Position Summary

In order to make an application, simply read through the following job description and make sure to attach relevant documents. We are seeking a highly experienced and visionary leader of CMC & Manufacturing to lead our cell therapy development programs. The successful candidate help lead CMC strategy, manage process development and manufacturing activities, and play a key role in advancing programs into first-in-human clinical trials. This role requires demonstrated success in bringing at least one cell therapy program from preclinical through IND and into clinical trials. Key Responsibilities lead/support the development and implementation of CMC strategy for cell therapy programs. Lead process development and optimization for iPSC- or MSC-derived products and drive process development, scale-up, and tech transfer. Contribute to regulatory filings (CMC sections of IND/CTA). Collaborate with CMC, R&D, QC, QA, and clinical teams across China and the U.S. to ensure a seamless transition from preclinical to clinical development. Support resource planning, budgeting, and project management for CMC deliverables. Provide strategic leadership to ensure clinical readiness and robust supply chain for first-in-human studies. Qualifications PhD (preferred) or MS in Cell Biology, Immunology, Bioengineering, or related field. 8+ years of biotech/pharma experience with at least 5 years in cell therapy CMC leadership. Hands-on experience with iPSC/MSC biology, process development, and GMP compliance. Proven track record of advancing programs into IND/clinical development. Deep knowledge of GMP regulations, regulatory expectations, and cell therapy manufacturing platforms. Excellent leadership, communication, and cross-functional team management skills. Strong interpersonal and communication skills; ability to thrive in a fast-paced, collaborative biotech environment. Strong leadership, project management, and cross-functional communication skills.

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