Quality Inspector 1st Shift

Crossroadsstaffing; Camarillo (CA); On-site; USD 48,000 - 70,000; Full time

Job summary

Crossroadsstaffing in Camarillo, CA seeks a Quality Inspector to support the packaging area with strict adherence to GMP, FDA, and DEA standards. You will review Master Batch Records, verify labels, and perform in-process inspections to ensure product quality before release.

The role requires a HS Diploma or GED, experience in QA/QC, and proficiency with MS Office. Work will be performed on-site in a pharmaceutical manufacturing setting with attention to regulatory compliance.

Qualifications

• H.S. diploma or GED required; familiarity with quality systems.
• Experience with QA/QC processes and GMP/FDA expectations.
• Ability to read and follow SOPs and regulatory requirements.
• Proficient with MS Office for data entry and reporting.

Responsibilities

• Provide quality-support to the packaging area in line with GMP, FDA, and DEA compliance.
• Review Master Batch Records and confirm accuracy prior to packaging runs.
• Verify and release components, quantities, and product lot numbers for production.
• Inspect packaging labels, inserts/outserts, and tray box labels for accuracy.
• Conduct line verifications and in-process inspections at designated intervals.
• Prepare release stickers and ensure proper inventory labeling and reconciliation.
• Document quality data in required spreadsheets and maintain records.

Skills

Measurement instruments

Quality assurance

Quality control

SOP literacy

Education

HS Diploma or GED

Tools

MS Office

Job description

Great Opportunity Available in Camarillo

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. Working knowledge of measurement instruments. Prior quality assurance or control exp. Knowledge of federal and state regulations. Proficient in MS Office.

Skills Preferred

1 year exp pharmaceutical manufacturing preferred. Proficient in ISO, FDA and GMP.