- 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