The Manufacturing Downstream Lead (Associate III-IV) is responsible for prioritizing daily schedule requirements and executing manufacturing operations within a fast-paced cGMP cleanroom environment. Serving as the main operational point of contact inside the cleanroom, this role leads core downstream processing activities-including chromatography, tangential flow filtration (TFF), filtration techniques, and product filling. The position is also instrument
The Manufacturing Downstream Lead (Associate III-IV) is responsible for prioritizing daily schedule requirements and executing manufacturing operations within a fast-paced cGMP cleanroom environment. Serving as the main operational point of contact inside the cleanroom, this role leads core downstream processing activities-including chromatography, tangential flow filtration (TFF), filtration techniques, and product filling. The position is also instrument
The Quality Assurance Specialist II provides comprehensive quality oversight for clinical and commercial cell and gene therapy manufacturing operations. This role integrates batch disposition, material management, QA floor support, and document control to ensure strict adherence to Good Manufacturing Practices (cGMP) and applicable regulatory standards. The position serves as a technical resource for continuous quality improvement, deviation/CAPA oversight
The Quality Assurance Specialist II provides comprehensive quality oversight for clinical and commercial cell and gene therapy manufacturing operations. This role integrates batch disposition, material management, QA floor support, and document control to ensure strict adherence to Good Manufacturing Practices (cGMP) and applicable regulatory standards. The position serves as a technical resource for continuous quality improvement, deviation/CAPA oversight
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