Zimmer Biomet-posted 2 months ago
$65,000 - $75,000/Yr
Full-time
Farmingdale, NJ
5,001-10,000 employees
Miscellaneous Manufacturing

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.

  • Works with the quality engineers supporting day to day operations, Non Conformance Reports-(NCRs), Out of Tolerance Gage Reports, Customer Complaints, Corrective and Preventive Action- (CAPA) development and implementation, Operational Procedures revisions and Continuous Improvement (CI) initiatives.
  • Actively supports and participates in special projects.
  • Identify, report and seek corrections for calibration out of tolerance (OOT) incidents in a timely manner.
  • Participate in investigations: Non Conformance Report (NCR), Out of Tolerance, and Customer Complaints.
  • Publish Metric Trending Plans for Calibration and assist with Corrective and Preventive Action (CAPA) resolution.
  • Assist with revising Operational Procedures and Continuous Improvement (CI) initiatives.
  • Deliver training to other team members that will perform tasks related to the same area.
  • Participate in department and cross functional meetings in the absence of the QA Calibration Engineer.
  • Execute validation protocols, gage repeatability and reproducibility (R&R) testing, data analysis and complete the required reports.
  • Complete Vertex, CMM programming and SPC template completion.
  • High school diploma or GED is required.
  • 3 years of relevant experience preferred.
  • Proficient technical writing abilities.
  • Broad knowledge of good documentation practices and good manufacturing processes.
  • Ability to read and interpret blue prints and drawings.
  • Knowledgeable in the area of Geometric, Dimensioning & Tolerancing (GD&T).
  • Excellent communication, organization and problem solving skills.
  • Able to work with minimum supervision and under pressure.
  • Takes initiative and makes good judgment in the performance of duties.
  • Computer literate: Microsoft Word, Excel and Power Point.
  • ASQ Quality Technician Certification is highly desirable.
  • Knowledge in FDA & ISO regulations are a plus.
  • Development opportunities
  • Robust employee resource groups (ERGs)
  • Flexible working environment
  • Location specific competitive total rewards
  • Wellness incentives
  • Culture of recognition and performance awards
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