Posted in Other about 2 hours ago.
Location: Philadelphia, Pennsylvania
University Overview
The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's Best Large Employers in 2023.
Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play.
The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
The principal responsibilities encompass clinical-scale processing of cells, involving the isolation, genetic modification, expansion, formulation, and cryopreservation of specific human hematopoietic cell fractions. Additionally, the role involves the isolation, expansion, and cryopreservation of tumor cell populations. The incumbent will play a pivotal role in developing and implementing cell-based assays aimed at enhancing clinical cell products.
This position additionally requires providing technical support for in vitro and in vivo experiments, encompassing molecular biology, cell culture, and flow cytometry, for the benefit of post-doctoral fellows and graduate students within the laboratory. Beyond these duties, the individual will contribute to the development and validation of standard operating procedures (SOPs) critical for modifying and upscaling cell products in preparation for clinical manufacturing. This encompasses the execution of assays, data analysis, presentation of findings, and overall laboratory management, including the oversight of materials and equipment. Additionally, the role involves training others in various techniques and procedures and engaging with vendors.
Proficiency in handling and processing primary clinical samples, expertise in genetic engineering through viral or non-viral delivery methods, multi-color flow cytometry, general laboratory operations, and familiarity with animal experimentation are prerequisites for this position. The successful candidate must possess extensive organizational skills, troubleshooting capabilities, effective communication skills, teamwork ethos, a commitment to accurate documentation, and a strong sense of personal responsibility.
This Human Genome Editing Research Specialist C/D position requires a dynamic individual with a strong background in genome editing, laboratory management, and collaborative research efforts in the field of cell and gene therapy. The ability to meet the specified qualifications is crucial for the success of this position in advancing the goals of the Center for Cellular Immunotherapy.
In addition, the Research Specialist D position requires an individual with advanced expertise, leadership capabilities, and a strategic vision to drive the laboratory's success. The increased level of responsibility involves leading complex projects, navigating regulatory landscapes, and contributing significantly to the advancement of the center's objectives.
Qualifications
Research Specialist C- Bachelor of Science and 3 to 5 years of experience or equivalent combination of education and experience is required.
Research Specialist D- Masters of Science in Biology and 3 to 5 years of experience or equivalent combination of education and experience is required. PhD preferred.
Additional Qualifications:
relevant experience in molecular biology, cell culture, flow cytometry, and human genome editing technique
Demonstrated experience in managing a laboratory and supporting multiple research projects
Proficiency in clinical-scale cell processing for isolation, genetic modification, expansion, formulation, and cryopreservation of human hematopoietic cell fractions
Expertise in isolation, expansion, and cryopreservation of tumor cell populations
Hands-on experience with in vitro and in vivo experiments, including molecular biology, cell culture, and flow cytometry
Proven track record of adherence to regulatory standards and guidelines, especially in the context of clinical cell product development
Experience in the development and implementation of assays supporting research activities
Ability to contribute to the development and validation of standard operating procedures (SOPs) for cell product modification and upscaling crucial for clinical manufacturing
Excellent written and verbal communication skills, with the ability to convey complex scientific information clearly to diverse audiences
Interpersonal skills to collaborate effectively with post-doctoral fellows, graduate students, and other team members
Strong organizational skills for the efficient management of laboratory space, equipment, software, protocols, and documentation
Experience in handling and processing primary clinical samples, genetic engineering using viral or non-viral delivery methods, and multi-color flow cytometry
Troubleshooting capabilities to address challenges related to laboratory operations, experimental procedures, and data analysis
Ability to work collaboratively in a team, including training others in techniques and procedures
Cross-functional collaboration with other labs for the translation of new processes and genetically-engineered cellular products to the clinic
Personal responsibility for accurate documentation, performance of assays, data analysis, and presentation of findings
This position is contingent upon grant funding.
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