Head of Quality Assurance

Domo Ventures W.L.L.; Manama; On-site; BHD 30,000 - 70,000; Full time

Job summary

An established industry player in the pharmaceutical sector is seeking a Head of Quality Assurance to lead quality operations in Bahrain. This pivotal role involves ensuring compliance with national and international standards, managing quality management systems, and designing strategies to enhance pharmaceutical services. The ideal candidate will possess a Bachelor's degree in Pharmacy and a valid NHRA license, along with significant experience in quality assurance. Join a forward-thinking company where your expertise will drive excellence in quality and compliance, making a meaningful impact in the pharmaceutical landscape of Bahrain.

Qualifications

• Bachelor's degree in Pharmacy and valid NHRA license required.
• 5-10 years of experience in quality assurance in pharmaceuticals.

Responsibilities

• Manage quality operations to comply with national and international standards.
• Design strategies to limit noncompliance and monitor supply chain quality.
• Prepare periodic quality reports and assist in maintaining SOPs.

Skills

Quality Management Systems

Pharmaceutical Compliance

Auditing

Regulatory Standards

Education

Bachelor's degree in Pharmacy

NHRA License

Job description

A client of Domo Ventures is looking for a Head of Quality Assurance for the pharmaceutical industry in Bahrain. Preference given for applicants based in Bahrain

Title:

• Head of Quality Assurance ( Pharmaceutical )

Location:

• Manama, Kingdom of Bahrain

Qualifications:

• Bachelor's degree in Pharmacy
• Must have a valid NHRA license
• Applicants outside of Bahrain should be eligible to have an NHRA license as per the PQR

Experience:

• 5 to 10 years

Responsibilities

• Manage the quality Operations to ensure that a Quality Management System is planned, and maintained to comply with the national and international standards of MOH, NHRA, WHO GDP & GSP, and ISO.
• Evaluate information and verify that pharmaceutical products and services within the organization comply with national and international standards.
• Design new strategies to limit noncompliance with pharmaceutical services.
• Monitor the Quality of Supply Chain operations, GDP, and GSP activities and compliance with its standards.
• Initiate, review, and approve Quality Technical Agreements (QTA) with principal companies.
• Contribute to the review of principle companies' Distribution Agreements.
• Review and Approve the Business Continuity Plan.
• Contribute to relevant Committees such as the Quality Improvement & Occupational Safety Committee.
• Organize all Quality Committee Meetings as Management Review, and Quality Improvement meetings, and make recommendations to the committee based on best practice and current regulatory standards.
• Approve the initiation of pharmaceutical product destruction internally, and communicate with the principal companies and regulatory team for NHRA / MOH approvals for destruction.
• Ensures organizational compliance with required KPIs and mandated quality indicators, by doing Audits and Validation for both internal and external KPIs related to principal companies.
• Prepare periodic reports like Quality reports, internal audit reports, and other reports required by the management.
• Assist the Head of Departments in developing and maintaining records of policies, standard operating procedures, guidelines, forms, and other documents and ensure the circulation of current documents and the de-circulation of expired documents.