Zimmer Biomet is a global medical technology leader.
Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.What You Can ExpectResponsible 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 ZB to achieve Zimmer Biomet Quality goals.How You'll Create Impact Formulates procedures, specifications, and standards for Zimmer products and processes.
Develops and implements corrective/preventive 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 the required information and facilities to deliver quality products to Zimmer.
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.).
High attention to detail in analytics, presentations, and communication; including logical structuring.
Able to communicate in both oral and written form to multiple levels of the company.
Ability to deliver, meet deadlines, and have results orientation.
Excellent Microsoft Office skills (PowerPoint, Word, and Excel) Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods.
Ability to define project goals and objectives, and track and report progress against defined goals to project stakeholders across multiple functional groups (internal and external, such as suppliers).
Demonstrates characteristics of high potential for future development opportunities.
Your Background English proficiency is required (C1) B.S.
in engineering or an alternative Bachelor's degree program with certification as a quality engineer (e.g.
CQE).
0-3 years of work experience.
Combination of education and experience may be considered (in evaluating experience relative to requirements) Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred Fluent in English, both in written and oral communication.
Experience in medical device regulations is a plus .
Please note that you must submit your resume in English at the time of applying, or your application will not be considered.Travel Expectations Up to 10% EOE/M/F/Vet/Disability
