Job Requirements
- University Graduated with M.Pharm, B. Pharm or M.Sc. (Chemistry)
- Must be Fluent in English & Familiar with MS Office application
- Must be able to work with systematic procedures
Key Responsibilities
- To implement the proper documentation management system at site.
- To monitor compliance of cGMP and GDP.
- Preparation and review of SOPs related to Quality Assurance.
- Responsible for management of Master SOPs and controlled copies
- Co-ordination, monitoring and logging of QMS documents.
- To coordinate with the external and internal trainings, Responsible for preparation of Internal Faculty Group Training Plan.
- Responsible for Preparation of Self-Inspection schedule and follow up of compliances from auditee and review of compliance action.
Benefits:
- Working Hours – (8:30 AM to 4:30 PM)
- Off Days – Sunday, Alternate Saturday and Public Holidays
- Ferry and Lunch Provided
- Overtime Payment and Allowance
