Validation Engineer

ppChiesi 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 h3Chiesi Global Manufacturing Division /h3 pChiesi Group has three production plants: /p pbParma /b (Italy), the strategic hub for the production and distribution of our products, serving as an international supply center with exports to over 80 countries. Here, solid medicines such as tablets and dry powders for inhalers, solutions and suspensions for inhalations and sterile suspension vials for endotracheal administration are produced. /p pIn 2024, a new bBiotech Centre of Excellence /b has launched in Parma. The new facility is dedicated to developing and producing monoclonal antibodies, enzymes, and other proteins. /p pbBlois-La Chaussée Saint Victor plant /b (France), a center of excellence specializing in the production of Dry Powder Inhalers and Metered Dose Inhalers (MDIs). The site manages direct distribution to customers in the French market and exports to other markets, effectively meeting both local and international needs. /p pbSantana de Parnaiba /b (Brazil), specialized in the production of pressurized solutions and suspensions for inhalation therapy (pMDIs). Additionally, it has an area dedicated to nasal sprays for the European market. Santana produces pressurised solutions and suspensions for inhalation therapy (MDI). /p pIn 2025, a new investment in bNerviano /b (Italy) has been announced with the construction of a new facility which will be primarily dedicated to manufacturing carbon minimal inhalers (reinforcing the company’s commitment to both patients’ health and sustainable healthcare solutions), dry powder inhalers and sterile biological products. /p h3Who we are looking for /h3 h3This is what you will do /h3 pFor our new Site in Nerviano (Milan) we are looking for a new Validation Engineer. /p pThe bValidation Engineer /b is responsible for the execution and coordination of the Commissioning and Qualification activities relevant to Systems, Equipment, Facilities, and Utilities at the pharmaceutical manufacturing site, specialized in respiratory spray and bio-pharmaceuticals products. /p h3You will be responsible for /h3 ul liDevelop bValidation Master Plans (VMP) /b for Systems, Equipment, Facilities, and Utilities according to Chiesi standards. /li liSupport the Validation Manager in the bmanagement of the Commissioning and Qualification activities (FAT, SAT, DQ, IQ, OQ, PQ) /b. /li liPrepare, or oversight external partners in the preparation, of Qualification Protocols for Systems, Equipment, Facilities, and Utilities. /li liExecute, or oversight external partners in the execution, of Qualification Protocols for Systems, Equipment, Facilities, and Utilities. /li libOversight Equipment Vendors and Contractors /b in the execution of FAT, SAT and Commissioning activities, ensuring compliance to Chiesi standards. /li liReview and approve bFAT, SAT, Commissioning and Technical Documentation /b issued by Equipment Vendors and Contractors. /li liAssureb Data integrity /bapplication. /li liSupport the Validation Manager in the management and implementation of the bChange Controls /b on qualified Systems and Equipment. /li liCollaborate with cross-functional teams, including Engineering, Maintenance, Production, Quality Control and QA for CQ activities. /li /ul h3You will need to have /h3 ul liDegree in bEngineering, Pharmacy, Chemistry, or related scientific /b discipline. /li liMinimum b5 years of experience /b in pharmaceutical Commissioning and Qualification, preferably on blarge scale Projects /b. /li liSolid knowledge of bEU GMP, FDA CFR 21 Part 11, Annex 15, GAMP 5 /b, and validation best practices. /li liExperience with baseptic/sterile production /b, preferably in brespiratory devices and biopharmaceuticals /b. /li liDemonstrated experience in bSystems and Equipment Commissioning and Qualification /b, including HVAC/Cleanrooms, Clean media and Process Equipment. /li liExperience in bFAT, SAT and Commissioning /b activities. /li liStrong understanding of brisk management /b methodologies (e.g., FMEA, QRM). /li libFluent in English /b (written and spoken). Any other language will be considered as a plus. /li /ul h3We would prefer for you to have /h3 h3Technical Skills /h3 ul liCommissioning (FAT, SAT, Commissioning) and Qualification (DQ, IQ, OQ, PQ) protocols and lifecycle management. /li liTechnical knowledge of Systems, Equipment, Facilities, and Utilities of a pharmaceutical manufacturing site and relevant functionalities. /li liCompliance with global regulatory standards. /li liData integrity principles and Computerized System Validation (CSV). /li liDeviation and change control management. /li /ul h3Soft Skills /h3 ul liExcellent bcommunication and interpersonal /b skills. /li libProblem-solving mindset /band ability to work under pressure. /li liHigh attention to detail. /li liStrategic thinking with a bproactive, hands-on approach /b. /li liCross-functional collaboration and stakeholder management. /li liWilling to work in a bdynamic, challenging and friendly environment /b /li /ul h3Location /h3 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