Senior Product Development Engineer

by Trudell Medical International

Location: London, ON
Date Posted: Jun 16, 2024
Trudell Medical International

Job Description


Senior Product Development Engineer
 

Job Description

In this role, you will deliver on complex and/or multiple innovative medical device designs that provide exceptional value to our patients. Demonstrate expert proficiency with the tools and techniques of medical device design while mentoring less experienced engineers. Lead and/or advise cross functional teams to deliver new product development projects on plan, within target costs, and that meet or exceed our expectations for quality and innovation.

 

RESPONSIBILITIES INCLUDE:

DESIGN DEVELOPMENT & TESTING

  • Deliver more complex medical device designs, systems, and/or multiple designs simultaneously
  • Own and/or influence design control development for multiple products
  • Actively mentor less experienced engineers to improve their capability and optimize the delivery of medical device designs

 

DEVELOPMENT PROCESS

  • Lead and/or advise on multiple different invention disclosures including for new technologies or systems
  • Lead and/or advise on development of multiple project plans and/or where planning expertise is required to address deep uncertainty or new areas of development
  • Lead continuous improvement teams and deliver on continuous improvement initiatives that improve aspects of the new product development process
  • Initiate lessons learned processes at points during the product development process in order to capture opportunities for improvement

COLLABORATION
  • Plan and execute complex device projects and/or multiple projects simultaneously
  • Fulfill the role of Core Team Leader and ensure project teams are able to deliver on the agreed upon plan
  • Provide guidance to less experienced product development staff on all aspects of project planning and project leadership

REGULATORY & COMPLIANCE
  • Deliver development of complicated products and/or systems to achieve regulatory clearance and policy compliance
  • Identify opportunities for improvement to regulatory related activities to optimize product development and improve effectiveness

QUALIFICATIONS
  • Degree in Engineering (Mechanical, Mechatronic, Biomedical) or a related field of study
  • 10-15 years of product development and design experience
  • Professional Engineer (P.Eng) and in good standing with Professional Engineers Ontario (PEO)
  • Medical device industry experience, or a similarly regulated field, is an asset
  • Experience using CAD (Parts, Assemblies, Drawings, PDM, etc.)
  • Analysis skills (Risk, Tolerances, Statistical, Root Cause, etc.)
  • Modelling and Simulation (FEA, CFD, Mathematical, etc.)
  • Design Verification and Validation (Test Design, Functional, Usability, Compliance, etc.)
  • Design for Manufacture including molding, automated assembly, packaging, etc.
  • Prototyping with 3D Printing, Electronics, Traditional, etc.
  • Programming experience with Python, Matlab, Arduino, etc.
  • Knowledge with electronics (prototype PCB or breadboard, component selection, test, etc.)
  • Leadership and Mentoring skills
  • Project management experience
  • Expert level proficiency with the tools and techniques of medical device design

 

At an applicant’s request, TMI will make accommodation to its recruitment process to meet the needs of applicants with disabilities.


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