Senior Facilities Technician - GMP/CMMS Maintenance Pro

36 Dexcom International Limited; Athenry; On-site; EUR 50,000 - 65,000; Full time

Benefits offered by this job

Comprehensive benefits

Career development

Tuition reimbursement

Global growth opportunities

Job summary

Dexcom Ireland is seeking a data analyst to support Engineering, Quality and Operations by retrieving, compiling and analyzing technical data from internal systems. You will generate regular and ad-hoc reports and interpret information from drawings, schematics and process data to support investigations.

You will contribute to trend analysis, manage Non-Conformances, prepare controlled documents, and liaise with cross-functional teams to drive continuous improvement while ensuring GMP-compliant

Qualifications

• Minimum 4–6 years of related experience.
• Strong electrical or mechanical background.
• Proficiency with Maximo CMMS.
• Solid understanding of GMP standards.
• Experience with reporting.

Responsibilities

• Retrieve, compile, and analyze data from internal systems.
• Generate regular and ad-hoc reports for Engineering, Quality, and Operations.
• Interpret drawings, schematics, and process data for investigations.
• Support trend analysis and data evaluation for improvements.
• Assist in managing Non-Conformances with documentation.
• Prepare and review SOPs, work instructions, and reports.
• Collaborate with Engineering, Production, and Quality to gather information.
• Provide technical input on quality issues from hands-on experience.

Skills

Electrical background

Mechanical background

Maximo CMMS

GMP knowledge

Report writing

Independent and team player

Education

High School diploma

Tools

Maximo CMMS

Job description

Dexcom Ireland is seeking a data analyst to support Engineering, Quality and Operations by retrieving, compiling and analyzing technical data from internal systems. You will generate regular and ad-hoc reports and interpret information from drawings, schematics and process data to support investigations.

You will contribute to trend analysis, manage Non-Conformances, prepare controlled documents, and liaise with cross-functional teams to drive continuous improvement while ensuring GMP-compliant