Analytical Scientist I, cGMP Lab & Method Development

Doist; Verona (WI); On-site; USD 57,000 - 68,000; Full time

Job summary

Arrowhead Pharmaceuticals, Inc. is seeking an Associate Scientist I to join the CMC Analytical Development group in Wisconsin.

The role supports analytical testing for drug substance and drug product development and assists with method development, qualification, and release testing for GLP toxicology studies and cGMP clinical materials. Under the guidance of senior scientists, you will learn analytical techniques including HPLC, GC, FTIR, UV/Vis, LC/MS, and Karl Fischer, while supporting

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline.
• 0–2 years of laboratory experience.
• Basic understanding of analytical chemistry principles.
• Familiarity with analytical instrumentation through coursework or lab.
• Excellent written and verbal communication skills.

Responsibilities

• Follow cGMP guidelines, lab procedures and SOPs.
• Perform routine analytical testing to support batch release and stability studies.
• Assist with analytical method development, qualification, and validation.
• Learn and perform techniques including HPLC, GC, FTIR, UV/Vis, LC/MS, Karl Fischer.
• Prepare samples, reagents, and standards for testing.
• Document procedures and results in notebooks and electronic systems.
• Compile data and prepare certificates of analysis; assist with stability reports.
• Collaborate with cross-functional teams to meet timelines; maintain a safe lab.

Skills

Organizational skills

Communication skills

Team collaboration

Prioritization

Attention to detail

Education

Bachelor's degree in Chemistry

Bachelor's degree in Biochemistry

Bachelor's degree in Pharmaceutical Sciences

Tools

HPLC

GC

FTIR

UV/Vis

LC/MS

Karl Fischer

Job description

Arrowhead Pharmaceuticals, Inc. is seeking an Associate Scientist I to join the CMC Analytical Development group in Wisconsin.

The role supports analytical testing for drug substance and drug product development and assists with method development, qualification, and release testing for GLP toxicology studies and cGMP clinical materials. Under the guidance of senior scientists, you will learn analytical techniques including HPLC, GC, FTIR, UV/Vis, LC/MS, and Karl Fischer, while supporting