Quality Auditor

The Quality Auditor role is responsible to ensure optimum product quality by utilizing the appropriate metrology instrumentation, sampling plans, and inspection procedures to verify products meet or exceed drawings and specification requirements.

Key Responsibilities

• Inspects, measures, and records results on any products before, during, and after processing using various quality tools such as sampling plans and statistical process control (SPC).

• Examines product visually with unaided eyes or with microscope to ensure products are machined properly.

• Measures products for proper print dimensions manually or with computer-aided measuring equipment.

• Records and verifies inspection data in electronic SPC system and prints SPC reports.

• Notifies Quality Manager of deviations from specifications and initiates NCMR’s and Discrepant Material reports.

• Conducts a Set-Up Quality Audit for all job orders to ensure operator has proper documentation and materials. Reviews the Shop Pack to ascertain it is the proper purchase order, part, revision, material identification, and lot. Matches the blueprint revision letters and labels. Examines and measures initial run before authorizing a start in production.

• Conduct in-process inspections according to inspection plan to ensure processes comply to specification and reviewing SPC data.

• Conducts Final Inspection by visual examination and measurement in accordance with the sampling plan. Prints and reviews SPC reports per the work order. Authorizes shipping of product by verifying labels and certificate of compliance and signing the certificate of compliance.

• Perform gage R&R, and first articles, and may aide in validation data collection.

• Cross-trained in all Quality Department functions including receiving inspection, work order review, shipping verification, and other activities.

• Move MRB product to proper staging in ERP system.

• Perform other duties as directed.

  
  

Requirements for Consideration:

• High school diploma or GED is required.

• Prior experience in a manufacturing environment is preferred.

• Basic knowledge of computer skills including Microsoft Office Suite is preferred.

Working Conditions

Work Environment: Office and Manufacturing Plants as needed

Atmospheric Conditions: Indoors

Temperature Extremes: None

Materials, Tools and Equipment Used: Optical comparator, video inspection equipment, microscopes, various gages and measurement tool, personal computer.

AMETEK Engineered Medical Components (EMC) is a market leader in delivering optimal solutions for the medical device industry. AMETEK EMC provides its customers with over 40 years of experience in: product design and development, precision engineering, pre-production to commercialized manufacturing, supply chain management, and quality assurance for cable assemblies and custom interconnects, laser processed polymers, catheter assemblies and sub-components, laser processed metals including NiTi and metal post processing. EMC’s experience has been applied to virtually all medical device markets from Electrophysiology to Neuromodulation, Cardiac Rhythm Management to Patient Monitoring, Ultrasound to Electrosurgical, and Diabetes to Peripheral Vascular.

AMETEK EMC's expertise stems from its passion for innovation and collaboration with customers to address complex challenges and produce optimal solutions. It does this by leveraging dynamic and innovative capabilities, collaborative engineering, and technical expertise with a proven record of excellence in solution delivery for new and existing products.