PCoordinating QC laboratory activities, responsible to ensure compliance to cGxP and Novartis standards for topic within area of responsibility (during development, transfer, release and stability), including safety testing, monitoring and trending. Participating to Pilot Plant build-up phase as key team member for GMP quality control laboratories, as well as support for development laboratories.brProvide guidance, support and leadership for implementation of analytical standards. /ph3About the Role /h3pbKey Responsibilities: /b /pulliEnsure quality, compliance, and efficiency in team operations while aligning with site strategies. /liliAct as the primary contact to address and manage laboratory issues related to equipment, analysis, compliance, and operational challenges. /liliPlan and coordinate lab activities, ensuring timely release of materials and products, proper inventory management, and adherence to site lead times. /liliCreate capacity plans to meet business objectives, optimize laboratory performance, and proactively ensure team compliance with HSE and operational procedures. /liliOversee analytical activities, including data review, batch release, analytical method lifecycle (validation, transfer, troubleshooting), and stability studies in collaboration with the Analytical Development Team. /liliMaintain inspection readiness, supervise compliance with cGxP, Good Laboratory Practices (GLPs), ALCOA+ principles, and manage deviations, CAPAs, and Change Controls as required. /liliLead and develop team members by monitoring training compliance, ensuring qualifications for GMP tasks, fostering a culture of engagement and accountability, and supporting talent development. /liliPromote a positive and motivated work environment by providing constructive feedback, coaching, and modeling cultural aspirations aligned with company values. /liliMaster’s degree (preferred) or equivalent in Pharmacy, Chemistry, or a similar scientific field. /lili5+ years of experience in a similar role within a GMP-regulated laboratory environment. /liliStrong background in analytical laboratory operations and quality management systems, with knowledge of Good Documentation Practices and Data Integrity principles. /liliExperience in the nuclear medicine industry (preferred). /liliHighly organized, detail-oriented, and accuracy-focused with the ability to work independently as a self-starter. /liliProven personal ethics, responsibility, and dedication to purpose. /liliExcellent written and verbal communication skills, including experience interacting professionally with external vendors or business partners. /liliStrong familiarity with GMP compliance and laboratory workflows. /li /ulpbWhy Novartis? /bOur 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: will receive: /b You can find everything you need to know about our benefits and rewards in the Novartis Life /ppHandbook. to Diversity and Inclusion /b: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. /ppbJoin our Novartis Network: /bIf 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: /ppstrongWhy Novartis: /strong 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. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? /ppstrongJoin our Novartis Network: /strong 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: /ppIT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl /ppFunctional Area Research Development /ppJob Type Full time /ppEmployment Type Regular /ppShift Work No /ppNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. /p #J-18808-Ljbffr