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Banc Mediolanum compta amb la xarxa líder d’Agents Financers a Espanya.I ara és la teva oportunitat de formar part d’ella.Busquem un/a professional que desitgi construir el seu projecte personar al sector de la banca.Com a Family Banker®, la nostre figura d’A

Contratamos y formamos a agentes inmobiliarios independientes. ¿POR QUÉ NO UNIRSE A NOSOTROS? El sector inmobiliario está en pleno auge. SAFTI ofrece la oportunidad de trabajar como agente inmobiliario independiente a quienes lo deseen. ¡Apoyándose en la red inmobiliaria SAFTI, se beneficiará de una formación inmobiliaria completa que le permitirá iniciar su nueva actividad profesional con toda tranquilidad! Trabajando de forma independiente, usted es su propio jefe y gestiona sus propias horas de trabajo. Référent sur votre zone, vous accompagnez vos clients vendeurs et acquéreurs pendant toute la durée de vie de leur projet immobilier : prospection, rendez-vous de prise de mandat, visites, négociation, etc... De este modo, contribuirá a la realización de proyectos inmobiliarios, con una rutina diaria que nunca es la misma. Convirtiéndote en agente comercial inmobiliario SAFTI: ?Trabajas de forma autónoma y gestionas tu propio horario de trabajo. ?Acompañará a sus clientes vendedores y compradores a lo largo de la vida de su proyecto inmobiliario: prospección, citas de mandato, visitas, negociaciones, etc. Nuestro programa de formación único y nuestro apoyo dedicado permitirán a cada uno prosperar en el negocio. ¿Desea combinar independencia, profesionalidad y proximidad? Tanto si es principiante como si es un agente inmobiliario experimentado, SAFTI puede adaptarse a sus necesidades y acompañarle en su proyecto. • ¿Está empezando o ya trabaja en el sector inmobiliario? Sea cual sea su perfil, la red SAFTI contrata agentes inmobiliarios en toda Francia., • Ante todo, buscamos las cualidades humanas que son la clave del éxito: aptitud para la venta, sentido del servicio al cliente y motivación.

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: The role will involve resolution of production problems, process optimisation and commissioning of new industrial facilities for the Group. Collaboration with Quality, Safety and Environment in the continuous auditing of processes based on technical knowledge of processes and facilities. Responsibilities: • Carry out operations related to the transfer and optimisation of industrial processes at Bioiberica's national and international plants, ensuring regulatory compliance by recording and evaluating the associated change control., • Collaborate in the preparation of reports derived from the evaluation of change requests, deviations and nonconformities affecting products, processes or equipment., • Collaborate with Engineering in defining user requirements for new production facilities and equipment., • Collaborate in reviewing the specifications of MMPPs, materials, in-process controls, intermediates and APIs produced, ensuring that their content corresponds to the DMF., • Collaborate as a member of the HACCP team in the identification, evaluation and control of significant hazards, ensuring compliance with current food safety regulations., • Participate in the verification and validation of the HACCP plan, ensuring the effectiveness of preventive and corrective measures., • Prepare manufacturing guidelines for new processes or optimisation of existing ones, as well as validation of processes prior to their industrial implementation., • Resolving production problems that require different solutions, collaborating in the monitoring of process optimisation projects, collaborating in the feasibility study of alternative MMPPs, collaborating with other areas of the company at a technical advisory level (commercial, customer service, RRAA)., • Possibility of participating in cross-functional projects that the company, based on your strengths and skills, may consider appropriate for you to participate in. About You: • A degree in Chemistry or Life Sciences, • Strong communication skills, • Fluent in English & Spanish What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

Importante hotel de Santa Susanna necesita incorporar un/a: GOBERNANTE/A DE HOTEL En dependencia de Dirección se encargará de: • Supervisar las tareas del equipo de pisos garantizando la correcta limpieza y orden., • Organizar y planificar los horarios del equipo a cargo., • Realizar inventarios periódicos y evaluar el rendimiento del personal., • Controlar los stocks y mantener ordenados los almacenes de cada planta., • Revisar y gestionar los listados de ocupación de los pisos., • Resolver las incidencias que surjan en la operativa diaria., • Asegurar el cumplimiento de las normativas de calidad e higiene, así como los protocolos internos del hotel. Requisitos: • Experiencia mínima de 3 años en puesto similar., • Valorable inglés. Se ofrece: • Contrato fijo discontinuo., • Jornada completa., • Salario según valores aportados.

Testo Industrial Services es uno de los proveedores líderes de servicios GxP en Europa. Entre ellas se incluyen la calibración, la cualificación, la validación, la garantía de calidad, formación GxP y asesoramiento normativo. Como filial de Testo SE & Co KGaA, tenemos más de 60 años de experiencia en el campo de los servicios a la industria farmacéutica. Actualmente seleccionamos un un/a Técnico/a Junior en Calibraciones para unirse a nuestro equipo y realizar servicios especializados en las instalaciones de uno de nuestros clientes del sector farmacéutico en la zona de Malgrat de Mar. Responsabilidades • Ejecución de calibraciones multivariable en equipos de medida térmicos, eléctricos y de presión., • Revisión y liberación interna de instrumentos de medición conforme a normativa vigente., • Gestión de datos en la base Testo y dentro del cliente, control de incidencias., • Elaboración precisa de certificados y documentación técnica. Se Ofrece: • Contrato indefinido desde el inicio, • Plan de carrera a tres años, • Horario jornada completa con horarios estables, • Plan de retribución flexible adaptado a tus necesidades, • Excelente ambiente de trabajo en un equipo multidisciplinar., • Beneficios como Ticket Restaurant. Se Requiere: • Formación técnica: Ingeniería Técnica o FP en electricidad/electrónica o similar., • No requiere experiencia previa, • Carnet de conducir Se valorará: • Experiencia en entornos #GMP y con clientes del sector farmacéutico., • Conocimiento de herramientas ofimáticas (Excel, gestión de bases de datos)., • Nivel medio de inglés técnico (lectura e interpretación de documentación)., • Capacidad de trabajo autónomo, orientación al cliente y habilidades interpersonales., • Residencia en la zona En Testo estamos comprometidos con la igualdad de oportunidades. Diversidad, Igualdad e inclusión se viven activamente. Tenemos un sentimiento único de "nosotros" en la empresa. Los objetivos y los retos se dominan juntos. Cada empleado contribuye al éxito de la empresa con su individualidad, la actitud adecuada y el corazón en el lugar correcto. Si te sientes identificado con estos valores y quieres dejar huella en un sector altamente regulado y tecnológico, ¡esperamos tu candidatura, esta es tu oportunidad!! Escríbenos.

¡Impulsa tu carrera en tecnología y telecomunicaciones con nosotros! ¿Te apasiona la tecnología y el mundo de las telecomunicaciones? ¿Tienes habilidades comerciales y te motiva conectar personas y empresas con soluciones innovadoras? ¿Te gustaría multiplicar tus ingresos? ¡Esta es tu oportunidad para crecer y destacar! ¿Quiénes somos? Somos una empresa líder en el sector de las telecomunicaciones, reconocida por nuestra innovación, excelencia en el servicio y un firme compromiso con el desarrollo profesional de cada miembro de nuestro equipo. Apostamos por el talento y la diversidad, y fomentamos un entorno donde tus ideas y tu crecimiento son nuestra prioridad. ¿Qué harás en nuestro equipo? Asesorarás a clientes sobre soluciones de internet, telefonía y servicios digitales, identificando sus necesidades y ofreciendo la mejor alternativa personalizada (B2B). Elaborarás presupuestos y gestionarás propuestas comerciales y opciones de financiación a medida. Gestión y ampliación de base de datos. Gestión de una cartera de clientes situada en Tarragona y prospección en la zona de Calella. Captación de clientes. Colaborarás con un equipo dinámico, donde cada día es una oportunidad para innovar y aprender. ¿Qué buscamos en ti? Experiencia previa en ventas, atención al cliente o asesoría comercial (idealmente en telecomunicaciones, tecnología o servicios). Pasión por la tecnología y capacidad para explicar conceptos técnicos de forma sencilla. Orientación a resultados, proactividad y espíritu de equipo. Excelentes habilidades de comunicación, negociación y empatía. Ganas de superarte y crecer en un sector en constante evolución. ¿Qué te ofrecemos? Contrato temporal con posibilidad de conversión a indefinido. Jornada completa de L-J de 09:00 a 14:00 y de 15:00 a 18:30h y viernes de 09:00 a 15:00h. Salario fijo de 22.428 euros brutos + comisiones, sin techo. Formación continua en productos, tecnología y habilidades comerciales, con acceso a certificaciones reconocidas. Oportunidades reales de desarrollo profesional y promoción interna: tu crecimiento es nuestro objetivo. Excelente ambiente de trabajo, joven, diverso y colaborativo. Beneficios sociales competitivos: seguro médico privado, descuentos exclusivos en nuestros productos y servicios, y programas de bienestar. Bonificaciones por desempeño: tu esfuerzo y resultados se ven recompensados. Eventos de equipo, afterworks y actividades sociales para que disfrutes cada día. ¿Por qué elegirnos? Aquí tu talento marca la diferencia. Valoramos tus ideas, te apoyamos en cada paso y te ofrecemos el entorno ideal para crecer profesionalmente en un sector que no deja de avanzar. ¡Únete y sé parte de una empresa donde tu futuro es tan importante como el presente!

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Ensure document traceability, correct management of deviations, CAPAs and changes, and provide support in audits, Regulatory Affairs and document release, minimising regulatory risks and ensuring compliance with international standards. Responsibilities: Review of GMP documentation (API technical backup): • Review and approve production spreadsheets, records and controls in accordance with GMP and PNT., • Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment)., • Coordinate the investigation, closure and verification of deviations and non-conformities., • Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan., • Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms., • Keep the document management system up to date in accordance with ICH Q7 and applicable regulations., • Participate in customer complaint investigations, ensuring feedback to the quality system., • Coordinate the change management process on the MasterControl platform., • Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities., • Ensure compliance with legal requirements for labelling and records., • Provide support in regulatory audits and inspections (EMA, FDA, AEMPS)., • Collaborate in the evaluation and approval of raw materials, critical services and auxiliary materials., • Participate in internal, customer and authority audits., • Prepare evidence, records and corrective action plans., • Prepare APR/PQR reports and management reviews., • Participate in continuous improvement projects., • Be the point of contact for customer enquiries and approvals., • Provide GMP training during onboarding and periodic training sessions., • Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them., • Report any risk situation in accordance with incident/accident management and quality event management procedures. About You: • Degree in Pharmacy, Chemistry, Biotechnology or similar., • Solid knowledge of GMP, ICH Q7, ISO and applicable regulations., • Training in Compliance and Regulatory Affairs is desirable., • Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable., • Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical)., • Experience in document management, audits, deviations and CAPAs., • Experience in Regulatory Affairs and supplier management is desirable., • Knowledge of the EU, FDA and EAEU regulatory environment and specific international regulations in destination countries. What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV to in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: • Take responsibility for managing the Industrial Manufacturing Control and Instrumentation System, both hardware and software, to ensure proper operation in accordance with corporate safety, quality and environmental standards., • Lead the implementation of the industrial manufacturing control system and take responsibility for its updating and supervision., • Motivate, drive and support change management in new programmes and practices, organisational behaviour, as well as technical solutions related to the processes under your responsibility., • Be responsible for the implementation and continuous improvement of your processes to strengthen the organisation's integrated management system for safety, quality, environment and sustainability., • Take responsibility for the department and manage the process of establishing the main directions and priorities in order to meet tight production deadlines and maintain plant availability, ensuring high levels of safety and quality as required., • Take responsibility for ensuring that engineering and maintenance activities are carried out in a timely manner and within budget, take an active role in obtaining supply contracts and, therefore, in controlling the budget., • Ensure that the organisation is at the forefront of new technologies in operational management. Ensure that Bioibérica's control and instrumentation facilities are state of the art. Responsibilities: • Ensure that all current safety, quality and environmental standards are applied in all activities carried out and ensure that other Bioibérica colleagues, internal and external suppliers involved in these activities also comply with them., • Manage the design, configuration and programming of the automated control system using SCADA Aveva System Platform or Intouch and Rockwell or Siemens PLCs., • Develop and implement control strategies to ensure the efficiency and safety of processes in the pharmaceutical industry., • Manage the integration of SCADA and PLC systems to enable effective communication and precise control of the equipment and processes involved in production., • Oversee the testing and commissioning of automation systems, ensuring their correct operation and compliance with quality, safety and environmental requirements., • Ensure that technical documentation is up to date, including control diagrams, user manuals, and validation procedures., • Comply with pharmaceutical industry standards and regulations, such as Good Manufacturing Practices (GMP) and system validation requirements (GAMP 5 and 21 CFR Part 11)., • Provide technical support and training to end users of automation systems., • Keep your knowledge up to date, both technically and legally, on issues related to GMPs, the environment, quality, occupational risk prevention, and industrial safety., • Maintain order and cleanliness in your workplace and in all areas where you carry out your activities. About You: • Experience working in the pharmaceutical environment and knowledge of the pharmaceutical and chemical business, manufacturing and quality processes (GxP compliance, validation and quality systems management, GMP Annex 11, 21CFR Part 11)., • University degree in Electrical Engineering, Electronic Engineering, Automation Engineering or related field, or CFGM/CFGS in Electrical Engineering., • Desirable: Aveva System Platform, Intouch Wonderware What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

Importante hotel situado en Pineda de Mar necesita incorporar un/a: ADJUNTO/A A DIRECCIÓN DE HOTEL En dependencia de Dirección se encargará de: · Supervisar y coordinar la operativa de todos los departamentos (Pisos, Cocina, Recepción y Mantenimiento), asegurando su funcionamiento y productividad. · Supervisar la implementación de los estándares de calidad y de procedimientos operativos en todas las área asegurando su cumplimiento. · Optimizar recursos y procesos para asegurar la satisfacción del cliente. · Coordinarse diariamente con los responsables de departamento. · Atender y gestionar quejas y reclamaciones y realizar un análisis para detectar áreas de mejora. · Analizar indicadores de gestión y proponer mejoras en los procesos. · Gestionar al personal a su cargo. · Colaborar con Dirección para garantizar la excelencia en el servicio. Requisitos: · Titulación universitaria en Turismo o similar. · Experiencia mínima de 5 años en puesto similar. · Dominio de inglés. Valorable francés. · Manejo de programas de Gestión Hotelera. · Capacidad de liderazgo, organización y toma de decisiones. Se ofrece: · Contrato fijo discontinuo. · Jornada completa. · Salario según valores aportados.

About Us: As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. About the Role: Ensure the proper administrative management of the Quality Assurance (QA) area, ensuring compliance with GMP requirements and applicable regulations, through the organisation, control and archiving of critical documentation, support in audits and coordination with other areas. Responsibilities: Document management and record control: • Create, review and update Standard Operating Procedures (SOPs)., • Control versions and ensure the correct distribution of current documents., • File physical and digital documentation in compliance with traceability requirements., • Record quality events in the system., • Follow up on actions arising from events (AI) and ensure compliance with deadlines., • Prepare periodic reports on quality indicators., • Monitor the release status of batches to ensure on-time deliveries to customers., • Coordinate with Production, Logistics and Customer Service to ensure availability., • Act as the QA liaison with the areas involved in order tracking., • Manage QA team schedules and meetings., • Prepare minutes and reports of quality-related meetings., • Maintain staff training records in the document management system (MasterControl)., • Coordinate the scheduling of courses and internal assessments related to the Quality area (GMP/HACCP/HALAL/GMP+, etc.)., • Prepare documentation required by authorities and auditors., • Organise evidence and records to facilitate review., • Know and apply current standards for safety, health, occupational risk prevention, quality, environment, energy efficiency, and ensure compliance., • Degree in Pharmacy, Chemistry, Biotechnology or similar., • Solid knowledge of GMP regulations and quality management systems., • Additional training in document management and compliance is desirable. What’s Next: If this sounds like a role that you would be interested in, then we would love to hear from you. Apply with a copy of your CV at the link below. *Please apply with your CV to in English where possible We value the support recruitment agencies provide, however we are unable to accept speculative CV’s from agencies we are not already engaged with. Closing Date: 5th January 2026 *Please note, closing dates are subject to change and, at time of high volume of applications, this may be brought forward. Other important information: Equality and diversity at Bioiberica: We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background. We expressly welcome applications from people with a wide range of perspectives and experiences. Our goal is to ensure equal opportunities and actively combat discrimination – both in the application process and in everyday working life.

Desde IMMACLÉ buscamos un/a Marketing Manager con visión estratégica y alta capacidad operativa, capaz de liderar y ejecutar iniciativas que impulsen el crecimiento, fortalezcan la presencia de la marca y potencien la experiencia de las futuras novias. Responsabilidades principales • Diseñar, liderar y ejecutar la estrategia de marketing digital orientada a adquisición y conversión de clientes potenciales., • Planificar y gestionar campañas de Paid Media (Meta Ads, Pinterest Ads y Google Ads), optimizando resultados y garantizando un flujo constante de leads cualificados., • Gestionar y supervisar la presencia en redes sociales, edición de vídeo, calendarios de contenido y desarrollo creativo junto al equipo., • Definir y mantener relaciones con influencers, creadoras de contenido y medios de comunicación para potenciar el alcance de la marca., • Crear contenido visual y narrativo alineado con la esencia de IMMACLÉ: moda nupcial, elegancia, sensibilidad y autenticidad., • Gestionar y responder mensajes directos de potenciales clientes con cercanía, cuidado y orientación hacia la experiencia de marca., • Medir y analizar KPIs de marketing, generando insights y propuestas de mejora continua. Requisitos • Experiencia demostrable en marketing digital, paid media y social media management (+2 años)., • Dominio de herramientas como Ads Manager, Google Ads, Google Sheets, Meta Business Suite, Canva, Cap Cut u otras herramientas de edición., • Conocimiento en estrategias de PR, colaboraciones e Influencer Marketing., • Alta sensibilidad visual y experiencia creando contenido atractivo y coherente con el universo de la marca., • Excelente comunicación en español, catalán e inglés., • Enfoque resolutivo, autonomía operativa y capacidad para priorizar en entornos dinámicos. Competencias clave • Visión estratégica combinada con una fuerte ejecución operativa., • Creatividad y entendimiento profundo de tendencias digitales y del sector moda/brides., • Pensamiento analítico y orientación a resultados (leads, citas, ventas)., • Habilidades de comunicación, empatía y trato exquisito con clientas., • Proactividad, organización y capacidad para trabajar mano a mano con un equipo pequeño pero muy ágil. Qué ofrecemos • Oportunidad de formar parte de una marca bridal líder y en crecimiento internacional., • Rol con gran autonomía creativa y alto impacto en los resultados del negocio., • Entorno joven, dinámico, y altamente creativo., • Participación en sesiones creativas, shootings y experiencias con el equipo de diseño y producto., • Oficinas en Canet de Mar, en un entorno inspirador y conectado con la cultura de la marca., • Bonus salarial basado en resultados y cumplimiento de objetivos de marketing. Afegir mes rollo salario basado en resultados.

Familia de 2 profesionales, uno de ellos Mdico, con horario variable.

Con nosotros viven nuestros gatitos Cleo y Giulio que nos acompaan desde ms de 10 aos. Hola! Somos Ari y Lauta, los paps de Lorenzo, un beb sper sonriente y dulce.

Necesito apoyo por un par de das de esta semana.

Tenemos 1 hijo Nio, No dudes en ponerte en contacto conmigo para concertar una cita.

Tengo dos criaturas un nio de 5 aos y una nia de 4, son simpticos y cariosos, necesito que los cuiden por norma general los sbados,.

Estamos buscando una chica que pueda cuidar a un nio de 4 aos el domingo de 3 a 4 horas por semana es un nio muy alegre y divertido queremos que en esas horas puedas divertirse en casa o en el parque o playa y tambin ayudarnos en los deberes de la casa pero lo bsico recoger juguetes y recoger el des

Hola soy madre de dos menores a mi cargo, hace un ao que nos vinimos a vivir a Sant Genis de Palafolls, por logstica y horarios necesito ha alguien que venga por las maanas , de lunes a viernes de 8h a 9h de la maana vivimos en ciudad jardn , y ellos siguen yendo al colegio e instituto en Pineda de

Tenemos un/a hijo/a (1 Nio, 3 aos).No dudes en ponerte en contacto conmigo para conocernos.

Hola somos una familia de 3 miembros, muy tranquilos y en busca de una persona que nos brinde seguridad en el cuidado de nuestro hijo.El nio se llama Adrin, es alguien muy tranquilo, curioso, juguetn pero sobre todo carioso, algo tmido en ocasiones pero sociable si se siente en confianza.Necesito cu

Tenemos un/a hijo/a (1 Nia, 0 aos).No dudes en ponerte en contacto conmigo para conocernos.

Hola! Buscamos niera para nuestro hijo de 2 meses, para los fines de semana de 10:00 a 19:00.

Tenemos una nia de 5 meses, muy espavilada, que se llama Nora.Necesitariamos una niera que nos pudiera ir a recoger a la nia a la guarderia a las 17 hasta las 18, con lo cual, solo seria 1hora por dia.No dudes en ponerte en contacto conmigo para conocernos.

Tengo 2 hijos (1 Nio y 1 Nia, 4 y 11 aos).No dudes en ponerte en contacto conmigo para conocernos.

Y estamos buscando a alguien que nos pueda ayudar algunas tardes despus del cole.Nuestras nias tienen (Lola, casi 3 aitos) y este ao empieza el cole de los grandes! Y (Mia, acaba de cumplir 16 meses) y va a la guardera.Hay das que no podemos recogerlas y queremos contar con alguien que pueda ir a bu

Som una famlia amb tres nens de 7, 5 i 3 anys, i estem buscant una persona de confiana que ens pugui donar un cop de m a lhora de dinar.La nostra idea s treure els nens del menjador escolar perqu puguin passar el migdia a casa, en un ambient ms tranquil i amb ms calma del que tenen a lescola.El que

Busco chica responsable que le gusten los peques mucho para estar con nuestra hija de 14 meses maanas o tardes de forma puntual.Jugar en casa ir al parque, dar merienda, acompaar a dormir en sus siestas.Es necesario tener coche porque vivimos en una casa con cuesta.

We have 1 child (1 boy, 0 years old).Feel free to contact me so we can make an appointment.

Ayudamos a más de 200 empresas y más de 20.Te incorporarás a un recurso municipal dirigido a mujeres cis y trans mayores de 16 años, orientado a ofrecer apoyo integral en igualdad, prevención y atención de las violencias machistas, atención psicológica, asesoramiento jurídico y acompañamie

Importante hotel situado en Pineda de Mar necesita incorporar un/a:. Manejo de programas de Gestión Hotelera.

Alguna hora suelta para solapar con la madre y poder ir a trabajar.L alguna maana para llevarla al colegio.

We are looking for someone for one or two afternoons to take care of my four years old son.He will not need much care because he will be accompanied but we want someone who speaks English to play and be with him and a friend of him too.Just to play with both in english.

Tenemos un/a hijo/a (1 Nio, 9 aos).No dudes en ponerte en contacto conmigo para conocernos.

Somos una familia de 3, un nio de 8 aos, tranquilo, obediente, respetuoso.Yo soy mdico anestesista del hospital de Calella, horario variable durante el mes.De momento algunas veces llevar a mi hijo al cole o buscarlo a la hora de salida!.

Buscamos a alguien qu acompane a nuestra hija al colegio todas las mananas, desde Can Reig hasta la escuela de Sant Pol.

Necesito ayuda los lunes -miercoles-viernes por la maana porque entro a trabajar muy temprano.Sera llegar a casa 6:15 de la maana, ayudarme con las cosas de casa hasta que la nia se despierte para vestirse, desayunar y llevarla al cole!! Tambin posibilidad de ms das en funcin de mi trabajo.

Somos brasileos y no tenemos familia cerca, as que en algn momento necesitamos un momento de ayuda para mantener a nuestro hijo ocupado.

Estoy buscando canguro habitual de lunes a viernes.Una hora por la maana actualmente.Con ampliacion de horas en dias de festivo escolar.

Deportista!y muy amigable!es comprometido!necesito cuidado infantil de Lunes a Viernes!de 5horas a 9!de la Maana!!para poder llevarlo al cole.

As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Review and approve production spreadsheets, records and controls in accordance with GMP and PNT. Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment). Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan. Document management system and quality assurance (API technical backup): Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities. Ensure compliance with legal requirements for labelling and records. Maintain up-to-date records of supplier approval and monitoring. Quality management system monitoring: Participate in continuous improvement projects. Coordinate with purchasing and the QA Supplier Manager to ensure supply reliability. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Training in Compliance and Regulatory Affairs is desirable. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical). com in English where possible We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background.

As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Review and approve production spreadsheets, records and controls in accordance with GMP and PNT. Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment). Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan. Document management system and quality assurance (API technical backup): Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities. Ensure compliance with legal requirements for labelling and records. Maintain up-to-date records of supplier approval and monitoring. Quality management system monitoring: Participate in continuous improvement projects. Coordinate with purchasing and the QA Supplier Manager to ensure supply reliability. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Training in Compliance and Regulatory Affairs is desirable. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical). com in English where possible We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background.

Contratamos y formamos a agentes inmobiliarios independientes. ¿POR QUÉ NO UNIRSE A NOSOTROS? ¿Por qué unirse a SAFTI? El sector inmobiliario está en pleno auge. SAFTI ofrece la oportunidad de trabajar como agente inmobiliario independiente a quienes lo deseen. ¡Apoyándose en la red inmobiliaria SAFTI, se beneficiará de una formación inmobiliaria completa que le permitirá iniciar su nueva actividad profesional con toda tranquilidad! TRABAJAR CON SAFTI Trabajando de forma independiente, usted es su propio jefe y gestiona sus propias horas de trabajo. Référent sur votre zone, vous accompagnez vos clients vendeurs et acquéreurs pendant toute la durée de vie de leur projet immobilier : prospection, rendez-vous de prise de mandat, visites, négociation, etc... De este modo, contribuirá a la realización de proyectos inmobiliarios, con una rutina diaria que nunca es la misma. Convirtiéndote en agente comercial inmobiliario SAFTI: ?Trabajas de forma autónoma y gestionas tu propio horario de trabajo. ?Acompañará a sus clientes vendedores y compradores a lo largo de la vida de su proyecto inmobiliario: prospección, citas de mandato, visitas, negociaciones, etc. Nuestro programa de formación único y nuestro apoyo dedicado permitirán a cada uno prosperar en el negocio. ¿Desea combinar independencia, profesionalidad y proximidad? Tanto si es principiante como si es un agente inmobiliario experimentado, SAFTI puede adaptarse a sus necesidades y acompañarle en su proyecto. Perfil • ¿Está empezando o ya trabaja en el sector inmobiliario? Sea cual sea su perfil, la red SAFTI contrata agentes inmobiliarios en toda Francia., • Ante todo, buscamos las cualidades humanas que son la clave del éxito: aptitud para la venta, sentido del servicio al cliente y motivación.

As a global life science company, taking care of human, animal and plant life has been our priority for 50 years. Today, we are a world leader in the production of heparin – the primary anticoagulant used to save approximately 100 million lives every year. We have also set the benchmark for the manufacture of APIs and functional ingredients for the pharmaceutical, nutraceutical, veterinary, animal nutrition and agricultural sectors. We work to innovate in human, animal, and plant health. We believe that partnership is the key to success and we support our partners across the healthcare, plant and animal health markets worldwide. Ensure regulatory compliance and quality in GMP processes, acting as QA and Compliance Manager and as backup for the API QA Technician. Review and approve production spreadsheets, records and controls in accordance with GMP and PNT. Verify the integrity, traceability and accuracy of critical data (processes, in-process controls, times, equipment). Supervise the investigation of OOS/OOT, ensuring immediate action, root cause analysis and action plan. Document management system and quality assurance (API technical backup): Prepare, review and control versions of SOPs, technical instructions, spreadsheets and GMP forms. Participate in customer complaint investigations, ensuring feedback to the quality system. Develop and control quality indicators and participate in management reviews. Assess potential impacts on quality and safety, validate regulatory compliance, and document execution and closure. Prepare and maintain documentation to be provided by QA for regulatory dossiers, site master files, certificates and documentation for authorities. Ensure compliance with legal requirements for labelling and records. Maintain up-to-date records of supplier approval and monitoring. Quality management system monitoring: Participate in continuous improvement projects. Coordinate with purchasing and the QA Supplier Manager to ensure supply reliability. Quality training and culture: Provide GMP training during onboarding and periodic training sessions. Promote a culture of quality through awareness-raising activities. Be familiar with and apply current regulations on safety, health, occupational risk prevention, quality, the environment and energy efficiency, and ensure compliance with them. Report any risk situation in accordance with incident/accident management and quality event management procedures. Training in Compliance and Regulatory Affairs is desirable. Internal Auditor certification in GMP, GLP, GDP, Quality Management Systems (food, feed) is desirable. Minimum 2 years in QA and Compliance in GMP environments (pharmaceutical, API, chemical). com in English where possible We value diversity and are committed to an inclusive working environment in which all employees are respected and supported regardless of gender, age, ethnic origin, religion, sexual orientation, disability, or social background.

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