CSV Engineers

Syspro Automation; Torrejón de Ardoz; A distancia; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading automation company is seeking CSV Engineers to contribute to exciting projects within a GMP environment. This role involves risk analysis, documentation management, and collaboration within a dynamic team. Candidates should possess significant experience in CSV validation and familiarity with the biotech sector. Flexibility in work options is obtainable, alongside professional growth opportunities.

Servicios

Permanent contract

Remote or hybrid work options

Professional development opportunities

Formación

• Minimum of 5 years of experience in CSV validation.
• Experience in biotech industry and knowledge of cGMP.
• Strong skills in documentation management and communication.

Responsabilidades

• Conduct risk analysis and define validation plans.
• Review documentation for compliance.
• Define and document qualification tests.

Conocimientos

Documentation management

Communication

Proactive attitude

Ability to work independently

Teamwork

Knowledge of cGMP

English Level B2

Herramientas

Microsoft Word

Microsoft Excel

DeltaV systems

Kneat documentary platform

Descripción del empleo

In Syspro Automation we are looking for CSV (Computerized System Validation) Engineers to join a multidisciplinary team working in challenging automation projects within a GMP environment.

Main responsibilities :

• Conduct risk analysis and define validation plans for various process equipments in the pharmaceutical industry.
• Review documentation of the equipments to ensure compliance with the validation plan.
• Define, execute and document qualification tests.
• Manage and document deviations and changes.

Required skills and experience :

• Minimum of 5 years of experience in CSV validation.
• Strong skills in managing and creating documentation (Microsoft Word and Excel).
• Excellent communication skills and proactive attitude.
• Ability to work independently and as part of a team.
• Experience within the biotech industry with knowledge of current Good Manufacturing Procedures (cGMP).
• English level B2 or better.

Skills that would be a plus :

• Experience with DeltaV systems is a strong plus.
• Knowledge of Kneat documentary platform is a plus.

We offer :

• Permanent contract.
• Remote or hybrid work options in our offices in Nigrán, Madrid and Lisbon.
• Integration into a young and highly skilled team.
• Opportunities for professional development and continuous training.