Supervisor - Biomanufacturing, Downstream/mRNA
Core
Lead downstream/mRNA biomanufacturing operations in a cGMP environment, ensuring batch readiness, schedule adherence, and quality compliance for biologics production.
Role type
Supervisor, Biomanufacturing (Downstream/mRNA)
Builds
Clinical and commercial biologics (mRNA) via chromatography, filtration, and filling
Domain
Biopharmaceuticals / Biologics / mRNA
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
cGMP compliance, chromatography, tangential flow filtration (TFF), viral reduction/filtration, batch manufacturing, deviation investigations, change control, cleanroom operations, equipment qualification/validation, resource allocation, team leadership, continuous improvement
Preferred skills
None stated
Technologies
Single-use systems, column chromatography, TFF, filtration systems
Responsibilities
Oversee manufacturing operations for schedule and quality; lead, develop, and evaluate staff; author and maintain cGMP documentation; support internal, client, and regulatory audits; maintain Quality System and cleanroom operations; coordinate scheduling and resource allocation
Seniority
Supervisor, hands-on IC with team leadership