• Supervision and management of a range of studies in a GLP/GMP accredited facilities• Planning of studies, responsibility for accurate performance and analysis of the study results.• Quality improvement of different procedures and processes. • Analysis and optimization of work processes and SOP's.• Experienced in pre-clinical research• Good Manufacturing Practice. • Good Laboratory Practice.• Close attention to details; ability for multi-tasking.• Highly ability to adapt to changing priorities Particularely interested in the fields of research, pharma and biotech.- As a person, I am positive & sociable. - Curious, ambitious and a fast learner. - Hard worker, who takes my work seriously and aiming for a continuous personal and professional improvement. - Tend to fit in easily and have good experience working both individually and as a team player.