- Legend Biotech USA, Inc. (Raritan, NJ)
- …floor quality oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. This ... Provide Quality oversight of all aspects of the cell therapy clinical manufacturing process.Support manufacturing activities for cGMP compliance through spot… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …technical activities within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. This role will ... activities including data or document review, risk assessments, CAPAs, and continuous improvement activities. They will be a subject matter expert for the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …position will be responsible for providing operational support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will partner ... support of GMP investigations, change controls, document control, process improvement , process validation and data management.Partners with Operational Excellence to… more
- Formation Bio (New York, NY)
- …review and approval of batch records, release testing, and other quality-related documentation . Foster a culture of continuous improvement and development within ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …quality systems and cGMP requirements.Review and approve SOPs, and other documentation .Drive continuous improvement .Have advanced computer skills to increase ... management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Insmed Incorporated (NJ)
- …compliant state throughout their lifecycle a plus .Familiarity with validation of documentation , audit readiness, and continuous improvement of CSV processes. ... compliance with GxP regulations and industry standardsFamiliarity with validation of documentation , audit readiness, and continuous improvement of CSV processes… more
- Christus Health (Tyler, TX)
- …hospital through in-service training and educational resources. Program Development and Improvement : Contribute to the development and improvement of lactation ... ensuring they align with current evidence-based guidelines. Participate in quality improvement initiatives and audits to enhance patient outcomes and satisfaction.… more
- Christus Health (Henderson, TX)
- Description Summary: Performs clinical testing in assigned section/s such as general laboratory, Blood Bank and Microbiology sections, with all duties necessary for ... accurate and timely results including quality control, performance improvement , proficiency testing, and preventative maintenance of equipment. Recognizes abnormal… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the development of manufacturing processes including appropriate documentation .Drive continuous improvement of manufacturing operations leveraging ... operations team responsible for production of autologous CAR-T products for clinical and commercial operation in a controlled current Good Manufacturing Practice… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …change control process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will ... quality systems and cGMP requirements.Review change controls, SOPs, and other documentation .Require minimal direction to complete tasks, knows how to get resources… more
