Responsibilities: * Manage existing client relationships * Generate leads through cold calling & field sales * Close deals with B2B/B2C customers * Meet revenue targets * Acquire new clients via business dev
Experienced QA professional for medical device (IOL) manufacturing. Must have strong knowledge of ISO 13485, CE certification, and international regulatory standards. Experience in documentation, audits, and device licensing preferred. Required Candidate profile Candidates with 0–5 yrs QA experience, hands-on with audits, documentation & regulatory submissions.