About this opportunity
Moderna lists this Sr. Manufacturing Associate I, Drug Substance Operations opportunity in norwood, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Role
Senior Manufacturing Associate I in mRNA and LNP drug substance operations, responsible for executing GMP manufacturing processes for clinical and commercial vaccines.
Core responsibilities
aseptic processing, formulation, filling, dispensing, and documentation compliance within sterile environments; utilizing manufacturing systems such as SAP, VEEVA, Delta V, and LIMS; and performing training and troubleshooting.
Qualifications
HS Diploma with 8+ years industry experience, or STEM degree with 4+ years, demonstrating strong GMP knowledge.
Requirements
adherence to safety and GMP standards, precise task execution, and understanding of equipment and process controls.
HighValue
GMP manufacturing, aseptic processing of mRNA/LNP (including chromatography, filtration, nano-mixing), clinical and commercial scale, regulated environment, cross-functional collaboration with quality, engineering, and validation teams, and experience with manufacturing support systems.
Work setup
On-site with a 70/30 in-office model; no travel specified.
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Worksite address
norwood, MA, 02062, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.