Quality Control Associate

UCSD Layoff from Career Appointment: Apply by 6/03/2026 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor. Reassignment Applicants: Eligible Reassignment clients should contact their Disability Counselor for assistance. Description Under supervision, the QC Associate will focus on QC activities supporting the manufacturing of cell therapy products. This includes release and stability testing of cell therapy products, maintaining the QC laboratory and instruments, authoring and revising standard operating procedures (SOPs) & certificates of analysis, and managing off-site testing of QC samples. Will perform environmental monitoring of the production suites as needed. Works on research data reporting assignments that are of moderate diversity in scope. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Performs other duties as assigned. Minimum Qualifications Six (6) years of related experience, education/training, OR a Bachelor's degree in related area (scientific discipline) plus two years of related experience/training. Working knowledge of research function. Knowledge of test methods used to test cell therapy products or similar characterization assays. Skills to communicate complex information in a clear and concise manner both verbally and in writing. Willingness to adhere to established UCSD guidelines for safety and environmental issues. Working skills in analysis and consultation. Strong analytical and critical thinking skills, with the ability to quickly analyze problems. Experience using basic laboratory equipment; knowledge of safe laboratory procedures. Working skills in statistical analysis, systems programming, database design and data security measures. Strong organizational skills with ability to prioritize tasks and to work under the pressure of multiple demands. Preferred Qualifications Familiarity with the Miltenyi CliniMACs or similar flow cytometry devices, QPCR intruments, and absorbance readers. Hands-on experience in a pharmaceutical, biotech, drug manufacturing, or academic environment is required, with knowledge of clean room practices being essential. Strong skills using FlowLogic, MACSQuantify, FACS DIVA, or similar, as well as MS Word and Excel. Working knowledge of laboratory Good Manufacturing Practice (GMP), Food and Drug Administration (FDA), United States Pharmacopeial Convention (USP), and International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) Regulations. Environmental monitoring experience a plus. Special Conditions Employment is subject to a criminal background check. Willingness to work in Biosafety Level II environment where biological (including infectious agents and blood borne pathogens) hazards are present. Willingness to work with embryonic stem cells, work with viruses that are infectious to humans, including adeno-associated viruses, Sendai viruses, and lentiviral vectors which are derived from human immunodeficiency virus (HIV). Must be able to work various hours and locations based on business needs. Pay Transparency Act Annual Full Pay Range: Unclassified - No data available (will be prorated if the appointment percentage is less than 100%) Hourly Equivalent: Unclassified - No data available Factors in determining the appropriate compensation for a role include experience, skills, knowledge, abilities, education, licensure and certifications, and other business and organizational needs. The Hiring Pay Scale referenced in the job posting is the budgeted salary or hourly range that the University reasonably expects to pay for this position. The Annual Full Pay Range may be broader than what the University anticipates to pay for this position, based on internal equity, budget, and collective bargaining agreements (when applicable). #J-18808-Ljbffr