Quality Engineering Technician

Zimmer GmbH; Farmingdale (NJ); On-site; USD 60,000 - 80,000; Full time

Job summary

Une entreprise leader en technologie médicale recherche un support qualité pour participer aux opérations quotidiennes et s'assurer que les procédures sont respectées. Le poste exige une interaction active dans divers projets et une connaissance approfondie des systèmes de qualité et des réglementations. Ce rôle nécessite des compétences en technique écrite et une expérience dans la résolution de problèmes dans un environnement de fabrication.

Qualifications

• Au moins cinq ans d'expérience pertinente.
• Connaissance des réglementations FDA et ISO est un plus.
• Capacité à lire et interpréter des plans et dessins.

Responsibilities

• Soutenir les ingénieurs qualité dans les opérations quotidiennes.
• Participer aux investigations liées aux NCRs et aux plaintes des clients.
• Développer et publier des plans de suivi de métriques pour la calibration.

Skills

Technical writing

Documentation practices

Problem-solving

Communication

Education

High school diploma or GED

ASQ Quality Technician Certification

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.

What You Can Expect

Supports quality engineers in daily operations, including 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 participates in special projects. Performs all duties in compliance with company procedures, GMPs, SOPs, and other relevant regulations.

How You'll Create Impact

• Identify, report, and address calibration out of tolerance (OOT) incidents promptly.
• Participate in investigations related to NCRs, OOT, and Customer Complaints.
• Develop and publish metric trending plans for calibration; assist with CAPA resolution.
• Assist in revising operational procedures and CI initiatives.
• Deliver training to team members on relevant tasks.
• Participate in department and cross-functional meetings as needed, especially in the absence of the QA Calibration Engineer.
• Execute validation protocols, perform Gage R&R testing, analyze data, and prepare reports.
• Complete Vertex, CMM programming, and SPC template documentation.

This list is not exhaustive and may not include all essential functions for the role.

What Makes You Stand Out

• Proficient in technical writing.
• Strong knowledge of good documentation practices and manufacturing processes.
• Ability to read and interpret blueprints and drawings.
• Knowledge of Geometric Dimensioning & Tolerancing (GD&T).
• Excellent communication, organization, and problem-solving skills.
• Ability to work independently and under pressure.
• Initiative and sound judgment in performing duties.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Knowledge of FDA and ISO regulations is a plus.

Your Background

• High school diploma or GED required.
• At least five years of relevant experience.
• ASQ Quality Technician Certification is highly desirable.

Travel Expectations

Less than 5% travel expected.

EOE/M/F/Vet/Disability