Job Information
Zimmer Biomet Quality Engineer I in Bogota, Colombia
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
What You Can Expect
Responsible 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 Zimmer Biomet to implement Zimmer Biomet Quality goals.
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How You'll Create Impact
Formulates procedures, specifications, and standards for Zimmer products and processes.
Develops and implements corrective/preventative action plans.
Collects and analyzes data for gauge and product evaluation.
Identifies critical personnel, gauges, procedures, and materials needed for the completion of servicing activities.
Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet.
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.).
Ability to deliver, meet deadlines and have results orientation.
Able to communicate both orally and in written form to multiple levels of the company.
Demonstrates characteristics of high potential for future development opportunities.
Ability to identify updates to risk files, hazard analyses, and risk controls based on post-market findings
Microsoft Office Suite
Your Background
B.S. in engineering or an alternative Bachelor’s degree program
Minimum 1 year of relevant work experience.
Knowledge of FDA QSR (21 CFR 820), ISO 13485, and ISO 14971 preferred.
Knowledge of design controls, risk management, FMEA, CAPA, root cause investigation and statistical analysis.
Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred
Travel Expectations
EOE/M/F/Vet/Disability