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.

This job was published 4 months ago

Qa Validation Technician

Randstad España

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

Job Description

- Efficiently execute computerized system validations under GMP/GLP regulations and GAMP 5 methodologies.
- Ensure alignment with FDA and EMA regulations.
- Develop and review the validation documentation lifecycle (Validation Plans, URS, DQ/IQ/OQ/PQ, and Summary Reports).
- Draft and update Standard Operating Procedures (SOPs) specific to the quality system in their area.
- Act as the computerized systems administrator within the Technical Management area, ensuring access control and traceability.
- Lead improvement proposals for validation processes and implement technological solutions that optimize the QA area.

University Degree in Health Sciences, Engineering, Pharmacy, or similar.
Minimum 2 years of experience in Quality Assurance departments within the pharmaceutical sector.
English B2
Own vehicle to access the facilities.
Analytical profile, with technical leadership capacity and attention to detail.

View original advert (Spanish)

- Ejecutar de manera eficiente las validaciones de sistemas informatizados bajo normativas GMP/GLP y metodologías GAMP 5.
- Asegurar la alineación con las regulaciones de la FDA y las EMA.
- Desarrollar y revisar el ciclo de vida de la documentación de validación (Planes de Validación, URS, DQ/IQ/OQ/PQ e Informes de Resumen).
- Redactar y actualizar los Procedimientos Normalizados de Trabajo (PNTs) específicos del sistema de calidad en su área.
- Actuar como administrador de sistemas informatizados dentro del área de Dirección Técnica, asegurando el control de accesos y la trazabilidad.
- Liderar propuestas de mejora en los procesos de validación e implementar soluciones tecnológicas que optimicen el área de QA.

Grado Universitario en Ciencias de la Salud, Ingeniería, Farmacia o similar.
Mínimo 2 años de experiencia en departamentos de Garantía de Calidad en el sector farmacéutico.
Inglés B2
Vehículo propio para acceder a las instalaciones.
Perfil analítico, con capacidad de liderazgo técnico y orientación al detalle.