Join an international team that accelerates drug discovery and development through scientific excellence and integrated CRO/CDMO solutions — helping our partners Resumen del Puesto** El Analista de Laboratorio Químico - Tratamiento de Muestra es responsable de la preparación y análisis inicial de muestras de diversas matrices (alimentos, aguas) de acuerdo con procedimientos operativos estándar y normas de calidad en metodologías para metales, proximales y análisis químico generales. Este rol es fundamental para garantizar la integridad y confiabilidad de los resultados de laboratorio en ALS Group USA, Corp. Responsabilidades del Puesto** * Recibir, registrar y etiquetar muestras de manera precisa y oportuna, asegurando la trazabilidad. * Realizar la preparación de muestras mediante técnicas como titulación, digestión, extracción y filtración, utilizando equipos especializados. * Operar y mantener equipos de laboratorio como balanzas analíticas, hornos y agitadores, siguiendo los protocolos establecidos. * Preparar reactivos y soluciones estándar, verificando su calidad y caducidad. * Entregar resultados según lo requerido. * Mantener un ambiente de trabajo limpio y organizado, asegurando el cumplimiento de las normas de seguridad e higiene. * Documentar detalladamente todos los procedimientos realizados, resultados obtenidos y cualquier desviación observada. * Colaborar con otros miembros del equipo para optimizar los flujos de trabajo y resolver problemas técnicos. * Identificar y reportar cualquier anomalía en las muestras o equipos al supervisor. * Adherirse estrictamente a los sistemas de gestión de calidad (ISO 17025) y procedimientos internos de ALS Group USA, Corp. Calificaciones del Puesto** * Título técnico o universitario en Química, Ingeniería Química, Químico Farmacéutico Biólogo o campo relacionado. * Experiencia mínima de 1-2 años en un laboratorio químico, preferiblemente en el tratamiento y preparación de muestras en alimento. * Conocimiento sólido de técnicas de preparación de muestras y manejo de equipos de laboratorio. * Familiaridad con normas de calidad (ISO 17025) y buenas prácticas de laboratorio (BPL). * Habilidad para seguir instrucciones detalladas y trabajar de forma independiente o en equipo. * Atención al detalle, precisión y habilidades organizativas. * Capacidad para levantar y mover objetos de hasta 20 kg ocasionalmente. * Conocimiento básico de software de laboratorio y Microsoft Office. * Disponibilidad para trabajar en horarios rotativos o fines de semana si es necesario. At Nuvisan, everything revolves around one central question: How can we bring new therapeutics to the patients who need them faster? As a science-driven CRO/CDMO, we support the full spectrum of drug discovery and development. To succeed, we rely on people who are curious, take ownership and want to make a meaningful impact as part of a team. If you are looking for an environment that combines scientific excellence, collaboration and real opportunities to grow, you have come to the right place. Everyone Matters As part of ALS, Nuvisan is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued. Nuvisan welcomes applications from people with all levels of ability. Reasonable adjustments to support candidates throughout the recruitment process are available upon request Eligibility To be eligible to work at Nuvisan you must be a citizen or permanent resident of the country you are applying for, or either hold or be able to obtain, a valid working visa. How to apply Please apply online and upload your detailed resume. We will contact you as soon as possible after reviewing your application. Your partner of choice in bringing therapeutics to life Nuvisan is a full-service contract research organisation (CRO) and development and manufacturing organisation (CDMO) with state-of-the-art laboratories in Germany and France. Our pharmaceutical, biotechnology, venture capital and non-profit clients partner with us because our high-quality end-to-end solutions and scientific expertise enable us to streamline and accelerate drug discovery and development – from ensuring target understanding to helping bring therapeutics to life. Founded over 40 years ago by a team of pharma industry innovators, Nuvisan has established a reputation for expertise and professionalism. Our team leaders have extensive experience in the biopharma industry, and our unique centres of excellence – for drug discovery in Berlin, formulation and GMP manufacturing in Sophia Antipolis, and our bioanalysis hub in Neu-Ulm – enable our experienced scientists to help guide and advance projects. We know how to discover, develop and bring the next generation of medicines to market. At the same time, we are committed to flexibility, transparency and collaboration in our approach, working closely with you to adapt to your individual needs, minimise risks and help deliver your project. Didn’t see the right job for you today? We'd still love to hear from you. With a team of more than 20,000 employees across 70 countries, it takes all kinds of skills and expertise to make a company like ours thrive – and not all of them are in labs! We’re all about people – so show us who you are and why you're passionate about working with us by submitting your resume, and we’ll keep it on file for future opportunities. Want to know more? Check out our careers page to find out about the benefits of joining our team, and don’t forget to follow us on LinkedIn for the latest updates!

Analista Laboratorio químico - tratamiento muestra.

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