Senior Analytical QA Lead — Methods & Compliance

Scorpion Therapeutics; Lebanon (IN); On-site; USD 125,000 - 175,000; Full time

Job summary

Lilly Medicines Foundry in Carmel, IN is seeking a Sr. Principal Associate for Analytical Quality Assurance to provide quality oversight across GMP testing and analytical development with internal and external partners.

The role ensures the quality management system is followed, supports method development/validation, and leads QA initiatives that improve data integrity and regulatory compliance across multiple projects.

Qualifications

• Bachelor's degree and 5+ years of QA laboratory experience in pharma.
• Strong knowledge of GMP and quality management systems.
• Experience with analytical method development and validation.

Responsibilities

• Provide quality oversight in analytical testing and audits.
• Oversee method verification, qualification, and validation.
• Ensure quality systems are implemented and continuously improved.
• Evaluate incident impact on material quality and data integrity.
• Review GMP documentation and ensure technical review.
• Collaborate with Lilly quality organizations to share best practices.
• Promote a positive quality culture in lab areas.
• Lead process improvement projects across multiple business areas.

Skills

Quality Assurance

Analytical Method Validation

Documentation Review

Education

Bachelor's degree in related field

Job description

Lilly Medicines Foundry in Carmel, IN is seeking a Sr. Principal Associate for Analytical Quality Assurance to provide quality oversight across GMP testing and analytical development with internal and external partners.

The role ensures the quality management system is followed, supports method development/validation, and leads QA initiatives that improve data integrity and regulatory compliance across multiple projects.