Scientist I - Process Development
Core
Scientist I supporting Process Development projects in a CDMO, focusing on formulation design, process design, and scale-up for small molecules and biologics.
Role type
Scientist I (Process Development)
Builds
Pharmaceutical development projects for biopharma clients
Domain
Biopharma / CDMO / Process Development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
wet chemistry, cGMP knowledge, aseptic manufacturing, bulk intermediate manufacturing, medical device manufacturing, HPLC/UPLC, UV-Vis spectroscopy, Flowcam, Karl Fischer titration, DSC/FDM, SOP drafting, batch record management
Preferred skills
MS Office, SmartSheets, LabX, Empower, leading junior scientists
Technologies
HPLC, UPLC, UV-Vis, Flowcam, Karl Fischer, DSC, FDM, SmartSheets, LabX, Empower
Responsibilities
Support formulation design, sterile filtration, lyophilization, and post-processing; perform in-process and finished product testing; execute technology transfer and scale-up activities; draft and review batch records, protocols, and reports; maintain SOPs and controlled documents; lead and train junior level scientists.
Seniority
Entry-level to Mid-level (0-5 years experience)