Quality Control Associate
$34.29 - $61.02 per hourUniversity of California San Diego
Payroll Title: RSCH DATA ANL 2 RP Department: Sanford Stem Cell Institute Hiring Pay Scale $34.29 - $61.02 / Hour Worksite: Campus Appointment Type: Career Appointment Percent: 100% Union: RP Contract Total Openings: 1 Work Schedule: Days, 8-Hour Shifts, Monday-Friday #139933 Quality Control Associate Extended Deadline: Mon 6/29/2026 Apply Now UC San Diego values and welcomes people from all backgrounds. If you are interested in being part of our team, possess the needed licensure and certifications, andfeel that you have most of the qualifications and/or transferable skills for a job opening, we strongly encourage you to apply. 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 In 2022, businessman and philanthropist T. Denny Sanford committed $150 million to the creation of the Sanford Stem Cell Institute at UC San Diego. This gift combines current infrastructure with new Centers intended to leverage the advantages of space-based science, including expansion and, in some ways, quite literally launch stem cell research and regenerative medicine at UC San Diego into new spaces, endeavors, and training of future stem cell scientists. Sanford Stem Cell Institute provides essential physical and human resources needed to leverage stem cell research currently being conducted at UC San Diego. Due to the complexity of regenerative medicine projects and substantial institutional investment, daily Sanford Stem Cell Institute personnel work with all 9 Vice Chancellor areas: Academic Affairs; Research Affairs; Equality, Diversity, and Inclusion; Student Affairs; Marine Sciences; Health Sciences; Health System; Chief Financial Officer; Advancement; Resource Management and Planning. As part of UC San Diego, Sanford Stem Cell Institute motivates University-wide change, sustainability, and partnership, focusing on creating the structure under which various innovative regenerative medicine units and initiatives are developed. The new UC San Diego Sanford Stem Cell Institute builds upon a $100 million gift in 2013 from T. Denny Sanford that established UC San Diego as a leader in developing and delivering the therapeutic promise of human stem cells - special cells with the ability to develop into many different cell types and which, when modified and repurposed, have the potential to treat, remedy or cure a vast array of conditions and diseases. The new UC San Diego Sanford Stem Cell Institute includes six (6) stem cell Centers led by Center Directors and Deputy Directors and one (1) Brain Tumor and Neuro-Restoration Program. 1.Sanford Integrated Space Stem Cell Orbital Research (ISSCOR) Center, for stem cell research that will be conducted in a laboratory bay located aboard the International Space Station currently in low-Earth orbit. 2.Sanford Stem Cell Fitness and Space Medicine Center, which conducts in-depth space fitness and orbital medicine that can benefit both astronauts and people living on Earth. 3.Sanford Stem Cell Innovation Center, which will support regenerative medicine company development, including contract research in low-Earth orbit. 4.Sanford Stem Cell Discovery Center, which conducts basic and translational stem cell research. 5.Sanford Advanced Therapy Center, which provides fundamental tools and services to move basic research findings to next stages, such as early phase trials. 6.Sanford Stem Cell Clinical Center, which conducts research to accelerate relevant drug and therapy development in regenerative medicine, including clinical trials. The Advanced Cell Therapy Laboratory (ACTL), housed under the Sanford Advanced Therapy Center (SATC), offers expert assistance and hands-on services to investigators who require cGLP/cGMP systems and facilities. We aid in the transition from research and development to compliant and clinically-relevant manufacture of cell therapy products for IND-enabling studies or Phase I/II trials.We provide assistance with cell banking, process development and scale-up, product characterization, document writing, product stability assessment, and packaging. 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 judgmentwithin 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). Apply Now If employed by the University of California, you will be required to comply with our Policy on Vaccination Programs, which may be amended or revised from time to time. Federal, state, or local public health directives may impose additional requirements. If applicable, life-support certifications (BLS, NRP, ACLS, etc.) must include hands-on practice and in-person skills assessment; online-only certification is not acceptable. UC San Diego Health Sciences is comprised of our School of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, The Herbert Wertheim School of Public Health and Human Longevity Science, and our Student Health and Well-Being Department. We have long been at the forefront of translational - or "bench-to-bedside" - research, transforming patient care through discovery and innovation leading to new drugs and technologies. Translational research is carried out every day in the hundreds of clinical trials of promising new therapies offered through UC San Diego Health, and in the drive of our researchers and clinician-scientists who are committed to having a significant impact on patient care. We invite you to join our team! Applications/Resumes are accepted for current job openings only. For full consideration on any job, applications must be received prior to the initial closing date. If a job has an extended deadline, applications/resumes will be considered during the extension period; however, a job may be filled before the extended date is reached. To foster the best possible working and learning environment, UC San Diego strives to cultivate a rich and diverse environment, inclusive and supportive of all students, faculty, staff and visitors. For more information, please visit UC San Diego Principles of Community . The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. For the University of California's Anti-Discrimination Policy, please visit: UC San Diego is a smoke and tobacco free environment. Please visit smokefree.ucsd.edu for more information. UC San Diego Health maintains a marijuana and drug free environment. Employees may be subject to drug screening. Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer. a. "Misconduct" means any violation of the policies governing employee conduct at the applicant's previous place of employment, including, but not limited to, violations of policies prohibiting sexual harassment, sexual assault, or other forms of harassment, or discrimination, as defined by the employer. For reference, below are UC's policies addressing some forms of misconduct: UC Sexual Violence and Sexual Harassment Policy UC Anti-Discrimination Policy Abusive Conduct in the Workplace
- ...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...SuggestedHourly pay
- Careers for the Changemakers At UC San Diego, we prefer the road less traveled. And it has led us to remarkable new ways of seeing and making a difference in the world. Being part of something greater, of serving a larger mission of innovation and care — that's the ...SuggestedWorldwide
- ...school and industry). Education - BS/BA/MS in a related scientific discipline or some science related college coursework. The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures,...Suggested
$19 - $26.5 per hour
Job Title Quality Control Associate I, Flow Cytometry (PM Shift) Location San Diego About Us Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm...SuggestedHourly payFull timeWork experience placementLocal areaShift work$23.55 - $31.5 per hour
Job Summary At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The QC Associate II for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following...SuggestedFull timeTemporary workPart timeWork experience placement$34.29 - $61.02 per hour
Quality Control Associate (#139933) Apply Deadline: Fri 6/12/2026. Job Details Title: RSCH DATA ANL 2 RP Department: Sanford Stem Cell Institute Pay Scale: $34.29 - $61.02 / Hour Worksite: Campus Appointment Type: Career Appointment Percent: 100% Union: RP Contract...Hourly payContract workMonday to FridayDay shift- USLA BioLegend, Inc. is seeking a Quality Control Associate I for Flow Cytometry on the PM Shift in San Diego. The role involves testing high-quality reagents while following SOPs and ISO requirements. Candidates should be motivated science enthusiasts ready to work in...Shift work
$75k - $95k
The Quality Control Associate III, Sample Management is responsible for the receipt, tracking, storage, distribution, and disposal of samples in a controlled laboratory or regulated environment. This role ensures sample integrity, accurate documentation, and compliance...$19 - $26.5 per hour
BioLegend, Inc. is hiring a Quality Control Associate in San Diego, California. The role involves testing high-quality products such as antibodies and proteins while ensuring compliance with SOPs and ISO requirements. The ideal candidate should have lab experience and skills...$23 - $35 per hour
Quality Associate - San Diego Location: San Diego, CA Pay Rate: $23.00 - $35.00 per hour (based on experience) Shift: 2:30 PM - 11:00 PM (... ...manufacturing environment 3+ years of experience in quality control, performing visual and mechanical inspections 3+ years of experience...Hourly payContract workFor contractorsLocal areaShift workAfternoon shift- ...QUALITY SYSTEMS & DOCUMENTATION SPECIALIST Looking to join a cutting edge medical device team paving the way in a very unique product line? The Quality Systems & Document Control Specialist is the central steward of our Quality Management System and a key partner across...Local areaImmediate start
$24 - $45.5 per hour
...Job Title: Quality Systems Specialist Job Description This role supports Quality Assurance operations in a GMP-regulated pharmaceutical... ...regulatory and internal quality standards. Perform document control activities, including managing logbooks, standard operating procedures...Contract workTemporary work- Position Quality System Specialist I Location San Diego, CA Duration 12 Months Total... ...coordination and management of the document control and change management process and... ...Qualifications High School Diploma or GED required, Associate's or Bachelor's Degree strongly...Local areaShift workDay shift
- Quality Control Specialist (Temp) Location: San Diego, CA Duration: 12 Months Contract Total Hours/week: 40.00 Shift: 1St Shift We are... ...all required techniques, equipment operation, and software associated with testing, data analysis, and reporting. Complete all...Contract workTemporary workShift workDay shift
- MillenniumSoft Inc is seeking a Quality System Specialist I in San Diego, CA. This role... ...with regulations, and managing document control processes. The ideal candidate will have... ...or GED, with a strong preference for an Associate's or Bachelor's Degree, and a minimum of...
- Performance Label International Inc in San Diego is seeking a Rewinder/Quality Control Assistant to join their dynamic team. This role is essential for ensuring high-quality products in an innovative environment. Candidates should have a strong attention to detail, basic...
$19 - $26.5 per hour
BioLegend is seeking an Associate for their Quality Control group in San Diego, California. The candidate will be responsible for testing high quality reagents, including antibodies and proteins, utilizing techniques such as flow cytometry, immunohistochemistry, and ELISA...Hourly pay$65.2k - $101.95k
Job Overview Noblis MSD is seeking a Quality Assurance Analyst to support the Naval Information... ...Engineering Facility (NIEF). The Associate will be responsible for inspections and... ...including quality assurance and quality control of all incoming, in-process, and final delivery...Full timeInterim roleLocal area$90k - $110k
...interest. We’re looking for a strategic and analytically driven Quality Assurance professional to join the Customer Operations team and... ...focused on proactively identifying quality signals, designing control strategies and QA programs, and influencing stakeholders to...Work at officeRemote workFlexible hours$85k - $89k
Quality Assurance Specialist II - San Diego By Catalent, Inc., a leading global contract development and manufacturing organization (CDMO... ...and update documents related to material management quality control, batch records, compliance, and validation systems. Participate...Contract work$33 per hour
Adecco is hiring immediately for a Quality Assurance Associate with a local client in San Diego, CA ! Apply now if you meet the qualifications listed... ...for just-in-time labeling processes Manage document control activities, including issuance, scanning, filing, and archiving...Hourly payTemporary workLocal areaImmediate startShift work$100k - $118k
...supporting off-hours GMP manufacturing. As a Quality Assurance Specialist at Capricor, you... ...quality records, logbooks, forms, and associated documentation as authorized. Identify,... ...Support investigations, CAPAs, change controls, and quality risk assessments as required...Shift workNight shift- ...of science and delivering life-changing treatments to patients and families who need them most. Position Summary The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor’s...Work at office
- ...pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most. The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in...
- Cooley LLP is seeking an IP US Filing Specialist (Quality Control) to join their IP Services team in San Diego. This role involves quality control functions for US patent filings and full support to patent attorneys, agents, and clients. The ideal candidate will have 3+...Work at office
- We’re looking for someone organized, detail-oriented, and proactive to join our Quality Control team. This is an administrative position based at our Corporate Office , supporting licensing, training, and compliance across the company. You’ll play a key part in making sure...Work at office
- Lloyd Pest Control is seeking a detail-oriented administrative professional for their Quality Control team in San Diego, California. This position involves processing licenses, maintaining records, communicating training schedules, and assisting in compliance. We're looking...
$32 - $38 per hour
Quality Control Analyst II or III - Microbiology About this position OrganaBio was founded in 2018 with the mission to become the hub for tissue sourcing, clinical sample processing and contract manufacturing services to support cell and gene therapy developers around the...Hourly payContract workMonday to FridayFlexible hours- ...) Reviews production batch records, logbooks and other associated documents Performs Quality verification of just-in-time labeling activities Performs... ...SOPs Participates in Quality programs, procedures and controls to ensure that products conform to established...Contract work
$60k - $90k
...Job Title and Information Risk, Quality, and Performance Analyst (Internal Job Profile Code: TCS015, P3, Band 6) – Maximus TCS (Technology... ...with audit readiness, process documentation, and quality controls to ensure artifacts meet agency and federal oversight expectations...Contract work
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