This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
We are seeking a motivated, technically skilled, and communicative System Engineer to take ownership of our AVEVA PI Data Historian and Rotronic Monitoring Systems (RMS). In this critical role, you will act as the System Owner for both platforms, ensuring their reliable operation in a highly regulated GMP environment. You will work closely with manufacturing, engineering, quality, automation, and IT teams while driving system improvements, compliance activities, and strategic projects. This is an excellent opportunity for a hands-on engineer who combines strong technical expertise with leadership capabilities and enjoys working in a complex pharmaceutical production environment.
Job Responsibility
Serve as the System Owner for AVEVA PI and Rotronic Monitoring Systems (RMS)
Ensure reliable operation and lifecycle management of both systems across the Basel and Kaiseraugst sites
Manage system performance, availability, maintenance, and continuous improvement activities
Create, review, and maintain validation and qualification documentation
Ensure compliance with GMP, GxP, CSV, and internal quality standards
Support audits and inspections and coordinate remediation activities where required
Lead Incident, Problem, Change, and Deviation Management processes
Coordinate service providers and internal stakeholders to ensure timely issue resolution
Drive continuous service improvements and operational excellence
Lead and contribute to system-related projects and upgrades
Implement and configure equipment interfaces to the AVEVA PI platform
Connect manufacturing and laboratory equipment to the production domain via Active Directory
Collaborate closely with automation, manufacturing, quality, and IT teams
Requirements
Degree, Technician Certification, or completed vocational training in Computer Science / Information Technology, Automation Engineering, Electrical Engineering or a comparable technical discipline
Strong hands-on experience with the AVEVA PI Platform
Advanced knowledge of PI System configuration and interface implementation
Experience with PLC and Process Control Systems, preferably Siemens S7
Experience with Computerized System Validation (CSV) and IT Qualification
Good understanding of Active Directory environments
Experience working in regulated pharmaceutical manufacturing environments
Proven experience within Pharmaceutical Production and GxP-regulated environments
Experience in Project Management
Strong understanding of system lifecycle management and compliance requirements
Experience managing cross-functional stakeholders and vendors