OverviewThis role utilizes chemistry laboratory skills to test and measure products or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia.ResponsibilitiesExecutes analyses on excipients, raw materials, finished products, and packaging per internal SOPs and applicable pharmacopeias.Conducts stability studies, process and method validations, and activities related to tech transfer of pharmaceutical products.Performs instrument qualification and re-qualification (IQ/OQ/PQ) according to internal procedures.Records analytical data in compliance with ALCOA+ principles and data integrity requirements.Reviews GMP documentation, batch records, analytical reports, and certificates for completeness and compliance.Collaborates with QA, Production, and R&D; supports method transfers, troubleshooting, and safe lab/5S practices.Participates in audits and inspections by providing data and responses; contributes to CAPA, deviations, change control, and SOP updates.Tracks KPIs: on-time completion and right-first-time rates, data integrity compliance, audit outcomes, documentation quality, and continuous improvement impact.Essential RequirementsDegree in ChemistrySolid technical-scientific knowledge of pharmaceutical/chemical QC or equivalent analysisPrevious experience working in a laboratory environment in the pharmaceutical industryExperience in GMP environmentFluent in Italian and EnglishWhy Novartis?Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-cultureYou will receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewardsCommitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representation of the patients and communities we serve.Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkWhy Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureJoin our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/networkBenefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewardsSeniority levelEntry levelEmployment typeFull-timeJob functionManagement and ManufacturingIndustries: Pharmaceutical ManufacturingReferrals increase your chances of interviewing at Novartis Contract Manufacturing by 2xGet notified about new Pilot jobs in Ivrea, Piedmont, Italy.We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr