Instrumentation Specialist II

OverviewThe 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 - Saturday, 10pm - 9am Essential Functions and ResponsibilitiesPerform preventative, routine and corrective maintenance of CTU's, process utility systems, and manufacturinglaboratory 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 BMSQEMS.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, mechanicalplumbing piping diagrams, Piping & Instrumentation Diagrams (P&IDs)Write incidentdeviation 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 andor repair of equipment.Provide "On-Call" support as needed.Must adhere to Iovance Biotherapeutics' core values, policies, procedures, and business ply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.Perform miscellaneous duties as assigned. Required Education, Skills, and KnowledgeBachelor'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 BioPharmaLife Sciences is highly desirable.Experience working under ISOIEC 17025 andor ANSINCSL 3 management systems is preferred.Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations is preferred.

Created: 2024-11-09