Ruth Goldberg
About Ruth Goldberg
Ruth Goldberg is a Quality Process and Risk Management Team Leader with a PhD in Cell Biology and Immunology from Technion. She has over a decade of experience in leadership roles within the biotech industry, focusing on quality regulatory aspects and methods development.
Current Role at Biosense Webster
Ruth Goldberg serves as the Quality Process and Risk Management Team Leader at Biosense Webster. She has held this position since 2024, contributing to the organization’s commitment to quality and risk management in medical technologies. Her role involves overseeing quality processes and ensuring compliance with regulatory standards.
Previous Experience at Biosense Webster
Prior to her current role, Ruth Goldberg worked at Biosense Webster as the Escalations and Standards NPD Quality Lead from 2022 to 2024. In this capacity, she focused on managing quality escalations and establishing standards for new product development, enhancing operational efficiency and product reliability.
Experience at Pluristem Therapeutics
Ruth Goldberg has extensive experience at Pluristem Therapeutics, where she held multiple positions. She served as the Associate Director of Bioassays and Translational Medicine for nine months in 2022-2023, and prior to that, she was the Compliance and Methods Validations Manager from 2018 to 2022. Her tenure at Pluristem also included roles as Method Development and Validation Manager and QC Method Development and Validations Manager, totaling over a decade of service.
Educational Background in Medical Sciences
Ruth Goldberg has a robust educational background from Technion - Israel Institute of Technology. She earned her PhD in Cell Biology and Immunology from 2001 to 2005. Prior to her doctorate, she completed her MSc in Medical Sciences from 1999 to 2001 and a BSc in Biology from 1996 to 1999, establishing a strong foundation in the life sciences.
Leadership and Industry Expertise
Ruth Goldberg possesses over a decade of leadership experience in the biotech industry, specializing in quality-regulatory aspects and methods development/validations. Her skills encompass Biotechnology, Life Sciences, Quality Assurance, Quality Systems, and the Pharmaceutical Industry. She has experience managing both direct and indirect teams, including vendors and subcontractors, demonstrating her capability in team leadership and project management.