R&d Project Manager, Tracheostomy

**Date**:20 Dec 2024

**Location**: Kamunting, 08, MY

**Company**:Teleflex

**Expected Travel**: None

**Requisition ID**: 11574

**About Teleflex Incorporated**

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of 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.

Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck - trusted brands united by a common sense of purpose.

**Global Operations -** Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

**Position Summary**

**Principal Responsibilities**
- 1. Manage the development, planning, and execution of design-related projects (both NPD and Sustaining). Create project plans, charters, schedules, and other project specific documentation. Assess project feasibility, cost estimates and business impact and risks.
2. Ensure alignment and governance to corporate NPD and Sustaining processes.
3. Engage the appropriate technical resources and departmental leaders to identify deliverables, resources requirement, milestones, timelines, risks, and mitigation plans.
4. Own and execute technical deliverables within the project as required.
5. Collaborate with project team, business unit, and workstream/shared services leads, as well as functional leaders from operations, regulatory, quality, and clinical functions to finance to ensure efficient execution of a shared strategy.
6. Ensure overall compliance; promote creative solutions; ensure on-time completion of individual tasks and project workstream goals.
7. Lead/ coordinate project activities with Regulatory Affairs, Clinical Medical Affairs, Sterility Assurance, Global Packaging, Global Biocompatibility, and other shared service teams as required.
8. Communicate effectively with leadership to ensure clear expectations, demonstrate progress, and identify issues. Provide progress updates and regular reporting to business and functions leadership.
9. Through the implementation of project management and productivity tools, maintain and track progress and produce applicable reports.
10. Plan and oversee the implementation of new components/modified designs with strategic sourcing and manufacturing project leads.
11. Create project charters in the project management database (Planview); maintain project information and provide status updates within database. Utilize various project management software and tools as required for project plan creation, scheduling and reporting.
12. As required, coordinate a project portfolio review across multiple projects. This may include smaller technical projects led by engineering across a particular product family. Provide consistent high-level project leadership, maintain an understanding of project status, and report progress.
13. Partner with other project leaders to ensure coordination of activities and timelines, facilitating efficient use of resources.
14. Partner with Quality, Operations and Regulatory as well as IT project management to develop systems and IT tools requirements to support effective standard processes.
15. Facilitate regularly scheduled meetings, take meeting minutes with action items, and follow up with SMEs on expected deliverables.
16. And any other assignment / task as deemed fit.

**Education / Experience Requirements**
- Qualification:
a) Bachelor’s degree in a business or science discipline or equivalent education/experience required.
b) Minimum 4 years’ experience in Project Management, PMP Certification preferred.
- Experience
a) Minimum 4 years project management experience preferably in the medical device and/or FDA regulated industry.
b) R&D or engineering experience/knowledge and relevant experience in project management and proficiency in project management software and tools.
c) Exceptional interpersonal and communication skills, with the ability to collaborate and influence at all levels of the organization
d) Excellent verbal/ written communication and presentation skills. Demonstrated ability to communicate to various levels of management succinctly and accurately and across the organization
e) Ability to