Job Description
-Coordinate, prepare, or review regulatory submissions for domestic or international projects.
-Interpret regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures.
-Prepare or direct the preparation of additional information or responses as requested by regulatory agencies.
-Prepare leaflets in Persian and English for medicines and supplements.
-Coordinate in preparing artworks for packaging materials.
-Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review.
-Identify relevant guidance documents, international standards, or consensus standards and provide interpretive assistance.
-Obtain and distribute updated information regarding domestic or international laws, guidelines, or standards.
-Write or update standard operating procedures, work instructions, or policies.
