Quality Control Manager
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About the Role
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.
Key Skills for This Role
Full Job Posting
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 QC 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.
- 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 & Requirements
- Education: B. Pharm and M. Pharm
- QA Certification is an advantage.
- 3 to 4 years of solid experience in Pharmaceutical QC and QA within a GMP-regulated organization (mandatory).
- 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.
- Only candidate who has quality Control experience in pharmaceutical sector will be preferred.
- Apply directly or share your CV at [email protected]
- we look forward to considering your candidacy.
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