ImmunityBio
Principal Scientist, Upstream Process Science
Louisville, CO · Principal
Stay score
odds of building a lasting career here
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
Personalize to your clock →Employer immigration record
from this employer's Department of Labor filings
Files H-1B transfers
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
Community outcomes
No reports yet — be the first to help the next applicant.
About the role
- This role serves as a technical expert for specific unit operations within the upstream manufacturing process, including both microbial and cell culture seed expansions and bioreactor operations across multiple cell lines.
Responsibilities
- The Principal Scientist, Upstream Process Sciences role will manage the team responsible for upstream process development, process characterization, and scientific support activities for GMP manufacturing.
- This role is also responsible for designing and executing process development experiments to design a robust and scalable clinical and commercial production process.
- Manage the day-to-day activities of the team to include the hiring and training of new team members, coaching employees and monitoring performance
- Guide and advise other technical staff in risk assessment, Design of Experiments (DOE), process characterization, process validation, and process monitoring activities.
- Provide input for development programs, and collaborate with discovery, formulation, analytical, quality, regulatory and manufacturing teams.
- Perform ad-hoc and cross-functional duties and/or projects, as assigned, to support business needs and provide developmental opportunities.
- Performs ad-hoc and cross-functional duties and/or projects assigned to support business needs and provide developmental opportunities.
Requirements
- Extensive experience in method development, method validation, and method transfer is required.
- Fundamental knowledge of cell and molecular biology, immunology, and/or virology
- Master-level technical knowledge of microbial, cell culture, and harvest operations affecting product quality.
Nice to have
- 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.
- Provide high-level technical knowledge in the development of batch, fed batch, and perfusion processes for inoculum expansion and biologics production operations.
- Provide project coordination and high-level technical expertise in process development, process improvement, scale-up, and tech transfer activities.
- Draft, review and approve technical protocols, reports, and manufacturing deviation investigations.
- Present activities and results interdepartmentally, and to senior management.
- Author and review process-related regulatory submissions.
Skills
- This position works on site, in Louisville, CO.
- Regular work schedule is Monday - Friday, within standard business hours. Flexibility is available with manager approval.
- Occasional travel may be required, up to 10%.
- 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
- 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
Compensation
- The annual base pay range for this position is below.
Company info
- At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace.
Visa & Work Authorization
- 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
This listing is sourced directly from ImmunityBio's careers page and normalized into a canonical job model.