Officer (QMS)

We are looking for a detail-oriented Officer (QMS) to support and maintain the Quality Management System in the pharmaceutical industry. The candidate will be responsible for quality documentation, SOP management, compliance monitoring, and implementation of GMP standards to ensure effective quality system operations.

• Maintain and update Quality Management System (QMS) documentation.
• Prepare, review, and control SOPs and quality-related documents.
• Handle deviations, CAPA, change control, and document control activities.
• Maintain training records and ensure GMP compliance.
• Assist in internal audits, external audits, and regulatory inspections.
• Monitor quality records and ensure proper documentation practices.
• Coordinate with QA, QC, Production, and other departments.

• Education: B.Pharma, M.Pharma, B.Sc., or M.Sc. in Chemistry, Microbiology, Biochemistry, or a relevant scientific discipline.
• Male candidates required.
• Relevant experience in pharmaceutical QA/QMS operations preferred.
• Knowledge of GMP, WHO-GMP, SOPs, and regulatory guidelines.
• Understanding of CAPA, deviations, change control, and audit procedures.
• Good documentation, communication, and analytical skills.
• Basic knowledge of MS Office and quality documentation systems.

• Competitive salary based on qualifications and experience.
• Performance-based incentives, where applicable.
• Career growth opportunities in Quality Assurance.
• Professional training and skill development.
• Exposure to pharmaceutical quality systems and regulatory compliance.