Scientist II, Quality Control

Scorpion Therapeutics; Madison (WI); On-site; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics in Madison, WI is seeking a Scientist II in Quality Control to support analytical method validation, transfer, and testing of raw materials, in-process samples, finished drug substances, and drug products for biopharma applications.

The role emphasizes leading analytical projects, developing and optimizing methods across LCMS, HPLC/UPHPLC, GC, FTIR, UV/Vis, and KF, preparing technical documentation, mentoring junior staff, and interpreting stability data for API and drug

Qualifications

• MS in Chemistry with 5+ years or BS with 8+ years laboratory experience.
• proficiency in analytical techniques, cGMP, ICH, and CDER standards.
• strong attention to detail and independent work capability.

Responsibilities

• lead and coordinate analytical projects
• perform method development and optimization (LCMS, HPLC/UPHPLC, GC, FTIR, UV/Vis, KF)
• prepare technical documentation
• mentor junior staff
• interpret data related to API and drug product stability

Skills

Analytical method development

cGMP knowledge

ICH/CDER standards

Attention to detail

Independent work

Project leadership

Education

MS in Chemistry

BS in Chemistry

Tools

LCMS

HPLC/UPHPLC

GC

FTIR

UV/Vis

KF

Job description

Role

Scientist II in Quality Control supporting analytical method validation, transfer, and testing of raw materials, in-process samples, finished drug substances, and drug products for biopharma applications.

Responsibilities

• lead and coordinate analytical projects
• perform method development and optimization (LCMS, HPLC/UPHPLC, GC, FTIR, UV/Vis, KF)
• prepare technical documentation
• mentor junior staff
• interpret data related to API and drug product stability

Requirements

• MS in Chemistry with 5+ years or BS with 8+ years laboratory experience
• proficiency in analytical techniques, cGMP, ICH, and CDER standards
• strong attention to detail and independent work capability

High-Value

• biopharma QC
• analytical validation
• multiple sophisticated techniques
• experience supporting API and drug product release
• team leadership
• technical coordination

WorkSetup

not specified.