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Nuestro equipo de ingeniería de mantenimiento y fiabilidad es una pieza clave del compromiso de Amazon con la innovación. Este equipo se asegura de que las herramientas y tecnologías que utilizamos evolucionen y se adapten a los cambios al mismo ritmo que Amazon. Como técnico/a sénior de ingeniería de mantenimiento y fiabilidad, nos ayudarás a ir siempre un paso por delante, adoptando las últimas tecnologías e identificando formas nuevas y más eficientes de trabajar. En este puesto, prestarás especial atención a nuestros procesos de seguridad y salud laboral para ayudar a cumplir los exigentes estándares por los que nos regimos y pondrás en marcha mejoras para continuar avanzando. Key job responsibilities • Aplicar las mejores prácticas en el uso seguro de los equipos y supervisar al personal para garantizar que todos siguen los procedimientos de seguridad y salud laboral correctamente., • Realizar inspecciones de seguridad, evaluaciones de riesgos y auditorías periódicas para identificar y mitigar peligros potenciales en el entorno de trabajo., • Garantizar el rendimiento seguro de los dispositivos mediante comprobaciones visuales, controles de estado y tareas de mantenimiento preventivo, asegurando el cumplimiento de las normativas de prevención de riesgos laborales., • Supervisar al personal técnico que esté de turno para apoyar su desarrollo en materia de seguridad y actuar como primer punto de contacto para las cuestiones de WHS relacionadas con los equipos de mantenimiento y fiabilidad., • Resolver problemas en los equipos para reducir los tiempos en los que las operaciones se detienen, priorizando siempre la seguridad de las personas y el cumplimiento normativo., • Ayudar a encontrar formas de mejorar constantemente los sistemas de gestión de seguridad y salud, homogeneizando los procesos y estándares WHS en toda la red de la UE. A day in the life Serás responsable de la supervisión de los procesos para velar por el cumplimiento de las normativas de seguridad y salud laboral, así como garantizar que se lleva a cabo el mantenimiento preventivo pertinente para aumentar el tiempo de actividad de los equipos de forma segura. A partir de lo que observes en tus turnos, propondrás mejoras destinadas a incrementar la seguridad, la eficiencia y la productividad de nuestros sistemas y, más adelante, implantarás dichos cambios en todos nuestros centros de la UE. • Experiencia relevante en el área de la automatización o con equipos de manipulación de materiales, con enfoque en su operación segura., • Título de bachillerato., • Experiencia previa relevante en un puesto de dirección técnica con responsabilidades en seguridad y salud laboral., • Experiencia relevante en la identificación de riesgos y aplicación de medidas preventivas en entornos industriales o logísticos., • Conocimiento de normativas de prevención de riesgos laborales y procedimientos de seguridad (LOTO, permisos de trabajo, evaluaciones de riesgos)., • Nivel avanzado de español, tanto oral como escrito, y conocimientos básicos del inglés., • Experiencia en la realización de auditorías de seguridad y en la gestión de planes de acción correctivos en entornos con multitud de contratistas y en diferentes ubicaciones., • Conocimiento de los requisitos normativos de seguridad de máquinas (marcado CE, directivas de máquinas)., • Experiencia en el manejo de sistemas informáticos de gestión de seguridad y salud (registro de incidentes, investigación de accidentes, planificación de acciones preventivas)., • Titulación universitaria, preferentemente en una disciplina técnica, de prevención de riesgos laborales o ingeniería de seguridad., • Formación específica en prevención de riesgos laborales (Técnico Superior en PRL o equivalente). Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice (_) to know more about how we collect, use and transfer the personal data of our candidates. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit _ for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.

Are you experienced in technical Translations? Are you open to work on site, in Madrid? Take a look! ORTEC ENGINEERING is the engineering subsidiary of ORTEC GROUP. We are an European leader in engineering, linguistics, risk and project management. The ORTEC branch in Spain is specialized in Engineering services, maintenance engineering, integrated logistics support, supportability, reliability and maintainability engineering and technical translations. Our team is in charge of developing engineering studies for the creation, update or optimization of aircraft Maintenance Programs, using specific methodologies, for different customers - main European aircraft manufacturers or vendors. Our Linguistics Department is looking for Freelance or Staff employee technical translators specialized in, and with demonstrate experience in, translating documents from French to German (FRàGE) to reinforce our in-house translations teams in our production center in Madrid. We are looking for translators with experience in technical translation, from FRENCH to GERMAN and vice versa, and technical documentation like aircraft maintenance manuals, industrial installations instructions, ground vehicles maintenance or other similar technical language- related translations. JOB DESCRIPTION You will be mainly involved in: Analysis of source documentation authored in French or German, in collaboration and close contact with our technical authors. Translation from French to German and from German to French. Management of translation memories in automatic translations software (TRADOS). Cross-check processes in accordance with our Quality Assurance processes. PROFILE We are looking for candidates whose profile matches the following characteristics: Translation or Interpretation studies Experience in translations of technical texts from Spanish and English into German or French Experience in the translation of technical texts from other languages, such as English. Knowledge in Simplified Technical English (STE) standard Experience in maintenance manuals and / or real maintenance experience. Systems or structures general knowledge, systems operation, structural repairs, data sheets or other technical domains. Use of translations software e.g. TRADOS STUDIO XML / SGML authoring experience Expert in Microsoft Office Good organizational skills Ability to focus on priorities and deliver on time to agreed standards Service-oriented attitude Excellent oral and written communication skills in the different languages. And a strong team spirit! If you match these skills, you are located in Spain and want to work as in-house translator in our offices in Madrid, don't hesitate to apply for this job offer. At Ortec Engineering we are proud to consider Diversity and Inclusion as essential elements in everything we do. We are committed to our Equal Employment Opportunity policy without regard to race, color, ethnicity, gender, age, sexual orientation, gender identity, religion, or disability. Note: Through your active application in this Selection Process via LinkedIn, you authorize the processing and use of your personal data, including your LinkedIn profile, in accordance with the ORTEC GROUP DATA PROTECTION POLICY available at https://ortec-group.com/en/gdpr/

Territory includes but not limited to: All of EU countries as needed The Regional Medical Director (RMD) is an integral member of the metabolic/obesity clinical sciences group, who assists and extends Clinical Sciences across the metabolic portfolio on assigned studies at the regional level. Duties and Responsibilities: • Site engagement and training o A cadence of touchpoints with sites on a regular basis o Meeting with sites and presenting at PSVs, SIVs o Retraining as needed (e.g., due to amendments) • Recruitment issues o Site identification/recruitment: Meeting with potential sites, in collaboration with CTL, to discuss the program/assess of their interest o Patient recruitment issues (ongoing oversight): Meeting with sites, in collaboration with CTL, to help understand the hurdles with recruitment at their site and trouble shooting • Answering questions from sites o Helping address site medical/clinical questions as a first line for those questions that are straightforward or previously addressed or to help coordinate a response with the Medical Director for those that are not straightforward/new  This includes referencing and updating the FAQ, as applicable  Medical Director should always be copied on the email correspondence for oversight • Assisting with eligibility assessments o Help perform eligibility checks or address urgent eligibility questions prior to randomization • Assisting with query closure o Helping site understand what is needed to close a medical query if there is a misunderstanding from the site regarding what is needed  Feedback should also be provided to the study team if the query text could be improved for clarity o Helping ensure that the information that we must have to describe a safety event is sufficient, including:  Ensuring that all information has been gathered as expected (i.e., the site has taken all reasonable steps to obtain the information, etc.) in collaboration with the CRA, if additional support is needed during escalation process  Ensure that all questions have been answered/follow-up assessments have been done  This may include requesting additional assessments for a complete evaluation/specialist consultation, etc. • Protocol Deviations o In collaboration with the CTL, retrain the site, to prevent future deviations/address any misunderstandings by the site • Retention issues o Helping to ensure that the site has followed up with patients in the event of lost to follow-up / all appropriate steps have been taken (in collaboration with the CTL) and that any protocol specific requirements have been met • Missing assessments o For instance, in PNH studies, help to ensure that all LDH values that are not done/unable to be performed are rapidly chased to ensure a repeat is done as quickly as possible, in collaboration with the CRA/CTL o For other studies, may require help in working with site to obtain any key missing assessments (eg, images, PK samples, biomarker samples), in collaboration with the CRA/CTL • Laboratory reference range o In collaboration with the CRA, ensure that the laboratory reference ranges are provided for local laboratory data • Site issues o Discussion with the sites for any potential quality issues /concerns requiring physician to physician discussion (first line)  The global medical director can be pulled in if the issue cannot be easily resolved • Attend CSTs, if possible, • Weekly meetings with medical director (if possible) or weekly communication with medical director, at a minimum, • May provide clinical assistance and feedback on PI interest in proposed studies at the local level Qualifications and Experience: • MD PhD, or PharmD; MD strongly preferred, • 8+ years of industry clinical development experience, • Expertise in clinical trials and clinical development, • Strong understanding of the Metabolic/Obesity clinical research landscape and implementation and conduct of these clinical trials, • Demonstrated ability to develop and maintain excellent working relationships with both internal stakeholders and study investigators and site staff, • Demonstrated ability to work well in cross functional and geographically diverse teams, • Ability to communicate and work independently with scientific/technical personnel with excellent oral presentation skills, • Ability to think critically, and demonstrated troubleshooting and problem-solving skills, • Excellent initiative and judgment, and demonstrated ability to positively represent Regeneron in a compliant manner, • Cross cultural awareness and fluent in the local language of primary country assignment in addition to English, • Computer skills including Excel, Word, and PowerPoint, • A willingness to travel up to 65%, which may include local, regional and international travel, • Valid driver’s license

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a Desarrollo Galénico - Inyectables para una empresa del sector industrial con sede en Madrid. ¿Qué harás? • Desarrollo farmacéutico de productos inyectables estériles (soluciones, suspensiones, liofilizados, formulaciones peptídicas y complejas), incluyendo estudios de preformulación, optimización y escalado bajo normativa GMP., • Diseño, ejecución y transferencia de procesos de fabricación, participando en validaciones, soporte a producción y asegurando el cumplimiento regulatorio e ICH., • Gestión y análisis de datos experimentales y documentación técnica, elaborando protocolos, informes, SOPs y batch records, y aplicando metodologías de Quality by Design (QbD) para la mejora continua., • Colaboración multidisciplinar y liderazgo de proyectos, con una actitud proactiva, creativa y orientada a la resolución de problemas, asumiendo la responsabilidad y seguimiento integral de los proyectos hasta su finalización. ¿Qué buscamos? • Graduado en Farmacia, Química o similar., • Nivel de Ingles tanto oral como escrito alto., • Se requieren de 1-3 años de experiencia en desarrollo de formulaciones de inyectables. ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo., • Retribución flexible., • Banda Salarial; Según experiencia aportada por los candidatos (30k-40k).

About the Company Si desea conocer los requisitos para este puesto, siga leyendo para obtener toda la información relevante.The NSG Group is one of the world's largest manufacturers of glass and glazing products for architectural, automotive and established creative technology to support NSG group's future growth. With around 27,000 permanent employees, we have principal operations around the world and sales in over 100 countries. About the Role As a Production Team leader your purpose will be responsible for you for ensuring line efficiencies, personal utilisation, quality and safety in our site in Sagunto. The job holder will report to the Production Manager Sagunto and cooperate with the rest of Production Team Leaders as well as with the management team. In this position, the manager will be responsible for: Lead and develop the team under your supervision, identifying potential and fostering growth among team members, including Process Improvers, Supervisors, line coordinators, and others. Ensure daily, weekly and monthly production targets are met whilst quality and EHS standard are respected. Ensure the system contains accurate information for precise reporting of plant status. Coordinate production tests, production changes, and line improvements. Provide solutions to high-level issues within the facilities. Collaborate with your team (SLs, PIs, Supervisors) to resolve problems within your area of responsibility. Work with MICs, SLs, PIs, and other plant personnel on special projects related to your area of responsibility. Perform any other duties and tasks in line with the responsibilities of the position. Requirements A degree in Industrial Engineering, Mechanical Engineering, or a related field is often required. Advanced degrees or certifications in management or automotive engineering are a plus. Strong knowledge of automotive manufacturing processes, quality control, and production planning. Familiarity with lean manufacturing principles and Six Sigma methodologies is highly desirable. Training in continuous improvement methodologies such as Kaizen, 5 S, and other process optimization techniques. Used to work in a multicultural, future-oriented environment. Fluent in English (Oral and written) and Spanish. xqbhyrx Business acumen, basic financial knowledge. Nice to have SAP knowledge Preventive resource (Risk prevention official basic degree) Knowledge on ISO 14001, IATF What we offer The opportunity to grow in an international and dynamic environment Competitive salary + variable compensation Flexible working hours Life insurance provided by company Optional medical insurance managed by company Meal benefits (canteen)

We are looking for a CTO to lead the development and industrialization of our SOEC technology, with our 2028 go-to-market in sight. Our roadmap is demanding and clearly defined: we will be scaling our technology by orders of magnitude over the coming years, going through several validation milestones, design freeze and end of development before reaching the market. The new CTO will join at a critical moment along that path: not at the very beginning, where everything is exploration, nor at the very end, where everything is execution, but at the point where scientific rigor and industrial discipline must coexist every day. We are looking for someone capable of combining two things that rarely come together: the scientific rigor to solve the technological challenges still ahead of us in MEA (Membrane Electrode Assembly), Stack and Balance of Plant, and the discipline of New Product Introduction to bring the technology from the lab to the industrial product. You will have three direct reports leading the MEA, Stack and Bo P areas: people with judgment, autonomy and deep knowledge of their field. Your challenge will not be to build the team from scratch, but to take it to the next level: aligning them around the roadmap, professionalizing the way we develop product, and building, together with them, the technical culture with which Kerionics will reach the market. Nor is this a role for silent execution. We are looking for someone capable of acting as the CEO's technical right hand: bringing top-level judgment, following the defined strategy and, when necessary, challenging it with arguments when you believe something has been wrongly decided. You will report to the CEO, but we expect from you the professional maturity to co-build with him, not just to execute. That technical honesty is part of the job. Why this role matters (and what's in it for you) Technical leadership of a European deeptech scale-up. You will lead the development of one of the most efficient technologies on the market for decarbonizing energy-intensive industries. Few roles allow this much technical, commercial and environmental impact at the same time. A solid team and a project with real backing. Although we are not yet in a commercial phase, Kerionics already has financial backing from deeptech-specialized funds such as Inno Energy, top-tier industrial and scientific partners, and participation in strategic European projects. We are in a moment of active growth, opening new conversations with private investors to support the next phase of development. You join a project with clear direction, a consolidated team and a defined path to market. A real voice in strategy. You are not just another report: you are part of the management committee that sets the direction of the company. You take part in strategic and investment decisions, and we expect you to challenge whatever needs to be challenged. You will report to the CEO, but your technical opinion carries weight in shaping where Kerionics is heading. A real transition to market. In just a few years, you will live the full cycle: from prototype to product, from lab to industrial plant, from first customer to deployment. What you will do Your mission is to lead Kerionics' technical development and ensure we reach 2028 with an industrializable, reliable and competitive product. You will lead the cross‑functional technical development of our SOEC technology, integrating progress across the MEA, Stack and Bo P areas into a coherent product vision. You will ensure that the development process follows a New Product Introduction (NPI) logic, with clear stage gates, defined technical pass/fail criteria and traceability of decisions. You will lead the transition from R&D to industrialization, maintaining the scientific rigor that the product needs at each phase. Team and technical culture You will directly lead the MEA, Stack and Bo P managers, supporting their priorities and unblocking what they need to move forward. You will build a technical culture grounded in data, intellectual honesty and accountability for results. You will play an active role in technical hiring decisions and in the professional development of your team. Solving critical technical problems You will provide top‑level technical judgment on the open challenges of the product. You will lead decision‑making on problems that affect more than one area (MEA‑Stack interfaces, Stack‑Bo P integration, system thermal behavior). You will make technical decisions with incomplete data when context demands it. Technology strategy and partnership with the CEO You will be the technical reference in the management committee, taking an active part in shaping the strategic direction of the company. You will support the CEO on technical decisions that go beyond his own field of expertise, offering honest judgment even when it contradicts what was previously defined. You will represent Kerionics before technology partners, research centers, investors and industrial customers whenever technical depth is needed. Industrialization and quality You will coordinate with the Industrial Project Manager on the product aspects that affect the design of our future industrial plant. You will work closely with the Quality & Testing Manager (who reports to the CEO) to ensure that validation criteria are aligned with the technical reality of the product. What we are looking for Must-haves Advanced degree in Engineering (Chemical, Mechanical, Materials, Energy) or Materials Science / Chemistry. A Ph D will be highly valued. Relevant experience in high‑temperature electrochemical systems, with at least 5 years of knowledge in SOEC, SOFC, fuel cells or equivalent technologies. At least 3 years of experience leading product development from R&D toward industrialization (TRL advancement, stage gates, NPI or similar processes). Experience leading multidisciplinary technical teams. Solid knowledge of at least one of the three pillars of the product: MEA and high‑temperature ceramic materials, stack design and validation, or Balance of Plant in complex energy systems. We don't expect equivalent depth in all three, but we do expect the ability to hold demanding technical conversations across all of them. Fluent English (oral and written), professional level for technical discussions and external representation of the company. Availability to relocate to Valencia within a maximum of 2‑3 months. We value individual cases: if you need more time due to family circumstances, let's talk. Valid work permit for Spain. We are looking for someone who… Has the technical judgment to say no to a good project when it doesn't fit the strategy, and to say yes to a hard project when the evidence supports it. Knows how to operate under uncertainty, making decisions with incomplete data without falling into paralysis or improvisation. Is capable of challenging the CEO with arguments when needed, while always remaining loyal to the agreed strategy. Combines scientific rigor with industrial sense of urgency: understands that the best technical product is worthless if it doesn't reach the market on time. Leads through context and example, not through micromanagement. Stays hands‑on when needed: not afraid to get into the technical detail with the team, while always thinking two steps ahead and anticipating what's coming next. Stays current with developments in AI and integrates them critically into their professional work, both as a thinking partner and as a tool to accelerate technical and team productivity. Has the professional maturity to join an already formed team and earn its trust through knowledge and respect, not through hierarchy. Not required, but you'll surprise us if you also… Have previous experience as a CTO, VP of R&D or Head of Technology in a deeptech scale‑up. Have lived through a complete industrial scale‑up process (from TRL 5‑6 to TRL 8‑9) in electrochemical, energy or advanced materials technologies. Have experience in Kerionics' target industrial sectors (steel, cement, petrochemicals, ceramics, glass, paper) or have worked on industrial decarbonization projects. What we offer €70-80 K gross per year, depending on experience and fit. Variable bonus of up to 25% of the fixed salary, tied to company and area objectives. Stock option plan. Details to be discussed during the process. Relocation support package for candidates moving to Valencia. 22 working days of holiday plus the Christmas period. The opportunity to lead the technical development of one of the most promising technologies for industrial decarbonization in Europe. A direct voice in the management committee and in shaping the strategic direction of the company. An already‑formed technical team, with consolidated managers and a clear roadmap toward 2028. Cross‑learning sessions across teams: you'll learn from your team and share what you know. Annual training budget tailored to your needs. Enrichment through the cultural diversity of our team: you'll work alongside people from India, the UK, France, Pakistan, Mexico, Argentina, Colombia, Ecuador… Every Friday, from 11:00 to 12:00, we break the routine and share a good Valencian esmorzaret. A moment to disconnect, laugh and celebrate the small wins of the week. A direct contribution to industrial decarbonization through the most efficient SOEC technology on the market. #J-18808-Ljbffr

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a Desarrollo Galénico - Inyectables para una empresa del sector industrial con sede en Madrid. ¿Qué harás? Desarrollo farmacéutico de productos inyectables estériles (soluciones, suspensiones, liofilizados, formulaciones peptídicas y complejas), incluyendo estudios de preformulación, optimización y escalado bajo normativa GMP. Diseño, ejecución y transferencia de procesos de fabricación, participando en validaciones, soporte a producción y asegurando el cumplimiento regulatorio e ICH. Gestión y análisis de datos experimentales y documentación técnica, elaborando protocolos, informes, SOPs y batch records, y aplicando metodologías de Quality by Design (Qb D) para la mejora continua. Colaboración multidisciplinar y liderazgo de proyectos, con una actitud proactiva, creativa y orientada a la resolución de problemas, asumiendo la responsabilidad y seguimiento integral de los proyectos hasta su finalización. ¿Qué buscamos? Graduado en Farmacia, Química o similar. Nivel de Ingles tanto oral como escrito alto. Se requieren de 1-3 años de experiencia en desarrollo de formulaciones de inyectables. ¿Qué ofrecemos? Contrato indefinido con cliente final. Salario competitivo. Retribución flexible. Banda Salarial; Según experiencia aportada por los candidatos (30k-40k).

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a Desarrollo Galénico - Inyectables para una empresa del sector industrial con sede en Madrid. Asegúrese de presentar su candidatura con toda la información solicitada, tal como se expone en la descripción del puesto a continuación. ¿Qué harás? • Desarrollo farmacéutico de productos inyectables estériles (soluciones, suspensiones, liofilizados, formulaciones peptídicas y complejas), incluyendo estudios de preformulación, optimización y escalado bajo normativa GMP., • Diseño, ejecución y transferencia de procesos de fabricación, participando en validaciones, soporte a producción y asegurando el cumplimiento regulatorio e ICH., • Gestión y análisis de datos experimentales y documentación técnica, elaborando protocolos, informes, SOPs y batch records, y aplicando metodologías de Quality by Design (QbD) para la mejora continua., • Colaboración multidisciplinar y liderazgo de proyectos, con una actitud proactiva, creativa y orientada a la resolución de problemas, asumiendo la responsabilidad y seguimiento integral de los proyectos hasta su finalización. ¿Qué buscamos? • Graduado en Farmacia, Química o similar., • Nivel de Ingles tanto oral como escrito alto., • Se requieren de 1-3 años de experiencia en desarrollo de formulaciones de inyectables. ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo. xcskxlj, • Retribución flexible., • Banda Salarial; Según experiencia aportada por los candidatos (30k-40k).

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a Desarrollo Galénico - Inyectables para una empresa del sector industrial con sede en Madrid. ¿Qué harás? • Desarrollo farmacéutico de productos inyectables estériles (soluciones, suspensiones, liofilizados, formulaciones peptídicas y complejas), incluyendo estudios de preformulación, optimización y escalado bajo normativa GMP., • Diseño, ejecución y transferencia de procesos de fabricación, participando en validaciones, soporte a producción y asegurando el cumplimiento regulatorio e ICH., • Gestión y análisis de datos experimentales y documentación técnica, elaborando protocolos, informes, SOPs y batch records, y aplicando metodologías de Quality by Design (QbD) para la mejora continua., • Colaboración multidisciplinar y liderazgo de proyectos, con una actitud proactiva, creativa y orientada a la resolución de problemas, asumiendo la responsabilidad y seguimiento integral de los proyectos hasta su finalización. ¿Qué buscamos? • Graduado en Farmacia, Química o similar., • Nivel de Ingles tanto oral como escrito alto., • Se requieren de 1-3 años de experiencia en desarrollo de formulaciones de inyectables. ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo., • Retribución flexible., • Banda Salarial; Según experiencia aportada por los candidatos (30k-40k).

Desde la división de Química&Pharma nos encontramos en la búsqueda de un/a Técnico/a Desarrollo Galénico - Inyectables para una empresa del sector industrial con sede en Madrid. ¿Qué harás? • Desarrollo farmacéutico de productos inyectables estériles (soluciones, suspensiones, liofilizados, formulaciones peptídicas y complejas), incluyendo estudios de preformulación, optimización y escalado bajo normativa GMP., • Diseño, ejecución y transferencia de procesos de fabricación, participando en validaciones, soporte a producción y asegurando el cumplimiento regulatorio e ICH., • Gestión y análisis de datos experimentales y documentación técnica, elaborando protocolos, informes, SOPs y batch records, y aplicando metodologías de Quality by Design (QbD) para la mejora continua., • Colaboración multidisciplinar y liderazgo de proyectos, con una actitud proactiva, creativa y orientada a la resolución de problemas, asumiendo la responsabilidad y seguimiento integral de los proyectos hasta su finalización. ¿Qué buscamos? • Graduado en Farmacia, Química o similar., • Nivel de Ingles tanto oral como escrito alto., • Se requieren de 1-3 años de experiencia en desarrollo de formulaciones de inyectables. ¿Qué ofrecemos? • Contrato indefinido con cliente final., • Salario competitivo., • Retribución flexible., • Banda Salarial; Según experiencia aportada por los candidatos (30k-40k).

Se necesita un profesional para trabajar como gerocultor o auxiliar de enfermería en un centro residencial en Llíria. También se colabora en el traslado de los residentes a terapias o actividades, se administra la medicación oral indicada por enfermería y se apoya en el trabajo asistencial gene