Ellen Rønneberg's Location
Oslo, NO
Ellen Rønneberg's Work
- Head of Unit, Reliable Supply @ Norwegian Medicines Agency
- Head of Section, Regulatory Affairs @ Norwegian Medicines Agency
- Senior Advisor, Quality Assessor @ Norwegian Medicines Agency
- Director CMC, Regulatory Affairs @ Pronova BioPharma - now part of BASF
- Manager CMC Documentation, Regulatory Affairs @ GE HealthCare
- Registration officer, Quality documenation, Drug Regulatory Affairs @ GE HealthCare
- Research scientist, Pharmaceutical R and D @ GE HealthCare
- Sales representative @ MSD
Ellen Rønneberg's Education
- Universitetet i Oslo (UiO) / University of Oslo
(Psycology- Basic courses at bachelor's level)
2009 - 2011 - Universitetet i Oslo (UiO) / University of Oslo
M.Sc.Pharm (Pharmacology)
1981 - 1986 - Universitetet i Oslo (UiO) / University of Oslo
(Mathematics and natural sciences)
1980 - 1981
Ellen Rønneberg's Skills
- Pharmaceutical Industry
- Regulatory Affairs
- GMP
- Regulatory Submissions
- Quality System
- Technology Transfer
- Product Development
- Chemistry
- Pharmaceutics
- Manufacturing
Ellen Rønneberg's Summary
Ellen Rønneberg, based in Oslo, NO, is currently a Head of Unit, Reliable Supply at Norwegian Medicines Agency, bringing experience from previous roles at Norwegian Medicines Agency, Pronova BioPharma and GE Healthcare. Ellen Rønneberg holds a 2009 - 2011 Universitetet i Oslo (UiO) / University of Oslo. With a robust skill set that includes Pharmaceutical Industry, Regulatory Affairs, GMP, Regulatory Submissions, Quality System and more, Ellen Rønneberg contributes valuable insights to the industry. Ellen Rønneberg has 2 emails on RocketReach.
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