Job Description
- Preparing the requested logs and archiving them.
- Preparing and adjusting the list of all MMR and all SOPs in the company.
- Pursuing the approval of the quality assurance system documentation and communicating it to the relevant units.
Requirements
- Proficient in preparing guidelines.
- At least three years of relevant experience in the pharmaceutical industry.
- Bachelor's or Master's degree, preferably in one of the related fields.
- Minimum age: 26 years old.
- Proficient in ICDL.
- Relative proficiency in English.
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