Senior Development Engineer

ICONMA, LLC

  • Warsaw, IN
  • Today
  • $1 Per Hour
  • Instant Apply
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Skills

  • ABET (Accreditation Board for Engineering and Technology)unmatched
  • Analysis Skillsunmatched
  • Biomedicineunmatched
  • Communication Skillsunmatched
  • Cross-Functionalunmatched
  • Design Failure Mode and Effects Analysis (DFMEA)unmatched
  • Design Verificationunmatched
  • Documentationunmatched
  • Functional Analysisunmatched
  • Geometric Dimensioning and Tolerancingunmatched
  • Health Planunmatched
  • Healthcareunmatched
  • Manufacturingunmatched
  • Materials Engineeringunmatched
  • Medical Equipmentunmatched
  • Medical Recordsunmatched
  • Microsoft Officeunmatched
  • Organizational Skillsunmatched
  • Process Developmentunmatched
  • Product Designunmatched
  • Regulationsunmatched
  • Riskunmatched
  • Team Playerunmatched
  • Technical Writingunmatched
  • Testingunmatched
  • Validation Testingunmatched
  • Writing Skillsunmatched

Description

Our client, a Medical Devices / Healthcare company, is looking for a Senior Development Engineer for their Remote location.
 
Responsibilities:

  • Responsible for the post market activities of existing Design History Files for Medical Devices under the direction of a project leader or manager. 
  • Author and Review existing Design History Files, identify scope, and mark gaps where necessary documents are missing
  • Utilize Vault Systems to manage Document workflow
  • Generate or analyze and update existing risk documentation (DFMEA or risk tables)
  • Coordinate, prepare, and conduct design reviews with cross-functional teams
  • Perform functional relationship analyses (FRA) and tolerance stack-ups
  • Generate comprehensive protocols to test/analyze the product for design verification and design validation (V&V)
  • Update prints and other design and manufacturing elements
 
Requirements:
  • Previous system experience with Vault is preferred.
  • Excellent communication, teamwork, and organizational skills are essential. 
  • Candidates must be self-starters and self-motivators.
  • Familiarity with Vault Systems
  • Familiarity with drafting standards and geometric dimensioning and tolerancing (GD&T)
  • Strong Background in DHF documentation authoring and executing for Medical Devices
  • Ability to effectively work within a team to expedite completion of critical project tasks with cross functional groups including Regulatory and Quality
  • Establishing a process method which meets performance and quality requirements
  • Ability to give clear and concise oral presentations
  • Technical writing
  • Microsoft Office Suite
  • B.S. degree from an ABET accredited school (or global equivalent) in Biomedical, Mechanical, or Materials engineering, or equivalent.
 
Why Should You Apply?

Numbers & Facts

LocationWarsaw, IN
Salary$1 Per Hour

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