CLEEVEN is a European consulting and engineering company built around two core beliefs:
* The excellence of European engineers should drive global competitiveness.
* Our human mission is to support our consultants in both their professional and personal development.
In Switzerland, we support leading industrial and pharmaceutical organizations through high-value engineering, digital transformation, automation, and IT projects.
We are currently looking for a System Engineer / System Owner to support critical manufacturing and monitoring systems within a highly regulated pharmaceutical environment.
In this role, you will be responsible for the lifecycle management, compliance, and continuous improvement of industrial data historian and monitoring platforms, while acting as a key interface between IT, automation, engineering, and production teams.
Mission Objectives
* Act as the System Owner for critical manufacturing systems, including AVEVA PI and environmental monitoring platforms.
* Ensure the reliability, availability, and compliance of the systems under your responsibility.
* Maintain and update validation and qualification documentation in accordance with GxP requirements.
* Manage incidents, problems, changes, and deviations through established quality processes.
* Support service management activities and coordinate with internal and external stakeholders.
* Lead or contribute to technical and compliance-related projects.
* Support regulatory audits and inspections.
* Design, implement, and maintain interfaces between production equipment and the AVEVA PI platform.
* Integrate manufacturing equipment into the production IT environment and Active Directory domain.
* Drive continuous improvement initiatives to enhance system performance and operational efficiency.
Key Skills
* Hands‑on experience with AVEVA PI / PI System.
* Experience configuring and maintaining PI interfaces and data acquisition solutions.
* Solid understanding of industrial automation environments, including PLCs and process control systems (Siemens S7 preferred).
* Experience with Computerized System Validation (CSV) and IT qualification activities.
* Previous experience within a pharmaceutical, biotech, or other regulated GxP environment.
* Good knowledge of Active Directory environments.
* Strong stakeholder management and communication skills.
* Ability to work effectively in cross‑functional and matrix organizations.
* Fluent English, German is a big plus
Nice to Have
* Experience with Rotronic Monitoring System (RMS).
* Knowledge of network infrastructure and industrial networking concepts.
* Experience with VMware virtualization technologies.
* Familiarity with backup and recovery solutions such as Acronis.
* AVEVA PI certification.
Profile
* Degree or technical qualification in Computer Science, Automation, Engineering, or a related field.
* Proven experience managing critical manufacturing or industrial IT systems.
* Strong analytical and problem‑solving skills.
* Comfortable working in regulated environments with high quality and compliance standards.
* Able to communicate effectively with technical and non‑technical stakeholders.
* Autonomous, organized, and proactive.
* Team player with a collaborative mindset.
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