Iovance Biotherapeutics, Inc. · 6 hours ago
Quality Control Analyst I, Analytical [Contract to Hire]
Philadelphia, PA
Contract
Onsite
Entry Level
2+ years expIovance Biotherapeutics is a company focused on cell therapy products, seeking a Quality Control Analyst I to support quality control testing operations. The role involves performing GMP Quality Control laboratory testing, data analysis, and providing training to new personnel while ensuring compliance with applicable regulations.
BiotechnologyClinical TrialsHealth CareHealth DiagnosticsMedical
Responsibilities
Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations
Perform data analysis and final result reporting to support product lot release with adherence to turnaround times
Act as a subject matter expert (SME) on one or more assays and train new laboratory personnel
Support thorough GMP investigations for out-of-specification test results and other quality events
Support technical problem-solving for issues pertaining to GMP Quality Control
Support product stability programs, including execution of stability testing and final reporting of stability data
Initiate and support revisions of documentation, such as SOP, protocols and reports
Initiate and support quality records such as deviations, laboratory investigations, CAPAs, and change controls
Perform peer review of laboratory data and logbooks
Update trending data sheet, as required
Operate at a consistent and high level of efficiency, while producing high-quality and accurate results
Support Health Authority inspections
Provide input to functional laboratory team meetings
Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics
Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations
Perform miscellaneous duties as assigned
Qualification
Required
Minimum of a bachelor's degree in biology, Biochemistry, Microbiology, Chemistry, or related scientific field or equivalent combination of education and experience
Minimum two (2) years of GMP experience in the pharmaceutical industry within a Quality Control role
Solid understanding and functional knowledge with hands-on experience with at least one of the following: Multicolor Flow Cytometry, Cell-based ELISA, cell culture with cell enumeration (NC-200)
Experience in technical writing (e.g., test methods, SOPs, protocols, etc.)
Detail-oriented with strong technical skills
High level of ownership and accountability
Demonstrate a sense of urgency; ability to recognize time sensitivity
Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
Preferred
Experience with cell therapy products is a plus and/or relevant technical skills (NC 200, ELISA, and/or Flow)
Company
Iovance Biotherapeutics, Inc.
Iovance Biotherapeutics (NASDAQ: IOVA) aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapies for patients with cancer.
501-1000 employees
H1B Sponsorship
Iovance Biotherapeutics, Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (12)
2024 (11)
2023 (7)
2022 (7)
2021 (2)
2020 (2)
Funding
Current Stage
Public CompanyTotal Funding
$1.58B2024-02-20Post Ipo Equity· $211M
2023-07-10Post Ipo Equity· $150M
2020-05-27Post Ipo Equity· $603.7M
Leadership Team
Jean-Marc Bellemin
Chief Financial Officer
Cheryl Aranda
Executive Assistant to Chief Medical Officer
Recent News
2025-12-29
2025-12-07
2025-11-11
Company data provided by crunchbase