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EI&C MES System Engineer (7118)

CTC Resourcing Solutions AG 01.10.2026 Déposer ma candidature
Entreprise
CTC Resourcing Solutions AG
Date
01.10.2026
Référence
361063

Role Overview

Join an international company operating in a highly regulated industrial environment to serve as a key technical resource. This is a 100% site-based position in Visp, offered initially for 12 months with the possibility of extension.

Key Responsibilities

  • Maintain, govern, and continuously improve 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 requirements.
  • 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 and 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.

Required Skills & Qualifications

  • Degree in Automation Engineering, Information Technology, Computer Science, Electrical Engineering, or a related technical discipline.
  • Proven experience with MES, Manufacturing IT, OT, or automation systems within a GMP-regulated pharmaceutical, biotech, or life sciences environment.
  • Strong understanding of manufacturing processes, batch execution, and electronic records management.
  • Experience supporting system implementations, enhancements, upgrades, and operational support activities.
  • Familiarity with GAMP, GMP, data integrity, and computerized system validation (CSV) practices.
  • T/OT background with strong understanding of manufacturing system architectures.
  • Experience with Manufacturing Execution Systems (e.g., PAS-X, Syncade, PharmaSuite, Opcenter, or similar platforms).
  • Knowledge of OT infrastructure, industrial networking, virtualization technologies (VMware), and server environments.
  • Understanding of system integration concepts and interfaces between MES, ERP, historians, and automation platforms.
  • Knowledge of cybersecurity principles and best practices within manufacturing environments.
  • Experience with GxP documentation and change management processes.
  • Fluent in English and/or German.

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