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 ExpectProvide first level Quality Engineering support to production.
Role model quality compliance best practices on shift.
Be the primary point of contact for any quality excursions and act immediately to control all affected product and resolve the non-conformance.
Work with Engineering on new equipment and program releases.How You'll Create ImpactDisposition all non-conforming lots on hold in a timely manner and fully compliant to procedure.Assess all product builders in training for certification readiness.Analyse all gage calibration failures for impact to product and conduct follow-up activities as necessary to control all affected product.Support Engineering through review of program First Article Lay-outs and through qualification of new equipment.Conduct test Method Validations on product acceptance activities.Analyse and report out on all quality performance metrics and take action to address any adverse trends.Support the cleanroom monitoring program and investigate and respond to any out of control eventsAct as the primary Quality point of contact on shift and coach and mentor all production personnel onQuality compliance best practices.Analyse the impact of unscheduled maintenance on the validated state of any process and ensure that the process has been returned to its validated state prior to release of equipment back to production.Support site transformational projects as necessary.Lead yellow belt teams to investigate and resolve any quality compliance or performance issues, as needed.What Makes You Stand OutAdvanced knowledge of the following measurement devices: caliper, micrometer, and optical comparator.In depth knowledge of Good Manufacturing Practices.Familiarity with QSR and FDA requirements.Should be familiar with general dimensioning and tolerances (GD &T).
A knowledge and proficiency in coordinate measuring machine (CMM) operations would be usefulFamiliarity with computer production tracking software or spreadsheet manipulation.Your BackgroundDiploma in Quality or related field.Previous experience in a quality related role desirableEOE/M/F/Vet/Disability