CareerPlan

Pharmaceutical Development Senior Associate Scientist I

Kansas City, MO, USFull-time2026-11-12 → 2026-11-13
On-site

Core

Support formulation design and development of oral solid drug products in a GMP environment.

Role type

Senior Associate Scientist (Pharmaceutical Development)

Builds

Oral solid drug products for clinical trials and market

Domain

Pharmaceutical manufacturing / Oral drug delivery

Required skills

GMP compliance, formulation design, laboratory techniques, technical documentation, process execution, deviation management, scientific reasoning

Preferred skills

Solids development experience, Master's degree in life/physical science, 2+ years experience

Technologies

GMP systems, laboratory equipment

Responsibilities

Train others on procedures and lab techniques, execute efficiency improvement projects, conduct work in GMP areas with minimal supervision, draft technical documents (notebooks, protocols, batch records), perform parallel review of GMP documents, propose deviations based on sound judgment

Seniority

Associate, hands-on IC