Overview. . Reporting to the Senior Director of Program Management, the Program Management Intern is responsible for supporting the Program Manage Team in finalizing integrated project plans (IPPs). IPPs are used by Program Management to directly track and drive early-stage and late-stage programs to successful completion. Essential Functions and Responsibilities. . This intern position will be responsible for transferring older IPPs into a new t...
Overview. The Director of Drug Safety Operations reports to the Head of Drug Safety Operations and will work collaboratively within the Drug Safety department, cross-functionally with other departments, and with partner companies to achieve department and company goals. . This position is responsible for supporting Iovance study teams and contributing to the pharmacovigilance activities of all Iovance products. This shall include ensuring the est...
Overview. . Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. The Quality Control Analyst will support quality control testing operations at Iovance’s integrated Cell Therapy Center (iCTC). The Quality Control testing programs include, but are not limited to, in-process, final drug product, and stability testing with a focus on cell therapy products. We are ...
Overview. The senior CMC Biostatistician will be a statistical resource for. developing and commercializing cell therapies in oncology. This will include direct support in the design and analysis of process and analytical CMC activities and manufacturing and quality control. . Essential Functions and Responsibilities. Provide statistical design and analysis supporting Process Development (including process development, process characterization, v...
Overview. Iovance is seeking an Associate Director, External Quality Control to provide strategic, technical, and operational leadership for external QC-related activities. The Associate Director will provide oversight of external testing vendors, build and maintain business continuity plans, support methods transfers to external vendors, and perform technical feasibility assessments, for the Company's cell therapy and biotherapeutic assets. . Es...
Overview. . Iovance is seeking a Specialist, Quality Systems who has experience in Quality Systems, QA, or Compliance in Pharmaceutical and/or Biotechnology companies. This individual will be responsible for maintaining Quality Systems at Iovance’s manufacturing facility to ensure GMP compliance in accordance with country regulations and guidelines, as well as the company’s policies and procedures. S/he will be an innovative, self-sufficient, sel...
Overview. Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Supervisor, Quality Control Logistics - Sample Management, who will be responsible for sample inventory management as well as internal and external sample distribution, including storage and shipping of QC samples under appropriate conditions. The position will be based at Iovanc...
Overview. Iovance is seeking a highly motivated individual for the position of GMP Quality Assurance Associate, Documentation at. Iovance’s IOVA. A facility located within American Red Cross in Philadelphia, PA. This position is responsible for the Quality Assurance documentation related activities in support of the manufacturing/testing operations and ensuring compliance to quality objectives and regulatory requirements. This individual will be ...
Overview. . The Quality Control Analyst will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. This position will work a weekend 2nd shift. (10 hr shifts Sun-Wed, 2PM-1230AM). to support manufacturing weekend activities. . S...
Overview. . The Senior Plant Engineer is responsible for the operation and optimization of the equipment, systems and utilities of a cGMP Cell Therapy Manufacturing Facility. Collaborate with Maintenance and Metrology groups to develop programs for equipment maintenance and calibrations. Coordinate with the Facilities, Engineering, Operations and Quality teams to ensure maximum uptime and efficiency of all systems and equipment. . Primary Respons...
Overview. . The Quality Control Analyst will support quality control testing operations at Iovance’s Cell Therapy Center (iCTC). The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, and sterility techniques. This position will work a weekend 2nd shift. (10 hr shifts Wed-Sat, 2PM-1230AM). to support manufacturing weekend activities. . S...
Overview. . The Metrology Specialist is responsible for calibrating and repairing equipment and systems supporting cGMP Manufacturing, Laboratories, and Warehouse. Perform calibrations using appropriate procedures and standards for various utilities, equipment, and instruments. Essential Functions and Responsibilities. . Calibrate, adjust, and maintain measuring and indicating instruments to meet set standards. Some calibrations will be performed...
