Zimmer Biomet Careers is hiring for a Quality Engineer I position in Bangalore, Karnataka. This is an entry-level Quality & Regulatory role focused on product quality, testing, inspections, corrective/preventive actions, supplier coordination, and quality standards in the medical-device industry.
Job Overview
| Particular | Details |
|---|---|
| Company | Zimmer Biomet |
| Job Role | Quality Engineer I |
| Job ID | 11668 |
| Location | Bangalore, Karnataka, India |
| Department | Quality & Regulatory |
| Job Type | Full-Time |
| Experience Level | Entry Level |
| Work Mode | Hybrid |
| Office Requirement | 3 days in office |
| Shift Timing | 11:00 AM – 8:00 PM |
| Education | Bachelor’s degree in Engineering or alternative degree + CQE certification |
| Travel | Up to 20% |
| Key Areas | Quality Engineering, CAPA, FMEA, GD&T, Product Testing, Inspection |
About the Role
The Quality Engineer I is an entry-level position responsible for ensuring that products meet established requirements and standards through appropriate audit, inspection, and testing activities.
The role involves collaboration with different departments, suppliers, regulatory agencies, and external experts to support Zimmer Biomet’s quality objectives.
Key Responsibilities
The selected candidate will be expected to:
- Develop procedures, specifications, and standards for products and processes.
- Develop and implement corrective and preventive action plans.
- Collect and analyze data for gauge and product evaluation.
- Identify personnel, gauges, procedures, and materials required for new products.
- Ensure suppliers have the necessary information and facilities to deliver quality products.
- Support product quality and inspection activities.
- Work with multiple internal and external stakeholders.
Eligibility & Qualifications
Candidates should have:
- A Bachelor’s degree in Engineering, or an alternative Bachelor’s degree with a Certified Quality Engineer (CQE) qualification.
- Knowledge of quality engineering principles.
- Familiarity with FMEA (Failure Mode and Effects Analysis).
- Ability to work with CMMs (Coordinate Measuring Machines).
- Ability to develop and implement CAPA (Corrective and Preventive Action).
- Strong written and verbal communication skills.
Preferred Skills
The following skills can strengthen a candidate’s profile:
- GD&T (Geometric Dimensioning & Tolerancing)
- Blueprint reading
- QSR/ISO regulations
- Product testing and inspection methods
- Design assurance
- Medical-device industry knowledge
- Orthopedic industry experience
- Microsoft Office Suite
- Experience with optical comparators
- Experience with CMMs
A Certified Quality Engineer (CQE) certification and medical-device/orthopedic industry experience are preferred according to the listing.
Who Should Apply?
This position is particularly suitable for candidates with:
- An engineering background.
- An interest in Quality Engineering and regulatory processes.
- Knowledge of manufacturing or product testing.
- Familiarity with FMEA, CAPA, GD&T, or quality standards.
- Strong analytical and communication skills.
- An ability to collaborate with engineering, suppliers, and other teams.
Candidates should also be comfortable working in a structured quality environment where documentation and accuracy matter. Because apparently a medical device is one of those things where “close enough” isn’t an acceptable engineering philosophy.
Work Location & Schedule
Location: Bangalore, Karnataka, India
Work Model: Hybrid, with 3 days in the office
Shift: 11:00 AM – 8:00 PM
Travel: Up to 20%
Career Opportunity
Zimmer Biomet operates in the medical-technology industry, and this role provides exposure to quality engineering, product testing, supplier quality, regulatory requirements, CAPA, FMEA, and product inspection.
For candidates interested in medical-device manufacturing and quality engineering, the position can provide a strong foundation in regulated product development and quality systems.
FAQs
Is this a software engineering role?
No. This is a Quality & Regulatory position focused on product quality, testing, inspection, manufacturing processes, and regulatory requirements.
Is the position suitable for freshers?
The listing describes the position as entry level, but it does not provide a specific years-of-experience requirement. Candidates should evaluate their qualifications against the stated engineering/CQE and quality-related requirements.
Is CQE mandatory?
The listing states a Bachelor’s degree in Engineering or an alternative Bachelor’s degree program with certification as a Quality Engineer, such as CQE. It separately says CQE is preferred.
Is medical-device experience mandatory?
No. Medical-device and orthopedic-industry experience are described as preferred, rather than explicitly mandatory.
What is the work mode?
The position is hybrid, with 3 days in the Bangalore office.
What are the working hours?
The listed shift timing is 11:00 AM to 8:00 PM.
Is travel required?
Yes. The listing states that travel may be up to 20%.
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Final Thoughts
The Zimmer Biomet Quality Engineer I position is a good entry-level opportunity for engineering graduates interested in quality engineering, manufacturing, medical devices, product testing, and regulatory compliance.
The strongest candidates will likely be those who can demonstrate knowledge of FMEA, CAPA, GD&T, CMMs, quality standards, testing methods, and structured problem-solving, along with strong communication skills.