Reliability Engineer (Quebec) (Quebec City)

Responsibilities Working with R&D;, quality assurance and manufacturing teams to develop reliability requirements (including requirements cascade), develop and implement comprehensive reliability test plans for IVD medical devices that align with product development and production processes. Developing reliability plans and requirements, leading and facilitating Design Failure Mode and Effects Analysis (DFMEA). Designing and developing test methods and fixtures to assess the performance and durability of IVD devices. Writing test protocols, training personnel on test procedure, analyzing data and creating final reports. Conducting reliability tests and documenting results, including environmental, lifecycle, and accelerated aging tests, to evaluate product performance under different conditions and in compliance with relevant regulatory standards and guidelines. Analyzing test results and providing detailed reports, identifying areas for improvement and potential risks. Serving as the subject matter expert and technical representative for the reliability engineering function in project teams. Recommending design or test methods and statistical process control procedures for achieving required levels of product reliability. Leading and directing multiple projects in a quick-paced, cross-functional workplace. Participating in design reviews and working with engineering to drive DFR (Design for Reliability) process and tools and support in defining and executing reliability plans. Reviewing device failures, performing root cause investigations, and documenting results in a failure reporting, analysis, and corrective action (FRACAS) system. Compiling and analyzing performance reports and process control statistics; investigating and analyzing relevant variables potentially affecting product and processes. Qualifications Familiarity with design for reliability and reliability engineering. Working knowledge of regulations and best practices for medical device development such as ISO 13485 and 21 CFR 820 as well as IEC 61010, IEC 60601, IEC 62506, IEEE 1413 and IEEE 1332. Ability to generate data and perform life data analysis. Knowledge of building fixtures and performing Life Data Analysis for in-vitro diagnostics medical products. Ability to manage multiple projects and prioritize tasks effectively. Ability to communicate effectively with other engineers, managers, and stakeholders. Demonstrated ability to lead, motivate, and collaborate with technical teams and drive results. Ability to identify and solve complex problems related to design for reliability. Ability to analyze data and identify patterns to develop solutions for potential problems. Strong understanding of engineering principles and familiarity with relevant software and tools. Ability to identify and assess risks that can cause delays to project timelines or increase project costs. Ability to develop process and methodology to model system and subsystem reliability. Ability to work with development teams to drive effective FMEA's and risk reduction. Required Skills Bachelor’s degree (Advanced degree preferred) in Mechanical /Electrical /Reliability Engineering or related discipline. 10+ years reliability engineering experience in highly regulated industry preferably in a medical device industry. Previous experience creating custom verification tests and fixtures. Previous experience planning verification tests (DoE, sample size selection, etc.). Experience in Reliability and statistical analysis software like Reliasoft/PTC Windchill/Minitab. #J-18808-Ljbffr Apply on Kit Job: kitjob.ca/job/2ptydp