Job Summary We are seeking a highly qualified and experienced Senior Quality Assurance Specialist to join our pharmaceutical team. The successful candidate will be responsible for ensuring compliance with GMP standards, maintaining quality systems, supporting audits and inspections, and driving continuous improvement initiatives across manufacturing and quality operations.
Key Responsibilities Ensure full compliance with GMP, regulatory requirements, and company quality standards. Review and approve batch manufacturing records and related documentation. Handle and investigate deviations, OOS, change controls, and CAPA processes. Participate in and support internal and external audits and regulatory inspections. Monitor and maintain the effectiveness of the Quality Management System (QMS). Review and approve SOPs, protocols, and validation reports. Conduct risk assessments and implement corrective and preventive actions. Provide training and guidance to junior QA staff. Coordinate with production, QC, and other departments to ensure product quality and compliance. Support continuous improvement initiatives and quality performance monitoring.

Job Requirements Bachelor's degree in Pharmacy, Science, or a related field. Minimum 5–7 years of experience in Quality Assurance within the pharmaceutical industry. Strong knowledge of GMP, GDP, and pharmaceutical regulatory standards. Experience in deviation investigation, CAPA, change control, and risk management. Familiarity with validation, qualification, and documentation control systems. Experience with regulatory inspections and audit readiness. Strong analytical and problem-solving skills. Excellent communication and leadership abilities. Ability to work under pressure and manage multiple priorities. Very good command of English (written and spoken).