Design Quality Assurance Specialist
Il y a 2 mois
About Zimmer Biomet
Zimmer Biomet is a global medical technology leader dedicated to enhancing patient mobility and quality of life. With a rich history spanning nearly 100 years, our company has been at the forefront of innovation, driving our mission forward with each passing day.
Our Commitment to Excellence
We are committed to creating an environment where every team member feels included, respected, empowered, and recognized. Our focus on development opportunities, robust employee resource groups, a flexible working environment, location-specific competitive total rewards, wellness incentives, and a culture of recognition and performance awards sets us apart as a leader in the industry.
Job Summary
We are seeking a highly skilled Design Quality Assurance Specialist to join our team. As a key member of our quality assurance team, you will be responsible for ensuring that our products conform to established requirements and standards through appropriate audit, inspection, and test activities.
Key Responsibilities
- Formulate procedures, specifications, and standards for Zimmer products and processes.
- Develop and implement corrective/preventative action plans.
- Collect and analyze data for gauge and product evaluation.
- Identify critical personnel, gauges, procedures, and materials needed for the completion of new products.
- Ensure that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet.
Requirements
- Bachelor's degree in engineering or an alternative degree with a certification as a quality engineer (e.g. CQE).
- Proven track record in working as a Certified Quality Engineer (CQE) in the medical devices industry.
- 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.
- Ability to communicate both orally and in written form to multiple levels of the company.
- 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 able to use optical comparators and CMMs.
About You
We are looking for a highly motivated and experienced individual who is passionate about quality assurance and has a strong background in the medical devices industry. If you are a team player with excellent communication skills and a proven track record of delivering results, we encourage you to apply for this exciting opportunity.
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