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Quality Head – Pharmaceutical Manufacturing

TALENT ONE EMPLOYMENT SERVICES
Posted 6 days ago, valid for 9 days
Location

Dubai, Dubai

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The position of Quality Head in Pharmaceutical Manufacturing is available in the UAE, offering a full-time role.
  • Candidates should have a Bachelor’s or Master’s degree in Pharmacy and a minimum of 10 years of progressive experience in pharmaceutical Quality Assurance and Quality Control.
  • The successful applicant will lead QA and QC operations, ensuring compliance with GMP, GDP, and regulatory requirements while managing team performance and development.
  • Proven leadership experience and strong knowledge of quality management systems are essential, with Qualified Person experience being highly preferred.
  • Salary details are not specified, but the role emphasizes the importance of effective leadership and collaboration with various departments to maintain efficient operations.

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 QualityAssurance and Quality Control functions at a pharmaceutical manufacturing site.The role will ensure robust quality systems, inspection readiness andcompliance 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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