Label Control and Packaging Supervisor

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About the role

This position is responsible for supervising Nivagen label control and packaging area. Works in SAP system and Quality system to perform inspection testing of incoming labelling and packaging components. Supervising the packaging team to provide oversight of Packaging and making sure that AQL’s support finished product release. The position is a liaison with the warehouse, customer service and manufacturing for incoming goods both finished product and incoming components. The position is responsible for implementing Nivagen inspection and testing quality standards for labelling and incoming packaging components, while leading the packaging QA team to meet Nivagen timelines. ESSENTIAL DUTIES AND RESPONSIBILITIES • Manage the Label Control Program ensuring that finished product is appropriately labeled to the correct versions and timelines. This includes management of specifications, inspections, and release of labelling in SAP. • Manage the Packaging Component Specification program by obtaining documentation for components that have product contact from project managers, engineers, or purchasing. • Prepare or review change controls to introduce product/components into Nivagen Quality System. • Develop quality inspection criteria for finished products to include label review, temperature requirements, and destructive testing for quality attributes, if applicable. • Create documentation for Quality inspection of each packaging component against supplier drawings, supporting documentation and physical testing. • Work with Engineer and Operations for component acceptability testing on the line in conjunction of writing component specifications for approval. • Sample and inspect incoming drug products and/or components against quality standards. Record and review documentation for accuracy and completeness. • Maintain the initial and final documentation in the electronic management system. • Disposition of product/component after quality review of inspection criteria • Set up metadata in SAP of new drug products and establish workflows for inspection criteria in the documentation quality system. • Interact with Purchasing and Supplier for investigations into non conformances, writing deviations, and SCAR reports. • Track labelling and packaging components supplier performance and assist in quality agreements. • Maintain all working areas in a clean and orderly state. Assure products are stored, segregated and clearly labeled. • Ensures timely release of products in compliance with established standards. • Assist in the QA release process, ensuring products meet established quality standards before release for production. • Demonstrate proactive leadership through GMP regular audits, monitoring, and enhancing the efficiency and effectiveness of QA release procedures. • Review/approve documents as a Quality Subject Matter Expert (SME). • Develop and uphold Standard Operating Procedures (SOP) and protocols, ensuring they align with quality practices and meet regulatory requirements. • Review batch records for accuracy and completeness for product disposition. Ensure that corrections are made in a timely manner. • Apply a working knowledge of statistical based sampling plans. • Write reports and provide information needed to investigate, document and close deviation. QUALIFICATIONS To perform this job, the individual must have FDA 21Part210/211 knowledge. Quality inspection experience in component or final product inspection is required. Experience in a pharmaceutical environment is required (3 years minimum) Self-motivated and proactive in preparing documentation and testing products. EDUCATION AND EXPERIENCE Knowledge of quality assurance in the drug industry with emphasis on contract manufacturing requirements

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