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Senior Scientist, Radiochemistry

Telix Pharmaceuticals Limited
Full-time
On-site
Los Angeles, CA
Clinical Research and Development

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Role Summary

Senior Scientist, Radiochemistry responsible for hands-on radiolabeling of antibodies and antibody fragments with radiometals and for the conjugation of biomolecules with metal chelators. This role requires a strong foundation in radiochemistry, protein biochemistry, and antibody characterization. Supports preclinical research activities in cancer theranostics and therapeutic applications, and contributes to translational development and early CMC scale-up initiatives. Serves as the site Radiation Safety Officer (RSO) and ensures compliance with radiation safety regulations and internal practices.

Responsibilities

  • Radiochemistry & Conjugation
    • Perform and optimize radiolabeling of antibodies and antibody fragments with therapeutic and diagnostic radiometals (e.g., 177-Lu, 225-Ac, 89-Zr, 64-Cu, etc.).
    • Conduct chemical conjugation of antibodies with metal chelators (e.g., DOTA, DOTAGA, DTPA, DFO, MACROPA).
    • Develop reproducible and scalable labeling protocols for preclinical and translational applications.
    • Design and execute quality control assays (HPLC, iTLC, SEC, SDS-PAGE).
    • Develop and transfer analytical methods to support preclinical studies and CMC activities.
  • Protein Biochemistry
    • Apply biochemical expertise in antibody/protein handling, purification, and characterization.
    • Assess protein integrity and stability following conjugation and radiolabeling.
    • Support analytical method development for protein-radiometal conjugates.
  • Preclinical & Development Support
    • Collaborate with in-vivo biology team to support in vitro and in vivo studies.
    • Provide input into CMC scale-up activities.
    • Contribute to IND-enabling activities, including process documentation and technology transfer.
  • Radiation Safety
    • Serve as the site’s Radiation Safety Officer (RSO).
    • Maintain compliance with local, state, and federal radiation safety regulations.
    • Implement radiation safety procedures, train laboratory staff, and maintain required records and licenses.

Qualifications

  • Required:
    • Bachelors plus 8+ years, Masters plus 6+ years, Ph.D. plus 5+ years in Chemistry, Biochemistry, Radiochemistry, Pharmaceutical Sciences, or related field.
    • 3+ years of laboratory experience in radiolabeling of biologics, metal chelator chemistry, and related QC techniques.
    • Strong background in protein biochemistry, including antibody purification, conjugation, and characterization.
    • Experience with analytical methods commonly applied in radiopharmaceutical and protein characterization.
    • Prior or current qualification as Radiation Safety Officer (or equivalent experience).
    • Knowledge of regulations governing radiation safety.
    • Strong documentation, organizational, and communication skills.
  • Preferred:
    • Experience with preclinical radiopharmaceutical development in oncology.
    • Familiarity with CMC scale-up activities and regulatory documentation.
    • Experience with GMP or GLP environments.

Skills

  • Safety Mindset: Demonstrates strict adherence to radiation safety protocols and laboratory best practices.
  • Scientific Rigor: Applies a detail-oriented and methodical approach to experimental design, execution, and data analysis.
  • Collaboration: Works effectively across multidisciplinary teams, fostering open communication and knowledge sharing.
  • Accountability: Takes ownership of projects and responsibilities, delivering on commitments in a timely manner.
  • Adaptability: Adjusts to evolving project priorities, regulatory requirements, and organizational needs.
  • Problem-Solving: Approaches technical challenges with creativity and persistence, identifying practical solutions.
  • Communication: Clearly communicates experimental results, documentation, and regulatory materials to internal stakeholders and collaborators.