
This role serves as the Quality Unit Representative for a global life sciences company, overseeing the Quality Management System for a diverse portfolio of regulated products including OTC sterile eyedrops, dietary supplements, and cosmetics. The position is responsible for maintaining regulatory compliance with FDA standards, managing contract manufacturer audits, and performing final batch releases. Key duties include reviewing product labeling, leading adverse event reporting investigations, and acting as the Tier 2 escalation point for complex customer quality inquiries. The role appeals to professionals seeking to leverage their expertise in sterile manufacturing and regulatory affairs within a stable, 179-year-old organization. The position offers a supportive work environment with comprehensive benefits and the opportunity to drive quality standards across a global supply chain.














