Quality Head – Pharmaceutical Manufacturing
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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
Bachelors or Masters 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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