SeniorFull TimeEN
Expected Travel: None
Requisition ID: 13787
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™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
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.
1. As technical lead and project manager which responsible to lead process improvement for assembly process activities, inclusive of the manual assembly, semi automated and fully automated processes and equipment
2. Establish a holistic approach and road map for process development on new project and existing process improvement opportunity.
3. Manage a portfolio of projects ensuring effective allocation of resources and tracking the progress update on individual project
4. Coordinate technical training for team members upon SME development.
5. Support new products, transfers, and existing production process development.
6. Research, investigate, test and develop new manufacturing process technology including manufacturing and testing equipment thus provides improvement for current process.
7. Drive technical project to completion by ensuring overall design of the equipment meets requirements, overseeing project, and maximizing project resources to ensure milestones are met on a timely basis
8. Manage resources to ensure the successful completion of an assigned project.
9. Manage the project to keep it on track and within approved budget. Ensures technical decisions are appropriate to meet all requirements and cost-effective for manufacturing requirements.
10. Identifies potential for process or quality improvements during development of new process, product transfer or new project introduction.
11. To ensure the implementation and maintenance within the workplace of an effective management for occupational safety and health consistent with the Occupational Safety and Health Act 1994 and other legislative requirements.
Qualification :
Bachelor’s Degree in Mechanical Engineering or equivalent technical discipline, or an advanced degree, or equivalent work experience.
Experience :
a) Minimum 8 years working experience, preferably in a Medical Device / Manufacturing Industries and demonstrated expertise or with in-depth knowledge in relevant Engineering discipline and Project Management
b) 3 years project leadership experience, across the full spectrum of product / process development. Experience as the lead for manufacturing process development on medical device and proficient in technical writing of protocols and reports. Familiar with medical terminology, medical / clinical research methodology. Significant experience in product verification and validation testing, new product development of the medical device and rapid prototyping.
c) Recognized as an influential business partner. Has strong facilitation skills and the ability to communicate effectively to varied audiences to gain support or resolve issues. Makes effective presentations on complex or sensitive topics to top management and/or other key stakeholders.
d) Advanced interpersonal and communication skills, both written and verbal, with the ability to work as a team player and team builder. Highly self-motivated, minimal day to day supervision. Excellent collaborator and able to quickly establish effective relationships with people across all levels.
e) Stage-gate product / process development process experience and ability to leverage and/or engage others to accomplish projects
f) It will be an advantage to have relevant experience from the Medical Device industry including FDA requirements, Design Control, Process Validation and ISO 13485.
g) Ability to Influence scientific thinking and direction of projects
h) Proficient in manufacturing process control with strong analytical and statistical skills
Note: As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time.
Teleflex is an equal opportunities employer.
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.
