VIR Consultant
Newark, DE
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Job Description :
  • Experience Medical Device Industry
  • Experience transferring Product Manufacturing processes across sites, Relocation of equipment’s, new equipment’s, CAPA projects and Remediation projects etc.
  • Develops and executes Engineering studies and Process validation protocols and Summary reports (Installation Qualification, Operation Qualification, Process Qualification and Test Method Validation).
  • Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
  • Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
  • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
  • Adapts machine or equipment design to factory and production conditions.
  • May incorporate inspection and test requirements into the production plan.
  • Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
  • Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques.
  • Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.


Client : VIR
             

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