cGMP Lab & Facilities Coordinator

University of Southern California; Glendale (CA); On-site; USD 55,000 - 62,000; Full time

Job summary

The University of Southern California (USC) seeks a dynamic Facility Coordinator for its cGMP facility within the Keck School of Medicine. You will oversee cGMP lab spaces, ensure compliant operations, and support the development of cell and gene therapies.

Responsibilities include operations, maintenance, qualification/validation, calibration, and coordination with contractors, vendors, and safety programs. A related degree and 3+ years of experience are required.

Qualifications

• Strong knowledge of laboratory procedures, techniques and testing in specialized scientific fields.
• Excellent written and verbal communication, able to work independently and in a team.

Responsibilities

• Supports cGMP lab and ancillary spaces operations, qualification, maintenance (shutdowns), risk assessments, and troubleshooting for building systems and equipment.
• Performs repairs, emergency and preventive maintenance, and oversees outside contractors.
• Supports equipment commissioning, qualification and validation activities including testing and documentation.
• Conducts routine laboratory procedures and tests with high quality results, e.g., media formulations and Elisa testing.
• Supervises staff in absence of Facilities Manager, assists in planning and workload prioritization.
• Coordinates environmental health and safety programs and coordinates security surveys.
• Prepares space and equipment analysis and contributes to long-range planning.
• Coordinates construction, renovation, and telecommunication projects and staff training as needed.

Skills

Lab procedures knowledge

Communication skills

Education

Degree in related specialized scientific field

Job description

The University of Southern California (USC) seeks a dynamic Facility Coordinator for its cGMP facility within the Keck School of Medicine. You will oversee cGMP lab spaces, ensure compliant operations, and support the development of cell and gene therapies.

Responsibilities include operations, maintenance, qualification/validation, calibration, and coordination with contractors, vendors, and safety programs. A related degree and 3+ years of experience are required.