Quality Systems Technician I at Theragenics Corp – Buford, Georgia

Be part of a mission that matters—join Theragenics as a Quality Systems Technician I and help drive the production of life-saving radiopharmaceuticals used in cutting-edge cancer treatments. In this critical role, you'll operate advanced cyclotron systems to support the development of precision-targeted therapies, contributing directly to the creation of medical devices that improve and extend lives. If you're passionate about technology, accuracy, and making a meaningful impact in healthcare, this is your opportunity to help shape the future of patient care.

Company Overview

At Theragenics, we're passionate about transforming healthcare and enhancing patient outcomes. Our commitment to innovation drives us to push the boundaries of what's possible, ensuring a brighter future for patients everywhere.

Theragenics is a leader in developing medical devices that focus on minimally invasive treatments for cancer, blood vessel procedures, and surgical applications. The company is based in Atlanta, Georgia, and has facilities in Costa Rica, Texas, and Massachusetts. Theragenics proudly operates Arrotek, a visionary medical device design consultancy in the U.S. and Ireland, dedicated to pioneering minimally invasive solutions that enhance lives.

Position Summary

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 as requested by the Manager of Quality and Regulatory Affairs or Team Leader.

Key Responsibilities

• Conduct incoming acceptance activities and release components to production
• Evaluate and release finished products
• Review Material History Records and Device History Records for completeness, accuracy, and regulatory compliance
• Write Standard Operating Procedures as requested by the Team Leader
• Identify process/product nonconformities and ensure corrective actions are implemented
• Perform scheduled calibrations on testing and measuring instruments
• Verify in-process forms and equipment parameters
• Conduct internal audits and assist in improving processes and production
• Train hourly manufacturing personnel in quality system requirements
• Inform Team Leader of corrective actions needed in production areas
• Work mandatory overtime as required

Education

• High School Diploma/GED required
• Associate or Technical Degree preferred (e.g., Technical, Chemistry, or Scientific fields)

Experience

• 2–3 years of related experience
• Background in science, chemistry, or quality control preferred
• Experience in medical device manufacturing preferred

Knowledge, Skills & Abilities

• Strong written, verbal, interpersonal, math, chemistry, and computer skills
• Ability to troubleshoot and conduct investigations
• High attention to detail
• Skilled in visual inspection and handling small parts with calipers, micrometers, and other measuring tools
• Ability to perform repetitive and routine inspections while maintaining quality and concentration
• Ability to prioritize multiple tasks without constant supervision
• Willingness to work mandatory overtime
• Ability to perform light lifting

Why Join Us

• Career growth opportunities
• Work on innovative projects with global impact
• Collaborative and supportive culture
• Competitive benefits package
• Purpose-driven work that directly improves patient care

Ready to make a difference? Apply today and be part of something extraordinary.

“We don’t just ship inventory; we deliver care.”