Quality Control Job for Life Science Candidates at ImmunityBio
Searching for a high-growth quality control job in the biotech industry? This full-time job in USA offers an exciting opportunity for life sciences candidates to join ImmunityBio Careers as an Associate, Quality Control Analytical in Culver City, California. This is a strong job opportunity for life science graduates seeking hands-on GMP laboratory experience while contributing to cutting-edge oncology and immunotherapy products.
Company Overview
ImmunityBio, Inc. is a commercial-stage biotechnology company focused on developing cell and immunotherapy products designed to strengthen the body’s natural immune system. The company’s mission is to harness and amplify both branches of the immune system to eliminate cancerous or infected cells while building long-term immunological memory. Through innovative therapies and vaccines, ImmunityBio aims to transform cancer treatment by targeting the host immune response rather than solely the disease.
Job Details:
- Job Title: Associate, Quality Control Analytical
- Company: ImmunityBio, Inc. (NASDAQ: IBRX)
- Location: Culver City, California, United States
- Employment Type: Full-Time
- Job Requisition ID: R2856
- Work Environment: Onsite
Quality Control Job Summary
The Associate, Quality Control Analytical (QCA) is responsible for executing analytical assays in support of product release across ImmunityBio’s oncology platforms. The role requires close collaboration with cross-functional teams, including Quality Assurance, Facilities/Engineering, and Process Sciences, to ensure compliance, efficiency, and inspection readiness within a GMP-regulated environment.
Essential Functions
- Schedule, process, and test raw materials, in-process, release, and stability samples in accordance with turnaround time (TAT) requirements
- Support method development, qualification, validation, and transfer activities
- Maintain GMP laboratory testing readiness, including assay setup, equipment ownership, and inventory management
- Support new equipment installation and Operational Qualification (IQ/OQ) activities
- Contribute to Continued Process Verification (CPV) programs for fusion drug products
- Review product-specific Bills of Materials (BOM) and raw material testing strategies
- Adhere to and improve SOPs, protocols, and analytical test methods
- Ensure compliance with GxP standards and maintain a state of inspection readiness
- Lead or support Out-of-Specification (OOS) and Out-of-Trend (OOT) investigations and implement corrective and preventive actions (CAPA)
- Troubleshoot and improve assay performance as needed
- Review testing performed by other team members
- Track and trend Key Performance Indicators (KPIs) to ensure business continuity
- Participate in Continuous Improvement (CI) initiatives and Gemba walk activities
- Interface with internal and external auditors to support positive audit outcomes
- Support Environmental Health & Safety (EH&S) standards
- Contribute to ad-hoc and cross-functional projects as required
Education & Experience
- Bachelor’s degree in a Life Sciences discipline required
- Minimum of 1 year of experience in a GMP-regulated biologics or pharmaceutical environment required
- Experience with compendial standards (USP, EP) and FDA guidelines preferred
Knowledge, Skills, & Abilities
- Knowledge of USP, EP, FDA, 21 CFR 210/211, and ICH guidelines
- Foundational understanding of chemistry and molecular biology
- Strong technical writing skills, including preparation of SOPs, validation protocols, analytical reports, and method development documentation
- Effective verbal and written communication skills
- Strong organizational skills with the ability to manage multiple priorities and deadlines
- Proactive, solution-oriented mindset with accountability and urgency
- Strong proficiency in Microsoft Word, Excel, and PowerPoint (Visio and Monday.com preferred)
- Demonstrates professionalism, reliability, teamwork, and openness to feedback
Working Environment
- Onsite GMP analytical laboratory environment
- Proper use of personal protective equipment (PPE) required
- Flexible schedule, including potential off-hours, overtime, second shift, or weekend work as needed
- Occasional travel (approximately 10%) between Culver City and El Segundo offices
Compensation for Quality Control Job
Hourly base pay range: $32.00 – $35.00 per hour
- $32.00: Entry-level qualifications
- $35.00: Highly experienced candidates
This position is also eligible for a discretionary bonus and equity award. Compensation is based on qualifications, experience, and geographic considerations.
