EMED Technologies Corporation is seeking a Quality Assurance and Regulatory Affairs Specialist to support the company's QMS and ensure compliance with applicable regulations. You will work closely with CA/QA/RA leadership and cross-functional teams to maintain documentation, CAPA, and audit readiness. The role emphasizes document control, CAPA investigations, handling nonconforming product, customer complaints, and quality metrics reporting, with opportunities to engage in internal and supplier

Also on the board Same function, level within a rung

Level

Lead

Location

New York, NY

Occupation

Regulatory Affairs Specialists

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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