Materials Management Associate II

Materials management specialist focused on cGMP operations within a biopharma setting, ensuring inventory control, compliance, and regulatory readiness.

• Oversee receipt, inspection, disposition, storage, and shipping of controlled materials for cell and gene therapy manufacturing;
• Support investigations, change controls, CAPAs, and supplier qualification;
• Coordinate with manufacturing and QA/QC to ensure material availability and compliance;
• Maintain accurate inventory records, perform cycle counts, monitor storage conditions, and facilitate material releases.

• Associate or bachelor’s in life sciences or supply chain, with at least 4 years’ experience in regulated environments;
• Strong knowledge of cGMP, GMP/GDP, traceability, data integrity, and warehouse controls;
• Experience in biotech/pharma industries;
• Proficiency with inventory systems, Microsoft Office, and ERP.

• Familiarity with OE/5S and regulated industry standards.

• cGMP compliance, biotech/pharma experience, cell and gene therapy production support, inventory management, temperature-sensitive material handling, collaboration with manufacturing and quality teams.

• Physical capacity for manual handling;
• may require working outside regular hours and handling hazardous materials.