Senior Quality Control Laboratory Technician

Responsibilities:

The Quality Control Laboratory Technician position is a technical support and/or collaboration role in tasks related to Quality Control equipment to meet the main objectives of the Alcobendas plant regarding:

• Leading the projects included in the equipment-related validation master plan, as well as validations of new products, re-validations, cleaning validations, services, and analytical transfers, meeting established deadlines, providing technical knowledge, and ensuring required timelines are met.

• Evaluation of the technical characteristics of new equipment available on the market and management of their purchase.

• Planning and performing calibration, preventive and corrective maintenance of laboratory equipment.

• Knowing and technically supervising chemical analyses and samples arriving at the laboratory, ensuring the review and approval of analytical data (e.g., product analysis, service samples, cleaning of parts/equipment, stability samples).

• Collaborating in resolving laboratory system incidents and analytical investigations and deviations, properly identifying root causes and establishing action plans to prevent recurrence, as well as the technical documentation associated with the position.

• Actively collaborating to ensure the laboratory quality system is maintained according to established quality standards.

Basic requirements:

• A university degree in Chemical Sciences, other Health Sciences degrees (Pharmacy, Biology), or Chemical Engineering is required.

• A minimum of 3 years of experience in a GMP quality control laboratory is required, including experience with different laboratory equipment and analytical techniques, and experience qualifying/validating laboratory or manufacturing equipment is required.

• Fluent English, both spoken and written (C1).

• Work schedule: afternoon shift (3:05 PM - 11:15 PM), Monday to Friday.

Additional skills/preferences:

• Personal skills: Teamwork, customer orientation (internal/external), initiative and decision-making, good oral and written communication, active listening, and problem-solving skills.

• Organizational skills: Ability to organize one's workplace and daily activities to ensure maximum quality. Ensuring a safe environment to prevent incidents and/or accidents. Attention to detail. Ability to handle multiple tasks simultaneously and prioritize objectives.

• Technical skills: Knowledge of Good Manufacturing Practices, policies, and GMP procedures. Ability to work in a highly regulated environment.

• Computer skills: User-level knowledge of office software, as well as knowledge of the computer systems that control daily activities.

full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

Responsabilidades:

La posición del Técnico de Laboratorios de Control de Calidad es una posición de soporte técnico y/o colaboración en las tareas relacionadas con los equipos de Control de Calidad para cumplir con los objetivos principales de la planta de Alcobendas relativos a:

• Liderar los proyectos incluidos en el plan maestro de validación relacionados con los equipos del laboratorio asi como validaciones de nuevos productos, re-validaciones, validaciones de limpiezas, servicios y transferencias analíticas cumpliendo con los plazos establecidos aportando el conocimiento técnico y asegurando que se cumplen los plazos requeridos.

• Evaluación de las características técnicas de nuevos equipos disponibles en el mercado y gestión de la compra de los mismos.

• Planificar y realizar la calibración, mantenimientos preventivos y correctivos de los equipos del laboratorio.

• Conocer y supervisar técnicamente los análisis químicos y las muestras que llegan al laboratorio asegurando la revisión y aprobación de los datos analíticos (por ejemplo, análisis de producto, de muestras de servicios, de limpiezas de piezas/equipos, de muestras de estabilidad).

• Colaborar en la resolución de incidencias de sistemas del laboratorio e investigaciones analíticas y desviaciones, identificando adecuadas causas raíz y estableciendo planes de acción que eviten recurrencias, así como la documentación técnica asociada a su puesto de trabajo.

• Colaborar activamente en que el sistema de calidad del laboratorio se mantiene de acuerdo con los estándares de calidad establecido.

Requisitos básicos:

• Se requiere formación universitaria en Ciencias Químicas, en otras licenciaturas de Ciencia de la Salud (Farmacia, Biología) o en Ingeniería Química.

• Se requiere experiencia mínima de 3 años en un laboratorio de control de calidad GMP, contando con experiencia en los diferentes equipos de laboratorio y técnicas analíticas y es requerida experiencia cualificando/validando equipos de laboratorio o fabricación.

• Nivel de inglés fluido hablado y escrito (C1).

• Trabajo en turno de tarde (15:05-23:15) de lunes a viernes.

Habilidades adicionales/preferencias:

• Habilidades personales: Trabajo en equipo, orientación al cliente (interno/externo) iniciativa y toma de decisiones, buena comunicación oral y escrita, saber escuchar, capacidad para resolución de problemas.

• Habilidades organizativas: Cualidades para organizar su lugar de trabajo y sus actividades diarias con el fin de garantizar la máxima calidad. Asegurar un ambiente seguro para evitar incidentes y/o accidentes. Atención al detalle. Capacidad para trabajar con varios temas a la vez y priorizar objetivos.

• Habilidades técnicas: Conocimiento en las normas de correcta fabricación, políticas y procedimientos GMP. Capacidad para trabajar en un ambiente altamente regulado.

• Habilidades en Herramientas Informáticas: Conocimientos de Software Ofimático al nivel de usuario, así como conocimiento de los sistemas informáticos que controlan las actividades que ejecuta diariamente.

full-time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly