Manufacturing Associate I
Moderna
October 1, 2026
Full-time
On-site
Norwood, MA
Operations
Role: Manufacturing Associate I in mRNA and LNP drug substance operations, executing GMP manufacturing processes for clinical and commercial vaccine products. Responsibilities: perform aseptic processing, formulation, filling, and dispensing of drug substance using Moderna-specific technologies; follow SOPs, batch records, and GMP regulations; ensure documentation compliance and maintain a clean, controlled environment; operate manufacturing support systems; adhere to safety and waste procedures. Requirements: HS Diploma with 3-5 yearsβ industry experience, or STEM degree with minimal experience; ability to learn GMP regulations; on-site role with no travel specified. HighValue: GMP manufacturing, aseptic processing of mRNA/LNP biologics, clinical and commercial vaccine production, clean-room environment, batch documentation, and equipment operation. Work setup: 100% onsite; safety, data integrity, and environmental compliance emphasized.