Quality Engineer II

JOB DESCRIPTION:

Job Summary

Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, or quality goals

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.

This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.

Expected Areas of Competence (i.e., knowledge, skills and abilities)

· 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
· Proficient in blueprint reading and geometric dimensioning and tolerancing, thorough understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs.

Education/Experience Requirements

· B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE).
· Minimum 1 year of relevant work experience.
· Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred

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