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 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.
The Supervisor will oversee daily quality related tasks at manufacturing floor. This role involves ensuring compliance with industry regulations, written procedures and work instruction, finding out noncompliance at shop floor and in cross functional team activities and to highlight/resolve them following appropriate procedures. This role requires managing quality inspectors at shop floor who are testing product quality with respect to written specification. This role is responsible to ensure high quality products are being manufactured by ensuring all in-process quality related checks performed at specified intervals. This role also requires reviewing and ensuring completeness of all manufacturing batch records prior to release of finished products in market. The Supervisor will collaborate with other departments to drive continuous improvement.
- Bachelor’s degree in engineering, Life Sciences, or a related field.
- Minimum of 2-3 years of experience in the medical device or related industries.
- Strong knowledge of USFDA regulations, ISO 13485, and GMP standards.
- Proven ability to lead and develop a high-performing team.
- Good problem-solving, organizational, and communication skills.
- Proficiency in relevant software and tools (MS Office); SAP shall be an additional benefit.
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.