Manufacturing Associate II
Core
Perform routine unit operations including formulation, sterile filtration, aseptic filling, and visual inspection in a cGMP manufacturing environment.
Role type
Manufacturing Associate II (DP Operations)
Builds
Pharmaceutical products (mRNA therapeutics)
Domain
Biopharma / Manufacturing
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
cGMP compliance, aseptic technique, SOP adherence, in-process controls, deviation reporting, equipment cleaning, documentation (ALCOA+), cross-functional collaboration
Preferred skills
GMP manufacturing experience, cleanroom gowning, continuous improvement, peer mentoring
Technologies
MES, eBR, disinfectants
Responsibilities
Perform formulation, sterile filtration, vial/syringe filling, and visual inspection; conduct equipment checks and facility cleaning; complete accurate batch records and logbooks; identify and escalate deviations; support SOP development and continuous improvement; maintain compliance with cGMP, safety, and gowning requirements; train and mentor peers.
Seniority
Mid-level, hands-on IC