cGMP Quality Control Associate

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.

USCs 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 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 candidates 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.

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 theBackground Screening Policy Appendix Dfor 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 or by email at. Inquiries will be treated as confidential to the extent permitted by law.

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