Medical Device Integration Specialist

2 weeks ago


Montreal, Quebec, Canada Noze Full time

Noze is a revolutionary healthcare company pushing the boundaries of medical technology. We are seeking a skilled Medical Device Integration Specialist to join our team.

Salary: $120,000 - $180,000 per year, depending on experience and qualifications.

Job Description:

Company Overview:

We're a pioneering healthcare company focused on decoding the body's hidden language to elevate human health. Our mission is to bridge the gap between hardware, data science, and chemistry to bring the sense of smell to the forefront of medicine.

Your Role:

You will play a pivotal part in advancing our mission by designing and building test platforms for evaluating individual components and whole systems, leading data collection and evaluation efforts.

Responsibilities:

  • Designing, validating, and building test benches to ensure efficient testing processes.
  • Collaborating with development teams to identify and scrutinize complex hardware, software, and system-level requirements, driving innovation and quality.
  • Developing performance studies to evaluate the functionality, reliability, and safety of medical devices, guaranteeing compliance with regulatory standards.
  • Utilizing exploratory test techniques to provide early feedback throughout the design and development process, enhancing product quality.
  • Designing and developing test tools to support efficient and systematic testing, ensuring seamless integration with existing systems.
  • Performing data analysis and participating in design reviews to inform product development and improvement.
  • Collaborating with cross-functional teams to refine and improve product testing, promoting a culture of excellence.
  • SUPPORTING quality control processes and establishing standardized testing procedures to maintain consistency and efficiency.
  • Participating in the assessment of potential product hazards, ensuring a safe and reliable product for users.
  • Collaborating with external certified labs to ensure compliance with regulatory and quality standards, maintaining industry-leading standards.
  • Drafting and maintaining design history files to document critical design decisions and testing outcomes.

Requirements:

  • Bachelor's or Master's degree in biomedical, mechanical engineering, or related fields.
  • At least 3 years of experience in systems testing, product development, prototyping, or design, with a proven track record of delivering high-quality results.
  • Experience with dev/eval boards, test equipment, and rapid testing and evaluation of subsystems and parts.
  • Strong analytical skills and proficiency with test equipment and data analysis software.
  • Experience working under a quality management system and drafting technical documentation.
  • Knowledge of QMS standards and CAD software such as Solidworks.
  • Experience in rapid prototyping tools and testing medical devices.


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