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QC Specialist

Location: Windsor, CT, United States
Date Posted:

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The Quality Control Specialist performs inspections and analytical tests, throughout the
manufacturing process to ensure compliance to specifications under the supervision of Quality
Management. Other tasks may include review of documentation for final product release and works independently on assigned projects or tasks to support the Quality System.
8am - 4:30pm Monday - Friday
  • Perform incoming inspection of raw materials in accordance with raw material specifications.
  • Maintain all specification files (customer & raw materials)
  • Makes final approval of products for shipment.
  • Performs inspection and testing of products.
  • Conducts finished product audits.
  • Consults manufacturing on quality issues in Converting and Coating operations.
  • Coordinates shipments with Customer Service, Shipping, Converting, and Quality.
  • Records, charts and analyzes test data for comparison purposes.
  • Tests finished products in accordance with Product Requirement Sheet, (PRS), and Tech 11.
  • Types of tests include, but are not limited to peel, shear, tack and adhesion to release.
  • May perform additional tests to meet customer's certification requirements.
  • Reviews and approves testing performed by other Quality Assurance technicians.
  • Prepares non-conforming reports and reports findings to Quality Engineer and Quality Assurance Manager.
  • Input raw material and finished product test requirements in ERP system.
  • Perform usage decisions in ERP system based on raw material and finished product test/inspection results.
  • Initiate internal and supplier complaints for non-conforming material.
  • Consults and communicates with managers on quality issues
  • Provides the appropriate training and assistance, as needed.
Essential Skills / Experience / Qualifications:
  • Excellent communication and able to collaborate and work well with others.
  • Proficient use of Microsoft Office suite of products (Word, Excel).
  • Knowledge of ISO standards (e.g. ISO 9001 and ISO 13485).
  • Must be able to evaluate quality based on the use and interpretation of product/process specifications.
  • Must be able to evaluate quality based on product specifications and alert manufacturing when product is non-conforming.
  • Proficient technical writing
Desirable Skills / Experience / Qualifications:
  • 3 years experience in Quality Assurance or Quality Control.
  • 2 years experience in medical device or industrial manufacturing.
Work Environment / Physical Demands:
Manufacturing / Laboratory environment, standing for long periods.