Sr. Manufacturing Associate , Drug Substance Operations
Listed on 2026-09-14
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer
Role
Senior Manufacturing Associate I in mRNA and LNP drug substance operations, responsible for executing GMP manufacturing processes for clinical and commercial vaccines.
Core responsibilitiesaseptic 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.
QualificationsHS Diploma with 8+ years industry experience, or STEM degree with 4+ years, demonstrating strong GMP knowledge.
Requirementsadherence to safety and GMP standards, precise task execution, and understanding of equipment and process controls.
High ValueGMP 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 setupOn-site with a 70/30 in-office model; no travel specified.
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