8006BR - Supplier Quality Engineer  (Jobs - Full Time Jobs)

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Ad ID 158800  In Category: Jobs > Full Time Jobs

8006BR - Supplier Quality Engineer

8006BR - Supplier Quality Engineer LOCATION: Mahwah, NJ (RELOCATION AVAILABLE) (07430) 50% Travel SPONSORSHIP AVAILABLE

This is a retainer based executive search, our client is a global leader in medical technology that consist of orthopedic products in over 120 countries. This position is for a Supplier Quality Engineer based in Mahwah, NJ. If you are interested please send your resume and I will reply ASAP.



POSTION DETAILS

Salary Range: $75k to 85K Plus a 6K bonus

Best Industry: Engineering , Engineering Consulting , Medical Device ,Technical Support

Best Department: Engineering , Medical Devices , Project Management

50% Travel

SPONSORSHIP AVAILABLE/H1b Transfers

RELOCATION AVAILABLE

4 year degree required

5-10 years experience



JOB DESCRIPTION:

1. Responsible for providing technical support to internal customers and suppliers for activities related to supplier quality system assessment, performance evaluation and supplier development.

2. Will work with internal customers and suppliers in support of supplier selection, supplier development and certification, and the establishment of process equivalence.



ESSENTIAL DUTIES AND RESPONSIBILITIES:

Liase with internal customers to support supplier development and certification.

Lead and performs supplier quality system audits on new and existing suppliers to 21CFR 820, ISO 13485:2003 and other applicable Standards to assess a suppliers' capabilities and ability to meet Corporate and regulatory requirements.

Work with new and existing suppliers develop internal processes and controls using; 6 sigma tools, root cause analysis, process capability assessment (Cpk), process validation, statistical techniques, gage R&R, pFMEA, control plans, and mistake-proofing (poke-yoke).

Work with new and existing suppliers in support of supplier certification activities, including product source and skip-lot inspection.

Assist in the development, review, approval, implementation and/or training of process and equipment validations.

Issue corrective action requests to suppliers in response to audit findings and/or internal Stryker issues.

Ensure effective closure, by working with suppliers to ensure comprehension, development, and execution of corrective/preventive action with regards to any nonconformities cited during audits.

Maintain supplier database, files and approved supplier list (ASL).

Develop and conduct effective training programs on related QA topics



ADDITIONAL INFORMATION:

CQE, CQA, and/or Black belt certification preferred.

Project Management experience.

High level of PC Proficiency.

Strong interpersonal, organizational and written/verbal communication skills.

Ability to understand technical drawings and GD&T.

Self starter with demonstrated analytical and problem solving skills.

Ability to manage multiple tasks in a fast paced environment.

Self-motivated with the ability to effectively work with others in various coordinate disciplines, on multi-national teams, and to prioritize tasks in a deadline-driven environment.



CANDIDATE MUST HAVE:

5+ years experience in a medical device or other regulated industry.

Bachelor's degree in Mechanical or Industrial Engineering.

Related Link : (None)
Target State : New Jersey
Target City  : Mahwah
Ad Owner Name: The Barron/Carlington Group
Contact Phone: (None)
Contact Email: gg@barronsys.com
Last Update  : 2008/08/08 10:17:54 AM
Number of Views: 23



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