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Henriette Pasgaard Bertelsen

Consultant

Quality Assurance
GMP/ GDP
Deviations and CAPA
Change Control
Project Coordination
Qualification
Cleaning Validation
Data Analysis
ISO-standard 15189
Eudralex vol. 4

Henriette holds a Ph.D. in Molecular Biology from Aarhus University. She has 6 years of experience with Quality and Compliance from pharmaceutical production, healthcare analysis, research, and education.  

Most recently, she worked as a dQP and production academic at the Cytostatic Production, Regions Apoteket Gødstrup, where she performed quality control and release of cytostatic products and was responsible for cleaning, hygiene, and equipment qualification, managing risk assessments, Change Controls, and deviations. Previously, at Fertin Pharma A/S, she served as a Specialist, contributing to GMP compliance, cleaning validation and qualification of new equipment. She developed and optimized new or existing cleaning methods in pharmaceutical production, handled Change Controls as well as deviations and CAPA. At the Clinical Genetics Department, Vejle Hospital, she performed data analysis, prepared patient reports, and oversaw molecular biology analyses, ensuring adherence to ISO standards.

“As a person, I am well organized and positive. I quickly acquire new knowledge and try to create a common consensus for the given task. I thrive in an environment where people across professional groups value each other's strengths and different competencies, to achieve the best solution for the client.”