Role
Support drug product development for Moderna’s sterile biologics, focusing on process development, scale-up, and formulation optimization for clinical and future commercial supply.
Responsibilities
- Conduct studies on manufacturing scale-up processes (freeze/thaw, mixing, lyophilization, transport)
- Evaluate material compatibility
- Collaborate on toxicology and stability fills
- Plan and execute experiments (including DoE)
- Troubleshoot manufacturing issues
- Perform characterization techniques (opacity testing, microscopy, particle sizing)
- Ensure long-term stability of vialed products, with documentation in ELN
Qualifications
- Master’s or Bachelor’s in Chemical, Biochemical, Biomedical Engineering, Pharmaceutical Sciences, or related fields
- 0-2 years post-Master’s or 2+ years post-Bachelor’s experience
- Strong lab skills
- Knowledge of DoE and nucleic acid chemistry advantageous
Preferred
- BioPharma experience
- Nanoparticle formulation
- GMP familiarity
- Willingness to travel up to 20%
High-Value
- Biologics
- mRNA modalities
- Clinical stage (preclinical or early-phase)
- Aseptic processing
- Process characterization
- Collaboration with analytical and manufacturing teams
Work setup
Collaborative environment with hybrid onsite/work-from-home model.
#J-18808-LjbffrEngineer II, Drug Product Development in norwood at Unknown Company
This position is listed as full time and hybrid.