Bachelors degree in biology or a related field and seven years of experience or masters degree in biology or a related field with five years of experience. Doctoral degree in biology or related field with two years of experience.
Job Description:
Process Development Experimental Design & Optimization
Lead the design optimization and scale-up of automated closed-system processes for dendritic cell CAR T autologous T cells and stem cell-based products.
Evaluate and integrate novel technologies (e.g. automated selection and transduction systems closed culture platforms) to enhance robustness reproducibility and compliance with GMP standards.
Develop and optimize RNA synthesis workflows including IVT purification and capping strategies to support preclinical and clinical supply.
Collaborate with formulation scientists to establish scalable reproducible LNP formulation processes tailored for diverse therapeutic payloads.
Define and monitor critical process parameters (CPPs) and critical quality attributes (CQAs) to ensure consistent product quality and regulatory readiness.
Partner with the manufacturing team for operator training and investigations.
Author process development and qualification protocols and manufacturing batch record in accordance with phase-appropriate GMP standards. Facilitates effective dialogue across manufacturing quality and clinical teams ensuring process development priorities are understood and integrated into program timelines
Provides scientific and strategic leadership for the analytical function mentoring junior scientists and fostering a culture of rigor accountability and innovation
Collaborate with equipment vendors CDMOs and technology providers to evaluate platforms execute tech transfers and manage deliverables.
Research Compliance GMP Alignment & Documentation
Administer biological research activities in accordance with approved protocols bio-safety requirements and institutional policies.
Author and maintain process development documentation qualification protocols standard operating procedures (SOPs) and manufacturing batch records as applicable.
Support alignment with phase-appropriate GMP expectations and regulatory readiness for translational research activities.
Laboratory Operations & Personnel Supervision
Manage daily laboratory operations including the cultivation and study of live specimens equipment use and resource coordination.
Train and direct the work of research staff postdoctoral fellows graduate students and technical personnel.
Support operator training deviation investigations and continuous improvement initiatives in collaboration with manufacturing and research teams.
Collaborate with equipment vendors CDMOs and technology providers to evaluate platforms execute tech transfers and manage deliverables.
Collaborate with interdisciplinary teams to analyze scientific and operational challenges and recommend solutions.
Support technology transfer activities and manage deliverables with external collaborators.
Scientific Communication & Research Support
Maintain accurate laboratory records and analyze research data in accordance with institutional and funding requirements.
Prepare reports presentations and documentation to communicate research results to internal and external stakeholders.
Contribute to grant applications manuscripts and other research advancement activities as assigned.
Expected Salary:
$70600-$80200
Required Qualifications:
Bachelors degree in biology or a related field and seven years of experience or masters degree in biology or a related field with five years of experience. Doctoral degree in biology or related field with two years of experience.
Preferred:
Hands-on expertise with closed-system cell processing platforms (e.g. CliniMACS Prodigy DynaSelector equivalent) and associated unit operations.
Experience in RNA manufacturing (IVT purification) and LNP formulation techniques.
Demonstrated track record of leading process development from research to GMP readiness.
Strong understanding of GMP principles regulatory expectations (FDA/EMA/ICH) and quality systems.
Excellent leadership project management and communication skills with a proven ability to collaborate across disciplines.
Special Instructions to Applicants:
For consideration please complete an application and include a cover letter resume and the names and email addresses of three to five references.
The University of Florida is an Equal Employment Opportunity Employer.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
This requisition has been reposted. Previous applicants are still under consideration and need not apply.
Health Assessment Required:
Yes
Required Experience:
IC
Classification Title:Process Scientist/Biological Scientist IIIClassification Minimum Requirements:Bachelors degree in biology or a related field and seven years of experience or masters degree in biology or a related field with five years of experience. Doctoral degree in biology or related field w...
Classification Title:
Process Scientist/Biological Scientist III
Classification Minimum Requirements:
Bachelors degree in biology or a related field and seven years of experience or masters degree in biology or a related field with five years of experience. Doctoral degree in biology or related field with two years of experience.
Job Description:
Process Development Experimental Design & Optimization
Lead the design optimization and scale-up of automated closed-system processes for dendritic cell CAR T autologous T cells and stem cell-based products.
Evaluate and integrate novel technologies (e.g. automated selection and transduction systems closed culture platforms) to enhance robustness reproducibility and compliance with GMP standards.
Develop and optimize RNA synthesis workflows including IVT purification and capping strategies to support preclinical and clinical supply.
Collaborate with formulation scientists to establish scalable reproducible LNP formulation processes tailored for diverse therapeutic payloads.
Define and monitor critical process parameters (CPPs) and critical quality attributes (CQAs) to ensure consistent product quality and regulatory readiness.
Partner with the manufacturing team for operator training and investigations.
Author process development and qualification protocols and manufacturing batch record in accordance with phase-appropriate GMP standards. Facilitates effective dialogue across manufacturing quality and clinical teams ensuring process development priorities are understood and integrated into program timelines
Provides scientific and strategic leadership for the analytical function mentoring junior scientists and fostering a culture of rigor accountability and innovation
Collaborate with equipment vendors CDMOs and technology providers to evaluate platforms execute tech transfers and manage deliverables.
Research Compliance GMP Alignment & Documentation
Administer biological research activities in accordance with approved protocols bio-safety requirements and institutional policies.
Author and maintain process development documentation qualification protocols standard operating procedures (SOPs) and manufacturing batch records as applicable.
Support alignment with phase-appropriate GMP expectations and regulatory readiness for translational research activities.
Laboratory Operations & Personnel Supervision
Manage daily laboratory operations including the cultivation and study of live specimens equipment use and resource coordination.
Train and direct the work of research staff postdoctoral fellows graduate students and technical personnel.
Support operator training deviation investigations and continuous improvement initiatives in collaboration with manufacturing and research teams.
Collaborate with equipment vendors CDMOs and technology providers to evaluate platforms execute tech transfers and manage deliverables.
Collaborate with interdisciplinary teams to analyze scientific and operational challenges and recommend solutions.
Support technology transfer activities and manage deliverables with external collaborators.
Scientific Communication & Research Support
Maintain accurate laboratory records and analyze research data in accordance with institutional and funding requirements.
Prepare reports presentations and documentation to communicate research results to internal and external stakeholders.
Contribute to grant applications manuscripts and other research advancement activities as assigned.
Expected Salary:
$70600-$80200
Required Qualifications:
Bachelors degree in biology or a related field and seven years of experience or masters degree in biology or a related field with five years of experience. Doctoral degree in biology or related field with two years of experience.
Preferred:
Hands-on expertise with closed-system cell processing platforms (e.g. CliniMACS Prodigy DynaSelector equivalent) and associated unit operations.
Experience in RNA manufacturing (IVT purification) and LNP formulation techniques.
Demonstrated track record of leading process development from research to GMP readiness.
Strong understanding of GMP principles regulatory expectations (FDA/EMA/ICH) and quality systems.
Excellent leadership project management and communication skills with a proven ability to collaborate across disciplines.
Special Instructions to Applicants:
For consideration please complete an application and include a cover letter resume and the names and email addresses of three to five references.
The University of Florida is an Equal Employment Opportunity Employer.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
This requisition has been reposted. Previous applicants are still under consideration and need not apply.
Job Location:
Monthly Salary:
Posted on:
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