Quality Engineer II
Description
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.
How You'll Create Impact
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What Makes You Stand Out
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Your Background
- B.S. in engineering or an alternative Bachelor’s degree (Biomedical, Mechanical or other Engineering also considered).
- Minimum 1 year of relevant work experience in manufacturing.
- Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience in manufacturing plant (medical devices, pharma, metalworking).
- Hands - on experience in process validation (IQ-OQ/PQ)
Nice to have:
- Experience in medical devices.
- Knowledge of ISO 13485/21CFR 820
- CQE or similar quality certification
- Experience with mesuring equiptment.
Travel Expectations
Travel: 20%
Hybrid role: 4 days per motnh on site in Bogotá.
Schedule: Monday to friday. 8:00am - 5:00pm.
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EOE/M/F/Vet/Disability
