Work Flexibility Hybrid What will you do Technical Responsibilities Lead technical team members in research design development modification and evaluation of modules assemblies or subsystems Apply advanced engineering theories principles and concepts across various products within business Translate user needs to design inputs specifications and produce system architectural level layouts and platform designs Assess current technologies and capabilities prototyping testing et al for the organization Med Device Compliance Divisional expert with extensive experience applying industry standards for device development Lead the development of standards and regulations working closely with functions within and across business General Responsibilities Lead cooperative efforts with R D Quality Manufacturing Regulatory Clinical Marketing and Project Management to ensure project success Lead and support team members to create or improve procedures policies processes systems and technology requirements Hold team accountable to deliver high quality results with passion energy and drive to meet business priorities Mentor develop and influence across business intentionally building divisional relationships What will you need Minimum Qualifications Bachelor of Science in Engineering Mechanical Engineering or Bio Medical 13 years of work experience Broad base of experience in Implementing design methodologies such as DFM Reliability Systems Design High degree of experience in medical device design or designing in a highly regulated industry and ability to utilize Solid Modeling and CAE tools to optimize the design In-depth knowledge of materials manufacturing and processing methods and technologies to support complex product development Ability to communicate complex plans and technical information to team members within and across businesses Preferred Qualifications Communication skills Ability to lead and manage Travel Percentage 20

📌 Principal Engineer (Haryana)
🏢 Stryker
📍 Haryana