Director of Isotope CMC & Radiochemistry

Oklo Inc

Austin (TX)

On-site

USD 170,000 - 250,000

Full time

12 days ago
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Benefits offered by this job

Flexible time off
Equity
Bonuses
401(k)
Health insurance
HSA
FSA
Wellness credits

Job summary

Oklo Inc. is seeking a Director of Chemistry, Manufacturing and Controls (CMC) to lead the radiochemistry team and scale isotope production in Austin, TX.

The role focuses on Lu-177, Am-241, and Ra-226 processing, process development, technology transfer, and regulatory readiness in a cGMP environment. You will build a multidisciplinary team, establish manufacturing controls, and drive continuous improvement across analytics, validation, and lifecycle management in collaboration with Quality,

Qualifications

  • Master's degree in a closely related technical discipline required.
  • 10+ years in radiochemistry or isotope production with regulated environments.
  • Experience with cGMP manufacturing and regulatory frameworks (FDA/NRC/DOE).
  • Proven ability to lead technical teams and manage lifecycle of processes.

Responsibilities

  • Lead radiochemistry and CMC organization for isotope process development and lifecycle management.
  • Oversee Lu-177 production and Am-241/Ra-226 processing, including purification and waste minimization.
  • Establish technical basis for manufacturing processes and controls.
  • Drive technology transfer, analytic strategy, and regulatory support.
  • Build and mentor a high-performing radiochemistry team and ensure safety and quality.

Skills

Radiochemistry expertise
Leadership
Analytical strategy
Process development
Cross-functional collaboration
Problem solving

Education

Master's in Radiochemistry / Chemistry / Chemical Eng

Job description

Oklo Inc. is seeking a Director of Chemistry, Manufacturing and Controls (CMC) to lead the radiochemistry team and scale isotope production in Austin, TX.

The role focuses on Lu-177, Am-241, and Ra-226 processing, process development, technology transfer, and regulatory readiness in a cGMP environment. You will build a multidisciplinary team, establish manufacturing controls, and drive continuous improvement across analytics, validation, and lifecycle management in collaboration with Quality,

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