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Elena Narmontaite

Analytical Methods Development And Quality Control Manager at Northway Biotech

Elena Narmontaite has extensive experience in the biopharmaceutical field, currently serving as the Analytical Methods Development and Quality Control Manager at Biotechpharma UAB since January 2014. In this role, Elena leads a team responsible for the development, qualification, and transfer of analytical methods for investigational medicinal products and active pharmaceutical ingredients. Prior experience includes roles at Teva SICOR Biotech UAB where Elena functioned as an R&D Senior Biotechnologist-Researcher, focusing on method validation and stability studies, as well as the Head of the Biochemical and Physico-chemical Control Group. Earlier positions included contributions to stability studies at SICOR Biotech UAB and HPLC method development at the National Veterinary Laboratory. Elena holds a Master's degree and a Bachelor's degree in Bioengineering from Vilnius Gediminas Technical University.

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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


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Vilnius, Lithuania

Employees

51-200

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