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.

Syspro Automation is an engineering company focused on GMP Automation, working globally with offices in Spain, Portugal, Switzerland and the United States.

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 8 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 C1 or better.

Skills that would be a plus:

- Knowledge of Kneat documentary platform is a plus.
- Spanish or portuguese language is also a plus.

We offer:

- Permanent contract.
- Integration into a young and highly skilled team.
- Opportunities for professional development and continuous training.

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📌 Csv senior validation engineers (Comunidad de Madrid)
🏢 Syspro Automation
📍 Comunidad de Madrid