Senior IT Quality Systems Analyst

Benefits

Parental leave

Not verified

Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

Not verified checked Jun 13, 2026

Salary

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401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)

$116,543 U.S. median for this role

Projected growth (BLS Employment Projections)

+9.8% - Much faster than average

Matched to SOC 15-1252 - Software Engineering aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Engineering From the posting source checked Jun 20, 2026

Seniority

Senior From the posting source checked Jun 20, 2026

Schedule

Shift type

Not verified

Weekend work

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Company

Company stage

Public-company From the posting source checked Jun 20, 2026

Equity

Offered Verified - SEC 10-K source checked Jun 20, 2026

Application

Cover letter

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Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Senior IT Quality Systems Analyst Philadelphia, PA 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. Essential Functions and 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

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