QA Expert

BioSun Pharmed Tehran

Posted a month ago

Job Description

- Gathering Pharmacovigilance and ADR reports - Supervision of quality processes - Develop professional relationships with MOH staff and proactively - Review documents as CTD, PMFs, to fulfill MOH requirement for registration - Familiar with TTAC portal of MOH and material registration. - Review product printing materials, labeling, specification sheets with applicable regulations and policies - Provision of SOPs

Requirements

- Minimum 3 years of experience in field of Pharma - Familiar with Validation and Qualification - Familiar with GMP rules - Excellent Fluency in English in all skills - Strong communication skills - Good command of computer knowledge (MS. Office) - Teamwork spirit and responsibility

Job Category:

Quality Control, QA & Inspection

Employement type:

Full Time

Job Category:

Quality Control, QA & Inspection

Employement type:

Full Time

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