PpDate: 20 Apr 2026 /p pBusiness Area: Industrial Operations HSE /p pJob Type: Direct Employee /p pContract Type: Permanent /p pLocation: Parma, IT /p h3Subject Matter Expert Process Validation Life Cycle Management – Respiratory Orals Small Mol. /h3 h3This is what you will do /h3 pYou will act as subject matter expert for process validation and technical maintenance activities, supporting industrialization, product technology transfer and life‑cycle management for respiratory, oral and small molecule products. /p pYou will provide specialist technical support to RD, Operations, Quality and external stakeholders, including contract manufacturers and subcontractors, ensuring robust and compliant manufacturing processes throughout the product lifecycle. As part of RD product teams and the extended technical team, you will support industrial process validation activities and coordinate technical maintenance on in‑market products, contributing to solutions aligned with quality requirements and business needs. /p h3You will be responsible for /h3 ul liParticipating in technology transfer processes between different Chiesi group sites (RD included) and/or subcontractors operated by Global TechOPS with a focus on process validation and all the propaedeutic activities. /li liCollaborating in designing technology transfer documents and matrices, supporting the identification of scientific rationales to be reported in quality and regulatory documentation. /li liFinalizing the industrialization of new products within the RD product teams (as a member of the extended technical team) and structuring the industrial process validation. /li liExecutive responsibility for technology transfer activities between different Chiesi group sites (RD included) and/or subcontractors operated by Global TechOPS, both for primary and secondary technology transfer activities, with a focus on process validation and all the propaedeutic activities. /li liScouting for new equipment/technologies and tools to improve manufacturing execution and process robustness. /li liBeing the key reference person for Global TechOPS functions (incl. plant site process SME – Parma, Blois, Santana, Nerviano Virtual plant), supporting with technical expertise for maintenance activities for in‑market products, regarding maintenance needs collection, planning and execution, challenges identification, supporting geo‑expansion and module X maintenance. /li liBeing the key reference person in Global TechOPS functions for product lifecycle, reporting to dedicated governance bodies. /li liSupporting Chiesi functions (global and local) in preparation for audits (inspection readiness streams). /li liParticipating constructively or coordinating extended teams and work‑package development meetings (e.g., ETTs, technical maintenance, operative teams). /li liSupporting the development and evolution of Chiesi products toward sustainability‑driven initiatives, through the eco‑friendly challenge and performing product sustainability assessment and defining improvement plans. /li liProviding scientific evaluation and effective methodological support in problem‑solving, contributing in a significant way to root cause identification. /li liParticipating constructively in extended teams for task forces. /li /ul h3You will need to have /h3 ul liBachelor’s degree in Pharmaceutical Sciences, Chemical Engineering, Biological Sciences or related field. /li li5+ years pharmaceutical/biotech industry experience in drug product manufacturing, with at least 3 years in a similar role or in manufacturing/technology and analytical quality/QC area. /li liFluency in written and verbal communication in English. /li liWillingness to travel up to 30%; business trips may vary depending on project/business needs. /li /ul h3We would prefer for you to have /h3 ul liDirect experience on respiratory products (DPI and/or pMDI) and/or oral solid and small molecules. /li liDirect and solid experience in process validation and lifecycle management activities. /li liExperience working in multicultural and multinational environments. /li liExperience working within a CRO or CMO environment. /li /ul h3Technical Skills /h3 ul liDemonstrated strength in problem‑solving, and interpersonal communication, with proven ability to work effectively across diverse technical, business, and operational functions. /li liSolid understanding of the pharmaceutical industry and end‑to‑end drug product manufacturing. /li liExperience in pharmaceutical or biotech MSAT process development and/or GMP manufacturing. /li liStrong working knowledge of current regulations, quality expectations, and industry trends related to manufacturing and testing. /li /ul h3Soft Skills /h3 ul liAbility to lead cross‑functional project teams in an international environment, including internal and external manufacturing (CMOs/CDMOs). /li liWork and think proactively to support business continuity. /li liStrong interpersonal skills and ability to interact with different stakeholders. /li /ul h3Location /h3 pThe primary work location is Parma (Italy). The role offers flexibility, combining on‑site presence with remote work. /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