Are you eager to lead innovation in stem cell manufacturing? Are you experienced with stem cells, and scalable bioreactor based manufacturing processes? As a Senior Process Engineer at Cellistic, youll play a key role in developing and optimizing GMP compliant processes for cutting edge stem cell therapies. Cellistic is growing, and were looking for passionate team members who believe in the power of engineered cells as medicines, challenge the status quo, and thrive on bringing novel ideas to life. The position As a Senior Process Engineer, you will drive the development of a novel allogeneic chimeric antigen receptor T (CAR T) cell manufacturing process. The Senior Process Engineer will serve as the process subject matter expert, lead development, and coordinate the integration of multiple unit operations. In this role you will focus on the scale up (and automation) of bio processes for manufacturing products from pluripotent stem cells to CAR T cells. The candidate will lead a multidisciplinary project team to execute the development plan, and support the technology transfer to GMP manufacturing team. This role will collaborate closely with multiple cross functional teams including Analytical Development, Research, Supply Chain. As a major part of the job responsibility includes hands on processes development, the preferred candidate is a highly motivated researcher with desire to work in a laboratory focused role. Responsibilities: Develop pioneer processes and introduce state of the art technologies to manufacture iPSC derived T cells therapeutics. Evaluate and implement technology to enhance consistency, scalability and cGMP compliance of bio processes for manufacturing iPSC derived T cell therapeutics. Leverage high throughput experimental designs and equipment (from deep well plates to small scale bioreactors) to optimize cellular differentiation and optimize for product quality Develop scale down models for process optimization studies. Evaluate and implement process analytic technologies (PAT) for improved monitoring and control of stem cell bio processes. Responsible to plan technical work packages and deliver them according to quality and delivery targets, in alignment with the project manager. Write protocols, technical reports, and Standard Operating Procedures (SOPs). Participate in technology transfer of processes and equipment to the Manufacturing group. Collaborate with project teams to integrate processes. Ability to manage various priorities in a fast paced and growing environment Document, share, present and communicate study results at meetings and in other formats Qualifications: Ph.D. and 10+ years or MS and 15+ years of experience in bioengineering, chemical engineering, biology, biochemistry or related field Must have industry and project management experience; direct, hands on industrial upstream experience (ideally in gene and/or cell therapy process development), Strong industrial upstream processing knowledge requi