Scientist (all levels) – Radiopharmaceutical

Aktis Oncology Inc • Boston, MA

10d • $108,000 - $167,200 • Onsite

About The Position

Aktis Oncology is seeking highly motivated scientists to support manufacturing and QC development of AKTIS Oncology’s proprietary radiopharmaceutical drug products. The candidate will be part of radiolabeling development, formulation optimization, and establishment of initial analytical methods within the RPD group. These roles are critical in ensuring product quality, regulatory compliance, and successful advancement of radiopharmaceutical programs from early development through clinical manufacturing. The position(s) will collaborate closely with cross-functional team members to ensure timely delivery of robust manufacturing protocols in support of technology transfer activities. The ideal candidate has hands-on experience in radiolabeling and handling radioactive materials and radiopharmaceutical analytical techniques. This role requires full-time on-site presence at the Aktis Boston office.

Requirements

• Minimum BS in chemistry, engineering or related field, with relevant industry experience
• Hands-on experience with metal chelation chemistry, radiolabeling methods and handling radioactive materials.
• Experience analyzing radiolabeled compounds, experience with gamma detectors, UV- and radio-HPLC
• Experience with protein solubility, binding assays, and drug product formulation
• Experience with HPLC troubleshooting and maintenance
• Project management and organizational skills, proven track record of setting priorities, and ability to work independently and as a team member.
• Strong desire to be part of a mission‐oriented company leading transformative change for patients.
• Proven demonstration of transparent communication and fostering open and diverse debate.
• Ability to work with agility and manage ambiguity.
• Personifies positive energy and exemplifies respect.

Responsibilities

• Radiolabeling and analytical method development of Aktis’ radioactive drug products for pre-clinical and early phase clinical use.
• Participate in day-to-day laboratory operations, including radiation safety.
• Write development reports that can be used for transfer of technology and regulatory filing.
• Take on new challenges willingly and build a culture of rigor and data-driven decision making to bring novel therapies to the clinic
• Demonstrate high standards for scientific rigor, team behaviors, excellence and a culture of innovation that is fully aligned with company objectives
• Operate and maintain radio-HPLC systems, detectors, and analytical instruments

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level