As a sr. process engineer global MSAT contractor, you will contribute to advancing CAR-T manufacturing processes and technology transfers within a decentralized manufacturing model. Your expertise will play a key role in ensuring the transition of lab-scale processes into robust, GMP-compliant manufacturing systems. You will face challenges such as process characterization, lifecycle validation, and regulatory documentation, requiring a strong background in cell and gene therapy, automated bioreactors, and GMP manufacturing.
What You Will Do:
- Act: as a subject matter expert on automated CAR-T manufacturing processes and technology transfers.
- Develop: and execute plans for lifecycle process validation activities and product comparability assessments.
- Lead: process characterization studies, including protocol design, data analysis, and technical report preparation.
- Collaborate: with process development and CMC teams to translate lab-scale processes into GMP-ready manufacturing systems.
- Prepare: and review CMC documentation, including validation protocols, comparability reports, and regulatory filing sections.