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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: 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.

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.

Formación a cargo de la empresa. Si tienes experiencia en mantenimiento electromecánico en líneas automáticas y buscas un proyecto estable en la provincia de Girona, queremos conocerte.

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 experie

Beneficios: seguro médico privado de empresa Condiciones generales: • Contrato indefinido (con período de prueba de 3 meses) • Categoría según experiencia (oficial de 1ª, 2ª o 3ª) • Formación a cargo de la empresa • Imprescindible conocimientos de español y catalán Si ti

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 experie

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.

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.

Desde HELPOINT garantizamos la igualdad y no discriminación por razón de sexo, género, raza, religión, discapacidad, edad y orientación sexual en nuestros procesos de selección, para obtener un mejor aprovechamiento de las capacidades de las personas en toda su diversidad, evitando cualquier t

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 experie

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 experie

Ubicación: Bonmatí (Girona) Sector: bollería industrial⏱️ Turnos rotativos: • 7 días de mañana • 7 días de descanso • 7 días de noche • 5 días de descanso • 7 días de tarde • 2 días de descanso Salario: 28. BONMATÍ (Girona) – Técnicos/as electromecánicos/as

Ubicación: Bonmatí (Girona) Sector: bollería industrial⏱️ Turnos rotativos: • 7 días de mañana • 7 días de descanso • 7 días de noche • 5 días de descanso • 7 días de tarde • 2 días de descanso Salario: 28. BONMATÍ (Girona) – Técnicos/as electromecánicos/as

BONMATÍ (Girona) – Técnicos/as electromecánicos/as OFERTA BONMATÍ (Girona) – Sector bollería Buscamos técnicos/as electromecánicos/as con experiencia eléctrica en líneas automáticas de producción para planta de bollería industrial en la zona de Bonmatí (Girona). Ubicación: Bo

Ubicación: Bonmatí (Girona) Sector: bollería industrial⏱️ Turnos rotativos: • 7 días de mañana • 7 días de descanso • 7 días de noche • 5 días de descanso • 7 días de tarde • 2 días de descanso Salario: 28. BONMATÍ (Girona) – Técnicos/as electromecánicos/as

Experiencia como soldador/a de al menos 2 años.

HELPOINT -Es una consultoría única especializada en la selección de perfiles de oficios y profesionales cualificados.Damos cobertura a nivel nacional e internacional conectando el talento que necesitan nuestros clientes.Somos especialistas en procesos derivados de la trayectoria laboral de la emp

Servicios Profesionales de Recursos Humanos.Seleccionamos y contratamos profesionales para cubrir necesidades temporales.Limpieza, lijado, decapado y aplicación de imprimaciones.Uso de maquinaria como pistolas de aire comprimido, granalladoras o equipos de lijado industrial.Aplicación de recubrimi

Formación profesional de Grado Medio o Superior en Instalaciones Frigoríficas, Climatización, Mantenimiento Industrial o similar.

Si te apasiona la seguridad industrial, el cumplimiento normativo y quieres aportar tu experiencia en la protección de instalaciones frente a incendios, ¡queremos conocerte! Da el siguiente paso en tu carrera profesional y ayúdanos a hacer de la prevención una prioridad para todos/as. Experienci

Experiencia como pontor/a de coches de al menos 2 años. Limpieza, desengrasado, lijado, enmasillado y aparejado de la superficie del vehículo. Pulido, encerado y abrillantado para lograr un acabado uniforme y de alta calidad.

Feines de manteniment de vehicles fent operacions de canvi d’oli, frens, pneumàtics. Des de Talent Services (Grupo Castilla) estem gestionant una posició de Mecànic/a per a una important i consolidada empresa del sector automoció, ubicada a Blanes. Horari de dilluns a divendres de 09:00h a 13:

Experiencia mínima de uno o dos años en mantenimientos preventivos y correctivos. Ejecutar el mantenimiento preventivo y correctivo de la maquinaria. Mantenimiento general instalaciones empresa.

Buscas empleo en peones agrícolas? En Palafolls te esperan nuevas oportunidades este diciembre.

Mezclar cemento, arena y otros componentes para elaborar mortero o concreto. Asistir en la colocación de pilares, vigas, y otras estructuras metálicas o de hormigón. Vehículo propio para desplazarse al puesto de trabajo.

Trabajos de mantenimiento de señalización, identificación y etiquetado de equipo y/o espacios. Trabajos de mantenimiento correctivo por la detección y resolución de averías durante su jornada de trabajo. Un/a técnico/a de mantenimiento para empresa del sector metal, ubicada en la zona de Pala

Realizar un mantenimiento preventivo. Jornada completa de 40 horas semanales, en horario de mañana de 6 a 14h, con lo descansos establecidos por ley. Reparar y sustituir componentes eléctricos.

Servicios Profesionales de Recursos Humanos.Seleccionamos y contratamos profesionales para cubrir necesidades temporales.Garantizar el cumplimiento de normativas.Administrar y controlar la documentación de obra.Coordinar y realizar el seguimiento de facturación.Elaborar y actualizar reportes de co

Servicios Profesionales de Recursos Humanos.Seleccionamos y contratamos profesionales para cubrir necesidades temporales.Desde la oficina RAS INTERIM BLANES seleccionamos PEONES/AS para empresa del sector de RECICLAJE ubicada en SANT FELIU DE BUIXALLEU.Transportar, organizar y

Servicios Profesionales de Recursos Humanos.Seleccionamos y contratamos profesionales para cubrir necesidades temporales.Cortar, doblar, moldear y dar forma a chapas metálicas según planos y especificaciones técnicas.Unir piezas de chapa metálica mediante soldadura, remachado o atornillado.Coloc

Jornada completa de 40 horas semanales con los descansos establecidos por ley. Experiencia previa en el sector del metal de al menos un año. Valorable carnet de carretillas, de pala excavadora y pulpo.

Realización de controles visuales de calidad para detectar defectos simples. Soporte a operarios y técnicos en tareas sencillas (preparación de piezas, entrega de herramientas, limpieza de zona). Carga y descarga de mercancía de forma manual o con transpaleta.

Necesitamos incorporar un/a operario/a electricista para trabajar en empresa del sector de servicio situada a la zona de Malgrat de Mar.

Buscas empleo en electricistas? En Malgrat de Mar te esperan nuevas oportunidades este diciembre.

Vols formar part d’una empresa consolidada i compromesa amb l’excel·lència en el servei al client? A.Seràs l’encarregat/da de realitzar intervencions tècniques.Busquem un/a professional amb capacitat per diagnosticar i solucionar problemes tècnics de manera eficient, amb vocació de serve

We are young, we are cool… We are NOW!”.En Bershka, empresa comprometida con la igualdad de oportunidades, buscamos una persona que se incorpore al equipo de Automatistas.Cómo es el día a día en tu puesto?.Gestión y coordinación de la parte automatizada del centro de distribución.Control y

Taller mecánico con mas de 10 años de trayectoria ubicado en Girona requiere:.Un responsable del mantenimiento y reparación de vehículos.Sus tareas diarias incluirán el diagnosis de fallos, ejecución de reparaciones y mantenimiento preventivo, así como la atención al cliente para asegurar su

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 manu

El nostre propòsit és impulsar un nou model de construcció més eficient, sostenible i respectuós amb l’entorn, sempre amb un alt nivell de qualitat i atenció al detall.Gestió i actualització de la informació comercial de l’empresa.Atenció a clients: assessorament, visites tècniques i

We are young, we are cool… We are NOW!”.En Bershka, empresa comprometida con la igualdad de oportunidades, buscamos un Project Manager para dar apoyo puntual al equipo de Obras para cubrir una baja.Cómo es el día a día en tu puesto?.Desde el rol de promotor, serás el responsable máximo de c

En Altorecruit colaboramos con compañías industriales líderes en plásticos de ingeniería, ayudándolas a identificar y atraer el mejor talento en posiciones clave.Para una planta industrial ubicada en Girona , buscamos un/a Electromecánico/a con experiencia en mantenimiento industr

Técnic@ de Prevención de Riesgos Laborales en GEFA PREVEN servicio de prevención de riesgos laborales.Las funciones a realizar consistirán en el desempeño de las siguientes tareas: Diseñar e implantar el Plan de Prevención en las empresas clientes.Elaborar la evaluación de puestos de trabaj

Técnic@ de Prevención de Riesgos Laborales en GEFA PREVEN servicio de prevención de riesgos laborales.Las funciones a realizar consistirán en el desempeño de las siguientes tareas: Diseñar e implantar el Plan de Prevención en las empresas clientes.Elaborar la evaluación de puestos de trabaj

AXXON selecciona, per una important empresa industrial multinacional, referent global en el desenvolupament i producció de materials compostos avançats i solucions d’enginyeria, un/a: EXPERT/A GLOBAL EN SUPPLY CHAIN (H/D).El seu enfocament combina rendiment, sostenibilitat i innovació contínu

Vols formar part d’una empresa consolidada i compromesa amb l’excel·lència en el servei al client? A IEC busquem una persona responsable, resolutiva i amb ganes de créixer professionalment per incorporar-se al nostre equip tècnic.QUINA SERIA LA TEVA MISSIÓ? Seràs l’encarregat/da de rea