Jovita D Sa
About Jovita D Sa
Jovita D Sa is a Validation Specialist at Bristol-Myers Squibb in New Jersey, with extensive experience in CAPA and LIMS systems.
Title
Jovita D Sa is a Validation Specialist currently employed at Bristol-Myers Squibb in New Jersey, United States.
Education and Expertise
Jovita D Sa completed her MCA in Computer Science from Visvesvaraya Technological University, attending from 2003 to 2006. She is certified as a LabWare LIMS V6 Administrator since 2009 and as a V7 Administrator since 2017. Additionally, she holds certification in LabWare LIMS Basic since 2017.
Professional Experience
With a strong background in pharmaceutical software validation, Jovita has been working as a Validation Specialist since May 2011. Her role involves developing Requirement Specifications, Validation Plans, Test Plans, Test Scripts, and Summary Reports. Jovita has extensive experience with CAPA and LIMS systems, including LabWare LIMS and STARLIMS v10.
Technical Proficiency
Jovita is proficient in using Mercury Quality Center, Win Runner, and Test Director for manual testing. She is experienced in defect tracking, analysis, management, and reporting using Quality Center and Test Director, and has solid skills in various types of testing including GUI, Functional, Integration, System, Performance, and Regression testing.
Regulatory Knowledge
Jovita D Sa holds sound knowledge of regulatory standards such as 21 CFR Part 11, 21 CFR Part 210/211, 21 CFR Part 820, cGxP, and SDLC regulations, ensuring compliance in her validation work.