Support and maintain the Quality Management System (QMS) to ensure compliance with GMP, ISO standards, and regulatory requirements in a pharmaceutical environment.

• Quality Management System (QMS) & Compliance Maintain QMS documentation, SOPs, and master records in line with ISO 22716 and regulatory requirements.
• Training & Capability Development Develop and conduct GMP and SOP training. Ensure all training records are accurate and up to date.
• Supplier Quality Management Assess and qualify suppliers to ensure compliance with quality standards.
• Equipment, Facility & Environmental Control Oversee equipment calibration, maintenance, and environmental controls (cleaning, pest control, monitoring).
• Audit Management & Compliance Assurance Support internal, external, and customer audits. Perform root cause analysis and implement CAPA.
• Deviat...