Senior Principal QA Lead, Analytical Foundry

BioSpace; Lebanon (IN); On-site; USD 65,000 - 169,000; Full time

Benefits offered by this job

401(k) plan

Pension

Vacation benefits

Well-being programs

Job summary

Lilly is building the Medicine Foundry in Indiana to accelerate manufacturing and drug development. The Sr. Principal Associate for Analytical Quality Assurance will ensure analytical data quality, support GMP testing, and maintain the quality management system for the Foundry as it nears completion.

This role requires strong QA leadership, favorable regulatory knowledge, and collaboration with external contract labs to uphold global quality standards in a fast-paced environment.

Qualifications

• Bachelor’s degree in Pharmacy, Chemistry, Biology, or related field.
• Minimum 5 years of technical laboratory experience with QA in pharma preferred.
• Strong knowledge of analytical method development/validation and GMP expectations.

Responsibilities

• Provide quality oversight of Analytical testing and qualification activities.
• Lead quality assessments of GMP documentation and deviations.
• Ensure quality systems are in place and followed across the Foundry lab.

Education

Bachelor’s degree in Pharmacy, Chemistry, Biology, or related field

Tools

Analytical method development

GMP compliance

Quality system management

Job description

Lilly is building the Medicine Foundry in Indiana to accelerate manufacturing and drug development. The Sr. Principal Associate for Analytical Quality Assurance will ensure analytical data quality, support GMP testing, and maintain the quality management system for the Foundry as it nears completion.

This role requires strong QA leadership, favorable regulatory knowledge, and collaboration with external contract labs to uphold global quality standards in a fast-paced environment.