A double masters, 8 plus years experienced and highly demonstrated working professional in the Pharmaceutical industry with strong background in Validations, QA, Analytical Testing, and QC data review. Knowledge in practical aspects of writing and executing validation protocols in Cleaning, Process and Equipment, and Technical writing skills.Expertise in Review of Validation Protocols and Reports, Review of IQ,OQ, PQ data, QC data, and Stability data, Management of Change Controls, Investigations, Deviations, CAPAs, Internal audits, Supporting Regulatory audits and External audits, Generation and review of SOPs, GMP Training Coordination,Ensuring the CGMP Compliance, Skilled in Analytical Method Developments, Validations, Cleaning Method Validations, Writing Validation Protocols, and Reports. Immense knowledge on GMP(s), GDP(s), and GLP (s).Hardworking, Potential Team Player, Strong Organisational Skills, Effective Communicational Skills, Results Oriented, Analytical Thinking and Proven track record of achieving exceptional results in tight deadlines while paying strong attention to detail without compromising on Quality.