Interplex Medical assists OEM's to maintain their leadership status in the medical marketplace. Interplex Medical is an award-winning full-service contract engineering company that is 100% dedicated to the design, development and manufacturing of medical devices. At the crossroads of experience and innovation, we create out-of-the-box enabling technologies within the highly regulated medical business sector.
Interplex Medical continues to provide comprehensive and complex engineering solutions in major markets, such as: endoscopic, laparoscopic, cardiovascular, orthopedic, urological, gynecological, neurovascular, interventional and peripheral vascular, gastrointestinal, including electrophysiology and pulmonary. Interplex Industries global family of companies includes medical design and contract manufacturing outsourcing services with facilities in the United States, Mexico and Scotland.
This global footprint provides unparalleled capabilities and services unmatched by the competition.
Interplex Medical continues to provide comprehensive and complex engineering solutions in major markets, such as: endoscopic, laparoscopic, cardiovascular, orthopedic, urological, gynecological, neurovascular, interventional and peripheral vascular, gastrointestinal, including electrophysiology and pulmonary. Interplex Industries global family of companies includes medical design and contract manufacturing outsourcing services with facilities in the United States, Mexico and Scotland.
This global footprint provides unparalleled capabilities and services unmatched by the competition.
Services
We excel at creating cardiology, gynecology, pulmonary, urology, endoscopy and laparoscopy products that are high-quality and cost-effective.
This is accomplished by adhering to a disciplined approach of problem solving and the integration of best practices within the medical device industry.
Clear communication and total transparency are paramount to maintaining expectations and meeting customer needs and project requirements.
Each program is assigned a program manager to ensure all deliverables are being met, including detailed project updates sent weekly.
This is accomplished by adhering to a disciplined approach of problem solving and the integration of best practices within the medical device industry.
Clear communication and total transparency are paramount to maintaining expectations and meeting customer needs and project requirements.
Each program is assigned a program manager to ensure all deliverables are being met, including detailed project updates sent weekly.
As an ISO 13485 certified and FDA registered medical device manufacturer, Interplex Medical excels at providing an optimal level of support for each customer based on their production needs.
We provide a seamless transition [from product development into steady-state production] utilizing processes that are continually benchmarked for efficiencies and effectiveness.
Through the use of value-added tools; such as Theory of Constraints (TOC), 5S Methodology and Continual Improvement Processes (CIP), Interplex Medical thinks 'lean' right from the beginning.
We provide a seamless transition [from product development into steady-state production] utilizing processes that are continually benchmarked for efficiencies and effectiveness.
Through the use of value-added tools; such as Theory of Constraints (TOC), 5S Methodology and Continual Improvement Processes (CIP), Interplex Medical thinks 'lean' right from the beginning.
7-10 years experience in designing surgical instruments in the fields of cardiology, cardiovascular surgery, endoscopy, laparoscopy, and orthopedics.
Knowledge of catheter based products and mechanical disposable devices are desirable.
Design and develop instruments for a wide variety of device OEMs Communicate with customers and surgeons to understand clinical requirements.
Ensure compliance with FDA regulations, and support 510(k) submissions or IDE clinical studies.
Experience in the creation of solid models (SolidWorks), analyzing designs (COSMOS) and detailed drawings for new designs, maintain design control documentation and project files adhering to FDA and ISO design control requirements.
Knowledge of catheter based products and mechanical disposable devices are desirable.
Design and develop instruments for a wide variety of device OEMs Communicate with customers and surgeons to understand clinical requirements.
Ensure compliance with FDA regulations, and support 510(k) submissions or IDE clinical studies.
Experience in the creation of solid models (SolidWorks), analyzing designs (COSMOS) and detailed drawings for new designs, maintain design control documentation and project files adhering to FDA and ISO design control requirements.
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