Sandoz
- Pharma, Chemie und Medizintechnik
- Biochemiestraße 10, 6250 Kundl, Österreich
- https://www.sandoz.com/careers
- jobs.austria@sandoz.com
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- ATU32425809
Principal Scientist (d/f/m)
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
We are looking for you as an experienced Principal Scientist in Pharmaceutical Development to join our team in Sandoz Development Center in Kundl, Austria. We focus on development of oral and parenteral dosage forms. Your responsibilities include, but are not limited to:
Aufgaben
You will lead and coordinate pre-formulation, formulation and process development tasks and represent pharmaceutical development in the project team of assigned projects.
You are accountable for managing all pharmaceutical development related activities of Drug Product development incl. pre-formulation, Quality by Design formulation and process development, technology transfers.
Design, plan, perform and documentation as well as statistical analysis and interpretation of scientific experiments to drive development of final drug product and manufacturing process for solid and liquid dosage forms applying QbD principles with special focus on rigorous DoE
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 documentation for regulatory submissions and you will interact with authorities, act as technical expert in audits, inspections etc.
Qualifikation
3-5 years of hands-on industry experience in formulation, preformulation, deformulation and manufacturing process development
Proficient in using statystical tools like Minitab, Design Expert etc.
Excellent understanding of regulatory expectations and requirements including EMA, US FDA, ANVISA, PMDA
Expert understanding of Data Integrity, cGMP, ICH guidelines and regulatory requirements
Experience working 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), basic German skills are an advantage
Externer Link
https://www.sandoz.com/careers/career-search/job-details/REQ-10000327/principal-scientist-dfm/Gehalt
- Mindestgehalt pro Monat laut Kollektivvertrag:
- 4300 €
- Ungefähres Jahresgehalt abhängig von der Qualifikation:
- 60212 €
Zusatzleistungen
- Flexible Arbeitszeit
- Kinderbetreuung
- Mitarbeiterparkplatz
- Vergünstigtes Mittagessen
- Weiterbildungsmöglichkeiten
- Beschäftigungsart:
- Vollzeit
- Position im Unternehmen:
- Berufserfahrung
- Niveau Schul-/Studienabschluss:
- Berufsfeld:
- Chemie, Biotechnologie, Lebensmittel, Kunststoffe
- Befristung:
- Unbefristet
- Erwarteter Arbeitsbeginn:
- Sobald als möglich
- Veröffentlicht:
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