Job opportunity

MES System Engineer / MES System Engineeress

Proclinical Visp October 2, 2026

Join a Leading Manufacturing Environment

Proclinical is excited to announce a contract position for a MES System Engineer (EI&C) based in Switzerland. Your expertise in Manufacturing Execution Systems will be crucial in supporting compliance, enhancing efficiency, and achieving operational excellence. This role offers the opportunity to contribute to the digitalization and optimization of manufacturing processes within a dynamic environment.

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

  • Maintain, govern, and enhance MES standards, templates, best practices, and system architectures across manufacturing sites.
  • Provide technical support for MES operations, including troubleshooting, performance monitoring, incident resolution, and system optimization.
  • Support MES enhancements, upgrades, deployments, and lifecycle management activities.
  • Ensure GMP-compliant electronic batch records, manufacturing workflows, and system documentation are maintained according to regulatory requirements.
  • Develop and review GxP documentation, including specifications, risk assessments, test documentation, change controls, and SOPs.
  • Collaborate with Automation, IT, Validation, Quality, and Manufacturing teams to implement and maintain MES solutions aligned with business needs.
  • Support integration of MES with automation systems, historians, ERP platforms, and other manufacturing applications.
  • Participate in commissioning, qualification, validation, and system release activities.
  • Analyze manufacturing processes to identify opportunities for digitalization, standardization, and continuous improvement.
  • Ensure system reliability, data integrity, cybersecurity, and compliance with company standards and regulatory expectations.
  • Support audits, inspections, and periodic reviews related to MES systems and electronic records.

Key Skills and Requirements

  • Degree in Automation Engineering, Information Technology, Computer Science, Electrical Engineering, or a related technical field.
  • Experience with MES, Manufacturing IT, OT, or automation systems in a GMP-regulated pharmaceutical, biotech, or life sciences environment.
  • Strong understanding of manufacturing processes, batch execution, and electronic records management.
  • Familiarity with GAMP, GMP, data integrity, and computerized system validation (CSV) practices.
  • IT-OT background with knowledge of manufacturing system architectures.
  • Experience with MES platforms such as PAS-X, Syncade, PharmaSuite, Opcenter, or similar systems.
  • Knowledge of OT infrastructure, industrial networking, virtualization technologies (e.g., VMware), and server environments.
  • Understanding of system integration concepts between MES, ERP, historians, and automation platforms.
  • Awareness of cybersecurity principles and best practices in manufacturing environments.
  • Proficiency in GxP documentation and change management processes.
  • Fluency in English and/or German.

Apply Now

If you are interested in this exciting opportunity, please apply online using the form below. Only applications matching the job profile will be considered.

Proclinical is a leading life sciences recruiter focused on matching exceptional talent with outstanding positions across the globe. Proclinical acts as an Employment Agency in relation to this vacancy. By submitting your application, you confirm that you have read and understood our privacy policy, which outlines how we process and safeguard your data - https://www.proclinical.com/privacy-policy.

Work locationVisp, Switzerland

Application Form

Please enter your information in the following form and attach your resume (CV)

Only pdf, Word, or OpenOffice file. Maximum file size: 3 MB.