Quality Assurance Document Control Specialist I [Contract to Hire]

Iovance Biotherapeutics(3 months ago)

Philadelphia, PAOnsiteFull TimeJunior$61,328 - $82,238 (estimated)Quality Assurance

About this role

The Quality Assurance Specialist I, Document Control at Iovance's iCTC in Philadelphia is a full-time on-site role supporting the facility's Quality Document Control program. The position ensures compliance with quality objectives and regulatory standards in a manufacturing lab and office environment. The role supports cross-functional teams, provides eDMS user assistance, and participates in audits and record archival activities.

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Required Skills

Document Control
Lot Issuance
Batch Records
Label Generation
eDMS
Archival
Audit Support
MS Office
Problem Solving
Communication

+5 more

Qualifications

Bachelor's Degree In Life Sciences
Advanced Degree

About Iovance Biotherapeutics

iovance.com

Iovance 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.