Company Overview
Headquartered in suburban Atlanta, Georgia, Artivion, Inc. specializes in developing innovative medical devices aimed at addressing challenging cardiac and vascular conditions. Our Austin facility houses a diverse team dedicated to producing the On-X Mechanical Heart Valves. With over 1,400 employees globally and manufacturing sites in Atlanta, Austin, and Hechingen, Germany, Artivion serves healthcare professionals in over 100 countries. For more details, visit our website at www.artivion.com.
Position Objective:
Responsible for providing process engineering support for the Machine Shop and act as a backup to any/all other manufacturing departments. Supports manufacturing operations to ensure consistent adherence to the standard operating procedures and business continuity. Initiates process improvement initiatives to improve the efficiency of current manufacturing processes, as well as developing new processes to improve manufacturing efficiency. Supports new product launches by collaborating with other functional areas and providing process engineering expertise during the implementation of processes or equipment.
Responsibilities:
Process Engineering Support:
- Own manufacturing processes to ensure stable, efficient, and compliant production in an FDA/ISO-regulated environment.
- Provide production support by troubleshooting processes and equipment, performing root cause analysis, and delivering technical leadership and training to production teams to ensure effective execution and sustainment.
- Develop and maintain manufacturing documentation (SOPs, work instructions, drawings, etc.), ensuring audit readiness and traceability.
- Lead process validation (IQ/OQ/PQ), PFMEA, and risk management to ensure robust and compliant processes.
- Partner with Quality to resolve nonconformances, drive CAPA to resolve issues and prevent recurrence
- Provide technical ownership for suppliers, including component/process qualification, issue resolution, and driving improvements in supplier quality and performance.
- Coordinate Engineering Change Notices (ECN) with managerial oversight for process & equipment changes and process impact of material changes.
- Ability to read and update CAD drawings, Solid Model assemblies, and machine schematics to troubleshoot problems and implement solutions
- Perform additional duties as assigned by Manager.
Continuous improvement:
- Identify improvement opportunities through data analysis, operator feedback, and observation; implement data-driven improvements to enhance yield, throughput, and uptime.
- Monitor and improve performance using SPC and capability analysis (Cp/Cpk); establish and maintain process control limits.
New Process/Product Implementation:
- Support equipment and tooling selection, qualification, and implementation, including automation where applicable.
- Lead design transfer and new product introduction (NPI), ensuring manufacturability, scalability, and alignment between R&D and operations.
- Provides engineering support for new equipment start-up, debug and process validation. As required, conducts process evaluations and validations under guidance of senior engineers and quality engineering.
Other responsibilities as assigned.
Qualifications:
Required:
- Bachelor’s degree in Engineering (Mechanical, Chemical, Biomedical, Industrial or related field of engineering).
- 2-5 years of medical device, tissue product, or related engineering experience (1-3 years with Masters in Engineering).
- Data-Driven Problem Solving: Demonstrated understanding of problem-solving tools including; root cause analysis (5-why, fishbone) and Statistical process control (SPC), etc Typically requires 2-5 years of medical device, tissue product or related engineering experience (1-3 years with Masters in Engineering).
- Process Optimization / Lean Mfg.: Demonstrated execution of lean principles, cycle time / throughput improvement, yield improvement, workflow optimization, etc.
- Cross-Functional Collaboration: ability to work cross-functionally with operators, quality, regulatory and management teams; train operators and implement new processes, etc.
Required:
- CNC / Machining Knowledge: basic understanding of CNC milling, turning, lathes, lapping, multi-axis machining, etc. is preferred
- CAD/CAM & Programming Proficiency: basic understanding of CAM Software (Mastercam), how to generate/optimize toolpaths, and machine code (G-code)
Benefits:
- Comprehensive Medical, Dental, and Vision
- Life Insurance
- Supplemental Benefits
- 401(k) with both Traditional and Roth options available
- Employee Stock Purchase Plan (ESPP)
- 10 Paid Company Holidays
- Competitive PTO plan
- Tuition Reimbursement
Equal Employment Opportunity Employer (EEO):
We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected status under applicable law.
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Skills Required
- Bachelor's degree in Mechanical, Chemical, Biomedical, Industrial, or related engineering field
- 2-5 years of medical device, tissue product, or related engineering experience; 1-3 years with a Master's degree
- Understanding of data-driven problem-solving tools, including root cause analysis, 5-Why, fishbone, and statistical process control
- Experience executing lean manufacturing principles and improving cycle time, throughput, yield, or workflow
- Ability to collaborate cross-functionally with operators, quality, regulatory, and management teams; train operators and implement processes
- Basic knowledge of CNC milling, turning, lathes, lapping, and multi-axis machining
- Basic understanding of CAM software such as Mastercam, toolpath generation and optimization, and G-code
What We Do
Artivion is a leader in the manufacturing, processing, and distribution of medical devices and implantable tissues used in cardiac and vascular surgical procedures focused on aortic repair. Our purpose is to develop simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with diseases of the aorta and deliver breakthrough technologies of unsurpassed quality that have far-reaching impact. Our decades of expertise in treating aortic diseases—coupled with our recent acquisitions and partnerships—have empowered us to offer cardiac and vascular surgeons a suite of aortic-centric solutions such as cryopreserved cardiac and vascular allografts, surgical sealants, prosthetic heart valves, and aortic stents and stent-grafts. Artivion has over 1,250 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas, and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America.
