Radiochemist

Company Description Eckert & Ziegler Radiopharma Inc. is a radiopharmaceutical company headquartered at 25 Upton Drive in Wilmington, Massachusetts. The company operates in the United States, supporting the development and production of nuclear medicine products and services. Team members contribute to solutions used in medical diagnostics and therapy. The Wilmington site offers laboratory and production environments for scientific, technical, and quality-focused professionals. Eckert & Ziegler Radiopharma Inc. provides opportunities to work in a regulated, safety‑conscious setting with a focus on patient care and innovation. Role Description The Radiochemist will work full time on‑site in Wilmington, MA, supporting the development, synthesis, and production of radiopharmaceuticals. Daily responsibilities include performing radiochemical syntheses, preparing and handling radioactive materials, and carrying out routine and non‑routine laboratory procedures in accordance with established protocols and safety regulations. The role involves executing and documenting quality control tests, maintaining accurate batch records, calibrating and maintaining laboratory equipment, and assisting with method development and process optimization. The Radiochemist will collaborate with cross‑functional teams, follow Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards, and support troubleshooting, investigations, and continuous improvement activities. The position also includes participating in radiation safety practices, training, and audits to ensure compliance with internal policies and regulatory requirements. Qualifications Strong foundation in radiochemistry and radiopharmaceutical science, with demonstrated ability to perform radiolabeling, synthesis, and characterization of radioactive compounds. Hands‑on laboratory skills, including solution preparation, sample handling, use of analytical instruments (e.g., HPLC, GC, gamma counters), and adherence to GLP/GMP requirements. Experience with quality control testing, including assay, purity, identity, sterility, and endotoxin testing, and the ability to accurately document and interpret QC data. Knowledge of nuclear science principles, radiation physics, and radiation safety procedures, including working with sealed and unsealed sources under regulatory guidelines. Bachelor’s or Master’s degree in Chemistry, Radiochemistry, Nuclear Chemistry, Pharmaceutical Sciences, or a related scientific discipline (PhD is a plus). Familiarity with FDA, USP, and other regulatory expectations for radiopharmaceuticals or sterile drug products is desirable. Strong problem‑solving and troubleshooting abilities, with attention to detail and a commitment to data integrity and documentation accuracy. Effective communication and teamwork skills, with the ability to follow written procedures and collaborate in a multidisciplinary, safety‑focused environment. Previous experience in a radiopharmacy, nuclear medicine, pharmaceutical manufacturing, or related regulated environment is preferred. #J-18808-Ljbffr Eckert & Ziegler Radiopharma Inc