Job Description

• Follow-ups with MOH and IFDA on files review and ensures timely submission of additional documentation requested • Review documents as CTD, PMFs, to fulfill MOH requirement for registration • Familiar with TTAC portal of MOH and material registration. • Develop professional relationships with MOH staff and proactively monitor relevant governmental bodies to identify changes in legislation/regulations • Supervision of quality processes • Familiar and provision of SOPs • Review product printing materials, labeling, specification sheets with applicable regulations and policies. • Supervising all product quality activities according to internal and external standards such as GMP and …

Requirements

• Pharm.D. Pharmacist Female/male • Having minimum 5 years of experience in pharmaceutical industries • Familiar with the field of Probiotics • Interest and experienced in QA and regulatory affairs • Strong communication skills and high team work value • Good command of English and computer skills • Location: Tehran office and Goldasht Karaj plant

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