Instrumentation Engineer

Merck Sharp & Dohme Corp

Carlow, Ireland
Hybrid
Bachelor's degree in instrumentation engineering
Minimum 5 years pharmaceutical manufacturing experience
Proficiency with cmms/ccms management tools
Merck Sharp & Dohme Corp is seeking an Instrumentation Engineer in Carlow, Ireland, to manage site-wide calibration and gas detection programs, ensuring compliance with regulatory standards. The role requires a strong background in pharmaceutical manufacturing, data management, and cross-functional collaboration

Job Summary

  • This role serves as the subject matter expert for site-wide calibration and gas detection programs within a GMP sterile fill facility.
  • The engineer will manage CMMS configurations, ensure ALCOA+ compliant documentation, and lead root cause analyses for equipment failures.
  • Candidates must uphold data integrity standards and collaborate across Production, Quality, EHS, and Engineering teams to drive operational excellence.

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking an Instrumentation Engineer in Carlow, Ireland, to manage site-wide calibration and gas detection programs, ensuring compliance with regulatory standards. The role requires a strong background in pharmaceutical manufacturing, data management, and cross-functional collaboration.

Skills & Requirements

Must-have

  • Bachelor's degree in Instrumentation Engineering
  • Minimum 5 years pharmaceutical manufacturing experience
  • Proficiency with CMMS/CCMS management tools
  • Solid understanding of GMP and data integrity
  • Experience with gas detection systems
  • Root cause analysis (RCA) and troubleshooting skills

Nice-to-have

  • Lean Six Sigma methodology experience
  • Cross-functional collaboration abilities
  • Continuous improvement mindset
  • Strong leadership and delegation skills
  • Willingness to support team growth

Key Requirements

  • Bachelor's degree in manufacturing/mechanical/electrical/instrumentation engineering
  • Minimum 5 years in pharmaceutical manufacturing preferred
  • Practical knowledge of routine maintenance in GMP Sterile Fill Facility

Work Rights

Not specified

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