Assistant Scientist – Assistant Director, Vector Manufacturing and Process & Ana
University of Florida, Gainesville, FL, United States
Classification Title
Assistant Scientist – Assistant Director, Vector Manufacturing and Process & Analytical Development
Classification Minimum Requirements Ph.D. in a relevant scientific field
Job Description The Assistant Scientist serving as Assistant Director of Vector Manufacturing and Process & Analytical Development supports the strategic expansion of UF’s gene therapy manufacturing capabilities. This position provides advanced scientific expertise and operational leadership in vector production, process optimization, technology transfer, and analytical method development at the Powell Gene Therapy Center. The role ensures high-quality, scalable, and compliant production of viral vectors to support preclinical, IND-enabling, and early-phase clinical programs.
Essential Functions
Vector Manufacturing Leadership
Oversee and guide AAV vector manufacturing operations.
Ensure manufacturing activities meet scientific, quality, and safety standards.
Lead troubleshooting and implement CAPA strategies.
Process Development & Technology Transfer
Design and execute process development studies.
Implement new manufacturing technologies.
Coordinate technology transfer across groups.
Analytical Method Development
Lead development and qualification of analytical assays.
Support QC release and regulatory documentation.
Ensure analytical comparability and product quality.
Documentation, Regulatory & Quality Support
Prepare SOPs, batch records, and technical reports.
Support IND and CMC submissions.
Maintain regulatory-compliant documentation.
Team Leadership, Training & Collaboration
Mentor staff and trainees.
Coordinate cross-functional communication.
Represent PGTC in scientific and operational meetings.
Expected Salary Commensurate with education and experience
Required Qualifications
Ph.D. in a relevant scientific field
Experience with AAV or viral vector production and analytics.
Strong scientific leadership and problem-solving skills.
Preferred
Experience with IND-enabling studies and CMC documentation.
Hands-on experience with bioreactors, chromatography, and analytics.
Supervisory experience and familiarity with GLP/GMP systems.
Health Assessment Required: Yes
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Classification Minimum Requirements Ph.D. in a relevant scientific field
Job Description The Assistant Scientist serving as Assistant Director of Vector Manufacturing and Process & Analytical Development supports the strategic expansion of UF’s gene therapy manufacturing capabilities. This position provides advanced scientific expertise and operational leadership in vector production, process optimization, technology transfer, and analytical method development at the Powell Gene Therapy Center. The role ensures high-quality, scalable, and compliant production of viral vectors to support preclinical, IND-enabling, and early-phase clinical programs.
Essential Functions
Vector Manufacturing Leadership
Oversee and guide AAV vector manufacturing operations.
Ensure manufacturing activities meet scientific, quality, and safety standards.
Lead troubleshooting and implement CAPA strategies.
Process Development & Technology Transfer
Design and execute process development studies.
Implement new manufacturing technologies.
Coordinate technology transfer across groups.
Analytical Method Development
Lead development and qualification of analytical assays.
Support QC release and regulatory documentation.
Ensure analytical comparability and product quality.
Documentation, Regulatory & Quality Support
Prepare SOPs, batch records, and technical reports.
Support IND and CMC submissions.
Maintain regulatory-compliant documentation.
Team Leadership, Training & Collaboration
Mentor staff and trainees.
Coordinate cross-functional communication.
Represent PGTC in scientific and operational meetings.
Expected Salary Commensurate with education and experience
Required Qualifications
Ph.D. in a relevant scientific field
Experience with AAV or viral vector production and analytics.
Strong scientific leadership and problem-solving skills.
Preferred
Experience with IND-enabling studies and CMC documentation.
Hands-on experience with bioreactors, chromatography, and analytics.
Supervisory experience and familiarity with GLP/GMP systems.
Health Assessment Required: Yes
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