Teams at ImmunityBio

The Manager will oversee Capex projects in GMP environments, ensuring compliance with regulations, managing contractors, and leading engineering initiatives for manufacturing operations.

Provide legal support for clinical research by drafting, reviewing, and negotiating Clinical Trial Agreements and related vendor and commercial contracts. Ensure compliance with FDA, GCP, HIPAA, GDPR and other regulations; develop templates, SOPs, and negotiation playbooks; advise internal stakeholders on risk mitigation; assist with informed consent review; deliver training and lead process-improvement and cross-functional projects.

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