Associate Scientist III, Analytical Development

The Position

This position is in the Analytical Development (AD) Group within the CMC Manufacturing Organization. An Associate Scientist III will support method development/validation activities for new drug substances and drug product. They will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies.

• Know and adhere to cGMP policies and procedures and relevant SOPs
• Independently provide accurate analytical results in support of projects
• Meet project timelines and deliverables
• Perform testing of samples to support batch release and stability studies
• Perform portions of analytical techniques, such as HPLC, GC, FTIR, UV/Vis, LC/MS, KF, etc.
• Assist with the design and initiation for development of analytical methods and improvement of existing ones
• Handle, analyze and characterize chemicals, pharmaceuticals, and related organic molecules
• Evaluate and interpret scientific data and provide significance
• Independently design and execute non-routine experiments
• Analyze data/results and propose appropriate follow-up
• Compile data tables, certificate 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 working 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; team-oriented
• Flexibility with changing priorities

• Master’s Degree

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