As a leading provider of medical technologies, Teleflex is driven by its purpose to improve the health and quality of people's lives. With a vision to become the most trusted partner in healthcare, the company offers a diverse portfolio with solutions in therapy areas including anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology.
We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Position Summary
The Global QA Operations Manager will oversee the Logistics & Distribution (L&D) process to ensure product quality is maintained throughout the Teleflex distribution process and across all global distribution centers and entities.
Key Responsibilities:
* Support the Global QA L&D Operations process in conjunction with Global Operations, Global Logistics & Distribution, and Global Quality.
* Provide support to Global Distribution Centres to ensure adherence to required regulatory and corporate compliance systems.
* Manage strategic programs as part of the Global QA Logistics & Distribution organisation.
* Detect, identify, correct, and prevent problems within the relevant quality system elements.
* Develop roadmaps/methodologies to move from current state to future state, including changes and implications to existing architecture and systems.
* Lead the Global L&D QA team, including key talent development, mentoring, coaching, effective organisational structure development, and motivation of personnel.
* Implement Supplier Controls & Management in the 3PL network and develop strategy for support of Supplier Quality in Regional offices.
* Provide guidance and recommendations on Quality requirements and the implementation and adherence to those requirements.
* Lead a diverse team from multiple cultures by sustaining an inclusive and empowered organization that adapts to business needs.
Requirements:
* B.S Degree in Science, Medical Technology, or related discipline.
* 10+ years experience in Quality Assurance and/or Regulatory Affairs of medical products.
* Extensive knowledge of FDA/ISO/CE QMS & Regulatory Requirements with proven audit experience.
* Broad Range of Quality experience including Supplier Management, Post Market, and Distribution.
* Proven People Management of multi-site teams.
Specialized Skills / Other Requirements:
* Excellent IT skills & knowledge – MS applications, systems knowledge, WMS knowledge, SAP.
* Strong project management skills and experience in leading virtual teams.
* Process-focused and results-driven.
* Excellent communication, problem-solving, and interpersonal skills across all organisation levels.
* Self-driven and ability to work independently and/or as a team player.
Salary: Estimated $100,000 - $120,000 per year
Travel: Up to 20% required
Company Culture: Embracing diversity and fostering inclusivity, with a focus on innovative thinking and entrepreneurship.