Engineer II, Drug Product Development

Role: Support drug product development for Moderna's sterile biologics, focusing on process development, scale-up, and container compatibility to enable clinical and commercial supply. Responsibilities: conduct scale-up studies, develop protocols for material compatibility, collaborate on toxicology and stability operations, plan and execute experiments (including DoE), troubleshoot manufacturing issues, and perform characterization techniques (opacity testing, microscopy, particle sizing). Requirements: Master’s or Bachelor’s in Chemical, Biochemical, Biomedical Engineering, Pharmaceutical Sciences, or Materials Science; 0–2 years post-Master’s or 2+ years post-Bachelor’s experience; strong lab skills, knowledge of DoE, and familiarity with nucleic acid chemistry is a plus. Preferred: industry experience in Biopharma or biotech, GMP knowledge, ability to travel up to 20%. HighValue: biologics, sterile drug processes, drug product stability, scale-up, technology transfer, collaboration with analytical, manufacturing, and regulatory teams. Work setup: not specified, travel up to 20%.