Jobs at ImmunityBio

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

The Manufacturing Specialist oversees biological manufacturing processes, ensuring adherence to cGMP. Responsibilities include leading operations, troubleshooting, and training staff while improving production processes.

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

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

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

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.

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.

The Senior Director of Talent and Culture leads HR strategies, oversees recruitment, performance management, and cultural initiatives to enhance employee engagement and retention within a biotechnology company.

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

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

The Senior Biostatistician will oversee statistical analyses and reporting of clinical trial data, ensuring quality and compliance with regulatory standards while mentoring junior staff.

The Senior Statistical Programmer leads statistical programming for clinical trial data, ensures quality and standards, mentors junior staff, and handles regulatory submissions.

The Clinical Trials Associate will support the administration of clinical trials, ensuring compliance with regulations, maintaining documentation, and facilitating communication between clinical sites and the operations team.

The Clinical Trials Manager oversees clinical studies, manages protocol compliance, develops study documents, supports site management, and assists in staff training and clinical trial updates.

The Uro Oncology Business Manager drives adoption of Anktiva in clinics and hospitals, builds relationships, and trains healthcare providers on treatment.