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Supplier Quality Engineer II

TekWissen LLC

  • Warsaw, IN
  • 12 days ago
  • $37.75

Highlights

client has operations in more than 40 countries around the world Job Title: Supplier Quality Engineer II Work Location: Warsaw, IN Duration: 7 Months Job Type: Temporary Assignment Work Type: Onsite Job Description: Job Summary Responsible for gathering relevant, factual information and data in order to solve quality related problems. Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and able to use optical comparators and CMMs.

Numbers & Facts

LocationWarsaw, IN
IndustryComputer/IT Services
Salary$37.75
Company Size100 to 499 employees
Year Founded2009
Websitehttp://www.tekwissen.com/

Description

Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Client designs, develops, manufactures and markets orthopedics products, including knee, hip, shoulder, elbow, foot and ankle artificial joints and dental prostheses. client has operations in more than 40 countries around the world
Job Title: Supplier Quality Engineer II
Work Location: Warsaw, IN
Duration: 7 Months
Job Type: Temporary Assignment
Work Type: Onsite
Job Description:
Job Summary
Responsible for gathering relevant, factual information and data in order to solve quality related problems. Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents. Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Work effectively/ productively with all departments by developing a team atmosphere. Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Client to implement Client Quality goals.
Principal Duties and Responsibilities:
  • Evaluating process methods and equipment to meet performance and quality requirements.
  • Establishing quality plans for equipment and processes for general and specific product performance needs.
  • Monitoring performance of processes to standards. Applying ISO and QSR requirements to processes and procedures for Client and outside suppliers.
  • Working with suppliers on new product introduction to insurer that quality and performance requirements are fulfilled.
  • Assisting Manufacturing, Sourcing and Development in the interpretation and application of regulations.
  • Developing and maintaining department and project budgets.
Skills:
Expected Areas of Competence:
  • Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
  • Facilitates team efforts on quality engineering projects. Ability to deliver, meet deadlines and have results orientation.
  • Able to communicate both orally and in written form to multiple levels of the company.
  • Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and able to use optical comparators and CMMs.
  • Knowledge of statistics, process control, and process capability.
  • Full working knowledge of all supporting department needs and capabilities, including the ability to discern when inaccurate information is supplied and offer ideas for how to correct it.
  • Thorough knowledge base of existing Client products and a basic understanding of competitive products.
Education:
Education/Experience Requirements:
  • Bachelor's in engineering or an alternative Bachelor's degree program with certification as a quality engineer (e.g. CQE).
  • Certification as a quality engineer (e.g. CQE) or the Reliability Engineer Certification (CRE) granted through the American Society of Quality (ASQ) preferred.
  • 5-years' experience in a Quality Engineering role and Medical device strongly preferred, or an equivalent combination of education and experience.
  • Combination of education and experience may be considered (in evaluating experience relative to requirements).
TekWissen Group is an equal opportunity employer supporting workforce diversity.

About Company

WE THE TEKWISSEN PEOPLE

TekWissen offers you a broader portfolio of services, industry-leading solutions, and the meaningful innovations that give you greater flexibility and speed to respond to market dynamics, reduced costs and risk to improve enterprise performance, and increased productivity to enable growth.

To keep pace with global market demands, TekWissen keeps its finger on the pulse of change. Our organized approach to guiding a project from its inception to closure. Managing projects is becoming more and more important as we enter the digital era. To cope with the pace that this transition demands, a method is required to manage projects so they can yield quality work, while incorporating efficient use of time and resources.

Project involves identifying which quality standards are relevant to the project and determining how to satisfy them.

It is important to perform quality planning during the Planning Process and should be done alongside the other project planning processes because changes in the quality will likely require changes in the other planning processes, or the desired product quality may require a detailed risk analysis of an identified problem. It is important to remember that quality should be planned, designed, then built in, not added on after the fact.

Capabilities and accomplishments in one TekWissen business enhance the opportunity for success in the others. Put simply, TekWissen's unique combination of attributes promotes success.



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