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Adeas Hr busca un EXPERTO DE PROCESOS (Compounding) para liderar, transferir y poner en marcha procesos estériles de producción en una multinacional farmacéutica con foco en GMP y FDA. Coordinará lotes técnicos, media fills y actividades de transferencia, asegurando cumplimiento y documentación GMP durante todo el proyecto. El candidato ideal tiene 5+ años en industria farmacéutica, experiencia en transferencia de tecnología, y dominio de MES/SAP/Track Wise. #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.The PositionAbout The RoleAs a Technical Lead Assay Development, you will steer complex, global, and cross-functional diagnostic projects with significant strategic impact and risk potential. You will provide technical leadership to a laboratory team, applying deep scientific expertise to advance core lab technology assay development. In this role, you will analyze R&D results, champion new diagnostic innovations, drive agile cross-functional collaboration, and pioneer creative solutions beyond conventional approaches. In this role, your work will be focused on the Elecsys/cobas e instrument platform.Key ResponsibilitiesProject Leadership & Technical Steering (40%): Lead and drive technical development within complex, global cross-functional projects involving intricate interface management and long-term strategic impacts. Participate in program and agile ceremonies, collaborate with Product Owners on schedules, and hold accountability for technical PI planning contributionsTeam Leadership & Scientific Expertise (20%): Provide technical guidance to a laboratory team and support the development of IVD assays and assay components. Define the competence standards required for operational success and align requirements with team leadsDecision Support & Risk Management (10%): Prepare data-driven analyses and information to facilitate key decision-making while assessing and interpreting product and project risksInnovation & Continuous Improvement (10%): Monitor emerging trends and technologies in the diagnostic field, proposing applications for IVD solutions and fostering technical growth within agile teamsStakeholder Collaboration & Networking (10%): Build strong partnerships across internal departments and external collaborators. Help build a vibrant Technical Lead community across functional customer areasResults Analysis & Scientific Dissemination (5%): Analyze and interpret R&D outcomes, present findings to key functional committees, and support academic/scientific publicationsInnovative Problem Solving (5%): Independently design and execute innovative solutions outside of established frameworksQualifications & RequirementsEducation & ExperienceEducation: Master's degree with 5-7 years of professional experience in developing diagnostic solutions, OR a PhD in Biochemistry or a closely related scientific fieldTechnical Experience: Demonstrated experience in assay development or in-vitro diagnostic (IVD) solution design, alongside experience in technical supervision/mentorshipMatrix Leadership: Experience providing technical direction within complex matrix organizational structuresLanguages: Business fluent in English (written and spoken)Specialist Knowledge & Core CompetenciesDeep expertise in IVD assay development and technical solution architectureAdvanced scientific, analytical, and complex problem-solving capabilitiesStrong technical stakeholder management, dependency management, and cross-functional alignment skillsProven communication, presentation, and task delegation skillsStrategic mindset with the ability to make timely, well-reasoned decisions under uncertaintyOpenness to agile ways of working and cultural transformationOpenness to travel within Europe on a regular basis particularly during the on-boardingWho we areA healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.Let's build a healthier future, together. Roche is an Equal Opportunity Employer.#J-18808-Ljbffr

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA.Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L.The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do:Providing cutting-edge end-to-end services.Offering extensive expertise in biologics.We are looking for a new person to join the team as a DSP Manufacturing Team Leader in our brand new facilities in Sant Quirze del Vallès:MAIN RESPONSIBILITIES:Team Leadership & Development: Supervise and guide DSP technicians and engineers, promoting continuous professional growth through training and problem-solving support.Encourage proactive communication within the team and with other departments to resolve operational issues.DSP Project Management & Cross-Department Collaboration: Plan, coordinate, and execute downstream processing projects, ensuring quality, timelines, and efficiency while collaborating with R&D, QA, QC, and MSAT teams during tech transfers.Manage the integration of new processes or modifications to existing ones, ensuring successful implementation and validation.Process Optimization & Protocol Development: Develop and implement improvements in protein purification processes (centrifugation, filtration, chromatography), and create standardized protocols to enhance yield and reproducibility.Use data-driven approaches to identify process bottlenecks, implement corrective actions, and drive continuous improvements in throughput, yield, and product purity.Regulatory Compliance and Quality Standards: Ensure all DSP operations comply with GMP regulatory standards, maintaining the highest quality and safety in all processes.Regularly review and update standard operating procedures (SOPs) to stay current with evolving industry regulations, internal best practices, and audit findings.Ensure that all data, from batch records to test results, is accurately documented, and that all documentation meet regulatory and quality requirements.Performance Monitoring & Resource Management: Monitor KPIs (e.G., protein yield, cycle time, cost), manage resource allocation effectively, and ensure availability of required equipment to optimize operations.Ensure the availability and functionality of required equipment and reagents, overseeing maintenance schedules and troubleshooting issues in collaboration with the maintenance team.REQUIREMENTS:Bachelor’s degree in biotechnology, Biology, Chemistry, Chemical Engineering, or related fields and master’s degree or specialization in areas related to bioprocessing, protein engineering, or biotechnology.At least 5 years of experience in a GMP manufacturing environment, with a minimum of 2 years in a leadership or supervisory role in downstream processing (DSP) and protein purification.Solid experience in purification techniques such as chromatography, filtration, centrifugation, and other separation techniques.Familiarity with laboratory and production equipment used in DSP, including its operation and maintenance and experience in process optimization and troubleshooting technical issues during purification processes.Knowledge of Good Manufacturing Practices (GMP) principles, regulations, and quality standards in the pharmaceutical or biotechnology industry.Ability to plan, coordinate, and execute DSP projects while ensuring adherence to timelines, costs, and quality standards.Knowledge and experience in regulatory compliance with international standards (FDA, EMA, etc.), particularly within GMP production environments.Fluency in English (both written and spoken) is required, as most technical documentation and regulatory standards are in English.Flexibility in working hours may be needed to accommodate project timelines and cross-departmental collaboration.#J-18808-Ljbffr

Umi vale Activa , mutua colaboradora de la Seguridad Social que garantiza el asesoramiento a las empresas y la asistencia a la protección de los/as trabajadores/as, precisa un/a Graduado/a o Licenciado/a en Medicina. De entre otras, y en dependencia directa del responsable de área se encargará de las siguientes funciones: Asistenciales Asistencia médica de urgencia y programada en consulta de AT. Recepción del paciente (anamnesis, evolución y seguimiento). Determinación de contingencia. Exploración según protocolos y pruebas complementarias. Diagnóstico, aplicación y seguimiento del tratamiento. Valoración capacidad funcional. Gestión Bajas, Altas, HAD (Pdx, remisión a especialistas, RHB, Psicología, IQ). Incomparecencias. Propuestas de alta de incapacidad, conformidad pagos directos, ATRIUM, informes médicos (paciente o INSS) e información de enfermedades profesionales. Consentimientos firmados. Control de procesos de centros concertados. Control telefónico (delegada). Atención telefónica de consultas, llamadas a SME y relaciones con organismos públicos (INSS, Inspección). Colaborar en procedimientos judiciales. Recomendaciones buenos hábitos de salud que procedan. RX, conservar material y equipos sanitarios. Programación gestión trabajo (agenda y de citas, correo), informar actuaciones en NEOS, revisión y supervisión bajas activas, colaboración en métodos de trabajo, control gasto asistencial, colaboración lucha contra el fraude. Horario Jornada completa. De lunes a viernes, turnos rotativos de mañanas y tardes (8h-15h y 13h-20h), más doblajes (8h-20h) para coberturas de vacaciones, formación e imprevistos. #J-18808-Ljbffr

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, m RNA and p DNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, m RNA and p DNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000 L, another for microbial and yeast up to 1000 L, and a third are for m RNA up to 50 L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: Providing cutting-edge end-to-end services. Offering extensive expertise in biologics. We are looking for a new person to join the team as a DSP Manufacturing Team Leader in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: Team Leadership & Development: Supervise and guide DSP technicians and engineers, promoting continuous professional growth through training and problem-solving support. Encourage proactive communication within the team and with other departments to resolve operational issues. DSP Project Management & Cross-Department Collaboration: Plan, coordinate, and execute downstream processing projects, ensuring quality, timelines, and efficiency while collaborating with R&D, QA, QC, and MSAT teams during tech transfers. Manage the integration of new processes or modifications to existing ones, ensuring successful implementation and validation. Process Optimization & Protocol Development: Develop and implement improvements in protein purification processes (centrifugation, filtration, chromatography), and create standardized protocols to enhance yield and reproducibility. Use data-driven approaches to identify process bottlenecks, implement corrective actions, and drive continuous improvements in throughput, yield, and product purity. Regulatory Compliance and Quality Standards: Ensure all DSP operations comply with GMP regulatory standards, maintaining the highest quality and safety in all processes. Regularly review and update standard operating procedures (SOPs) to stay current with evolving industry regulations, internal best practices, and audit findings. Ensure that all data, from batch records to test results, is accurately documented, and that all documentation meet regulatory and quality requirements. Performance Monitoring & Resource Management: Monitor KPIs (e.G., protein yield, cycle time, cost), manage resource allocation effectively, and ensure availability of required equipment to optimize operations. Ensure the availability and functionality of required equipment and reagents, overseeing maintenance schedules and troubleshooting issues in collaboration with the maintenance team. REQUIREMENTS: Bachelor’s degree in biotechnology, Biology, Chemistry, Chemical Engineering, or related fields and master’s degree or specialization in areas related to bioprocessing, protein engineering, or biotechnology. At least 5 years of experience in a GMP manufacturing environment, with a minimum of 2 years in a leadership or supervisory role in downstream processing (DSP) and protein purification. Solid experience in purification techniques such as chromatography, filtration, centrifugation, and other separation techniques. Familiarity with laboratory and production equipment used in DSP, including its operation and maintenance and experience in process optimization and troubleshooting technical issues during purification processes. Knowledge of Good Manufacturing Practices (GMP) principles, regulations, and quality standards in the pharmaceutical or biotechnology industry. Ability to plan, coordinate, and execute DSP projects while ensuring adherence to timelines, costs, and quality standards. Knowledge and experience in regulatory compliance with international standards (FDA, EMA, etc.), particularly within GMP production environments. Fluency in English (both written and spoken) is required, as most technical documentation and regulatory standards are in English. Flexibility in working hours may be needed to accommodate project timelines and cross-departmental collaboration. #J-18808-Ljbffr

Se busca médico con formación en pediatría para incorporarse en Xàtiva (Valencia). El puesto consiste en atender a pacientes en edad infantil, realizar valoraciones clínicas, hacer seguimiento de su evolución y coordinarse con el resto del equipo sanitario para ofrecer una atención adecuada. El horario establecido es de 8:00 a 15:00 horas. El contrato es de tipo temporal y la jornada es completa. La persona seleccionada desarrollará su actividad en consulta, manteniendo un trato cercano con las familias y garantizando en todo momento una asistencia responsable y adaptada a las necesidades de cada menor. Se valorará la capacidad de comunicación, la organización y el trabajo en equipo en un entorno sanitario dinámico.

¿Buscas trabajo en salud y bienestar? Este mes de octubre surgen nuevas oportunidades para enfermería y medicina en Xàtiva. ¡Inscríbete gratis hoy mismo!

Se busca médico para cubrir urgencias hospitalarias en Xàtiva (Valencia), con atención continuada y guardias. El puesto requiere disponibilidad para trabajar en turnos que incluyen fines de semana, garantizando así la cobertura asistencial necesaria en todo momento. El contrato es de tipo temporal, a jornada completa, bajo una modalidad contractual de otros contratos. La persona seleccionada se integrará en el servicio de urgencias para atender las necesidades asistenciales que se presenten durante el turno. Se valorará la capacidad de adaptación a distintos horarios y la disposición para asumir guardias. El entorno de trabajo exige compromiso y responsabilidad en la atención al paciente, así como coordinación con el resto del equipo sanitario.

• Assistència a les persones residents en les activitats de la vida diària que no puguin realitzar per si mateixes i efectuar aquelles tasques encaminades a la seva atenció personal i del seu entorn- Col·laboraració amb la infermeria, si escau, en la distribució de la medicació, presa de constants, mesurament de diüresi, preparació d'elements per a anàlisis, vigilància de les sondes, cures i qualsevol altra tasca o cura que requereixi- Comunicació al seu immediat superior i emplenar tots els registres derivats de l'atenció als usuaris complint amb els protocols assistencials i pautes mostrades en el full d'auxiliars/HAI Permisos de conduir: b. espanyol (parlat Superior, escrit Superior), català (parlat Superior, escrit Superior)

Leanbio SL in Spain is seeking a DSP Manufacturing Team Leader for our new Sant Quirze del Vallès facility. You will supervise DSP technicians and engineers, drive process development, and ensure safe, compliant production of therapeutic biologics across mammalian, microbial and m RNA processes. The role requires 5+ years in GMP manufacturing with leadership, expertise in chromatography, filtration, centrifugation, and strong collaboration with R&D, QA, QC and MSAT. #J-18808-Ljbffr

Se busca cubrir un puesto de terapia ocupacional en L'Olleria para desarrollar tareas dentro del plan general de actividades de un centro. Entre las funciones principales están participar en actividades auxiliares de psicomotricidad, lenguaje, dinámicas y rehabilitación personal y social de los residentes, así como colaborar en el seguimiento o la evaluación de su proceso recuperador o asistencial. También se incluye la participación en las áreas de ocio y tiempo libre, y la colaboración en programas de formación e información dirigidos a las familias y a las instituciones. Además, la persona seleccionada realizará todas aquellas actividades relacionadas con lo anterior que le sean solicitadas. Es necesario contar con titulación universitaria en terapia ocupacional. Se valorará experiencia previa en residencias de la tercera edad. Las condiciones del puesto incluyen contrato indefinido, jornada completa y horario partido de lunes a viernes.

Fundada en 2017 en Barcelona, Innovamat cuenta con 31000 docentes de más de 3300 centros educativos de España, Estados Unidos, México, Italia, Chile, Ecuador, Colombia, Brasil y Perú, que hacen que más de 720000 alumnos aprendan matemáticas fomentando la comprensión profunda y el desarrollo c

Fundada en 2017 en Barcelona, Innovamat cuenta con 31000 docentes de más de 3300 centros educativos de España, Estados Unidos, México, Italia, Chile, Ecuador, Colombia, Brasil y Perú, que hacen que más de alumnos aprendan matemáticas fomentando la comprensión profunda y el desarrollo competen

Innovamat Education, SL busca un perfil fullstack orientado a producto para unirse al equipo Editorial Tech. Trabajarás en herramientas internas y flujos de creación, colaborando con múltiples equipos para acelerar proyectos y mejorar la calidad educativa de nuestras soluciones. Se valorará experiencia integrando IA y LLMs, pensamiento crítico, y capacidad para traducir necesidades de stakeholders en soluciones prácticas, en un entorno internacional en crecimiento. #J-18808-Ljbffr

Se busca psicólogo o psicóloga clínica para incorporación en Xàtiva (Valencia). Es imprescindible contar con la especialidad en Psicología Clínica (P.I.R) para poder desempeñar las funciones propias del puesto dentro del ámbito sanitario. La jornada será completa, con horario de 8:00 a 15:00 horas. El contrato será de tipo temporal y la modalidad contractual se encuadra dentro de otros contratos. Se valorará la capacidad de trabajo en equipo, la responsabilidad y la implicación en el desarrollo de las tareas clínicas diarias. Las personas interesadas deben adjuntar su currículum para completar el proceso de selección.

Seeking a caregiver for a full-time substitution role in a nursing home, assisting elderly residents with daily activities and promoting their autonomy.

CELO is seeking a Martech Manager to evolve and connect the marketing technology stack, including Magnolia CMS, Prestashop, Shopify, Hub Spot and Zapier, plus custom or third-party tools. You will own end-to-end web projects, coordinating internal teams and external providers to deliver robust digital solutions. You will optimize Hub Spot workflows, implement technical SEO, manage budgets for tools and integrations, and document and test new solutions. #J-18808-Ljbffr

Se busca enfermero o enfermera con formación específica en salud mental para incorporarse mediante un contrato temporal a jornada completa en Xàtiva (Valencia). La persona seleccionada desarrollará su labor en un entorno sanitario, atendiendo a pacientes que requieren cuidados especializados en el ámbito de la salud mental. Entre las funciones principales se encuentran la valoración y seguimiento de los usuarios, la administración de tratamientos, la elaboración de informes clínicos y la coordinación con el resto del equipo asistencial. Es imprescindible contar con la titulación correspondiente y capacidad para trabajar de forma organizada y cercana con los pacientes. La categoría profesional asociada a este puesto corresponde al nivel máximo dentro del equipo, lo que implica asumir responsabilidades de supervisión y apoyo al personal. Se valora la experiencia previa en contextos similares y la disponibilidad para incorporación ágil.

¿Buscas trabajo en salud y bienestar? Este mes de octubre surgen nuevas oportunidades para psicología en Xàtiva. ¡Inscríbete gratis hoy mismo!

KLINEA Biotech & Pharma Engineering busca un Project Manager para liderar proyectos de ingeniería farmacéutica.Serás responsable de cumplir objetivos de funcionalidad, costo, cronograma y alcance, asegurando cumplimiento de normativas y estándares de seguridad y medio ambiente.El profesional

¿Buscas trabajo en ayuda a la dependencia? Este mes de octubre surgen nuevas oportunidades para trabajadores y educadores sociales en Xàtiva. ¡Inscríbete gratis hoy mismo!

Lavado, planchado, organización y cuidado de la ropa. Apoyo en el cuidado de nuestra hija de 4 años.

Caring for animals in natural reserves or zoos, including cleaning, feeding, administering medication, and customer interaction.

Buscas trabajo en servicio doméstico? Este mes de octubre surgen nuevas oportunidades para cuidado de niños en Ronda.

Manager Senior de Seguridad y Salud de Centro Logístico, Health and Safety M/F En Amazon, necesitamos personas con talento y experiencia que nos ayuden a operar de forma segura y eficiente.Como Senior Responsable de Workplace Health and Safety (WHS), tu función es clave para impulsar mejoras estra