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.