Quality Inspector: Process Improvements & Compliance

Theragenics Corporation; Buford (GA); On-site; USD 42,000 - 65,000; Full time

Job summary

Theragenics Corporation in Buford, GA is seeking a Quality Inspector responsible for incoming inspection of components and process chemicals, in-process inspections, troubleshooting, and final product releases across manufacturing.

The role includes training responsibilities, calibrations, internal audits, and maintaining quality system requirements. Requires high school diploma; associate/technical degree preferred; 2–3 years related experience; medical device manufacturing experience preferred.

Qualifications

• High School Diploma or GED required; associate/technical degree preferred.
• 2–3 years related experience in quality control or manufacturing.
• Experience in medical device manufacturing is preferred.
• Good math, chemistry, and computer skills; strong attention to detail.

Responsibilities

• Perform incoming inspection and release components to production.
• Evaluate and release finished product, including regulatory records review.
• Identify nonconformities and implement short-term corrective actions.
• Perform scheduled calibrations on testing instruments.
• Assist in training hourly staff on quality system requirements.
• Support internal audits and process improvement efforts.
• Communicate corrective action needs to Team Leader.

Skills

Attention to detail

Troubleshooting

Written and verbal communication

Chemistry knowledge

Computer skills

Education

High School Diploma/GED

Associate or Technical Degree

Tools

Calipers

Micrometers

Measuring instruments

Job description

Theragenics Corporation in Buford, GA is seeking a Quality Inspector responsible for incoming inspection of components and process chemicals, in-process inspections, troubleshooting, and final product releases across manufacturing.

The role includes training responsibilities, calibrations, internal audits, and maintaining quality system requirements. Requires high school diploma; associate/technical degree preferred; 2–3 years related experience; medical device manufacturing experience preferred.