Sofie Vercammen Email
Registration Officer and label responsible @ Certiplant
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Sofie Vercammen Location
- Flanders, Belgium
Sofie Vercammen Work
- Registration Officer and label responsible @ (September 2016 - Present)
- Senior QA officer @ Toxikon Europe (January 2016 - September 2016)
- QA assistant @ Toxikon Europe (April 2013 - January 2016)
- QA assistent @ Qplus consult bvba (November 2012 - April 2013)
- QA-specialist @ Landen Pharmachem (July 2011 - October 2012)
- QC-specialist @ Landen Pharmachem nv (August 2010 - July 2011)
- process assistent @ (August 2006 - May 2009)
Sofie Vercammen Education
- KHLeuven
Pharmaceutical assistant
2009-2010 - KHLim
Bachelor's degree (Chemistry)
2003-2006 - KCST
Sciences-Mathematics
1997-2003
Sofie Vercammen Skills
- Biotechnology
- CAPA
- Change Management
- Chemistry
- Corrective and Preventive Action (CAPA)
- FDA
- GLP
- GMP
- HPLC
- Life Sciences
- Microsoft Excel
- Microsoft Office
- Microsoft Word
- Pharmaceutical Industry
- Pharmaceutics
- PowerPoint
- Project Management
- Quality Assurance
- Quality Control
- Quality System
- Regulatory Affairs
- SOP
- Strategic Planning
- U.S. Food and Drug Administration (FDA)
- Validation
- Corrective And Preventive Action Capa
- U.S. Food And Drug Administration Fda
- Corrective and Preventive Action
- u.s. Food and Drug Administration
Sofie Vercammen Summary
- Sofie Vercammen, based in Flanders, Belgium, is currently a Registration Officer and label responsible at Certiplant. Sofie Vercammen brings experience from previous roles at Toxikon Europe, Qplus consult bvba and Landen Pharmachem. Sofie Vercammen holds a 2009 - 2010 Pharmaceutical assistant @ KHLeuven. With a robust skill set that includes Biotechnology, CAPA, Change Management, Chemistry, Corrective and Preventive Action (CAPA) and more.
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