JOB DESCRIPTION
A: Purpose and Scope
The Engineer is to work within a regulated quality system environment to oversee and improve manufacturing processes to produce medical devices. The manufacturing engineer's responsibilities include identifying areas for improvement, maintaining high levels of manufacturing and product quality, implementation of new product and processes, as well as ensuring cost-efficiency and conformance with regulatory standards. The Engineer will work with new and existing suppliers to identify specifications and processes. The Engineer will write, execute, and report engineering verification and validation protocols in support of the implementation of manufacturing processes.
(Full time, 8+ years’ experience, strong in mechanical fixture design and implementation of production processes)
B: Responsibilities
JOB REQUIREMENTS
A: Skills & Abilities
B: Education and Training
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