QMS Manager

About the role

The QMS Manager will lead the implementation, maintenance, and continuous improvement of the Quality Management System at our Landhi pharmaceutical plant. This role ensures compliance with corporate quality policies, GMP standards, and regulatory requirements while supporting all departments in quality‑related activities.

Key responsibilities

• Manage and maintain the site’s Quality Management System, including the Site Master File and Quality Manual.
• Oversee preparation, review, revision, and control of SOPs and other quality documents.
• Ensure compliance with corporate quality policies, GMP requirements, and regulatory expectations.
• Coordinate training programs and verify timely completion of employee training requirements.
• Implement and monitor Quality Risk Management processes.
• Lead continuous improvement projects and quality system enhancements.
• Support departments with documentation, compliance, and quality‑related activities.
• Develop and coach the QMS team through performance management and training.

Required profile

• Science graduate or Master’s degree, preferably Chemistry or Pharmacy.
• 6‑8 years of experience in Quality Assurance or Quality Management Systems within a regulated environment.
• Strong knowledge of GMP, regulatory requirements, and quality management principles.
• Demonstrated leadership and team‑management abilities.
• Excellent communication, analytical, and problem‑solving skills.

Required skills

• Proficiency with Microsoft Office applications.
• Experience using quality management documentation systems.
• Knowledge of GMP and regulatory standards.