Demonstrated ability and knowledge of WMS and ERP. Solid dosage form and/or liquids manufacturing knowledge preferred. Strong Inventory/warehouse and safety best practices. Production planning/materials management/supply chain processes. Must have knowledge of Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), Drug Enforcement Administration (DEA), and other applicable regulatory requirements. General knowledge of the pharmaceutical industry, brand and/or generics (preferred). Demonstrated experience working in a regulated supply chain environment Knowledge: Knowledge of DEA, FDA, OSHA and relevant state and federal regulations. Qualifications Education/ Experience: Bachelor's degree in a related field and a minimum of five (5) years' supervisory experience in a high volume manufacturing and warehouse environment. Assists with new employee training for Production, Packaging or Warehouse personnel to ensure that individuals have a thorough understanding of DEA requirements. Ensures employee cross-functional development, regulatory education and compliance, and warehouse/production best practices. Provides supervision, guidance and training to the Warehouse Operators, Controlled Substance Coordinators and Vault Cage Monitors. Responsible for implementing corrective actions identified during investigations, audits or DEA inspections. Ensures all material movement and documentation is completed in an accurate and timely manner. Monitors and maintains DEA compliance within warehouse operations. Responsible for inventory accuracy and cycle count program in support of Operations and Fiscal responsibility. Manages controlled substance cage and vault inventory and investigates and reports any discrepancies to the DEA Compliance group. Develops and enforces policies and practices to ensure materials are secured and transported properly within the plant. Manages the room clearance process for controlled substances ensuring both compliance and operational effectiveness. Strong communication and partnering with Planning, Quality and Production to ensure support of business objectives. This includes receiving, pulling samples, pulling manufacturing orders, manufacturing returns, shipping, product destruction, and any other inventory movements. Key Accountabilities: Coordinates and oversees activities and schedules related to movement of materials with-in the plant. Responsible for adherence to all regulatory requirements. Oversees receiving, in-process and shipping activities. This position is responsible for the logistics of controlled and non-controlled substance products, including providing support to ensure adherence to the production plan and management of inventories. Job Summary This position manages warehouse and controlled substance operations, including: inventory control, storage and product movement for the plant Manufacturing and Packaging departments. Qualitest is an operating company of Endo International plc (NASDAQ: ENDP) (TSX: ENL), a global specialty healthcare company focused on improving patients' lives while creating shareholder value. Featuring a growing portfolio of over 600 products, the company is focused on manufacturing and marketing in specialty categories that include oral solid dose controlled substances, liquids, and semi solids. Company Name: Endo Pharmaceuticals Qualitest, headquartered in Huntsville, AL, provides affordable, high-quality generic pharmaceuticals.
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