Sterile Supervisor

ppSelect how often (in days) to receive an alert: /p pDepartment: Plant Operations Italy, Parma Site /p pBusiness Area: Industrial Operations HSE /p pJob Type: Direct Employee /p pContract Type: Permanent /p pLocation: Milano, IT /p pbAbout us /b /p 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 pbGlobal Technical Operations Supply /b /p 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 pWe are seeking an experienced and highly motivatedbSterile Production Supervisor /bto join a unique greenfield project focused onbbiologics manufacturing /b. /p pThis role offers the opportunity to contribute not only to daily sterile operations, but also to thebdesign, implementation, and start-up of a next-generation sterile production department /b. /p pThe 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. /p pThis is a rare opportunity to be part of absite built from the ground up /b, contributing to technical excellence, compliance, and long-term operational success. /p h3You will be responsible for /h3 pbProject Start-up Phase /b /p ul liContribute tobprocess and facility design discussions /b, ensuring manufacturability and GMP compliance. /li liSupportblayout review, equipment URS definition, and operational input /b during design and procurement phases. /li liParticipate inbFAT/SAT, commissioning, and qualification activities /b for sterile biologics manufacturing lines. /li liCollaborate with MST, Engineering, QA, and Validation teams to define robust operational workflows. /li liContribute to the development ofbSOPs, batch records, training programs, and aseptic practices /b. /li /ul pbOperational Phase /b /p ul liSupervise day-to-daybsterile biologics manufacturing operations /b (e.g., aseptic processing, filtration, filling, formulation). /li liEnsure compliance withbGMP, Annex 1, and aseptic processing standards /b. /li liLead and coach operators in cleanroom behaviors, gowning practices, and aseptic techniques. /li liMonitor production performance, deviations, and investigations; drive timely resolution and continuous improvement. /li liSupport media fills, environmental monitoring oversight, and inspection readiness activities. /li liPromote a strongbquality and safety culture /b within the department. /li /ul h3You will need to have /h3 ul liDegree in Biotechnology, Pharmacy, Biology, Chemical Engineering, or related scientific disciplines /li liMinimumb3-5 years of experience /b in sterile pharmaceutical manufacturing. /li liProven hands‑on experience inbbiologics manufacturing /b (e.g., aseptic processing, sterile filtration, fill‑finish, upstream/downstream interfaces). /li liKnowledge ofbGMP and Annex 1 requirements /b. /li liDeep understanding ofbaseptic techniques and contamination control strategy /b. /li liFamiliarity withbprocess validation and equipment qualification /b. /li liStrong documentation and deviation management capabilities. /li /ul h3We would prefer for you to have /h3 ul liExperience inbstart-up, scale-up, or facility expansion projects /b is desirable. /li liExposure to isolators, cleanroom qualification, and media fill execution is a strong advantage. /li /ul h3Location /h3 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,qualificationsand internal equity considerations. /p pIn addition, we offer a comprehensive benefits package inclining pension, private medical insurance, wellbeing programme, flexible benefits programme. /p pbWhat we offer /b /p 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 h3DISCOVER ALL OUR JOB OPPORTUNITIES /h3 h3Screen readers cannot read the following searchable map. /h3 pTo activate drag with keyboard, press Alt + Enter. Once in keyboard drag state, use the arrow keys to move the marker. To complete the drag, press the Enter key. To cancel, press Escape. 1 Job /p /p #J-18808-Ljbffr