Job Summary
This is a hybrid position at Inogen facilities located in Plano, TX or Beverly, MA.
Responsible for the development and execution of regulatory strategy for Inogen products. The Director of Regulatory Affairs will lead a team and activities resulting in obtaining and maintaining regulatory approval in support of Inogen business objectives and applicable global medical device regulations.
The position plays a critical role in supporting Inogen’s ambitious global growth objectives and will work closely with internal stakeholders such as R&D, Clinical, Commercial, Operations, and Quality, as well as external stakeholders such as FDA, Notified Bodies, etc.
Responsibilities:
Knowledge, Skills, and Abilities:
Qualifications: (Education and Experience)
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.
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