Scientist I, Research &Development

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 Scientist I position will aid in the development and generation of new novel therapeutics/vaccines intended for pre-clinical and cGMP-manufacturing use. The role is responsible for performing research and development work related to numerous expression system-based immunotherapies, including viral vector platforms and mRNA. The role will primarily be involved with the cloning of new gene-therapy vectors, subsequent vector characterization, cell culture optimization, and troubleshooting issues related to such pre-clinical manufacturing processes. The Scientist I will perform bio-assay development experiments, careful documentation of methods and materials and results, writing technical reports, and effectively communicating findings to other teams. This role is also responsible for aiding in the design and execution of product development experiments that lead to a robust and scalable clinical and commercial production process. Essential Functions Support Research and Development projects designed to generate pre-clinical material characterization, design of experiments (DOE), and defining critical process parameters. Identify and propose process optimization, continuous improvement projects and support initiatives. Support scale-up and technology transfer of new products and processes into cGMP manufacturing. Apply analytical skills to evaluate and interpret complex issues and data sets utilizing multiple sources of qualitative information and quantitative research. Support product specific data trending programs. Author and review technical protocols/reports, tech transfer documents, SOPs and MBRs. Lead and participate in team meetings and present results intra- and interdepartmentally. Provide support and technical insight for process-related issues and investigations, including non-conformance product impact assessments, root cause analysis, change control, and process optimization. Design and execute experiments, and compile results/statistical data analysis for scaled-down lab processes to enable process troubleshooting, support process robustness and characterization studies, and develop process improvements Bench-scale study ownership including the collection and interpretation of data from bench scale experiments with minimal oversight. Conducts daily tasks associated with development and characterization of novel human therapeutics. Responsible for laboratory equipment maintenance programs. Meticulously maintains experimental records with detailed observations. Conducts additional laboratory work and projects, as needed. Support preclinical studies by evaluating basic health status of animals and reporting abnormalities to the appropriate personnel Support the lab by performing activities such as maintaining lab equipment, ordering and stocking supplies, and maintaining inventory 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 Cell Biology, Microbiology, Biology, or other life science or related field with 10+ years of experience including direct experience in upstream and/or downstream processes Master’s degree in Cell Biology, Microbiology, Biology, or other life science or related field with 8+ years of experience in biopharmaceutical-based process development and/or GMP manufacturing operations including direct experience in upstream processes required; or PhD degree in Cell Biology, Microbiology, Biology, or other life science or related field with 1+ experience in biopharmaceutical-based process development and/or GMP manufacturing operations including direct experience in upstream processes preferred. Experience with molecular cloning, human tissue culture, and viral vector construction required Experience working with viruses in a BSL-2 viral laboratory required Experience in molecular biology/cloning, RNA biology, cell biology, tissue culture and cell-based methods, with a proven track record of achievement required Knowledge, Skills, & Abilities Strong initiative, problem solving, attention to detail, ability to effectively organize and prioritize are required. Ability to work with Quality and Manufacturing groups to ensure a compliant manufacturing environment and work collaboratively with other team members to support the transfer of biological drug processes from R&D/Product Development to Manufacturing. Adapts to rapidly changing work environment and shift in priorities. Possess good interpersonal and strong written/verbal communication skills. Manage multiple assignments and processes with excellent skills in prioritizing and time management. Possess the ability to multitask and work independently or in a team environment with minimal supervision. Good computer skills in word processing, spreadsheets, and database software applications, including MS Office (Word, Excel), Visio and statistical software including JMP. Strong aptitude for problem solving, technical writing and ability to effectively participate on teams. Possess a high level of honesty and integrity, highly motivated and detail-oriented. Comfortable/Willing to work with small rodent research animals Working Environment / Physical Environment This role works on site This role works in both lab and cleanroom environments. Occasional travel may be required to support technical transfer of processes. This position works on-site in a research lab and adjacent vivarium and will include exposure to small rodent animal models. This role works in both lab and occasional cleanroom environments May include off-hour work and flexible work scheduling. 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. $110,000 (entry-level qualifications) to $121,000 (highly experienced) annually 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. ImmunityBio is a leading registration-stage immuno-oncology and infectious disease company activating both the innate (natural killer cell and macrophage) and adaptive (T cell) immune system. We are developing molecular and product platforms including N-803, Aldoxorubicin, and a second-generation adenovirus vector, based upon our three key modalities of activating natural killer (‘NK’) and T cells, tumoricidal macrophages, and memory T cells. Please be aware of fraud or scams from individuals, organizations, and/or internet sites claiming to represent ImmunityBio in recruitment activities. We have an established recruitment process which is required for all posted positions by ImmunityBio prior to issuing an offer of employment. This ImmunityBio process requires formal interviews conducted live with personnel representing ImmunityBio and never requires payments or fees from job applicants. In the event that you receive a suspicious phone call, email or Linked InMail message about recruiting on behalf of ImmuntiyBio, unless it’s from an authorized recruiting associate, do not provide any personal information and never pay any fees. Qualified and interested candidates should apply to current openings directly through this ImmunityBio website. ImmunityBio accepts no responsibility for costs or charges incurred as a result of fraudulent activity.