Job description:

We are looking for an experienced DeltaV Automation Engineer to support the design, implementation, commissioning, and qualification of automation solutions for major CAPEX projects. You will work closely with Engineering, Operations, Validation, Quality, and Project teams to deliver reliable and GxP-compliant automation systems from design through startup.

• Design and implement Emerson DeltaV automation solutions for CAPEX projects.
• Configure control strategies, system interfaces, graphics, alarms, and process automation applications within the DeltaV environment.
• Develop and maintain GxP-compliant engineering and validation documentation in accordance with site and company standards.
• Integrate DeltaV with process equipment, PLCs, utility systems, MES, and other plant systems.
• Support and execute FAT, SAT, commissioning, IQ/OQ, qualification, and startup activities.
• Troubleshoot automation, communication, integration, and control-system issues throughout the project lifecycle.
• Ensure compliance with GMP, data integrity, change management, and validation requirements.
• Collaborate with multidisciplinary teams to ensure successful and timely project delivery.

About the customer:

Our client is an international organization within the pharmaceutical and life sciences sector, with a strong presence in Switzerland. The Visp site supports large-scale manufacturing, technology transfer, and major investment in modern facilities and automation infrastructure. Teams work across Engineering, Operations, Quality, Validation, and Project Management to deliver safe, compliant, and reliable solutions. The environment is technically demanding and strongly focused on GMP, operational excellence, and continuous improvement, offering exposure to significant CAPEX projects and advanced automation technologies.

Requirements:

• Degree in Automation Engineering, Electrical Engineering, or a related technical discipline.
• Strong hands-on experience with Emerson DeltaV engineering and configuration.
• Proven experience creating and maintaining GxP documentation within pharmaceutical, biotech, life sciences, or another regulated environment.
• Good understanding of commissioning, qualification, and validation processes.
• Experience with process automation, control-system integration, and industrial communication interfaces.
• Strong troubleshooting, root-cause analysis, and problem-solving skills.
• Previous experience working within CAPEX project environments.
• Ability to work effectively with Engineering, Operations, Validation, Quality, and external project partners.
• Good English skills, German is beneficial.