Kosal Keo

Strategic Advisor To The Board at Boston Technology Research

Kosal Keo has extensive work experience in various roles and companies. Kosal is the Founder and Chief Product Officer of Sware since June 2019. Prior to that, they were the Founder and Chief Executive Officer of Boston Technology Research from May 2014 to May 2019.

Before their entrepreneurial ventures, Kosal worked at Sanofi as an Associate Director from 2008 to 2013, where they were responsible for IT Quality, Risk management, Change management, Validation, Security, and compliance functions. Kosal developed and oversaw compliance programs across R&D groups, such as PharmaCovigelence, Clinical, Research and Development, and Medicals affairs.

Kosal also has experience in Compliance Validation as a Compliance Validation Manager at Valcom Group Inc from 2003 to 2005. Prior to that, they worked as a QA Validation Specialist at Wyeth from 2000 to 2003 and as a Validation Engineer at PAREXEL from 1999 to 2000.

Kosal began their career as a Micro-validation Lab engineer at EMD Millipore, where they worked from 1996 to 1999.

Overall, Kosal Keo has a diverse background in compliance, validation, and executive roles, and has consistently demonstrated strong leadership and expertise in the pharmaceutical industry.

Kosal Keo attended the University of Massachusetts Lowell from 1995 to 1999, where they pursued a BS degree in Biotechnology.

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Boston, United States

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Boston Technology Research

Everything you need to manage the compliance of the systems you rely on most. BTR (Boston Technology Research) is a regulatory technology company serving healthcare, life sciences and SaMD. We provide enterprise-wide solutions that automate how companies ensure compliance with domestic and international regulatory requirements. BTR is headquartered in Chelsea, MA with a global workforce located throughout North America, Europe and Asia. BTR was founded by the same leaders who took Veeva and the life sciences industry into the cloud. We’re validation pioneers in the industry transition to Computer Systems Assurance (CSA), building the software needed to actualize the FDA’s vision for Industry 4.0.


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51-200

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