Daisy Rentzing Email & Phone Number

Delft, South Holland, Netherlands

Leiden, South Holland, Netherlands

 Coordination of all related activities for late-stage and commercial projects for viral and microbial safety (VMS) Representing VMS in interdepartmental meetings and external meetings (e.g. CMOs and external labs)  Translate sampling, testing and documentation requirements from QA, DS and DP manufacturing into aligned plans for implementation either onsite or at CMOs and external labs Maintain overviews of qualifications, verifications, validations Review manufacturing and test data in support of continuous process verification  Support regulatory filing activities (EMA and FDA) by performing data verifications and confirming integrity of source documents

Leiden, South Holland, Netherlands

 Coordination of all related activities for transfer of viral and microbial safety assays to manufacturing sites and contract laboratories worldwide Maintain overviews of qualifications, verifications, validations Supporting role in analytical transfer plans, GAP assessments, sampling plans, specification documents, verification/validation protocols and reports

Leiden, South Holland, Netherlands

 Planning and coordination of all QC related activities for release and stability testing of clinical trial material Authoring documentation (sampling plans, CoA’s, shipping documents) Review specification documents, protocols, reports Contact with external labs for outsourcing activities Develop and maintain KPI’s LIMS Subject Matter Expert

Leiden, South Holland, Netherlands

 Production and material planning Batch file review GMP support for the production department (quality issues, investigations, change controls)

Zeewolde, Flevoland, Netherlands

 Planning and coordination of all operational activities for theproduction, packaging and randomisation of clinical trial material Distribution of clinical trial material Design of patient packaging  Contact with clients and preparation of quotations in collaboration with Business Development

Leiden, South Holland, Netherlands

 Review of lab experiments (method verification, cleaning verification, release analysis and stability) Review of production batch files and shipment batch records Review of analytical equipment qualifications (i.e. IQ, OQ. PQ) Review of study protocols, SOP’s, reports Release of raw materials Major contributor to continuous improvement of procedures Training of personnel Internal and external QA audits

Leiden, South Holland, Netherlands

 Supervising QC technicians  Management of the analytical laboratory and equipment Improvement of analytical procedures Coordination of quality issues

Leiden, South Holland, Netherlands

Coordination of 2 projects (including productions, method development, validations, release analysis and stability studies)

Leiden, South Holland, Netherlands

 Method development and validation Writing protocols and reports Performing analysis (e.g. HPLC, UV, Karl Fisher) for release and stability

Weesp, North Holland, Netherlands

 Coordination of stability testing for commercial products including protocol and report writing Validation of HPLC methods Performing analysis (HPLC, dissolution, disintegration, UV) LIMS template manager

Roelofarendsveen, South Holland, Netherlands

 Advise and support companies in the food industry to successfully implement and maintain their quality (HACCP) system Performing chemical and microbiological analyses

Weesp, North Holland, Netherlands

HPLC method development and validation for analysis of tissue and blood samples

Chemical Engineering

Medical Microbiology And Bacteriology

Food Technology

Havo