Associate - Quality Systems

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.

What You Will Achieve In this role, you will: .

• Knowledge of GMP Document and Record Management, including document issuance, retrieval, archival, retention, and disposition.
• Knowledge of PDOCs, SDS, p-Log, Therefore, CICR, and electronic document management systems.
• Knowledge of official print management, audit trail review, metadata verification, document scanning, and record tracking.
• Understanding of Document Lifecycle Management, including document creation, review, approval, issuance, archival, retrieval, retention, and obsolescence.