Newton Colmore Consulting is seeking a Regulatory Affairs Engineer for Cambridge, to support medical devices across diverse projects. You will work at the intersection of design, innovation and compliance, partnering with design engineers, scientists and project teams to ground development in robust regulatory thinking.
You will apply ISO 9001, ISO 13485 and FDA 21 CFR 820 knowledge, develop regulatory strategies, interpret requirements, track changes and contribute to the quality management
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This opportunity is for the Regulatory Strategy Engineer – Medical Devices role at Newton Colmore Consulting.
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This posting is for the Regulatory Strategy Engineer – Medical Devices role at Newton Colmore Consulting, based in Cambridge, England, United Kingdom.