Sally Jennings serves as the Regulatory Affairs Manager at Cochlear since January 2018, overseeing EU MDR submissions, international registrations, special projects, and regulatory reporting, along with managing Regulatory Intelligence. Prior roles at Cochlear include Principal Regulatory Affairs Specialist, contributing to ANZ, APAC, and EU AIMDD regulatory submissions and supporting EU MDR certification. Sally's earlier experience includes various positions at Abbott Diagnostics from April 2005 to January 2018, including QA RA Manager and Senior QA RA Associate. Sally Jennings holds a Doctor of Philosophy (PhD) in Organic Chemistry from La Trobe University, earned between 1981 and 1990.
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