R&D Engineering Associate, Co-op/New Grad

Boston Scientific•Mississauga, ON

1d•Hybrid

About The Position

In our Research & Development Engineering Department, our Engineers focus on the ideation, design, prototyping, and manufacturing transfer of cutting-edge devices for use in medical procedures. Our R&D Engineers are directly involved with obtaining regulatory approval and patents as well as actively participating in clinical research studies.

Requirements

Actively enrolled in an Engineering degree, or a recent graduate from a Bachelor's degree in Electrical, Biomedical, or Computer Engineering
Exposure to laboratory or engineering test environments, including use of standard measurement tools/instruments
Demonstrated ability to prepare technical documentation (e.g., drawings, work instructions, or reports)
Internship, co-op, or project experience involving product design, testing, or development

Nice To Haves

Strong interest in biomedical technology
Custom PCB design and analog circuit design
Motivated self-starter with a hands-on approach
Ability to work independently and with a diverse group of Engineers and Clinicians
Excellent communication skills, both written and oral
Strong leadership and problem-solving skills
Positive attitude and enthusiasm
Six Sigma or LEAN knowledge
Experience with SolidWorks and Minitab
Experience in a highly regulated manufacturing environment
Knowledge of ISO 13485

Responsibilities

Assist in the development of devices through prototyping, testing, and 3D modeling.
Create and conduct verification and validation testing to validate design requirements and concepts.
Prepare regulatory filings to various government bodies alongside our IP and Regulatory Affairs teams.
Support clinical trials of devices and work with external suppliers and clinicians.
Aid in the development and provision of technical documentation by preparing drawings, writing work instructions, and presenting technical insights.
Monitor safety practices and ensure ISO 13485 and FDA compliance while collaborating with cross functional teams to meet product timelines.
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Other duties as required.