Mechanical Design Engineer; Medical Device) Security Clearance

Position: Mechanical Design Engineer (Medical??????? Device) with Security Clearance
Mechanical Design Engineer - Vascular Devices)

* Location:

100% ONSITE - Tempe, Arizona (85283)

* Type: W2 contract (NO C2C OR THIRD PARTY will be considered)

* Pay Rate:
Negotiable depending on direct related experience UP to $48 - $53/hour

* Duration: 9 months contract

* Work Authorization:
Must be currently located and authorized to work in the United States without CURRENT Visa transfer or sponsorship requirements. KEY AREAS OF RESPONSIBILITY:

What you will do:

Technical Responsibilities:
* Research, design, develop, modify, and verify components and systems for medical devices with minimal supervision.

* Translate user needs to design inputs/ specifications and produce system-level designs.

* Develop and analyze solutions, prototyping one or more options to provide proof of concept.

* Apply fundamental and some advanced concepts, practices and procedures for problem solving.

* Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements.

* Develop bench testing methods, conduct measurement system analysis, and develop DOE.

* Conduct research and studies to support product design. Business Responsibilities:
* Demonstrate advanced understanding of customer needs and design inputs.

* Demonstrate proficiency with product's intended use and clinical procedures.

* Learn how the financial models are constructed

* Support Voice of Customer sessions internally and with clinicians to develop an understanding of customer needs

* Apply understanding of customer needs to development of robust and appropriate design inputs.

* Understand the product's intended use and clinical procedures.

* Apply understanding of the impact of design decisions on production metrics (COGS, yield, etc.). Med Device Compliance:
* Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements.

* Independently create or refine engineering documentation, such as the Design History file.

* Follow R&D procedures like design controls and risk management, per the Quality Management System.

PREFERRED QUALIFICATIONS:

What you will need (strongly desired):
Technical

Skills:

* Vascular device engineering preferred

* Technical ability to develop and optimize designs for medical device assemblies, incorporating DFM principles and clinical feedback and knowledge.

* Ability to communicate basic plans and technical information to team members, leaders, and project managers

* Technical knowledge in creating product test fixtures and developing test methods for verification and validation activities

* Fundamental knowledge and understanding of engineering practices, tools, and design principles within a regulated environment.

* Demonstrated ability to influence and drive results through others. Work Authorization:
Must be currently located and authorized to work in the United States without current transfer or future sponsorship requirements.

- No C2C or third-party candidates. ~
*** Kelly does not expense relocation/interview costs.
*** Important information:
To be immediately considered, please send an updated version of your resume to .