Lissette L.

Lissette L.

Research Investigator @ Bristol Myers Squibb

About Lissette L.

Lissette L. is a Research Investigator at Bristol Myers Squibb in Manatí, Puerto Rico, with extensive experience in quality systems, laboratory investigations, and technical writing.

Current Job at Bristol Myers Squibb

Lissette L. currently holds the position of Research Investigator at Bristol Myers Squibb in Manatí, Puerto Rico. In this role, she leverages her extensive experience in laboratory investigations, quality systems, and technical writing. Her hands-on expertise in areas such as GMPs and GLPs, equipment qualification, and analytical data approval directly supports the research and development efforts at the company.

Previous Experience at Amgen

In 2020, Lissette L. worked as a Product Development Scientist at Amgen in the United States for a brief period of four months. During her tenure, she contributed to product development initiatives, applying her skills in method transfer, chemical analysis, and process improvement. This role was notable for its focus on innovative product workflows and adherence to regulatory standards.

Role at Johnson & Johnson

Lissette L. spent 16 years at Johnson & Johnson as a QC Analyst in Las Piedras, Puerto Rico, from 2003 to 2019. Throughout her long tenure, she was involved in quality control processes, SOP management, change control, and CAPA implementation. Her experience at Johnson & Johnson provided a solid foundation in quality tools, equipment qualification, and environmental monitoring.

Educational Background in Chemical Engineering

Lissette L. completed her Master's degree in Chemical Engineering from the University of Puerto Rico-Mayaguez. Her academic background provided a deep understanding of chemical processes, quality systems, and technical documentation. This education has been instrumental in her ability to handle complex laboratory investigations and develop thorough technical documentation.

Hands-On Experience and Technical Skills

Lissette L. has accumulated vast hands-on experience in laboratory investigations, GMPs and GLPs, Six Sigma, 21 CFR, USP/NF, and EP. She is proficient in LabWare LIMS Validation and LIMS Master Data Configuration. Her technical skills include developing and maintaining quality systems, performing equipment qualifications, and managing method transfers. Additionally, she excels in chemical analysis, technical writing, and bilingual communication in English and Spanish.

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