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Quality Control Analyst II

Equal Opportunity EmployerPurpose of Position:The position involves the performing of routine and non-routine analyses of raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance to other QC Analysts. The individual troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required.Key Responsibilities:Understands importance and priority of EHS and takes personal responsibility for their own safety; looks out for the safety of colleagues and avoidance of all incidents; willingly engages in and embraces activities to improve EHS performance in the working environment.Test and analyze samples in a timely manner in support of project plans in accordance to cGMP guidelinesReview analytical data for compliance with specifications and cGMP guidelinesAssist in development of experimental procedures and protocolsDevelop/revise documentation such as SOP, testing procedures and material specificationsProvide training and guidance to other analystsJob Knowledge Required:BS in chemistry, biology or related discipline2-5 years experience as a QC analyst/chemist in a GMP environment preferredExperience and familiarity with analytical testing equipment and methodology including HPLC, Karl Fischer, Spectrophotometry (UV/VIS, IR, NMR), and possibly LCMS.
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CEO of Nitto Denko
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Hideo Takasaki
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Our mission is to continue to build value for our customers, as they progress through drug development into commercialization. And as a member of the Nitto Denko Corporation (www.nitto.com), Avecia is committed to the future of the oligonucleotide...

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Full-time, on-site
DATE POSTED
August 8, 2024

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