Celeste Miranda
About Celeste Miranda
Celeste Miranda is a Validation Engineer at Bristol-Myers Squibb with over 7 years of experience at the company. She has also worked at Amgen and gained early career experience through internships at Bristol-Myers Squibb and Fluor Corporation.
Current Title and Role
Celeste Miranda holds the title of Validation Engineer at Bristol-Myers Squibb. In this role, she is responsible for overseeing and ensuring the validation of manufacturing processes and equipment. Her work directly contributes to the compliance and quality standards essential in the pharmaceutical industry.
Professional Experience at Bristol-Myers Squibb
Celeste Miranda has been employed at Bristol-Myers Squibb for over 7 years, beginning her tenure in April 2016. She currently serves as a Validation Engineer and was previously an engineering intern in 2014, a position she held for 2 months. In her current and prior roles, she has gained extensive experience in the pharmaceutical manufacturing sector.
Past Role at Amgen
Prior to her current role, Celeste Miranda worked at Amgen for a brief period. From 2015 to 2016, she was employed as a Manufacturing Associate for 6 months. This role allowed her to gain critical experience in the manufacturing processes and operations within the biopharmaceutical industry.
Early Career Internships
Celeste Miranda built a foundation for her career through strategic internships. In 2013, she completed a 3-month engineering internship at Fluor Corporation, providing her with initial exposure to engineering principles and industry practices. The following year, she spent 2 months as an engineering intern at Bristol-Myers Squibb, further enhancing her technical skills and familiarity with the pharmaceutical field.