Stability and Analytical Methods Validation Specialist

I perform and document stability studies for pharmaceutical products and participate in analytical method validation activities. I evaluate analytical results and conduct laboratory analyses according to established procedures.

I prepare and review technical documentation, analytical records, and reports. I use HPLC and UV-Vis spectrophotometry while supporting pharmaceutical quality control activities and laboratory compliance.

I performed analytical method validation activities and supported the evaluation of analytical data. I conducted laboratory testing in accordance with established analytical procedures.

I prepared technical documentation and analytical reports. I also supported pharmaceutical quality control activities within the laboratory.

I performed analysis and testing of pharmaceutical raw materials. I conducted physicochemical analyses according to established laboratory procedures.

I documented laboratory results and contributed to quality control processes for pharmaceutical materials.

I performed in-process controls, including authorization and verification of activities in production and packaging areas. I conducted physicochemical analysis of raw materials, water systems, and packaging materials.

I supported microbiological analysis of finished products, raw materials, water systems, and stability samples. I also performed area monitoring and personnel and equipment swabbing.

I performed conditioning and packaging activities for pharmaceutical products. I worked in production areas involved in filling liquid and semisolid products.

I operated automatic filling and capping equipment and supported routine pharmaceutical production operations.

Bachelor's Degree in Chemistry and Pharmacy in progress.