Job Description
- Managing continuous and active professional collaboration with Iran MoH.
- Managing all the quality assurance procedures.
- Supervising and following up on all technical and scientific affairs of manufacturing of under-license products.
- Supporting the technical performance and obtaining legal permission for the manufacturing of products.
- Establishing fluent and open interaction and cooperation with other departments of the company.
- Preparing regulatory documents (CTD, DMF, PMF, etc.).
Requirements
- Pharmacist (PharmD).
- Knowledge of quality assurance.
- Familiar with regulations, rules, instructions, and policies of the Food and Drug Administration of Iran.
- Previous experience in writing of CTD and DMF.
- At least 2 years of experience in similar positions.
- Fluency in writing, reading, and speaking English.
- Good knowledge of Microsoft Office.
- Sense of human relations, capability to work as a member of the team.
- Ability to undertake multiple tasks at the same time without losing focus.
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