Key responsibilities include performing sampling and inspection of in-process and finished pharmaceutical products according to approved procedures, specifications, and quality expectations; supporting and facilitating finished product labeling activities, including label coordination, verification, reconciliation support, documentation, and escalation of labeling discrepancies as assigned; reviewing GMP documentation, including master batch production records, room logs, equipment logs, inspection records, forms, checklists, and other quality-related documents for accuracy, completeness, and compliance; supporting manufacturing and receiving activities by verifying materials, components, documentation, supplier-related information, or inspection requirements as assigned; assisting with investigations related to deviations, documentation discrepancies, process concerns, product issues, supplier concerns, label discrepancies, complaints, or other quality events; supporting corrective and preventive action activities, including fact gathering, follow-up, implementation support, and effectiveness checks; supporting quality management system activities, including document control, training program management, record review, quality data entry, metrics, and trending; identifying and escalating potential deviations, documentation errors, missing information, product defects, material concerns, label mismatches, or process issues to the appropriate Quality or operational leader; working cross-functionally with Production, Warehouse, Receiving, QC, QA, and leadership to support compliant operations, timely issue resolution, and product quality; maintaining accurate, timely, legible, complete, and attributable documentation in accordance with GDP expectations; following all applicable cGMP, GDP, FDA, OSHA, DEA, company procedure, safety, PPE, and quality system requirements; supporting continuous improvement by identifying recurring issues, communicating improvement opportunities, and participating in process or quality system improvements; and performing other duties as assigned based on business and quality needs. What success looks like includes understanding that QA support directly impacts patient safety, product quality, product release, and regulatory compliance; reviewing documentation carefully and catching missing, inconsistent, incomplete, or inaccurate information before it creates a larger issue; identifying product, material, label, documentation, or process concerns and escalating appropriately instead of making assumptions or unsupported decisions; maintaining objectivity, professionalism, and confidentiality when supporting investigations, CAPAs, complaints, or quality events; communicating clearly with Production, Warehouse, Receiving, QC, QA, and leadership, especially when priorities shift or concerns need follow-up; staying organized while managing multiple tasks, open items, deadlines, and documentation requirements; following SOPs and work instructions exactly and understanding the importance of cGMP, GDP, and data integrity; demonstrating accountability, curiosity, and willingness to learn broader quality systems and pharmaceutical manufacturing processes; showing motivation to grow within Quality Assurance and take on additional QMS, investigation, documentation, or floor support responsibilities over time.