Product Development Engineering Specialist

Trudell Medical International; London; On-site; CAD 90,000 - 130,000; Full time

Job summary

Trudell Medical International in London, Ontario, seeks a Product Development Engineering Specialist to design mechanical/electromechanical medical devices, act as DRE, and drive development projects on plan and cost targets. You’ll mentor engineers, deliver design documentation, and ensure regulatory compliance across the development lifecycle.

Ideal candidates have 5–10 years in product development, CAD/PDM proficiency, and hands-on modelling, testing, and prototyping with an emphasis on

Qualifications

• Degree in Engineering (Mechanical, Mechatronic, Biomedical) or related field.
• 5–10 years of product development and design experience.
• Medical device industry experience or similar regulated field is an asset.
• CAD proficiency with parts, assemblies, drawings and PDM.
• Experience with risk, tolerances, statistics and root cause analysis.
• Modelling and simulation with FEA/CFD or equivalent.
• Design verification/validation testing and DIN design controls experience.
• Design for manufacture including molding and automated assembly.
• Materials selection, costing, prototyping (3D printing, electronics).
• Programming (Python, Matlab, Arduino) and electronics prototyping.

Responsibilities

• Design mechanical or electromechanical solutions to support device design.
• Act as Design Responsible Engineer (DRE) and maintain design controls.
• Create and manage Product Design Specifications and design documentation.
• Develop invention disclosures and project plans for new product development.
• Lead continuous improvement and transfer product to manufacturing with feedback.
• Collaborate with senior engineers to align tasks with the project plan.
• Ensure compliance with standards, regulations, and policies for clearance.
• Uphold health and safety regulations in all development activities.

Skills

CAD

Analysis

Prototyping

Python

Matlab

Design for Manufacture

Project management

Mentoring

Education

Engineering degree

Tools

CAD

PDM

FEA

CFD

Matlab

Python

Arduino

Job description

At Trudell Medical International (TMI), we pride ourselves on our passion for finding innovative and creative solutions which has enabled us to develop medical devices that continue to make a difference in the lives of people around the world. Situated within a modern facility located in beautiful London, Ontario, TMI offers a comfortable work environment with a respectful and family-oriented culture.

As an employee of Trudell Medical International, not only will you contribute to the development of products at the cutting edge of medical device technology, but you will also have the opportunity to perform challenging work alongside a first-rate group of dedicated professionals.

PRODUCT DEVELOPMENT ENGINEERING SPECIALIST

Job Purpose

Deliver innovative medical device designs that provide exceptional value to our patients. Demonstrate proficiency with the tools and techniques of medical device design while developing mentoring skills to guide less experienced engineers. Influence 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

• With oversight from Senior, Principal Engineer or Product Development Project Lead, design mechanical or electromechanical solutions to support device design
• Act as Design Responsible Engineer (DRE) and maintain and create the Product Design Specification and all design controls
• Apply standardized problem-solving tools to identify a design problem and propose solutions before implementation

DEVELOPMENT PROCESS

• Develop full invention disclosures within the Intellectual Property development process as lead inventor
• Develop complete project plans that accurately reflect the scope and deliverables required for a given project
• Deliver continuous improvement initiatives that improve aspects of the new product development process as part of a continuous improvement team
• Transfer product to manufacturing and revise design/process based on feedback until the product has reached target production yields and throughput

COLLABORATION

• With support from Senior, Principal Engineer or Product Development Project Lead, plan design to achieve a developed product
• Coordinate with Product Development Project Lead to align design and development tasks to the overall project plan

REGULATORY & POLICY

• Deliver device development projects in full compliance with all applicable standards, regulations, and policies to achieve clearance.
• Adapt to and challenge regulations as appropriate to find the best path to clearance

HEALTH & SAFETY

• Ensure compliance with relevant health and safety legislation, including the Workplace Safety and Insurance Act, the Occupational Health and Safety Act, etc.

Qualifications

• Degree in Engineering (Mechanical, Mechatronic, Biomedical) or a related field of study
• 5-10 years of product development and design experience
• Medical device industry experience, or a similarly regulated field, is an asset
• CAD (Parts, Assemblies, Drawings, PDM, etc.)
• Analysis (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 (Molding, automated assembly, packaging, etc.)
• Materials selection (Polymers, additives, properties, safety, etc.)
• Costing (COGS)
• Prototyping (3D Printing, Electronics, Traditional, etc.)
• Programming (Python, Matlab, Arduino...etc.)
• Electronics (prototype PCB or breadboard, component selection, test, etc.)
• Experience with mentoring and leading teams
• Project management experience
• Proficient with 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.

Trudell Medical International is committed to providing fair and equitable compensation opportunities to all teammates. The range displayed on each job posting reflects the target for new hire salaries for the advertised position. Within the range, individual compensation is determined by job-related skills and knowledge, relevant professional, lived experience, and/or work location. Our compensation policies and practices are designed to allow our colleagues’ growth and salary progression as they develop in their role. As a candidate, you are encouraged to ask compensation-related questions and have an open dialogue with your recruiter, who can provide specific details for this role and share more information about our total rewards package.

As part of our recruitment process, we may use AI tools to screen applicants and assist in evaluating candidate qualifications. All final hiring decisions are made by our recruitment team.

We are an equal opportunity employer and it is important to our Company that all its employees, including those with disabilities, find our workplace to be welcoming and supportive. If you are a candidate with a disability who requires accommodations during the recruitment process, please let us know.