The Manager, Site Planning will develop and manage the Master Schedule for Beam Therapeutics in North Carolina, coordinating input from various departments including Manufacturing, Quality, and Supply Chain. They will ensure seamless integration of scheduled activities and maintain clear communication about updates and changes. This role may also involve selecting and implementing scheduling software aligned with company needs.

The Quality Control Specialist will lead analytical method implementation for GMP testing in a new laboratory. Responsibilities include maintenance of the QC lab, performing release and stability testing, training junior analysts, and overseeing instrument qualifications and troubleshooting. The role requires collaboration for timely analysis completion and data integrity management.

Senior Research Associate with a strong background in analytical method development and sample testing for non-GMP lot release, stability, and characterization of cell and gene therapy products using lipid nanoparticle (LNP) delivery. Responsibilities include developing and optimizing analytical methods, executing sample testing, collaborating with cross-functional teams, and supporting external testing labs. Qualifications include a relevant degree and experience in analytical method development.