Jessica Rios

Tech II QA

Cardinal Health

07.2010 - Current

Responsible for verifying, inspecting, dispositioning, and documenting results of all the in-process and final pack product inspections as per applicable procedures including line clearances.
Follow the appropriate QCIC's, drawings or specifications, S.O.P.'s, TM, and determines the disposition of subassemblies and finished goods. Ensures non-conformant product is identified and segregated. Escalates issues to supervisor when non-conformances are issued.
Performs validation protocol inspections as per business needs.
Inspect all first articles, following the appropriate QCIC's, drawings or specifications, S.O.P.'s, TM, and determines the disposition of such goods.
The incumbent performs line clearances, including label room, and ensures documentation completeness according to procedures.
Maintains quality control records, procedures, and other documentation accurate, updated and properly organized files.
Responsible for assuring that all shop orders are accompanied with the corresponding copy of Non-Conformance Reports when applicable.
Maintains all equipment used for testing and measuring, and keeps the working area in a clean, well-organized condition.
Performs review of shop orders for completeness and accuracy.
Inspects pallet configuration, quantity and information at finished goods staging area as required.
Submits DCN’s when updates to controlled documents is required.
Produces printed labels per instructions contained in the Label Control Room
Ensures that all labels are correctly printed according to the Device Master Records, including specifications, drawings, procedures, and electronic files.
Assists in training of new Quality Inspectors.
Agile and PRMS knowledge.
Provide support to the Incoming and Product Release Area as require