Scientist I, RNA
Core
Onboarding new technical transfer activities for Drug Substance life cycles from development through clinical and commercial applications, focusing on process review and implementation into GMP spaces for RNA work streams.
Role type
Scientist I, RNA Technical Operations
Builds
Scalable and reliable GMP Operations for RNA-based therapies
Domain
Biopharma / RNA manufacturing / Drug Substance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
RNA manufacturing, experimental design, data analysis, biologics downstream bioprocessing, GMP compliance, technical writing, change controls, quality event investigations
Preferred skills
RNA/LNP program support, regulatory guidelines (CMC), automated purification systems (AKTA, KrosFlo), automated method text instructions (Unicorn, Repligen Recipe Editor)
Technologies
AKTA systems, KrosFlo systems, Unicorn, Repligen Recipe Editor
Responsibilities
Execute working plans or studies with oversight through all phases of the process (pre-clinical to clinical), aid in onboarding of RNA technical transfers, collaborate cross-functionally to achieve manufacturing and quality goals, execute change controls and aid in quality event investigations, align with evolving business priorities
Seniority
Individual Contributor, entry to mid-level