The design, supervision and execution of quality control studies of Biological Products including chromatography and HPLC. At least 3 years of experience with these techniques is required.
The management of the assigned projects keeping the deadlines and establishing a direct communication with the client
Technical document management associated with the studies ( standard procedures, certificates of analysis, deviations, OOS’s, CAPA’s, etc.)
The direction and supervision of the experimental work of the technical staff in charge.
Requirements :
Degree in Biochemistry, Biotechnology, Chemistry or related
Experience in HPLC methods.
Experience in working in quality Control in Pharmaceutical Company and GMP environments is a must.
Knowledge of electrophoretic techniques, Western-Blot and ELISAs and Quality Control of Proteins will be a plus.