Global Regulatory Affairs Specialist – Medical Devices

A prominent medical device company is seeking a Regulatory Affairs Specialist to manage a variety of regulatory activities related to medical devices and Software as a Medical Device (SaMD). This role involves leading regulatory submissions, collaborating with international teams, and ensuring compliance with US, EU, and Canadian regulations. The ideal candidate will have a Bachelor's Degree in a related field and at least 2 years of experience in the medical device industry.

Strong organizational and communication skills are essential for success in this fast-paced work environment.
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