To perform QC release testing for raw material and finished products within a GMP laboratory.

Performed release testing for metered dose and dry powder inhalers per STP and FDA regulations.Performed APSD/DDU research testing for API blends and soft mist inhaler devices.

Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.

Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.

Aided in facilitating information to students in introductory courses of chemistry and physics.Attended multiple CRLA certified training seminars for proper tutoring techniques and lessons.