OriGen Biomedical
Carissa Bishop is a seasoned professional in regulatory affairs with a comprehensive background in biomedical and quality control environments. Currently serving as a Regulatory Affairs Project Manager and previously as a Senior Regulatory Specialist at OriGen Biomedical since December 2022, Carissa has developed expertise in regulatory processes. Prior experience includes roles at Luminex Corporation, where Carissa held positions as Regulatory Affairs Associate II and Quality Control Associate from November 2018 to December 2022, and at Veridia Diagnostics as a Medical Laboratory Technician from October 2017 to November 2018. Carissa's academic foundation includes a Bachelor of Arts from Southwestern University, where studies were complemented by experience as a Teacher's Assistant and Undergraduate Student Researcher from January 2015 to May 2017.
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OriGen Biomedical
OriGen Biomedical, Inc. is a small, privately-held medical device manufacturer founded in 1997 and headquartered in Austin, Texas. They manufacture a range of products to treat respiratory distress, cancer, genetic conditions, and other life-threatening diseases.