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Assist in the development of medical devices.
Designs, runs, and gathers data for a series of experiments.
Analyzes and documents test results in a laboratory notebook.
Participates in design control and market requirements.
Responsible for processing Engineering Change Orders (ECO's).
Assists with implementing design control requirements.
Supports laboratory and clinical research.
Supports production and manufacturing.
Vendor contracts and specification development.
Interface with other departments such as Customer Service and Sales/Marketing, Manufacturing, Regulatory and Quality. Qualifications