Boston Scientific-posted about 7 hours ago
Full-time • Entry Level
5,001-10,000 employees

Assesses process capabilities and innovates and implements process improvements for discrete, well-defined processes. Writes clean and concise work instructions that can be understood by product builders. Contributes to technical reports, validations, and qualifications by capturing experimental results. Assists in completing proper documentation to meet quality systems requirements. (e.g., BOM's, Routers, FMEA's, etc.) Writes validation protocols and reports applicable to new processes. Gathers and provides technical data for technical reviews. Oversees development builds associated with the project using special work requests. Assists in developing qualified production lines. Provides Design for Manufacturability (DFM) input to the engineering print package. Contributes ideas to or generates Intellectual Property submissions. May train manufacturing personnel when required as part of a validation

  • Assesses process capabilities
  • Innovates and implements process improvements
  • Writes work instructions
  • Contributes to technical reports, validations, and qualifications
  • Completes documentation to meet quality systems requirements
  • Writes validation protocols and reports
  • Gathers and provides technical data for technical reviews
  • Oversees development builds
  • Assists in developing qualified production lines
  • Provides Design for Manufacturability (DFM) input
  • Contributes ideas to or generates Intellectual Property submissions
  • May train manufacturing personnel
  • BS in Engineering required
  • 0-2 years of related experience
  • Experience contributing to complex projects
  • Knowledge in statistical analysis
  • Design of Experiments (DOE) experience
  • Failure modes analysis
  • Fully Bilingual
  • Silicone Molding
  • CAD knowledge
  • Equipment integration
  • Vision systems development
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