Manufacturing Associate II / III, Purification (Days)
Core
Execute daily manufacturing activities including column chromatography, viral filtration, ultra-filtration, and bulk dispensing of drug substance in a cGMP clean environment.
Role type
Manufacturing Associate (Downstream/Purification)
Builds
Drug substance for biotherapies
Domain
Biomanufacturing / Pharmaceutical
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Operating process equipment, executing validation protocols, cGMP data documentation, aseptic/cleanroom operations, process automation software (DeltaV, LIMS), pipetting
Preferred skills
Understanding of aseptic environments, process automation systems, pipetting experience
Responsibilities
Operate process equipment and execute validation protocols, document cGMP data and deviations, create and revise batch records and equipment logbooks, assist in in-process sampling and analysis, maintain clean and safe work environment, participate in training and development initiatives
Seniority
Entry Level