Associate, Quality Control Analytical

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient’s immune system and treat the host rather than just the disease.

Why ImmunityBio?
• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
• Work with a collaborative team with the ability to work across different areas of the company.
• Ability to join a growing company with professional development opportunities.

Position Summary

The Associate, Quality Control Analytical in the Quality Control department is responsible for ensuring the timely execution of Quality Control Analytical assays in support of product release across all of ImmunityBio’s oncology and vaccine product platforms. This position will train on and perform a variety of molecular biology, and/or chemistry assays including but not limited to cell culture, qPCR, flow cytometry, cytotoxicity, visual inspection and/or Compendial test methods in the evaluation of product quality.   

Essential Functions

• Ensure and support a safe working environment for work areas.
• Perform testing of assigned lot release and stability samples to meet expected turnaround time requirements. 
• Participate in method qualification, validation and transfer activities.
• Support instrument installation and operational qualification activities (IOQ).
• Ensure a compliant workspace by adhering to and enforcing GxP requirements.
• Ensure the integrity of all data generated.
• Maintain laboratory equipment, supplies and inventory inclusive of cleaning and sanitization of equipment and restocking of supplies.
• Assist in authoring and working collaboratively on documentation such as protocols, reports, SOPs and test methods as needed. 
• Ensure timely escalation of all assay related challenges/issues and assist in developing countermeasures to improve performance. 
• Track / trend key performance indicators and identify adverse events in testing and escalate as needed to prevent reoccurrence. 
• Participate in continuous improvement activities to help improve the overall operations of the testing labs. 
• Maintain analytical laboratory in a state of control, compliance, and inspection readiness. Interface with all auditors (internal and external) to ensure positive audit outcomes.
• Partner with colleagues in various departments (e.g., AD/PD, Facilities, Engineering, QA and Regulatory) to ensure achievement of company goals.
• Adheres to Standard Operating Procedures (SOPs) and cGMP guidelines.
• Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities.

Education & Experience

• Bachelor’s degree in a life sciences discipline with 1+ years of relevant experience required.
• Experience in a GMP regulated Biologics or Pharmaceutical environment is preferred.
• Knowledge of cell and molecular biology, immunology, and/or virology is preferred.
• Experience in cGMP aseptic processing facility is preferred.
• Good understanding and demonstration of aseptic techniques is preferred.

Knowledge, Skills, & Abilities

• Proficient communicator (written and verbal)
• Ability to proactively take initiative to remove roadblocks that interfere with the completion of assigned tasks
• Able to be timeline focused
• Proficient in Microsoft Word, Project, and Excel
• Strong problem-solving skills with demonstrated attention to detail
• Strong verbal, written, and interpersonal communication skills
• Proficiency in computer use and Microsoft Office applications
• Attention to detail with strong analytical and problem solving skills
• Well-developed written and oral communication skills
• Motivated to work in a team environment
• Ability to perform troubleshooting and develop solutions to problems of moderate scope in complexity
• Ability to operate in a fast-paced, multi-disciplinary industrial environment
• Ability to work efficiently in a highly interactive, goal-oriented team environment
• Able to be flexible in order to meet the demands of a multi-product clinical phase biopharmaceutical company.
• Exceptional organization and time-management skills
• Ability to multi-task across multiple functional areas and retain flexibility in a dynamic environment
• Consistently deliver on commitments

Working Environment / Physical Environment

• This position works onsite and depending on location may need to travel to other buildings
• This position works in a lab environment.
• Regular work schedule is Monday – Friday, within standard business hours.  Flexibility is available with manager approval.
• Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer.
• Must have ability to perform work while wearing the appropriate gowning material for cleanroom environments.
• Ability to work on unscheduled days occasionally to support the dynamic schedule and relevant timelines.
• Ability to manage up to fifty (50) pounds at a time and stand for extended periods of time while wearing appropriate clean room gowning material and appropriate personal protective equipment is required

This position is eligible for a discretionary bonus and equity award. The hourly base pay range for this position is below. The specific rate will depend on the successful candidate’s qualifications, prior experience as well as geographic location.

$32.00 (entry-level qualifications) to $35.00 (highly experienced) per hour

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day •  We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.