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Added 3 mins ago
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Corvita Biomedical

R&D Biomedical Engineer

Toronto, ON, Canada

Job type: Full-time
Apply by: Mar 20, 2027
Posting language: English
Posted: Sep 21, 2026

Apply About employer

Applications open in a new tab.

Original job description

Company: Corvita Biomedical Inc.

Location: Greater Toronto Area, Ontario, Canada - Hybrid

Employment: Full-time, permanent

Experience: Early-career to intermediate; relevant co-op and research experience considered

Reports to: Head of Engineering

Start date: As soon as mutually agreed

About Corvita Biomedical

Corvita Biomedical Inc. is a mission-driven medical device startup transforming neonatal healthcare globally. We are developing the ARK Incubator, designed to democratize access to intensive care for premature and critically ill newborns. Our technology addresses the global crisis where millions of infants die annually due to lack of access to proper neonatal intensive care, particularly in underserved communities, rural areas, and humanitarian settings. As a member of our team, you'll have the unique opportunity to directly impact infant mortality rates and health outcomes on a global scale.

Role Summary

We are seeking a Biomedical Engineer to support system integration and multidisciplinary R&D for ARK. The role connects physiological and user needs with measurable engineering requirements, sensor behaviour, subsystem interfaces, test methods, and verification evidence.

This is not a general clinical, quality, or regulatory catch-all role. You will provide biomedical context and hands-on engineering support to the software and mechanical teams and own defined integration and test work packages. Production software, released mechanical design, PCB and firmware implementation, ML models, and regulatory submissions remain with their respective owners.

Key ResponsibilitiesSystems engineering and integration

Translate approved user and clinical needs into measurable system and subsystem requirements with defined acceptance criteria.
Maintain assigned requirements, interface definitions, assumptions, and traceability through design reviews and verification.
Develop interface matrices and integration plans covering sensors, embedded electronics, software, mechanical features, data outputs, alarms, and accessories.

Biomedical sensing and applied research

Support selection, characterization, and integration of physiological and environmental sensors relevant to ARK.
Develop bench methods to assess signal quality, accuracy, repeatability, latency, drift, calibration, noise, motion artefact, and failure behaviour.
Analyze biosignals and sensor data using Python, MATLAB, or equivalent tools, documenting algorithms, assumptions, limitations, and results.
Investigate sensor-to-patient and sensor-to-device interfaces, including contact pressure, placement, materials, cable effects, motion, temperature, and usability constraints.

Software engineering

Define biomedical data semantics, including units, ranges, sampling needs, timing, quality flags, error states, and expected sensor behaviour.
Create reference calculations, analysis scripts, test vectors, simulated inputs, and sensor or device emulators for development and verification.
Review software behaviour against biomedical requirements and help develop objective acceptance tests.
Provide domain context and curated test data to the ML and Data team, which retains ownership of model training, validation, deployment, and monitoring.

Mechanical engineering support

Convert biomedical and use-environment needs into mechanical design inputs concerning sensor placement, patient contact, caregiver access, cable management, cleaning, serviceability, and human interaction.
Review CAD, drawings, prototypes, and tolerance decisions for their effect on sensor performance, usability, integration, and testability.

Required Qualifications

Bachelor's degree in Biomedical Engineering, Systems Engineering, Mechatronics, Electrical Engineering with biomedical experience, or a related discipline.
Applied understanding of physiology, sensors, measurement systems, signal acquisition, sampling, filtering, noise, calibration, and uncertainty.
Experience using Python, MATLAB, or an equivalent environment for data analysis and repeatable engineering tests.
Ability to turn ambiguous needs into measurable requirements, testable interfaces, and practical experiments.

Preferred Qualifications

Co-op, research, or industry experience with a medical device, patient-monitoring product, incubator, diagnostic system, wearable, or regulated electromechanical product.
Experience with biosignal acquisition, motion-artifact reduction, physiological monitoring, or sensor-to-skin interfaces.
Familiarity with medical-device design controls, requirements traceability, verification, risk management, and controlled documentation.
Familiarity with ISO 13485, ISO 14971, IEC 60601, IEC 62304, or IEC 62366-1 concepts.
Experience with Git, automated test scripts, structured datasets, statistics, uncertainty analysis, or test-equipment automation.
Exposure to human factors, biological evaluation, cleaning or disinfection constraints, or neonatal-care environments.
Experience collaborating with clinicians, external laboratories, research partners, or contract manufacturers.

What We Offer

Meaningful ownership of defined work in an early-stage medical-device program.
Hands-on exposure to requirements, prototyping, integration, verification, and manufacturing preparation.
Close collaboration with engineering, clinical, quality, regulatory, and manufacturing contributors.
Hybrid work with regular access to Corvita's Greater Toronto Area development environment.
The opportunity to help establish practical engineering processes as the team grows.

How to Apply

Please email the following to [email protected]:

Resume or CV.
A brief cover letter explaining your interest and relevant experience.
An optional portfolio, publication, public repository, or non-confidential work sample showing biomedical sensing, systems integration, software support, or mechanical support.

Please do not include confidential or proprietary information from a current or former employer. Applications will be reviewed on a rolling basis until the position is filled.

Apply About employer

More about this job

Responsibilities

The role involves translating clinical needs into measurable system requirements and managing integration plans for sensors, software, and mechanical subsystems. You will provide biomedical domain expertise to support multidisciplinary teams in developing and verifying the ARK neonatal incubator.

Requirements

Candidates must hold a bachelor's degree in Biomedical, Systems, Mechatronics, or Electrical Engineering with a strong understanding of physiology and measurement systems. Proficiency in Python or MATLAB for data analysis and the ability to define testable engineering requirements are essential.

Skills

Biomedical engineering
Systems engineering
Python
MATLAB
Sensor integration
Signal acquisition
Data analysis
Requirements traceability
Medical device design
Physiological monitoring
Verification and validation
Risk management
Mechatronics
Embedded electronics
Statistical analysis

Benefits

Meaningful ownership of work
Hands-on exposure to medical device development
Collaborative environment

Visa sponsorship

Not detected in the job text

Keywords

Biomedical Engineering
Systems Engineering
Mechatronics
Electrical Engineering
Medical Device
ARK Incubator
Neonatal Healthcare
Sensor Characterization
Signal Processing
Python
MATLAB
ISO 13485
ISO 14971
IEC 60601
IEC 62304
IEC 62366-1
Requirements Traceability
Verification
Validation
Risk Management
Biosignal Acquisition
Data Analysis
Human Factors
Prototyping
Mechanical Design
Firmware
Machine Learning
Git
Statistical Analysis
Clinical Collaboration

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