Nichole has extensive experience in both heavily regulated and research markets and has demonstrated results in building effective processes and systems to enable both. Prior to IDT, Nichole spent 6 years with SCIEX, where she led as the Vice President of QA/RA, strategically directing the establishment, implementation, and maintenance of adherent QA/RA systems as well as building regulatory strategies for medical device launches in key markets.
Nichole also played a leading role in driving forward SCIEX’s D+I strategy –an initiative she is deeply passionate about– and helped the team deliver tremendous impact in 2022. Prior to joining SCIEX, Nichole managed the global regulatory affairs team at Boston Scientific’s Urology and Pelvic Health Division for 10 years.
Nichole holds a Bachelor of Science in Biomedical Engineering from Western New England College in Springfield, MA, U.S.A.
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