a degree in Bioprocess engineering and in Management Jolanda Muurman works in
the (bio)pharmaceutical industry since 2000. She started her career in the
quality unit of one of the top 10 pharmaceutical companies. Her first steps
were in the area of pharmaceutical packaging and the critical aspects of
printed packaging materials. From there she moved on to parenteral and biotech
product. For five years she has worked for a CMO in the field of Bulk Drug
Substance manufacturing and Fill Finish of Investigational Medicinal Products. Combined with a manufacturing back ground and
thorough understanding of GMP and Quality Assurance in biopharmaceutical
product development, she has worked as a Qualified Person for IMP’s in the
different stages 1, 2 and 3 of clinical product development. She speaks English
passions are GMP-trainings:
Biotech manufacturing processes
Risk Based Product development
But she also works in the field of:
development and design
She is providing standardized training but also tailor-made sessions
adapted to the specific needs of the client and the company.
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