Job Detail

Senior Manager, Associate Director External Collaboration

Inseriert am: 11.08.2020

SUMMARY


This position is within the Global Biologics External Manufacturing in the Technical Operation Department. The position will play a leading role in the collaboration between Incyte and MorphoSys to ensure successful launch and commercialization of Tafasitamab in the EU according to the expected time-lines. In addition, the incumbent will support the integration of MorphoSys and Tafasitamab external manufacturing partners (CMOs) into the Incyte supply chain. Tafasitamab is an investigational monoclonal antibody currently in clinical development for the treatment of B cell malignancies.


DUTIES AND RESPONSABILITIES



  • In collaboration with MorphoSys, lead a team for the commercialization and the launch for Tafasitamab IN EU and other regions


  • Technical and business customer liaison between Incyte and Morphosys


  • Work closely with supply chain to ensure the launch readiness


  • Responsible for developing processes and structures to supportlaunch workstreams


  • Close engagement with cross-functional counterparts and teams; serving as a key interface with the Supply Chain and the external partner


  • Single point of contact for Morphosys in terms of forecast and demand planning


  • In collaboration with supply chain, develop an inventory strategy to ensure product supply to all markets


  • Accountable for converting demand planning forecast into production / inventory requirement for external suppliers


  • Review and assess RFPs, Contracts and Statement of Works from technical & management point of view


  • Establish, manage and oversee all aspects of the relationship with Biologics co-manufacturing partners


  • Manage and track POs and budgets


  • Develop and implement product cost reduction


  • Lead the negotiations and subsequent maintenance of the contractual pricing and content on new and contract renewals


  • Work effectively in a matrix organization


  • Manage and/or create internal documents and SOP’s to ensure cGMP compliance


  • Implement commercial “GXP’s” guidelines and requirements for biologics

    Contribute positively to a strong culture of business integrity and ethics


  • Act within compliance and legal requirements as well as within company guidelines


  • Delegate to: Global Biologics Commercial Manufacturing

    REQUIREMENTS


  • Bachelor’s degree required; MBA or advanced degree preferred


  • Experience in Pharmaceutical or Biotech organization


  • Experience in Project/Program management in life sciences organizations


  • Background and understanding of supply chain management principles such as Production Planning, Purchasing, Forecasting and Logistics


  • English fluency written and spoken, French and/or German is a plus


  • Excellent communication skills


  • Natural problem solver and negotiator


  • Strong analytical, organizational and execution skills


  • Ability to work both independently and as part of a team is essential


  • Proficiency in usual Microsoft applications


  • Excellent written and verbal skills


  • Available to travel




Disclaimer:  The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications.  Management reserves the right to change or modify such duties as required.


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