Sr. Officer - Quality Assurance

Roles & Responsibilities
• Perform and oversee equipment qualification activities including IQ, OQ, and PQ
• Ensure qualification documentation is prepared and maintained as per cGMP and regulatory requirements
• Review qualification protocols, reports, and related quality documentation
• Coordinate with engineering, production, and validation teams for qualification and compliance activities
• Ensure adherence to regulatory guidelines and internal quality standards
• Support audit and inspection readiness by maintaining accurate qualification records
• Assist in deviation management, CAPA implementation, and change control activities related to equipment qualification
• Participate in continuous quality improvement and compliance initiatives

Qualification
• B.Pharm / M.Pharm

Experience
• 3–6 years of experience in Quality Assurance within pharmaceutical manufacturing
• Hands-on experience in equipment qualification and validation processes

Skills
• Strong knowledge of cGMP and pharmaceutical regulatory compliance
• Experience in equipment qualification documentation and validation protocols
• Understanding of quality systems including deviation, CAPA, and change control
• Strong analytical, documentation, and problem-solving skills
• Good communication and cross-functional coordination abilities

About the Organization
Kwality Pharmaceuticals is a well-established pharmaceutical manufacturing company known for producing high-quality formulations for domestic and international markets. The organization focuses on regulatory compliance, advanced manufacturing practices, and continuous improvement to ensure global quality standards.