Soju Joseph Email & Phone Number | As a Regulatory Affairs Specialist-CMC Lead at QLife Pharma, I have been instrumental in optimizing regulatory processes and driving global compliance for the organization. With 8 years of experience in the pharmaceutical industry, I have a proven track record of successfully navigating complex regulatory environments and delivering regulatory strategies that drive product approvals and ensure compliance with stringent guidelines. I have streamlined the CMC review process, resulting in a remarkable 60% reduction in the time required to compile and submit dossiers to Health Authorities. I have also led the development of product pathways from early stages through the full life cycle, registering over 130 products in multiple markets. Additionally, I have implemented system improvements and cost saving measures that have increased productivity by 40% and reduced production costs by 30%. I hold an Mtech in Pharmaceutical Operations and Management from Birla Institute of Technology and Science, Pilani, and I possess core competencies in regulatory strategy development, standard operating procedure, and CMC regulatory affairs. My career goal is to leverage my expertise and leadership skills to drive regulatory excellence for a forward-thinking pharmaceutical organization. I am passionate about optimizing regulatory processes, fostering innovation, and ensuring a smooth run of regulatory activities.

Soju Joseph

As a Regulatory Affairs Specialist-CMC Lead at QLife Pharma, I have been instrumental in optimizing...
Zone 57, Doha, Qatar

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Soju Joseph’s Email soju.joseph@cipla.com

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Soju Joseph’s Location Zone 57, Doha, Qatar

Soju Joseph’s Current Industry Qlife Pharma

Soju Joseph’s Prior Industry Cipla

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Regulatory Affairs Specialist-Cmc Lead

2018-01-01 00:00:00 - Present

Assistant Manager- Regulatory Affairs

2015-01-01 00:00:00 - 2018-01-01 00:00:00

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Soju Joseph is a As a Regulatory Affairs Specialist-CMC Lead at QLife Pharma, I have been instrumental in optimizing regulatory processes and driving global compliance for the organization. With 8 years of experience in the pharmaceutical industry, I have a proven track record of successfully navigating complex regulatory environments and delivering regulatory strategies that drive product approvals and ensure compliance with stringent guidelines. I have streamlined the CMC review process, resulting in a remarkable 60% reduction in the time required to compile and submit dossiers to Health Authorities. I have also led the development of product pathways from early stages through the full life cycle, registering over 130 products in multiple markets. Additionally, I have implemented system improvements and cost saving measures that have increased productivity by 40% and reduced production costs by 30%. I hold an Mtech in Pharmaceutical Operations and Management from Birla Institute of Technology and Science, Pilani, and I possess core competencies in regulatory strategy development, standard operating procedure, and CMC regulatory affairs. My career goal is to leverage my expertise and leadership skills to drive regulatory excellence for a forward-thinking pharmaceutical organization. I am passionate about optimizing regulatory processes, fostering innovation, and ensuring a smooth run of regulatory activities.