Quality Inspector

Theragenics Corporation

Buford (GA)

On-site

USD 42,000 - 65,000

Full time

39 hours ago
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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

Come Join Our Team!

We are seeking a dynamic Quality Inspector to join our team. The Quality Inspector is responsible for incoming inspection of cold components and process chemicals, monitoring in-process inspections, troubleshooting and analyzing problems for solutions, and final product releases of all manufacturing processes. Conducts training about 10% as requested by the Manager of Quality and Regulatory Affairs or Team Leader.

  • Conducts incoming acceptance activities and releases components to production.
  • Evaluates and releases finished product.
  • Reviews Material History Records and Device History Records for completeness, accuracy and Regulatory Compliance and Control.
  • Writes Standard Operating Procedures as requested by the Team Leader.
  • Identifies process/product nonconformities and ensures short term corrective actions are developed and implemented.
  • Performs scheduled calibrations on testing and measuring instruments.
  • Evaluates in-process forms and equipment parameters for verification.
  • Conducts internal audits and assist in improving process and production.
  • Assists in training hourly manufacturing personnel in the requirements of the quality system.
  • Informs Team Leader if corrective actions are needed in production areas.
  • Works mandatory overtime as required.
Essential Duties And Responsibilities Include
  • Conducts incoming acceptance activities and releases components to production.
  • Evaluates and releases finished product.
  • Reviews Material History Records and Device History Records for completeness, accuracy and Regulatory Compliance and Control.
  • Writes Standard Operating Procedures as requested by the Team Leader.
  • Identifies process/product nonconformities and ensures short term corrective actions are developed and implemented.
  • Performs scheduled calibrations on testing and measuring instruments.
  • Evaluates in-process forms and equipment parameters for verification.
  • Conducts internal audits and assist in improving process and production.
  • Assists in training hourly manufacturing personnel in the requirements of the quality system.
  • Informs Team Leader if corrective actions are needed in production areas.
  • Works mandatory overtime as required.
Education

High School Diploma/GED Required

Experience

Associate or Technical Degree Preferred

2 – 3 years related experience.

Experience In Science/Chemistry Or Quality Control Preferred Not Required

Experience in medical device manufacturing preferred. (helpful)

Additionally
  • Good written, verbal, interpersonal, general math, chemistry, and computer skills.
  • Ability to troubleshoot and conduct investigations.
  • Ability to pay close attention to detail.
  • Ability to visually inspect and handle small parts with calipers, micrometers and other measuring tools
  • Ablility to perform repetitive and routine inspections while maintaining high level of quality and concentration.
  • Ability to perform and prioritize multiple duties and tasks without direct and constant supervision.
  • Ability to perform light lifting.
  • Ability to work overtime as workload dictates.
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