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Current Experience

  • Head Global Product Supply

    Since January 2016
    • definition and execution of the global product Manufacturing Strategy to ensure robust market supply • selection of external manufacturers and 3rd party alliance & Performance Management • definition of integrated strategic and operational Manufacturing plans • cross-functional launch management • definition of Manufacturing life cycle management Strategy • Definition and execution of the global product manufacturing strategy to ensure robust market supply • Selection of external manufacturers and 3rd party alliance & performance management • Definition of integrated strategic and operational manufacturing plans • Cross-functional launch management • Definition of manufacturing life cycle management strategy

Past Experience

  • Head Global Technical Project Management

    June 2014 --- December 2015
    • disciplinary Leader of a group of global technical project leaders in four countries and Project Management office • accountability for technical progress several development and life-cycle programs for sandoz Biopharmaceuticals and support of development projects for novartis pharma and third parties • dual reporting line into head global technical development and head global Pharmaceutical and device development • resource management for two departments; fte Planning and responsibility for a development budget of >60 musd p.a.

  • Global Program Leader

    January 2009 --- June 2014
    global lead for development programs of biosimilar compounds; lead of multidisciplinary global program teams; provide strategic Leadership; lead development of integrated strategic(commercial/development) and operational development plans for development programs with the objective to optimize value, time, resources and risks; lead scenario generation, contingency Planning, conflict resolution and the process of decision-making within the team

  • Liaison Manager RegCMC

    April 2007 --- December 2008
    lead of global regcmc project teams; compilation of technical submission Documentation for biopharmaceutical development projects; strategic guidance to project teams

  • Regulatory Consultant

    September 2004 --- March 2007
    regulatory Consulting to clients on Pharmaceutical Development projects

  • Scientist

    March 2001 --- August 2004
    Scientist in development of biopharmaceutical compounds.


LinkedIn Assessment :
BiopharmaceuticalsPharmaceutical DevelopmentImmunologyInternational Project ManagementBiosimilar DevelopmentCMC Regulatory AffairsCross-functional team leadershipMedical DevicesArzneimittelzulassungMonoclonal AntibodiesRegulatory affairsCMO selectionDevice DevelopmentCombination ProductsTechnical Project ManagementStrategic LeadershipProject LeadershipMedizinprodukteBiopharmazeutikaProduktentwicklungProjektmanagementBiowissenschaftenGMPImmunologieAbteilungsValidation


  • Diploma in Chemistry from Ruprecht-Karls-Universität Heidelberg / University of Heidelberg in 2000
  • PhD in Biology from Ruprecht-Karls-Universität Heidelberg / University of Heidelberg in 2000
  • in from MPI Biochemie Martinsried in 0000
  • in from MPI Biochemie Martinsried in 0000


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    12 weeks
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position :    100% FTE
  • International:

Area / Region



Driving License
  • No

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