Riya Mavi
About Riya Mavi
Riya Mavi is a Senior Validation Engineer at Bristol-Myers Squibb with over a decade of experience in the pharmaceutical and medical manufacturing industries.
Current Role at Bristol-Myers Squibb
Riya Mavi is currently serving as a Senior Validation Engineer at Bristol-Myers Squibb in New Jersey. With over seven years at this pharmaceutical giant, she has been instrumental in leading validation efforts to ensure compliance with regulatory standards. Her role involves extensive work on projects that have supported the successful launch of new pharmaceutical products, leveraging her deep expertise in validation engineering within the pharmaceutical sector.
Past Experience at Baxter International
Riya Mavi worked as a Validation Engineer at Baxter International Inc. for three years from 2013 to 2016. Located in Vernon Hill, IL, this role enabled her to hone her skills in ensuring compliance with regulatory standards and contributed to the validation processes essential in pharmaceutical manufacturing. This period was critical in shaping her career, providing her with substantial experience that she carried forward into her current role.
Early Career at APP Pharmaceuticals
Riya Mavi began her career in validation engineering at APP Pharmaceuticals in Barceloneta, Puerto Rico, where she worked for two years from 2011 to 2013. During her tenure, she was responsible for various validation projects essential to the company's manufacturing processes. This role laid the foundation for her extensive expertise in the field, particularly in ensuring regulatory compliance in pharmaceutical manufacturing.
Expertise in Validation Engineering
Riya Mavi has accumulated over a decade of experience in validation engineering, particularly within the pharmaceutical and medical manufacturing industries. Her primary responsibilities have revolved around ensuring that pharmaceutical manufacturing processes comply with stringent regulatory standards. This extensive background underlines her capability in contributing to the successful launch of new pharmaceutical products through meticulous validation projects.