Perform routine as well as non-routine evaluation of raw materials, intermediate and finished pharmaceutical formulations along with packaging components as per SOPs.
Ensure to get familiar with standard analytical lab equipment usage in pharmaceutical industry.
Compile and record data for documentation needed for testing and reports preparation.
Implement development method and validation protocols.
Review and update SOPs related to quality control.
Ensure regulatory compliance working with GLP and GMP environment.
Interact with Operations, Quality Assurance and R&D.
Operate and implement analytical lab instrumentation.
Maintain and manage accurate and precise documentation.
Support insuring testing to be in compliance with schedules by team oriented processing.
Conduct laboratory evaluation of samples.
Record data on computer following standard operating methods.
Update and calibrate lab analysis instrumentation.
Comply with standard procedures and quality control to improve products.
Conduct regular computations, update records and develop reports.