Quality Assurance Document Control Specialist I [Contract to Hire]
Iovance Biotherapeutics
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.
Skills
Qualifications
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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About Iovance Biotherapeutics
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
Unlock Company Insights
View leadership team, funding history,
and employee contacts for Iovance Biotherapeutics.
Salary
$61k – $82k
per year
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