Precision QA Technician – Medical Devices (2nd Shift)

Becton Dickinson NA; El Paso (TX); On-site; USD 42,000 - 64,000; Full time

Job summary

BD is seeking a Quality Control Inspector to perform in-process, final, and incoming inspections of medical devices and components. You will test, document results, and report non-conformances in a regulated environment.

You will work with production, engineering, and QA teams, supporting CAPA and audits while adhering to GMP, ISO 13485, and FDA requirements. This role requires attention to detail and accuracy.

Qualifications

• High school diploma or GED required; 1–3 years in QC/QA in regulated industry preferred.
• Experience reading blueprints, schematics, and specs.
• Familiar with GMP, ISO 13485, and FDA 21 CFR Part 820. Bonus for prior audits.
• Proficient with MS Office and QA documentation tools.
• Strong attention to detail and analytical skills; able to document clearly.

Responsibilities

• Conduct in-process, final, and incoming inspections per procedures.
• Perform visual, dimensional, functional, and material verification tests.
• Document results accurately; report non-conformances.
• Initiate NCRs and assist investigation/disposition of non-conforming materials.
• Use calipers, micrometers, gauges, and other QC tools.
• Support CAPA activities and root cause analysis as needed.
• Develop and revise inspection procedures and QA docs.
• Comply with GMP and quality system regs (ISO 13485, FDA 21 CFR 820).
• Collaborate with production, engineering, and R&D to resolve issues.
• Participate in internal and external audits.

Skills

Quality control

Documentation

Blueprint reading

Measurement tools

GMP/ISO knowledge

Attention to detail

Problem solving

Team collaboration

Education

High school diploma or GED

Associate's degree in a technical field

Tools

Calipers

Micrometers

Gauges

Testing equipment

Job description

BD is seeking a Quality Control Inspector to perform in-process, final, and incoming inspections of medical devices and components. You will test, document results, and report non-conformances in a regulated environment.

You will work with production, engineering, and QA teams, supporting CAPA and audits while adhering to GMP, ISO 13485, and FDA requirements. This role requires attention to detail and accuracy.