A dynamic and highly motivated professional with experience of handling validation of systems and software associated with Life Science - Clinical Data Solutions, Discovery & Lab Informatics and Technology Services for Regulated Environment for Bio-Pharma companies (Pharmaceutical, Bio-technology, Medical Devices), Contract Research Organisations and Product companies. At the moment, I am working in capacity of Validation Lead and have expertise in EU Annex 11 and 21 CFR Part 11 regulations and FDA regulations. I have worked on multiple assignments which includes though not limited to, drafting business requirement document, test script analysis, test log drafting for OQ, IQ and PQ, documenting traceability matrix and data analysis.SpecialtiesStrong Technical Skills, Good Leadership Skills, Excellent Communication, Out of the Box Thinking, Willingness to Learn, Self-motivated,Highly Ethical and Trustworthy