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 Management System (QMS) 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

-QMS Maintenance: ensure and update the Quality Management System under medical device sector regulations (ISO 13485 and MDR).

-Audits: support the preparation, coordination, and execution of internal and external audits (notified bodies and inspections).

-Data and ERP Management: daily control of technical documentation, quality records, and product traceability through the ERP system.

-Cross-functional Quality Assurance: supervise that the required quality levels are met across all operational areas of the company.

-Education: Higher Vocational Training (FPII) in the chemical/laboratory field or University Degree (Chemistry, Biology, Biotechnology, Engineering, or similar).

-Experience: junior profile with 2 years of experience in laboratory environments, preferably in quality control/management departments.

-Languages: advanced level of English (B2-C1) for the management of international technical documentation.

-Skills: methodical, rigorous, organized person with the ability to communicate with other departments.

View original advert (Spanish)

-Mantenimiento del SGC: asegurar y actualizar el Sistema de Gestión de Calidad bajo las normativas del sector medical device (ISO 13485 y MDR).

-Auditorías: apoyar en la preparación, coordinación y ejecución de auditorías internas y externas (organismos notificados e inspecciones).

-Gestión de datos y ERP, controlar diariamente la documentación técnica, registros de calidad y trazabilidad del producto a través del sistema ERP.

-Garantía de calidad transversal: supervisar que se cumplan los niveles de calidad exigidos en todas las áreas operativas de la compañía.

-Formación: Ciclo Formativo de Grado Superior (FPII) del ámbito químico/laboratorio o Grado Universitario (Química, Biología, Biotecnología, Ingeniería o similar).

-Experiencia: perfil junior con experiencia de 2 años en entornos de laboratorio, preferiblemente en departamentos de control/gestión de calidad.