QC Leader, Gene Therapy Start-up & Compliance

Eli Lilly and Company

Lebanon (IN)

Sur place

USD 125 000 - 202 000

Plein temps

Il y a 5 jours
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Avantages offerts par ce poste

401(k) eligibility
Pension
Vacation benefits
Health benefits
Flexible spending accounts

Résumé du poste

Lilly in Lebanon, Indiana, seeks a Site QC Lead to drive quality control strategies for LP2's advanced therapies startup and ongoing operations. You will oversee internal and external testing, ensure timely release of materials, and partner with site leadership and CDMOs to meet safety and regulatory standards.

You'll mentor QC staff, manage day-to-day workload, drive inspection readiness, and align with GMP commitments to deliver compliant testing for clinical and commercial supply.

Qualifications

  • Bachelor's degree in a science field (chemistry, microbiology, biology) required.
  • 8+ years of cGMP commercial manufacturing experience in QC or related disciplines.
  • 8+ years of direct laboratory leadership and supervision of QC personnel.

Responsabilités

  • Set site QC strategy for internal and external laboratory operations.
  • Lead startup and ongoing operations, coordinating with GFD and construction teams.
  • Oversee external partner testing ensuring quality and regulatory readiness.
  • Ensure compliance with procedures and regulatory commitments; support inspections.
  • Develop QC staff through mentoring and career planning.

Connaissances

Laboratory leadership
cGMP knowledge
Regulatory inspection readiness

Formation

Bachelor's degree in a science field (chemistry, microbiology, biology)

Description du poste

Lilly in Lebanon, Indiana, seeks a Site QC Lead to drive quality control strategies for LP2's advanced therapies startup and ongoing operations. You will oversee internal and external testing, ensure timely release of materials, and partner with site leadership and CDMOs to meet safety and regulatory standards.

You'll mentor QC staff, manage day-to-day workload, drive inspection readiness, and align with GMP commitments to deliver compliant testing for clinical and commercial supply.

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