Francia D.
About Francia D.
Francia D. is a Manager of QA, Drug Product Disposition at Bristol Myers Squibb in Summit, New Jersey, with expertise in GMP, CAPA, and OTC cosmetic manufacturing.
Current Role at Bristol Myers Squibb
Francia D. currently holds the position of Manager, QA, Drug Product Disposition at Bristol Myers Squibb in Summit, New Jersey, United States. In this role, Francia oversees the quality assurance processes for drug product disposition, ensuring compliance with industry standards and regulations. Her responsibilities include implementing and maintaining GMP (Good Manufacturing Practices) and CAPA (Corrective and Preventive Actions) to ensure the highest quality of pharmaceutical products.
Previous Experience at Bristol Myers Squibb
Before her current role, Francia D. served as Sr. Specialist, QA - Drug Product Disposition at Bristol Myers Squibb from 2019 to 2021. During her tenure, she was responsible for quality assurance activities related to drug product disposition in Summit, NJ. Her role included the development and management of SOPs, along with ensuring the adherence to GMP and CAPA protocols.
Past Position at Celgene
Francia D. was employed as a QA Specialist at Celgene from 2018 to 2019 in Warren, New Jersey. In this capacity, she gained valuable experience in the pharmaceutical quality assurance field. Her responsibilities involved supervising quality assurance protocols and performing rigorous checks to maintain high standards in drug manufacturing processes.
Work at Bentley Laboratories, LLC
Between 2015 and 2018, Francia D. worked as a Quality Assurance Document Specialist at Bentley Laboratories, LLC. Over her three-year tenure, she focused on the creation and management of key quality assurance documentation. Her role also included involvement in OTC (Over-the-Counter) cosmetic manufacturing, ensuring the production adhered to established quality standards.
Educational Background and Professional Training
Francia D. earned a Master’s degree in Pharmaceutical Management from the New Jersey Institute of Technology, completing her studies between 2018 and 2020. Prior to that, she obtained a Bachelor of Arts in Humanities and Justice from John Jay College (CUNY), finishing in 2011. Her formal education has equipped her with a robust foundation in pharmaceutical management and humanities.
Industry Skills and Expertise
Throughout her career, Francia D. has developed expertise in GMP (Good Manufacturing Practices) and CAPA (Corrective and Preventive Actions). She is proficient in Microsoft Office applications and has a solid background in customer service within the pharmaceutical industry. Her experience includes quality assurance leadership, OTC cosmetic manufacturing, and the creation and management of SOPs.