Sr. Director, Clinical and Pre Clinical Quality Assurance

Sana Biotechnology(29 days ago)

HybridFull TimeDirector$240,000 - $310,000Quality

About this role

Senior Director of Quality (GLP/GCP) at Sana Biotechnology will report to the Chief Medical Officer and lead the company’s strategic quality approach for GLP- and GCP-regulated nonclinical and clinical work. The role is responsible for establishing phase-appropriate quality programs and translating strategy into operational policies, procedures, and training to meet global regulatory and industry standards. This position is based in Cambridge, MA with an in-office schedule of three days per week and may require some travel.

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Required Skills

Quality Strategy
GLP Compliance
GCP Compliance
QMS Management
Auditing
Vendor Management
CAPA Management
Training Programs
Regulatory Compliance
Risk Management

+4 more

Qualifications

Bachelor's Degree
Advanced Degree (Preferred)

About Sana Biotechnology

sana.com

Sana Biotechnology engineers cells to repair or control genes in diseased cells or to replace missing or damaged cells, aiming to address the underlying causes of disease. The company develops cell- and gene-based therapeutic platforms — spanning in vivo and ex vivo approaches — to create durable, curative treatments across a range of indications. Sana combines platform R&D with preclinical and clinical programs to advance engineered-cell medicines toward scalable, restorative therapies.