Technologist III, Downstream Manufacturing - Biologics - Eurofins CDMO Alphora, Inc.
Core
Execute downstream cGMP manufacturing of novel biologics and therapeutics, ensuring compliance and process transfer.
Role type
Senior IC manufacturing technologist (downstream biologics)
Builds
Novel biologics and therapeutic products for pharmaceutical clients
Domain
Biopharmaceutical CDMO / Bioprocessing
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
chromatography, tangential flow filtration (TFF), depth filtration, nanofiltration, viral inactivation, protein bioconjugation, aseptic techniques, cGMP compliance, commissioning/qualification/validation (CQV), Cytiva UNICORN software
Preferred skills
bioconjugation, large-scale TFF
Technologies
AKTA Ready Gradient, AKTA Readyflux, Cytiva UNICORN
Responsibilities
Operate advanced purification equipment; execute downstream processing steps; perform in-process sampling and basic analytical tests; assist in technical investigations and root cause analysis; write and review batch records, SOPs, and cGMP documentation; author and execute CQV protocols; coordinate material handoffs with Upstream, QA, and QC teams.
Seniority
Mid-level, hands-on IC
