Pharma Equipment Maintenance Coordinator

Chiesi Farmaceutici S.p.A.

Milano

In loco

EUR 35.100 - 42.900

Tempo pieno

14 giorni+

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Vantaggi offerti da questo lavoro

Pension

Private medical insurance

Wellbeing programme

Flexible benefits programme

Relocation support

Descrizione del lavoro

Chiesi Farmaceutici S.p.A. in Milano, IT is seeking a maintenance/engineering specialist for the Global Technical Operations & Supply division.

The role focuses on coordinating maintenance for pharmaceutical aerosol production lines, ensuring asset reliability and GMP compliance, and collaborating across engineering, QA, and validation teams. Ideal candidates bring 3–5 years in pharma maintenance, strong CMMS experience, and knowledge of GMP regulations.

Competenze

Minimum 3–5 years of maintenance or engineering experience in the pharmaceutical industry.
Strong knowledge of preventive, predictive, and corrective maintenance methodologies.
Experience with pharmaceutical manufacturing and packaging equipment, preferably MDI or aerosol production lines.
Good understanding of GMP regulations, engineering documentation, and pharmaceutical quality systems.
Experience with CMMS systems.
Knowledge of pneumatic, mechanical, electrical, and automated production systems.
Strong troubleshooting, analytical, and problem-solving skills.
English knowledge.

Mansioni

Coordinating preventive, predictive, and corrective maintenance activities for manufacturing and packaging equipment.
Ensuring maximum equipment availability and reliability while minimizing production downtime.
Planning maintenance interventions in collaboration with production and planning to optimize manufacturing schedules.
Coordinating maintenance technicians and external contractors to ensure safe and efficient execution of maintenance activities.
Monitoring equipment performance and identifying opportunities for reliability improvement through root cause analysis and continuous improvement initiatives.
Supporting troubleshooting activities.
Managing maintenance documentation, work orders, spare parts, and equipment history using the site's CMMS.
Supporting equipment qualification, commissioning, FAT/SAT, validation, and start-up activities for new production lines.
Managing investigations related to equipment failures, deviations, CAPAs, Change Controls, and Risk Assessments.
Ensuring maintenance activities comply with GMP requirements, safety regulations, and company engineering standards.
Collaborating with Automation and Engineering teams to optimize equipment performance and implement technical improvements.
Supporting regulatory inspections and internal audits by ensuring maintenance documentation is complete and inspection-ready.
Monitoring maintenance KPIs and implementing strategies to improve OEE, reliability, and maintenance efficiency.