Job DescriptionWe are seeking an experiencedSenior Systems Engineerwith deep technical expertise to lead system?level architecture, integration, and verification activities for complex electromechanical medical systems. This role is suited for an engineer who thrives in multidisciplinary environments, understands the interactions between hardware, firmware, software, and clinical workflows, and can drive robust system design from concept through commercialization.Role OverviewAs a Senior Systems Engineer, you will be responsible for end?to?end technical ownership across the full product development lifecycle. You will translate stakeholder inputs into system requirements, define architecture, lead integration activities, and develop verification and validation strategies for high?reliability medical systems. You will work cross?functionally with mechanical, electrical, software, quality, regulatory, cybersecurity, and clinical teams, ensuring system functionality, safety, and regulatory compliance.You will also mentor junior engineers, challenge design proposals through structured reviews, and lead the identification and resolution of system?level behaviour issues across new and legacy product lines.Key Technical ResponsibilitiesDefine and maintain system requirements, ensuring full traceability from User Needs through verification and validation.Lead system architecture development, including interface definitions, subsystem interactions, control strategies, and design constraints.Drive system integration activities, ensuring hardware, embedded software, and mechanical components interface correctly under all operating conditions.Develop comprehensive verification test strategies, including test protocols, acceptance criteria, and risk?based testing approaches.Execute system characterization activities to confirm performance across environmental, mechanical, and clinical use conditions.Conduct failure analysis, root?cause investigation, and drive corrective actions in alignment with DFSS, FMEA, and other reliability tools.Evaluate trade?offs between performance, safety, cost, manufacturability, and regulatory constraints during design decision?making.Lead cross?functional design reviews, challenge assumptions, and ensure system robustness through disciplined engineering rigor.Support regulatory submissions by providing system documentation, trace matrices, risk analyses, and verification evidence.Required BackgroundBachelor's degree in Engineering or a related technical field (Mechanical, Electrical, Systems, Biomedical, Mechatronics, etc.).5+ years of experience in systems engineering for electromechanical medical devices, IVD instrumentation, lab automation, or similarly regulated system architectures.Demonstrated experience developing requirements, architectures, and integration strategies in multidisciplinary engineering environments.Strong familiarity with safety?critical design and risk management methodologies (FMEA, DFSS, fault tree analysis).Ability to synthesize complex technical data, identify system?level issues, and develop actionable solutions.Excellent communication skills with the ability to present complex engineering decisions clearly to technical and non?technical stakeholders.Experience collaborating with global teams and external design or technology partners.The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.