Quality Systems Engineer, Senior

Department: Quality

Employment Type: Full Time

Location: Gainesville, FL

Reporting To: Director Quality Management Systems

Description

Key Responsibilities

• Quality Systems and Regulatory Compliance:
  •  Know and apply the Quality System and any appropriate Federal and International standards (FDA, ISO 13485, MDSAP, EU MDR, etc.)
  •  Provide leadership and strategy for the team in the overall administration and maintenance of the QMS processes, ensuring alignment with organizational goals.
  •  Ensure that Quality Management Systems documentation meets the required guidelines for maintaining FDA compliance and ISO/EC/MDR certification.
  • Support the strategic initiatives of the company to achieve and maintain regulatory compliance.
• Corrective and Preventive Action: 
  • Oversees CAPA system, including maintenance, development and system validation. 
  • Develops and facilitates continuous training and development for the CAPA process, including root cause analysis and verification of effectiveness. 
  • Responsible for the reporting of CAPA system KPIs during Quality Systems Governance and Management Review.
  • Operates as lead Subject Matter Expert during internal/external audits and inspections..
• Product/Process Nonconformance: 
  • Oversees NC system, including maintenance, development and system validation. 
  • Supports cross-functional teams with investigations, root cause analysis, escalation decisions, and dispositions.
  • Operates as lead Subject Matter Expert during internal/external audits and inspections. 
• Product Corrections and Removals: 
  • Oversees the process for product event escalations, health hazard evaluation, and execution of product corrections and removals. 
  • Provides guidance and drives cross-functional collaboration to make timely decisions, based upon product risk.  
  • Supports cross-functional teams with investigations, root cause analysis, escalation decisions, and final decisions.
  • Operates as lead Subject Matter Expert during internal/external audits and inspections. 
• Training and Cross-Functional Responsibilities: 
  • Oversees the Learning Management Solution (LMS), including maintenance, development and system validation. 
  • Develop training and competency solutions to meet the needs of the company and its Quality Management System.
  • Monitors Quality Systems training curricula for completeness, appropriateness and execution. 
  • Responsible for the reporting of LMS system KPIs during Quality Systems Governance and Management Review. 
  • Operates as lead Subject Matter Expert during internal/external audits and inspections. 
• Data Analytics & Reporting Responsibilities: 
  • Assist with the development of training materials and documentation to ensure effective dissemination of knowledge to team members and stakeholders.
  • Responsible for compiling process data for presentation during Quality Systems Governance and Management Reviews. 
  • Facilitates Quality Systems Governance and Management Review meetings in accordance with company procedures.  

Skills Knowledge and Expertise

• Bachelor’s Degree in Engineering or related science from an accredited institution required; Master’s Degree preferred. 

• Minimum of 6 years full-time medical device engineering/quality/regulatory technical experience. This experience shall be in addition to any college internships. Relevant experience in other areas may be considered.
• Experience in Change Management documentation systems preferred.
• Experience in electronic Quality Management Systems solutions (e.g. SmartSolve IQVIA, Cornerstone, Teamcenter).
• Experience in data management and reporting utilizing PowerBI. 
• Professional Certification through the American Society for Quality (ASQ) or equivalent in Auditing for Medical Devices.
• Experience in software validation, operating within a Quality Management System

• Demonstrated ability to lead cross-functional teams and project
• Demonstrated ability to communic