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As a key member of the executive team, the Senior Vice President (SVP) of Regulatory Affairs, and Quality will play a pivotal leadership role in leading our regulatory affairs and quality assurance function with distinction, integrity, and strategic foresight. You will be responsible for developing and implementing robust regulatory strategies that align with our business objectives, ensuring timely regulatory submissions, fostering and maintaining strong relationships with the FDA and other international regulatory agencies, and fostering a culture of quality excellence accountability and continuous improvement throughout the organization. Additionally, you will oversee the optimization of our quality management systems, driving efficiencies, mitigating risks to safeguard our reputation, and navigating complex regulatory landscapes for RNA exon editing programs.