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

• 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

• Master’s Degree

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