Quality SR. Officer (QMS)

We are looking for a qualified and detail-oriented Quality Senior Officer (QMS) to manage and maintain the Quality Management System (QMS) in the pharmaceutical industry. The candidate will be responsible for ensuring regulatory compliance, maintaining quality documentation, coordinating audits, and implementing quality procedures in accordance with GMP and applicable regulatory standards.

• Maintain and monitor the Pharmaceutical Quality Management System (QMS).
• Prepare, review, and control SOPs and quality-related documents.
• Handle deviations, CAPA, change control, and document control.
• Coordinate internal audits, external audits, and regulatory inspections.
• Monitor training records and ensure GMP compliance.
• Maintain quality records, reports, and documentation.
• Support continuous improvement of quality systems.

• Education: B.Pharma, M.Pharma, B.Sc., or M.Sc. in Chemistry, Microbiology, Biochemistry, or a relevant scientific discipline.
• Male and female candidates can apply.
• Relevant experience in pharmaceutical QA/QMS operations.
• Good knowledge of GMP, WHO-GMP, and regulatory guidelines.
• Experience in SOP management, CAPA, deviations, change control, and audits.
• Strong documentation, communication, and analytical skills.
• Proficiency in MS Office and quality documentation systems.

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