Full-Time

Executive Director

PSC Process Development

Confirmed live in the last 24 hours

Sana Biotechnology

Sana Biotechnology

201-500 employees

Develops cell-based therapies and gene technologies

Biotechnology

Senior

Cambridge, MA, USA

Requirements
  • PhD in a life Scientific Discipline or engineering filed with 15+ years of experience in academic research and/or industry
  • Deep expertise and industry experience in cell therapy process development principals including DOE and experience with current technologies in PSC process development and manufacturing
  • Experience overseeing the transfer of a cell therapy process for cGMP manufacturing to internal facility and external CDMO with a quality/compliance mindset
  • Knowledge and understanding of regulatory guidelines and experience supporting regulatory filings and interactions
  • CMC team leadership experience managing cell therapy programs through product life cycle from pre IND through clinical and commercialization stages
  • Highly proficient at communicating and influencing individuals across all levels of an organization and multidisciplinary teams while prioritizing multiple projects and meeting deadlines
  • Demonstrated ability to mentor scientists and engineers, engage in crucial conversations by providing and receiving feedback to support the growth and development of direct reports
  • Proven track-record of organizational leadership, functional buildup and management
Responsibilities
  • Provide strategic and technical CMC leadership for developing innovative, scalable expansion and differentiation processes to manufacture PSC derived cell therapy products
  • Provide oversight of activities required to ensure successful transfer and execution of differentiation processes in GMP manufacturing, including oversight of external CDMOs
  • Drive technical advancements through collaborations with suppliers, academic research institutions and industry consortiums
  • Hire, develop and mentor a talented team of scientists and engineers with a vision of setting industry-leading scientific standards and innovation
  • Drive curiosity, scientific rigor and leverage excellent problem-solving skills across a fast-paced performance driven environment
  • Develop the content of relevant CMC sections of regulatory dossiers, support regulatory interactions and queries
  • Serve as a cross-functional, matrix CMC leader for PSC programs
  • Collaborate with Sana colleagues in Research, Translational Sciences, Clinical and Technical Operations and effectively manage stakeholders across the organization to align strategy and approach to rapidly advance Sana’s PSC pipeline
  • Partner with the Program Team Leader to ensure achievement of program deliverables
  • Manage the functional component of business planning and own budget accountability for the group
  • Contribute to developing the organization strategy, cultivate opportunities for career development, champion the Sana culture and make it a great place to work

Sana Biotechnology, Inc. specializes in utilizing engineered cells as medicines to address various diseases and developing novel delivery technologies to repair and control genes in cells. The company also focuses on enabling broader access to therapies through scalable manufacturing solutions.

Company Stage

IPO

Total Funding

$865M

Headquarters

Seattle, Washington

Founded

2018

Growth & Insights
Headcount

6 month growth

-9%

1 year growth

-19%

2 year growth

-13%