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QA Line Inspector

The job is located in the City of Bell, California and is currently in transition for 12-16 weeks from Culver City.
Basic Purpose

Perform finished product inspection to ensure products distributed to customer meet specifications. Functions include but not limited to: Inspect production line before start of production; Inspect finished products; Approve production set-up; Verify information on the batch records; Provide assistance to Production for self-inspection; Prepare and file batch records; Maintain Finished Product Standards; Perform any other functions requested by any Quality Department Supervisor.

Responsibilities

 

  1. Prepare product standards with proper information and submit to lead/supervisor for approval. After new revision is approved, remove previous product standard from the cabinet.
  2. Verify components used on each filing line are labeled properly
  3. Perform production line in-process inspections in accordance with current specifications. Record inspection result on Finished Product Inspection in a timely manner ( at the time is being performed, no back dated information is allowed)
  4. Submit Component Reconciliation and Yield (F084) for OTC products immediately after each product is completed.
  5. Monitor and verify calibration of equipment used to test or inspect materials; any equipment issue must be reported to immediate supervisor in a timely manner.
  6. Pull QC approved retains, validation and stability samples as required.
  7. File documentation and production batch records
  8. Enter retain samples information into the retain samples log and maintain retain samples (each work order must have its own retain sample)
  9. Record any unusual incident in comment section for each component during finished product inspection.
  10. Initiate a QA HOLD, if product fails to meets requirements
  11. Prepare and check the batch record to ensure all required documents are completed
  12. Submit batch record to QA Lead for review within 24 hours of work order completion
  13. Other duties and responsibilities as may be required by immediate supervisor or management team. Work with minimal supervision; must be responsible and able to timely initiate appropriate work activities
  14. Assist the head of Quality Department to ensure quality records meet FDA and ISO 9001-2000 requirements.
  15. Help manage all aspects of the quality program
  16. Assist in preparation for different audits, i.e. FDA, ISO, NSF/Organic, IASC, Kosher, GFCO, etc.
                             


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