Lymari Sanchez
About Lymari Sanchez
Lymari Sanchez is the Associate Director of Manufacturing Science & Technology at Bristol Myers Squibb in New Jersey, with extensive experience in pharmaceutical validation and engineering.
Company
Lymari Sanchez is currently associated with Bristol Myers Squibb, a global biopharmaceutical company known for its focus on discovering, developing, and delivering innovative medicines. She has been with Bristol Myers Squibb since April 2016, contributing to the company's mission of advancing research and development in the healthcare sector. Her role is based in New Jersey, United States.
Title
Lymari Sanchez holds the title of Associate Director, Manufacturing Science & Technology at Bristol Myers Squibb. In this capacity, she is involved in overseeing key processes and technology within the manufacturing domain, ensuring high standards of quality and efficiency in production.
Education and Expertise
Lymari Sanchez has a strong educational background with a Bachelor of Engineering (B.E.) in Chemical Engineering from the University of Puerto Rico, earned between 1995 and 2001. She has extensive experience in oral solid dosage (OSD) process and cleaning validation, equipment and computer system validation, and change control within the pharmaceutical industry. Her skill set is further enhanced by her involvement in Corrective and Preventive Action (CAPA) and experience working with the U.S. Food and Drug Administration (FDA).
Professional Background
Lymari Sanchez has a diverse professional background in the pharmaceutical industry. Her previous roles include Pharmaceutical Technologist Specialist III at Actavis plc in Fajardo, PR (2015-2016), Formulator at Neolpharma PR in Caguas (2013-2015), and Validation Consultant at Conde InduServices Corp. (2012-2013). She also served as Senior Technical Services Scientist at McNeil Consumer Healthcare in Las Piedras, PR (2010-2012) and Senior Validation Specialist at Echo Consulting Group (2006-2010). Earlier in her career, she was a Pharmaceutical Technology Validation Specialist II at Watson Laboratories in Humacao, PR (2004-2006) and a Product Transfer Scientist II at MOVA Pharmaceuticals in Manati, PR (2001-2004).
Achievements
Throughout her career, Lymari Sanchez has demonstrated a consistent ability to manage complex manufacturing and validation processes in the pharmaceutical industry. She has successfully led initiatives in OSD process and cleaning validation, and equipment and computer system validation. Her work in change control and Corrective and Preventive Action (CAPA) has been pivotal in maintaining high standards of compliance and operational efficiency. Her collaborations with the U.S. Food and Drug Administration (FDA) underscore her expertise in regulatory affairs and quality assurance.