Job Description:

• Manages Current Good Manufacturing Practices (cGMP) facility and reagent preparation for the human pancreatic islet isolation.

• Assists during human islet isolation process.

• Prepares supplies in the cGMP facility and routinely checks supplies inventory.

• Performs quality control and release criteria tests of final islet product in compliance with internal Standard Operating Procedures (SOPs), lab policies and applicable regulations.

• Assists in equipment maintenance and troubleshooting.

• Assists in materials preparation, washing and sterilization.

• Assists in drafting and improvements of SOPs and other laboratory documentation.

• Organizes data into professional format, summarizes results, and presents data to PI and in lab meetings.

• Maintains clear, accurate, complete, and timely reports of experiments.

• Maintains records to ensure compliance with biosafety, radiation safety, animal protocols, compliance reports, instrument maintenance, and supply orders.

• Notifies PI of any potential violations of regulations.

  Coordinates compliance with institutional, state, and federal regulatory policies, procedures, directives, and mandates.

• Participates in research with laboratory animals.

• Supports data collection and analytical needs of research projects. Conducts literature reviews and helps write reports and manuscripts. Ensures project compliance with different policies, procedures, directives, and mandates.
• Takes responsibility for the following non-laboratory duties: transcribing and coding data; developing data collection instruments; presenting research; and recruiting and scheduling research subjects. Acquires higher-level skills and knowledge in the process.
• Performs other related work as needed.

Preferred Qualifications

Experience:

• Experience in laboratory rodent handling and aseptic techniques in rodent survival surgery.

Technical Skills or Knowledge:

• Basic laboratory skills: pipetting, buffer/reagents preparation, basic laboratory equipment use.
• Mammalian cell culture procedures.
• Regulatory policies and procedures and grant preparation.
• Microsoft Office and statistical software.
• Deep knowledge of aseptic techniques.
• cGMP/cGLP regulations related to laboratory work.
• Sterilization techniques.

Preferred Competencies

• Problem-solving and analytical skills.
• Work independently and as part of a team.
• Verbal and written communication skills.

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Application Documents

• Resume/CV (required)
• Cover Letter (required)

The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, status as an individual with a disability, protected veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.

Staff Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via the Applicant Inquiry Form.

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