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Job PurposeThis 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.Main Tasks and Responsibilities• 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.Requirements neededEducation • Bachelor's or master's degree in computer science, Information Systems, QM or related field and/or related working experience.Experience & personal attributes• 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)Work locations: Straumann Group offices inMadrid/Wroclaw/Curitiba - Hybrid, with 2 remote working days/week Remote from Spain with some travel for business meetings to Madrid expected All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.Employment Type: Full Time Alternative Locations: 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 : Navarra || Spain : 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 Travel Percentage: 0 - 10% Requisition ID: 20070Job SummaryJob number: 20070Date posted : Profession: Information TechnologyEmployment type: Full Time

table.MiTabla { max-width: 1020px;}Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunity fostering an inclusive environment where diversity makes us be outstanding.Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Global Quality Manager like you.What your responsibilities will beIssue and review Global Quality Policies and ensure its implementation in all the sites within Biopharma Business UnitStay updated on industry trends and advancements in quality management practices to drive innovation and improvementFoster harmonization of Quality Systems across Biopharma sites Coordinate the implementation of electronic Quality Management SystemsCoordinate global Quality projects and initiativesCoordinate global Quality working groups comprised by different key users of the sites of BiopharmaManage digitalization projects Perform oversight of Quality Systems and escalate risks detected to Senior ManagementEvaluate new applicable regulations and ensure its timely implementationContinuous support to the Quality areas of BiopharmaWho you areTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).Bachelor’s Degree in Health Sciences or a related field5-10 years of experience managing quality systems is requiredAnalytical and problem-solving abilitiesExcellent written and verbal communication skillsExperience in project managementAbility to facilitate changeDevelops collaborative working relationshipsGood understanding of regulatory requirements and quality standards relevant to Biological productsInternational experienceWillingness to travel internationally as neededAmbitious, results-oriented, business-minded personWhat we offerIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.Information about Grifols is available at you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!We look forward to receiving your application!We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.Grifols is an equal opportunity employer. xcskxlj Flexibility for U Program: Hybrid ModelFlexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).Benefits package Contract of Employment: Permanent position#LI-ER1#LI-HybridLocation: SPAIN : España : Sant Cugat del Valles || SPAIN : España : Aigües de Vilaju ga || SPAIN : España : Barcelona || SPAIN : España : Coslada (Madrid) || SPAIN : España : Derio || SPAIN : España : En Remoto || SPAIN : España : En Remoto || SPAIN : España : Expat || SPAIN : España : Leioa || SPAIN : España : Mondragón (Arrasate) || SPAIN : España : Parets del Valles || SPAIN : España : Santa Cruz de Tenerife || SPAIN : España : Santiago Compostela || SPAIN : España : Sevilla || SPAIN : España : Torres de Cotillas || SPAIN : España : Valencia || SPAIN : España : Zaragoza:[[cust_building]]Learn more about Grifols

Tipo de Contrato: Temporal tiempo completoNúmero de solicitud de puesto: 544163¿Te gustaría unirte a un equipo internacional que trabaja para mejorar el futuro del sector de la salud? ¿Quieres contribuir a mejorar la vida de millones de personas? Grifols es una compañía global del sector de la salud que desde 1909 mejora la salud y el bienestar de las personas en todo el mundo. Somos líderes en medicamentos hemoderivados y medicina transfusional y desarrollamos, producimos y comercializamos medicamentos, soluciones y servicios innovadores en más de 110 países y regiones.Creamos que la diversidad aporta valor a nuestro negocio, a nuestros equipos y a nuestra cultura. Estamos comprometidos con la igualdad de oportunidades y nuestra misión es ofrecer un entorno inclusivo donde las diferencias sumen a nuestra compañía.Instituto Grifols es una empresa especializada en la investigación, desarrollo, producción de proteínas plasmáticas purificadas con propiedades terapéuticas que se obtienen a partir de fraccionamiento del plasma humano y en el área de Producción se precisa incorporar a un/a Operario/a de Fibrin Sealant.Cuáles serán tus responsabilidades- Realizarás la filtración y las cromatografías y UF.- Te encargarás de realizar determinaciones PH.- Te responsabilizarás de las filtración y centrifugación y limpieza de maquinaria.- Dispones de Bachillerato o CFGM con experiencia. Se valorará que tengas CFGM/CFGS rama Química o similar con experiencia en áreas de Producción dentro del sector Químico/Farmacéutico, con conocimientos de normativa GMP.- Tienes conocimientos de MS Office a nivel de usuario.- Horario: 12H, turnos rotativos.- Paquete de beneficios.Formar parte de Grifols significa la oportunidad de trabajar en un entorno de proyección internacional dónde se promueve la igualdad de oportunidades.Significa la oportunidad de desarrollarte profesionalmente, de disponer de formación continua y de integrarte en un equipo de profesionales en el que la aportación individual de cada uno cuenta. Nuestro compromiso es mantener un entorno que favorezca el desarrollo profesional de nuestros empleados en un buen ambiente de trabajo.El capital humano de Grifols es clave tanto en el desarrollo de las actividades como en el proceso de expansión de la compañía.Si estás interesado/a en crecer con nosotros y tu perfil encaja con esta oportunidad profesional, mándanos tu cv.Ubicación: SPAIN : España : Parets del Valles || SPAIN : España : Aigües de Vilajuïga || SPAIN : España : Barcelona || SPAIN : España : Coslada (Madrid) || SPAIN : España : Derio || SPAIN : España : En Remoto || SPAIN : España : En Remoto || SPAIN : España : Expat || SPAIN : España : Leioa || SPAIN : España : Mondragón (Arrasate) || SPAIN : España : Sant Cugat del Valles || SPAIN : España : Santa Cruz de Tenerife || SPAIN : España : Santiago Compostela || SPAIN : España : Sevilla || SPAIN : España : Torres de Cotillas || SPAIN : España : Valencia || SPAIN : España : Zaragoza : [[cust_building]]#J-18808-Ljbffr

Buenas habilidades de comunicación y resolución de problemas. Desarrollo profesional en ambiente internacional y multilingüe. Ofrecer soporte técnico/a y soluciones IT a usuarios/as que presenten algún problema relacionado con la informática a través de teléfono, e-mail o intranet.

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Es una oportunidad de formar parte de un proyecto con impacto directo en el crecimiento del negocio, donde tus ideas cuentan, los datos guían las decisiones y cada acción tiene resultados visibles. Las personas que concurran a los procesos de selección y evaluación serán valoradas en base a los

Buenas habilidades de comunicación y resolución de problemas. Seleccionamos varios perfiles de agente Service Desk con francés e inglés para incorporación inmediata. Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbr