Associate Principal Scientist, Mixed Modality Product Development
Core
Developing parenteral dosage forms (injections, implants, inhaled, ocular) for small, intermediate, and large molecules from preclinical toxicology studies to commercialization.
Role type
Associate Principal Scientist (R4), biologics sterile product development
Builds
Robust drug product composition, scalable process, primary packaging, and regulatory filings for non-oral drug products
Domain
Biopharmaceuticals / Parenteral Drug Delivery
Required skills
Biologics process development, Cell Line Development, Design of Experiments (DOE), Downstream Process Development, Drug Delivery, Drug Product Development, Expression Vectors, Molecular Biology, Particle Engineering, Pharmaceutical Formulations, Pharmaceutical Process Development, Product Formulation, Technology Transfer, Toxicology
Preferred skills
Surface science, colloid science, particle engineering, ADC formulations, high concentration formulations, process scale up, modeling, regulatory filings
Technologies
None explicitly listed beyond general scientific domains
Responsibilities
Lead innovative approaches for biologics sterile product development via experimental design and data analysis; Support early and late-stage candidates in formulation, packaging, and compatibility characterization; Lead project activities at external manufacturing sites including tech transfers; Mentor scientists and drive organizational strategic objectives
Seniority
Senior, hands-on IC with strategic leadership
