CSV/CQV Validation Engineers

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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 3 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:

• Spanish language is 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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