CSV Engineers

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.