Manage QA operations during manufacturing, ensuring compliance with cGMP, conducting batch record reviews, and overseeing quality assurance processes.

The Sr. Director, Public Relations will develop and execute communication strategies, manage media relations, and support executive leaders in conveying company objectives.

The QC Associate will execute GMP-compliant testing of cell therapy products, manage cell culture, draft SOPs, coordinate lab equipment maintenance, and support quality investigations.

The Principal Scientist will lead translational strategies for clinical programs, integrating biomarker data to inform clinical decisions and ensure compliance with regulatory standards.

The Manager will lead corporate communications and digital media efforts, curate content, manage editorial calendars, and engage audiences across multiple platforms.

The Director of Investor Relations will develop and execute a strategic IR program, manage communications, support events, and collaborate with senior executives and financial communities.

The Senior Director, Statistical Programming oversees design and delivery of statistical programming solutions for clinical trials, ensuring CDISC compliance and managing programming teams.

As a QC Associate, you will execute GMP-compliant environmental monitoring, manage lab supplies, support QC data tracking, and maintain lab equipment.

As a Senior People Partner, you will guide the Commercial organization in talent strategy, workforce planning, performance management, and cultural initiatives during the company's growth phase towards commercial launch.

As a Scientist, you'll execute protein and molecular biology engineering strategies, collaborating with a team to develop cancer therapies and advance therapeutic candidates.

The Senior Scientist will develop and manage clinical biomarker assays, ensuring compliance and integrating new technologies while interpreting data and supervising others.

The Office Manager oversees daily operations, supports executive staff, manages facilities, tracks Purchase Orders, and coordinates events and travel.

The Associate Director will manage the clinical supply chain, ensuring timely supply of trial materials while developing strategies, overseeing operations, and fostering vendor relations for Arcellx's cell therapy pipeline.