QA Operations Lead – GMP & Start-up Pharma Site

712 Lly Lebanon Adv Therapies; Lebanon (IN); On-site; USD 66,000 - 172,000; Full time

Benefits offered by this job

401(k) participation

Medical, dental, vision benefits

Well-being programs

Job summary

Lilly is seeking a Quality Assurance Operational Support Representative for the LP2 site in Lebanon, Indiana. The role ensures GMP compliance and oversees daily QA operations, including non-conformance investigations, change control proposals, and batch disposition for clinical and commercial supply.

Responsibilities include leading quality reviews, mentoring staff, and supporting inspections readiness with regulatory agencies.

Qualifications

• Requires a Bachelor’s degree in a science, engineering, computer, or pharmaceutical related field or equivalent industry experience.
• 3+ years in pharmaceutical manufacturing quality assurance roles.
• Authorized to work in the United States full-time.

Responsibilities

• Provide leadership and guidance on quality matters and regulatory compliance.
• Review and approve documents to ensure GMP and local procedures.
• Oversee verification of manufacturing equipment and facilities from requirements through testing.
• Mentor and coach operations staff on quality topics and data integrity.

Skills

Leadership

Good documentation practices

Data integrity

Regulatory compliance

Education

Bachelor's degree in science/engineering/pharma or related field

Tools

Kneat

Veeva Vault

SAP

Manufacturing execution systems

Job description

Lilly is seeking a Quality Assurance Operational Support Representative for the LP2 site in Lebanon, Indiana. The role ensures GMP compliance and oversees daily QA operations, including non-conformance investigations, change control proposals, and batch disposition for clinical and commercial supply.

Responsibilities include leading quality reviews, mentoring staff, and supporting inspections readiness with regulatory agencies.