Plan, design and perform experiments to characterize pharmaceutical micro- and nanosuspensions, including illustration, interpretation and reporting of results
Develop and validate QC methods for particle and powder characterization to analyze drug products, drug substances and excipients
Provide raw data documentation, evaluation and results interpretation of scientific experiments with high focus on quality
Meet quality, quantity and timelines in all assigned projects
Actively contribute to analytical method transfer to other development sites, production or contract laboratories
Contribute to maintenance of infrastructure and equipment
Work according to appropriate SOPs, GMP, Quality Directives, Health and Safety (HSE) regulations and internal guidelines
Du solltest haben:
Technical education (HTL, FH) or BS / MS in analytical chemistry or equivalent
1 -2 years’ minimum proven experience in pharmaceutical industry, preferred in analytical development in the field of QC and/or particle characterization
Good scientific or technical knowledge in analytical science, in particular in QC and particle/powder characterization techniques
Good knowledge in English and German (oral and in writing)
Ability to perform in a highly dynamic environment
