Ms. Jolanda Muurman 

Bio

With 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 and Dutch.

  • Her real passions are GMP-trainings:
  • GMP trainings
  • Biotech manufacturing processes
  • Risk Based Product development
  • Validation

But she also works in the field of:

  • Training development and design

She is providing standardized training but also tailor-made sessions adapted to the specific needs of the client and the company.

Languages: Dutch & English

References: SynCo Biopartners, Pharming, Janssen Vaccines & Prevention, Biotech Training Facility