לוח משרות דרושים רפואה ופארמה התמחות, לחיפוש זה נמצאו 5 משרות

Required Verification Intern
Job Description Summary
Contributes to the design, development, and verification of Point of Care Ultrasound products and systems.
Responsible for supporting enhancements to existing products and components by identifying issues, implementing improvements, and validating performance.
Works collaboratively within the team, taking ownership of assigned tasks and ensuring high quality deliverables that meet defined requirements and timelines.
Roles and Responsibilities:
Execute laboratory and field validation testing, including test setup, data acquisition, clinical review of datasets and analysis to support product design and verification.
Design and develop test environments, including test setups, instrumentation systems, and supporting test software.
Identify issues, analyze results, and contribute to improvements in product performance, reliability, and quality.
Collaborate with cross-functional teams to ensure alignment between testing activities and product requirements.
Apply and continuously expand technical knowledge within the domain to effectively perform assigned tasks and support team objectives.
Follow established engineering processes and standards while taking ownership of task execution and deliverables.
Work with some autonomy to resolve technical issues within established procedures Consults more senior team members for issues outside of defined instructions/parameters.
Communicate technical and clinical information clearly to team members and stakeholders.
Collaborate and communicate with the team and potentially leads a junior team if needed.
Develop strong customer relationships and serve as the interface between customer and us.

The internship program provides a learning experience, mentoring and valuable work experience in the field of clinical trials. We provide our interns the opportunity to work on meaningful assignments and make sure that they gain real world experiences (in the areas of Regulatory & Finance and Supply & CRA support).

This program provides comprehensive trial and site administration experience. Under the oversight of the Clinical Operation Manager Leads/Clinical Operation Managers and Clinical Trial Coordinators, the person prepares, collates, distributes and archives clinical documents. The Interns supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.