Mechanical Engineer Medical Device

Position: Mechanical Engineer with Medical Device
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 Para metrics 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

Thanks & Regards,

B. Mahesh

Sr. US IT Recruiter

Kaav Inc.
3925 75th St, Suite 101 A, Aurora, IL - 60504

Email:  :: P:

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