Quality Engineer I

Quality Engineer

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.

As a Quality Engineer in this role, you will be responsible for evaluating product conformity of medical devices throughout their lifecycle at the distribution center. Employee will oversee activities from receiving, installation, servicing, and end of life from a quality perspective to ensure user and patient safety.

• Perform receiving product inspections a. Follow established procedures and processes to determine compliance of product b. Document and report nonconforming product through Nonconformance Reports (NCR)

• Support creation, revision, and implementation of processes and written instructions
• Review servicing records for work performed on product
• Performs other tasks within the functional work area, as instructed by the Supervisor or Designee. 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.

Expected Areas of Competence (i.e., knowledge, skills and abilities)

• Must possess good communication (oral and written) skills.
• Team work and customer focus oriented.
• Computer literate with proficiency in the use of MS Office Suite (Word, Excel, PowerPoint, etc.) or similar office applications.

Education/Experience Requirements

• 1-3 years experience in a regulated environment, preferably in the medical device field
• Experience performing product inspections preferred
• Experience working within a quality team, with a basic understanding of the associated standards and regulations preferred

Licenses/Certifications
• Bachelor's or Associates degree preferred

EOE/M/F/Vet/Disability