The QC Support technician, CAR-T Manufacturing is an executing function with responsibilities within QC area related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
Major Responsibilities:
You will support the daily QC analyses:
...
- You will control, disinfect and clean the materials/equipment needed for the QC analyses.
- You will help out with the internal transfer of the materials from the logistic center to the in process lab.
- You will help out with the handling of the waste from the lab.
- You will support the transport of the samples (QC release, QC retain, EM) at different temperatures (room temperature, cooled transport).
- You will support the EM analyses in grade C and grade D.
- You will utilize an electronic system (LIMS) for execution and accurate documentation of the disinfection and cleaning of the equipment or document your performed tasks in a correct way in logbooks and forms.
- You execute the activities in a strictly regulated environment.
- You perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
- Other duties will be assigned, as necessary
toon meer
The QC Support technician, CAR-T Manufacturing is an executing function with responsibilities within QC area related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
Major Responsibilities:
You will support the daily QC analyses:
- You will control, disinfect and clean the materials/equipment needed for the QC analyses.
- You will help out with the internal transfer of the materials from the logistic center to the in process lab.
- You will help out with the handling of the waste from the lab.
- You will support the transport of the samples (QC release, QC retain, EM) at different temperatures (room temperature, cooled transport).
- You will support the EM analyses in grade C and grade D.
- You will utilize an electronic system (LIMS) for execution and accurate documentation of the disinfection and cleaning of the equipment or document your performed tasks in a correct way in logbooks and forms.
- You execute the activities in a strictly regulated environment.
- You perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
...
- Other duties will be assigned, as necessary
toon meer