Quality Engineer I
Careers.zimmerbiomet.com
Apply to this jobAt 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
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.
How You'll Create Impact
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.
What Makes You Stand Out
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
Physical Requirements
EOE/M/F/Vet/Disability
Summary
Evaluate product conformity, perform inspections, support process creation, ensure safety and compliance.
Job title
Quality Engineer I
Experience level
1-3 years
Minimum experience
1+ years exp
Industry
medical technology
Location requirements
Olive Branch, Mississippi, United States, on-site work only
Salary
Not specified
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
Olive Branch, MS 38654, USA