GMP Project & Logistics Coordinator

Job Summary The GMP is dedicated to the production of clinical-grade stem cell therapies, gene therapy products, and pharmaceutical formulations for use in clinical trials and novel or routine patient treatments. Operating under strict regulatory standards, the facility ensures compliance with current Good Manufacturing Practices (cGMP) while supporting translational research, product development, and technology transfer. In addition to manufacturing, the facility contributes to scholarly innovation by advancing biomanufacturing methods and collaborating with investigators to bring promising therapies from bench to bedside. The Project Manager will assist with programmatic activities, The position will be responsible for fostering and managing internal and external partnership and apply evidenced-based project management expertise to organize multiple workstreams simultaneously. Apply By Date : 10/16/2026 by 11:59pm Minimum Qualifications - For full consideration, applicants are encouraged to upload license and/or certification if required of the position Project management certification from a reputable organization such as PMP, CSM or ACP to include a qualifying exam and / or quality assurance processes like Six Sigma or Lean or equivalent project management experience required. Bachelor's degree in related area and/or equivalent experience/training. At least two (2) years of experience working in a clinical lab, GMP facility, and/or regulated setting. At least two (2) years of experience managing client projects. At least two (2) years of experience implementing operational improvements projects. Working knowledge of project management principles, theories, and concepts. Demonstrated ability and/or skills creating and formatting spreadsheets and databases. Demonstrated ability to anticipate obstacles and plan for contingencies. Strong organizational skills. Strong time management skills. Ability to assess complex projects, project timelines, available resources, and budget information Preferred Qualifications Experience in cell and gene therapy manufacturing. Knowledge or ability to understand University fund accounting, generally accepted accounting principles, and government auditing standards. Experience with grant/core financial management, logistical supply chain management, and data sharing methodologies. Key Responsibilities 50% - Project Management 50% - Program Logistics Department Overview The Good Manufacturing Practice Facility (GMP) is a recognized as the largest academic GMP in Northern California. The GMP team reports to Stem Cell Program leadership; the Stem Cell Program is an internationally recognized basic, translational science and clinical research program committed to finding treatments and cures for debilitating human diseases and injuries utilizing the full range of human stem cells. The program includes affiliates from numerous departments across the Sacramento and Davis campuses. The purpose of the Good Manufacturing Practice (GMP) Facility is to manufacture clinical grade stem cell and other cellular therapy products, gene therapy products, pharmaceutical products and formulations for novel or routine patient treatments and clinical trials, and to perform scholarly research and development when appropriate. POSITION INFORMATION Salary or Pay Range: $3,440.00 - $6,328.00 Salary Frequency: Bi-Weekly Salary Grade: 123 UC Job Title: PROJECT MGT PROFL 3 RP UC Job Code: 005252 Number of Positions: 1 Appointment Type: Staff: Career Percentage of Time: 100% Shift (Work Schedule): Day Location: UCD Inst for Regenerative Cure (HSP041) Union Representation: RP - Research and Public Service Professionals Benefits Eligible: Yes This position is 100% on-site Benefits Outstanding benefits and perks are among the many rewards of working for the University of California. UC Davis offers a full range of benefits, resources and programs to help you bring your best self to work, as well as to help you and your family…

View the full posting and apply