📌 Técnico/a de PLM
📅 Fecha límite para aplicar: 11/05/2026
⏳ Temporal: 12 meses
🧩 ¿En qué consiste el puesto?
Buscamos un/a Técnico/a de PLM para unirse al equipo de MSAT de GSK Aranda, con ganas de aprender y crecer en el ámbito de la gestión del ciclo de vida de producto y proceso (PLM) dentro de un entorno farmacéutico altamente regulado.
Trabajarás dando soporte a actividades técnicas clave relacionadas con PLM, colaborando estrechamente con otras áreas de la planta y participando en proyectos reales que impactan directamente en la introducción, mantenimiento y mejora de nuestros productos.
Es una oportunidad ideal si ya tienes experiencia en industria farmacéutica y quieres profundizar en PLM, procesos, datos y cumplimiento GMP.
🔍 ¿Qué harás en tu día a día?
- Dar soporte técnico a actividades de PLM (Product / Process Lifecycle Management) en distintas etapas del ciclo de vida del producto: productos comerciales establecidos, cambios, transferencias o nuevos lanzamientos.
- Colaborar en la elaboración, despliegue y mantenimiento de documentación técnica asociada a PLM (normas (GQSOPs), protocolos, informes, evaluaciones, etc.).
- Participar en evaluaciones de riesgos (por ejemplo, TRAs o MRAs), aprendiendo a identificar impactos técnicos y de proceso.
- Apoyar en actividades de control de cambios, ayudando a evaluar impactos y a asegurar la trazabilidad documental. Colaborar en el análisis de tendencias y monitorización de datos de proceso, dentro de dinámicas de mejora continua.
- Participar en investigaciones derivadas de desviaciones, tendencias o eventos de calidad, contribuyendo al análisis de causas raíz junto al equipo. Dar soporte en actividades de cualificación de equipos analíticos, así como en el mantenimiento de su estado de control.
- Asistir a foros y reuniones locales (desviaciones, validaciones, CPV, PPR, etc.) como parte de tu desarrollo técnico y formativo. Interactuar con diferentes áreas de la planta y, de forma puntual, con equipos globales.
📈 A medida que ganes experiencia y autonomía, el rol te permitirá asumir responsabilidades cada vez mayores dentro del ecosistema de PLM.
✅ ¿Qué buscamos en ti?
Requisitos necesarios
- Titulación universitaria en Ingeniería, Ciencias de la Salud, Química, Biotecnología o similares.
- Sólida experiencia en la industria farmacéutica, preferiblemente en áreas técnicas como Producción, MSAT o Calidad.
- Conocimientos intermedios/avanzados de GMP y entorno regulado.
- Interés real por la gestión del ciclo de vida de producto/proceso (PLM) y por entender cómo se conectan procesos, datos y calidad.
- Capacidad de aprendizaje, actitud proactiva y ganas de desarrollarte en un entorno técnico exigente.
- Nivel intermedio/alto de inglés (mínimo, B2).
- Buenas habilidades de comunicación y trabajo en equipo.
Requisitos valorables
- Experiencia previa en validación o cualificación de equipos, sistemas o procesos.
- Conocimientos en evaluaciones de riesgos, controles de cambios o desviaciones.
- Familiaridad con análisis de datos, tendencias de proceso o herramientas digitales.
- Formación complementaria o máster en Industria Farmacéutica o áreas afines.
🎯 Si buscas un puesto con recorrido, aprendizaje continuo y exposición real a procesos clave de la industria farmacéutica, este puede ser tu siguiente paso. ¡Anímate a aplicar!
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Healthcare Strength — Health coverage is presented as comprehensive, spanning medical, dental, vision, disability, life insurance, and mental health benefits. The breadth of coverage is repeatedly framed as a standout element of the overall rewards experience.
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Retirement Support — Retirement offerings are described as robust, anchored by a 401(k) plan and additional savings vehicles such as employee stock purchase programs. Employer contributions and savings options are portrayed as meaningful supports for long-term financial security.
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