Responsibilities include project management of CMC development programs, acting as primary contact for international clients, and facilitating project success through proactive measures. The role involves project controlling, compiling summary documents, and managing subcontractors.
Requirements
- Master's degree in Pharmaceutical Sciences, Life Sciences, Project Management, or a related field
- Proven experience (>5 years) in project management within the pharmaceutical or biotechnology industry
- In-depth knowledge of pharmaceutical development processes, including preclinical, clinical, regulatory, and manufacturing phases in combination with a strong understanding of regulatory guidelines (FDA, EMA, etc.)
- Excellent team management skills, with the ability to inspire and motivate cross-functional teams
- Proficiency in project management tools and software
- Demonstrated ability to manage multiple projects simultaneously while maintaining attention to detail and meeting deadlines
- High degree of reliability and organizational skills in combination with strong analytical and conceptual skills
- In depth computer skills, ideally experience with project management software
- Excellent communication and presentation skills in German and English with pronounced client orientation
- Willingness to travel and flexibility
Benefits
- Responsible and varied tasks in a motivating working environment
- A permanent position in a dynamically growing international life science group with approx.175 employees
- Optimal induction and training opportunities as well as individual development options
- Appreciation, openness and respect as well as a lively feedback culture
- Flat hierarchies, short decision-making processes and flexibility
- Comprehensive health management
- Job-Bike leasing
- Regular company and team events