Within the boundaries given by a strategic portfolio team you are responsible for leading cross functional teams involved with the development of around 5-10 generic products. You report directly to the Vice President Global Project Management.
You:
- prepare a project execution plan including budget and timelines,
- deliver the project in line with the appropriate quality standards, agreed deadlines and scope,
- are in the lead of a multidisciplinary project team, which includes representatives of several departments, such as Regulatory Affairs, Intellectual Property, API Procurement, Quality Assurance and delegates of the Drug Substance and Drug Product R&D groups,
- are in close contact with the Business Development Managers to align customer’s needs with project execution,
- safeguard that products could easily be implemented in the commercial chain together with the Operational teams,
- clearly oversee and safeguard the projects strategy and are able to discuss impact of changes in strategy, planning and budget with senior management,
- inform the senior stakeholders of the company pro-actively as they are heavenly involved and together you agree on any risks or delays that occur in the project,
- are responsible for the operating plan for the project. This is a comprehensive list of all the studies and activities anticipated to be required to result in a successful registration package,
- are responsible, during the registration phase, for a clear transfer of the developed product to the commercial chain. The goal is that the project can efficiently be handled in the commercial chain.
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