Regulatory Affairs Lead — Medical Device CIP Programs
6AM City, LLC
6AM City, LLC is looking for a Senior Regulatory Affairs Specialist to lead regulatory strategies for Material Cost Improvement Projects. Applicants should have over 5 years of experience in the medical device sector, ensuring compliance with US and international regulations. This role requires collaboration with Quality Assurance and other departments to streamline regulatory submissions. Strong problem-solving skills and expertise in technical writing are essential. A Bachelor’s degree in Science or Engineering is required. #J-18808-Ljbffr 6AM City, LLC
Vacancy posted 4 days ago
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