Sr. Manufacturing Associate I, Drug Substance Operations

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 include 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.