Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | Department Description: |
| 2 | Department Description: Dr. Brian Shy ‘s Research Laboratory is dedicated to advancing the therapeut | ||||
| > | ic application of genome and epigenome engineering tools for a wide range of indications, including | ||||
| > | cancer, rare diseases, infectious diseases, autoimmunity, and transplant-related conditions. The suc | ||||
| > | cessful outcomes from the research are transferred to the Cellular Therapy Development (CTD) Laborat | ||||
| > | ory, where cellular therapy manufacturing processes are developed before transfer over to the GMP fa | ||||
| > | cility. Job Summary: The Lab Operations Specialist will be an integral member within the Operational | ||||
| > | Team, functioning under the guidance and supervision of the Operations Manager. They will play an a | ||||
| > | ctive role in executing operational tasks within the UCSF Human Islet and Cellular Transplantation F | ||||
| > | acility (HICTF), a GMP facility dedicated to the manufacture of experimental cell therapies. In addi | ||||
| > | tion, they will support the daily maintenance of process development lab and support requests from D | ||||
| > | r. Shy’s research lab, while ensuring compliance with UCSF policies, regulations, and safety standar | ||||
| > | ds. The Lab Operations Specialist will serve as a point of contact for the labs and support key admi | ||||
| > | nistrative functions, including coordinating laboratory schedules to ensure smooth and efficient ope | ||||
| > | rations. They will also assist with maintaining and scheduling equipment maintenance and repairs, an | ||||
| > | d help facilitate clear communication and collaboration between research groups, core facilities, ve | ||||
| > | ndors, and lab teams. The Lab Operations Specialist will play a vital role by supporting the work of | ||||
| > | cellular therapy process development and manufacturing teams. Key duties include assisting with the | ||||
| > | establishment and upkeep of Standard Operating Procedures (SOPs) for equipment, techniques, and saf | ||||
| > | ety protocols; processing order requests, overseeing the receipt, shipping, and handling of inventor | ||||
| > | y, which includes materials, chemicals, gases, and equipment. They will also assist with restocking | ||||
| > | supplies, maintaining a clean and organized laboratory environment; supporting the monitoring and re | ||||
| > | sponse to alarms and out-of-specification conditions related to equipment and laboratory environment | ||||
| > | al conditions. Additionally, they will assist with SOP and EH&S compliance, including investigations | ||||
| > | , audits, corrective actions, and process improvements. Support deviations, change controls, and com | ||||
| > | pliance documentation.. | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | Dr. Brian Shy ‘s Research Laboratory is dedicated to advancing the therapeutic application of genom |
| > | e and epigenome engineering tools for a wide range of indications, including cancer, rare diseases, | ||||
| > | infectious diseases, autoimmunity, and transplant-related conditions. The successful outcomes from t | ||||
| > | he research are transferred to the Cellular Therapy Development (CTD) Laboratory, where cellular the | ||||
| > | rapy manufacturing processes are developed before transfer over to the GMP facility. | ||||
| 5 | Required Qualifications: - Associate degree in Science, Technology, Engineering, Nursing or Math-rel | 4 | |||
| > | ated field and/or at least 2 years of experience research lab or drug manufacturing lab operations o | ||||
| > | r an equivalent combination of education and experience - Knowledge in basic laboratory procedures a | ||||
| > | nd skills (documentation, reagent handling, equipment troubleshooting) - Good interpersonal and comm | ||||
| > | unication skills - Able to multi-task and prioritize activities effectively - Able to work independe | ||||
| > | ntly and as part of a team Preferred Qualifications: - Experience in research lab or drug manufactur | ||||
| > | ing lab operations - Knowledge of aseptic techniques | ||||
| 5 | Job Summary: | ||||
| 6 | |||||
| 7 | The Lab Operations Specialist will be an integral member within the Operational Team, functioning u | ||||
| > | nder the guidance and supervision of the Operations Manager. They will play an active role in execut | ||||
| > | ing operational tasks within the UCSF Human Islet and Cellular Transplantation Facility (HICTF), a G | ||||
| > | MP facility dedicated to the manufacture of experimental cell therapies. In addition, they will supp | ||||
| > | ort the daily maintenance of process development lab and support requests from Dr. Shy’s research la | ||||
| > | b, while ensuring compliance with UCSF policies, regulations, and safety standards. | ||||
| 8 | |||||
| 9 | The Lab Operations Specialist will serve as a point of contact for the labs and support key adminis | ||||
| > | trative functions, including coordinating laboratory schedules to ensure smooth and efficient operat | ||||
| > | ions. They will also assist with maintaining and scheduling equipment maintenance and repairs, and h | ||||
| > | elp facilitate clear communication and collaboration between research groups, core facilities, vendo | ||||
| > | rs, and lab teams. | ||||
| 10 | |||||
| 11 | The Lab Operations Specialist will play a vital role by supporting the work of cellular therapy pro | ||||
| > | cess development and manufacturing teams. Key duties include assisting with the establishment and up | ||||
| > | keep of Standard Operating Procedures (SOPs) for equipment, techniques, and safety protocols; proces | ||||
| > | sing order requests, overseeing the receipt, shipping, and handling of inventory, which includes mat | ||||
| > | erials, chemicals, gases, and equipment. They will also assist with restocking supplies, maintaining | ||||
| > | a clean and organized laboratory environment; supporting the monitoring and response to alarms and | ||||
| > | out-of-specification conditions related to equipment and laboratory environmental conditions. Additi | ||||
| > | onally, they will assist with SOP and EH&S compliance, including investigations, audits, corrective | ||||
| > | actions, and process improvements. Support deviations, change controls, and compliance documentation | ||||
| > | .. | ||||