Associate Quality Control Specialist, Document Control [Contract to Hire]

Iovance Biotherapeutics(22 days ago)

Philadelphia, PAOnsiteFull TimeJunior$61,248 - $82,170 (estimated)Quality Control

About this role

The Associate Quality Control Specialist, Document Control role is based at Iovance’s Cell Therapy Center (iCTC) in Philadelphia, PA and requires full-time onsite work on a Wednesday–Saturday schedule. The position supports the site’s quality document control program to help ensure alignment with quality objectives and applicable regulatory expectations in a manufacturing and office environment.

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Required Skills

Document Control
GMP Documentation
EDMS
Archiving
Audit Support
Regulatory Compliance
Change Management
Microsoft Office
Metrics Tracking
Process Improvement

+3 more

Qualifications

Bachelor’s Degree in Life Sciences

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.