Northway Biotech
Samuel Akinwande has extensive experience in the biotech and pharmaceutical industries. samuel is currently working as a Principal Associate Scientist at Northway Biotech, where they focus on the development and manufacturing of biopharmaceuticals. samuel'sresponsibilities include analytical development, stability studies, prototype building, and method qualification. Prior to this role, Samuel worked as a Senior Associate Scientist at Northway Biotech and as a Research Analytical Scientist at Integral Biosystems. samuel also has experience as a Senior Analytical Chemist at Cambrex Corp and as an Analytical Chemist II at Eurofins Alphora. Earlier in their career, Samuel worked as a Quality Control Chemist at Piramal Pharma Solutions and as a Chemist at York University. samuel began their career as a Pharmaceutical Manufacturing Associate at Novopharm Pharmaceutical Ind. Overall, Samuel has a strong background in method development, validation, and analysis within the biotech and pharmaceutical sectors.
Samuel Akinwande completed a Bachelor of Science (B.Sc.) in Analytical chemistry/ Applied Biochemistry from York University between 2009 and 2014. samuel later pursued a Master of Science (MS) in Medicinal and Pharmaceutical Chemistry at The Ohio State University from 2020 to 2021. Additionally, in the same period, they obtained a Pharmacy Graduate Certificate in Regulatory Affairs in Drug Development from the University of Cincinnati.
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Northway Biotech
Northway Biotech is a Contract Development and Manufacturing Organization (CDMO) located in Waltham, MA, USA, and Vilnius, Lithuania, EU. Extensive expertise in drug substance and drug product development, as well as GMP compliant manufacturing, makes us exceptionally well-versed in all aspects of the biopharmaceutical value chain – from gene to drug manufacturing in microbial and mammalian expressions systems. Our customers appreciate our ability to react rapidly to unexpected project changes, adjusting timelines, and availability of additional capabilities to meet our customers' evolving needs. We are deeply invested in providing high-quality, world-class contract development and manufacturing services with vast flexibility and responsiveness backed by a strong foundation in science and technology innovation. Northway Biotech end-to-end services include: Cell Line (Mammalian & Microbial) Development Analytical Methods Development Formulation Development Upstream & Downstream Process Development (USP & DSP) cGMP Manufacturing of Biologics & Biosimilars (Drug Substance, Drug Product) cGMP Master and Working Cell Bank Manufacturing cGMP pDNA Manufacturing Fill & Finish (F&F) Quality Assurance, Quality Control, and Regulatory CMC Support