Operario De Producción Y Bodega — Turnos Rotativos

Servimos S.A.S

Bogotá ciudad

Sur place

COP 40 000 000 - 90 000 000

Plein temps

14 jours+

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Résumé du poste

Zimmer Biomet is seeking a Quality Engineer to ensure products meet established requirements through audits, inspections, and testing. You will interact with multiple departments and external suppliers to implement quality goals.

The role requires a CQE certification, a B.S. in engineering, and at least one year of experience. Travel up to 20% is expected and collaboration across teams is essential.

Qualifications

  • B.S. in engineering or an equivalent with CQE certification.
  • Minimum 1 year of relevant work experience.
  • CQE certification and orthopedic medical device experience preferred.

Responsabilités

  • 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.

Connaissances

Team collaboration
Deadline-oriented
Written and oral communication
FMEA
QSR/ISO regulations

Formation

Bachelor of Science in Engineering
Certified Quality Engineer (CQE)

Outils

CMMs
Optical comparators
Geometric Dimensioning and Tolerancing
Microsoft Office Suite

Description du poste

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
Principal Duties and Responsibilities:
  • 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
Expected Areas of Competence (i.e., knowledge, skills and abilities)
  • 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
Education/Experience Requirements
  • 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 preferred
Travel Expectations

20%

EOE/M/F/Vet/Disability

EOE/M/F/Vet/Disability

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