IB Temporary - Associate , Quality Control

NantWorks (the "Company") is the parentcompany of various private and public entities that are changinghow we work, live and play. We focus on three main categories: lifesciences; energy & renewables; and media & technology. We investin strategies that improve our core capabilities and in brandnew industries, poised to change mankind for the better. Bycapturing tomorrow's opportunities through scientific processes andentrepreneurial philosophies, we are at the forefront of emerginghigh-growth technologies across a wide range of industries.

The Company is a mandatory vaccination employer for COVID-19 and its variants. The Company requires that its employees be fully vaccinated as of their start date. If you require a medical or religious accommodation we will engage in the interactive process with you. Proof of vaccination will be required prior to start. If we make you an offer and you are not yet vaccinated, we will accommodate a delay in start date. The Company may also mandate that its employees receive vaccine boosters, and all accommodation laws will be followed.

Position Summary

The IB Temporary - Associate 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, ELISA, qPCR, HPLC, icIEF, CE-SDS techniques 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.
• May conduct other Quality Control related duties as assigned.

Education & Experience

• Bachelor's degree in a life sciences discipline with 3+ years of relevant experience required.
• Experience in a GMP regulated Biologics or Pharmaceutical environment preferred.
• Experience in cGMP aseptic processing facility is preferred.

Knowledge, Skills, & Abilities

• Knowledge of cell and molecular biology, immunology, and/or virology.
• Proficiency and understanding and demonstration of aseptic techniques.
• 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

• Flexibility in working schedule, i.e., occasional off-hours, second shift, and weekends.
• Exposure to onsite in-lab environment.
• Regular work schedule is Monday - Friday, within standard business hours. Flexibility is available with manager approval.
• Will require occasional weekend and holiday work to meet business needs.
• Ability to gown and gain entry to manufacturing areas and be in the cleanroom environment for extended periods of time.

This position is eligible for a discretionary bonus and equity award. The annual 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.

$32.40 (entry-level qualifications) to $36.00 (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.