Global Regulatory Strategy Lead – Medical Devices

A leading medical device company is seeking a Principal Regulatory Affairs Specialist to oversee regulatory strategy and ensure compliance for their portfolio of devices. The ideal candidate will have at least 7 years of experience in regulatory affairs, particularly with Class II or III medical devices, and possess strong communication skills. Responsibilities include managing regulatory submissions, mentoring team members, authoring technical reports, and collaborating with various departments.

This role offers the opportunity to influence and navigate complex regulatory environments, making a direct impact on patient access to innovative solutions.
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