Senior Regulatory & Quality Lead, FDA 510(k) & ISO 13485
Essenlix
A fast-growing medical device company in New Jersey seeks a Senior Regulatory Affairs & Quality Systems Manager. This role requires leading FDA 510(k) submissions, ensuring compliance with quality standards, and managing cross-functional teams. Candidates should have a relevant Bachelor's degree and at least 5 years of experience in regulatory affairs and quality systems, including knowledge of FDA regulations and ISO certifications. Competitive salary and benefits offered. #J-18808-Ljbffr Essenlix
Vacancy posted 1 day ago
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