Valentine has over nine years of experience in medical devices, biotechnology, and pharmaceutical manufacturing, with expertise in quality assurance, process validation, technical transfer, scale-up, and root cause analysis. She has held positions within pharmaceutical manufacturing organizations in North America and Europe, including serving as a Manufacturing Science and Technology Drug Product Subject Matter Expert (MSAT DP SME). She holds a master’s degree in industrial engineering as well as a bachelor’s degree in medical laboratory technologies.
At STERIS Life Sciences, Valentine provides technical support for cleaning, cleaning validation, and contamination control. She is also responsible for consulting on the consumables portfolio, with a focus on critical environment applications, prioritizing the European region. In addition, Valentine engages with industry peers and regulatory trends as an active member of A3P.
