Analytical Development Scientist III — Method Dev & QC Support

Scorpion Therapeutics; Madison (WI); On-site; USD 78,000 - 90,000; Full time

Job summary

Scorpion Therapeutics in Madison, WI is seeking an Associate Scientist III to join the Analytical Development group. You will support method development/validation for new drug substances and products, and assist testing for GLP toxicology and cGMP clinical trial material release, as well as stability studies.

You will implement non-routine experiments, analyze data, and prepare COAs, stability reports, and SOPs.

Qualifications

• Bachelor’s degree in Chemistry or related field required.
• 4 years of experience in a chemistry lab setting required.
• Familiar with analytical instrumentation and cGMP practices.
• Ability to analyze data and propose follow-up actions.
• Strong attention to detail and team orientation.
• Flexibility with changing priorities.

Responsibilities

• Know and adhere to cGMP policies and SOPs.
• Independently provide accurate analytical results for projects.
• Meet project timelines and deliverables.
• Test samples to support batch release and stability studies.
• Perform portions of analytical techniques (HPLC, GC, FTIR, UV/Vis, LC/MS, KF).
• Assist with development and improvement of analytical methods.
• Handle and characterize chemicals and related molecules.
• Evaluate data and provide significance.
• Design and execute non-routine experiments.
• Analyze results and propose follow-up actions.
• Compile data tables, COA, and develop stability reports.
• Write analytical methods, protocols, and SOPs.
• Calibrate, maintain, and troubleshoot analytical equipment.

Skills

Data analysis

Data interpretation

Attention to detail

Team oriented

Education

Bachelor’s in Chemistry

Master’s Degree

Tools

HPLC

GC

FTIR

UV/Vis

LC-MS

KF

Job description

Scorpion Therapeutics in Madison, WI is seeking an Associate Scientist III to join the Analytical Development group. You will support method development/validation for new drug substances and products, and assist testing for GLP toxicology and cGMP clinical trial material release, as well as stability studies.

You will implement non-routine experiments, analyze data, and prepare COAs, stability reports, and SOPs.