Principal Manufacturing Engineer

Posted Thursday, December 4, 2025 at 5:00 AM

Atri Cure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use Atri Cure technologies for the treatment of Afib and reduction of Afib related complications. Atri Cure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib.

Atri Cure’s Atri Clip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. Atri Cure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. Atri Cure’s cryo

ICE cryo

SPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit  or follow us on Twitter @Atri Cure.

We foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.

This Position is located in Mason/Cincinnati OH and will be onsite. Must be able to commute or relocate to Cincinnati OH for this position to be considered.

A Principal Manufacturing Engineer is a high level, experienced manufacturing/process engineer and is accountable for developing and maintaining capable and stable manufacturing processes to meet product quality standards/requirements. The role is responsible for process development and improvement, and tooling and fixture development and improvement both internally at Atri Cure, and externally at key suppliers. A principal manufacturing engineer may also be involved in development of process analytics for preemptive defect control, process documentation and process layout & material logistic flow.

• Experienced member of the manufacturing engineering team responsible for the development, qualification, implementation and support of new manufacturing processes and equipment
• Design and develop fixtures in CAD prototypes for manufacturing and assembly
• Is considered a subject matter expert in at least 2 major areas of manufacturing engineering
• Ensures continuous improvement in process, cost, quality and production
• Responsible for leading/mentoring members of the Manufacturing/Process Engineering Teams
• Supports and drives a DFM (design for manufacturability) focused culture within the PD teams and the operations organization
• Supports and drives a Lean processes and continuous improvement culture within the PD teams and the operations organization
• Develop business, operational and financial strategies, plans and programs that foster the achievement of organizational objectives
• Translate broad strategies into specific objectives and action plans
• Read blueprints and interpret technical specifications and illustrations
• Drive multiple initiatives at a rapid pace, making thoughtful recommendations with available data

• Regular and predictable worksite attendance
• Ability to work under fast-paced conditions
• Ability to make decisions and use good judgment
• Ability to prioritize various duties and multitask as required
• Ability to successfully work with others
• Additional duties as assigned

• Bachelor’s degree in Industrial Eng., Biomedical Engineering or Mechanical Eng. or equivalent is required
• 15+ years (10 years + Masters) of experience:
• Experience in development of new manufacturing processes and the tooling/equipment required to implement the processes
• Demonstrated ability to design in CAD and prototype manufacturing/assembly fixtures
• Knowledge base in Lean Processes and Continuous Improvement
• Experience in Design for Manufacturability
• Experience with medical device design and manufacture
• Experience with process validation
• Previous class II or class III Medical Device manufacturing experience
• Possess a…