PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. SUMMARY: The Document Control Specialist is responsible for managing controlled documents in compliance with regulatory requirements. The Specialist supports audits, runs training reports, and assists with GMP Training and routing changes for contract manufacturing organizations. Strong communication, organizational, and technical skills are essential for success in this role, which requires a detail-oriented approach and the ability to work both independently and in a team environment. Work Schedule: Monday - Friday 8:30am-5pm
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