Quality Assurance Specialist I, Raw Material Release. Sunday to Wednesday [Contract to Hire]
Iovance Biotherapeutics(2 months ago)
About this role
The Quality Assurance Specialist I, Raw Material Release is an entry-level QA role supporting material handling and release within a regulated biopharma (cell and gene therapy) environment. The position is based onsite across office and manufacturing areas and works closely with cross-functional teams. It contributes to maintaining regulatory compliance and supports the Quality department’s processes and controls.
Required Skills
- cGMP
- Documentation Review
- Batch Records
- Deviations
- Document Revision
- Material Disposition
- Labeling
- Lot Closure
- QMS
- Microsoft Word
+7 more
Qualifications
- Bachelor's Degree in Science, Engineering or Related Discipline
- Advanced Degree
About Iovance Biotherapeutics
iovance.comIovance Biotherapeutics is a clinical-stage biopharmaceutical company developing tumor-infiltrating lymphocyte (TIL) therapies that harness a patient’s own immune cells to recognize and kill diverse cancer cells. Its lead product, AMTAGVI (lifileucel), has received U.S. FDA accelerated approval for defined indications, and the company is advancing multiple clinical trials across solid tumors. Iovance builds and operates cell therapy manufacturing and Iovance Cell Therapy Centers to support production and commercialization, and partners with academic and industry collaborators to advance next‑generation T‑cell platforms. The company also provides patient resources, an expanded-access policy, and information about its pipeline and research.
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