22 feb
Importante grupo
Estado de México
Responsibilities: 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 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 field.
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.
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