● Managing registration and variation of all products and regulatory affairs of the company.
● Regular contact with principal suppliers of the company to be assured about safety, quality, and continuous supply of needed importation.
● Managing continuous and active professional collaboration with Iran MoH, external stakeholders, and Iranian distributors.
● Managing all the quality assurance procedures.
● Managing all pharmacovigilance procedures as QPPV.
● Supervising and following up on all technical and scientific affairs of importing vaccines, biologic products and medical devices.
● Participating in internal and external inspections, and GMP visits.
● Supporting the technical performance and obtain legal permission for importation and clearance of products.
● Establishing fluent and open interaction and cooperation with other departments of company.
Requirements
● Pharmacist (PharmD).
● Knowledge of QA, pharmacovigilance, and international regulations.
● Familiar with regulations, rules, instructions, and policies of the Food and Drug Administration of Iran.
● At least 3 years of experience in similar positions.
● Fluency in writing, reading, and speaking English.
● Ability to travel within the country and abroad.
● High level of 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 team leader.
● Ability to undertake multiple tasks at the same time without losing focus.