Company Overview
AMETEK, Inc. is a global leader in industrial technology solutions, serving a wide range of specialized markets with annual sales exceeding $7.0 billion.
With a workforce of approximately 21,000 employees across 35 countries, AMETEK is dedicated to solving its customers’ most complex challenges through innovative and differentiated technology solutions.
At the core of AMETEK’s success is the AMETEK Growth Model, which drives long-term, sustainable growth through four key strategies:
- Operational Excellence
- New Product Development
- Global and Market Expansion
- Strategic Acquisitions
These strategies are further strengthened by a disciplined focus on cash generation, capital deployment, and talent development, creating a scalable platform for continuous growth.
AMETEK operates through two primary business groups, each offering highly specialized technologies and holding leading positions in niche markets:
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Electronic Instruments Group (EIG) – Specializes in the design and manufacturing of advanced analytical, test, and measurement instrumentation for industries including aerospace, medical, power, energy, research, and industrial markets.
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Electromechanical Group (EMG) – Focuses on highly engineered solutions, including medical components and devices, automation systems, thermal management solutions, specialty metals, and electrical interconnects.
About the Job
The Quality Auditor Technician plays a crucial role in ensuring optimal product quality and assisting engineers in resolving quality-related issues. This position applies fundamental quality principles and industry best practices to enhance product standards and improve quality systems efficiently and effectively.
Key Responsibilities
- Conduct investigations and generate reports on technical data as needed.
- Identify and recommend solutions for quality issues, including RGA, CAPA, and NCMR.
- Inspect, measure, and document product quality at various stages of production.
- Record and verify inspection data in the electronic SPC system and generate reports.
- Alert the Quality Manager about deviations from specifications and initiate NCMRs and Discrepant Material Reports.
- Perform gage R&R, first article inspections, and validation data collection as required.
- Receive cross-training in all Quality Department functions, including receiving inspections, work order reviews, and shipping verification.
- Serve as a substitute for inspectors or technicians when necessary.
- Carry out additional tasks as assigned.
Requirements for Consideration
- High school diploma or GED required.
- Knowledge of ISO standards, GDP, GMP, and FDA QSRs is a plus.
- Strong attention to detail.
- Excellent verbal and written communication skills.
- Previous experience in a manufacturing environment.
- Basic computer proficiency, with familiarity in Microsoft Office Suite preferred.
- Ability to follow directions, take initiative, and work independently most of the time.
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