Quality Engineer I

Zimmer Biomet · Bengaluru

  • Experience1–3 yrs
  • SalaryNot disclosed
  • Work modehybrid
  • Leveljunior
  • Posted18 Sept 2026
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About Zimmer Biomet

Zimmer Biomet is hiring in Bengaluru in healthcare. This role looks for around 1+ years of experience.

Skills

  • medical device quality
  • risk management
  • design verification
  • design validation
  • design control
  • quality management
  • FMEA
  • CAPA
  • root cause analysis
  • regulatory submissions
  • quality audits
  • quality data analysis
  • Critical to Quality
  • supplier quality

The role

A quality engineer at a medical technology company assures device compliance through medical device quality, risk management, and design verification, and supports regulatory submissions and CAPA investigations. The role applies ISO 13485 and FDA 21 CFR Part 820 standards across product development and quality improvement.

Full 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

Job Summary

The Quality Engineer 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)

How You'll Create Impact

Principle Duties And Responsibilities

Ensure compliance with global regulations and recognized standards (e.g., FDA 21 CFR Part 820, ISO 13485, ISO 14971, EU MDR).Review, maintain and approve Design History Files (DHF) and Risk Management Files (RMF).Identify and mitigate design risks using FMEA and other tools.Support design verification and validation activities.Supports design and change control processes.Collaborate with design teams to embed quality standards.Author, review and approve documentation in Quality capacity.Define and control Critical to Quality (CTQ) characteristics.Assist with regulatory submissions and audits.Analyse quality data to identify trends and improvement areas.Support quality improvement initiatives.Support root cause investigations and CAPA activities.Supports design transfer and sourcing transfers with Supplier Quality counterparts.Supports customer complaints investigations.Management of product nonconformance, hold and field action records and activities.Support audit, inspection, and regulatory submission readiness activities as needed.

What Makes You Stand Out

Your Background

Education/Experience Requirements

Bachelor’s degree with 1-3 year’s of related experience.Familiarity with 21 CFR 820/ISO13485/IEC 62304 and other government/ISO standards preferred. Experience in regulated industries. Medical device experience preferred.Strong computer skills (MS Office Suite and Adobe).

Physical Requirements

Travel Expectations

EOE/M/F/Vet/Disability