Quality Engineer Ii (Bogotá)

What You Can Expect

Responsible for executing product failure root cause investigations according to integral requirements to drive product and regulatory compliance. Activities will include but are not limited to complaint evaluation and investigation, the filing of Medical Device & Vigilance Reports, tracking and trending of product quality, identification, execution, and closure of remedial actions, and other complaint handling activities for the global enterprise in compliance with applicable regulations and guidance requirements worldwide.

How You’ll Create Impact

• Perform root cause investigations to drive product improvement and quality.
• Write medical device and vigilance reports to competent authorities and notified bodies.
• Formulate procedures, specifications, and standards for Zimmer products and processes.
• Develop and implement corrective/preventative action plans.

What Makes You Stand Out

...