Pharmaceutical- Quality Assurance Supervisor
1 month ago
**Key Responsibilities**:
Responsible to actively participate in the quality, health, safety and environment aspects in IMC pharmaceutical warehouse. Internally check and ensure operations & in - house procedures to meet regulatory body guidelines and MAH requirements in compliance with cGxp.
1. Quality Management system: Assist in the development, implementation, and maintenance of quality management policies, instructions, and other related documents as required.
2. Regulatory Compliance : Strictly adhere to all Ministry Of Health Standards, QHSE guidelines, cGxP and internal standards and policies.
3. Audit Management and Participation : Actively participate in audits and manage follow-ups for closing audit reports.
4. Audit Management : Responsible to platform the audit follow - up for closing of audit reports.
5. Deviation Management : Responsible to raise deviation reports and manage CAPA for non - compliance observed during inspections.
6. Temperature Monitoring : Monitor storage area temperature, outbound delivery on daily and report deviations to the warehouse In-Charge and QA Manager.
7. Change Control : Responsible to handle and update change control process and related CAPAs.
8.Risk Management : Responsible to maintain and update the risk register as per mitigate plan.
9. Product Quality Complaint : Report product quality complaints to the manager and relevant suppliers, as per procedures.
10. Shipment Damage handling : Report any incoming shipment damage for assessment by the principle or supplier.
11. Product recall management: Supervise product recalls per MAH or MOPH notifications.
12. Shipment release : Manage trade or tender consignment release and dispositions for final batch distribution release.
13. Warehouse operations Management : Oversee daily warehouse quality operations.
14. Housekeeping & safety Compliance : Ensure safety regulations and proper housekeeping in the warehouse.
15. Training & development : Train warehouse employees on QMS and quality procedures.
16. QMS Documentation : Ensure proper management of QMS documentation, including SOPs.
17. SOP Development : Prepare and update operational and system - specific SOPs.
**Experience & Qualification**:
Minimum 3 -5 years as a QA supervisor or Manager in **pharma Industry**
Experience in (drug stores/ pharmaceutical manufacturing/ Supply Chain distribution is mandatory )..
Excellent knowledge in Good distribution practice and ISO 9001-2016 or TQM.
Experience in supplier's audits.
Experience in due diligence questionnaires.
Experience in technical agreements.
Having driving license.
Excellent command of English languages. Arabic is preferred
Bachelor's/ B.Sc. in sciences or Pharmacy
**ISO and QMS training certification is preferred.**
**Proficiency in Microsoft Office (Word, excel, PowerPoint).**
**Experience with Oracle ERP or WMS software is preferable.**
**Experience in handling warehouse temperature monitoring software is preferable.**
Pay: QAR7,000.00 - QAR8,000.00 per month
**Education**:
- Bachelor's (preferred)
**Experience**:
- pharmaceutical manufacturing or Supply Chain: 4 years (required)
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