Quality Head – Pharmaceutical Manufacturing

Industry: Pharmaceutical Manufacturing
Location: UAE
Employment Type: Full-Time

Role Purpose

We are seeking a strategic Quality Head to lead the Quality Assurance and Quality Control functions at a pharmaceutical manufacturing site. The role will ensure robust quality systems, inspection readiness and compliance with GMP, GDP and applicable local and international regulations.

Key Responsibilities

Lead and manage site-wide QA and QC operations, including team performance, capability development and succession planning.
Own and continuously improve the Quality Management System, including deviations, CAPA, change control, complaints, recalls and investigations.
Ensure compliance with cGMP, GDP, data integrity and applicable regulatory requirements.
Lead regulatory authority interactions, inspections, audit responses and follow-up actions.
Oversee batch review, certification and product release activities; QP responsibilities where applicable.
Manage validation, qualification, PQR, Site Master File and Validation Master Plan activities.
Oversee supplier qualification, quality agreements, audits and quality-risk management.
Establish quality KPIs and drive improvements in batch-release timelines, audit outcomes, CAPA effectiveness and deviation reduction.
Partner with Manufacturing, Engineering, Supply Chain and Regulatory Affairs to maintain compliant, efficient operations.
Support quality-related CAPEX, budget and strategic improvement initiatives.

Requirements

Bachelor’s or Master’s degree in Pharmacy.
Minimum 10 years of progressive experience in pharmaceutical Quality Assurance/Quality Control.
Proven leadership experience managing QA and QC teams in a pharmaceutical manufacturing site.
Strong knowledge of GMP, GDP, QMS, validation, audit management and regulatory inspections.
Qualified Person experience is highly preferred.
UAE/GCC pharmaceutical manufacturing experience is preferred.
Excellent leadership, stakeholder-management and English communication skills.

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المهارات المطلوبة

Quality Management System (QMS) ownership and improvementcGMP complianceGDP complianceData integrity managementRegulatory inspections and authority interactionsAudit management (internal, supplier, regulatory)Deviation, CAPA and change control managementBatch review, product certification and Qualified Person (QP) responsibilitiesValidation and qualification (VMP, Validation Master Plan, PQR)Supplier qualification, quality agreements and supplier auditsQuality metrics, KPI establishment and continuous improvementTeam leadership, capability development and succession planningStakeholder management and cross-functional partnering (Manufacturing, Engineering, Supply Chain, Regulatory Affairs)Pharmaceutical regulatory compliance (local and international)Quality-related CAPEX and budget oversight

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