Supervisor, Quality Systems

Quality Systems Supervisor

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure's Isolator Synergy Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure's AtriClip Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure's Hybrid AF Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure's cryoICE cryoSPHERE probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. 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.

POSITION SUMMARY :

This position will ensure the AtriCure Document Control system is compliant with domestic and international medical device quality system regulations. The Quality Systems Supervisor will assist in the management and establishment of policy in the document control and record retention systems. The Quality Systems Supervisor is responsible for leading and coordinating the activities of the Document Control team. This position can answer daily questions for the AtriCure organization regarding the document control system (i.e., MasterControl, PLM), record retention and document control. In the role of the Quality Systems Supervisor, this person will work with the entire AtriCure organization to ensure compliance with the AtriCure quality system and will be responsible for reporting to management issues revolving around quality system compliance. The Quality Systems Supervisor is responsible for identifying and implementing state-of-the-art solutions for document control, records management, and external standards maintenance / administration.

ESSENTIAL FUNCTIONS OF THE POSITION :

• Responsible for leading the configuration management and software validation of the quality software system.
• Responsible for identifying and implementing process improvements to the document control system
• Responsible for processing Document Change Notices or Advanced Task Packets through the quality system
• Responsible for quality systems records filing, maintenance, and retention of all files (e.g., design history files, device history records, and other quality system records) per domestic and international regulatory requirements
• Responsible for understanding and ensuring compliance with all domestic and international medical device quality system regulations and standards, where appropriate
• Responsible for ensuring all document control processes are compliant with AtriCure quality system and company policies
• Provide training on how to utilize the document control system to new hires, transfers, co-ops, etc. This includes training on the various processes and systems used (e.g. MasterControl, DocuWare, filing, e-forms, signature cards, record retention, etc.)
• Provide support to users with timely responses to questions regarding Document Control processes
• Coordinate and manage the transfer of quality system records to and from the offsite storage facility, Iron Mountain
• Identify and escalate issues
• Responsible for administering external standards management as assigned
• Serve as the MasterControl expert, proactively assessing and identifying new features or methods to enhance efficiency and compliance
• Collaborate with the organization to tailor or cre