Allogene Therapeutics

HQ
South San Francisco
Total Offices: 2
382 Total Employees

Allogene Therapeutics Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers accidental death & dismemberment insurance

Offers life insurance

Offers company equity

Offers performance bonuses

Offers employee stock purchase plan

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers Health Savings Account (HSA)

Offers generous parental leave

Career Growth + Development

Provides customized development tracks

Work-Life Balance + Wellbeing

Offers generous PTO

Provides paid sick days

Provides paid holidays

Offers an Employee Assistance Program (EAP)

Offers gym membership

Company Culture

Offers a remote work program

Provides free snacks and drinks

Offers diversity-based Employee Resource Groups

5 Days AgoSaved
In-Office
Newark, CA, USA
Biotech
Provide QA leadership and oversight for CMOs and material suppliers; support GMP manufacturing, disposition, audits, investigations, change control, quality agreements, regulatory submissions, analytical transfers, and continuous improvement activities.
10 Days AgoSaved
In-Office
South San Francisco, CA, USA
Biotech
Lead and grow Process Sciences teams to develop robust CAR-T drug substance and drug product processes. Drive DoE/QbD-based process characterization, risk assessments, GMP documentation, technology transfer, and regulatory filing support (IND–BLA). Mentor staff, collaborate cross-functionally and with external partners, and represent the organization in publications and conferences to advance platform process knowledge and commercialization readiness.
10 Days AgoSaved
In-Office
South San Francisco, CA, USA
Biotech
Lead product characterization strategy and author regulatory product characterization from IND to BLA for allogeneic CAR T cell products. Drive innovation in analytical methods, collaborate with Process Science, Quality, and Regulatory to define CQAs and control strategies, and characterize gene editing/insertion impacts. Mentor staff, maintain high-quality documentation, and support regulatory interactions while staying current with field and regulatory guidance.