Jaswant Singh is a strategic professional with over 16 years of rich and qualitative experience, specializing in Qualification and Validation, primarily within the Pharmaceutical sector. His expertise encompasses a comprehensive understanding of computer system applications validation, regulatory compliance, risk assessment, Qualification/Validation and quality assurance. He possesses a strong background in guiding projects through various stages of the Software Development Life Cycle (SDLC) and Software Testing Life Cycle (STLC), while adhering to regulations such as 21 CFR Part 11 and EU annex 11. Jaswant has a proven track record of driving process improvements, conducting risk assessments, and maintaining compliance with FDA Regulations. His proficiency extends to preparing and implementing Quality Management Systems, Qualification, Validation, and review procedures for Equipment, Facility, Utilities, Products, and Processes. He holds substantial experience in Validations and Qualification of different dosage forms, including Sterile and Non-Sterile formulations. Jaswant's expertise further includes audits for regulatory bodies such as USFDA, MHRA, WHO and EU-GMP. Throughout his career, Jaswant has been dedicated to operational excellence and regulatory compliance, consistently meeting and exceeding organizational goals. He is recognized for his ability to identify improvement areas, lead teams, and streamline processes to ensure quality assurance and compliance with the latest technological advancements and regulations. Jaswant Singh's core competencies lie in Quality Assurance, Validation Planning & Execution, Process Improvements, Cost Optimization, Compliance Management, and Team Management. He has a solid record of delivering results in various senior roles, demonstrating his commitment to excellence in the field.