Melissa Sanchez

Staff Regulatory Affairs Specialist at Werfen

Melissa Sanchez is a seasoned regulatory affairs professional with extensive experience in managing and implementing regulatory functions across various organizations. Currently serving as a Staff Regulatory Affairs Specialist at Werfen since January 2023, Melissa focuses on regulatory strategies and product registrations to ensure compliance with U.S. regulations. Prior to this, Melissa held progressive roles at Asuragen, where responsibilities included regulatory affairs management and strategic documentation improvements. Melissa's expertise also encompasses project management and technical writing, demonstrated through roles at Mirna Therapeutics and Thermo Fisher Scientific, where high-quality documentation and compliance with ISO standards were paramount. Melissa holds a Bachelor's Degree in Biomedical Science from Texas A&M University.

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Werfen

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Werfen is a global leader in in vitro diagnostics (IVD) in the specialties of Hemostasis, Critical Care and Autoimmunity. Our core business is dedicated to R&D, manufacturing and distribution of diagnostic systems for hospitals and clinical laboratories. Our other areas of expertise include Original Equipment Manufacturing, IVD & Clinical Software, Clinical Chemistry, Infusion Therapy, and Medical Devices Distribution.


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Headquarters

Barcelona, Spain

Employees

5,001-10,000

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