Lavoro Novartis

Job Description SummaryTo lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head...

SummaryThe IT Site Business Partner for Technical Research and Development to be based in Ivrea, Italy captures IT demand, collaborates with IT functions, and supports the implementation of digital strategies at the Ivrea site. The role contributes to the Product Roadmap, supports global rollouts an...

RLT Analytical Product Project Leader (m/f/d) Job ID: REQ-10015150Jul 11, 2024Location: Ivrea, ItalySummary Role Purpose: Define, lead and manage the analytical project strategy including the overall analytical control strategy for Drug Substance(s) and radiopharmaceutical parenteral Drug Product(s)...

SummaryLocation: Ivrea, ItalyRole Purpose: Define, lead and manage the analytical project strategy including the overall analytical control strategy for Drug Substance(s) and radiopharmaceutical parenteral Drug Product(s) in line with the overall CMC project development plan; ensure project specific...

SummaryResponsible for Engineering activities including planning and coordination of maintenance & calibration activities, project execution and continuous improvement at site level (e.G. buildings, process equipment, utilities, automation).About the RoleStrategy & Organizational DevelopmentEnsures ...

Summary To lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible...

SummaryResponsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well as any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging validation, process...

SummaryLocation: Ivrea, ItalyRole Purpose: Leads and manages all Drug Product (DP) project activities linked to the development of radiopharmaceutical parenterals (both ready to use and freeze dried products). Supports & coaches team members, participates in scientific teams and contributes to the o...

To lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible for ens...

To support the Site Head in analyzing the site Finance KPI’s by developing robust financial planning & detailed tracking processes, driving day-to-day process improvement, and ensuring strict compliance with the NAM / TechOps Accounting Manual in close collaboration with the Finance teams in the Ope...

Job Description SummaryContributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team, c...

SummaryCreate and drive with scientific & technological excellence the formulation development in close collaboration with operations, analytics, engineering and relevant SMEs, QA and the project DPPL. Development activities includes among others: formulation and process-design, control strategy, qu...

Novartis is at the forefront of transforming lives through radioligand therapy in nuclear medicine, combatting several prevalent cancer types. If you’re passionate about pushing the boundaries of this industry and creating innovative, life-saving medicines for cancer patients, consider joining us as...

Job Description SummaryThe Clinical Supply Chain Manager partners with the Clinical Trial Supply Manager team to ensure continuous supply of Investigational Medicinal Product (IMP) for assigned clinical trials through effective monitoring and maintenance. Has operational end-to-end responsibility fo...

-Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team, contributes to operatio...