Principal Scientist (m/f)

REFERENZNUMMER:

323169/11

IHRE AUFGABEN:

-Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances and drug products
-Responsible for analytical methods development, validation, stability and release testing and transfer activities of drug substance and formulated drug product
-Contribute to the overall analytical project strategy
-Write analytical documents (e.g. Analytical methods, Validation reports, Stability reports)
-Author, review and approve GMP relevant documents (e.g. analytical methods, raw data, SOPs, qualification reports for analytical instruments etc.)
-Review analytical batch records according to SOPs

IHRE QUALIFIKATIONEN:

-PhD in analytical chemistry or equivalent
-Profound experience in the pharmaceutical industry, experience in analytical development is of advantage
-Strong scientific knowledge in analytical development
-Fluency in English (oral and in writing)
-GMP knowledge (work history in cGMP environment) is desirable

WEITERE QUALIFIKATIONEN:

R&D scientist