Senior IT Quality Systems Analyst

Iovance Biotherapeutics•Philadelphia, PA

7h•Onsite

About The Position

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview This position reports to the Director IT, Tech Ops and Quality. The Senior Quality Systems Analyst is a hands-on technical and operational lead responsible for the strategy, administration, support, validation, and continuous improvement of Quality and Laboratory systems in a GxP-regulated pharmaceutical manufacturing environment. This role serves as a subject matter expert for enterprise Quality systems, especially the LIMS and QMS platforms, and partners closely with Quality, Manufacturing, QC Laboratories, MSAT, R&D, IT and other departments to deliver compliant, scalable, and efficient digital solutions that support product quality, data integrity, and regulatory commitments.

Requirements

Bachelor’s degree in Computer Science, Engineering, Life Sciences, or a related discipline.
8+ years of hands-on experience in biotech, pharmaceutical, or other regulated life sciences environments supporting Quality Systems, LIMS, QMS, or manufacturing information systems.
Experience working in a GxP-regulated environment with strong knowledge of computer system validation, SDLC, and change control processes.
Strong knowledge of pharmaceutical business processes, 21 CFR Part 11, Annex 11, ALCOA+ data integrity principles, and regulatory compliance expectations.
Hands-on experience with LIMS and QMS platforms, including configuration, administration, workflows, and support.
Experience with laboratory instrument integration, interfaces, and enterprise system connectivity using file-based integrations, APIs, web services, or middleware.
Strong interpersonal, presentation, analytical, and communication skills with the ability to work effectively across technical and business teams.
Demonstrated sense of urgency, strong problem-solving capability, and ability to work independently as well as collaboratively.

Nice To Haves

Experience with cell and gene therapy or pharmaceutical manufacturing environments preferred.
Direct experience with platforms such as LabVantage LIMS, MasterControl QMS, MES, Sample Management software and/or CMMS (Blue Mountain) is preferred.
Experience designing or supporting end-to-end digital lab and quality ecosystems, including integrations with ERP, ELN, CDS, or other enterprise systems.
Technical experience with SQL, scripting, database management, or advanced integration technologies is a plus.
Experience supporting multi-site or global operations and leading digital transformation initiatives is preferred.
Relevant certifications in GxP, CSV, quality systems, or related disciplines are desirable.

Responsibilities

Lead the selection, deployment, administration, support, and continuous improvement of computer-based systems supporting 24x7 Manufacturing Operations, Laboratory, and Quality Management processes.
Serve as the subject matter expert and system owner for Quality and Laboratory platforms, including LIMS and QMS solutions.
Perform operational support activities for critical GxP systems, including end-user support, monitoring, troubleshooting, issue resolution, break-fix activities, and performance optimization.
Lead system lifecycle management activities, including configuration, upgrades, patching, change management, deviations, and maintenance of inspection-ready documentation.
Architect, implement, and maintain system integrations and interfaces, including laboratory instrument connectivity and data exchange between lab equipment and enterprise applications.
Lead computer system validation activities in accordance with FDA, EMA, GAMP 5, and internal quality standards, including risk assessments, validation planning, and execution of IQ/OQ/PQ documentation.
Ensure compliance with 21 CFR Part 11, Annex 11, ALCOA+ data integrity principles, and other applicable regulatory requirements.
Drive continuous improvement and digital transformation initiatives that improve operational efficiency, audit readiness, system reliability, and cost effectiveness.
Support investigations, root cause analysis, CAPAs, and remediation activities related to system issues, data discrepancies, or process deviations.
Provide technical leadership, mentoring, and knowledge sharing across Quality Systems initiatives.
Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics and perform miscellaneous duties as assigned.