Quality Engineer Ii

Contract Duration: 01/04/2027 - 01/03/2028
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, and experts outside to implement
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 to

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
Travel Requirements
Up to 20%