Principal Scientist
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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