Arthrex’s corporate headquarters is located in Naples, Florida where visitors will find a vibrant atmosphere of rapid product innovation, medical research and surgeon collaboration. The sprawling campus houses corporate and manufacturing operations, as well as Arthrex’s premier Medical Education Center, which serves as an education destination for surgeons from around the world to learn about new products and techniques through hands-on surgical skills training programs.

Arthrex Ave Maria, FL, USA
Mar 20, 2020
Please note, this internship is located in Ave Maria, FL and is not benefit eligible. The ideal candidate will be available to start in Spring 2020. Main Objective: To develop skills such as preparing materials for analysis and testing per Quality System Requirements. Essential Duties and Responsibilities: Create reagents and materials necessary for Laboratory tests Perform tests and assays as required per established procedures Assist with Laboratory maintenance and cleaning Provide contributors with research information and updates Maintain sample receipt and log in database Assist in maintaining the Biological Safety Laboratory systems and documentation Incidental Duties: The above statements describe the general nature and level of work being performed in this job. They are not intended to be an exhaustive list of all duties, and indeed additional responsibilities may be assigned, as required, by management. Education and Experience:...
Arthrex Santa Barbara, CA, USA
Aug 20, 2019
Job - Full time
Responsible for full life cycle development of Class I and II medical devices, which includes initiation, design, development, execution, verification/validation, release, and product maintenance.  Recognized as key technical resource.   ESSENTIAL DUTIES AND RESPONSIBILITIES:   Support team efforts in establishing program design inputs and/or requirements, ensuring compliance to Arthrex QMS and global standards and regulatory requirements Manage completion of Design Control Documentation: Traceability Matrix; Risk Management File; Verification and Validation Plans and Protocols; etc. Support team efforts in product complaints review, root cause failure analysis activities Support team efforts to develop, track and monitor functional systems needs and reliability throughout a products life cycle, making recommendations on corrective actions and/or potential enhancements. Develops and manages product compliance initiatives to relevant standards...