Address
Form of workJob Description
Hiring For Mechanical Engineer with Medical Device
C2C, Fulltime
Location: Philips, Orlando FL ( On-site )
Exp: 15+
Responsibilities
Mechanical Engineer
will be a member of the Product Development staff and be involved in the design, development,
and maintenance of new MRI compatible products.
Responsible for the mechanical design of future generations of MR Patient Care products
Coordinates and mentor junior engineers in research, design, development, and implementation of product
architerctures
Connect and align with project management on project content, timeline and costs
Responsible for requirements, design, implementation, test and integration of module/sub-system in accordance
with the higher level requirements and specifications
Conduct concept & feasibility studies. Lead the introduction of new technologies
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 technical issues using methodical problem solving techniques and provide root cause / 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.
Network with colleagues within BU and beyond and maintain external contacts for benchmarking, new
technologies, tooling, design methods, and reflects them to the HW-group
Draws up personal schedule and reports on progress
We are looking for
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 an engineering
discipline.
At least 15 years of engineering design experience.
Experienced in designing mobile and portable electronic enclosures.
Familiarity with Current ISO standards family that apply to Medical Devices.
Ability to interface with internal stakeholders 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 analyze designs for static and dynamic stresses.
Experience in using 3D Parametric tools (Creo, Solidworks, etc.).
Knowledgeable of ASME Y14.100 Engineering Practices.
Proficient in Geometric, Design and Tolerancing (GD&T) principles.
Experience with design reviews based on failure modes (DFMEA)
Experience with design of experiments (DOE)
Experience with requirements deconstruction from subassemblies to components.
Experienced in rapid prototyping techniques (CNC Machining, 3D Printing, Sheet Metal, etc.)
Ability to understand and debug problems across hardware/software / system boundaries
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 and Creo Parametrics 8.
Experience in the field of Medical Devices product design e.g. CT, MR, X-Ray, Mammography systems etc. will be
an added advantage
Exposure to International Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE is a plus
Interested Candidates Can Send their Resume to mahesh.b@kaavinc.com
Thanks & Regards,
B. Mahesh
Sr. US IT Recruiter
Kaav Inc.3925 75th St, Suite 101 A, Aurora, IL 60504
Email: mahesh.b@kaavinc.com :: P: 847-450-7769
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