QA Inspector II - Medical Devices, On-Site

Becton Dickinson NA; Covington (GA); On-site; USD 42,000 - 65,000; Full time

Job summary

Becton, Dickinson and Company (BD) is hiring a Quality Assurance Tech 2 to perform routine quality inspections, tests and documentation, ensuring medical devices meet stringent regulatory standards. You will support production by addressing non-conformances and upholding quality systems.

Responsibilities include in-process and final inspections, CAPA investigations, and collaboration with manufacturing to sustain a culture of quality and compliance with GMP and ISO 13485 requirements.

Qualifications

• High school diploma or equivalent; associate degree preferred.
• 2–4 years in quality assurance or quality control in medical devices.
• Read blueprints and interpret schematics accurately.
• Use inspection tools like calipers, micrometers, gauges and optical comparators.
• GMP, ISO 13485 and 21 CFR Part 820 knowledge.
• Proficient with Microsoft Office Suite.

Responsibilities

• Conduct in-process and final inspections of medical devices per procedures.
• Perform visual, dimensional, and functional tests using appropriate tools.
• Document inspection results and maintain records per quality system.
• Identify non-conforming materials, segregate and disposition as needed.
• Assist in CAPA investigations and root cause analysis.
• Collaborate with production to address quality concerns.
• Review and update quality documentation and forms.
• Support internal and external audits with required documentation.
• Adhere to safety guidelines and maintain clean work environment.
• Operate and maintain quality control equipment and calibration.

Skills

Attention to detail

Communication

Independent worker

Team player

Education

High school diploma or equivalent

Associate's degree (technical field)

Tools

Calipers

Micrometers

Gauges

Optical comparators

Microsoft Office

Job description

Becton, Dickinson and Company (BD) is hiring a Quality Assurance Tech 2 to perform routine quality inspections, tests and documentation, ensuring medical devices meet stringent regulatory standards. You will support production by addressing non-conformances and upholding quality systems.

Responsibilities include in-process and final inspections, CAPA investigations, and collaboration with manufacturing to sustain a culture of quality and compliance with GMP and ISO 13485 requirements.