Top Tech Jobs & Startup Jobs in Los Angeles, CA

The Senior Automation Engineer leads automation systems integration, oversees project implementation, collaborates across disciplines, and provides technical support for biologics manufacturing.

Perform and lead QC analytical testing (lot release and stability) using molecular biology and chemistry assays (ELISA, HPLC, icIEF, CE-SDS, cell culture). Support method qualification/validation, IOQ, data integrity, OOS investigations, technical transfer, and GMP/GxP compliance. Interface cross-functionally and maintain inspection readiness.

Perform and support QC analytical assays (e.g., cell culture, qPCR, flow cytometry, cytotoxicity) for lot release and stability under cGMP; maintain lab equipment and documentation; support validations, IOQs, audits, and continuous improvement to ensure compliant, inspection-ready operations.

Senior HR leader who designs and executes talent and culture strategies across global teams, leading acquisition, onboarding, performance management, employee engagement, HR analytics, succession planning, compliance, employee relations, and HR technology to support biotech R&D and commercial operations.

Lead end-to-end recruiting for assigned roles at ImmunityBio, partnering with hiring managers and HR to design structured interviews, source talent, manage candidate experience, and ensure compliant hiring. Develop evaluation frameworks, coach interviewers, facilitate selection decisions, extend offers, and support onboarding while contributing to diversity sourcing and cross-functional projects.

The Executive Assistant & Office Manager supports C-suite leaders, manages executive calendars, oversees office operations, and handles financial responsibilities, ensuring efficient organizational function.

The Director of Commercial QCA oversees quality control programs to ensure product compliance and reliability, managing teams and laboratory operations.

Support environmental monitoring programs for sterile product manufacturing, oversee compliance, conduct testing, and provide guidance to junior analysts in a GMP setting.

Coordinate stability and reference programs including scheduling, data trending, and protocol drafting, while maintaining controlled documents and equipment.

The Senior Associate, Document Control is responsible for managing electronic and physical record documentation, ensuring compliance, and providing training support in a biopharmaceutical environment.