Garonit Pharmaceutical
The QC Chemist is an analytical role responsible for HPLC testing, data analysis, and documentation in a cGMP pharmaceutical quality control laboratory. This position supports finished product testing, investigations, and continuous improvement while ensuring compliance with regulatory and compendial standards.
Key Responsibilities Perform HPLC sample preparation, testing, and data analysis
Review and report analytical data in compliance with USP/ICH/cGMP requirements
Maintain and troubleshoot HPLC instrumentation
Execute compendial and non-compendial testing
Support investigations, CAPA, change controls, validations, and stability programs
Ensure laboratory safety and compliance
Qualifications Bachelor’s degree in Chemistry or related discipline with 5 years HPLC experience or Master’s degree with 3+ years HPLC experience
Hands-on experience with Empower 3
Experience working in anFDA-regulated, cGMP environment
Knowledge of USP monographs, method development, and validation
Strong attention to detail and documentation skills
Excellent written and verbal communication skills
#J-18808-Ljbffr
Key Responsibilities Perform HPLC sample preparation, testing, and data analysis
Review and report analytical data in compliance with USP/ICH/cGMP requirements
Maintain and troubleshoot HPLC instrumentation
Execute compendial and non-compendial testing
Support investigations, CAPA, change controls, validations, and stability programs
Ensure laboratory safety and compliance
Qualifications Bachelor’s degree in Chemistry or related discipline with 5 years HPLC experience or Master’s degree with 3+ years HPLC experience
Hands-on experience with Empower 3
Experience working in anFDA-regulated, cGMP environment
Knowledge of USP monographs, method development, and validation
Strong attention to detail and documentation skills
Excellent written and verbal communication skills
#J-18808-Ljbffr