University of Chicago
Microbiome Quality Control Technician
University of Chicago, Chicago, Illinois, United States, 60601
Laboratory Research Assistant
The Duchossois Family Institute (DFI) at the University of Chicago is using cutting-edge technologies and developing facilities to accelerate research and introduce novel interventions that optimize microbiome-mediated host defenses, with the goal of enhancing health. By developing new knowledge about the interactions between the human body and the microbiome, the DFI is breaking new ground that will lead to therapies that increase resistance to a wide range of diseases. The job performs routine laboratory data collection and analysis to support clinical research, and assists in specialty research involving animals, MRI technologies, histology, among others. Responsibilities Perform in-process QC tasks (CFU viability, USP 61/62, media production) for drug substances and drug products. Operate and maintain laboratory equipment such as anaerobic chambers, Biological Safety Cabinets, spectrophotometers, and pH meters. Document QC tasks clearly and accurately on controlled forms and electronic systems (LIMS). Participate in environmental monitoring of the cGMP facility. Assist in investigations related to deviations and out-of-specification (OOS) results. Maintain laboratory supply inventory and preventive maintenance / calibration schedule. Perform routine maintenance of lab equipment including setup, cleaning, and appropriate care. Maintain the highest standards of laboratory workplace safety and product quality. Meet all training requirements for applicable Standard Operating Procedures (SOPs). Follow verbal and written instructions and procedures for processes and equipment. Identify and report non-conforming events in a timely manner. Comply with regulations set forth in SOPs. Perform peer review of cGMP manufacturing activities. Prepares quality and safety control measures for the laboratory, such as checks of equipment, temperature control, and documentation of quality improvement projects. Under a limited degree of supervision, provides support to clinical research studies. Has general awareness of safety, quality control, and quality assurance procedures. Maintains quality and safety control measures for the laboratory. Conducts new tests and researches on new technologies for implementation in the laboratory. Solves routine or standard problems relating to the collection and management of patient results and data. Performs other related work as needed. Minimum Qualifications Education:
Minimum requirements include a college or university degree in related field. Work Experience:
Minimum requirements include knowledge and skills developed through
Certifications:
--- Preferred Qualifications Education:
B.S. degree in Chemical engineering or Biology is highly preferred. Experience:
Hands-on experience operating laboratory equipment is highly desirable. This includes operation of anaerobic chambers and working inside Biosafety Cabinets. Preferred Competencies Strong analytical and problem-solving skills. Ability to work independently and in a collaborative team environment. Strong ability to collaborate with cross functional teams. Ability to work under cGMP guidelines for extended periods of time. Cleanliness, organization, good laboratory skills, excellent record keeping, and Good Documentation Practices (GDP). Working Conditions Office Setting Environment. Laboratory/cleanroom environment. Application Documents Resume (required) Cover Letter (preferred) When applying, the documents
MUST
be uploaded via the
My Experience
page, in the section titled
Application Documents
of the application.
The Duchossois Family Institute (DFI) at the University of Chicago is using cutting-edge technologies and developing facilities to accelerate research and introduce novel interventions that optimize microbiome-mediated host defenses, with the goal of enhancing health. By developing new knowledge about the interactions between the human body and the microbiome, the DFI is breaking new ground that will lead to therapies that increase resistance to a wide range of diseases. The job performs routine laboratory data collection and analysis to support clinical research, and assists in specialty research involving animals, MRI technologies, histology, among others. Responsibilities Perform in-process QC tasks (CFU viability, USP 61/62, media production) for drug substances and drug products. Operate and maintain laboratory equipment such as anaerobic chambers, Biological Safety Cabinets, spectrophotometers, and pH meters. Document QC tasks clearly and accurately on controlled forms and electronic systems (LIMS). Participate in environmental monitoring of the cGMP facility. Assist in investigations related to deviations and out-of-specification (OOS) results. Maintain laboratory supply inventory and preventive maintenance / calibration schedule. Perform routine maintenance of lab equipment including setup, cleaning, and appropriate care. Maintain the highest standards of laboratory workplace safety and product quality. Meet all training requirements for applicable Standard Operating Procedures (SOPs). Follow verbal and written instructions and procedures for processes and equipment. Identify and report non-conforming events in a timely manner. Comply with regulations set forth in SOPs. Perform peer review of cGMP manufacturing activities. Prepares quality and safety control measures for the laboratory, such as checks of equipment, temperature control, and documentation of quality improvement projects. Under a limited degree of supervision, provides support to clinical research studies. Has general awareness of safety, quality control, and quality assurance procedures. Maintains quality and safety control measures for the laboratory. Conducts new tests and researches on new technologies for implementation in the laboratory. Solves routine or standard problems relating to the collection and management of patient results and data. Performs other related work as needed. Minimum Qualifications Education:
Minimum requirements include a college or university degree in related field. Work Experience:
Minimum requirements include knowledge and skills developed through
Certifications:
--- Preferred Qualifications Education:
B.S. degree in Chemical engineering or Biology is highly preferred. Experience:
Hands-on experience operating laboratory equipment is highly desirable. This includes operation of anaerobic chambers and working inside Biosafety Cabinets. Preferred Competencies Strong analytical and problem-solving skills. Ability to work independently and in a collaborative team environment. Strong ability to collaborate with cross functional teams. Ability to work under cGMP guidelines for extended periods of time. Cleanliness, organization, good laboratory skills, excellent record keeping, and Good Documentation Practices (GDP). Working Conditions Office Setting Environment. Laboratory/cleanroom environment. Application Documents Resume (required) Cover Letter (preferred) When applying, the documents
MUST
be uploaded via the
My Experience
page, in the section titled
Application Documents
of the application.