Radiopharmaceutical Development Scientist – Tech Transfer Lead

Hartmann Young

Utah

On-site

USD 120,000 - 180,000

Full time

48 hours ago
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Benefits offered by this job

Competitive compensation
Scientific ownership
Collaborative culture

Job summary

Hartmann Young partners with a growing radiopharmaceutical biotechnology company to recruit a Scientist or Senior Scientist for Radiopharmaceutical Development & Technology Transfer in Salt Lake City, Utah. You will drive development, optimization, and transfer of manufacturing processes to GMP sites and collaborate with CMC, Manufacturing, Quality, Regulatory, and external CDMO partners.

The role emphasizes hands-on process development, cross-functional leadership, and external partner

Qualifications

  • PhD with 4+ years of experience, MSc with 8+ years, or BSc with 10+ years.
  • Hands-on experience with radioactive materials.
  • Experience in radiopharmaceutical process development and manufacturing.
  • Strong understanding of cGMP principles and GMP operations.
  • Experience transferring technology to internal/external sites.
  • Excellent technical writing and cross-functional collaboration skills.

Responsibilities

  • Develop and optimise radiopharmaceutical production processes.
  • Lead technology transfer activities to GMP sites and CDMOs.
  • Design qualification, verification and validation strategies.
  • Prepare development reports, protocols, and regulatory content.
  • Support investigations and CAPA with root-cause analysis.
  • Ensure data integrity and regulatory compliance.

Skills

Radiopharmaceutical process dev
Technology transfer
cGMP/GMP
External partner management
Technical writing

Education

PhD in a relevant science
MSc in a relevant science
BSc in a relevant science

Tools

LIMS
Chromatography systems

Job description

Hartmann Young partners with a growing radiopharmaceutical biotechnology company to recruit a Scientist or Senior Scientist for Radiopharmaceutical Development & Technology Transfer in Salt Lake City, Utah. You will drive development, optimization, and transfer of manufacturing processes to GMP sites and collaborate with CMC, Manufacturing, Quality, Regulatory, and external CDMO partners.

The role emphasizes hands-on process development, cross-functional leadership, and external partner

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