Marmon Technologies India Private Limited As a part of the global industrial organization Marmon Holdings which is backed by Berkshire Hathaway you ll be doing things that matter leading at every level and winning a better way We re committed to making a positive impact on the world providing you with diverse learning and working opportunities and fostering a culture where everyone s empowered to be their best This Senior Lead Engineer for Microaire is responsible for providing technical leadership and direction across Sustaining and Innovation Engineering projects overseeing design changes product enhancements and new solution development This role drives complex problem-solving mentors junior engineers and ensures design integrity from concept to validation Senior Lead Engineer partners with engineering leadership to define strategies for product improvement cost optimization and innovation while maintaining compliance with engineering standards and business objectives Mandatory Skills 5 years experience in driving execution of complex design changes including model and drawing revisions design justifications tolerance stack-ups verification testing and root cause analyses 5 years Advanced proficiency in SolidWorks or equivalent CAD software for complex assemblies tolerance stack-up analysis and design optimization 3 to 5 years experience in deep understanding of GD T per ANSI Y14 5 tolerance analysis and mechanical stress evaluation for high-precision components Strong communication interpersonal skills and ability to work in a fast-paced workplace and manage multiple priorities Desired Skills Lead and oversee Change Request and Change Order processes ensuring effective prioritization technical accuracy and cross-functional alignment Drive execution of complex design changes including model and drawing revisions design justifications tolerance stack-ups verification testing and root cause analyses Manage and approve design control documentation updates related to post-market activities ensuring traceability through Risk Analysis Product Trace Matrices and Usability Engineering records Provide technical oversight for regulatory support activities including review of Technical Files FDA notifications and OUS market submissions to ensure design compliance Partner with Product Innovation and Strategy teams to lead user evaluations design validations and technical feasibility studies for new or modified products Mentor and guide the Design Verification team in developing and validating robust test methods analyzing results and ensuring design intent is fully verified Collaborate with Manufacturing Engineering to oversee Design Transfer activities ensuring design robustness manufacturability and adherence to quality standards Engage and manage relationships with external partners and suppliers providing technical direction for materials components and prototypes Lead cross-functional collaboration with Quality Regulatory Project Management and Testing teams to ensure timely completion of engineering deliverables and adherence to design control processes Provide technical mentorship to junior engineers fostering continuous improvement in design practices and documentation rigor Advanced proficiency in SolidWorks or equivalent CAD software for complex assemblies tolerance stack-up analysis and design optimization Deep understanding of GD T per ANSI Y14 5 tolerance analysis and mechanical stress evaluation for high-precision components Expertise in designing and validating mechanical systems with strong understanding of materials mechanical behavior and manufacturing constraints Strong knowledge of fabrication and process capabilities machining molding casting surface finishing and their impact on design for manufacturability DFM and design for assembly DFA Understanding of lifecycle reliability factors such as corrosion resistance fatigue wear and sterilization effects in reusable instruments Experience leading Design Verification and Validation DV V test method development and data-driven design decisions Comprehensive understanding of ISO 13485 ISO 14971 CFR 21 Part 820 30 and IEC 62366 requirements with demonstrated application in product development and documentation Experience supporting regulatory submissions Technical Files FDA notifications OUS registrations from a design perspective Proven ability to lead cross-functional design reviews mentor engineers and guide design control documentation Strong communication presentation and decision-making skills High proficiency in MS Office Project and engineering software used for analysis and documentation Demonstrated ability to manage multiple projects set technical priorities and ensure compliance with business and regulatory requirements Opportunities for Growth Take ownership of cross-functional engineering and validation projects with exposure to medical systems aligned with U S norms Deepen expertise in validation engineering statistical data analysis and workflow automation using Smartsheet SharePoint and ERP tools Build leadership by mentoring junior engineers improving processes and driving data-based decision-making across global teams Progress into senior roles such as Engineering Manager or Technical Manager based on performance with leadership and mentoring opportunities Required Qualifications Graduation in Mechanical Engineering or equivalent work experience with 8 -10 Years Min 5 years of exp in projects working with US businesses Medical device product development experience is added advantage A seasoned result-oriented engineer who can work independently once given direction has good rapport with coworkers can listen be creative and is detailed oriented Strong analytical and problem-solving abilities with keen attention to detail accuracy and flexibility to adapt quickly to changing business needs and project priorities Excellent communication and interpersonal skills with the ability to convey technical information clearly collaborate effectively across functions and work both independently and in team leadership roles Maintains a good attitude persistence and drive focused on finding a way to accomplish the objectives Following receipt of a conditional offer of employment candidates will be required to complete additional job-related screening processes as permitted or required by applicable law