Pharma Maintenance Coordinator - GMP & MDI Equipment

Chiesi Group; Lombardia; On-site; EUR 35,000 - 43,000; Full time

Benefits offered by this job

pension

private medical insurance

wellbeing programme

flexible benefits programme

Job summary

Chiesi Group in Nerviano, Milan, is seeking an experienced maintenance/engineering professional to coordinate maintenance activities for pharmaceutical production lines. The role emphasizes GMP-compliant operations and collaboration across production, QA, and engineering teams.

You will ensure asset reliability, lead technicians and contractors, support qualification and start-up, and drive continuous improvements using CMMS data and KPIs.

Qualifications

• Technical diploma and 3-5 years in pharmaceutical maintenance/engineering.
• Experience with pharmaceutical manufacturing equipment and GMP documentation.
• Capable of troubleshooting and problem solving with CMMS use.

Responsibilities

• Coordinate preventive, predictive, and corrective maintenance for manufacturing and packaging equipment.
• Maximize equipment availability and minimize downtime.
• Plan maintenance interventions with production and planning to optimize schedules.
• Coordinate maintenance technicians and external contractors safely.
• Monitor equipment performance and drive improvements through RCA and continuous improvement.
• Support debugging, qualification, FAT/SAT, validation, and start-up activities.
• Maintain maintenance documentation, work orders, spare parts, and equipment history in CMMS.
• Assist regulatory inspections and internal audits with complete documentation.
• Track KPIs to improve OEE, reliability, and maintenance efficiency.

Skills

Maintenance engineering

GMP knowledge

CMMS experience

Troubleshooting

English knowledge

Education

Technical diploma

Tools

CMMS systems

Job description

Chiesi Group in Nerviano, Milan, is seeking an experienced maintenance/engineering professional to coordinate maintenance activities for pharmaceutical production lines. The role emphasizes GMP-compliant operations and collaboration across production, QA, and engineering teams.

You will ensure asset reliability, lead technicians and contractors, support qualification and start-up, and drive continuous improvements using CMMS data and KPIs.