Job Description

- Analysis (SDS-PAGE, Real time PCR, …) - Documentation (preparing analysis report, COA, new SOP’s, review of other SOP’s according to manager or supervisor order) - Search for new products analytical methods - Collaboration in AMV & CV teams

Requirements

- At least 3 years of experience in in Pharmaceutical Industry - Mastering the process of controlling biological and chemical process of products - Ability to provide and implement the applicable procedures and guidelines for the Quality Control system - Proficiency in analyzing barriers and potential problems in the field of the Quality Control process - Ability to make decisions in crucial situations to remove barriers to work - Good teamwork abilities - Punctual Having a strong "can-do" attitude.

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