Jackelyn Lozano
About Jackelyn Lozano
Jackelyn Lozano is a Regulatory Affairs Analyst specializing in the Latin American market, currently working at Bristol-Myers Squibb in New York.
Company
Jackelyn Lozano is currently employed at Bristol-Myers Squibb. She works as a Regulatory Affairs Analyst for the Latin American region, focusing on mature brands. Her position is based in New York, New York, United States. Bristol-Myers Squibb is a well-known pharmaceutical company engaged in the discovery, development, and delivery of innovative medicines.
Title
Jackelyn Lozano holds the title of Regulatory Affairs Analyst for the Latam Region Mature Brands at Bristol-Myers Squibb. Her role involves navigating regulatory requirements and ensuring compliance for mature brands within the Latin American market.
Education and Expertise
Jackelyn Lozano has a solid educational background, having studied at a university from 2008 to 2012 for four years. She specializes in regulatory affairs, focusing on the Latin American market, and has accumulated over eight years of experience in this field. Her expertise spans both the pharmaceutical and medical device industries, enabling her to navigate complex regulatory landscapes effectively.
Professional Background
Jackelyn Lozano's professional journey began in regulatory affairs as a trainee at B. Braun Medical in 2013. She then moved to Bristol-Myers Squibb, serving as a Regulatory Affairs Trainee for the Latam Region Mature Brands from 2013 to 2015. Afterwards, she gained experience as a Regulatory Affairs Analyst at Quimica Suiza in 2015 for eight months, before rejoining Bristol-Myers Squibb in her current role. Additionally, she has worked in the Molecular Biology, Microbiology, and Biotechnology Laboratory as a research student for two years while at university.
Regulatory Affairs Experience
Jackelyn Lozano has extensive experience in regulatory affairs, particularly in the Latin American region. She has been working in this field for over eight years, dealing with both pharmaceuticals and medical devices. Her responsibilities include ensuring that mature brands comply with regional regulatory requirements, a role she has continuously fulfilled at Bristol-Myers Squibb since 2013.