Category
Regulatory, Quality and Clinical
Description
Your responsibilities
- 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
- strong target orientation
- excellent interpersonal communication skills
- willingness to travel