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Associate Director, Regulatory Affairs
The Associate Director, Regulator Affairs will be part of the Global Regulatory Affairs team, and be responsible for supporting the team in creating and executing regulatory strategies and objectives in alignment with business needs. This includes the preparation of regulatory submissions required to market new or modified medical devices, and related regulatory affairs activities, such as development, execution and management of procedures and systems designed to ensure that the company’s overall product development process, including clinical studies, addresses all regulatory requirements as well as the objectives of the business. The Associate Director, Regulator Affairs will primarily support the company’s US regulatory activities, but will al


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