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Receiving Inspector II

Job in Newark, New Castle County, Delaware, 19711, USA
Listing for: Synerfac Technical Staffing Internal
Full Time position
Listed on 2026-07-09
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA
Salary/Wage Range or Industry Benchmark: 40000 - 55000 USD Yearly USD 40000.00 55000.00 YEAR
Job Description & How to Apply Below

Job Description

Our client is seeking a detail-oriented Receiving Inspector to join their team in Newark, DE. This position plays a critical role in ensuring incoming materials and components meet quality standards through inspection, documentation review, and collaboration with suppliers and internal teams to support manufacturing operations.

  • Perform incoming inspection of purchased materials, components, and equipment, including visual, dimensional, quantity, and documentation verification against specifications, BOMs, and purchase orders.
  • Review supplier certifications and quality documentation, record inspection results in PLM systems, generate nonconformance reports (NCEs), and participate in MRB and corrective action processes.
  • Communicate with suppliers and internal teams to resolve quality discrepancies, maintain material status control, and support product release activities within ERP systems.
  • Conduct first article inspections, prioritize daily inspection activities, maintain accurate training records, and support production schedules through reliable attendance and overtime as needed.
Requirements
  • High school diploma/GED or Associate degree preferred, with 1-2 years of manufacturing, quality assurance, or related experience.
  • Experience in a manufacturing environment with knowledge of quality inspection tools, blueprint/schematic reading, and product specifications.
  • Proficiency with Microsoft Office, ERP systems, and data entry; experience with Oracle ERP, Agile PLM, or FDA-regulated medical device environments is a plus.
  • Strong attention to detail, communication, and documentation skills, with an understanding of GMP/GDP practices and the ability to work independently or as part of a team.
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