Senior Materials Management Associate

Role:
Senior Materials Management Associate responsible for receiving, inspecting, verifying, and managing raw materials, supplies, and hazardous substances in a GMP-regulated biopharma environment. Objectives include ensuring accurate inventory control, compliance with GMP procedures, and safe handling of materials.

Responsibilities encompass visual inspections, recording transactions in SAP, conducting sampling for analysis, preparing shipment materials, maintaining data accuracy, and resolving routine issues independently.

Requirements: high school diploma (associates or trade school preferred), valid driver’s license, experience in regulated environments like pharma or biotech, and handling hazardous materials. Forklift experience is preferred but trainable.

High-value specifics include GMP compliance, GMP form completion, raw material sampling, and inventory management within a biopharma manufacturing setting.

Location:

Devens, MA; work setup involves on-site operations with potential safety and compliance responsibilities.

As a Senior Materials Management Associate, you will play an important part at Bristol Myers Squibb in Harvard, MA, United States.