Randstad is a global leader in the HR services industry, specializing in recruitment, staffing, and outsourcing solutions across 39 countries. As one of the world's largest HR providers, the company operates at a massive scale, connecting millions of candidates with opportunities in sectors ranging from technology and engineering to healthcare and logistics.

In Spain, Randstad maintains one of the most extensive professional networks in the country, with a presence in nearly every major city. For international professionals, Randstad serves as a primary entry point into the Spanish labor market, offering specialized recruitment services through divisions like Randstad Technologies and Randstad Professionals, which frequently handle roles for multinational clients requiring English or other foreign languages.

Founded in 1960 by Frits Goldschmeding in the Netherlands, Randstad has grown from a small local operation into the world's largest HR service provider. The company expanded into Spain in the 1990s and has since solidified its position through major acquisitions like Vedior.

For international professionals

Operates a vast network of over 200 offices across Spain, providing local support in almost every province.
Features specialized divisions for IT, Engineering, and Life Sciences that are highly relevant for skilled international workers.
Acts as a primary recruiter for many Fortune 500 companies established in Spain.
Provides a wide variety of contract types, including permanent placements and long-term outsourcing projects.

Pharmaceutical Technology - Internship - Curious Talent

Randstad España

This job was originally posted in Spanish and automatically translated to English. You'll most likely need Spanish to apply.

Job Description

Ready to apply your magic and break barriers with us? Join a global team of curious minds dedicated to creating, improving, and prolonging lives through innovative solutions in Healthcare, Life Science, and Electronics.

Your Role:

- We are looking for individuals with initiative, curiosity, digital and statistical skills who are familiar with the GMP environment and oral solid dosage manufacturing processes.

In our team, your role will be:

- Collaborate in the preparation and updating of manufacturing process lifecycle documentation (Process Control Strategy – PCS, Continuous Process Verification – CPV) and cleaning validation, working with real process data from the start.
- Participate in process and cleaning improvement projects, learning to use historical data and digital tools to identify optimization opportunities.
- Provide support for process and cleaning investigations that arise during routine manufacturing, analyzing process information and learning how data-driven decisions are made in a GMP environment.
- Assist in the collection, organization, and analysis of data for quality investigations and for the tracking of corrective and preventive actions (CAPAs).
- Work cross-functionally with Production, Quality, and Engineering teams, developing a global vision of the production process and the use of shared digital knowledge.

Who you are:

- University degree in Health Sciences.

- Basic knowledge of statistics and a curiosity for data analysis, with an interest in learning how to analyze and visualize data.

- Proficiency in Excel, Word, and PowerPoint.

- Motivation to develop yourself in a digital, data-driven, and continuous improvement environment.

- Fluent English, both spoken and written.

A one-year, full-time, paid internship contract is offered.

View original advert (Spanish)

¿Listo para aplicar tu magia y romper barreras con nosotros? Únete a un equipo global de mentes curiosas dedicado a crear, mejorar y prolongar vidas a través de soluciones innovadoras en Healthcare, Life Science y Electronics.

Tu Rol:

-Buscamos personas con iniciativa, curiosidad, habilidades digitales y estadísticas que conozca el entorno GMP y familiarizado con los procesos de fabricación de formas sólidas orales.

En nuestro equipo tu rol será:

- Colaborar en la preparación y actualización de documentación del ciclo de vida de los procesos de fabricación (Process Control Strategy ¿ PCS, Continuous Process Verification ¿ CPV) y validación de limpieza, trabajando con datos reales de proceso desde el inicio.
- Participar en proyectos de mejora de procesos y de limpiezas, aprendiendo a usar datos históricos y herramientas digitales para identificar oportunidades de optimización.
- Dar soporte a las investigaciones de proceso y limpieza que surjan durante la fabricación rutinaria, analizando información de proceso y aprendiendo cómo se toman decisiones basadas en datos en un entorno GMP.
- Ayudar en la recopilación, organización y análisis de datos para investigaciones de calidad y para el seguimiento de acciones correctivas y preventivas (CAPAs).
- Trabajar de forma transversal con equipos de Producción, Calidad e Ingeniería, desarrollando una visión global del proceso productivo y del uso del conocimiento digital compartido.

Quién eres:

- Titulación universitaria en Ciencias de la Salud.

- Conocimientos básicos de estadística y curiosidad por el análisis de datos, con interés en aprender a analizar y visualizar datos..

- Buen manejo de Excel, Word y PowerPoint.

- Motivación por desarrollarte en un entorno digital, data¿driven y de mejora continua.