Systems Integration Engineer

2 weeks ago

Montreal, Quebec, Canada Noze Full time
About the Role

We are seeking a highly skilled Systems Integration Engineer to join our team at Noze. As a key member of our Product team, you will play a pivotal role in advancing our mission to elevate human health by unlocking the digital sense of smell.

As a Systems Integration Engineer, you will be responsible for designing, developing, validating, and building various prototypes and commercially-ready devices. Our designs are informed by a wide array of knowledge, from mechanical design to hardware, fluid mechanics, chemistry, and physiology. We value data-driven processes, and as a medical company, every aspect of our devices must meet the highest standards.

Key Responsibilities
  • Design and build test platforms for evaluating both individual components and whole systems.
  • Collaborate closely with the development team to identify, comprehend, and scrutinize complex hardware, software, and system-level requirements.
  • Develop, execute, and document detailed performance studies to evaluate the functionality, reliability, and safety of medical devices in accordance with quality and safety standards.
  • Use exploratory test techniques to provide early feedback throughout the design and development process.
  • Design and develop insightful methods and test tools—both manual and automated—to support efficient and systematic testing.
  • Perform data analysis and participate in design reviews to discuss implementation details and suggest improvements or new features.
  • Collaborate with cross-functional teams, including firmware, AI, sensor, and aroma engineering teams, to refine and improve product testing.
  • Support the quality control process by establishing standardized testing procedures, conducting testing and inspections, and analyzing test data.
  • Participate in the assessment of potential product hazards and devise appropriate tests to verify mitigation of identified risks.
  • Collaborate with external certified labs to ensure compliance with regulatory and quality standards for clinical use.
  • Draft and maintain design history files in accordance with QMS and regulatory requirements, including design requirements, technical specifications, verification and validation test reports, and risk assessment documentation.
Requirements
  • Bachelor's or Master's degree in biomedical / mechanical engineering, or related fields.
  • 3+ years of experience in systems testing, product development, prototyping, or design, ideally within a startup or fast-paced research environment.
  • Experience with dev/eval boards and rapid testing and evaluation of subsystems and parts for the design of electrical and mechanical systems.
  • Strong analytical skills, leveraging advanced characterization techniques (e.g., FTIR spectroscopy, Mass spectrometry).
  • Proficiency with test equipment such as oscilloscope, logic analyzer, and other specialized test equipment.
  • Excel in processing and analyzing large datasets using statistical software packages (e.g. Python), with a passion for data visualization tools.
  • Experience working under a quality management system (QMS), drafting technical documentation for a design history file (DHF), and knowledge of QMS standards.
  • Embrace emerging technologies, demonstrate a hunger for continuous learning, and excel at adapting to evolving research objectives and priorities.
What We Offer
  • The opportunity to join a forward-thinking company surrounded by a collaborative team of innovative thinkers.
  • A rewarding career path with diverse opportunities for professional growth.
  • A competitive compensation and benefits package including employer-paid health and dental benefits for regular, full-time employees.
  • A generous learning and development budget to attend conferences, classes, and other events.
  • A bunch of other perks that involve food, fun, and travel.

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