Quality Inspector

ADP; Buford (GA); On-site; USD 42,000 - 56,000; Full time

Job summary

ADP in Buford, GA is seeking a Quality Inspector to perform incoming inspections of cold components and process chemicals, monitor in-process inspections, and approve final releases across manufacturing processes.

The role includes training about 10% as requested by management, plus SOP writing and ongoing audits. Requirements include 2–3 years of related experience and a High School diploma; an Associate/Technical degree is preferred.

Qualifications

• High School Diploma or GED required; Associate/Technical degree preferred.
• 2–3 years related experience; medical device manufacturing preferred.

Responsibilities

• Perform incoming inspection and release components to production.
• Evaluate and release finished product.
• Review Material History Records and Device History Records for regulatory compliance and control.
• Write Standard Operating Procedures as requested by the Team Leader.
• Identify process/product nonconformities and ensure short term corrective actions are developed and implemented.
• Perform scheduled calibrations on testing and measuring instruments.
• Evaluate in-process forms and equipment parameters for verification.
• Conduct internal audits and assist in improving process and production.
• Assist in training hourly manufacturing personnel in the requirements of the quality system.
• Inform Team Leader if corrective actions are needed in production areas.
• Work overtime as required.

Skills

Attention to detail

Troubleshooting

Chemistry knowledge

Computer skills

Education

High School Diploma or GED

Associate or Technical Degree preferred

Tools

Calipers

Measuring tools

Micrometers

Job description

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Quality Inspector

Full Time Individual Contributor Buford, GA, US

2 days ago Requisition ID: 1251

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.

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

Associate or Technical Degree Preferred

Experience

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.