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.

Quality Manager

Randstad España

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

Job Description

Do you have experience in pharmaceutical or food quality and are looking for a position in Ciudad Real? Randstad Professional is looking for a profile like yours!

- Management of the quality team.
- Analyze deviations, anomalies, and detected non-conformities, validating and communicating conclusions and monitoring corrective actions.
- Evaluate change controls with the Regulatory Affairs department and other involved departments.
- Evaluate batch records and propose their release.
- Monitor and/or validate production material lists.
- Establish the implementation of validation processes in accordance with internal and international standards.
- Establish the validation and/or qualification programs to be carried out, including documentation, responsibilities, necessary actions, etc., as well as monitoring and evaluating results according to the defined program and involved departments.
- Participate in the establishment of the protocol and verify the validation report of procedures, facility qualification, analytics, modification control, etc.
- Participate in and provide support for audits.
- Participate in the preparation and collection of quality indicators.
- Use and maintain in good condition the manual and mechanical tools required for the development of assigned tasks.
- Ensure the updating and reliability of the department's databases.
- Comply with current regulations regarding data protection and access to information.
- Carry out work in accordance with established procedures and current regulations regarding occupational risk prevention.

- At least 3 years in a similar QC/QA lead position.
- Degree in Pharmacy, Chemistry, or similar.

- Competitive salary
- Stable position
- Schedule from 7:00 to 15:00

View original advert (Spanish)

¿Tienes experiencia en calidad farmacéutico o alimenticia y buscas una posición en Ciudad Real? Pues desde Randstad Professional buscamos un perfil como el tuyo!

- Gestión del equipo de calidad.
- Analizar las desviaciones, anomalías y no conformidades detectadas, validando y comunicando las conclusiones y realizando el seguimiento de las acciones correctivas.
- Evaluar los controles de cambio con el departamento de Regulatory Affairs y demás departamentos implicados.
- Evaluar los expedientes de lote y proponer su liberación.
- Realizar el seguimiento y/ o validación de las listas de materiales de producción.
- Establecer la puesta en marcha de los procesos de validación conforme a los estándares internos e internacionales.
- Establecer los programas de validaciones y/o cualificaciones a realizar, incluyendo la documentación, las responsabilidades, las acciones necesarias, etc., así como llevar acabo su seguimiento y evaluación de resultados,
según el programa definido y los departamentos implicados.
- Participar en el establecimiento del protocolo y verificar el informe de validación de los procedimientos, cualificación de las instalaciones, analíticas, control de las modificaciones, etc.
- Participar y dar soporte en auditorías.
- Participar en la preparación y recopilación de los indicadores de calidad.
- Utilizar y mantener en buen estado, las herramientas manuales y mecánicas requeridas para el desarrollo de los trabajos asignados.
- Velar por la actualización y la fiabilidad de las bases de datos del departamento.
- Cumplir la normativa vigente en materia de protección de datos y acceso a la información.
- Desarrollar su trabajo conforme a los procedimientos establecidos y la normativa vigente en materia de prevención
de riesgos laborales.