Jobs · Engineering · California

Manufacturing Engineer

Cytek Biosciences · Fremont, CA · 3 wk ago
EngineeringFull-time

Essential Duties And Responsibilities

  • Directs personnel in the troubleshooting of Optics, fluidics and equipment components used in Integration, subassembly, and final test process.
  • Takes lead in identifying problems and pursuing plans toward their resolution to improve quality, waste, and equipment efficiency in production process.
  • Able to handle projects of a moderate to large scope requiring extensive cross functional coordination.
  • Responsible for handling several assignments (project & process duties) simultaneously.
  • Be responsible for all associated documentation, including however not limited to, the following validations, Operations Procedures, Preventive Maintenance schedules, Engineering Change Notifications, spare parts listings, etc.
  • Provide adequate support of the introduction of new products into manufacturing while supporting the production of existing products.
  • Perform and document field failure investigations, identify root causes, reduce process scrap, and participate in corrective and preventive action efforts.
  • Lead continuous improvement projects to support cost reduction, on-time delivery, customer complaints and production capacity goals.
  • Perform documented training and coaching to reduce instrument down time and increase output.
  • Resolve and determine root cause of technical mechanical, optical, and electrical issues encountered in Production during Assembly and Test.
  • Collaborate cross-functionally with development, supply chain and production teams to deliver product and process solutions and improvements that achieve company objectives.
  • Reduce labor hours/unit, manufacturing lead time and failure at installation.
  • Keep an accurate inventory in the manufacturing production floor.

Requirements & Qualifications

  • Six Sigma certification (greenbelt or blackbelt) preferred.
  • BS Degree in Mechanical or Industrial Engineering with minimum 3 years' experiences supporting system integration/ testing or equivalent.
  • Understanding ISO13485 is desired.
  • Familiarity with Medical Device Manufacturing environment is desired.
  • Knowledge of PCBA, Lasers, optics and fluidic systems is a plus.
  • Must possess good written and verbal communication skills, and be able to adapt quickly to changes, prioritize and execute multiple tasks in the fast-paced environment.
  • Statistical Expertise: Proficiency in applying Design of Experiment statistical approaches during process optimization and scale-up.
  • Familiarity with statistical software for data analysis.
  • Experimental Design: Proven experience in designing and executing experiments, drawing meaningful conclusions, and providing recommendations based on experimental data.

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