Quality Control Inspector

Job Summary:

The Quality Control Inspector I is responsible for inspecting, testing, and auditing raw materials and finished products, as well as releasing finished products.


* Attention to detail is an expectation.


* Demonstration of commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures.


* Inspect and release raw materials, components, sub-assemblies, and finished devices according to procedure.


* Drives continuous improvement activities with cross-functional team members.


* Generate non-conformances and escalate to the Material Review Board in a timely manner.


* Interacts with production areas, manufacturing and design engineering, marketing, quality, and management.

Job Duties:


* Promotes a work environment of continuous improvement that supports CQ Medical's Quality Policy, Quality System, and the appropriate regulations.


* Assists with communicating business-related issues or opportunities for improvement to management.


* Accountable for compliance with applicable US and International regulations and directives including, but not limited to, Food & Drug Administration (FDA), Canadian and European Union regulations.


* Works in a team environment to achieve metrics.


* Interprets engineering drawings, schematic diagrams, sampling tables, or formulas and confers with management or engineering staff to determine quality and reliability standards.


* Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, mechanical, or chemical characteristics.


* Records test data, applying statistical quality control procedures using GMP documentation practices.


* Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability.


* Quarantines all incoming material until testing is accepted.


* Quarantines all non-conforming material during any step of the manufacturing process until the Material Review Board dispositions the material.


* Purging of records as required.


* Maintains a neat and organized work area.


* Remains current on all required training.


* Conducts calibrations and works with 3^rd party calibration providers to ensure inspection equipment meets specifications.


* Conducts transactions in the Quality Management System and/or ERP system to detail the disposition of incoming and in-process materials.

Working Conditions:


* 50 lbs.

of lifting required for this role


* Hearing protection, safety glasses, safety shoes, and gloves are required for this role


* Required exposure to biohazard

Job Qualifications:


* Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.


* Ability to write routine repo...