Jobs at Adicet Bio, Inc

Leads cross-functional biotech program management, developing integrated timelines, tracking milestones, managing risks, budgets, resources, documentation, governance, and stakeholder communication. The role supports drug development programs, facilitates team decision-making, drives issue resolution and continuous improvement, and may supervise junior program managers. Collaboration includes China-based stakeholders and oncology, autoimmune disease, or cell therapy programs.

Lead and build the QA Operations team to ensure cGMP compliance for clinical manufacturing. Oversee lot disposition, validations, quality investigations, audits, training, raw material QA, and support regulatory submissions. Collaborate cross-functionally to manage quality systems, risk management, and continuous improvement to support CMC and clinical activities.

Coordinate and execute in vivo and ex vivo nonclinical studies (efficacy, PK/PD, safety) using murine xenograft and humanized models. Contribute to study design and timelines, collaborate with CROs, perform necropsies and tissue processing, run downstream assays (flow cytometry, qPCR/ddPCR, ELISA), maintain experimental records, troubleshoot technical challenges, and support program advancement.