Participation in the preparation of the validation documents, execution of the validation protocol (FAT) for a medical device assembly equipment. Direct collaboration with customer team to prepare, conduct tests and finalize the dossier. Writing of functional specifications and risk analysis. Contribution to the revision of a standardized validation file.

Participation in quality system maintenance. Internal audits in production department. Mapping of monitoring plan. Consolidation and monitoring of key performance indicators (KPI). Extraction of data from forms and ERP, set up pivot tables and trend curves (in Microsoft Excel). Update of mission sheets.

Analyses of speciality gas mixtures under ISO 17025 and 17034 standards.

Leading of the Analytical Chemistry Group for development, validation and routine measurement activities of analytical methods aiming at quantification of regulated analytes in food/beverages/water matrices.

Group supervisor. Development, validation and routine measurement activities for analytical methods aiming at trace level compounds (aroma, harmful smoke constituents) quantification in complex matrices (smoke, aerosol, tobacco, indoor air).

Analytical support for manufacturing of food products. Development of quantitative analytical methods for flavour compounds in food matrices and encapsulated systems.