cGMP Vector Manufacturing Associate

University of Southern CaliforniaLos Angeles, CA
1d$38 - $39

About The Position

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 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.

Requirements

  • 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.
  • 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.
  • Bachelor's degree In Biotechnology and/or Biological Science
  • 3 years

Nice To Haves

  • Master's degree
  • 4 years
  • Biotechnology and/or Biological Science, Viral Vector Production

Responsibilities

  • 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.

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Number of Employees

5,001-10,000 employees

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