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Quality Assurance Engineer I
hace 2 meses
Zimmer Biomet is a leader in the medical technology sector, dedicated to enhancing patient mobility through innovative products and solutions. Our commitment to quality and excellence has been at the forefront of our mission for nearly a century.
Role Overview
As a Quality Engineer I, you will play a crucial role in ensuring that our products meet established standards and requirements. This position involves collaboration with various departments, suppliers, and external experts to achieve our quality objectives.
Key Responsibilities
- Develop and establish procedures, specifications, and standards for Zimmer Biomet products and processes.
- Implement corrective and preventive action plans to address quality issues.
- Collect and analyze data for product evaluation and gauge performance.
- Identify essential personnel, gauges, procedures, and materials necessary for new product development.
- Ensure suppliers are equipped with the necessary information and resources to deliver high-quality products.
- Proficiency in English (C1 level).
- Bachelor's degree in engineering or a related field, with certification as a quality engineer (e.g., CQE).
- 0-3 years of relevant work experience.
- Certification as a Quality Engineer (CQE) and experience in the medical device sector, particularly in orthopedics, is preferred.
- Strong understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methodologies.
- Excellent skills in Microsoft Office Suite (PowerPoint, Word, Excel).
- Ability to communicate effectively in both written and oral formats across various levels of the organization.
- Demonstrated potential for future development opportunities.
- Up to 10% travel may be required.
