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 5 months ago

Senior Quality Assurance Specialist

Randstad España

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

Job Description

Maintain and improve the Quality Management System in accordance with ISO 13485 (Medical Devices), ISO 22716 (Cosmetics - GMP), and other applicable regulations (FDA, ANVISA, etc.).
Manage and track Non-Conformities, CAPAs (Corrective and Preventive Actions), and deviations.
Prepare, review, and approve key documentation (procedures, work instructions, specifications, validation and qualification protocols).
Lead and participate in internal and external audits (certification, clients, suppliers).
Review and approve manufacturing batches for release.

Education: Bachelor's degree in Pharmacy, Chemistry, Biology, or similar.
Experience: Minimum 3-5 years of experience as a QA Technician/Specialist in the Medical Devices sector (essential) and/or Cosmetics (highly valued).
Proficiency in the ISO 13485 standard.

Stable contract, with an attractive remuneration package and social benefits.
You will be part of an innovative company in continuous growth.
100% on-site position.

View original advert (Spanish)

Mantener y mejorar el Sistema de Gestión de la Calidad de acuerdo con las normativas ISO 13485 (Dispositivos Médicos), ISO 22716 (Cosméticos - GMP) y otras regulaciones aplicables (FDA, ANVISA, etc.).
Gestionar y realizar el seguimiento de No Conformidades, CAPAs (Acciones Correctivas y Preventivas), y desviaciones.
Elaborar, revisar y aprobar documentación clave (procedimientos, instrucciones de trabajo, especificaciones, protocolos de validación y cualificación).
Liderar y participar en auditorías internas y externas (certificación, clientes, proveedores).
Revisar y aprobar los lotes de fabricación para su liberación.