OrganOx is a global medical device company focused on organ technology. The Senior Regulatory Affairs Specialist will lead regulatory submissions for North America, support ISO/GMP compliance, and collaborate with R&D, Manufacturing and QA to advance OrganOx products. The role is flexible remote or hybrid on-site in Madison, NJ with up to 5% travel. Ideal candidates have 3–8 years in regulatory affairs for Class II/III devices and SaMD/SiMD.

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Level

Manager L7

Location

Atlanta, GA

Occupation

Regulatory Affairs Specialists

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

2 days ago

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