Quality Engineer

The Quality Engineer will play a key role in supporting the launch and transfer of manufacturing processes at a new Costa Rica site, ensuring products meet established quality standards. Responsibilities include formulating procedures, developing corrective actions, conducting audits and inspections, and collaborating with suppliers and internal teams. The role requires a B.S. in engineering or a related degree with quality engineering certification, at least one year of relevant experience, and proficiency in QSR/ISO regulations, FMEA, and product testing methods. Familiarity with Microsoft Office Suite, blueprint reading, and geometric dimensioning and tolerancing is essential. Experience in the medical device, particularly orthopaedic, industry, and Certified Quality Engineer (CQE) certification are preferred. Travel up to 20% may be required.

The Quality Engineer at Zimmer Biomet will play a pivotal role in supporting the launch and implementation of new products at the Costa Rica site. This position is responsible for ensuring that all Zimmer Biomet products meet established quality standards through rigorous audits, inspections, and testing. The role involves collaborating with various departments, suppliers, and external experts to achieve quality goals and maintain compliance with regulatory requirements. Candidates will contribute to the development and implementation of quality management systems, support process transfers, and help drive continuous improvement in product manufacturing. The position offers opportunities for professional growth within a supportive and inclusive work environment.

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

This role is part of the combined Operation Quality team supporting the launch of a new Costa Rica site and the initial transfer of manufacturing equipment, processes, and product manufacturing implementation. Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities, and for supporting the use of specific QMS tools required to launch the processes. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals during site implementation.

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.

This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.

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

• Up to 20%

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 assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities.
• Play a key role in shaping procedures, specifications, and standards for Zimmer products and processes.
• Develop and implement corrective and preventative action plans to address quality issues.
• Collect and analyse data for gauge and product evaluation to ensure product quality.
• Identify critical personnel, gauges, procedures, and materials needed for new product completion.
• Ensure that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet.
• Collaborate cross-functionally to implement Zimmer Biomet Quality goals during site implementation.

Skills:

• Ability to work within a team environment and build relationships with internal and external stakeholders such as suppliers and regulatory agencies.
• Proficiency in Microsoft Office Suite, blueprint reading, and geometric dimensioning and tolerancing.
• Thorough understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods.
• Experience using optical comparators and CMMs is required.
• Certified Quality Engineer (CQE) and experience in the medical device, particularly Orthopaedic industry, are preferred.

Education:

• A B.S. in engineering or an alternative Bachelor’s degree programme with certification as a quality engineer (e.g. CQE) is required.