quality control chemist
Glaxo Saudi Arabia
Total des années d'expérience :6 years, 11 Mois
participating in quality management system activities related to audits, CAPA, process validation, risk assessment, documents management, change control.
Routine testing of Stability samples & finished
products and raw materials as per the defined procedures and ensuring
Good manufacturing practices (GMP) are
maintained throughout all process.
• Calibration of various instruments such as HPLC,
Analytical balance & pH meter
• Process validation (as per ICH Guidelines or any
Country specific requirements).
• Method transfer Documentation
• Provide Training for the operation of lab Instruments.
• Working on SAP (Result Recording).
• Out-Of-Specification investigation (Second
Analysis).
• Review Log Books and the usage records of
standards.
• Maintaining Temperature and humidity records of
Stability Walk in rooms/chambers.
Routine testing of Stability samples & finished
products as per the defined procedures and ensuring
Good manufacturing practices (GMP) are
maintained throughout all process.
• Calibration of various instruments such as HPLC,
Analytical balance & pH meter
• Process validation (as per ICH Guidelines or any
Country specific requirements).
• Method transfer Documentation
• Provide Training for the operation of lab Instruments.
• Working on SAP (Result Recording).
• Out-Of-Specification investigation (Second
Analysis).
• Review Log Books and the usage records of
standards.
• Maintaining Temperature and humidity records of
Stability Walk in rooms/chambers.