Quality Engineer I

Zimmer Biomet

Bengaluru

Hybrid

INR 300,000 - 460,000

Full time

3 days ago
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Job summary

Zimmer Biomet in Bengaluru is seeking an entry-level Quality Engineer I to assure products meet requirements through audit, inspection, and test activities. You will collaborate with multiple functions and suppliers to implement quality goals.

The role involves formulating procedures, data analysis for gauge and product evaluation, and supporting CAPA processes. The site offers hybrid work and opportunities to grow in a global medical technology leader.

Qualifications

  • B.S. in engineering and CQE certification preferred.
  • Experience with FMEA and GD&T is desirable.
  • Ability to use CMMs and optical comparators for inspection.
  • Strong written and verbal communication skills.
  • CAPA development and implementation experience is a plus.
  • Familiarity with QSR/ISO regulations and product testing methods.

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.

Skills

Team collaboration
Oral and written communication
Results oriented
MS Office proficiency

Education

B.S. in engineering
CQE certification

Tools

CMMs
Optical comparators
Geometric Dimensioning & Tolerancing (GD&T)
Blueprint reading
FMEA
QSR/ISO regulations

Job 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

The Quality Engineer I is an entry level position 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.

Work Location: Bangalore

Work Mode: Hybrid (3 Days in office)

Shift Timing - 11:00 AM - 8:00 PM

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
  • Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing and inspection methods, and ability 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).
  • Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred
  • Familiarity with FMEA (Failure Mode & Effects Analysis).
  • Ability to use CMMs (Coordinate Measuring Machines).
  • Ability to develop and implement CAPA (Corrective & Preventive Action).
  • Strong oral and written communication
  • Good to have:
    • Understanding of Geometric Dimensioning & Tolerancing (GD&T).
    • Blueprint reading. QSR/ISO regulations. product testing methods.
    • Medical Device Industry experience.
Travel Expectations

Up to 20%

EOE/M/F/Vet/Disability

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