Radiopharmaceutical Development Scientist: Radiolabeling & QC

Aktis Oncology; Boston (MA); On-site; USD 110,000 - 170,000; Full time

Job summary

Aktis Oncology, Inc. is seeking highly motivated scientists to support manufacturing and QC development of AKTIS Oncology’s proprietary radiopharmaceutical drug products.

You will contribute to radiolabeling development, formulation optimization, and analytical method establishment in the RPD group, with full‑time on‑site work at the Aktis Boston office. The role emphasizes regulatory readiness, cross‑functional collaboration, and robust manufacturing protocols to transfer technology and advance

Qualifications

• Minimum BS in chemistry, engineering or related field with relevant industry experience.
• Hands‑on experience with radiolabeling methods and handling radioactive materials.
• Experience analyzing radiolabeled compounds with gamma detectors and HPLC.
• Experience with protein solubility, binding assays, and drug product formulation.

Responsibilities

• Radiolabeling and analytical method development of radioactive drug products for pre‑clinical and early phase clinical use.
• Participate in day‑to‑day laboratory operations, including radiation safety.
• Write development reports for technology transfer and regulatory filing.
• Take on new challenges and foster data‑driven decisions to bring therapies to the clinic.
• Demonstrate scientific rigor and collaboration aligned with company objectives.
• Operate and maintain radio‑HPLC systems, detectors, and analytical instruments.

Skills

Radiolabeling

Analytical method development

Radiation safety

HPLC operation

Project management

Independent work

Education

BS in Chemistry or related field

Tools

Radio‑HPLC systems

Detectors (gamma, UV)

HPLC troubleshooting

Job description

Aktis Oncology, Inc. is seeking highly motivated scientists to support manufacturing and QC development of AKTIS Oncology’s proprietary radiopharmaceutical drug products.

You will contribute to radiolabeling development, formulation optimization, and analytical method establishment in the RPD group, with full‑time on‑site work at the Aktis Boston office. The role emphasizes regulatory readiness, cross‑functional collaboration, and robust manufacturing protocols to transfer technology and advance