Description
Energetic and trilingual quality engineer (member of OIQ) with experience in medical devices, pharmaceuticals and the bottling industry. Offers work experience in a highly regulated (FDA) pharmaceutical environment using Good manufacturing practices (GMP), Good laboratory practices (GLP), Good documentation practices (GDP) as well as Health and Safety issues (CSST). Solid record in designing and validating changes which improves productivity or flow-through and increases compliance with external or internal process requirements. Has worked internationally and on new technology implementation, process development and new product launches, and is familiar with multidisciplinary and multi-cultural teams and matrix organizational structures. Good manager and team-player who communicates clearly and is fluent in French, English and Persian.
