Iovance Biotherapeutics, Inc. Benefits Overview

Manages GMP and contracted manufacturing operations for protein-based products, specializing in downstream processing, formulation, fill-finish, and lyophilization. Oversees process development, technology transfer, scale-up, validation, COGS improvements, manufacturing readiness, quality investigations, regulatory CMC support, and data management. Collaborates globally with CMOs, Quality, Regulatory, Supply Chain, and technical teams while supporting audits, product lifecycle activities, and staff development.

Own the architecture and hands-on implementation of an enterprise Windows endpoint platform using Intune, Autopilot, Entra ID, PowerShell, and Microsoft 365. Responsibilities include device provisioning, configuration and compliance policies, application packaging, remediation, performance baselines, driver management, documentation, and support-team training. The role also builds SharePoint Online solutions, Power Automate workflows, and Microsoft Forms integrations for business processes, while partnering with security, quality, and business stakeholders in a regulated biotech environment.

Contract Statistical Programmer to develop, validate, and maintain SAS/R programs producing SDTM/ADaM datasets and TLFs per CDISC and regulatory standards. Support analyses for safety reports, submissions, and ad hoc requests; perform QC, documentation, automation, and collaborate with biostatistics and data management in a GxP-compliant environment.