About me

As a seasoned Quality Assurance leader with over two decades of dedicated experience in the pharmaceutical industry, I, Mahaboob Subhani Sayed, currently serve as Senior Manager of Quality Assurance at Laurus Labs Limited. My career has been defined by a steadfast commitment to regulatory excellence, operational integrity, and the advancement of quality management systems that ensure patient safety and compliance with global standards such as GMP and FDA. Specializing in regulatory compliance, validation, audits, and technology transfer, I have honed my expertise in managing complex investigations—including Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and Corrective and Preventive Actions (CAPA)—while leading cross-functional teams to foster a culture of continuous improvement. My proficiency extends to vendor management, quality risk management, and the validation of cleaning processes, analytical methods, and computerized systems. I am adept at leveraging tools like APQR, Minitab for statistical analysis, and implementing lean methodologies to enhance efficiency and reliability across supply chains. Throughout my professional journey, I have held pivotal roles at esteemed organizations such as Laurus Labs, Lantech Pharmaceuticals, Granules Omnichem (now Ajibio-Pharma), Hetero Drugs, Aurobindo Pharma, Allana Group, Mylan Laboratories, and Nagarjuna AgroChem. In these capacities, I have spearheaded vendor qualifications, conducted internal and external audits, overseen technology transfers for CDMO and CRO projects, and ensured seamless compliance during regulatory inspections. My contributions have consistently driven process optimizations, strengthened client relationships, and upheld the highest standards of data integrity and product quality. Holding a Master's degree in Organic Chemistry, I am further distinguished by certifications in Total Quality Management & ISO 9000, an Advanced Diploma in Pharmaceutical Quality Assurance Management, and Lean Six Sigma Green Belt. I remain at the forefront of industry advancements through participation in seminars and webinars on topics ranging from FDA compliance overviews to WHO GMP transitions and technical writing skills. Driven by a passion for excellence and innovation in pharmaceutical quality, I am committed to mentoring teams, setting strategic KPIs, and navigating the evolving landscape of global regulations. I invite you to explore my insights and connect on how we can collaborate to elevate quality standards in the industry