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Manufacturing Associate I, Drug Substance Operations

Moderna
September 17, 2026
Full-time
On-site
Norwood, MA
Operations
Role: Manufacturing Associate I in Drug Substance Operations, responsible for producing mRNA drug substance within a GMP-regulated environment. Objectives include executing manufacturing processes with precision, maintaining compliance, and supporting aseptic operations such as formulation, filtration, and filling. Responsibilities involve following detailed procedures, performing cleanroom tasks, real-time documentation, equipment operation, and maintaining safety and cleanliness standards. Requirements: Bachelor’s in STEM with 0-1 years or relevant industry experience; strong attention to detail; disciplined execution; ability to work in a GMP cleanroom; excellent communication and teamwork skills. Preferred: Experience in biopharma manufacturing, digital tools (SAP, Veeva, LIMS), and continuous improvement mindset. High-Value: biologics/mRNA, GMP drug substance manufacturing, error prevention, real-time data documentation, and cross-functional collaboration. Work setup: Onsite; no travel specified.