Experienced pharmaceutical professional with a strong background in CSV (Computer System Validation) and expertise in Pharma 4.0 and Digitization. Proficient in implementing and managing CSV processes to ensure compliance with regulatory standards. Skilled in leveraging digital technologies to optimize pharmaceutical operations and enhance efficiency. Proven ability to adapt to evolving industry trends and drive innovation in the pharmaceutical sector
Requirements Gathering
To utilize my comprehensive expertise in CSV (Computer System Validation), Pharma 4.0, Digitization, and project management within the pharmaceutical domain. Seeking a strategic role where I can lead and execute initiatives to enhance operational effectiveness, ensure regulatory compliance, and drive digital transformation. Committed to leveraging my project management skills to oversee successful implementation of innovative solutions, fostering collaboration across teams, and delivering tangible results in alignment with organizational objectives.
Notice Period: 2-Months
Date of Birth: 06/13/86
Nationality: Indian
Marital Status: Married
HPLC/UPLC, ELN, LIMS, Dissolution ICPMS, LCMS, Particle size distribution 2000s and 3000s, Surface area analyzer, TGA, DSC, AAS, XRD (Bruker and Pan analytical) UV, IR, KF titrator, pH meter and other instruments. Well versed in: 21 CFR part 11 compliance, ICH guidelines, Audit preparation and Laboratory compliance. Review and compliance of QMS like, OOS/OOT, Laboratory incidents