Trabajos cafeteria en en Campo OlivarCrear alertas

In a nutshell Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. Position: Senior QA Specialist Location: Valencia (on-site) Experience: 3-5 years of experience in Quality Assurance within the pharmaceutical industry Want to know more? Are you looking to take the next step in your Quality Assurance career in a demanding, dynamic pharmaceutical environment focused on excellence? At BioNanopharma, we are looking for a Senior QA Specialist to play a key role in quality oversight, regulatory compliance, and continuous improvement across our operations. If you have experience in GMP-regulated environments, enjoy working with technical rigor, and are motivated by collaborating across teams to ensure the highest quality standards, we would love to hear from you. Your mission will be to actively support the effective execution and oversight of Quality Assurance activities, contributing to the maintenance of the Quality Management System, documentation management, deviation handling, CAPA follow-up, audit readiness, and regulatory compliance. In addition, you may support Deputy QP-related activities when required. What are we looking for? We are looking for a professional with solid experience in Quality Assurance, a strong compliance mindset, analytical capabilities, and a continuous improvement approach. We want someone who combines quality vision, attention to detail, cross-functional collaboration, and commitment to both regulatory and business standards. The challenge! Support the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) in line with GMP requirements and internal procedures. Manage and maintain QA documentation, including SOPs, work instructions, templates, records, and other controlled documents. Review quality records and provide quality oversight of manufacturing and associated operations. Ensure compliance with approved procedures and applicable regulatory requirements. Participate in the management of deviations, incidents, non-conformities, change controls, and CAPAs. Support investigations, root cause analysis, and follow-up of corrective and preventive actions. Support the preparation, coordination, and follow-up of internal audits, external audits, customer audits, and regulatory inspections. Monitor compliance with applicable pharmaceutical regulations, GMP standards, and internal quality policies. Collaborate cross-functionally to ensure quality requirements are integrated into daily operations and decision-making. Support the design and delivery of training related to GMP, quality procedures, and compliance standards. Contribute to the monitoring of quality KPIs and continuous improvement initiatives within the QA area. Support Deputy QP-related activities when required, according to qualification, business needs, and the applicable regulatory framework. What do you need? ~ University degree in Pharmacy, Chemistry, Biotechnology, Health Sciences, or a related field. ~3-5 years of experience in Quality Assurance within the pharmaceutical industry. ~ Previous experience in GMP-regulated manufacturing environments. ~ Solid knowledge of Quality Management Systems (QMS). ~ Experience in quality documentation management. ~ Knowledge of deviations, CAPAs, change controls, and non-conformities. ~ Experience supporting audits, inspections, and inspection readiness. ~ Knowledge of root cause analysis and pharmaceutical QA operations. ~ Fluent Spanish and English. ~ Knowledge of or exposure to Deputy QP responsibilities will be highly valued. ~ FDA knowledge is a plus. What do we value in you? Customer centricity Speed with quality Adaptability to change and flexibility Innovation Leadership and teamwork Effective communication Growth mindset Business orientation Compliance, integrity, and sustainability We also expect you to: Act with a strong quality and compliance mindset in all activities. Demonstrate rigor, accuracy, and discipline in documentation and QA processes. Collaborate effectively with cross-functional stakeholders. Escalate quality risks and compliance concerns in a timely and constructive manner. Balance operational agility with quality and regulatory requirements. Show accountability, ownership, and reliability in assigned responsibilities. Promote continuous improvement, integrity, and teamwork across the organization. Our benefits! Permanent contract Flexible working hours Free on-site cafeteria On-site parking Professional development and continuous training What’s the selection process like? ~ Initial contact by phone or email. ~1 or 2 interviews (on-site/virtual) with HR and the Technical Management team. ~ Ongoing communication about your application status. Do you think this role is not for you? If this opportunity is not the right fit for you at the moment, we encourage you to stay tuned for future opportunities at BioNanoPharma and share this role with people in your network who may be interested. xcskxlj EQUAL OPPORTUNITIES COMMITMENT At BioNanoPharma, we are committed to fostering an inclusive and diverse workplace and to providing equal opportunities for all candidates. We do not discriminate on the basis of gender, gender identity or expression, ethnicity, nationality, religion, sexual orientation, disability, age, or any other characteristic protected by applicable law.

In a nutshell ¿Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en "Solicitar". Position: Senior QA Specialist Location: Valencia (on-site) Experience: 3-5 years of experience in Quality Assurance within the pharmaceutical industry Want to know more? Are you looking to take the next step in your Quality Assurance career in a demanding, dynamic pharmaceutical environment focused on excellence? At BioNanopharma, we are looking for a Senior QA Specialist to play a key role in quality oversight, regulatory compliance, and continuous improvement across our operations. If you have experience in GMP-regulated environments, enjoy working with technical rigor, and are motivated by collaborating across teams to ensure the highest quality standards, we would love to hear from you. Your mission will be to actively support the effective execution and oversight of Quality Assurance activities, contributing to the maintenance of the Quality Management System, documentation management, deviation handling, CAPA follow-up, audit readiness, and regulatory compliance. In addition, you may support Deputy QP-related activities when required. What are we looking for? We are looking for a professional with solid experience in Quality Assurance, a strong compliance mindset, analytical capabilities, and a continuous improvement approach. We want someone who combines quality vision, attention to detail, cross-functional collaboration, and commitment to both regulatory and business standards. The challenge! Support the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) in line with GMP requirements and internal procedures. Manage and maintain QA documentation, including SOPs, work instructions, templates, records, and other controlled documents. Review quality records and provide quality oversight of manufacturing and associated operations. Ensure compliance with approved procedures and applicable regulatory requirements. Participate in the management of deviations, incidents, non-conformities, change controls, and CAPAs. Support investigations, root cause analysis, and follow-up of corrective and preventive actions. Support the preparation, coordination, and follow-up of internal audits, external audits, customer audits, and regulatory inspections. Monitor compliance with applicable pharmaceutical regulations, GMP standards, and internal quality policies. Collaborate cross-functionally to ensure quality requirements are integrated into daily operations and decision-making. Support the design and delivery of training related to GMP, quality procedures, and compliance standards. Contribute to the monitoring of quality KPIs and continuous improvement initiatives within the QA area. Support Deputy QP-related activities when required, according to qualification, business needs, and the applicable regulatory framework. What do you need? ~ University degree in Pharmacy, Chemistry, Biotechnology, Health Sciences, or a related field. ~3-5 years of experience in Quality Assurance within the pharmaceutical industry. ~ Previous experience in GMP-regulated manufacturing environments. ~ Solid knowledge of Quality Management Systems (QMS). ~ Experience in quality documentation management. ~ Knowledge of deviations, CAPAs, change controls, and non-conformities. ~ Experience supporting audits, inspections, and inspection readiness. ~ Knowledge of root cause analysis and pharmaceutical QA operations. ~ Fluent Spanish and English. ~ Knowledge of or exposure to Deputy QP responsibilities will be highly valued. ~ FDA knowledge is a plus. What do we value in you? Customer centricity Speed with quality Adaptability to change and flexibility Innovation Leadership and teamwork Effective communication Growth mindset Business orientation Compliance, integrity, and sustainability We also expect you to: Act with a strong quality and compliance mindset in all activities. Demonstrate rigor, accuracy, and discipline in documentation and QA processes. Collaborate effectively with cross-functional stakeholders. Escalate quality risks and compliance concerns in a timely and constructive manner. Balance operational agility with quality and regulatory requirements. Show accountability, ownership, and reliability in assigned responsibilities. Promote continuous improvement, integrity, and teamwork across the organization. Our benefits! Permanent contract Flexible working hours Free on-site cafeteria On-site parking Professional development and continuous training What’s the selection process like? ~ Initial contact by phone or email. ~1 or 2 interviews (on-site/virtual) with HR and the Technical Management team. ~ Ongoing communication about your application status. Do you think this role is not for you? If this opportunity is not the right fit for you at the moment, we encourage you to stay tuned for future opportunities at BioNanoPharma and share this role with people in your network who may be interested. xcskxlj EQUAL OPPORTUNITIES COMMITMENT At BioNanoPharma, we are committed to fostering an inclusive and diverse workplace and to providing equal opportunities for all candidates. We do not discriminate on the basis of gender, gender identity or expression, ethnicity, nationality, religion, sexual orientation, disability, age, or any other characteristic protected by applicable law.

In a nutshell Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. Position: Senior QA Specialist Location: Valencia (on-site) Experience: 3-5 years of experience in Quality Assurance within the pharmaceutical industry Want to know more? Are you looking to take the next step in your Quality Assurance career in a demanding, dynamic pharmaceutical environment focused on excellence? At BioNanopharma, we are looking for a Senior QA Specialist to play a key role in quality oversight, regulatory compliance, and continuous improvement across our operations. If you have experience in GMP-regulated environments, enjoy working with technical rigor, and are motivated by collaborating across teams to ensure the highest quality standards, we would love to hear from you. Your mission will be to actively support the effective execution and oversight of Quality Assurance activities, contributing to the maintenance of the Quality Management System, documentation management, deviation handling, CAPA follow-up, audit readiness, and regulatory compliance. In addition, you may support Deputy QP-related activities when required. What are we looking for? We are looking for a professional with solid experience in Quality Assurance, a strong compliance mindset, analytical capabilities, and a continuous improvement approach. We want someone who combines quality vision, attention to detail, cross-functional collaboration, and commitment to both regulatory and business standards. The challenge! Support the implementation, maintenance, and continuous improvement of the Quality Management System (QMS) in line with GMP requirements and internal procedures. Manage and maintain QA documentation, including SOPs, work instructions, templates, records, and other controlled documents. Review quality records and provide quality oversight of manufacturing and associated operations. Ensure compliance with approved procedures and applicable regulatory requirements. Participate in the management of deviations, incidents, non-conformities, change controls, and CAPAs. Support investigations, root cause analysis, and follow-up of corrective and preventive actions. Support the preparation, coordination, and follow-up of internal audits, external audits, customer audits, and regulatory inspections. Monitor compliance with applicable pharmaceutical regulations, GMP standards, and internal quality policies. Collaborate cross-functionally to ensure quality requirements are integrated into daily operations and decision-making. Support the design and delivery of training related to GMP, quality procedures, and compliance standards. Contribute to the monitoring of quality KPIs and continuous improvement initiatives within the QA area. Support Deputy QP-related activities when required, according to qualification, business needs, and the applicable regulatory framework. What do you need? ~ University degree in Pharmacy, Chemistry, Biotechnology, Health Sciences, or a related field. ~3-5 years of experience in Quality Assurance within the pharmaceutical industry. ~ Previous experience in GMP-regulated manufacturing environments. ~ Solid knowledge of Quality Management Systems (QMS). ~ Experience in quality documentation management. ~ Knowledge of deviations, CAPAs, change controls, and non-conformities. ~ Experience supporting audits, inspections, and inspection readiness. ~ Knowledge of root cause analysis and pharmaceutical QA operations. ~ Fluent Spanish and English. ~ Knowledge of or exposure to Deputy QP responsibilities will be highly valued. ~ FDA knowledge is a plus. What do we value in you? Customer centricity Speed with quality Adaptability to change and flexibility Innovation Leadership and teamwork Effective communication Growth mindset Business orientation Compliance, integrity, and sustainability We also expect you to: Act with a strong quality and compliance mindset in all activities. Demonstrate rigor, accuracy, and discipline in documentation and QA processes. Collaborate effectively with cross-functional stakeholders. Escalate quality risks and compliance concerns in a timely and constructive manner. Balance operational agility with quality and regulatory requirements. Show accountability, ownership, and reliability in assigned responsibilities. Promote continuous improvement, integrity, and teamwork across the organization. Our benefits! Permanent contract Flexible working hours Free on-site cafeteria On-site parking Professional development and continuous training What’s the selection process like? ~ Initial contact by phone or email. ~1 or 2 interviews (on-site/virtual) with HR and the Technical Management team. ~ Ongoing communication about your application status. Do you think this role is not for you? If this opportunity is not the right fit for you at the moment, we encourage you to stay tuned for future opportunities at BioNanoPharma and share this role with people in your network who may be interested. xcskxlj EQUAL OPPORTUNITIES COMMITMENT At BioNanoPharma, we are committed to fostering an inclusive and diverse workplace and to providing equal opportunities for all candidates. We do not discriminate on the basis of gender, gender identity or expression, ethnicity, nationality, religion, sexual orientation, disability, age, or any other characteristic protected by applicable law.

Desarróllate profesionalmente con nosotros, la formación que impartimos cumple ampliamente con la normativa vigente adaptándose en todo momento a cualquier cambio tanto en contenidos como plazos, te ayudamos a forjar tu futuro en uno de los sectores más estables y con más proyección del mercad

Buscamos un perfil con experiencia real como cuadrista, metódico, con autonomía y orientado a trabajos de calidad. Mecanizado de envolventes (cajas, placas, carril DIN, canaleta, etc. Persona ordenada, responsable y con atención al detalle.

Desarróllate profesionalmente con nosotros, la formación que impartimos cumple ampliamente con la normativa vigente adaptándose en todo momento a cualquier cambio tanto en contenidos como plazos, te ayudamos a forjar tu futuro en uno de los sectores más estables y con más proyección del mercad

Atención al cliente telefónica y presencial. Buscamos incorporar un/a Administrativo/a con buen nivel de euskera en Markina. Formación en Grado Superior, Diplomatura en Administración o Graduado Social.

Experiencia presentando y defendiendo ideas frente a cliente. Puedes liderar proyectos de marca, coordinarte con estrategia, cuentas, creatividad y cliente, y mantener el nivel de exigencia en todo el proceso. Sensibilidad estratégica para entender negocio, posicionamiento, público, tono y arquite

Possibilitats de creixement i participació en decisions estratègiques. Grup Plana, grup operador referent en mobilitat de passatgers a Catalunya, cerca incorporar un/a. Planificació i coordinació de manteniment.

Generación de nuevos leads: realizar investigaciones para identificar clientes potenciales y generar leads de manera efectiva con el fin de construir una sólida cartera de clientes a través de diversas fuentes. Construcción de relaciones: tu objetivo será desarrollar y mantener relaciones con c

Conduct regular on-site assessments and audits of authorized dealers' service capabilities to ensure alignment with company standards and identify areas for development. Proven track record in aftermarket parts sales, customer relationship management, or experience in a similar PSSR (Product Support

Colaboración mercantil presencial en Valencia, con posibilidad de un día de teletrabajo a la semana. Remuneración a convenir según experiencia y valía. Grado en Derecho, Máster de Acceso y colegiación en vigor.

Si te encaja un rol administrativo con responsabilidad real, trato con cliente profesional y un entorno consolidado, nos encantará conocerte. Experiencia previa de al menos 3 años en. Se valorará positivamente el conocimiento en otros idiomas pero no es imprescindible.

We encourage all applicants, regardless of race, religion or belief (if any), color, nationality, ethnic or national origin, gender, gender identity, pregnancy and maternity, sexual orientation, age, marital and civil partnership status, or disability. Demonstrated Customer Orientation (commitment t

Gestión de retiradas de contratos realizados: coordinación de transportista, comprador y vendedor, verificación de documentos, seguimiento de pagos, resolución rápida y eficaz de incidencias. Mínimo de 3 años de experiencia laboral en alguno/s de los siguientes equipos:. Se encargará de g

Documentation: Create and maintain comprehensive documentation, including requirement documents, project plans, user manuals, and other relevant materials. Identify opportunities for process improvement and recommend enhancements. Advanced English fluency (written and spoken) - mandatory;.

Buscamos un/a Especialista en Murex con experiencia en entornos de Capital Markets para incorporarse a una iniciativa estratégica de Commodities dentro de Sistemas de Tesorería. La persona seleccionada participará en el diseño, desarrollo y mantenimiento de integraciones entre sistemas Front Off

Enviar CV + breve explicación de experiencia en el sector y video de 2 minutos explicado por qué tienes que ser tú. Si tienes experiencia real en el sector y sabes captar, negociar y cerrar operaciones, queremos conocerte. Estructura ya en funcionamiento.

This is a senior leadership role responsible for overseeing the end-to-end operational execution of Phase I–IV clinical trials, driving operational excellence, quality, compliance, and cross-functional collaboration within a dynamic R&D environment. This is an excellent opportunity to join a highl

Garantizar la correcta instalación, funcionamiento y mantenimiento de nuestras tecnologías en casa del cliente, asegurando la continuidad de sus procesos productivos. Experiencia en instalación o mantenimiento de maquinaria industrial. Si quieres desarrollar tu carrera en una compañía innovador

Desde Adecco selección estamos en la búsqueda de varios operarios/as o ayudantes/as de producción y mantenimiento para una empresa de mantenimiento industrial que colabora en la planta logística automatizada de un cliente multinacional del sector textil, ubicada en Holanda (Lelystad). Te gustar�

Contrato indefinido en una compañía puramente tecnológica, que forma parte de un gran grupo, solvente y en crecimiento. En los últimos cuatro años, hemos experimentado un crecimiento exponencial, duplicando nuestro volumen de negocio año tras año. Experiencia en asistencia técnica y soporte

En Kirey Solutio creemos en el valor de la diversidad y en la igualdad de oportunidades. Todas las candidaturas serán valoradas sin distinción de género, edad, origen, discapacidad, orientación sexual, identidad o expresión de género, religión o cualquier otra circunstancia personal o social.

En los últimos cuatro años, hemos experimentado un crecimiento exponencial, duplicando nuestro volumen de negocio año tras año. Contrato indefinido en una compañía puramente tecnológica, que forma parte de un gran grupo, solvente y en crecimiento. Esto nos ha permitido consolidarnos como un a

La persona seleccionada se incorporará al equipo técnico para realizar labores de mantenimiento, reparación y mejora de instalaciones industriales automatizadas, participando activamente en intervenciones en campo y en la resolución de incidencias técnicos/as. Si te motiva enfrentarte a nuevos

Más de 30 años de experiencia en mantenimiento aeronáutico y un futuro lleno de retos y crecimiento. Vivirás la operación desde dentro: planificación, producción, cliente, ingeniería, entendiendo el MRO 360º. Horario flexible de entrada y las ventajas de trabajar en una organización que en

Ofrecer soluciones tecnológicas, de negocio, estrategia, desarrollo y mantenimiento de aplicaciones, siendo un referente en consultoría. Experiencia hands-on en APIs, mensajería, eventos, diseño de interfaces y resolución de incidencias técnicas. Experiencia en integración de sistemas bancari

This role suits a hands-on architect who enjoys customer engagement, proactive delivery, and helping organisations achieve secure, healthy environments. Deliver workshops, assessments, and structured advisory engagements. Strong communication, documentation, and training skills.

Extensive experience in clinical project/program management within pharma or biotech, including leadership of global outsourced studies. The Senior Director ensures that all programs meet quality, timeline, budget, and regulatory expectations while shaping the long‑term operational model for outso

Te apasiona el deporte? Convierte tu tiempo libre en ingresos extra asistiendo a eventos deportivos en directo. Conocimientos básicos de las reglas del fútbol, principalmente, pero también de otros deportes. Entrada + gastos de desplazamiento cubiertos.

Queremos que cada persona, con independencia de su origen, sexo, raza, color, características genéticas, lengua, religión o convicciones, opiniones políticas o de cualquier otro tipo, nacimiento, discapacidad, edad u orientación e identidad sexual, sienta que puede desarrollarse profesionalment

Vas a trabajar identificando microseñales, entendiendo comportamientos humanos y asegurando que cada operación esté bien estructurada, documentada y ejecutada sin errores. Permitimos que propietarios con viviendas alquiladas conviertan sus rentas futuras en liquidez inmediata, sin tener que vende

No previous professional experience is required to apply to this role, however, working on this project will require you to pass the basic requirements and go through a standard assessment process. In order to be hired into the program, you’ll take a language assessment and an open book qualificat

Nos gustaría encontrar un/a Director/a de Cuentas especializado/a en comunicación de consumo con una experiencia total en agencias o consultoras especializadas de 7-8 años donde al menos el ultimo año haya ocupado la posición de director/a de cuentas. Elaborarás propuestas o planes para potenc

Vectalia es un Grupo Empresarial con más de cien años de experiencia, referente a nivel nacional en prestación de Servicios, Transporte y Movilidad con sede central en Alicante. Somos una empresa comprometida con la Igualdad de Oportunidades entre mujeres y hombres, creemos en el talento único d

Capacidad para entender y discutir arquitecturas en entornos distribuidos (Cloud/AWS) y su convivencia con sistemas Mainframe. Experiencia real en proyectos de Activos Digitales, entendiendo protocolos DLT, custodia institucional (MPC/HSM) y Smart Contracts. En } ReCodme ( aceleramos el desarrollo t

Atención al cliente (presencial y telefónica). Experiencia previa en Administración de Fincas. Asistencia a juntas de propietarios.

Creamos un entorno donde todas las personas son bienvenidas, independientemente de género, edad, religión, orientación sexual o cualquier otra condición. Además, el Arquitecto/a de Datos juega un papel de liderazgo técnico y colabora estrechamente con otros perfiles como analistas de datos, in

Experiencia en construcción de entornos Data Lake y Data Warehouse, definición de arquitecturas de datos y soluciones basadas en Microsoft Foundry, así como experiencia en entornos de payments. Te apetece formar parte de una compañía en pleno crecimiento? ¿Y trabajar rodeado del mejor TALENTO

Buscamos un abogado con 2 / 3 años de experiencia en. Licenciatura/Grado en Derecho y Máster de Acceso a la Abogacía.

Más de 2 años de experiencia relevante en sistemas de energía y conexiones a la red en España, preferiblemente en operador del sistema español (Red Eléctrica) o en un desarrollador de proyectos de energías renovables. The Green Recruitment Company está en búsqueda de un Grid Manager para tr

Creamos un entorno donde todas las personas son bienvenidas, independientemente de género, edad, religión, orientación sexual o cualquier otra condición. En Paradigma, valoramos tanto la experiencia como la actitud: buscamos personas con conocimientos en varias de las áreas clave y, sobre todo,

Si eres, un comunicador excepcional, te encanta trabajar en equipo y estás dispuesto a superar metas, ¡inscríbete en nuestra oferta!. Captar y establecer relaciones sólidas con los clientes, comprender sus necesidades a través de un análisis personalizado, ofreciéndole soluciones de Protecci�

En SEGULA Technologies buscamos incorporar un/a Jefe/a de Proyecto Solar (PSFV) para participar en un proyecto internacional dentro del sector de energías renovables. Si tienes experiencia liderando proyectos fotovoltaicos y te interesa formar parte de un entorno�

Prospección e identificación de nuevos partners entre los distribuidores de material eléctrico, y seguimiento de su evolución. Salario a comentar en la entrevista personal. Comunicación y gestión de incidencias con los clientes.

En particular, la organización está comprometida con la creación de un contexto favorable a la diversidad y avance en la erradicación de la discriminación de las personas LGTBI, independientemente de su orientación e identidad sexual o su expresión de género. Todos nuestros procesos de selec

Industria Alimentaria, en los ámbitos de la Ingeniería y la Consultoría Técnica, buscamos incorporar para nuestro equipo en Madrid a un/a CONSULTOR/A COMERCIAL SENIOR DE I+D+i. Estudios mínimos: Titulación Universitaria en Ingeniería, Economía o Ciencias, con especialización en ventas. Cono

Para sentirte a gusto en esta posición es necesario que seas una persona con espíritu emprendedor y pensar en grande, proactivo , con habilidades comunicativas, experiencia comercial, alta capacidad comunicativa. Nuestro objetivo es darte la oportunidad en un sector en continuo crecimiento y trans