Senior PCS 7 Automation Engineer - On-site Life Sciences

Us3 Consulting; Antwerpen; Sur place; EUR 70 000 - 95 000; Plein temps

Résumé du poste

Us3 Consulting is seeking a Senior PCS 7 Automation Engineer for an on-site assignment in Antwerp, Belgium. You will maintain, support, and optimize a Siemens PCS 7 process control environment within a highly regulated life sciences manufacturing setting.

The role combines hands-on technical work with documentation, validation activities, and collaboration with Quality, Engineering and Operations to ensure compliance and continuous improvement.

Qualifications

• Extensive hands-on experience with Siemens PCS 7 in an industrial process automation setting.
• Experience in GMP-regulated life sciences environments.
• Familiarity with validation activities, FAT/SAT and commissioning documentation.
• Strong communication and documentation skills.

Responsabilités

• Provide day-to-day technical support for a Siemens PCS 7 distributed control system within a live manufacturing environment.
• Diagnose automation issues, perform root cause analysis and implement robust, long-term solutions.
• Deliver small-scale system enhancements and modifications, coordinating implementation and validation.
• Work with Quality, Engineering and Operations to ensure changes meet regulatory requirements.
• Provide guidance on system performance, risk mitigation and continuous improvement opportunities.
• Maintain high-quality technical documentation and change records.
• Support safe, reliable operation of interconnected automation systems in a regulated production environment.

Connaissances

Siemens PCS 7

Industrial process automation

Stakeholder communication

Description du poste

Us3 Consulting is seeking a Senior PCS 7 Automation Engineer for an on-site assignment in Antwerp, Belgium. You will maintain, support, and optimize a Siemens PCS 7 process control environment within a highly regulated life sciences manufacturing setting.

The role combines hands-on technical work with documentation, validation activities, and collaboration with Quality, Engineering and Operations to ensure compliance and continuous improvement.