to drive, facilitate and coordinate all process and product development activities related to Pharmaceutical Development of complex generic products together with external and internal partners
to be the interface with CDOs for technical product development activities
to review project progress in line with associated budget
to monitor the preparation and review (when appropriate) the CMC section of regulatory files and interface with the regulatory group
to drive risk management through risk assessment and development of mitigation plans
to ensure appropriate communication within the project team and report on the project status
Your qualifications
Bachelor's or Master's degree or PhD in a scientific or related discipline, with significant previous experience in the life sciences, ideally in the pharmaceutical or biotech industry
fluent in German and English.
sound ability in using project management tools
well developed analytical and conceptual skills with a solution-orientated behaviour