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Quality Inspector 2nd Shift
Job ID:00004HM1
Category:Quality Control
Location:CA Camarillo
Hours:40 Monday to Friday 2pm to 1030pm
Pay:$19.16 $19.16
Great Opportunity Available in Camarillo
Job Description
The Quality Inspector will provide quality-support to the packaging area, to include oversight for adherence to GMPs FDA, and DEA compliance. The Quality Inspector will utilize practices and techniques within the disciplines of Quality Control, Quality Assurance, and Quality Improvement disciplines. Reads and understands written instructions and SOPs. Knows and understands applicable regulatory requirements that impact job performance. Makes sure relevant activities fall within SOP and regulatory requirements to ensure product conformity. Prioritizes multiple tasks simultaneously completes tasks in timely manner. Reviews Master Batch Record for accuracy prior to packaging run. Checks, verifies, corrects, and approves component and quantities release for production. Checks product lot number information. Reviews inserts and outserts product sample for accuracy. Reviews and approve tray box labels for accuracy. Issues correct labels for production run and quantity. Conducts line verifications. Conducts product in-process inspections at designated intervals. Performs final QA inspection for finished product release. Verifies Packaging Personnel reconciliation for accuracy on finished product release. Prepares print outer box release stickers when finished product is approved for release into inventory. Inspects Packaging Room CleanClear status approve its use for next packaging run. Performs Master Batch Record data entry in required spreadsheets. Receives label inventory reviewverify information data input. Reconciles label inventory sheets. Ensures required approved forms are available in vestibules for packaging personnel use. Performs quality duties as assigned.
Skills Required
HS Diploma or GED. Proficient in MS Office. Working knowledge of measurement instruments. Prior quality assurance or control exp. Able to prepare compliance reports or audit findings.
Skills Preferred
1 year exp pharmaceutical manufacturing preferred. Knowledge of federal and state laws, regulations and accreditation standards. Proficient in ISO, FDA and GMP. Knowledge of Six Sigma and SPC practices.