Sonia Ramos
About Sonia Ramos
Sonia Ramos is a Validation Specialist with over 25 years of experience in the pharmaceutical and healthcare industries, currently working at Vistapharm, Inc. and Bristol-Myers Squibb.
Title and Current Positions
Sonia Ramos holds the title of Validation Specialist. She is currently working at Vistapharm, Inc. in multiple managerial roles, including Manager Documentation and Document Control Manager. Additionally, she is a Validation Specialist at Bristol-Myers Squibb. She is also targeting QA Specialist and Quality Systems roles while leading QA/Quality Systems Processional Leadership projects.
Professional Background
Sonia Ramos has a professional background spanning more than 25 years in the pharmaceutical and healthcare industries. She began her career in 1990 at Mova Pharmaceutical as a Quality Administrative Assistant, where she worked for 7 years. She then worked as a Documentation Supervisor at Watson Laboratories Caribe Inc. for a decade. Following that, she served as a Documentation Coordinator at BD Caribe for 5 years and as a QA Supervisor at McNeil Healthcare LLC for 4 years. She has also held a Document Control Manager position at a private company.
Education and Expertise
Sonia Ramos studied at the University of Turabo, which laid the foundation for her extensive career. She has a robust background in validation processes and quality systems, gained through her varied roles in documentation management and quality assurance across multiple companies in the pharmaceutical and healthcare sectors.
Experience in Pharmaceutical Industry
With over 25 years in the pharmaceutical and healthcare industries, Sonia Ramos has held several integral roles. Her journey began in the early 1990s, with positions ranging from Quality Administrative Assistant to Documentation Supervisor. She has substantial experience managing documentation and quality systems, making her a seasoned professional in her field.