Mechanical Design Engineer II Role

22 hours ago

Hyderabad, Telangana, India Medtronic Full time

Transform Lives with Medtronic

We are seeking a skilled Mechanical Design Engineer II to join our team at the Medtronic Engineering and Innovation Center (MEIC). This is an exciting opportunity to contribute to the growth and development of our Global Manufacturing Group team.

As a member of the GO & SC group, you will collaborate closely with stakeholders on assigned tasks and projects, ensuring timely and successful completion. You will work closely with your counterparts in the US to deliver high-quality results.

A Day in the Life

At Medtronic, we strive to provide healthcare products that improve individuals' well-being. Our organization plays a vital role in this mission. With significant market demand for reliable medical devices, we need a Mechanical Design Engineer II who can ensure best-in-class quality and on-time delivery of products.

The ideal candidate will have expertise in working with stakeholders to set manufacturing processes and related deliverables. They will support designing manufacturing processes, procedures, and production layouts for assemblies, equipment installation, processing, machining, and material handling.

Key Responsibilities:

  • Supporting the design and development of manufacturing processes, procedures, and production layouts
  • Collaborating with stakeholders to set manufacturing processes and related deliverables
  • Identifying and communicating operations and program risks, driving risk mitigation activities as necessary
  • Preparing or reviewing validation plans, protocols, and procedures for transfer activities
  • Contributing to achieving Core Team/Project team goals and objectives, actively participating in Core Team/Project team meetings
  • Designing sequence of operations and specifying procedures for tool and equipment fabrication, product performance
  • Maintaining accountability and delivering projects/tasks assigned

Requirements

To be successful in this role, you will require:

  • Bachelor's degree in Mechanical Engineering with 5-8 years of relevant experience
  • Strong understanding of Master Validation, including Validation Master Planning, Installation Qualification, Operational Qualification, and Performance Qualification
  • Knowledge of GD&T and experience interpreting mechanical drawings
  • Working understanding of statistics, including sample size selection, data distribution analysis, capability calculations, Design of Experiments (DOE), and Analysis of Variation
  • Strong knowledge in Lean Manufacturing/Six Sigma methodologies
  • Thorough knowledge and effective application of Design for Manufacturability, Design for Inspectability, Validation Protocol and Report creation, SPC, Process Control Plans, MSA, Gauging applications, design, and construction, Sampling methodologies, Data Analysis
  • High degree of understanding/knowledge of Machining, Molding, Grinding, Forming, Assembly, Welding, Finishing, Cleaning, Passivating, Anodizing, Shot Peening, Mass Media Operations, Coatings, EDM, Casting, Forging, Polishing
  • Good understanding on inspection methods and procedures (Test Method validation TMV)
  • Experience with risk-management, including but not limited to Process Failure Mode Effects Analysis (pFMEA), Design Failure Mode Effects Analysis (dFMEA), fault tree analysis, or other risk-management tools
  • Experience in FDA 21 CFR Part 820 Medical Device Manufacturing, or ISO 13485 preferred
  • Knowledge on Engineering Change management processes and PLM-tools such as Agile, PTC Windchill preferred

Compensation Package

The estimated annual salary for this role is $95,000-$120,000, depending on experience and qualifications. We offer a comprehensive benefits package, including medical, dental, and vision insurance, 401(k) matching, and paid time off.

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