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.

Physicochemical Control Technician at Laboratorios Salvat

Randstad España

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

Job Description

At randstad, we are looking to incorporate a Quality Control Technician for Salvat

Under the supervision of the Physicochemical Control Manager, you will be responsible for:

Document Management: Review of analytical documentation generated in the laboratory and control in accordance with GMP and data integrity (ALCOA+).
SOPs: Drafting, reviewing, and updating Standard Operating Procedures and technical instructions.
Investigations and CAPAs: Leading investigations related to laboratory events, OOS, OOT, deviations, and complaints, defining CAPAs and Change Controls.
Laboratory Logistics: Stock management of reagents, consumables, and reference standards.
Coordination: Support in audits and inspections, and coordination with analysts and supervisors to optimize workflow.

Education: Degree in Chemistry, Pharmacy, or equivalent qualification.
Experience: Minimum 1 year in a pharmaceutical environment (QC).
Technical Knowledge: Familiarity with GMP regulations, analytical techniques (HPLC, GC, UV, etc.) at a user/support level, and handling of pharmacopoeias (Ph. Eur., USP).
Tools: Experience with chromatographic data acquisition systems, document management systems, and proficiency in MS Office. (Experience in SAP or LIMS will be positively valued).
Languages: English minimum level B2.

We are looking for a person with high attention to detail, planning ability, proactivity, a sense of responsibility, and excellent communication skills for teamwork.

What do we offer?

Substitution Contract + Permanent.
Work shift: Afternoon 14:30-22:30
Attractive Salary Range.
Joining a leading company in the Pharmaceutical world.
Career plan.

View original advert (Spanish)

Desde randstad estamos buscando incorporar a un Tecnico/a de Control de Calidad para Salvat

Bajo la supervisión del Responsable de Control Fisicoquímico, te encargarás de:

Gestión Documental: Revisión de la documentación analítica generada en el laboratorio y control conforme a GMP e integridad de datos (ALCOA+).
PNTs: Redacción, revisión y actualización de Procedimientos Normalizados de Trabajo e instrucciones técnicas.
Investigaciones y CAPAs: Liderar investigaciones relacionadas con eventos de laboratorio, OOS, OOT, desviaciones y reclamaciones, definiendo CAPAs y Controles de Cambios.
Logística de Laboratorio: Gestión de stock de reactivos, consumibles y patrones de referencia.
Coordinación: Soporte en auditorías e inspecciones, y coordinación con analistas y supervisores para optimizar el flujo de trabajo.

Formación: Grado en Química, Farmacia o titulación equivalente.
Experiencia: Mínimo 1 año en entorno farmacéutico (QC).
Conocimientos técnicos: Familiaridad con normativa GMP, técnicas analíticas (HPLC, GC, UV, etc.) a nivel usuario/soporte, y manejo de farmacopeas (Ph. Eur., USP).
Herramientas: Experiencia con sistemas de adquisición de datos cromatográficos, sistemas de gestión documental y dominio de MS Office. (Se valorará positivamente la experiencia en SAP o LIMS).
Idiomas: Inglés mínimo nivel B2.

Buscamos a una persona con alta atención al detalle, capacidad de planificación, proactividad, sentido de la responsabilidad y excelentes habilidades de comunicación para trabajar en equipo.