Marianne Hauge

Marianne Hauge has a diverse work experience spanning over several companies and roles.

Marianne started their career in 1990 at Dianalund as a Quality Assurance Manager, where they were responsible for implementing a complete quality system based on GMP and preparing the company for approval by the Danish Medicines Agency.

In 1992, they worked as a Regulatory Affairs Officer at Heigar & co A/S before becoming the Owner of PN Pharma in 1993.

From 1998 to 2001, they held roles as a Pharmaceutical Advisor at Eurovita A/S and as a Quality Assurance Manager at Eurovita International A/S.

Marianne then joined Nycomed Danmark in 2001 as a Regulatory Affairs Manager until 2008 when they became an International Regulatory Coordinator at Nycomed: a Takeda Company.

In 2008, they transitioned to Takeda Pharma A/S, where they held various positions including Associate Director, Head of Global Product Support Team, and eventually Associate Director, Europe RA LOC Liaison. Marianne'sresponsibilities included coordinating between global and local functions within Regulatory Affairs, networking, organizing international meetings, and leading a global product support team.

In 2022, they worked as the Head of Regulatory Affairs at Deerland Probiotics & Enzymes before assuming the same position at ADM Denmark A/S later in the year.

Marianne Hauge's extensive experience in Regulatory Affairs showcases their expertise in coordinating global and local functions, leading teams, and ensuring regulatory compliance.

Marianne Hauge completed their M.Sc.Pharm degree in Pharmacy from The Faculty of Pharmaceutical Sciences, University of Copenhagen, from 1979 to 1986. Marianne also obtained a Studentereksamen degree in Matematisk naturfaglig from Brønderslev Gymnasium og HF-kursus from 1975 to 1978. In 2022, they pursued Frivilligkoordinator studies at Ingerfair and VIA College.