QA Principal Scientist – Radioligand Manufacturing

100 Eli Lilly and Company

Indianapolis (IN)

On-site

USD 66,000 - 172,000

Full time

8 days ago

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Benefits offered by this job

401(k)
Pension
Vacation benefits
Medical, dental, vision
Flexible benefits

Job summary

Lilly in Indianapolis is seeking a Sr. Principal Scientist - QA to oversee QA responsibilities for radioligand drug product manufacturing. The role includes real-time batch record reviews, on-floor QA support, and final disposition of drug products to ensure GMP compliance and inspection readiness.

The ideal candidate holds a Bachelor's in a science/engineering field with 5+ years in pharma QA/QC, and is authorized to work in the United States. On-site role with opportunities to mentor QA staff.

Qualifications

  • Bachelor's degree in science, engineering, or related technical field.
  • 5+ years of experience in QA/QC roles in the pharmaceutical industry.
  • On-site role located in Indianapolis Radioligand Therapies.
  • Authorized to work in the United States on a full-time basis; no visa sponsorship provided.

Responsibilities

  • Provide QA oversight during aseptic drug product manufacturing.
  • Review batch records on the floor in real time and provide QA support.
  • Dispostion of drug product batches and drug substance intermediates.
  • Ensure GMP compliance and inspection readiness across operations.
  • Train floor QA personnel as SME and qualified trainer for tasks.

Skills

Independent work
Quality systems
Regulatory readiness
MES experience
Electronic batch release

Education

Bachelor's degree in science/engineering

Job description

Lilly in Indianapolis is seeking a Sr. Principal Scientist - QA to oversee QA responsibilities for radioligand drug product manufacturing. The role includes real-time batch record reviews, on-floor QA support, and final disposition of drug products to ensure GMP compliance and inspection readiness.

The ideal candidate holds a Bachelor's in a science/engineering field with 5+ years in pharma QA/QC, and is authorized to work in the United States. On-site role with opportunities to mentor QA staff.

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