Associate Scientist III, CMC Analytical Development

Responsibilities:
- Know and adhere to cGMP policies, procedures, and relevant SOPs
- Independently provide accurate analytical results supporting new and ongoing projects
- Meet project timelines and deliverables
- Perform testing for batch release and stability studies; support GLP Toxicology and cGMP clinical trial material release
- Perform analytical techniques including HPLC, GC, FTIR, UV/Vis, LC/MS, KF, etc.
- Assist with design and initiation of analytical method development and improvement
- Handle, analyze, and characterize chemicals, pharmaceuticals, and related organic molecules
- Evaluate and interpret scientific data; determine significance
- Design and execute non-routine experiments
- Analyze results and propose appropriate follow-up
- Compile data tables, certificates of analysis, and develop stability reports
- Write analytical test methods, protocols, and SOPs
- Calibrate, maintain, and troubleshoot analytical equipment

Requirements:
- Bachelor’s in Chemistry (or related area)
- 4 years of experience in a chemistry laboratory setting
- Familiar with analytical instrumentation, test methodology/validations, data acquisition systems, and cGMP policies/practices
- Ability to analyze/interpret data and propose follow-up
- Strong attention to detail
- Works well in a team environment; flexible with changing priorities

Preferred:
- Master’s Degree

Wisconsin pay range: $78,000 USD - $90,000 USD