Advisor - Translational Radiochemistry

Lilly

Indianapolis, Indiana, USA
$121,500 - $198,000; bonus: compyny bonus; benefit...
Gmp process development
Analytical method development
Radiopharmaceutical manufacturing
The selected candidate will manage and be a technical expert in the development, scale-up and tech transfer of GMP processes and analytical methods for radiopharmaceutical manufacturing, and the preparation and authorship of CMC-related documents required to support regulatory filings

Job Summary

  • The selected candidate will manage and be a technical expert in the development, scale-up and tech transfer of GMP processes and analytical methods for radiopharmaceutical manufacturing, and the preparation and authorship of CMC-related documents required to support regulatory filings.
  • Responsibilities include supporting early-phase radiopharmaceutical programs by leading tech transfer and post-validation development activities of GMP production processes and test methods, and authoring CMC regulatory documents for health authority filings.
  • Full-time equivalent employees will be eligible for a company bonus, a company-sponsored 401(k), pension, vacation benefits, and comprehensive medical, dental, vision, and prescription drug benefits.

Matching Summary

The selected candidate will manage and be a technical expert in the development, scale-up and tech transfer of GMP processes and analytical methods for radiopharmaceutical manufacturing, and the preparation and authorship of CMC-related documents required to support regulatory filings.

Salary

$121,500 - $198,000; Bonus: company bonus; Benefits: comprehensive benefit program

Skills & Requirements

Must-have

  • GMP process development
  • Analytical method development
  • Radiopharmaceutical manufacturing
  • CMC regulatory documents
  • Imaging radioisotopes
  • Therapeutic radioisotopes

Nice-to-have

  • Strong organization skills
  • Fast-paced environment
  • Cross-functional collaboration
  • Vendor relationship management
  • Environmental health and radioprotection

Key Requirements

  • PhD or MSc degree
  • 8+ years relevant industry experience (PhD)
  • 10+ years relevant industry experience (MSc)
  • Pharmaceutical GMP manufacturing experience
  • Experience with F-18, Ga-68, Lu-177, Ac-225
  • Ability to travel up to 50%

Work Rights

Not specified

Tailored Resume

Cover Letter