Are you a DeltaV Automation Engineer looking to shape the future of GMP-compliant manufacturing in Switzerland's thriving life sciences sector?

Proclinical is seeking an Automation Engineer to support pharmaceutical and biotech CAPEX projects in Switzerland. In this role, you will design, develop, and implement automation solutions using Emerson DeltaV systems while ensuring compliance with GMP, GAMP, and data integrity standards. This is a site-based position requiring collaboration across multidisciplinary teams to deliver robust automation solutions.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Design, develop, and implement Emerson DeltaV automation solutions for pharmaceutical and biotech projects.
• Configure DeltaV control modules, equipment modules, phases, recipes, graphics, alarms, and system interfaces following company standards.
• Develop and maintain automation documentation, including functional specifications, design specifications, test protocols, and validation records.
• Ensure compliance with GMP, GAMP, and data integrity requirements in all activities.
• Support system architecture design, hardware configuration, network integration, and interface development with third-party systems.
• Troubleshoot automation hardware, software, and communication issues during project execution and operational support.
• Participate in change control processes, deviation investigations, risk assessments, and continuous improvement initiatives.
• Collaborate with process engineering, IT-OT, validation, and operations teams to deliver fit-for-purpose automation solutions.
• Provide technical support during startup, handover, and operational phases of the project lifecycle.

Key Skills and Requirements:

• Degree in Automation Engineering, Electrical Engineering, Computer Science, or a related technical field.
• Experience with Emerson DeltaV automation systems in pharmaceutical, biotech, chemical, or industrial manufacturing environments.
• Strong understanding of process control systems, instrumentation, and automation architectures.
• Familiarity with GMP-regulated environments and validation activities.
• Knowledge of CAPEX project execution and commissioning processes is advantageous.
• Proficiency in Emerson DeltaV configuration and system administration.
• Experience with GxP documentation and computerized system validation (CSV).
• Skills in process control design, system integration, networking, and troubleshooting.
• Understanding of GMP, GAMP, and data integrity requirements.
• Fluency in German and/or English is required.

If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at o.worch@proclinical.com.

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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