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Instrument Test Technician 2 responsible for performing calibration, maintenance, and documentation of inspection, measurement, and test equipment (IM&TE) to ensure compliance with quality standards and regulatory requirements. Supports both lab and field equipment, maintaining audit readiness and operational efficiency.
Job Responsibility
Perform calibration, verification, and adjustment of electrical, mechanical, and dimensional equipment (e.g., balances, force testers, multimeters, calipers, Instron systems)
Execute calibrations following approved procedures, manufacturer guidelines, and traceability standards
Evaluate calibration results for out-of-tolerance conditions and measurement acceptability
Support calibration, tracking, and deployment of field service equipment
Accurately document calibration results and maintain audit-ready records, including certificates traceable to national/international standards
Assist in investigations for out-of-tolerance or calibration discrepancies
Schedule and coordinate calibration activities to reduce backlog and ensure timely equipment availability
Perform basic troubleshooting, preventive maintenance, and coordinate repairs for equipment issues
Requirements
Minimum 3+ years in calibration, metrology, or test equipment maintenance
Hands-on experience with IM&TE in regulated environments
Experience in medical device, biotech, or pharmaceutical sectors is a plus
Degree or relevant certification in Electronics, Mechanical Technology, Metrology, or equivalent experience
Familiarity with FDA 21 CFR Part 820 and ISO 13485 standards preferred
Proficiency with calibration and quality management systems is advantageous
Strong understanding of measurement science and calibration techniques
Proficiency in electrical and mechanical instrumentation
Ability to read and interpret technical drawings, specifications, and procedures
Familiarity with standard test equipment: multimeters, pressure gauges, scales, force testers, dimensional tools
Knowledge of root cause analysis and handling out-of-tolerance investigations
Nice to have
Experience in medical device, biotech, or pharmaceutical sectors is a plus
Familiarity with FDA 21 CFR Part 820 and ISO 13485 standards preferred
Proficiency with calibration and quality management systems is advantageous