player in the seed business, the company keeps a family spirit. This means 3 things: • it’s a people-oriented company where it is easy to communicate at all levels, • you will work closely with your colleagues and customers and will never be far from the fields, • as a result of its Japanese origins, you'll be working for a stable company with an emphasis on long-term. #J-18808-Ljbffr

Autohero busca Perito/a de Vehículos para trabajar en su taller de Ketzin, Alemania.Realizarás peritajes y reportes técnicos de vehículos, verificando daños y elaborando informes.Se ofrece contrato temporal de 24 meses, alojamiento incluido desde el primer día, 28 días de vacaciones, ayuda pa

Perito/a de Vehículos - Trabaja en Alemania.Perito/a / Inspector/a de Vehículos.Europa? ¿Tienes experiencia realizando peritajes y evaluaciones de vehículos?.Salario acorde al mercado y a la experiencia aportada.Ayuda económicapara el traslado, así como apoyo en la gestión documental.Cursos d

Medical Affairs Scientist/Medical Scientific Relations(MAS/MSR) function is responsible to create scientific partnership with local KOLs through a qualified approach that results in access and advocacy based on scientific evidence. In addition, he/she is the point of accountability for medical and scientific issues and initiatives related to therapeutic area. Medical Affairs Scientist /MSR (MAS/MSR) is accountable for developing and executing the country medical plan at local level that supports the strategic operating goals for the business. • Develop and consolidate a network of relationships with the KOL and Scientific Institutions at the local level, sharing the wealth of knowledge and technical skills in order to support the scientific and medical leadership of the company., • Be the in-field medical expert in the area of hematology tumours, • Facilitate medical and scientific field intelligence, to know investigators/potential investigators, understand competitive research activities in active or planned study sites, generate insights from investigators and identify opportunities for collaborations with key institutions and KOL leaders at local level, • Plans and executeslocal medical scientific strategic plans, as per their specialty role. Provide in country support for therapeutic areas. Promote to KOLs medical activities developed at the central level (e.g. medical education programs, congress, among others) to support the implementation of scientific strategies in their own territory, • Observation and assessment of competitor drug, • Attend relevant scientific meetings and Conferences, • Lead medical to medical communications in the field, • Disseminate scientific information to scientific community through 'Medical to Medical communication' (individual meetings and group), in line with company procedures, • Preparation of scientific talks and presentations., • Ensure that new clinical data on Pfizer medicine are promptly disseminated in the most accurate manner, compliant with the label of the product., • Ensure a strong medical and scientific presence for Pfizer in investigational sites and key scientific centers:, • Provide scientific and technical leadership to ensure professional and credible relationships with investigators, • Internal discussion of research grants proposal with above country medical team, • Provide support for adequate independent sponsored research, non-interventional studies and research grants planning and management., • Facilitation of clinical research and interventional phase 1-4 trials with Pfizer drugs., • Management of post-marketing studies (clinical trials, observational /pharmacoepidemiological studies, • Work in close collaboration with internal colleagues, • Support promotional activities on regional KOLs and Scientific Societies including active preparation and participation in symposia, opinion leaders’ meetings and advisory boards, • Aligns, supports and contributes to different internal stakeholders., • Support internal training of customer facing commercial colleagues, enhancing their knowledge, and understanding of clinical data and our medicines, • Provide scientific input to the cross functional team and contributes to company’s plans through actionable customers’ medical insights., • Keep internal activities, field interactions, and M2M communications correctly tracked through periodic reports, • Ensures conduct all of work in compliance with Pfizer internal policies and European / local regulation, codes of conduct and accepted standards of best practice in all activities and interactions (research, communications, unsolicited queries on off label use of drugs, …), • Degree in Health Sciences, • MD, MBA, PhDand/or expertise in Oncology strongly desired., • Previous experience as MSL/MSR desired, and Oncology/hematology local environment knowledge preferred, • Fluency in English required, • Background/clinical experience with Epidemiology, Oncology, Immunology, Clinical Trials, molecular biology, translational medicine preferred, • Excellent interpersonal, written and verbal, communication skills (scientific and non-scientific), • Previous experience in medical writing, submission of papers to peer review papers, • Strong customer orientation, science based, • Project management skills and capacity to work under strict deadlines, • Demonstrated ability to effectively work in a multi-functional team and good teamwork spirit, • Demonstrated ability to rapidly adopt and utilize new digital technology and other resources with medical customers and record medical interactions, • Working knowledge of Regulatory Affairs, Drug Safety, Legal and compliance, • Computer skills, • Interest and knowledge on innovation, as artificial intelligence (AI), digital environment, statistics..., • Willingness to travel as it is a field-based role.Possesses valid driver’s license, • Good understanding of the local healthcare environment at national and regional level, • Good understanding of drug development, clinical research, medical decision making and health environment, • Good knowledge of pharmacovigilance and regulatory legislation and how it impacts the product portfolio, • Good knowledge of drug development processes, • Good understanding of Clinical Research, • Type of position: Full time, regular, • Regional-based; position based in Andalusia, • European work permit necessary, • NO Relocation package available This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview. Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience. We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer iscommitted to celebratingthis,in all itsforms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here! Pfizer endeavors to make accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Se valorarán las candidaturas que puedan aportar certificados oficiales de discapacidad. To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers. #J-18808-Ljbffr

Job Description Medical Affairs Scientist/Medical Scientific Relations(MAS/MSR) function is responsible to create scientific partnership with local KOLs through a qualified approach that results in access and advocacy based on scientific evidence. In addition, he/she is the point of accountability for medical and scientific issues and initiatives related to therapeutic area. Medical Affairs Scientist /MSR (MAS/MSR) is accountable for developing and executing the country medical plan at local level that supports the strategic operating goals for the business. Main responsibilities Develop and consolidate a network of relationships with the KOL and Scientific Institutions at the local level, sharing the wealth of knowledge and technical skills in order to support the scientific and medical leadership of the company. Be the in-field medical expert in the area of hematology tumours Facilitate medical and scientific field intelligence, to know investigators/potential investigators, understand competitive research activities in active or planned study sites, generate insights from investigators and identify opportunities for collaborations with key institutions and KOL leaders at local level Plans and executeslocal medical scientific strategic plans, as per their specialty role. Provide in country support for therapeutic areas. Promote to KOLs medical activities developed at the central level (e.G. medical education programs, congress, among others) to support the implementation of scientific strategies in their own territory Observation and assessment of competitor drug Attend relevant scientific meetings and Conferences Lead medical to medical communications in the field Disseminate scientific information to scientific community through 'Medical to Medical communication' (individual meetings and group), in line with company procedures Preparation of scientific talks and presentations. Ensure that new clinical data on Pfizer medicine are promptly disseminated in the most accurate manner, compliant with the label of the product. Ensure a strong medical and scientific presence for Pfizer in investigational sites and key scientific centers: Provide scientific and technical leadership to ensure professional and credible relationships with investigators Internal discussion of research grants proposal with above country medical team Provide support for adequate independent sponsored research, non-interventional studies and research grants planning and management. Facilitation of clinical research and interventional phase 1-4 trials with Pfizer drugs. Management of post-marketing studies (clinical trials, observational /pharmacoepidemiological studies Work in close collaboration with internal colleagues Support promotional activities on regional KOLs and Scientific Societies including active preparation and participation in symposia, opinion leaders’ meetings and advisory boards Aligns, supports and contributes to different internal stakeholders. Support internal training of customer facing commercial colleagues, enhancing their knowledge, and understanding of clinical data and our medicines Provide scientific input to the cross functional team and contributes to company’s plans through actionable customers’ medical insights. Keep internal activities, field interactions, and M2 M communications correctly tracked through periodic reports Ensures conduct all of work in compliance with Pfizer internal policies and European / local regulation, codes of conduct and accepted standards of best practice in all activities and interactions (research, communications, unsolicited queries on off label use of drugs, …) Education, Skills And Professional Experience Degree in Health Sciences MD, MBA, Ph Dand/or expertise in Oncology strongly desired. Previous experience as MSL/MSR desired, and Oncology/hematology local environment knowledge preferred Fluency in English required Background/clinical experience with Epidemiology, Oncology, Immunology, Clinical Trials, molecular biology, translational medicine preferred Excellent interpersonal, written and verbal, communication skills (scientific and non-scientific) Previous experience in medical writing, submission of papers to peer review papers Strong customer orientation, science based Project management skills and capacity to work under strict deadlines Demonstrated ability to effectively work in a multi-functional team and good teamwork spirit Demonstrated ability to rapidly adopt and utilize new digital technology and other resources with medical customers and record medical interactions Working knowledge of Regulatory Affairs, Drug Safety, Legal and compliance Computer skills Interest and knowledge on innovation, as artificial intelligence (AI), digital environment, statistics... Willingness to travel as it is a field-based role. Possesses valid driver’s license Ideally, you also have: Good understanding of the local healthcare environment at national and regional level Good understanding of drug development, clinical research, medical decision making and health environment Good knowledge of pharmacovigilance and regulatory legislation and how it impacts the product portfolio Good knowledge of drug development processes Good understanding of Clinical Research Additional Information Type of position: Full time, regular Regional-based; position based in Andalusia European work permit necessary NO Relocation package available This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview. Purpose Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. Digital Transformation Strategy One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience. Flexibility We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Equal Employment Opportunity We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer iscommitted to celebratingthis,in all itsforms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. Disability Inclusion Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here! Pfizer endeavors to make accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Se valorarán las candidaturas que puedan aportar certificados oficiales de discapacidad. To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers. #J-18808-Ljbffr

Forward Deployed Engineer (Python, AI Systems)Spain (Madrid or Barcelona preferred) | HybridUp to 100k + performance bonus + equityWe're supporting one of our clients (an AI-native product company) in hiring a Forward Deployed Engineer to work at the intersection of engineering, AI systems, clients & product and enterprise deployments.This is not a traditional backend role.It's for engineers who want to build, ship, and deploy AI-powered systems directly into real client environments, fast.The RoleAs a Forward Deployed Engineer, you'll work closely with enterprise customers to design, implement, and deploy AI-driven workflows powered by LLMs and agent-based systems.You'll take ownership from architecture to production.This includes:Designing backend architectures in Python (FastAPI-heavy stack)Integrating AI systems (LLMs, RAG pipelines, structured outputs)Building APIs and microservices for client-specific workflowsDeploying scalable, containerized services (Docker, Kubernetes)Debugging production issues and improving system reliabilityTranslating business requirements into clean technical solutionsYou won't just ship code — you'll see it live, used, and scaled.What We're Looking ForStrong backend engineering fundamentals (Python preferred)Experience building and operating production systemsComfort with APIs, data modeling, and microservicesExperience integrating third-party systems or working client-facingCloud experience (AWS, GCP, or similar)Product mindset and high ownership mentalityBonus if you have:Experience working with LLMs or AI-powered systemsExperience with RAG or structured output generationExposure to container orchestration (Kubernetes)Who Thrives in This RoleEngineers who enjoy solving messy real-world problemsBuilders who like autonomy and ownershipPeople comfortable speaking to stakeholdersDevelopers who prefer impact over bureaucracyThis is a high-intensity, high-ownership environment.Not a maintenance role. Not a ticket factory.Compensation & SetupCompetitive base salary for Spain (up to 100k for the right profile)Performance-based bonus structureMeaningful equityHybrid model (Madrid or Barcelona preferred)If you're excited about deploying real AI systems into production environments — and want to work close to both product and customers — we'd love to speak.Apply directly or reach out for a confidential conversation.

This is a great opportunity to apply your leadership and expertise in pursuit of our mission to become the most customer-focused and innovative oral care company in the world. We are seeking an experienced CSV and Test Management Lead to drive the delivery of validated software solutions like SAP, Salesforce and other enterprise Applications and enable Global Test Management and capabilities for Straumann’s Global Business Applications department. The ideal candidate will bring deep CSV and Test Management expertise for Enterprise Business Applications like SAP, etc. As part of our digital transformation journey and business growth strategy, you will play a key role in contributing to major initiatives across the organization. You will report to the Head of Global Business Applications Processes, Toolchain, and Delivery. • Manage and review all levels of validation documentation (internal or external SDLC) in collaboration with all stakeholders Including Validation (Strategy) & Test Plans, User Requirements, Functional, Configuration, Installation Specifications, SOP’s and Qualification Documents like Test Specifications & records. Traceability Matrices, Risk Analysis, Validation Reports, etc., • Provide implementation or update project teams with computerized systems validation (CSV) guidance, • Continuous Improvement of CSV standards, considering best practices and regulatory changes to maintain compliance and improve validation processes in alignment with IT and QA departments., • Key role for defining, driving and implementation of Test Management for Business Application and other major initiatives like S/4HANA in alignment with Application Lifecycle Management Strategy, • Partner with Quality Assurance, Test Management and Compliance teams to align deliverables as CSV guidelines, • Coordinate local CSV and QA representatives to fulfill global CSV Compliance requirements., • Provide Training, guidance and coaching to all stakeholders for CSV standards, Test approaches, • Collaborate with functional teams in IT across SAP and other Business Application stakeholders and all relevant business representatives to ensure compliance and/or project quality., • Participate in internal and external audits if needed., • Bachelor's or master's degree in computer science, Information Systems, QM or related field and/or related working experience., • 10+ years of experience in CSV, QM, Test and Project Management, with at least 2 years in a leadership role., • Strong expertise in GxP requirements and guidelines like 21 CFR Part 11 regulations, GAMP 5 and Annex11 requirements for computerized systems., • Understanding, adapting and establishing GxP regulations, CSV and documentation best practices in regulated industries., • Strong Project- & Test management skills with the ability to adapt also solution-oriented compliance deliverables, • Familiar with several software development methodologies and the capability to adapt them for CSV, • Strong communication and stakeholder management skills, with the ability to build and maintain strong relationships across the organization and with external partners., • Capacity to face and adapt to challenges to overcome them (resilience), • Fluent English spoken and written, other languages are an asset (DE) Straumann Group offices in Madrid/Wroclaw - Hybrid, with 2 remote working days/week. Full Time • Spain : Madrid, • Brazil : Curitiba, • Poland : Gdansk, • Poland : Wroclaw, • Spain : Albacete, • Spain : Alcobendas, • Spain : Alicante, • Spain : Almería, • Spain : Araba, • Spain : Asturias, • Spain : Badajoz, • Spain : Barcelona, • Spain : Bilbao, • Spain : Burgos, • Spain : Cantabria, • Spain : Castelló, • Spain : Ciudad Real, • Spain : Cuenca, • Spain : Cáceres, • Spain : Cádiz, • Spain : Córdoba, • Spain : Gipuzkoa, • Spain : Girona, • Spain : Granada, • Spain : Guadalajara, • Spain : Huelva, • Spain : Huesca, • Spain : Illes Balears, • Spain : Jaén, • Spain : La Coruña, • Spain : La Rioja, • Spain : Las Palmas, • Spain : León, • Spain : Lleida, • Spain : Lugo, • Spain : Mendaro, • Spain : Murcia, • Spain : Málaga, • Spain : NavarraSpain : Ourense, • Spain : Palencia, • Spain : Pontevedra, • Spain : Salamanca, • Spain : Santa Cruz de Tenerife, • Spain : Segovia, • Spain : Sevilla, • Spain : Soria, • Spain : Tarragona, • Spain : Teruel, • Spain : Toledo, • Spain : Valencia, • Spain : Valladolid, • Spain : Zamora, • Spain : Zaragoza, • Spain : Ávila 0 - 10% All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability. #J-18808-Ljbffr

Adecco Outsourcing es una empresa comprometida con la igualdad perteneciente a The Adecco Group y especializada en la externalización de servicios cuyo valor añadido son los Recursos Humanos. En Adecco creemos en la igualdad de oportunidades y apostamos por el Talento Sin Etiquetas.

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