• Ness Ziona


about this position

  • To implement standards, methods and procedures in CMC processes
  • To follow in-house and external GMP manufacturing and support all related QA activities
  • Participate in the new product introduction process to determine requirements for documentation, materials, training, equipment.
  • To review and approve production batch records, Batch release
  • To lay down procedures for the preparation, approval, authorization, control and revision of SOPs
  • Responsible for training and implementation of SOPs
  • To maintain environmental monitoring tracking and trending, perform internal investigation in case of deviation.
  • Lead investigations related to Manufacture process / Equipment, CAPA’s, Change Control.
  • Review and approve calibration, IQ, OQ, PQ reports.
  • Review submission documents to ensure organization, clarity, accuracy, format and consistency.



    • Bachelor's Degree or higher within the Life Sciences space
    • 2+ years of experience within a quality role in a biologics focused environment
    • Experience in GMP manufacturing activities as review of batch records, OOS, CAPA, etc.
    • Expertise in GMP; strong working knowledge of FDA & EU and ICH regulations in relation to the manufacturing of biologics
    • Attention to details
    • Excellent written English skills
    • Participation in preparation of applications to regulatory authorities – an advantage

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