GMP Manufacturing QA Associate

Scorpion Therapeutics; Indianapolis (IN); On-site; USD 65,000 - 90,000; Full time

Job summary

Scorpion Therapeutics is seeking a Quality Assurance Associate for Manufacturing Operations to provide day-to-day QA oversight on GMP operations, change controls, and investigations on the production floor. The role emphasizes safe, compliant manufacturing and collaborative problem solving.

Initial location is Indianapolis, IN, with potential future site in Lebanon, IN. Travel expected 5–15%. On-call support nights/weekends/holidays may be required.

Qualifications

• BA/BS in Engineering, Science, or related field.
• Minimum 2 years in Biotech or Pharmaceutical FDA-regulated industry.
• Authorized to work in the United States; Lilly sponsorship not provided.

Responsibilities

• Participate in creating and maintaining a safe work environment.
• Foster a collaborative quality culture with cross-functional teams.
• Ensure GMP compliance across activities.
• Review GMP documentation including deviations and change controls.
• Work cross-functionally with plant teams for operational support and issue management.
• Assist with inspection readiness activities.
• Communicate effectively with internal and external stakeholders.

Skills

Quality Assurance

GMP knowledge

Documentation review

Root cause analysis

Cross-functional collaboration

Education

Bachelor's degree in Engineering or Science

Job description

Scorpion Therapeutics is seeking a Quality Assurance Associate for Manufacturing Operations to provide day-to-day QA oversight on GMP operations, change controls, and investigations on the production floor. The role emphasizes safe, compliant manufacturing and collaborative problem solving.

Initial location is Indianapolis, IN, with potential future site in Lebanon, IN. Travel expected 5–15%. On-call support nights/weekends/holidays may be required.