Sejal Chavda

I’m a detail-oriented lifesciences professional with 4+ years of academic and industry experience in regulatory compliance, data-driven consulting, stakeholder communication, and process optimization within highly regulated environments.

In my recent Process Sciences Associate role, I contributed to end-to-end protein purification implementation using AKTA and UNICORN systems, improving protein purity and lab throughput by 25%. I also supported method development and validation in compliance with cGMP standards, increasing data accuracy by 20%.

I’m especially focused on data integrity and workflow design—transitioning paper-based workflows to electronic lab notebooks (ELN) and LIMS to increase operational efficiency by 60%. I develop training documentation to support onboarding and knowledge transfer, and I conduct stakeholder meetings to align project goals and ensure regulatory compliance across QA/QC and process sciences.

Earlier, I strengthened my lab execution and documentation discipline through GLP-aligned work at NJIT, including NMR spectroscopy, distillation, and GLP lab data documentation that improved traceability and reduced data retrieval time by 30%. I also bring collaborative problem-solving from capstone work on secure digital systems and regulatory-compliant e-commerce processes, and I’m eager to bring value-driven leadership to the Infusion consulting team.