Quality Control Manager - Pharmaceuticals

Sky Pharma; Dubai; On-site; AED 320,000 - 640,000; Full time

Job summary

INFIKOR Group of Companies is seeking a detail-oriented Manager- Quality Assurance with hands-on GMP experience to lead QMS, deviations, CAPA, change controls, and audits within a commercial pharmaceutical setting in Dubai. A strong background in GMP/GDP compliance and regulatory liaison is required.

Education must include B. Pharm or M. Pharm; English is mandatory with Arabic/French/Russian as an advantage. Location is Dubai, UAE, with relocation considered for the right candidate.

Qualifications

• A minimum of 10 years of total experience, including at least 5 years in a QA role within a GMP-regulated pharmaceutical environment.
• QA Certification is an advantage.
• Understanding of GMP, GDP, and ICH Q10 Quality Systems is essential.
• Strong documentation and regulatory compliance skills.

Responsibilities

• Support 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.
• Ensure data integrity and compliance with applicable Health Authority requirements.
• Maintain GMP training records and training matrix.

Skills

Regulatory compliance

Documentation skills

Detail-oriented

GMP knowledge

Education

B. Pharm

M. Pharm

Job 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 relocate

Education: B. Pharm or M. Pharm (mandatory)

Company Over-View

INFIKOR 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 Summary

INFIKOR 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 Responsibilities

• Support 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.


• Ensure data integrity and compliance with applicable Health Authority requirements.


• Maintain GMP training records and training matrix.

Qualifications & Requirements

• Education: B. Pharm and M. Pharm


• QA 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