Radiopharmaceutical Development Scientist (All Levels) – On-Site

Aktis Oncology, Inc.; Boston (MA); On-site; USD 108,000 - 167,200; Full time

Job summary

Aktis Oncology is seeking scientists at all levels to support manufacturing and QC development of proprietary radiopharmaceutical drug products. The role involves radiolabeling, formulation optimization, and establishing analytical methods within the RPD group on-site at the Boston office.

The successful candidate will collaborate with cross-functional teams to ensure robust manufacturing protocols and timely technology transfer for regulatory filings, with hands-on experience in radiolabeling

Qualifications

• BS in chemistry, engineering or related field.
• Hands-on radiolabeling and handling radioactive materials.
• Experience with radiolabeled compounds, gamma detectors, UV- and radio-HPLC.
• Experience with protein solubility, binding assays, and drug product formulation.
• Strong project management and ability to work independently and as a team.
• Desire to work in a mission-oriented company advancing radiopharmaceuticals.

Responsibilities

• Radiolabeling and analytical method development 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 filings.
• Take on new challenges and promote data-driven decision making.
• Demonstrate scientific rigor and collaboration aligned with company objectives.
• Operate and maintain radio-HPLC systems, detectors, and analytical instruments.

Skills

Project management

Independent work

Team collaboration

Data-driven decision making

Scientific rigor

Education

Bachelor's degree in Chemistry/Engineering or related field

Tools

Radio-HPLC systems

Gamma detectors

Analytical instruments

Job description

Aktis Oncology is seeking scientists at all levels to support manufacturing and QC development of proprietary radiopharmaceutical drug products. The role involves radiolabeling, formulation optimization, and establishing analytical methods within the RPD group on-site at the Boston office.

The successful candidate will collaborate with cross-functional teams to ensure robust manufacturing protocols and timely technology transfer for regulatory filings, with hands-on experience in radiolabeling