Marie Wulff

Experience

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  Uppsala University

  Apr 1999 - Jun 2000

  Assistant Professor, Dept of Physical and Inorganic Pharmaceutical Chemistry

  Responsibility for examination, seminars, planning and conducting lectures for Chemistry course (10p) in first year within Pharmacy program for MSc students and BS students.

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  Medical Products Agency Läkemedelsverket

  Jan 2001 - Apr 2001

  Evaluator

  Evaluator at the Pharmacy and Biotechnology unit. Responsibilities included evaluation of the chemical-pharmaceutical documentation in applications for drug registration, both within the national and the EMEA approval procedures and participation in quality assurance of evaluations.

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  GE Healthcare

  Apr 2001 - Feb 2010

  Head of the Project Manager department in R&D (Bioprocess), line manager for 8 project managers. Responsible for the execution of the R&D project portfolio within Bioprocess area, ensuring the launches of new products and the maintenance of the existing product portfolio. Responsibility including planning, facilitating, tracking, reporting of projects/portfolio and management of personnel. Responsibility to take decisions and make priorities in the Project Portfolio in accordance with the business strategy. Show less Section Manager, Chromatographic Characterisation, section of 14 employees (2004-2006). Section Manager, Organic Chemistry, section of 9 employees (2003-2004).Manager responsibilities included management of personnel, budget planning and follow-up for section. Supplying projects with resources, know-how, technologies and methodologies within the fields of chromatography, separation technologies, media characterization, primary characterization, organic chemistry and coupling chemistry. Accountable for development of know-how, competencies, new technologies and methodologies according to the long term strategy outlined for the section. Show less

  • Portfolio Director Bioprocess

    Apr 2006 - Feb 2010

  • Section Manager R&D

    Apr 2003 - Mar 2006

  • Scientist R&D

    Apr 2001 - Mar 2003
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  GE Healthcare

  Sept 2010 - Jun 2014

  Line Manager for Quality Control (QC), a department of 90 employees divided into six sections. Responsible for quality control of incoming raw material, intermediates and all finished products manufactured within LS Chemical Production Uppsala. Responsibility also includes Environmental Lab (ISO 17025 accreditation) and Ware house. Head of the Project Management Office department in R&D encompassing 10 employees. Responsibility for project admin, Biotechnologies R&D project portfolio value analysis, budget/financial follow-up, project prioritization process, project management competency and management of personnel. Accountable for Strategic Customer R&D collaborations. Acting Head of Strategic Technologies function, line manager for 5 people, with responsibility for portfolio of long-term research initiatives, internal innovation processes and scouting of disruptive technologies.

  • Department Director Quality Control, Chemical Production

    Jul 2011 - Jun 2014

  • Portfolio Director and Head of PMO Biotechnologies

    Mar 2010 - Jul 2011

  • Head of Strategic Technologies (acting)

    Sept 2010 - May 2011
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  Maquet Getinge Group

  Jun 2014 - Dec 2015

  Director Project Portfolio & Asset Management

  Responsibility for development and implementation of global processes and tools for R&D Project Portfolio and Asset Management within Maquet Getinge Group, including optimization of the global R&D investments, realizing synergistic values through resource allocation and asset utilization.

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  Acute Care Therapies, Getinge Group

  Jan 2016 - Aug 2016

  Senior Director Program Management

  Line manager of global Project Manager department of 14 employees in CTO organization, Acute Care Therapies (ACT). Responsibility for ACT R&D project portfolio value analysis, budget/financial follow-up, project prioritization process, project management competency and management of personnel.

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  GE Healthcare

  Aug 2016 - Mar 2020

  Head of Product Governance and Compliance, Life Sciences

  Line manager of global organization of 75 employees in five teams. Organization supporting all Life Sciences businesses with Product Regulatory Compliance, Technical User Documentation, Product Life Cycle Management systems and Product Data Management processes.

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  Cytiva

  Apr 2020 - now

  Leading global organization of 250 employees divided into five departments. Organization innovating, developing and supporting products for protein purification. Head of global organization with 85 employees in five teams. Organization supporting business with Product Regulatory Compliance (non-MD products), Technical User Documentation, Product Life Cycle Management systems and processes.

  • Vice President, R&D Resins & Technology

    May 2023 - now

  • Head of Product Governance and Compliance

    Apr 2020 - Apr 2023