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Responsible for developing and maintaining manufacturing processes for metal components used in a drug delivery system. Collaborate with stakeholders to ensure product quality and safety. Support validation of processes and identify root causes of deviations. Review metal component designs and challenge specifications based on manufacturing capabilities.

Support two Vice Presidents with communicative, administrative, and practical tasks in a newly established area focused on digital transformation. Coordinate with global DSI team, manage calendars, plan review sessions, prepare budgets, maintain websites, support onboarding, ensure governance and compliance, manage purchases, and handle ad hoc tasks. Requires structured approach, proficiency in IT systems, and experience with budgets. Must be able to work independently, prioritize tasks, manage time effectively, and handle confidential information.

Lead and drive safety surveillance activities in development projects for rare diseases at Novo Nordisk. Chair cross-functional drug safety committees, prepare benefit risk assessments, develop study designs, and communicate with external parties. Collaborate with highly skilled colleagues and represent Safety Surveillance in cross-functional teams. Master's degree in Medicine or Natural Sciences required with several years of experience in Safety Surveillance and development in the pharmaceutical industry. Strong collaboration and communication skills are essential.