Key Responsibilities Identifying gaps in the acquired company’s compliance to Instructions and SOPs and defining strategy to close these gaps. Providing input to project goals and progress and recommending appropriate revisions. Communicating progress, risks, and trade-offs of technical deliverables to project leadership, and recommends revisions as needed. Completing complex or novel assignments requiring the development of new or improved techniques and procedures. Work is expected to result in efficient and effective integration of medical device technologies to the portfolio. Successfully completing engineering work in electrical design remediation, product design refinement, preparation of specifications, test method validation, and report preparation. Assessing the feasibility and soundness of alternative engineering processes, products, or equipment. Contributing to design hazard analysis, FMEA, and ensuring compliance with design control and risk management standard operating procedures. Completing clear and concise engineering documentation to facilitate knowledge transfer during product integration. Collaborating with external partners and suppliers to align component specifications, qualification and acceptance activities, testing protocols, and quality standards.
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Job Type
Full-time
Career Level
Mid Level