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Receiving Inspector II

Synerfac Technical Staffing

Newark, DE

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JOB DETAILS
SKILLS
Agile PLM / Oracle PLM (Product Lifecycle Management), Bill of Materials (BOM), Blueprints, Corrective Action, Data Entry, Detail Oriented, Documentation, Documentation Review, ERP (Enterprise Resource Planning), Establish Priorities, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), High School Diploma, Manufacturing, Manufacturing Operations, Medical Equipment, Microsoft Office, Operational Support, Oracle ERP, Product Lifecycle Management, Product Support, Production Schedule, Production Support, Purchase Orders, Purchasing/Procurement, Quality Assurance, Quality Control, Quality Metrics, Receiving Inspection, Record Keeping, Reporting Skills, Schematics, Team Player
LOCATION
Newark, DE
POSTED
3 days ago
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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Synerfac Technical Staffing

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