Still seeking for new challenges in the field of project management, regulatory affairs where I can bring in my knowledge gained from my work experience as a lab technician, lab head, study director and finally project manager/lead for regulatory affairs.Work ExperienceSince Aug 2012 SCC - Scientific Consulting Company Project manager for application of authorisation according to Article 33 and renewal for authorisation of plant protection products according to Article 43 under Regulation (EC) No 1107/2009. Responsible for communication with authorities (RMS/coRMS, EFSA and COM). Coordination of all sections relevant for the application of plant protection products, preparation and submission of different dossiers at EU level and coordination of any update according to regulatory requirements. Preparation and organization of pre-submission meetings.Disciplinary leadership of the project team and time management, as well as budget control.Performing STN literature searches according EFSA requirements for the registration of plant protection products.Preparation of different toxicological assessments, review and evaluation of the toxicological data.Preparation of dossiers (CSR and C+L) for chemicals for REACH. Entry of data into IUCLID database.Monitoring and preparation of biocompatibility dossiers for medical devices according ISO 10993 series.Study monitoring and interpretation of various toxicological study types. Definition of follow-up strategies.If you are interested in a full CV, please contact me.