In this role you will join an ongoing program which is focused on driving a strategy within the regulatory master data environment.
- Management of multiple complex and technical projects ensuring delivery within scopes, time and cost
- Liaison with senior management and other stakeholders
- Management of offshore teams located across Europe and North America
- 8+ years in Project/Program Management positions within the pharmaceutical industry is required
- Knowledge of and experience with ISO IDMP and EMA SPOR is required
- Strong knowledge of Master Data Management technologies is required
- Proven experience working within an Agile methodology is required
- Fluency in English is required
Does this sound like the perfect match to your experience? If so, send Swisslinx your application today!