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Operator II, Drug Substance - Downstream

Novo Nordisk
October 1, 2026
Full-time
On-site
Bloomington, IN
Operations
Role: Mid-level Manufacturing Operator responsible for executing drug substance manufacturing operations in a cGMP environment, supporting formulation, preparation, sanitization, and downstream processing for biopharmaceutical products. Responsibilities include equipment setup, aseptic processing, routine troubleshooting, cleaning, formulation of solutions, cell culture, and purification techniques, with a focus on ensuring product quality and compliance. Collaborates with senior team members and trains junior staff. Requirements: Bachelor’s degree in a related field with zero to minimal experience, or equivalent education with relevant experience; proficiency in GMP procedures, basic math, and understanding of biological or chemical principles. High-Value: Emphasis on biologics, cell/gene therapy, or recombinant protein production; work in upstream/downstream bioprocessing, formulation, and cleaning within a cGMP setting; night shift work (rotating 6PM-6:30AM); physical capacity for handling equipment and materials in a controlled cleanroom environment.