China jobs in Cerdanyola Del VallèsCreate job alerts

Como parte de nuestra estrategia de crecimiento internacional, buscamos un Business Development & Project Manager – Automotive Lighting, con un enfoque principal en reforzar nuestra presencia en China, al mismo tiempo que da soporte al desarrollo de negocio y a proyectos de clientes en otros merca

Tucai Group, está considerada como uno de los principales fabricantes de flexibles de conexión y válvulas para aplicaciones de gas, agua y combustible, con certificaciones reconocidas a nivel mundial y plantas en España, Bulgaria, China y Vietnam.La posición estará basada en nuestras oficinas

The Lancet Primary Care is seeking an in-house Senior Editor to oversee the creation and publication of original material for our online journal. Location options include London, Barcelona, India or China, with hybrid work from home and office. You will manage submissions and peer review, build global relationships, and contribute editorials. Applicants should have an MD/PhD or equivalent editorial experience, and embrace diversity in a collaborative environment. #J-18808-Ljbffr

Ayer Ofrecemos London Wall Madrid Shanghai_Tianshan Barcelona Chennai Guangdong_Kerry Plaza Beijing Full time R In-house Senior Editor (Maternity cover) Do you enjoy using science to drive change in the world? Join the team shaping The Lancet's gold open access primary care journal Location: London, Barcelona, India or China About our Team The Lancet Primary Care is part of The Lancet's family of world-renowned medical journals committed to publishing the best science for better lives. We handle high-quality research, reviews, and commentaries to drive thought leadership across all aspects of Primary care. We build solid relationships with research communities to ensure we offer, exciting, interesting and thought-provoking content. As an in-house Senior Editor, you will oversee the creation and publication of original material for our online journal. You will take ownership of overseeing submissions and performing quality peer review to ensure we publish high-quality content. You will build global relationships with experts in the community to disseminate and discuss practice-changing results from the field. At the Lancet we are deeply committed to fostering an inclusive environment. In our pursuit of excellence, we recognise the strength in varied perspectives, experiences, and backgrounds. As part of our ongoing efforts to enhance the diversity of our editorial team, we welcome applications from individuals who bring unique skills and perspectives to the role. • Managing peer review of high-quality research papers, and commissioning authors to ensure the successful production of new and engaging articles, • Developing and maintaining relationships with our global primary care community to attract high-quality research for the journal, • Attending conferences and events to represent the journal, keeping up to date with current developments in primary care and identifying potential topics of interest, • Writing editorials and other content for the journal as required., • Helping develop new initiatives for future development of the journal, • An MD or PhD with postdoctoral experience in a relevant subject, or, a postgraduate higher degree in a relevant discipline plus substantial editorial experience at a senior level on a peer reviewed STM journal, • Ability to demonstrate thorough knowledge of biological and medical sciences and broader social issues pertaining to Primary care, • Ability to engage and build relationships with external stakeholders, including medical and research professionals, a range of internal teams, and members of the media, • Excellent organisational skills and the ability to work efficiently to demanding press deadlines, • Excellent command of the English language and the ability to write in an engaging and interesting manner, • Proficiency with IT systems including MS Office, • Working remotely from home and at our office in a hybrid working style, • Working flexible hours - flexing the times you work in the day We are an equal opportunity employer with a commitment to help you succeed. Here, you will find an inclusive, agile, collaborative, innovative, and fun environment, where everyone has a part to play. Regardless of the team you join, we promote a diverse environment with co-workers who are passionate about what they do and how they do it. • Generous holiday allowance with the option to buy additional days, • Health screening, eye care vouchers and private medical benefits, • Wellbeing programs, • Life assurance, • Access to a competitive contributory pension scheme, • Long service awards, • Save As You Earn share option scheme, • Travel Season ticket loan, • Maternity, paternity, and shared parental leave, • Access to emergency care for both the elderly and children, • RECARES days, giving you time to support the charities and causes that matter to you, • Access to employee resource groups with dedicated time to volunteer, • Access to extensive learning and development resources, • Access to employee discounts via Perks at Work A global leader in information and analytics, we help researchers and healthcare professionals advance science and improve health outcomes for the benefit of society. Building on our publishing heritage, we combine quality information and vast data sets with analytics to support visionary science and research, health education and interactive learning, as well as exceptional healthcare and clinical practice. At Elsevier, your work contributes to the world's grand challenges and a more sustainable future. We harness innovative technologies to support science and healthcare to partner for a better world. If performed in any of the following locations: Barcelona, Madrid, Home Based - Madrid, Home Based - Barcelona, the base pay range is 38,300 - 63,600. This job may be subject to a collective labor agreement in Spain. Please consult with the hiring team for further details. We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. We are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our Applicant Request Support Form or please contact . We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law. USA Job Seekers: EEO Know Your Rights. RELX is a global provider of information-based analytics and decision tools for professional and business customers, enabling them to make better decisions, get better results and be more productive. Our purpose is to benefit society by developing products that help researchers advance scientific knowledge; doctors and nurses improve the lives of patients; lawyers promote the rule of law and achieve justice and fair results for their clients; businesses and governments prevent fraud; consumers access financial services and get fair prices on insurance; and customers learn about markets and complete transactions. Our purpose guides our actions beyond the products that we develop. It defines us as an company. Every day across RELX our employees are inspired to undertake initiatives that make unique contributions to society and the communities in which we operate. #J-18808-Ljbffr

Headquartered in Barcelona, we are a global pharmaceutical company with affiliates in Spain, Portugal, Italy, Germany, France, the UK, and the USA, as well as world-class production sites in Mexico and China supporting our global CMO business.

Demand Planner Applylocations: China-Remote Location-Shanghai: Spain-Barcelona: Germany-Waldbronn: Japan-Remote Location: China-Remote Location-Chengdutime type: Full timeposted on: Posted Todayjob requisition id: 4039205## Job DescriptionIntegrated Business Planning (IBP) brings together fo

Develop and execute Quantum Makers' promotion strategy in China, including WeChat promotion and Bilibili audience engagement, to grow brand awareness. Business development capability to identify and develop commercial opportunities in China Good understanding of Chinese Social Media High level

Alexion, based in Barcelona, seeks a GVAP China Strategic Access Lead to drive innovative access solutions for rare diseases in China, collaborating with AZ China and global teams to shape market access and pricing strategies. You will build cross-functional capabilities, engage payers and governmen

Importante Multinacional Farmacéutica, situada en Sant Cugat del Vallés precisa incorporar a su equipo: Como parte de la estructura de Operaciones de Calidad y reportando directamente al responsable del grupo de QA Shopfloor – Aseptic , el/la QA Compliance Officer – Aseptic será responsable de apoyar los procesos de toma de decisiones relacionados con los requisitos de calidad durante las fases de diseño y operación rutinaria de los procesos de Dispensing (dispensación), Compounding (preparación/formulación), Filling (llenado) y de los equipos auxiliares asociados al proyecto. • Apoyar la toma de decisiones relativas a los requisitos de calidad durante las fases de diseño, cualificación, validación y operación rutinaria de los procesos de Dispensing, Compounding, Filling y de los equipos auxiliares, incluida la integración de maquinaria., • Proporcionar supervisión de Aseguramiento de la Calidad (QA) en las operaciones de fabricación aséptica, garantizando el cumplimiento de los requisitos GMP y de los estándares internos de calidad., • Proporcionar soporte de QA en planta (shopfloor), evaluando incidentes de calidad y riesgos asociados al producto, y acordando con las funciones implicadas las medidas inmediatas de contención o corrección., • Liderar las investigaciones de desviaciones de fabricación y eventos de calidad, incluyendo la evaluación inicial, el análisis de causa raíz, la evaluación de recurrencia e impacto, la definición de medidas inmediatas de contención y acciones correctivas, la gestión de CAPA y su cierre dentro de los plazos establecidos., • Participar en la elaboración, revisión o aprobación de la documentación derivada de las decisiones tomadas durante las fases de diseño del proyecto, como justificaciones técnicas (rationales) y análisis de riesgos., • Garantizar el cumplimiento de las cGMP y de los requisitos regulatorios aplicables (FDA, EMA, China, Japón, etc.) en toda la documentación y los flujos de trabajo asociados., • Colaborar con los departamentos de Operaciones, Ingeniería, Validación y otras funciones para impulsar la excelencia en materia de calidad y mejorar el rendimiento operativo., • Titulación universitaria en Química, Bioquímica, Biología, Microbiología, Farmacia o un campo equivalente., • Es imprescindible contar con un mínimo de 5 años de experiencia en procesos asépticos y APS (Anexo I de las GMP de la UE, Guía FDA 2004 para la Industria, etc.)., • Se valorará positivamente la experiencia con productos combinados (por ejemplo, jeringa + autoinyector o PEN). #J-18808-Ljbffr