Job OverviewQA Specialist (Biotech) requires 3 years of experience in the biotech/pharmaceutical industry within research and development or commercial organizations.RequirementsPharmaceutical or Biotech industry experienceExperience with VeevaExperience in a cGMP manufacturing environmentFamiliarity with FDA regulationsKnowledge of Kneat, Slinshot, SAP, and Blue Mountain RAMKnowledge of manufacturing, batch record review, and/or analytical analyses for the biotech/pharmaceutical sectorDegree in Chemistry, Biology, or a related fieldResponsibilitiesPerform inspection and disposition of raw materials and componentsSupport incoming material release activities within the ERP system, ensuring compliance with applicable regulations and internal proceduresObtain Certificates of Analysis (CoA), Certificates of Compliance (CoC), and other required documentation from vendors in alignment with the Master SpecificationConduct thorough reviews of logbooks and Work Orders across Manufacturing, Engineering, Quality, and Warehouse departments to ensure entries are complete, accurate, and compliant with company policies and proceduresProvide QA review/approval of completed Manufacturing batch records in a timely manner and ensure the entries adhere to company policies and procedures#J-18808-Ljbffr
