Lobhana Mehta's Linkedin Analytics

A MSc. Biochemist with close to 10 years of experience in Biopharmaceutical industry with extensive cross functional team experience. Excellency in handeling documentation along with hands on experience in working with softwares like Document manager system(DMS), Quality Assurance management system(Trackwise/QAMS), Laboratory information management system(LIMS). Exposure in facing and successful managing Regulatory body Audits (eg: IMB, INVIMA etc.), FDA & Third Party audits. Sound knowledge about drug products(sterile injectables) manufacturing. Proficient in preparing Annual Product Quality Reports along with Process validation reports Good command over SAP for batch releases into market. Expertise in Training systems and audit compliance. Self directed work ethic in both individual contributor and team leadership roles. more than 1 year of experience in managing direct reports in matrixed environment.