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Are you a Quality Control Analyst interested in joining a big global pharmaceutical company? If you're ready to advance your career as a QC Analyst, we have the perfect opportunity for you. The QC Analyst uses techniques like HPLC and GC to check product purity and ensure regulatory compliance, guaranteeing the safety and effectiveness of medicines.
Job Responsibility:
GLP document preparation e.g. SOPs, Specification and Method of Analysis, Certificate of Analysis etc.
Good documentation practices and record keeping of all GMP documents / logs. (RM, PM, IP, FP sampling and testing)
Sampling and testing: RM, PM, FP and stability samples
Stability sample management and stability protocol preparation
Daily calibration and verification checks for QC instruments
Impurity and standard managements
Daily monitoring of data loggers and recording
Management of HPLC/GC Columns
Procurement of Laboratory chemicals & consumables
Requirements:
Familiarity with lab techniques like HPLC, GC, and spectroscopy
Understanding of Good Manufacturing Practices and regulatory guidelines
Ability to conduct precise and accurate testing
Ensuring accuracy in documentation and test results
Bachelor's degree in chemistry, biochemistry, pharmacy, or a related field
Proficiency in laboratory software and data management
Ability to clearly report and interpret test results