•Conducted Quality Control testing of raw materials, intermediate, final products and stability samples.•Implemented USP, customer, and company methods for drug analysis.•Processed samples to support production.•Organized stability sample testing program in Quality Control Department and reviewed stability testing protocols.•Evaluated other chemist reports and training other chemists.•Participated in the Supplier Certification program.•Performed routine calibration of QC and facilities instruments.•Prepared and revised of Test Methods and Specifications.•Developed and validated of new analytical Methods.

•Conducted various tests related to pharmaceutical analysis and performed special analyses and drafted reports, following exact procedures.•Implemented USP, customer, and company methods for drug analysis.•Processed samples to support production.•Evaluated other chemist reports.

•Conducted research in bioremediation research and development projects.•Assisted in QA / QC programming; performed SOP updates for analytical procedures.•Updated quality control log book and trained other chemists.•Helped Ph.D. students in setting up laboratory experiments.•Operated, maintained, and performed troubleshooting on laboratory instruments.•Maintained laboratory supplies and spare instrument parts.•Responsible for work-up and distribution of analytical data and corresponding reports.