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Senior Scientist (m/f/d)


Required qualifications:

  • Ph.D. in pharmaceutical sciences, biochemistry, chemical engineering or other related discipline with 3+ years' experience, MS in a similar discipline with 7+ years or BS with 10+ relevant experience
  • Drug product manufacturing process development experience including training on aseptic processing of sterile products

Key responsibilities:

  • Development of drug product formulation and manufacturing process
  • Design and execution of process characterization
  • Author protocols, development reports, risk assessment, and other technical documents
  • Technology transfer to pilot manufacturing sites for clinical supplies and subsequent technology transfer to commercial manufacture sites
  • Represent DPDO in cross functional matrix teams as it relates to biosimilar and novel biologic products within Teva
  • Coordinate, support and interface with GMP manufacturing facility or external contracting organization for the manufacture of drug product non-clinical and clinical batches
  • Provide technical support to troubleshooting issues with drug product processing technologies and equipment
  • Serve as a subject matter expert to support manufacturing operations with technical evaluation of change controls, deviations, corrective and preventative actions

» Job description

Teva Pharmaceutical Industries Ltd.
West Chester, Pennsylvania [Vereinigte Staaten]