GMP EMR Maintenance Engineer – Instrumentation & Calibration

Actalent; Oberwallis; Vor Ort; CHF 90.000 - 140.000; Vollzeit

Zusammenfassung

Actalent seeks an EMR Maintenance Engineer to oversee calibration, maintenance, and compliance of critical process instrumentation in a GMP-regulated environment.

The role focuses on hands-on calibration execution, record-keeping, and audit readiness across Pharma/Process Manufacturing settings, with cross-functional collaboration among Engineering, Production, Quality, and Maintenance teams.

Qualifikationen

• Minimum 5 years of hands-on experience in instrumentation, calibration, and maintenance.
• Experience working in a GMP-regulated environment.
• Strong understanding of calibration execution, documentation, and compliance requirements.
• Industry experience in Pharma, Chemical, Process Manufacturing, CDMO, or Oil & Gas.

Aufgaben

• Prepare, execute, and document calibration and preventive maintenance activities for process instrumentation.
• Manage calibration records and maintenance documentation using CMX Calibration Software.
• Ensure all activities comply with GMP requirements, site procedures, and regulatory standards.
• Support troubleshooting, diagnostics, and continuous improvement of instrumentation systems.
• Coordinate maintenance activities through SAP PM (Plant Maintenance).
• Review calibration documentation to ensure compliance and audit readiness.
• Collaborate with Engineering, Production, Quality, and Maintenance teams.
• Support investigations, change controls, deviations, and CAPA activities related to instrumentation and calibration.
• Contribute to maintaining high standards of safety, quality, and operational excellence.

Kenntnisse

Instrumentation & Calibration

GMP Compliance

Maintenance Execution

Ausbildung

Electrical/Automation Engineering

HF/FH or Apprenticeship

Tools

CMX Calibration Software

SAP PM (Plant Maintenance)

Jobbeschreibung

Actalent seeks an EMR Maintenance Engineer to oversee calibration, maintenance, and compliance of critical process instrumentation in a GMP-regulated environment.

The role focuses on hands-on calibration execution, record-keeping, and audit readiness across Pharma/Process Manufacturing settings, with cross-functional collaboration among Engineering, Production, Quality, and Maintenance teams.