AD, US Development Project Management. In-House

$500 million! That’s the savings Sandoz has provided in just two years to the US healthcare system as a result of the successful adoption of one of our oncology supportive care biosimilar into clinical practice. Sandoz has eight biosimilar approved globally – including four in the US – and more than ten in the pipe-line. Biosimilar may enable more patients to access advanced biologic medicines earlier, and Sandoz has proven that biosimilar offer significant savings for overburdened health systems. We are looking for curious, innovative, driven people to help us get these products into the market. Maybe that’s you.<br><br>Your responsibilities will include, but are not limited to: <br>• Responsible for defining and executing project strategies in alignment with US portfolio goals and assumptions<br>• Manage all in house development projects with critical portfolio impact to the US market (high risk, complex, and valuable). <br>• Plan and execute all project related activities by working directly with Sandoz Development Centers and required cross-functional teams including, Regulatory Affairs (RA), Product Development (PD) functions Quality Assurance (QA), Medical Affairs (MD), Intellectual Property (IP) and Manufacturing Science & Technology (MS&T) to evaluate all development related aspects of in house product development opportunities.<br>• Build relationships with Product Development Leadership and other pipe-line managers across Commercial PD organization; anticipate and address stakeholder needs<br>• As project owner, evaluate and communicate risks and challenges to Product Development and executive leaders. <br>• Prepare and execute risk mitigation plans with cross functional teams, when required.<br>• Propose and execute competitive strategies for project timelines, cost and quality, covering also the project strategies for development, regulatory as well as manufacturing and IP pathways. <br>• Monitor completion of key development tasks through milestone completion, quality gates, and stage gating processes<br><br>This position will be located at the Princeton site and will not have the ability to be located remotely. This position will require 20% travel as defined by the business (domestic and/ or international).<br><br> [#video#https://www.youtube.com/watch?v=8ZgyAWo0yg8 {#400,300#}#/video#]