Requirements
A minimum of 10 years of total experience, including at least 5 years in a QA role within a GMP-regulated pharmaceutical environment. Practical experience in deviation, CAPA, change control, document control, and audits is required. Understanding of GMP, GDP, and ICH Q10 Quality Systems is essential. Strong documentation and regulatory compliance skills.
Description
Job Title: Manager- Quality Assurance - Pharmaceuticals Company: INFIKOR Group of Companies Experience: A minimum of 10 years of total experience, including at least 5 years in a QA role within a GMP-regulated pharmaceutical environment Languages: English is must and Arabic, French or Russian is an advantage. Location: Dubai, UAE or willing to relocateEducation: B. Pharm or M. Pharm (mandatory)Company Over-ViewINFIKOR Group of Companies, we are a prominent pharmaceuticals group headquartered in Dubai, with a strong presence in the UAE, Ukraine, India, CIS Countries, Francophone Africa, GCC and Malaysia. Our company collaborates with industry leaders and operates in diverse international markets.Job SummaryINFIKOR Group of Companies is seeking a detail-oriented Junior QA Manager with hands-on experience in pharmaceutical GMP-based Quality Management Systems (QMS) within a commercial pharmaceutical company (manufacturer, MAH, or distributor).The role is strictly focused on GMP/GDP compliance, QMS documentation control, deviation and CAPA management, change control, audit readiness, and regulatory compliance.Applications from candidates with experience limited to R&D, GLP laboratories, CRO/clinical research, hospital pharmacy, or academic settings without GMP/QMS exposure will not be considered.Key ResponsibilitiesSupport the implementation and maintenance of the Pharmaceutical Quality Management System (QMS).Assist in preparing, reviewing, and controlling Pharmaceutical QA documentation (SOPs, forms, logs, checklists, records).Control and review SOPs, quality records, specifications, and quality agreements.Manage deviation, non-conformance, and quality complaint documentation.Track CAPA and Change Control processes through closure and effectiveness checks.Support internal audits and regulatory inspections.Maintain vendor qualification documentation (GMP/GDP compliance).Ensure data integrity and compliance with applicable Health Authority requirements.Maintain GMP training records and training matrix. Qualifications & RequirementsEducation: B. Pharm and M. PharmQA Certification is an advantage.A minimum of 10 years of total experience, including at least 5 years in a QA role within a GMP-regulated pharmaceutical environment Practical experience in deviation, CAPA, change control, document control, and audits is required.Understanding of GMP, GDP, and ICH Q10 Quality Systems is essential.Strong documentation and regulatory compliance skills