Expected Travel: None
Requisition ID: 5106
About Teleflex Incorporated
Teleflex is a global provider of clinically effective medical technologies designed to improve the health and quality of people's lives. We apply purpose driven innovation - a relentless pursuit of identifying unmet clinical needs - to benefit patients and healthcare providers. Our portfolio is diverse, with solutions in the fields of vascular and interventional access, interventional cardiology, surgical, anesthesia, cardiac care, interventional urology, urology, emergency medicine and respiratory care. Teleflex employees worldwide are united in the understanding that what we do every day makes a difference. 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
To manufacture/test medical device assemblies (including all lower level sub-assemblies and accessories) in a clean room environment. To utilize a wide range of equipment, fixtures, gages and hand tools to manufacture assemble and test medical device products. To maintain all logs, forms and resulting paperwork. To carry out all facets of medical device assembly including organization of work flow and training of personnel at all levels.
Principal Responsibilities
• Manufacture, inspect and package products following written processes
• Work at a pace that meets established time standards while making quality product
• Identify quality issues or workmanship deficiencies related to equipment, assembly and inspection processes, materials, sub-assemblies, and manufacturing environment
• Comply with GMP requirements by maintaining individual training records, completing data entry in production records in a timely and accurate manner, and adhering to documented manufacturing practices and procedures as defined in VSI Quality Systems Procedures
• Maintain a clean, safe and organized work environment
• Comply with all policies and procedures
• Perform other duties as assigned
• Cross-train across multiple operations within one or more than two operations or lines following the VSI training program
Note: 1.78% of this job involves direct R&D activities
Education / Experience Requirements
Subscribe to job alerts and upload your resume!
*By registering with our site, you agree to our
Terms and Privacy Policy.