Senior Radiochemist

1 month ago

Kuwait City Telix Pharmaceuticals Limited Full time
  • Interface with key stakeholders, including external CMOs, to manage the development of manufacturing and QC procedures for clinical-stage radiopharmaceutical assets in compliance with all applicable GMP regulations.
  • Manage the development and validation of manual or automated manufacturing procedures as required.
  • Manage the development and validation of non-compendial QC procedures as required.
  • Generate development, validation, method transfer, and various other types of protocols and reports.
  • Support regulatory filings via completion of CMC sections for INDs, NDAs, BLAs, and foreign equivalents.