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Quality Control Associate Two Jobs in California

Lonza

Senior Quality Control Associate

Vacaville, CA · On-site

$85K - $142K/yr

Senior Quality Control (QC) Associate will act as a team member of the Vacaville Quality Control Product Analytical & Bioassay Testing (PABT) department for testing/release of in-process, drug ...

Lonza

Senior Quality Control Associate

Vacaville, CA · On-site

$85K - $142K/yr

Senior Quality Control (QC) Associate will act as a team member of the Vacaville Quality Control Product Analytical & Bioassay Testing (PABT) department for testing/release of in-process, drug ...

Collabera

QC Associate I

San Diego, CA

Qualifications Education: BS/MS in Biology/Molecular Biology, biochemistry, chemistry or related discipline 2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based ...

Abzena Inc.

QC Associate I/II - Contract

San Diego, CA · On-site

$40 - $60/hr

The Quality Control (QC) Associate I / II is responsible for performing analytical testing and laboratory activities that support stability, qualification/validation, and supporting release testing ...

Grifols

Sr. Quality Associate I/II, QC

Clayton, CA

Schedule: First Shift Sr. Quality Associate I/II, QC: Position Summary: This role is responsible for the implementation, maintenance, and continuous improvement of the Laboratory Information ...

Grifols

Sr. Quality Associate I/II, QC

Clayton, CA

Experience managing, projects, teams, etc. is recommended Sr. Quality Associate II, QC - BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 6 yrs of ...

TekWissen LLC

Quality Control Scientist

Vacaville, CA · On-site

$20 - $25/hr

Job Title: QC Associate I / Quality Control Scientist Location: Vacaville, CA - 95688 Duration: 6 Months Job Type: Temporary Assignment Work Type: Onsite Summary With limited supervision, the QC ...

Alcon3Pl

Quality Control - Anaheim

Anaheim, CA · On-site

We are seeking an experience quality control asociate to add to our team in our Anaheim warehouse. This is a TEMP TO HIRE POSITION. Position Sumarry: Quality control (production operator) will be ...

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Quality Control Associate Two information

What is the difference between Quality Control Associate Two vs Quality Control Associate One?

AspectQuality Control Associate TwoQuality Control Associate One
Required CredentialsHigh school diploma or equivalent; some roles may require certifications in GMP or ISO standardsHigh school diploma or equivalent; basic understanding of quality standards
Work EnvironmentManufacturing or laboratory settings, often in regulated industriesSimilar environments, typically in labs or production areas
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing companiesCommonly used in similar industries, often as entry-level roles
Common Search & Comparison IntentYes, often compared to associate level roles to understand responsibilities and requirementsNo, usually the starting point for quality roles

Quality Control Associate Two typically requires more experience or certifications than Quality Control Associate One. It involves more responsibilities in quality inspections and compliance, making it suitable for those with some industry experience. Both roles are common in manufacturing and laboratory environments within regulated industries.

What cities in California are hiring for Quality Control Associate Two jobs? Cities in California with the most Quality Control Associate Two job openings:
Quality Control Associate Two jobs near you
cGMP Quality Control Associate

cGMP Quality Control Associate

University of Southern California

Los Angeles, CA • On-site

$37.72 - $38.50/hr

Full-time

Posted 5 days ago

University Of Southern California rating

8.3

Company rating: 8.3 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

96th of 539 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 comprises the faculty, students and staff that make the university what it is.
USC's Keck School of Medicine, current Good Manufacturing Practices (cGMP) facility is seeking a qualified cGMP Quality Control Associate to join the USC/CHLA cGMP facility. The successful candidate will play a vital role in conducting analytical testing, supporting product testing and documentation, and maintaining operations to ensure the quality and regulatory compliance of cell and gene therapy products. In addition, the cGMP Quality Control Associate will be responsible for the calibration and maintenance of laboratory equipment, drafting and reviewing Standard Operating Procedures (SOPs), and ensuring that the Quality Control (QC) laboratory remains inspection-ready at all times.
Job Accountabilities
  • Performs cell culture, media preparation, cryopreservation, cell expansion, and viral vector production under strict cGMP guidelines. Executes aseptic processing, (e.g., cell seeding, passaging, harvesting, and transduction using viral vectors). Works closely with manufacturing, PD, QA, and QC teams to align processes, troubleshoot issues, and enhance efficiency.
  • Assists in process optimization, scale-up, and validation to improve yield, efficiency, and reproducibility. Supports technology transfer from development to full-scale manufacturing. Performs data collection and analysis to refine production parameters and enhance process consistency. Participates in troubleshooting activities to identify process challenges and implement corrective actions.
  • Conducts routine cleaning, calibration, troubleshooting, and maintenance of equipment and analytical instruments to ensure compliance with cGMP standards. Manages inventory of reagents, raw materials, and supplies, ensuring availability for seamless production and testing operations.
  • Performs analytical testing for product release, stability, and in-process monitoring and support in assay qualification. Supports GMP documentation control, Corrective and Preventive Actions (CAPA) and change control processes to maintain quality standards. Assists in internal and external audits, batch record review, and deviation investigations to uphold regulatory and quality standards.
  • Assists in training operators and new team members on manufacturing procedures, QC testing, and process development protocols. Maintains compliance with all safety protocols, regulatory requirements, and workplace standards.
  • Encourages a workplace culture where all employees are valued, value others and have the opportunity to contribute through their ideas, words and actions, in accordance with the USC Code of Ethics.

Successful Candidates Must Demonstrate:
Degree in a directly related specialized scientific 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. Strong communication and writing skills with demonstrated ability to work as an individual contributor and in a dynamic team environment.
Salary Range:
The hourly rate range for this position is $37.72 - $38.50. 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.
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.
Minimum Education: Bachelor's degree In Biotechnology Or Biological Science
Minimum Experience: 3 years in cell therapy development
Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality control testing. Strong attention to detail and ability to follow standard operating procedures (SOPs) and Quality Assurance principles meticulously. Excellent communication and teamwork skills to collaborate effectively with cross-functional teams. Ability to troubleshoot and resolve technical issues in a timely manner. Knowledge of regulatory requirements and guidelines (e.g., FDA, EMA) related to cGMP.
Preferred Education: Master's degree
Preferred Experience: 4 years in cell therapy development
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$138100.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

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