Instrumentation & Equipment Specialist II

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 The Instrumentation and Equipment Specialist II is responsible for the maintenance, calibration and repair of equipment, utilities and systems supporting cGMP Manufacturing, Laboratories and Warehouse. Perform planned and corrective maintenance and calibration according to written instructions, diagnose issues in the field in real-time, propose corrective solutions, and complete and review related Facilities GMP documents.

Ensure the safety and compliance of all applicable systems. Shift: Wednesday to Saturday from 2200 to 0900 Essential Functions and

Responsibilities

Perform preventative, routine and corrective maintenance of CTU’s, process utility systems, and manufacturing/laboratory instruments. An understanding of calibration / metrology and the ability to calibrate, adjust, and maintain measuring and indicating instruments to conform to set standards is highly desirable. An understanding of PLC’s, HVAC, mechanical and electrical systems, and be able to troubleshoot and repair is highly desirable.

Perform routine inspections of the facility, equipment and systems. Monitor, investigate and respond to alarms generated from the BMS/QEMS. Knowledge in the use of a wide range of standards, including temperature, relative humidity, differential pressure, CO2, flow, conductivity, resistivity, speed, time, pressure, and weight is highly desirable.

Support Metrology to investigate OOT events using root cause analysis, metrics, technical knowledge and historical experience to identify and remediate. Ability to read and interpret engineering and architectural drawings, including floor plans, reflected ceiling plans, power plans, panel schedules, mechanical/plumbing piping diagrams, Piping & Instrumentation Diagrams (P&IDs) Write incident/deviation reports as necessary, perform root cause analyses and identify corrective actions as appropriate. Receive, filter and execute work order requests as necessary.

Ensure that any equipment repairs or maintenance activities are compliant with any applicable building codes. Work with external vendors for the service and/or repair of equipment. Provide “On-Call” support as needed.

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.

Required Education, Skills, and Knowledge Bachelor’s degree with 5 years of experience / Associates Degree with 10 years of experience is required. 5-10 years of related instrumentation and equipment experience in a GMP environment is required. Experience using Computerized Maintenance Management Software (Blue Mountain) is required.

Experience using Building Management Systems and Environmental Monitoring Systems (Siemens Desigo or Insight) is required. Must be able to wear appropriate clean room attire and all Personal Protective Equipment (PPE), i.e.

scrubs, gowning coverall, masks, gloves, etc. Excellent oral and written communication skills required. Must have valid driver’s license Preferred Education, Skills, and Knowledge Prior experience in cell therapy manufacturing or BioPharma/Life Sciences is highly desirable.

Experience working under ISO/IEC 17025 and/or ANSI/NCSL Z540.3 management systems is preferred. Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices