Senior Process Engineer – Mechanical Systems (Radiopharma)

Arrotek Medical Ltd; Buford (GA); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Competitive benefits

Job summary

Theragenics is seeking a Senior Process Engineer (Mechanical Systems) to design, optimize, and commission manufacturing processes and equipment for radiopharmaceutical production. You will work with Manufacturing, Chemistry, Radiation Safety, Validation, Quality Assurance, Facilities, and Process Development teams to improve performance and transfer new technologies into GMP environments.

You will lead qualification activities, develop process documentation, and drive improvements for safety,

Qualifications

• Bachelor’s or Master’s degree in Mechanical Engineering, Manufacturing Engineering, Bioengineering, or related field.
• 3–5 years in fixture design, process development, optimization, validation, or related engineering functions.
• Proficiency with CAD software such as SolidWorks for 3D models and 2D drawings.

Responsibilities

• Lead design, procurement, installation, commissioning, qualification, and continuous improvement of fixtures, tooling, equipment, and process systems.
• Develop PFDs, P&IDs, equipment layouts, and engineering specifications.
• Create detailed engineering drawings, 3D models, and BOMs using CAD software.
• Support preventive and predictive maintenance programs to maximize uptime.
• Collaborate with R&D to transfer radioisotope manufacturing processes into GMP operations.
• Prepare URS, FDS, and related engineering documentation.

Skills

Mechanical design

Process development

Troubleshooting

Team collaboration

Education

Bachelor’s or Master’s in Mechanical Engineering

Tools

SolidWorks

Job description

Theragenics is seeking a Senior Process Engineer (Mechanical Systems) to design, optimize, and commission manufacturing processes and equipment for radiopharmaceutical production. You will work with Manufacturing, Chemistry, Radiation Safety, Validation, Quality Assurance, Facilities, and Process Development teams to improve performance and transfer new technologies into GMP environments.

You will lead qualification activities, develop process documentation, and drive improvements for safety,