Overview Selution, in partnership with Cordis, specializes in the development of groundbreaking 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 As a Manufacturing Engineer Technician I (Second Shift), 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 and 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. Qualifications Qualifications • HS diploma or GED • 2+ years of related work experience in the medical device or pharmaceutical field, or an associate's degree and equivalent work experience. • Strong verbal and written communication skills with the ability to effectively communicate at multiple levels in the organization • Strong organization and follow-up skills, as well as attention to detail • Ability to make independent decisions • Knowledge of the validation verification process, Gage R&R, and a clear understanding of FDA's QSR and GMP • Basic proficiency in SolidWorks and computer-aided design a plus • Strong analytical, problem-solving, and project management skills • Fluent in English • Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA, and other federal, state, and local standards, including meeting qualitative and/or quantitative productivity standards • You must be able to lift and carry up to 25 lbs. Pay / Compensation The expected pre-tax pay rate for this position is $21.95–$27.50 per hour. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge, and location. US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.