Quality Systems Technician I

Theragenics Corp•Buford, GA

About The Position

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.

Requirements

High School Diploma/GED required
2–3 years of related experience
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

Nice To Haves

Associate or Technical Degree preferred (e.g., Technical, Chemistry, or Scientific fields)
Background in science, chemistry, or quality control preferred
Experience in medical device manufacturing preferred

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