cGMP Vector Manufacturing Associate

The USC/CHLA cGMP Facility is seeking a qualified cGMP Vector Manufacturing Associate to join the USC/CHLA cGMP Facility. The successful candidate will play a key role in the production and purification of viral vectors, including the execution and optimization of vector manufacturing processes, support of scale‑up activities, and preparation and documentation of all reagents in accordance with established protocols. In addition, the cGMP Vector Manufacturing Associate will be responsible for the calibration, troubleshooting, and maintenance of equipment and analytical instruments to ensure full compliance with current Good Manufacturing Practice (cGMP) standards. 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. Minimum Education: Bachelor’s degree In Biotechnology and/or Biological Science Minimum Experience: 3 years 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). 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 Preferred Field of Expertise: Biotechnology and/or Biological Science, Viral Vector Production 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. 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 View phone number on click.appcast.io, or by email at View email address on click.appcast.io. 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 #J-18808-Ljbffr Dormont Manufacturing Co