We are looking for a CSV / Automation Engineer with strong hands-on experience in Siemens PCS 7 to support the implementation, qualification and lifecycle management of automated manufacturing systems within a regulated GMP environment.
Key Responsibilities
- Support the design, configuration, testing and qualification of Siemens PCS 7 automation systems.
- Develop and review automation and CSV documentation, including URS, functional and design specifications, risk assessments, test protocols, traceability matrices and validation summary reports.
- Execute FAT, SAT, IQ, OQ and system integration testing for process control and automation systems.
- Ensure automated systems comply with GAMP 5, 21 CFR Part 11, EU GMP Annex 11 and data integrity requirements.
- Review system configurations, alarms, interlocks, recipes, audit trails, user access controls and electronic records.
- Investigate system deviations and support CAPA, change control, periodic review and system lifecycle activities.
- Work closely with Engineering, Manufacturing, Quality Assurance, IT, vendors and system integrators.
- Support automation troubleshooting, system upgrades, modifications and commissioning activities.
- Maintain validated system status throughout the equipment and system lifecycle.
Requirements
- Relevant experience supporting automation or computer system validation within pharmaceutical, biotechnology or other regulated manufacturing environments.
- Strong hands-on knowledge of Siemens PCS 7, including system architecture, configuration, testing and troubleshooting.
- Experience with DCS, PLC, SCADA, HMI, batch control systems or process automation.
- Familiarity with CSV documentation and the execution of IQ/OQ protocols.