On-site
Part Time
Senior Mechanical Engineer
You will report directly to the Senior Manager , Product Development. The MR Patient Care (MRPC) team is part of the Hospital Patient Monitoring (HPM) business unit. This position is based in Bangalore, India.
Your role:
The Senior Mechanical Engineer will be a member of the Product Development staff and be involved in the design, development, and maintenance of new and existing MRI compatible products.
Responsible for the Mechanical design of existing and future generations of MR Patient Care products.
Act as mechanical lead to review and provide oversight of R&D activities (i.e. internal and external support) developing products for the MRI.
Oversee compliance and V&V activities, including offsite test management.
Lead design reviews, FMEA analyses, and other DfX related activities.
Review and ensure adequacy of supplier qualification activities.
Analyze field issues using methodical problem solving techniques and provide solutions where required.
Actively participate on cross-functional/cross-business project teams through all phases of product development to ensure successful execution of innovative, best-in-class designs.
Coordinate local mechanical efforts, reliability and MR testing with other MRPC Sites
Lead MR testing resulting in appropriate MR-labeling of products
You're the right fit if:
The successful candidate will possess the following knowledge, skills education and experience:
Essential Requirements
Bachelor of Science degree required, (Masters of Science preferred) with a concentration in Mechanical Engineering discipline.
At least 8 years of engineering design experience.
Precision mechanism design competencies in product design and test.
Familiarity with Current ISO standards family that apply to medical devices.
Ability to interface with customers and be effective at managing suppliers.
Experienced in design of die castings, injection moldings, machinings and sheet metal.
Experience in using Finite Element Analysis (FEA) programs to analyse designs for dynamic stress analysis.
Experience in using 3D Parametric tools (Creo, Solidworks, etc.).
Knowledgeable of ASME Y14.100 Design Guidelines.
Experienced in applying Geometric, Design and Tolerancing (GD&T) Principles to drawings.
Experience with design reviews based on failure modes (DRBFM).
Experience with Fluid Flow analysis.
Experience with requirements deconstruction from subassemblies to components.
Desirable
Class 2 or Class 3 medical device development experience.
Understanding of global regulatory requirements for medical devices.
LEAN/Six Sigma certification or experience.
Familiarity with risk management through a full product development cycle from requirements to validation. Experience with DOORS requirement management tool a plus.
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