Quality Engineer

The Quality Engineer at Zimmer Biomet in Bangalore is an entry-level role responsible for ensuring products comply with quality standards through audits, inspections, and testing. The position involves collaborating with departments, suppliers, and external experts to implement quality goals. Key duties include conducting CAPA investigations, product evaluations, statistical analysis, and supporting process improvements. Candidates must have a bachelor’s degree and at least one year of related experience. Familiarity with 21 CFR 820/ISO13485 and experience in regulated industries are preferred. The role requires strong computer skills, particularly with MS Office Suite and Adobe, and the ability to work in a hybrid model with specific shift timings. Medical device experience and windchill familiarity are advantageous.

The Quality Engineer at Zimmer Biomet is an entry-level role focused on ensuring that products meet established requirements and standards through rigorous audit, inspection, and testing activities. This position plays a vital part in supporting the company’s mission to enhance patient mobility by maintaining high standards in quality management. The role involves collaborating with various departments and external experts to implement quality goals and support product development. Candidates will benefit from a flexible working environment, development opportunities, and a culture that values inclusion, recognition, and performance. The position is based in Bangalore and follows a hybrid work model.

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 Enginee 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 - 3:00 PM to 12:00 AM

How You'll Create Impact

• Perform CAPA investigations as assigned.
• Conduct product evaluations in a timely manner to support complaint investigations; Verification of product intended use, product related risk, probable root cause.
• Maintain and analyze department data; perform statistical analysis and identify the need for escalation and/or opportunities for improvement.
• Carry out effective resolution when tasked with difficult or unexpected situations in the workplace, as well as complex business challenges.
• Assist in establishing efficient and streamlined processes across the department.
• Assist in management and assessment of compliance to external standards within the quality management system.
• Provide support to Quality Department as requested and complete assigned tasks accurately and on time.
• Process engineering changes and support product development in design changes
• Other duties as assigned.

What Makes You Stand Out

Your Background

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

Physical Requirements

Travel Expectations

EOE/M/F/Vet/Disability

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

Responsibilities:

• Responsible for performing CAPA investigations as assigned.
• Conduct product evaluations in a timely manner to support complaint investigations and verify product intended use, risk, and probable root cause.
• Maintain and analyse department data, perform statistical analysis, and identify the need for escalation or opportunities for improvement.
• Carry out effective resolution when tasked with difficult or unexpected situations and complex business challenges.
• Assist in establishing efficient and streamlined processes across the department.
• Assist in management and assessment of compliance to external standards within the quality management system.
• Provide support to the Quality Department as requested and complete assigned tasks accurately and on time.
• Process engineering changes and support product development in design changes.

Skills:

• Familiarity with 21 CFR 820/ISO13485 and other government/ISO standards is preferred.
• Experience in regulated industries is required.
• Medical device experience is preferred.
• Experience with windchill is preferred.
• Strong computer skills, including proficiency with MS Office Suite and Adobe, are required.

Education:

• A Bachelor’s degree is required.