Coordinador De Producción Textil - Maquilas

Agencia De Empleo Cafam; Bogotá; Hybrid; COP 48.000.000 - 96.000.000; Vollzeit

Zusammenfassung

Zimmer Biomet is seeking a Quality Engineer to assure products conform to established requirements through audits, inspections and testing. You will interact with multiple departments and suppliers to achieve quality goals.

The role requires a CQE or equivalent engineering background, at least 1 year of experience, and the ability to work in a hybrid environment with up to 20% travel.

Qualifikationen

• B.S. in engineering or equivalent with CQE certification.
• Minimum 1 year relevant work experience.
• Certified Quality Engineer (CQE) and medical device experience preferred.

Aufgaben

• Formulates procedures, specifications, and standards for Zimmer products and processes.
• Develops and implements corrective/preventive action plans.
• Collects and analyzes data for gauge and product evaluation.
• Identifies critical personnel, gauges, procedures, and materials needed for new products.
• Ensures suppliers have information and facilities to deliver quality products.

Kenntnisse

Blueprint reading

GD&T

FMEA

MS Office

QSR/ISO knowledge

Ausbildung

B.S. in engineering

CQE certification

Tools

Optical comparators

CMMs

Jobbeschreibung

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

• 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 new products.
• 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.
• 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 are able to use optical comparators and CMMs

Your Background

• B.S. in engineering or an alternative Bachelor's degree program with certification as a quality engineer (e.g. CQE).
• Minimum 1 year of relevant work experience.
• Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preference.

Travel Expectations

• 20%
• Hybrid role.
• Monday to Friday (8:00am to 5:00pm).

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