Job Description
- Managing continuous and active professional collaboration with Iran MoH, external stakeholders, and Iranian distributors.
- Managing all the quality assurance procedures.
- Supervising and following up on all technical and scientific affairs of manufacturing of under-license supplementary products.
- Participating in internal and external inspections, and GMP visits.
- 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.
Requirements
- Pharmacist (PharmD).
- Knowledge of quality assurance.
- Familiar with regulations, rules, instructions, and policies of the Food and Drug Administration of Iran.
- At least 2 years of experience in similar positions.
- Fluency in writing, reading, and speaking English.
- Ability to travel within the country and abroad.
- High-level communication skills to deal with internal and external stakeholders.
- Good knowledge of Microsoft Office, especially Outlook.
- Sense of human relations, and 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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