Principal Scientist

Sandoz

Kundl, Austria

Your key responsibilities:

Your responsibilities include, but are not limited to:

  • You will lead and coordinate the analytical tasks and represent analytics in the project team of assigned projects;
  • You are accountable for managing all analytic related activities of Drug Product development incl. release and stability-testing, characterization of the API, method-development, -transfer and -validation, specification setting, know-how transfer etc.;
  • You will need to communicate effectively across organizational interfaces i.e. project-/program-management; line functions etc.;
  • You will proactively identify scientific, technological and GMP issues, propose creative solutions and communicate key issues to the appropriate management level;
  • You are responsible for high quality analytical registration documents for HA submissions and you will Interact with authorities, act as technical expert in audits, inspections etc.;
  • You are responsible for resource planning.

What you’ll bring to the role:

  • PhD with 3 years relevant experience of product development or MSc with 6 years relevant experience of product development or BSc or equivalent technical education with 12 years relevant experience of product development;
  • Previous experience in analytical areas in drug development in an industrial setting;
  • Proven leader with experience in managing multiple tasks;
  • Demonstrated excellent communication, presentation and management skills;
  • Excellent understanding of regulatory expectations and requirements;
  • Worked in interdisciplinary teams with excellent theoretical and scientific knowledge of product development;
  • Proven track record of creativity, problem solving and productivity;
  • Proficient scientific/technical writing skills;
  • Languages: Fluent in English (oral and written), skills in German are welcome.

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