At PathoFinder my main responsibilities are maintaining our ISO 13485 and IVDR 2017/746 certified QMS. My daily focus is set-up and review new procedures, documents. Review of technical files and to register our CE marked products.

At Medace my main responsibilities were maintaining our ISO 13485 certified QMS system and helping our clients to setup their own QMS. My daily focus is to help clients to bring their Medical Device faster to the market, by optimizing their quality system in the field of MDR and IVDR. I have setup new procedures and work instructions according to the new Regulations (MDR 2017/745 and IVDR 2017/746).When I started at Medace we were in a transition to a new facility. I played an important role in helping to build the new biomedical facility and getting our ISO certificate to the new location.

My main responsibilities were maintaining our ISO 13485 certified QMS system. Helping project and clients with QA and RA questions. Chemelot InSciTe biomedical became Medace.

As a technician at Pathofinder BV, located in Maastricht I worked on research and development of the Real Time Multiplex PCR-kit RespiFinder SMART 22 FAST. which detects up to 22 respiratory pathogens in a single MLPA PCR. After two years I stared working as a technician at the production department. Here I work on the manufacturing and preforming QC testing of our four product lines. The RealAccurate, the MultiFinder, the SmartFinder and the 2SMART.Since June 2013 I am also part of the Quality Assurance team. Here I am responsible for maintaining our QMS system. PathoFinder BV is ISO 13485 certified, and does have four products notified body certified.

Het uitvoeren van routine analytische werk op het laboratorium klinische chemie en hematologie.

Clinical heterogeneity of LMNA mutations with respect to the genetic background of the different LMNA isoforms

Mutation screening in nDNA subunits of Complex I of the OXPHOS system