BrightOwl Loader Loading


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

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 0
  • in from MPI Biochemie Martinsried in 0


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