Tests and Validations Specialists

About EERS EERS develops enabling hardware and software for noise management, hearing protection, audio clarity and voice intelligibility through devices that are comfortable and secure. We are experts in real‑time signal processing that builds applications for augmented hearing in industrial, medical, and consumer use cases. Our bio‑mechanical skills allow us to map and address the complexity of the human ear canal to build novel comfortable, usable, and manufacturable earpieces that are acoustically efficient. The EERS team is made up of experts in audiology, acoustics, embedded software, hardware design, bio‑mechanical, industrial design, and prototype assemblers capable of working on the smallest of form factors. Our head office is located in the heart of downtown Montréal. We offer competitive salaries as well as a great team environment with a hybrid WFH model. EERS is an equal‑opportunity employer committed to diversity. Job Description We are looking for a Tests and Validations Specialist to join our multidisciplinary R&D team and design state‑of‑the‑art communication system for use in the MRI room. We have just launched a very challenging and exciting new project which will allow the System Test Specialist to be directly involved in all phases of product design. Reporting to the Senior Hardware Design Engineer, and under supervision of the EMC specialist, the role will perform a variety of tasks ranging from design to execution of sub‑module tests in the laboratory to complete system testing in an MRI environment. The candidate will also have a direct impact on the design of the product family that we are currently defining. We are therefore looking for a versatile and passionate team member who is not afraid to take on multiple tasks. Duties and Responsibilities Define, plan, and execute validation tests for subsystems and the complete system, both in the laboratory and in an MRI environment. Collaborate closely with the development team to establish a test strategy aligned with product and regulatory requirements (e.g., IEC, ISO, FCC, FDA, Health Canada, 510(k), etc.). Collaborate with partners (engineers, physicians, clinical professionals, etc.) to understand customer needs and create innovative testing solutions for product validations. Collaborate with the Mechanical team for mechanical validations of the product. Develop testing and validation methodologies to simulate environmental testing in our laboratories. Create and maintain rigorous documentation of the test and validation strategy, specifications, and execution, as well as the analysis of all resulting data. Manage the coordination, execution, and monitoring of regulatory testing, including EMC testing in certified laboratories. Manage the coordination, execution, and monitoring of environmental testing performed in the MRI room. Contribute to the design by identifying potential failure modes to ensure required performance and long‑term product reliability. Provide the development team with Design for Validation and Test (DFT) recommendations. Develop the design and manage the manufacturing of automated test benches (validation and production) for the system and subsystems, including mechanical, electrical, and software aspects. Contribute to the continuous improvement of validation, traceability, and product quality processes. Bachelor’s or Master’s degree in Electrical Engineering, or related field. Qualifications 5+ years of experience in test engineering (methodology, planning, reliability, data analysis, etc.) Knowledge of the medical product development cycle for regulated products and the various control mechanisms. Proficiency in the use of laboratory equipment (oscilloscope, spectrum analyzer, VNA, etc.). Experience in designing automated test benches (PCBA, EOL, etc.) covering RF, EMC (EMI/EMC), and thermal management. Familiarity with automated test environments (Python, LabVIEW, etc.). Experience working closely with electrical and mechanical engineers and product designers. Assets Involvement in the testing and validation of complex products that have been marketed. Experience in medical product development. Experience with testing in an MRI environment or knowledge of the associated constraints (non‑ferromagnetism, interference, security, etc.). Soft Skills Ability to effectively communicate ideas and solutions in both French and English. Strong writing and documentation skills. Ability to work both individually and as part of a team in a fast‑paced environment. Excellent problem‑solving and analytical skills. Excellent time management and organizational skills; ability to contribute to multiple projects simultaneously. Depending on the daily tasks to be performed, working from home may be possible. However, as we often need laboratory equipment and great collaboration between the R&D teams is essential, the candidate must be able to come to the office with short notice if necessary. If you are meticulous, a problem solver, and a team player, you will feel right at home. Please send your cover letter and resume to OR submit them through our EERS Career platform. Seniority level Mid‑Senior level Employment type Full‑time Job function Quality Assurance Industries Industrial Machinery Manufacturing Referrals increase your chances of interviewing at EERS by 2x #J-18808-Ljbffr