Pharmaceutical in-depth knowledge and expertise in handling and implementing green propellants, specifically HFA 152a and 1234ze, in metered dose inhaler (MDI) formulations. My experience includes setting up production facilities and installing machinery optimized for the safe and efficient use of these environmentally friendly propellants. I have depth integrated knowledge about HFA 152a into MDI formulations, ensuring compliance with environmental regulations while maintaining product… Show more Pharmaceutical in-depth knowledge and expertise in handling and implementing green propellants, specifically HFA 152a and 1234ze, in metered dose inhaler (MDI) formulations. My experience includes setting up production facilities and installing machinery optimized for the safe and efficient use of these environmentally friendly propellants. I have depth integrated knowledge about HFA 152a into MDI formulations, ensuring compliance with environmental regulations while maintaining product efficacy. Additionally, I possess a strong understanding of the unique handling requirements, safety protocols, and machinery installation processes associated with HFA 152a and 1234ze propellants. My work has contributed to advancing sustainable practices in MDI production, reducing the environmental impact of pharmaceutical aerosols. This expertise positions me as a subject matter expert in the transition to eco-friendly propellant systems for inhalation therapies and also khave experience of different kind of new technology available in world related to MDI formulation. Show less

Pharmaceutical manufacturing expert with extensive experience 20+ years in MDIs and DPIs, specializing in optimizing production processes and ensuring regulatory compliance. I have a proven ability to implement effective CAPA strategies, significantly reducing defects and improving product quality. Skilled in managing Quality Management Systems (QMS) aligned with ISO 9001, ISO 13485, and cGMP standards. Proficient in troubleshooting and maintaining MDI/DPI machinery, leading to increased… Show more Pharmaceutical manufacturing expert with extensive experience 20+ years in MDIs and DPIs, specializing in optimizing production processes and ensuring regulatory compliance. I have a proven ability to implement effective CAPA strategies, significantly reducing defects and improving product quality. Skilled in managing Quality Management Systems (QMS) aligned with ISO 9001, ISO 13485, and cGMP standards. Proficient in troubleshooting and maintaining MDI/DPI machinery, leading to increased production efficiency and reduced downtime. My work has also contributed to successful regulatory approvals for new inhalation products. I hold certifications in Quality Engineering, Six Sigma, and ISO auditing, with a strong commitment to continuous improvement and operational excellence & During my tenure at Cipla, I successfully managed registration batches of Albuterol at Cipla's US Boston plant and oversaw commercial batches at Cipla's Morocco plant. I played a crucial role in launching the first approved ANDA Albuterol in Asia, marking a significant achievement for the company. My efforts were instrumental in navigating the challenges of launching this product during the critical period of COVID-19. I was a key member of the team that ensured the timely and successful execution of these projects. My work directly contributed to the approval and market entry of this essential medication. This experience underscores my ability to manage high-stakes projects under challenging circumstances. Show less

Responsible & Accountable for entire pMDI and DPI business & compliance