Senior Mechanical Engineer

<div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>Position Summary</b></H2></div><div><p>STERIS is a well-established company operating in the medical equipment industry, specifically in decontamination, sterilization, and infection prevention technologies. Recognized for its expertise, safe work environment, and high-quality standards, it plays a critical role in the healthcare supply chain by contributing to patient safety.

Are you looking to grow in a dynamic, innovative environment focused on operational excellence? Join the STERIS team!</p><p> </p><p>We are currently seeking a <strong>Senior Mechanical Engineer </strong>to join our <strong>Custom Engineering</strong> team in Beauport, Quebec.

Custom engineering plays a key role in the design and development of mechanical and electromechanical solutions tailored to the specific needs of our Life Sciences clients. As a design expert, the <strong>Engineer</strong> is involved throughout the entire project lifecycle, from analyzing client requirements to implementing solutions.

They actively participate in technical discussions with clients and contribute to strategic engineering decisions.</p><p> </p><p>Please note that this is a<strong> full-time, permanent and fully remote</strong> position.</p></div></div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>What you will do as a Senior Mechanical Engineer at STERIS</b></H2></div><div><div><ul><li>Design, develop, document, and implement mechanical and/or electromechanical solutions within a custom project environment;</li><li>Define and propose complete washing solutions tailored to client applications, taking into account technical, operational, and regulatory requirements;</li><li>Analyze clients’ technical needs and contribute to proposal preparation, including concept development, feasibility assessments, and cost estimates;</li><li>Actively participate in internal design reviews and technical reviews with clients;</li><li>Apply fundamental engineering principles in mechanics, statics, dynamics, thermodynamics, heat transfer, fluid mechanics, finite element analysis (FEA), and materials science to develop solutions for life sciences equipment;</li><li>Identify root causes of technical issues, propose sustainable solutions, and validate concepts in accordance with engineering best practices;</li><li>Apply DFMA (Design for Manufacturing and Assembly) principles to ensure robust, manufacturable, and optimized designs;</li><li>Collaborate closely with project management, manufacturing, quality, and procurement teams to ensure efficient and consistent project execution;</li><li>Clearly communicate complex technical concepts to both technical and non-technical audiences;Execute assignments with a high degree of autonomy while identifying risks and meeting project timelines;</li><li>Contribute to continuous improvement initiatives and the optimization of departmental processes.</li></ul></div></div></div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>The Experience, Skills and Abilities Needed</b></H2></div><div><p><span style="text-decoration: underline;">Required</span></p><ul><li>Bachelor's degree in Mechanical Engineering;</li><li>Professional Engineer (P.Eng.) designation and member in good standing with the engineering regulatory body in your province of residence;</li><li>7 to 10 years of relevant experience in mechanical design,</li><li>Proficiency with 3D design and modeling software, such as PTC Creo,SolidWorks, Autodesk Inventor, and CATIA, as well as 2D drafting software such as AutoCAD;</li><li>Strong understanding of manufacturing processes, including welded fabrications, machining, and assembly, with the ability to develop manufacturable and optimized designs in accordance with DFMA (Design for Manufacturing and Assembly) principles;</li><li>Excellent analytical, problem-solving, and technical decision-making skills;</li><li>Self-motivated, detail-oriented, customer-focused, and able to work effectively with minimal supervision;</li><li>Ability to share knowledge, recommend alternative solutions, and make sound technical decisions based on informed risk assessments;</li><li>Commitment to operational excellence, LEAN principles, and continuous improvement;</li><li>Ability to produce detailed, accurate, and high-quality technical documentation.</li></ul><p> </p><p><span style="text-decoration: underline;">Asset</span></p><ul><li>Experience with analysis and simulation software such as ANSYS for Finite Element Analysis (FEA), Computational Fluid Dynamics (CFD), thermal analysis, and related applications;</li><li>Knowledge of technical documentation, analysis, and communication tools, including Microsoft Office and PLM systems (e.g., Windchill, Vault) for technical data management and engineering change control</li><li>Knowledge in PTC Creo,</li></ul></div></div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>What we offer</b></H2></div><div><p>At STERIS, we offer a stimulating work environment with real opportunities for advancement! STERIS is a well-established company operating in the medical equipment field, specifically in decontamination, sterilization, and other infection prevention technologies.

This field directly impacts people’s health, which is why we make sure to surround ourselves with a rigorous team that adheres to the highest quality standards.</p><p> </p><p><span style="text-decoration: underline;">WHAT WE OFFER:</span></p><ul><li>Competitive compensation;</li><li>A range of employee benefits, including:<ul><li>A comprehensive and flexible group insurance plan – offering various options and approximately 90% covered by STERIS. This plan includes prescription drug coverage, vision care, paramedical services, and dental care;</li><li>Telemedicine services;</li><li>An Employee Assistance Program (EAP);</li><li>A bank of personal days (5 days);</li><li>A schedule of 12 holidays (including 8 statutory holidays);</li><li>A day off on your work anniversary;</li><li>A group RRSP with employer contributions from STERIS, up to 3% of annual salary;</li><li>A corporate bonus program;</li></ul></li><li>Typical workweek: Monday through Thursday with some roles eligible for an early finish Friday.</li><li>An experienced and multidisciplinary team;</li><li>A safe environment at the forefront of continuous improvement.</li></ul></div></div></div> <p>This position requires knowledge of English due to the nature of the duties involved, including regular communications outside the province of Quebec, training, email communications, and frequent meetings and interactions with English-only employees.

The employer has taken all reasonable steps to avoid imposing this language requirement, in accordance with the Charter of the French Language. </p><p>STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe.

For more information, visit <a href="https://www.steris.com">www.steris.com</a>. </p><p>STERIS strives to be an Equal Opportunity Employer. </p>