Mecánico/a vehículos - Eurofirms ETT - Sevilla

ph3Sobre Ardena /h3 pArdena es una organización global especializada en el desarrollo y fabricación por contrato (CDMO) y en investigación por contrato (CRO), centrada en el desarrollo de medicamentos de precisión. Apoyamos a compañías farmacéuticas y biotecnológicas en la puesta en el mercado de moléculas innovadoras y complejas. /p pEl Grupo Ardena cuenta con cinco centros en Europa y Estados Unidos, con más de 750 profesionales. Nuestras sedes europeas se encuentran en Oss y Assen (Países Bajos), Gante (Bélgica) y Pamplona (España), y contamos también con instalaciones en Somerset, Nueva Jersey (EE.UU.). /p pPara nuestra sede de Pamplona, buscamos incorporar un/a Técnico/a de Mantenimiento. /p h3DESCRIPCIÓN DEL PUESTO /h3 pbPuesto: /b Técnico/a de Mantenimiento /p pbDepartamento: /b Producción – Formulación y Mantenimiento /p pbUbicación: /b Pamplona, España /p pComo Técnico/a de Mantenimiento en Ardena, tu misión será garantizar el correcto funcionamiento, la fiabilidad y la disponibilidad de los equipos e instalaciones productivas en un entorno farmacéutico regulado. /p pTrabajarás asegurando el cumplimiento de los estándares GMP/GxP, en colaboración con equipos de Calidad, Producción y proveedores externos. /p h3Funciones principales /h3 ul liRealizar mantenimiento preventivo y correctivo de equipos e instalaciones. /li liParticipar en la cualificación de equipos según el plan establecido. /li liSupervisar proveedores externos, garantizando el cumplimiento de estándares de calidad y seguridad. /li liColaborar en proyectos de instalación, modificación y mejora de equipos e instalaciones. /li liDar soporte técnico a producción en ajustes e incidencias. /li liGarantizar el cumplimiento de las normas de seguridad, higiene y calidad. /li liRegistrar y mantener la documentación de mantenimiento conforme a GMP. /li liContribuir a iniciativas de mejora continua. /li /ul h3Perfil requerido /h3 pbRequisitos mínimos: /b /p ul liFP de Grado Superior en Mantenimiento Industrial, Electricidad o similar. /li liAl menos 1 año de experiencia en un puesto similar (entornos industriales, laboratorio o tecnología). /li liConocimientos en automatización eléctrica/electrónica. /li liManejo de herramientas informáticas. /li liNivel de inglés B1. /li liCapacidad de trabajo en equipo, comunicación y resolución de problemas. /li /ul pbSe valorará: /b /p ul liExperiencia en entornos regulados (GMP). /li liConocimientos de sistemas de gestión de mantenimiento. /li liExperiencia con equipos del sector farmacéutico o similar. /li liAlineación con los valores CARE de Ardena: Comunicación, Responsabilidad, Fiabilidad y Excelencia. /li /ul h3Qué ofrecemos /h3 ul liContrato indefinido a jornada completa. Trabajo a turnos según necesidades productivas. /li liSalario competitivo (entre 33.000 € y 45.000 € brutos anuales). /li liEntorno internacional y colaborativo. /li liOportunidades de desarrollo profesional y formación. /li liTrabajo con propósito en el sector farmacéutico. /li /ul h3Cómo aplicar /h3 p¿Quieres impulsar tu carrera en el desarrollo farmacéutico? Aplica ahora a través de la web de empleo de Ardena: careers.ardena.com /p h3About Ardena /h3 pArdena is a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO) specializing in precision medicine development. Ardena supports pharmaceutical and biotechnology companies in bringing innovative, complex molecules from discovery to market. /p pThe Ardena Group operates from five sites across Europe and the United States, employing more than 750 professionals. Ardena European sites are located in Oss and Assen (the Netherlands), Ghent (Belgium), and Pamplona (Spain). Ardena US facility is based in Somerset, New Jersey. /p h3Job Overview /h3 pbPosition: /b Maintenance Technician /p pbDepartment: /b Production – Formulation Maintenance /p pbLocation: /b Pamplona, Spain /p pArdena is hiring a Maintenance Technician to join the Production – Formulation Maintenance team at our Pamplona site. This role supports pharmaceutical development and manufacturing activities within a GMP-regulated environment. /p h3Role Description /h3 pAs a Maintenance Technician at Ardena, you will contribute to pharmaceutical operations by ensuring the proper functioning, reliability, and availability of production equipment and facilities. /p pYou will work in a regulated pharmaceutical environment, ensuring that all activities comply with GMP, GxP, and applicable standards, collaborating with cross-functional teams including Quality Assurance, Production, and external suppliers. /p h3Key Responsibilities /h3 ul liPerform preventive and corrective maintenance of equipment, installations, and machinery. /li liSupport equipment qualification activities in line with the annual plan. /li liSupervise external maintenance providers, ensuring compliance with quality and safety standards. /li liParticipate in installation, modification, and improvement projects of equipment and facilities. /li liSupport production teams in technical adjustments and troubleshooting. /li liEnsure compliance with health, safety, and hygiene standards. /li liMaintain proper documentation related to maintenance activities in accordance with GMP. /li liCollaborate with internal departments and contribute to continuous improvement initiatives. /li /ul h3Profile Qualifications /h3 pbRequired Qualifications: /b /p ul liHigher vocational training (FP Grado Superior) in Electrical Installations, Industrial Maintenance, or similar. /li liAt least 1 year of experience in a similar role within industrial, laboratory, or technological environments. /li liExperience working with electrical and electronic automation systems. /li liIT skills. /li liEnglish level B1. /li liStrong communication, teamwork, and problem-solving skills. /li /ul pbPreferred Qualifications: /b /p ul liExperience in GMP-regulated environments. /li liKnowledge of maintenance management systems. /li liExperience working with pharmaceutical or similar regulated equipment. /li liAlignment with Ardena’s CARE values: Communicative, Accountable, Reliable, and Excellent. /li /ul h3What Ardena Offers /h3 pArdena is a science-driven and people-focused employer. Working at Ardena means contributing to pharmaceutical projects that support the availability, safety, and quality of medicines for patients worldwide. /p pArdena offers an international working environment where employees are encouraged to develop their expertise, take ownership, and grow their careers. /p h3Benefits and perks include: /h3 ul liFull-time permanent contract (indefinite). Shift-based work may apply according to production needs. /li liCompetitive salary and benefits package. /li liGross annual salary range: 33.000 – 45.000€. /li liInternational and collaborative working environment. /li liOpportunities for professional development and training. /li liMeaningful work contributing to patient health. /li /ul h3How To Apply /h3 pReady to advance your career in pharmaceutical development? Apply now through the Ardena Careers website at careers.ardena.com. /p /p #J-18808-Ljbffr

pp We are looking for a results-driven, enthusiastic and proactive bUpstream Technician /bto join our Manufacturing Operations Department. /p pAs a bUSP Manufacturing Technician /b, your responsibilities will include: /p ul liEnsure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader. /li liEnsure the correct training of the personnel in charge. /li liPrepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms. /li liParticipate in internal / external audits as required by the Quality Assurance Department. /li liComply and ensure compliance with GMP standards within the work team. /li liRecord and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB). /li liInvestigate and propose new methods or process innovations to optimize and improve the work in the area. /li liEnsure proper compliance with regulations and correct completion of current documentation. /li liParticipate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager. /li liPerform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB). /li liSupervise the correct completion of the new equipment entry documentation. /li liSupervise the correct training of the personnel in charge, if any. /li liCarry out the distribution and supervision of daily activities. /li liWrite and keep updated the documentation associated with the production processes carried out in the USP area. /li liControl / monitoring of orders placed in the USP production area using ERP software. /li /ul pbEducation: /bBachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. /p pbLanguages: /bFluent in Spanishb. /bIntermediate level of English (Level B2 / First Certificate). /p pbBetween 1 and 2 years of experience in/with: /b /p ul liGMP/GLP regulations /li liWith bioreactors /li liCell Cultures /li liMicrobiological analysis techniques /li liUpstream production positions /li liBiotechnology / Biopharmaceutical Sector /li /ul pbOther requirements: /b /p ul liOpen to work in shifts. /li liA permanent and stable position in a competitive growing company. /li liA competitive time off package with 41 paid days of vacation. /li liFlexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.) /li liAll new hires who reside outside Navarra are provided with a relocation service and/or assistance. /li liCompany benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.) /li li3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees. /li liThe company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust. /li liWe encourage the participation of our employees in solidarity events such as charity races, social donations... /li liWe have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces. /li liWe have a high-impact work environment with flat hierarchies and short decision-making processes. /li li...And so much more! /li /ul pWe know it takes people with passion and a shared purpose to manufacture advanced medicines. /p pWe specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients /p pFrom development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. /p /p #J-18808-Ljbffr