Packaging QA Inspector: GMP & FDA Compliance

Crossroadsstaffing

Camarillo (CA)

Vor Ort

USD 48.000 - 70.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

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.

Qualifikationen

  • 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.

Aufgaben

  • 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.

Kenntnisse

Measurement instruments
Quality assurance
Quality control
SOP literacy

Ausbildung

HS Diploma or GED

Tools

MS Office

Jobbeschreibung

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.

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