Expected Travel: None
Requisition ID: 11500
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.
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.
Position Summary Principal Responsibilities1. Ensure Latex Plants conform to the Quality System Regulation (QSR), MDD or EU MDR, 93/42/ EEC,,ISO 13485:-2016 and other relevant Stds.
2. Assist Production in quality/regulatory requirements in manufacturing.
3. Manage routine QA activities in operation areas.
4. Ensure timely and adequate reporting.
5. Testing and release of products.
6. Initiate requests for and follow up on correction actions.
7. Assist QS Team to conduct internal as well as external audits whenever required.
8. Raise CAPA whenever required.
9. Support activities related to product recall or reporting of serious malfunction of products to regulatory bodies.
10. Manage handling of product non-conformities.
11. Ensure DHR is reviewed prior to final release and certification.
12. Manage soak test function
13. To ensure the implementation and maintenance, within the department, of an effective management for occupational safety and health consistent with the Occupational Safety and Health Act 1994 and other legislative requirements.
Qualification :
Degree in Science or Manufacturing Management System or related discipline.
Experience :
At least 5 years experience in quality field in medical device industry.
Good knowledge of the Quality System Regulation (QSR) and ISO Quality Management System.
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™, QuikClot™, LMA™, Pilling™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
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