Zimmer Biomet
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
What You Can Expect 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 Zimmer Biomet to implement Zimmer Biomet Quality goals.
How You’ll Create Impact
Helping with different supplier functionalities and project managing.
Formulates procedures, specifications, and standards for Zimmer products and processes.
Develops and implements corrective/preventative action plans.
Collects and analyzes data for gauge and product evaluation.
Maintains critical gauges, procedures, and materials needed to maintain existing products.
Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet.
What Makes You Stand Out
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.
Your Background
B.S. in Engineering.
Experience in the role.
Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred.
Travel Expectations
Up to 5%.
EOE/M/F/Vet/Disability
#J-18808-Ljbffr
What You Can Expect 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 Zimmer Biomet to implement Zimmer Biomet Quality goals.
How You’ll Create Impact
Helping with different supplier functionalities and project managing.
Formulates procedures, specifications, and standards for Zimmer products and processes.
Develops and implements corrective/preventative action plans.
Collects and analyzes data for gauge and product evaluation.
Maintains critical gauges, procedures, and materials needed to maintain existing products.
Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet.
What Makes You Stand Out
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.
Your Background
B.S. in Engineering.
Experience in the role.
Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred.
Travel Expectations
Up to 5%.
EOE/M/F/Vet/Disability
#J-18808-Ljbffr