EMD Millipore Corporation

The Senior Regulatory Expert will define the roadmap for global regulatory submissions for US Class I and II and EU Class A, B, and C in vitro diagnostic medical devices to global agencies and partners. Responsibilities include developing strategic frameworks for compliance across USA, EU, UK, Canada, Switzerland, and Asia Pacific regions.

The Senior Regulatory Expert - Medical Devices will oversee and define roadmap for the global regulatory submissions for US Class I and II and EU Class A, B and C in vitro diagnostic medical devices to global regulatory agencies and/or to commercial partners. Oversee and define r...