Traceability & Inventory Compliance Specialist

Star Health Manufacturing

LaBelle (FL)

Vor Ort

USD 45.000 - 65.000

Vollzeit

14 Tage+
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Zusammenfassung

Star Health Manufacturing is seeking an Inventory Management Specialist to oversee receipt, logging, and traceability of components, ingredients, and finished products in a cGMP environment. The role emphasizes lot control, segregation of quarantined materials, and accurate recordkeeping to support FDA inspections.

You will work with Quality Control to release materials, enforce FEFO/FIFO, and maintain system flags. Strong attention to detail and experience with WMS/ERP are essential.

Qualifikationen

  • High school diploma or GED required; associate/bachelor's preferred.
  • Experience in FDA-regulated inventory, warehousing, or materials management.
  • Knowledge of 21 CFR Parts 111, 117, 507 and GDP records.
  • Experience with WMS/ERP systems (SAP, Oracle, NetSuite, MS Dynamics).
  • Strong reading/writing of English; math and reconciliation skills.

Aufgaben

  • Receive, identify, and log incoming components, packaging, and ingredients with lot numbers.
  • Verify shipments against invoices, guarantees, POs, and CoAs.
  • Assign unique lot identifiers and track status (Quarantine, Approved, Rejected).
  • On receipt, place human dietary supplement ingredients into On Hold or Quarantine.
  • Maintain clear status labels and system flags for all inventory.
  • Move materials only with QC authorization and quarantine rejected items.
  • Ensure allergen segregation and proper FEFO/FIFO rotation.
  • Maintain forward/backward lot traceability and recall readiness.

Kenntnisse

Attention to detail
Math/reconciliation
English communication
GMP knowledge
Recordkeeping

Ausbildung

High school diploma or GED
Associate/Bachelor's preferred

Tools

SAP
Oracle
NetSuite
MS Dynamics

Jobbeschreibung

Star Health Manufacturing is seeking an Inventory Management Specialist to oversee receipt, logging, and traceability of components, ingredients, and finished products in a cGMP environment. The role emphasizes lot control, segregation of quarantined materials, and accurate recordkeeping to support FDA inspections.

You will work with Quality Control to release materials, enforce FEFO/FIFO, and maintain system flags. Strong attention to detail and experience with WMS/ERP are essential.

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