*Urgent requirement*

*Please send resume @ **bi...@tresourceinc.com* <bi...@tresourceinc.com>

Hi,

I have an urgent requirement with one of my clients, details given below.
If you find yourself suitable for the position, please send me your latest
updated resume along with contact details. Please include your employer
details as well.

*Job Title*

*Quality Engineer*

*Project Location*

*Minneapolis MN*

*Duration*

*6+Months*


*POSITION RESPONSIBILITIES: *

   - Provide Supplier Quality Engineering leadership to product development
   programs responsible for new medical device product (parts and materials)
   - Provide input to and align activities to program project planning
   - Provide technical expertise during supplier evaluation and selection
   - Lead efforts to characterize the supplier’s product
   - Lead efforts to characterize the supplier’s process
   - Coordinate with materials characterization and qualification
   activities into the product
   - Lead efforts to prepare the supplier’s product for production release
   - Facilitate transference of product from development to production.
   - Apply QSR 21CFR Part 820 (Medical Devices) to everyday application of
   Supplier Quality Engineering activities.
   - Define, establish and implement supplier quality assurance processes
   for medical device product.
   - Interface with Medtronic inspection, technical and engineering
   employees for the development and review of qualification and inspection
   processes and procedures.
   - Initiate and maintain appropriate corrective and preventive action per
   defined procedures.
   - Lead or participate in product, business process or quality system
   level improvement initiatives and activities including Global Supply Chain
   initiatives and Neuromodulation sector system development.
   - Collaborate with peers across Medtronic to achieve common supply chain
   and operational goals with shared suppliers.
   - Provide training and coaching to suppliers, or Medtronic personnel on
   Quality System Regulation, ISO and Neuromodulation quality systems
   requirements.
   - Participate in internal and supplier audits.
   - Travel as required to support assigned projects or other application
   work requirements.
   - Other duties as assigned.

*BASIC QUALIFICATIONS: *

   - *Bachelor’s degree in Engineering with 7+ years of experience OR*
   - *Master’s degree in Engineering with 5+ years of experience*
   - *5+ years supplier engineering experience*

*DESIRED/PREFERRED QUALIFICATIONS: *

   - Knowledge of one or more manufacturing processes such as contract
   manufacturing, finished device assembly, stamping/forming, injection
   molding, machining, extruding, coating, plating, foundry, etc.
   - Experience with Test Method Validation (Measurement Systems Analysis,
   Gage R&R, correlation and uncertainties) including gage and fixture design.
   - American Society for Quality Certified Quality Engineer and/or
   Certified Quality Auditor
   - Experience with data analysis software applications such as MiniTab,
   StatGraphics, SmartProfile or equivalent
   - Multiple engineering discipline (electronic, mechanical, chemical,
   etc.) experience is a plus
   - Experience in program or project leadership, and associated
   communication, presentation, team facilitation and influence management
   skills.
   - Knowledge, understanding and implementation experience with medical
   device quality systems, manufacturing operations, supplier quality, and
   regulatory requirements.
   - Demonstrated high proficiency with word-processor, spreadsheet, and
   database software









Thanks & Regards



*BIPIN RAJ *

Sr. US IT Recruiter (Talent Acquisition)

Technology Resource Group Inc

3736 Hills-Dale Court,
Santa Clara, CA 95051

Direct: 408-709-1760 Ext : 9818,



*G talk:* <G%20talk:> bipin.rgtal...@gmail.com

bi...@tresourceinc.com



                                              www.tech-resource.com

<https://www.linkedin.com/company/technology-resource-group-inc->
<https://twitter.com/TechResourceInc>

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