Elevate your career as a Quality Engineer with Zimmer Biomet. Focus on regulatory compliance, product quality, and design support in a collaborative environment.
Zimmer Biomet seeks a Quality Engineer I to ensure compliance and quality throughout the product lifecycle. This on-site role, requiring presence three days a week, works closely with multi-disciplinary teams to meet business objectives. Engage in design controls, risk management, and verification activities supporting patient mobility.
Key Responsibilities:
- Ensure compliance with FDA, ISO standards
- Collaborate on design and change control processes
- Review and maintain Design History and Risk Management Files
- Identify design risks using FMEA tools
- Analyze quality data for improvements
Requirements:
- B.S. in Engineering or related field
- Experience in design control and V&V activities
- Knowledge of risk management principles
- Strong communication and technical writing skills
- Familiarity with Windchill, Jira, and Minitab
Excite your potential by bringing quality assurance expertise to Zimmer Biomet, enhancing global health outcomes.
Quality Engineer at Zimmer Biomet in Montréal employer: Zimmer Biomet
At Zimmer Biomet, we pride ourselves on being an exceptional employer that fosters innovation and collaboration in the medical technology sector. Our commitment to employee development is reflected in our robust resource groups, flexible work environment, and competitive rewards tailored to our location. Join us to be part of a culture that values recognition, inclusivity, and the opportunity to make a meaningful impact on patients' lives worldwide.
