Drive standardization & deploy world-class solutions to drive improved quality and compliance
Recognized as a leading expert and internal thought leader in the designated QMS area with high-level knowledge and broad, comprehensive knowledge of other QMS disciplines
Leads major improvements to existing processes and develops or champions new systems, concepts, and procedures to solve unique and complex problems that have a broad impact on the business
Evaluate new regulations, guidelines and industry standards and their impact on ECMP QMS Workstream processes; plan and effectively implement plans across the business to maintain compliance
Establish a global community of practice for the designated QMS area or collaborate with responsible people to enhance the existing community of practice, including governance and oversight, to ensure compliance and consistency in relevant sub-processes applicable to the designated QMS area
Collaborate with process owners and stakeholders in corporate, divisions and sites to ensure the program is compliant, executable, and meets user needs
Ensure compliance of all process and digital improvements with all appropriate regulations and standards, including FDA, ISO 13485, CMDR, EU MDR and PMD Act
Interact and coordinate activities with other departments, external vendors, and customers
Influences and collaborates across stakeholder groups in the areas of process / system improvements, identify and implement opportunities
Drive quality culture improvements and foster collaboration to ensure functional teams work harmoniously and secure synergy and strengths across the global teams
Provides strategic direction and communication of the ECMP QMS work stream goals, directives, and policies to employees, creating a clear vision and positive, team-oriented environment resulting in the achievement of the company’s goals and increased profitability
Demonstrates technical leadership as an inter-departmental resource coaching and teaching other Integra Leaders across all functions and geographies
Perform other related duties as expected
Requirements
Bachelor’s Degree in Engineering, or Sciences or relevant Technical Field required
Master’s degree preferred
Minimum 10 years of experience in quality, manufacturing, or engineering, or equivalent education and years of experience
Strong experience leading deployment of enterprise quality management solutions
Experience in FDA controlled environment
Strong collaboration and facilitation skills and experience working in a matrix environment
Ability to interface with technical and non-technical personnel
Knowledge of FDA QMSR, ISO, MDSAP, EU MDR, PMD Act and other applicable standards and regulations