MES System Engineer

Source Group International

Oberwallis

Vor Ort

CHF 90.000 - 130.000

Vollzeit

vor 44 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Source Group International seeks an experienced MES System Engineer to support manufacturing systems in a GMP-regulated pharmaceutical/biotech environment. The role is a 1-year contract, on-site in Visp, with potential extension.

Responsibilities include maintaining MES architectures, enabling upgrades, validating systems, and ensuring data integrity across IT/OT and automation interfaces. Fluency in English and/or German is desirable.

Qualifikationen

  • Degree in automation, IT, CS, electrical engineering or related field.
  • Hands-on MES/Manufacturing IT/OT experience in pharma, biotech or life sciences.
  • Experience with MES platforms such as PAS-X, Syncade, PharmaSuite, Opcenter or similar.
  • Strong GMP, GAMP, GxP and CSV understanding.
  • Knowledge of manufacturing processes, batch execution and electronic records.
  • IT/OT infrastructure knowledge, industrial networking, VMware and servers.
  • Experience integrating MES with ERP, historians and automation platforms.
  • English and/or German language proficiency.

Aufgaben

  • Maintain and improve MES systems, standards and architectures.
  • Provide technical support, troubleshooting and optimization.
  • Support MES enhancements, upgrades, deployments and lifecycle activities.
  • Maintain electronic batch records and manufacturing workflows.
  • Prepare and review GxP documentation, risk assessments, testing docs, change controls and SOPs.
  • Support commissioning, qualification and validation.
  • Integrate MES with automation systems, historians, ERP and other apps.
  • Collaborate with Automation, IT, Validation, Quality and Manufacturing teams.
  • Ensure data integrity, cybersecurity and GMP compliance.

Kenntnisse

GMP knowledge
IT/OT networking
Data integrity
Cybersecurity awareness

Ausbildung

Degree in Automation Engineering, IT, Computer Science, Electrical Engineering or related

Tools

PAS-X
Syncade
PharmaSuite
Opcenter
VMware

Jobbeschreibung

We are looking for an experienced MES System Engineer to support manufacturing systems within a GMP-regulated pharmaceutical/biotech environment. This is 1 year contract with possibility of extension, on-site in Visp.

Key Responsibilities
  • Maintain and continuously improve MES systems, standards and architectures
  • Provide technical support, troubleshooting and system optimization
  • Support MES enhancements, upgrades, deployments and lifecycle activities
  • Maintain electronic batch records (EBR) and manufacturing workflows
  • Prepare and review GxP documentation, specifications, risk assessments, testing documentation, change controls and SOPs
  • Support commissioning, qualification and validation
  • Integrate MES with automation systems, historians, ERP and other manufacturing applications
  • Work closely with Automation, IT, Validation, Quality and Manufacturing teams
  • Ensure data integrity, cybersecurity and GMP compliance
Your Profile
  • Degree in Automation Engineering, IT, Computer Science, Electrical Engineering or a related discipline
  • Hands‑on experience with MES / Manufacturing IT / OT systems in a pharmaceutical, biotech or life sciences environment
  • Experience with MES platforms such as PAS-X, Syncade, PharmaSuite, Opcenter or similar
  • Good understanding of GMP, GAMP, GxP and CSV
  • Understanding of manufacturing processes, batch execution and electronic records
  • Knowledge of IT/OT infrastructure, industrial networking, VMware and server environments
  • Experience integrating MES with ERP, historians and automation platforms
  • English and/or German

We believe in equal opportunity for all and actively encourage applications from diverse backgrounds, experiences, and perspectives.

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