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Open nowFirst seen 5 days ago

Head of Quality Assurance

Domo Ventures W.L.L.511 open roles

Where
Manama, Capital Governorate, Bahrain
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Your applicationOpen nowHead of Quality AssuranceDomo Ventures W.L.L. · Manama, Capital Governorate, Bahrain

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The clock on this job

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Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: first seen 5 days ago

The posting

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

Industry

  • Healthcare/Medical/Pharmacy

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.

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