Quality Engineer - (V295711)

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. This is a contract position for one of the largest medical device companies globally.
Principal Duties and Responsibilities:
Formulates procedures, specifications, and standards for products and processes.
Develops and implements corrective/preventative action plans.
Collects and analyzes data for gauge and product evaluation.
Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.
Ensures that suppliers have necessary information and facilities to deliver quality products.
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.).
Ability to deliver, meet deadlines and have results orientation.
Able to communicate both orally and in written form to multiple levels of the company.
Demonstrates characteristics of high potential for future development opportunities.
Microsoft Office Suite
Basic knowledge of metrology, geometric dimensioning and tolerancing, Quality System Regulations/standards (ISO 9001) and calibration methods/systems.
Education/ Experience Requirements:
B.S. degree (engineering preferred) plus 2 years of experience in a Quality Engineering role. Supervisory experience strongly preferred.

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