$Not specified
Overview Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. Responsibilities The Manufacturing Engineering Technician II will be responsible for aiding in the development, evaluation, and optimization of manufacturing processes and methods, utilizing knowledge of product design, materials, fabrication processes, tooling, equipment, and quality control standards. As a Manufacturing Engineer Technician II, your responsibilities include: • Assist in the development of highly capable manufacturing processes for existing products in manufacturing • Ensure robust transition from product development through full rate production ensuring process stabilization. • Develop, and qualify new tooling and equipment. • Verification and validation of processes, machines, and equipment to meet requirements of Company procedures. IQ/OQ/PQ protocols. • Troubleshoot product/process related issues, perform root cause analysis to develop and implement corrective and preventative action plans. • Help execute the transfer, storage, and disposal of hazardous waste in strict compliance with CAL-OSHA, EPA, and Federal Hazardous Waste Regulations. • Assist in developing and overseeing detailed fabrication schedules for manufacturing runs, optimizing workflow efficiency while balancing resource availability and operational timelines. • Help manage end-to-end inventory control, including purchase order requests, while maintaining safety stock levels and contingency supplies for all fabrication module components, including specialized tools and chemical excipients. • Perform in-process sampling, microscopic visual inspection, and particle analytical testing to ensure adherence to rigorous manufacturing and safety standards. • Maintain compliance and execute the processing and packaging (vialing) of both internal and external microsphere batches, ensuring compliance with GMP and Cordis quality requirements.
This job posting was last updated on 10/22/2025