Sr Process Engineer (Mechanical Systems) – Radioisotope Manufact

Theragenics Corp•Buford, GA

6d•Onsite

About The Position

BE PART OF A MISSION THAT MATTERS Join Theragenics as a Senior Process Engineer (Mechanical Systems) and help advance the future of radiopharmaceutical manufacturing. In this critical role, you'll lead the design, optimization, commissioning, and continuous improvement of manufacturing processes and mechanical systems that support the production of life-saving radioisotope therapies. Your expertise will directly contribute to the development of innovative cancer treatments while ensuring safe, reliable, and GMP-compliant operations. If you're passionate about engineering excellence, process innovation, and making a meaningful impact on patient care, this is your opportunity to help shape the future of healthcare. 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, vascular interventions, and surgical applications. The company is headquartered in Atlanta, Georgia, with facilities in Costa Rica, Texas, and Massachusetts. Theragenics proudly operates Arrotek, a premier medical device design consultancy in the U.S. and Ireland, dedicated to pioneering minimally invasive solutions that improve lives. ROLE SUMMARY As a Senior Process Engineer (Mechanical Systems), you'll play a pivotal role in designing, developing, and optimizing manufacturing processes and equipment that support radiopharmaceutical research, development, and commercial production. Working closely with Manufacturing, Chemistry, Radiation Safety, Validation, Quality Assurance, Facilities, and Process Development teams, you'll implement engineering solutions that improve process performance, maximize equipment reliability, and support the successful transfer of new technologies into GMP manufacturing environments.

Requirements

Bachelor's or Master's degree in Mechanical Engineering, Manufacturing Engineering, Bioengineering, or a related engineering discipline.
3-5 years of experience in fixture design, process development, process optimization, validation, or related engineering functions.
Proficiency with CAD software such as SolidWorks for creating 3D models and 2D engineering drawings.
Strong understanding of mechanical systems, fluid mechanics, heat transfer, and process equipment design.
Knowledge of engineering change management and document control systems.
Strong troubleshooting, technical problem-solving, and root cause analysis skills.
Excellent written and verbal communication skills.
Ability to collaborate effectively within multidisciplinary teams.

Nice To Haves

Experience designing and installing automated manufacturing systems or production lines.
Experience working in highly regulated manufacturing environments, including pharmaceutical, medical device, biotechnology, or radiopharmaceutical industries.
Knowledge of GMP manufacturing practices and validation requirements.
Experience supporting qualification and commissioning activities for manufacturing equipment and facilities.
Familiarity with radiopharmaceutical manufacturing or radioactive material handling environments.

Responsibilities

Lead the design, procurement, installation, commissioning, qualification, and continuous improvement of fixtures, tooling, equipment, and process systems.
Develop process flow diagrams (PFDs), Piping & Instrumentation Diagrams (P&IDs), equipment layouts, and engineering specifications.
Create detailed engineering drawings, 3D models, and Bills of Materials (BOMs) using CAD software.
Support preventive and predictive maintenance programs to maximize equipment performance and uptime.
Partner with R&D teams to transfer new radioisotope manufacturing processes into commercial GMP operations.
Prepare User Requirement Specifications (URS), Functional Design Specifications (FDS), and related engineering documentation.
Support equipment qualification activities, including FAT, SAT, IQ, OQ, and PQ protocols.
Manage engineering change controls and contribute to validation activities.
Develop and maintain SOPs, maintenance procedures, and engineering standards.
Provide technical support for manufacturing operations, investigations, troubleshooting activities, and regulatory inspections.
Drive continuous improvement initiatives focused on safety, quality, efficiency, and reliability.