Associate Scientist I, Analytical Development

Scorpion Therapeutics; Madison (WI); On-site; USD 57,000 - 68,000; Full time

Benefits offered by this job

Competitive salaries

Excellent benefits

Job summary

Scorpion Therapeutics in Madison, WI is seeking an Associate Scientist I to support analytical testing for drug substance and product development (CMC Analytical Development). You will perform routine lab testing, method development/qualification, and release/stability testing for GLP toxicology studies and clinical trial materials.

Responsibilities include following cGMP, preparing samples, documenting results, collaborating with cross-functional teams, and maintaining a clean lab.

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• 0–2 years of laboratory experience (industry/academic/internship/co‑op).
• Basic understanding of analytical chemistry principles and lab techniques.
• Familiarity with analytical instrumentation (coursework or experience).
• Strong organizational skills and attention to detail.
• Excellent written and verbal communication skills.
• Ability to work independently and in a team.
• Ability to manage multiple priorities in a fast‑paced environment.

Responsibilities

• Follow cGMP guidelines, laboratory procedures, and applicable SOPs.
• Perform routine analytical testing to support batch release, stability studies, and development activities.
• Assist with analytical method development, qualification, and validation.
• Learn and perform analytical techniques including HPLC, GC, FTIR, UV/Vis, LC/MS, Karl Fischer, and other laboratory instrumentation.
• Prepare samples, reagents, and standards for testing.
• Accurately document procedures/results in lab notebooks and electronic systems.
• Compile data, prepare certificates of analysis, and assist with stability reports.
• Analyze data with guidance from senior team members.
• Calibrate, maintain, and perform basic troubleshooting of equipment.
• Collaborate with cross-functional teams to meet project timelines.
• Maintain a clean, organized, and safe laboratory environment.

Skills

Attention to detail

Strong communication

Teamwork

Independent worker

Education

Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field

Tools

HPLC

GC

FTIR

UV/Vis

LC/MS

Karl Fischer

Job description

The Associate Scientist I supports analytical testing for drug substance and drug product development (CMC Analytical Development), including routine laboratory testing, analytical method development/qualification, and release and stability testing for GLP toxicology studies and cGMP clinical trial materials.

Responsibilities

• Follow cGMP guidelines, laboratory procedures, and applicable SOPs.
• Perform routine analytical testing to support batch release, stability studies, and development activities.
• Assist with analytical method development, qualification, and validation.
• Learn and perform analytical techniques including HPLC, GC, FTIR, UV/Vis, LC/MS, Karl Fischer, and other laboratory instrumentation.
• Prepare samples, reagents, and standards for testing.
• Accurately document procedures/results in lab notebooks and electronic systems.
• Compile data, prepare certificates of analysis, and assist with stability reports.
• Analyze data with guidance from senior team members.
• Calibrate, maintain, and perform basic troubleshooting of equipment.
• Collaborate with cross-functional teams to meet project timelines.
• Maintain a clean, organized, and safe laboratory environment.

Requirements

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• 0–2 years of laboratory experience (industry/academic/internship/co‑op).
• Basic understanding of analytical chemistry principles and lab techniques.
• Familiarity with analytical instrumentation (coursework or experience).
• Strong organizational skills and attention to detail.
• Excellent written and verbal communication skills.
• Ability to work independently and in a team.
• Ability to manage multiple priorities in a fast‑paced environment.
• Candidates must have current, valid authorization to work in the country where this role is located.

Preferred

• Experience in a cGMP or regulated lab environment.
• Hands‑on chromatography or other analytical instrumentation experience.

Benefits/Compensation

• Wisconsin pay range: $57,000–$68,000 USD.
• Competitive salaries and an excellent benefit package.