Yolymar Mojica

Yolymar Mojica

Qc Microbiologist @ Bristol Myers Squibb

About Yolymar Mojica

Yolymar Mojica is a QC Microbiologist at Bristol-Myers Squibb in New Jersey, United States, with a background in microbiology and pharmaceutical research.

Title at Bristol-Myers Squibb

Yolymar Mojica currently holds the position of QC Microbiologist at Bristol-Myers Squibb in New Jersey, United States. Since joining the company in September 2015, Mojica has been involved in quality control processes related to microbiology, ensuring that pharmaceutical products meet strict quality and safety standards.

Previous Work Experience at AbbVie

Prior to her current role, Yolymar Mojica worked as a Microbiologist at AbbVie in North Chicago, Illinois. During her tenure from 2014 to 2015, which lasted 11 months, she conducted various microbiological tests and contributed to the development and validation of new pharmaceutical products as part of the quality assurance team.

Education and Research at University of Puerto Rico

Yolymar Mojica pursued her academic career at the University of Puerto Rico, where she was a Graduate Student Researcher from 2012 to 2015. She focused on research in microbiology and also earned a Masters in Pharmacy from the University of Puerto Rico School of Pharmacy between 2012 and 2014. Additionally, Mojica completed her undergraduate studies at Universidad De Puerto Rico, majoring in Molecular Biology, Physics, Organic Chemistry, Biology, and Statistics from 2006 to 2011.

Experience as a Manufacturing Technician at Patheon

In 2014, Yolymar Mojica worked at Patheon in Durham, North Carolina, as a Manufacturing Technician for 5 months. In this role, she was involved in the manufacturing processes of pharmaceutical products, ensuring compliance with industry standards and contributing to the efficiency of production operations.

Role as an Inspector at Bristol-Myers Squibb

Prior to her current role, Yolymar Mojica served as an Inspector at Bristol-Myers Squibb in New Jersey from 2011 to 2014. For three years, she was responsible for inspecting pharmaceutical products, ensuring they complied with regulatory standards and conducting quality control checks to maintain product integrity.

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