Senior Quality Inspector Advanced Manufacturing Job Henderson area,North Carolina USA,Quality Assurance

Senior Quality Inspector Advanced Manufacturing #2387

OXNC DIRECT HIRE Position Summary

Responsible for performing incoming, first article (FAI), in-process, and final inspection activities on precision machined and assembled medical device components in compliance with ISO 13485:2016 and FDA 21 CFR 820 (QMSR). Ensures products meet engineering drawings, specifications, and regulatory requirements prior to release.

This role has responsibility for inspection-based product acceptance decisions and support of nonconformance control activities.

Reporting Relationship

Reports to Head of Quality

Location:

In-person

Main Responsibilities

Product Inspection & Verification Perform incoming, first article (FAI), in-process, and final inspection according to procedures, drawings, and specifications. Verify dimensional, visual, and functional conformance of machined and assembled components. Ensure only conforming product is released to the next process or shipment.

Product Release Support Support product disposition decisions based on inspection results and applicable procedures. Communicate inspection results clearly to production and engineering personnel. Ensure product status (Accepted / Rejected / On Hold) is properly identified and controlled.

Nonconforming Product Control Identify, document, and segregate nonconforming materials or products in accordance with procedures. Initiate Nonconformance Reports (NCR) and support Material Review Board (MRB) disposition activities. Support root cause investigation and Corrective and Preventive Action (CAPA) activities as required. Ensure nonconforming product is effectively controlled to prevent unintended use, assembly, or shipment.

Measurement Equipment & Gage Management Verify calibration status prior to use of inspection equipment. Operate and maintain precision inspection tools and gauges. Ensure proper identification, traceability, storage, and handling of all inspection equipment. Support calibration coordination activities with internal or external calibration providers. Perform routine care, cleaning, and functional verification of inspection equipment.

Documentation & Data Integrity Record inspection results accurately in compliance with Good Documentation Practices (GDP). Ensure traceability and completeness of all inspection records. Support batch record review and product release documentation as required.

Quality System Support Support First Article Inspection (FAI), Measurement System Analysis (MSA), and process validation activities as required. Maintain product identification and traceability throughout inspection activities. Support continuous improvement of inspection methods and quality processes.

Workplace Compliance & 5S Maintain cleanliness and organization of inspection area in compliance with 5S and contamination control requirements. Follow safety, GMP, and regulatory requirements at all times. Report abnormal conditions, deviations, or potential quality risks in a timely manner.

Other Duties Perform other duties as assigned to support manufacturing, quality, and operational requirements.

Minimum Qualifications

Technical diploma or equivalent in Engineering, Manufacturing, or related field.
2+ years of inspection experience in machining, precision manufacturing, or regulated manufacturing environment (medical device preferred).
Ability to read and interpret engineering drawings, including basic GD&T.
Proficient in using precision measuring instruments, including but not limited to calipers, micrometers, height gauges, bore gauges, thread gauges, plug gauges, ring gauges, dial indicators, and surface roughness testers.
Ability to perform dimensional inspection using Coordinate Measuring Machines (CMM) (Hexagon preferred).
Ability to measure and inspect machined components with accuracy and consistency.
Familiarity with ISO 13485:2016 and FDA 21 CFR 820 (QMSR) preferred.
Strong attention to detail and Good Documentation Practices (GDP).
Ability to work independently and as part of a team in a fast-paced manufacturing environment.
Proficient in basic computer applications including Microsoft Office (Word, Excel, Outlook).
Ability to accurately enter inspection data, maintain electronic records, and work with basic manufacturing or quality systems such as ERP or similar systems (ERP/MES experience preferred).

Work Schedule / Employment Conditions

This position’s regular working hours are 7:00 AM to 3:30 PM. The role may require overtime, including extended weekday hours and occasional weekend work, based on production demands and business needs.

Work Environment

This position is an on-site position. It operates in both manufacturing and controlled inspection environments. The employee may be exposed to typical machining shop environments with background noise associated with production activities and fast-paced workflows.

Personal Protective Equipment (PPE) is required in designated areas and must be used in accordance with safety policies. PPE may include safety shoes, safety…