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.

Qara Specialist

Randstad España

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This position is responsible for maintaining and ensuring that the company's quality system complies with FDA, EU, ISO 13485, IEC 62304, and all international medical device and IVD market requirements. The QARA Specialist is also responsible for ensuring that products and their labeling meet all regulatory requirements (both domestic and international).
Key responsibilities include the independent management of QMS ISO standards and audits. Furthermore, the role will involve leading regulatory submissions to secure IVDR certification.
The successful candidate must possess a broad range of technical and scientific knowledge, with proven experience in ISO 13485 and IEC 62304. The ability to identify and quickly adapt to changing priorities is essential.

- Experience: Minimum of 5+ years of hands-on experience in QARA roles within the Medical Device, In Vitro Diagnostics (IVD), or digital health/SaMD industries.
- Education: Bachelor's or Master's degree in Biomedical Engineering, Computer Science, Biotechnology, Pharmacy, or a related scientific/technical discipline.
- CE-IVDR Expert: Deep knowledge and direct experience with the transition to and compliance with IVDR (EU 2017/746) and/or MDR (EU 2017/745).
- SaMD / Digital Health: Direct experience regulatory-filing for Software as a Medical Device (SaMD).
- Global Submissions: Proven track record preparing technical documentation for CE marking.