Careers that Change Lives
Be a part of the Medtronic Engineering and Innovation center (MEIC) by applying your skills to the growth and development & sustaining efforts of Medical Devices products at MEIC.
As a member of the MEIC team, you will collaborate with the broader Medical Devices engineering team, clinical and commercial teams globally. You will enable design & development of medical devices/products and the associated infrastructure & capability building elements in close conjunction with the Global teams
A Day in the Life
Manage a cross functional engineering technical team and provide leadership for design, development or optimization of products, processes, tooling and/or equipment by collaborating with the necessary stakeholders.
Responsible for all areas of mechanical development including Jigs & Fixture designs, Mold designs.
Work with engineers on critical issues, developing action plans and driving corrective actions
Provide a blend of people management and technical savviness. Should have worked on development of products and on successful delivery of solutions.
Review and verify technical drawings and specifications of mechanical parts and components, and to ensure that installation and operations conform to standards and requirements.
Should have knowledge of CTQs for review and verification of detailed multi-view drawings of assemblies and sub-assemblies
Must be able to support the global team in organic, blended, inorganic product development projects.
Support the technology road map of Medical Devices by proactively pitching for technology development and turnkey projects.
Develop junior members by coaching, empowering, reviewing results, both in technical areas and in “soft” skills.
Identify solution knowledge gaps within MEIC in Medical Devices solutions and prepare plans to address them ( strategic alliances and self-managed teams )
PRINCIPAL WORKING RELATIONSHIPS
The incumbent would work with the project management office at MEIC to ensure that resource forecasts, project metrics are correctly captured and presented to the leadership
Frequent interaction with team members from other disciplines, cross functional teams, to understand project requirements and to adhere to project schedules.
Possible interaction with clinicians, third-party vendors, manufacturers, and subcontractors.
EXPERIENCE
Experience of minimum of 15+ years in product development with at least a min of 10+ years in mechanical device development & verification.
KNOWLEDGE, SKILL, AND ABILITY
Experience in development of mechanical products, team building skills, talent management, conflict resolution, and global cross-functional stake holder management are critical to the role.
In-depth experience in CAD tools such as Pro-E Creo/Solid works is expected.
Expertise in Robust Modeling and Detailing practices following the ASME guidelines.
Strong Knowledge and application of GD&T including Tolerance stack-up analysis.
Strong knowledge of metal manufacturing processes. Knowledge on 3D printing and additive manufacturing technologies is an add-on.
Knowledge on Engineering Change management processes and PLM tools such as Agile, PTC Windchill is preferred.
Strong understanding of medical device standards, guidelines and regulations per ISO 13485, ISO 14971 and Design controls ( 21 CFR Part 820).
Strong knowledge of Engineering fundamentals and application of same during concept generation or re-design of products.
Able to effectively work with cross functional teams in a multinational matrix organization
Superior written and verbal communication skills required.
Good attitude and team player.
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