QA Director, Radiopharma Quality & Compliance

Eli Lilly and Company; Indianapolis (IN); Presencial; USD 125.000 - 183.000; Jornada completa

Descripción de la vacante

Lilly in Indianapolis is seeking a QA Associate Director/Director to provide leadership and oversight of a multi‑shift GMP operation that produces radioligand compounds. You will manage QA personnel, review records, and ensure regulatory inspections readiness.

The role partners with Technical Services for process qualification, drives continuous improvement, and fosters a strong quality culture across site operations.

Formación

• Bachelor’s degree in science/engineering/pharma or equivalent experience.
• 5+ years pharmaceutical leadership with QA experience, including cross‑functional work.

Responsabilidades

• Provide QA leadership for a multi‑shift GMP operation producing radioligand compounds.
• Oversee record review, release, and QA labs; ensure regulatory inspection readiness.
• Partner with Technical Services on process qualification and site objectives.

Conocimientos

Radiopharmaceuticals

Quality Management Systems

Regulatory requirements

GMP knowledge

Interpersonal communication

Educación

Bachelor's degree in science/engineering/pharma

Herramientas

Kneat

Veeva Vault

SAP

Manufacturing Execution Systems

Microsoft Office

Descripción del empleo

Lilly in Indianapolis is seeking a QA Associate Director/Director to provide leadership and oversight of a multi‑shift GMP operation that produces radioligand compounds. You will manage QA personnel, review records, and ensure regulatory inspections readiness.

The role partners with Technical Services for process qualification, drives continuous improvement, and fosters a strong quality culture across site operations.