Senior Executive – Quality Management System

About the role

CCL Pharmaceuticals is seeking a Senior Executive to lead the development, implementation, and continuous improvement of its Quality Management System (QMS). The role ensures compliance with regulatory requirements, PIC/S guidelines, and current Good Manufacturing Practices (cGMP) while supporting product quality and inspection readiness.

Key responsibilities

• Manage controlled quality documentation with high accuracy.
• Coordinate QMS processes across multiple stakeholders.
• Maintain QMS records and support vendor qualification activities.
• Facilitate internal, supplier, and contract manufacturing audits.
• Support Change Control, CAPA, Deviation, Risk Management, and document control systems.
• Organize quality governance meetings and follow up on action items.
• Deliver GMP awareness sessions and promote a quality‑focused culture.

Required profile

• Pharm.D or equivalent qualification from an HEC‑recognized institution.
• 3‑4 years of experience in Quality Assurance or Quality Management Systems within a reputable pharmaceutical organization.
• Strong understanding of QMS components such as Change Control, CAPA, Deviation Management, Risk Management, and Internal Audits.
• Familiarity with cGMP and PIC/S regulatory frameworks.

Required skills

• Quality Management System (QMS) documentation
• cGMP compliance
• PIC/S guidelines
• Change Control processes
• CAPA management
• Deviation handling
• Risk Management
• Internal Audit procedures