Jobs at ImmunityBio

Serve as a QC analytical subject matter expert to advise on method development, validation, transfer, and troubleshooting. Author and review SOPs, test methods, IND/BLA analytical sections, CoAs, OOS investigations, and batch release documentation. Review stability and lot release data, manage change controls and supplier notifications, collaborate with QA/regulatory and contract testing labs, and support data trending and quality investigations.

The Senior Compensation Partner designs and administers compensation programs, provides expert consultation to management on pay issues, ensures compliance, and supports strategic initiatives to attract and retain talent.

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

Manage day-to-day administration and support for GxP computerized systems, ensuring compliance with regulations and providing technical leadership for system deployments and upgrades.

The Senior Associate conducts environmental monitoring, microbiological testing, training, documentation, and supports lab compliance and operations.

Perform molecular biology and protein/RNA production to support immunotherapy R&D: cloning, PCR, plasmid prep, in vitro transcription, protein expression/purification, data recording, SOP adherence, and train junior staff.

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

The Senior Specialist in Quality Risk Management will oversee the QRM program, implement tools, deliver training, and ensure compliance in a GMP-regulated environment.

The Value Stream Quality Manager oversees product lifecycle quality, ensuring compliance with regulations for biotechnology products. They manage quality control and improvement processes while collaborating cross-functionally with various departments to support both internal and external GMP productions.

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

The Uro Oncology Business Manager drives treatment adoption of Anktiva among clinics and hospitals handling early-stage bladder cancer patients. Responsibilities include executing sales strategy, building customer relationships, training healthcare providers on drug administration, analyzing account performance, and collaborating with company partners.

The Senior GCP Auditor ensures compliance with GCP standards and regulations in clinical trials, oversees audits, and manages quality systems.

The Uro Oncology Business Manager drives clinical conviction and adoption of Anktiva, builds relationships with healthcare providers, and analyzes performance barriers to boost treatment adoption in their territory.

The Uro Oncology Business Manager will drive clinical conviction and treatment adoption of Anktiva within their territory, focusing on building relationships, analyzing account performance, and collaborating with partners.

Design and build full-stack applications with a focus on web and mobile systems, integrating AI technologies and containerized deployments.

The Uro Oncology Business Manager drives clinical conviction of Anktiva, focuses on treatment adoption, and builds relationships with healthcare providers within their territory.

The QA Engineer is responsible for test automation, software quality assurance, and platform reliability engineering, ensuring reliable and performant software delivery. They will design and maintain testing frameworks, validate AI workflows, and collaborate with multidisciplinary teams to uphold quality standards.

Design, develop, and maintain responsive UI/UX for web and mobile applications. Collaborate with teams to ensure seamless integration and optimize performance. Conduct user testing and contribute to architectural tooling for deployment.

Lead statistical strategies for clinical trials, ensuring regulatory compliance and guiding cross-functional teams in statistical methodologies and data management.