Beam Therapeutics - Quality Control

Associate Director, Product Quality Assurance sought for Cell and Gene Therapy programs in Cambridge, MA. This strategic Quality leader partners with CMC teams across the full product lifecycle, from development to commercialization. Requires 12+ years pharma/biotech experience, including 4+ year...

Seeking a Sr. Specialist I, Product Quality Assurance to provide critical Quality oversight at Beam’s advanced cell and gene therapy facility in Durham, NC. This role ensures GMP compliance for clinical and commercial manufacturing, requiring 10+ years in pharma/biotech with expertise in aseptic ...

Seeking a Director/Senior Director of Quality Control Automation & Digitalization in Cambridge, MA. Lead strategic transformation of QC operations through advanced lab automation and digital platforms. Requires 15+ years in pharma/biotech QC, 8+ years in leadership, and hands-on expertise with Ha...

Join Beam's innovative cell and gene therapy manufacturing team in Durham, NC. This senior Quality Assurance role provides critical GMP oversight for clinical and future commercial operations. We seek a scientific degree holder with 10+ years of pharma/biotech experience in manufacturing and qual...

Join our team as a Senior Specialist in Analytical Instrument Qualification. You will lead end-to-end qualification and lifecycle management for critical QC instruments across MA and NC GMP labs. The role requires deep expertise in analytical techniques, validation deliverables (URS, IQ/OQ/PQ), a...

Join Beam's Digital Quality team as a GxP Compliance & Data Integrity Specialist. You will ensure compliance for critical computerized systems (SaaS, IaaS, PaaS) and manufacturing platforms, partnering with cross-functional teams. This RTP-based role requires 8-10+ years in biotech/pharma QA/Vali...

Lead Quality Control strategy for innovative cell and gene therapy programs. This senior director role oversees analytical method lifecycle management and GMP testing across sites in Durham, NC, and Cambridge, MA. Requires 18+ years in pharma/biotech with strong QC leadership experience. Drive qu...

Lead global GMP/GXP compliance training initiatives for a biotech leader. Develop and implement effective training programs within a robust Quality Management System. This Durham-based role requires 8+ years of pharmaceutical industry experience and expertise in instructional design.