Senior Product Development Engineering Specialist - Design Support & Sustaining
- London, ON, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Experience
- 10-15 years of product development and design experience =
- Posting language
- English
- Posted
Original 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.
We’re actively searching for our next team member for the position of:
SENIOR PRODUCT DEVELOPMENT ENGINEERING SPECIALIST – DESIGN SUPPORT & SUSTAINING
Job Purpose
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. Influence 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
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.
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.
We’re actively searching for our next team member for the position of:
SENIOR PRODUCT DEVELOPMENT ENGINEERING SPECIALIST – DESIGN SUPPORT & SUSTAINING
Job Purpose
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. Influence 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
- Design efficient and effective mechanical and electromechanical systems and sub-systems to support product design. Acting as design responsible engineer (DRE) or as an advisor to more junior Engineers
- Actively mentor less experienced engineers to improve their capability and optimize the delivery of medical device designs
- Develop and maintain internal and external networks that can be leveraged to advance product development capabilities
- 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 with the SEED team to transfer product ideas into Phase 1 of product development
- Collaborate with the Marketing and Sales department to investigate incremental business ideas to capture the voice of the customer and develop a business case for strategic review
- 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
- Comply with relevant health and safety legislation, including the Workplace Safety and Insurance Act, the Occupational Health and Safety Act, etc.
- Identify areas for improvement with regards to Health and Safety within product development
- Degree in Engineering (Mechanical, Mechatronic, Biomedical) or a related field of study
- 10-15 years of product development and design experience =
- Experience working in a regulated industry an asset, e.g. medical device, pharmaceutical or aerospace
- 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 (molding, automated assembly, packaging, etc.)
- Prototyping (3D Printing, Electronics, Traditional, etc.)
- Programming (Python, Matlab, Arduino, etc.)
- Knowledge with electronics (prototype PCB or breadboard, component selection, test, etc.)
- Leadership and Mentoring skills
- Project management experience
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.
More about this job
Responsibilities
Lead and advise on complex medical device design and development, including mechanical and electromechanical systems, testing, regulatory compliance, and product development planning. Mentor engineers, guide cross-functional teams, contribute to invention disclosures, and improve development processes through continuous improvement and lessons learned.
Requirements
Requires an engineering degree in mechanical, mechatronic, biomedical, or a related field, along with 10–15 years of product development and design experience. Candidates should bring expertise in CAD, analysis and simulation, design verification and validation, manufacturing, prototyping, programming, electronics, leadership, mentoring, and project management; regulated-industry experience is an asset.
Skills
- Mechanical Design
- Electromechanical Systems
- Medical Device Development
- Computer-Aided Design (CAD)
- Risk Analysis
- Tolerance Analysis
- Statistical Analysis
- Root Cause Analysis
- Finite Element Analysis (FEA)
- Computational Fluid Dynamics (CFD)
- Design Verification and Validation
- Design for Manufacture
- Prototyping
- Programming
- Electronics
- Project Management
Visa sponsorship
Not detected in the job text
Categories
- Engineering
- Manufacturing
- Healthcare
- Management & Leadership
Keywords
- Medical Devices
- Product Development
- Mechanical Engineering
- Mechatronic Engineering
- Biomedical Engineering
- Design Support
- Sustaining Engineering
- Design Responsible Engineer
- Computer-Aided Design (CAD)
- Product Data Management (PDM)
- Risk Analysis
- Tolerance Analysis
- Statistical Analysis
- Root Cause Analysis
- Finite Element Analysis (FEA)
- Computational Fluid Dynamics (CFD)
- Mathematical Modeling
- Design Verification
- Design Validation
- Usability Testing
- Regulatory Clearance
- Design for Manufacture
- Automated Assembly
- 3D Printing
- Python
- MATLAB
- Arduino
- Printed Circuit Boards (PCB)
- Project Management
- Continuous Improvement