Senior Scientist
Sandoz
Kundl, Austria
Your responsibilities include, but are not limited to:
- Design, plan, perform and document scientific experiments as well as analysis and interpretation of the results to drive development and validation of analytical methods for solid and liquid dosage forms;
- Actively support product development with scientific input and generate scientific documents to hand over to internal and/or external partners;
- Report, interpret and present scientific/technical results to management;
- Participate in technical teams and fulfill assigned project tasks and responsibilities;
- Support generation of international registration documents;
- Ensuring adherence to requirements of cGMP, pharmacopoeias, health authorities and company quality system;
- Actively participate in knowledge exchange; train and mentor associate scientists and technicians, temporary employees, and employees under training/education.
What you’ll bring to the role:
- University degree in chemistry or pharmacy or related science with focus on analytical chemistry or equivalent;
- 5+ years of experience in pharma industry, preferably in analytical development, under GMP requirements;
- Strong background in development and validation of analytical methods, with hands-on experience in dissolution and chromatographic methods;
- A deep understanding of the pharmaceutical development requirements, analytical technological questions as well as scientific and process-oriented thinking;
- Passion for supporting the international scientific team in solving pharmaceutical challenge;
- Strength in organizational skills and proactive working, hands on attitude as well as excellent communication and team orientation are essential;
- Proficient in English (written and spoken), German is a plus.
Desirable requirements:
- Audit experience highly appreciated;
- Knowledge of dissolution apparatus USP4, IVIVC and QC dissolution method development.
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