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Sr R&D Engineer

Karwell Technologies

Maple Grove, MN

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JOB DETAILS
SKILLS
Bill of Materials (BOM), Biomedical Engineering, CAD/CAM (Computer-Aided Design/Computer-Aided Manufacturing), Catheterization, Coaching, Corrective Action, Document Management, Documentation, Feasibility Analysis, Geometric Dimensioning and Tolerancing, ISO (International Organization for Standardization), Materials Analysis, Mechanical Engineering, Medical Equipment, People Management, Problem Solving Skills, Product Design, Product Development, Product Engineering, Project Estimates, Regulations, Regulatory Submissions, Research & Development (R&D), Risk Analysis, Risk Management, SolidWorks, Team Player, Technical/Engineering Design, Tolerance Analysis, Windchill PLM Software
LOCATION
Maple Grove, MN
POSTED
30+ days ago
Job Description:
  • Independently conducts development work as part of a major research and/or development project.
  • Receives minimal technical direction/review on broad scope or complex projects.
  • Viewed as an expert in one or more in-house technologies.
  • Focused on next generation access and delivery catheter. 510k submission by next year .
  • Operating in a 510k submission lens .
Responsibilities:
  • Work with a small team of new product design engineers focused on the design of a new large bore delivery catheter.
  • Works independently to develop key deliverables as part of a 510k regulatory submission. Deliverables include, but not limited to: CAD design, detailed print packages, specification generation and rationale, specification mapping to essential design outputs, DFMEAs, tolerance analysis, device material assessment(s), and bill of materials.
  • Provides guidance to product and technology teams.
  • Assesses the feasibility and soundness of alternative engineering processes, products, or equipment.
  • Coordinates, manages, and documents project goals and progress and recommends appropriate revisions.
  • Develop and coach others on engineering documentation.
  • Demonstrates PDP/TPD system knowledge through coaching and delivery of high quality, high impact deliverables.
Qualifications:
  • Minimum of a bachelor's degree in mechanical or biomedical engineering (or other related technical discipline).
  • Experience working with medical devices (catheter or delivery systems is highly preferred).
  • 4+ years of experience in design assurance, new product development or related medical device / regulated industry experience.
  • Experienced in design controls, print packages, tolerance analysis, GD&T.
  • Windchill and SolidWorks experience (ability to create 2D drawings).
  • ISO 13485, ISO 14971 and Quality System Regulations understanding with a focus on Design Controls and Risk Analysis.
  • Experienced problem solver, capable of facilitating the problem-solving process.
  • Adaptable and effective collaborator in a team environment or in self-directed work.
  • Experience with design changes, complaint reduction, and corrective action.
Preferred Qualifications:
  • Experience working with catheter or delivery systems.
  • Quality Integration experience.
  • 510k regulatory experience.

About the Company

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Karwell Technologies