ph3About us /h3pChiesi 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 8000 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. /ppAt 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 Vantaggi Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact. /ppDiversity 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. /ph3Global Technical Operations Supply /h3pGlobal 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 Parnaiba (BR), and Nerviano (IT) - together with our Virtual Plant network of external partners. /ph3This is what you will do /h3pWe are seeking an experienced and highly motivated Sterile Production Supervisor to join a unique greenfield project focused on biologics manufacturing. /ppThis role offers the opportunity to contribute not only to daily sterile operations, but also to the design, implementation, and start-up of a next-generation sterile production department.



/ppThe successful candidate will play a key role in shaping processes, supporting equipment and facility design decisions, and establishing operational standards for a biologics manufacturing environment. /ppThis is a rare opportunity to be part of a site built from the ground up, contributing to technical excellence, compliance, and long-term operational success. /ph3You will be responsible for /h3ullibProject Start-up Phase /b Contribute to process and facility design discussions, ensuring manufacturability and GMP compliance. /liliSupport layout review, equipment URS definition, and operational input during design and procurement phases. /liliParticipate in FAT/SAT, commissioning, and qualification activities for sterile biologics manufacturing lines. /liliCollaborate with MST, Engineering, QA, and Validation teams to define robust operational workflows. /liliContribute to the development of SOPs, batch records, training programs, and aseptic practices. /liliSupervise day-to-day sterile biologics manufacturing operations (e.g., aseptic processing, filtration, filling, formulation). /liliEnsure compliance with GMP, Annex 1, and aseptic processing standards. /liliLead and coach operators in cleanroom behaviors, gowning practices, and aseptic techniques. /liliMonitor production performance, deviations, and investigations; drive timely resolution and continuous improvement. /liliSupport media fills, environmental monitoring oversight, and inspection readiness activities. /liliPromote a strong quality and safety culture within the department. /li /ulh3You will need to have /h3ulliDegree in Biotechnology, Pharmacy, Biology, Chemical Engineering, or related scientific disciplines /liliMinimum 3-5 years of experience in sterile pharmaceutical manufacturing. /liliProven hands-on experience in biologics manufacturing (e.g., aseptic processing,



sterile filtration, fill-finish, upstream/downstream interfaces). /liliKnowledge of GMP and Annex 1 requirements. /liliDeep understanding of aseptic techniques and contamination control strategy. /liliFamiliarity with process validation and equipment qualification. /liliStrong documentation and deviation management capabilities. /li /ulh3We would prefer for you to have /h3ulliExperience in start-up, scale-up, or facility expansion projects is desirable. /liliExposure to isolators, cleanroom qualification, and media fill execution is a strong advantage. /li /ulh3Location /h3pNerviano, Milano /ph3Compensation Range /h3pThe 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. /ph3What we offer /h3pNo 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. /ppWe 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. /ppChiesi 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

📌 Sterile Supervisor (Milano, IT)
🏢 Biopharma Careers
📍 Milano