QUALIFICATIONS

• Minimum of 5 years’ experience in mechanical device or product design, preferably within medical device R&D environments
• Bachelor’s degree in Mechanical Engineering required; Master’s degree preferred
• Professional Engineer (P.Eng) designation from EGBC preferred, or willingness to obtain licensure (alternative title may be provided until licensing is achieved)
• Extensive experience collaborating with design partners and external vendors
• Proficiency in SolidWorks and relevant add-ins
• Experience with plastic injection mold tooling design, including insert molding and over-molding techniques
• Strong project management skills with ability to meet deadlines in a fast-paced setting
• Demonstrated ability to work effectively in technical, team-oriented environments
• Sound independent engineering judgment and problem-solving abilities
• Excellent written communication skills with high attention to detail

WHY CONSIDER THIS OPPORTUNITY?

• Join a team dedicated to advancing patient care through innovative medical technology
• Engage in meaningful work that directly impacts healthcare outcomes
• Competitive salary range $100, 000 - $118,000 CAD, commensurate with experience and skills
• Eligibility for an annual performance bonus plan
• Comprehensive benefits including health spending account, paid time off, holidays, and retirement savings matching
  If you are a motivated Mechanical Engineer seeking to contribute to cutting-edge medical device innovation in a collaborative and supportive environment, we encourage you to apply.
  

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Job Types: Full-time, Permanent
Pay: $100,000.00-$120,000.00 per year
Work Location: In perso

ABOUT THE ROLE

Our client, a respected leader in medical device manufacturing, is seeking a Mechanical Engineer III to contribute to the design and development of innovative, high-quality medical devices and equipment. This role supports the commercialization of new products by delivering robust electromechanical assembly designs that meet clinical needs and regulatory standards.

KEY RESPONSIBILITIES

• Collaborate with external vendors to complete and validate design work, ensuring all deliverables meet product specifications and quality requirements
• Research and evaluate design options, conducting experiments to verify feasibility and performance
• Lead high-level design activities while coordinating detailed design efforts with partners
• Work closely with electrical and software engineering teams to create system-level designs
• Engage with global and internal manufacturing teams to optimize designs for manufacturability, reliability, and cost-efficiency
• Prepare and release product requirements, design specifications, and design descriptions in compliance with applicable medical device regulations and internal standards
• Maintain thorough engineering documentation in line with corporate policies
• Review product documentation for accuracy and clarity, including materials intended for customer use
• Participate in prototyping, testing, design validation, risk assessments, and regulatory submission activities
• Analyze product non-conformances and recommend design improvements using advanced problem-solving techniques
• Support intellectual property development initiatives