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Are you an experienced purpose-driven and business-minded pharmaceutical leader with expertise in drug regulatory affairs? Do you excel in a dynamic environment and want to be part of a rapidly growing organisation dedicated to improving the lives of people living with serious chronic diseases? If so, read on and apply today for a life-changing career. The position
The RA CMC organization is growing, and we are strengthening our leadership team with a new Director with strong experience and interest in Regulatory Life Cycle Management. As the Director for RA CMC LCM Biologics & Rare Diseases, you will play a pivotal role in shaping the future of RA CMC lifecycle management. We are looking for a dynamic and visionary leader to spearhead our team as the Director of a newly established area. This is your chance to significantly impact and develop an area responsible for regulatory CMC strategies, driving excellence in our pipeline, and delivering regulatory approvals in close collaboration with key stakeholders in Product Supply/CMC and Regulatory Affairs functions. You will report to the Vice President of RA CMC & Device and be part of the leadership team in RA CMC LCM Biologics & Rare Diseases and the extended leadership team in RA CMC & Device. In this position, you will be able to influence the future way of working in the ▶Novo Nordisk◀ Regulatory CMC and Device function. In this role you will: