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Weekend Biotech Quality Control Jobs in California

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 ...

Background in biotechnology, biopharmaceutical manufacturing, or QC laboratory environments. * Familiarity with GMP, GLP, HACCP, or food safety practices and their application in laboratory or ...

Our client is a leading biotechnology company that combines technological insight with world-class ... Job Title: QC Associate / Quality Control Analyst I Location: Vacaville, CA - 95688 Duration: 6 ...

Minimum of 3 years' experience in GMP pharma/biotech facility * Experience with Equipment ... weekends Base Hourly Range: * Scientist I: $30.01 - $41.27 * Scientist II: $34.70 - $47.77

Quality Control Scientist

Vista, CA · On-site

$30.01 - $41.27/hr

Minimum of 3 years' experience in GMP pharma/biotech facility * Experience with Equipment ... weekends Base Hourly Range: * Scientist I: $30.01 - $41.27 * Scientist II: $34.70 - $47.77

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Control Inspector inspects materials, parts, and products at different ...

Bachelor's or Master's Degree in Biology, Immunology or a related Science field * 4 to 6 years of biotech industry experience related to Quality Control * 2 years of experience supervising or leading ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

Bachelor's degree in chemistry or a related life sciences field * 5+ years' QC experience in biotech/pharma * 3+ years' experience in a biotech/pharma CDMO setting * 4+ years of project management ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

Showing results 21-40

Weekend Biotech Quality Control information

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Infographic showing various Weekend Biotech Quality Control job openings in California as of August 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 100% In-person job distribution.

cGMP Quality Control (QC) Specialist

Los Angeles, CA

University of Southern California
Colleges, Universities, and Professional Schools • 10K+ employees

$87K - $92K/yr

Full-time

Re-posted 26 days ago


University Of Southern California rating

8.2

Company rating: 8.2 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

154th of 633 rated colleges and universities


Job description

The University of Southern California (USC), founded in 1880, is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the "Trojan Family," which is comprised of the faculty, students and staff that make the university what it is.

USC's Keck School of Medicine, Department of Medicine is seeking a dynamic individual to work on the manufacturing of biologics and drugs for cell and gene therapy of internal/external users in the university's current Good Manufacturing Practices (cGMP) facility. The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and implementing quality control testing, assays, and procedures for materials and final cell therapy products manufacturing. The position will also be responsible for ensuring consistency with current Good Manufacturing Practice (cGMP) principles.

Job Accountabilities:

  • Supports cGMP manufacturing operations with responsibility for quality control. Performs cGMP batch release testing to ensure pharmaceuticals and biopharmaceuticals are of the highest possible quality before being applied to patients. Writes and reviews qualifications (e.g., installation, operation, performance), facility operation plans and reports, standard operating procedures, and batch records as required. Completes batch record documentation, all appropriate equipment log entries, and cGMP documentation.
  • Operates instrumentation needed for cell and gene therapy manufacturing (e.g., cell counters, bioreactors, centrifuges, biological safety cabinets). Assists in technology transfer of manufacturing processes from pre-clinical into cGMP environment.
  • Provides verification of facility operations and equipment, along with advanced problem-solving, troubleshooting, and consultation support, as needed. Supervises and directs junior staff to achieve project goals. Serves as a resource to cGMP facility management in identifying and assessing the appropriate complement of resources and support needed to successfully implement and execute projects.
  • Maintains confidentiality for patient identification, specimen labeling, and specimen verification during batch testing. Performs duties in a clean room environment, when needed and while fully gowned (e.g., mask, coverall, gloves), following cGMP guidelines and using aseptic techniques. Works with senior staff to ensure facilities' compliance with all applicable regulations.
  • Attends routine meetings with the management team for progress reports on projects, facility needs, and discussion of any other required items. Improves current methods and evaluates innovative techniques in quality control testing for cell therapy and biologics.
  • Promotes an environment that fosters inclusive relationships and creates unbiased opportunities for contributions through ideas, words, and actions that uphold principles of the USC Code of Ethics.
  • Performs other related duties as assigned or requested. The university reserves the right to add or change duties at any time.

Successful Candidates Must Demonstrate:

  • Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of all aspects of biotechnology and cell therapy. Demonstrated passion for solving complex scientific issues. Experience with Food and Drug Administration regulations and clinical trials. Extensive leadership experience.

Salary Range:

The annual base salary range for this position is $87,576.76 - $92,000. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

*This is a 3-year fixed-term position.

USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix Dfor specific employment screen implications for the position for which you are applying.

Minimum Education: Bachelor's degree

Minimum Experience: 3 years

Supervises: May lead one or more employees performing similar work

Minimum Field of Expertise: Bachelor's degree in a scientific discipline (e.g., pharmaceutical, biologics). Three years' experience in cellular or biological manufacturing with quality control responsibilities. Demonstrated knowledge base with Good Manufacturing Practices (e.g., cGMPs, GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work as an individual contributor and in a dynamic team environment. Excellent written and oral communication skills.

Preferred Education: Master's Degree

Preferred Experience: 5 Years

Preferred Field of Expertise: Biotechnology and life sciences

USC 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, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email at uschr@usc.edu. Inquiries will be treated as confidential to the extent permitted by law.

  • Notice of Non-discrimination
  • Employment Equity
  • Read USC's Clery Act Annual Security Report
  • USC is a smoke-free environment
  • Digital Accessibility

If you are a current USC employee, please apply to this USC job posting in Workday by copying and pasting this link into your browser:
https://wd5.myworkday.com/usc/d/inst/1$9925/9925$125114.htmld


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About University of Southern California

Sourced by ZipRecruiter

The University of Southern California (USC) is not a conventional company, but a private research university established in the heart of Los Angeles, CA, US. Founded in 1880, it's one of the oldest private research universities in California. USC operates in the education industry providing primary services of higher education, research, and community development. This prestigious institution offers a comprehensive array of undergraduate, graduate, and professional programs across various disciplines, including the humanities, social sciences, and STEM (Science, Technology, Engineering, and Mathematics). The University is guided by its commitment to foster creativity, innovation, leadership, and discovery through academic excellence.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Los Angeles , CA, US

Year founded

1880