Medical Device Quality Inspector (GDP & ISO)

Beacon Biosignals; Cleveland (OH); On-site; USD 38,572 - 44,083; Full time

Job summary

Beacon Biosignals is seeking a detail‑oriented Quality Inspector to join our Cleveland team. This hands‑on, in‑person contract role ensures GDP compliant inspection of components and devices, maintains accurate records, and flags nonconformances early to support audits and continuous improvement.

The ideal candidate has 1–2 years in medical device quality inspection, a high school diploma (associate degree preferred), familiarity with GDP and 21 CFR 820/ISO 13485, and strong communication.

Qualifications

• Experience in quality inspection in a medical device or regulated manufacturing environment.
• Familiarity with GDP and quality system requirements (e.g., 21 CFR 820, ISO 13485).
• Strong attention to detail and accuracy in documentation and data recording.

Responsibilities

• Perform incoming and final inspection of components, subassemblies, and finished devices per drawings and work instructions.
• Record inspection results and maintain device history records per GDP.
• Identify nonconforming material and escalate findings per nonconformance procedures.
• Conduct monthly quality inspections of manufacturing areas to ensure SOP compliance.
• Assist Quality Engineering with document control, audits, and investigations.
• Support equipment calibration tracking and upkeep.
• Stay current on applicable quality docs and requirements relevant to inspection.
• Participate in continuous improvement initiatives under Quality Engineering.

Skills

Attention to detail

Documentation accuracy

Communication skills

GDP knowledge

Quality systems knowledge

Education

High school diploma or equivalent

Associate’s degree preferred

Job description

Beacon Biosignals is seeking a detail‑oriented Quality Inspector to join our Cleveland team. This hands‑on, in‑person contract role ensures GDP compliant inspection of components and devices, maintains accurate records, and flags nonconformances early to support audits and continuous improvement.

The ideal candidate has 1–2 years in medical device quality inspection, a high school diploma (associate degree preferred), familiarity with GDP and 21 CFR 820/ISO 13485, and strong communication.