Manufacturing Associate I

Role: Manufacturing Associate I in Drug Substance Operations responsible for producing mRNA drug substance within a GMP environment. Core responsibilities include executing manufacturing operations such as aseptic processing, formulation, filtration, mixing, and filling; maintaining compliance with GMP standards; supporting equipment setup, cleaning, and documentation; and ensuring safety, cleanliness, and proper use of digital manufacturing systems (SAP, Veeva, DeltaV, etc.). Requirements: Bachelor's in STEM with 0-1 years or relevant industry experience; experience in biopharma or regulated environments preferred. High-value specifics: focus on mRNA drug manufacturing, GMP compliance, real-time documentation, and digital systems; onsite work with no specified travel. Collaboration involves working closely with cross-functional team members to ensure smooth manufacturing execution.