Product Development Engineer I — Medical Devices

MiRus®; Montreal (administrative region); On-site; CAD 92,000 - 128,000; Full time

Benefits offered by this job

401(k)

Dental insurance

Vision insurance

Disability insurance

Employee assistance program

Flexible spending account or Health FS

Health insurance

Life insurance

Paid time off

Job summary

MiRus is seeking a Product Development Engineer I to support design and development of medical devices within the R&D team. You will create CAD models, generate engineering prints, and perform analyses to ensure products meet specifications and regulatory requirements.

The role collaborates with engineering, marketing and manufacturing, with responsibility for documentation control and compliance under ISO13485 and FDA guidelines.

Qualifications

• BS in Mechanical Engineering or Bio-engineering or equivalent required.
• Experience in medical devices preferred.
• ISO13485 / FDA design control experience preferred.

Responsibilities

• Provide engineering support for projects including CAD modeling and detailed prints.
• Create and refine CAD models and detailed engineering prints (tolerances, GD&T).
• Perform engineering analyses including FEA, tolerance studies and FMEA.
• Conceptualize, design and develop new products such as implants and instrumentation.
• Ensure compliance with ISO and FDA QMS frameworks.
• Collaborate with engineering, marketing and manufacturing teams and manage documentation.

Skills

CAD modeling

Engineering analysis

Verbal communication

Time management

Problem solving

Education

BS in Mechanical Engineering

Tools

SolidWorks

Job description

MiRus is seeking a Product Development Engineer I to support design and development of medical devices within the R&D team. You will create CAD models, generate engineering prints, and perform analyses to ensure products meet specifications and regulatory requirements.

The role collaborates with engineering, marketing and manufacturing, with responsibility for documentation control and compliance under ISO13485 and FDA guidelines.