Specialist I, Quality Assurance, Supplier Quality - Cleveland
1 week ago

Job summary
This role supports the release of incoming materials in support of cGMP Operations as part of Abeona Therapeutics Inc.'s manufacturing facility in Cleveland OH.Responsibilities
- Perform routine activities associated with manufacturing cell and gene therapy products.
- Accurately review and approve controlled documents including suppliers Certificates of Analysis or Certificates of Conformity.
- Inspect incoming materials for accuracy and defects.
Job description
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