- 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.