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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