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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.

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

The Associate, Manufacturing supports biological manufacturing by adhering to cGMP guidelines, executing manufacturing processes, and collaborating cross-functionally to ensure quality operations.

The role involves managing clinical trial finances, ensuring compliance with GAAP, analyzing expenditures, and providing insights to optimize trial spending and resource allocation.

The QA Specialist ensures compliance and oversight of GMP processes in manufacturing, reviews documentation, conducts investigations, and leads continuous improvement efforts within quality systems to support biotech operations.

The Senior QA Specialist ensures compliance in QC labs, supervises analytical methods, and oversees quality assurance processes for microbiology and assays while collaborating with cross-functional teams.

The Program Manager oversees engineering projects from planning to execution, ensuring compliance with cGMP standards and coordinating cross-functional teams to meet project goals.

The Compensation Partner collaborates with HR and managers to manage compensation programs, conduct market analyses, ensure compliance, and educate team members.

Responsible for managing GMP investigations, ensuring product release timelines are met, leading training, and implementing continuous improvements in a dynamic environment.

Oversee clinical supply planning and logistics for clinical programs, working with various internal teams and external partners to ensure timely delivery of clinical materials.