Viral Vector cGMP Manufacturing Specialist

University of Southern California

Los Angeles (CA)

On-site

USD 52,000 - 54,000

Full time

14 days+
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Job summary

The University of Southern California (USC) seeks a cGMP Vector Manufacturing Associate to join the USC/CHLA cGMP Facility in downtown L.A. The position involves production and purification of viral vectors, with a strong emphasis on scale-up support and documentation.

You will calibrate and maintain equipment and support QC testing to ensure regulatory compliance. You will work with manufacturing, QA/QC, and PD teams to optimize processes, troubleshoot issues, and uphold cGMP standards in a

Qualifications

  • Bachelor's degree in Biotechnology or Biological Science required.
  • Experience with cGMP manufacturing and quality control testing preferred.
  • Strong attention to detail and ability to follow SOPs.

Responsibilities

  • Performs cell culture, media preparation, cryopreservation, and viral vector production under cGMP.
  • Assists in process optimization, scale-up, and validation to improve yield and reproducibility.
  • Maintains equipment and analytical instruments, conducts routine calibration and maintenance.
  • Performs analytical testing for product release and supports CAPA and change control processes.
  • Trains operators and team members on procedures and helps ensure safety and regulatory compliance.

Skills

Lab equipment handling
SOP compliance
Data analysis
Vision for quality

Education

Bachelor's degree in Biotechnology/Biology
Master's degree in Biotechnology (preferred)

Job description

The University of Southern California (USC) seeks a cGMP Vector Manufacturing Associate to join the USC/CHLA cGMP Facility in downtown L.A. The position involves production and purification of viral vectors, with a strong emphasis on scale-up support and documentation.

You will calibrate and maintain equipment and support QC testing to ensure regulatory compliance. You will work with manufacturing, QA/QC, and PD teams to optimize processes, troubleshoot issues, and uphold cGMP standards in a

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