PpSelect how often (in days) to receive an alert: /p pBusiness Area: Industrial Operations HSE /p pJob Type: Direct Employee /p pContract Type: Permanent /p pLocation: Milano, IT /p h3About us /h3 pChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here. /p pAt Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact. /p pDiversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better. /p h3Global Technical Operations Supply /h3 pGlobal Technical Operations Supply (Global TechOpS) is Chiesi’s global manufacturing and supply area, responsible for ensuring consistent, outstanding quality, service and value across our end‑to‑end supply chain. Global TechOpS oversees the entire lifecycle of the drug: from process optimization and industrialization, to manufacturing, engineering, quality oversight, and supply chain management. Throughout this journey, Operational Excellence drives continuous improvement. This end‑to‑end model is powered by our four manufacturing sites - Parma (IT), Blois (FR), Santana de Parnaíba (BR), and Nerviano (IT) - together with our Virtual Plant network of external partners. /p h3This is what you will do /h3 pYou will coordinate maintenance activities for manufacturing and packaging equipment dedicated to pharmaceutical aerosol products (Metered Dose Inhalers – MDIs) and inhalers for metered‑dose powders. You will ensure the reliability, availability, and compliance of production assets while supporting uninterrupted manufacturing operations in accordance with GMP standards. Working closely with production, engineering, QA, Validation, Automation, and EHS, you will oversee preventive and corrective maintenance activities, drive equipment performance improvements,



and contribute to operational excellence initiatives. /p h3You will be responsible for /h3 ul liCoordinating preventive, predictive, and corrective maintenance activities for manufacturing and packaging equipment. /li liEnsuring maximum equipment availability and reliability while minimizing production downtime. /li liPlanning maintenance interventions in collaboration with production and planning to optimize manufacturing schedules. /li liCoordinating maintenance technicians and external contractors to ensure safe and efficient execution of maintenance activities. /li liMonitoring equipment performance and identifying opportunities for reliability improvement through root cause analysis and continuous improvement initiatives. /li liSupporting troubleshooting activities. /li liManaging maintenance documentation, work orders, spare parts, and equipment history using the site's CMMS. /li liSupporting equipment qualification, commissioning, FAT/SAT, validation, and start‑up activities for new production lines. /li liManaging investigations related to equipment failures, deviations, CAPAs, Change Controls, and Risk Assessments. /li liEnsuring maintenance activities comply with GMP requirements, safety regulations, and company engineering standards. /li liCollaborating with Automation and Engineering teams to optimize equipment performance and implement technical improvements. /li liSupporting regulatory inspections and internal audits by ensuring maintenance documentation is complete and inspection‑ready. /li liMonitoring maintenance KPIs and implementing strategies to improve Overall Equipment Effectiveness (OEE), reliability, and maintenance efficiency. /li /ul h3You will need to have /h3 ul liMinimum 3–5 years of maintenance or engineering experience in the pharmaceutical industry, preferably within sterile, aerosol, or high‑speed manufacturing environments. /li liStrong knowledge of preventive, predictive, and corrective maintenance methodologies. /li liExperience with pharmaceutical manufacturing and packaging equipment, preferably MDI or aerosol production lines. /li liGood understanding of GMP regulations, engineering documentation, and pharmaceutical quality systems. /li liExperience with CMMS systems.



/li liKnowledge of pneumatic, mechanical, electrical, and automated production systems. /li liStrong troubleshooting, analytical, and problem‑solving skills. /li liEnglish knowledge. /li /ul h3We would prefer for you to have /h3 ul liExperience with PLC‑controlled equipment and industrial automation systems. /li liFamiliarity with Lean Manufacturing, TPM, Reliability Centered Maintenance (RCM), or Six Sigma methodologies. /li liExperience supporting engineering projects and continuous improvement programs. /li liKnowledge of risk management tools such as FMEA. /li liExperience supporting regulatory inspections by FDA, AIFA. /li liProject management experience and contractor supervision are considered a plus. /li /ul h3Location /h3 pMilano, IT /p h3Compensation Range /h3 pThe minimum salary for this role is € 39,000, aligned to our established salary framework. The final offer will reflect the candidate’s skills, experience, qualifications and internal equity considerations. /p pThis role is eligible to participate in an annual premio scheme, subject to company and individual performance. /p pIn addition, we offer a comprehensive benefits package including pension, private medical insurance, wellbeing programme, flexible benefits programme. /p h3What we offer /h3 pNo matter where your path starts at Chiesi, it leads to inspiring possibilities. Your future is our focus, and we are committed to nurturing your development in our dynamic, friendly environment with access to resources and training every step of the way. /p pWe provide top‑class benefits, including comprehensive healthcare programs, work‑life balance initiatives, and robust relocation support. Our salary package is competitive, comprising a basic salary, performance bonuses, and benefits benchmarked against the external market. Additionally, we offer flexible working arrangements, remote work options, and tax assistance services for foreign colleagues, all designed to help you thrive. /p pChiesi is an equal opportunity employer committed to hiring a diverse workforce at all levels of our business. All qualified applicants receive consideration for employment based on attitude and merit, without regard to race, national origin, age, sex, religion, disability, sexual orientation, marital status, military status, gender identity or expression, or any other basis protected by applicable laws. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination. /p /p #J-18808-Ljbffr

📌 Air products coordinator (Milano)
🏢 Chiesi Farmaceutici
📍 Milano