Director, MSAT

Sana Biotechnology Inc

Cambridge, MA

JOB DETAILS
SALARY
$200,000–$250,000 Per Year
SKILLS
Analysis Skills, Automation, Biology, Biomedical Engineering, Biotech and Pharmaceutical, Campaigns, Cleanroom, Communication Skills, Comparative Analysis, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Analysis, Detail Oriented, Diabetes, Establish Priorities, Experiment Design, GMP (Good Manufacturing Practices), ISO (International Organization for Standardization), Identify Issues, Lift/Move 25 Pounds, Manufacturing, Manufacturing Analysis, Manufacturing Technology, Medical Products, Mentoring, Multitasking, Operational Support, Phase I Clinical Trials, Presentation/Verbal Skills, Problem Solving Skills, Process Improvement, Python Programming/Scripting Language, R Programming Language, Regulatory Submissions, Root Cause Analysis, Staff Development, Stem Cells, Supply Chain, Team Lead/Manager, Team Player, Technical Strategy, Technical Writing, Technology Analysis, Time Management, Trend Analysis, Willing to Travel, Writing Skills
LOCATION
Cambridge, MA
POSTED
30+ days ago

About the role Sana Biotechnology is growing, and we are hiring new team members who believe in the potential of engineered cells as medicines, who are passionate about delivering the possible to patients, and who lead with the desire to work on novel ideas. As an MSAT Director, you will report to the Executive Director of MSAT and support manufacturing of Sana's stem cell-derived pancreatic islet cell program for persons with type 1 diabetes (SC451). You will lead an MSAT team responsible for the PSC seed train and differentiation to beta cells at an external partner. You will define and execute the technology transfer strategy in alignment with program timelines and provide your team with technical mentorship. Your team will provide technical coverage at an external manufacturing partner throughout the phase I manufacturing campaign including people-in-plant, executed batch record review, investigations, and batch summaries. You will collaborate with internal partners across Quality, External Manufacturing, and Supply Chain to complete batch disposition. You will draft applicable CMC sections of regulatory documents (IND module 3).

What you'll do

• Lead a team of 2-4 individuals supporting Phase I manufacturing of a PSC-derived pancreatic islet cell therapy product • Partner with CDMO technical team to achieve manufacturing readiness and address technical challenges • Oversee people-in-plant, manufacturing operator training, technical documentation, and process execution • Author CMC sections for regulatory filings (IND module 3) and other technical documents • Collaborate with Quality to close deviations, analyze manufacturing trends, and recommend process improvements • Lead investigations and troubleshoot process execution challenges including root cause analysis • Perform comparability studies in collaboration with Research and PD teams to assess technology transfer success • Engage in crucial conversations by providing and receiving feedback supporting the growth and development of team members • Demonstrate ability to engage and effectively influence team members across multidisciplinary teams while prioritizing multiple projects and meeting deadlines • Drive curiosity, scientific rigor and excellent problem-solving skills across a fast-paced performance driven environment

Innate ability to assess talent that will help grow the organization and add to Sana's culture

What we're looking for

BSc. in Chemical, Biological, or Biomedical Engineering plus 10 yrs or equivalent combination of education and work experience

• >5 year experience supporting early phase cell therapy manufacturing including technology transfers • Well versed with cGMP requirements and working in a regulated environment, including experience as person-in-plan and/or GMP operator • Knowledge of PSC culture and differentiation biology to pancreatic islets • Experience managing a team of >3 direct reports • Detail-oriented with good problem-solving, technical writing and verbal communication skills • Ability to effectively work in multidisciplinary teams, meet deadlines, and prioritize multiple projects • Aptitude for working in a self-driven, performance/results-oriented, fast-paced matrix environment

What will separate you from the crowd

• Experience with key cell therapy equipment and unit operations to support phase 1 clinical trials including cryopreservation • Working knowledge of statistical design of experiments (DoE) and RCA • Experience working in grade B / ISO 7 cleanroom • Understanding of analytical methods such as flow cytometry • Experience with cell therapy process closure and automation • Knowledge of single-use technologies as applicable to cell therapies • Familiarity with data analysis tools such as R, Python, JMP and FlowJo software

Requirements

• Travel to the manufacturing site ~25% of the time (Canada) • Some weekend work required • Lift up to 25 lbs • Work within a cleanroom environment

Compensation The base pay range for this position at commencement of employment is expected to be between $200,000 and $250,000/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience

About the Company

S

Sana Biotechnology Inc