Head of Quality – Pharmaceutical Manufacturing
Company Overview:
A state-of-the-art sterile pharmaceutical manufacturing facility in Abu Dhabi’s KEZAD industrial zone is seeking high-level expertise to lead its quality governance. We operate with an “educational family” philosophy, where technical management and pharmaceutical mastery are shared to ensure organizational success. At our facility, we believe that a robust Quality Management System (QMS) is the cornerstone of patient safety and technical innovation. Join our professional leadership team and contribute to an environment that values professional integrity, technical innovation in Information Technology, and the strategic oversight of our global manufacturing standards.
Job Description:
We are seeking an experienced Head of Quality to lead the full QMS for our sterile manufacturing facility. This role is fundamental to our regulatory framework, requiring a professional who can provide strategic oversight for QA, QC, and Validation operations. You will be responsible for managing batch releases, CAPA, and preparing for high-profile inspections (FDA, EMA, MOHAP) for management review. We are looking for a visionary leader with a strong background in sterile/GMP manufacturing who thrives in a high-compliance environment. This is a brilliant opportunity to drive quality strategy for a premier engineering and pharmaceutical firm within a structured and professional framework.
🔹 Key Responsibilities:
- Direct the full Quality Management System (QMS) setup and governance to ensure sterile manufacturing compliance.
- Manage batch releases, deviations, CAPA, and change control processes to support organizational sales of safe medical products.
- Lead the site’s preparation and representation during regulatory inspections, including FDA, EMA, and MOHAP.
- Liaise with the Human Resources department regarding the leadership and training of a high-performing quality team.
- Utilize advanced Information Technology tools for QMS tracking, KPI definition, and data integrity oversight.
🔹 Requirements:
- Bachelor’s Degree, Diploma, or Certificate in Pharmacy, Life Sciences, or a related field.
- 12 to 15+ years of professional experience in pharmaceutical quality, with 5–7+ years in a senior role.
- Expert knowledge of EU GMP, 21 CFR 210/211, and ICH guidelines within a sterile/GMP setting.
- Strong background in management of oncology or high-potency manufacturing is considered a plus.
- Professional background in education or training regarding international regulatory standards and validation protocols.
- Proven track record of successfully leading manufacturing facilities through global health authority inspections.
What We Offer:
- Monthly salary package ranging from AED 10,000 to 11,000 (Adjusted).
- A stable and influential leadership role within a premier Abu Dhabi pharmaceutical firm.
- Exposure to advanced oncology and high-potency sterile manufacturing technologies.
- Comprehensive benefits in accordance with UAE Labour Law.