Medical devices tester (1-Year Temporary Contract)

Randstad España; Barcelona; Presencial; EUR 42.000 - 64.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

On-site work

Competitive remuneration

Long-term continuity potential

Descripción de la vacante

Randstad España, on behalf of a leading biotechnology company in Barcelona, is seeking a Testing Specialist for its R&D department. You will participate in the evaluation and testing of an in vitro diagnostic instrument in the development phase.

You will help develop and implement test workflows according to IVD assay requirements, and contribute to testing biotech projects as a member of the R&D team. A degree in Biotechnology/Biomedicine and advanced English are required.

Formación

• English proficiency at an advanced level.
• Experience with IVD equipment, instrumentation or medical systems.
• Familiarity with ISO 9001, ISO 13485 and IVDR/FDA quality/regulatory regimes.
• Experience preparing technical documentation (specifications, test protocols, technical reports).

Responsabilidades

• Evaluate and test an in vitro diagnostic instrument in the development phase.
• Develop and implement test workflows on the instrument according to IVD assay requirements.
• Participate in testing biotech projects as a member of R&D.

Conocimientos

Advanced English

IVD knowledge

Educación

Degree in Biotechnology or Biomedicine

Descripción del empleo

An expanding, leading biotechnology company located in Barcelona is looking to recruit a Testing Specialist for its R&D department.

Functions:

• As a member of the R&D team, you will participate in the evaluation and testing of an in vitro diagnostic instrument in the development phase.
• You will be part of the development and implementation of test workflows on the instrument according to IVD assay requirements.
• You will participate in the testing of biotech projects as a member of R&D.

Requirements:

Degree in Biotechnology, Biomedicine, or similar.

Advanced level of English.

Experience working in a BSL-2 environment.

More than two years of experience with IVD equipment, instrumentation, or medical systems.

Experience in preparing technical documentation (specification documents, test protocols, technical reports, etc.).

Knowledge of quality systems (ISO9001, ISO13485) and IVD regulations (IVDR, FDA).

We Offer:

• You will be part of a high-performance team in a project of great interest and impact.
• Full-time position (Standard day shift shift), 100% on-site.
• Attractive remuneration package according to the experience provided.
• One-year temporary project with possibilities of indefinite continuity.

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