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 cleanroom environment.
Role type
Manufacturing Associate II/III (Purification)
Builds
Drug substance for biotherapies
Domain
Biotechnology / Biomanufacturing
Deliverable
physical/clinical work
Required skills
Operating process equipment, executing validation protocols, cGMP data documentation, aseptic/cleanroom operations, in-process sampling analysis, following SOPs, Good Documentation Practices (GDP)
Preferred skills
Process automation software (DeltaV, LIMS), pipetting experience, STEM background
Technologies
DeltaV, LIMS
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, hands-on IC